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<feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en"><id>http://publicationslist.org/data/david.wade/atom.xml</id><title>David Wade's Publications List</title>
<link rel="self" type="application/atom+xml" href="http://publicationslist.org/data/david.wade/atom.xml"/><link rel="alternate" type="text/html" href="http://publicationslist.org/david.wade"/><author><name>David Wade</name><uri>http://publicationslist.org/david.wade</uri></author><icon>$basepathfavicon.ico</icon><subtitle>Recent additions to David Wade's PublicationsList.org page</subtitle><logo>http://publicationslist.org/publications.png</logo><updated>2010-07-07T23:54:15Z</updated>

<entry>
<id>http://publicationslist.org/david.wade/refid67</id>
<updated>2010-07-07T23:51:58Z</updated>
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<title type='html'>Searching for Amelia Earhart at the Molecular Level:
Peptide AMELIAEARHART.</title>
<summary type='html'>This article proposes the synthesis and study of a peptide that is composed of 13 amino acids, and that has an amino acid composition and sequence that can be described with International Union of Pure and Applied Chemistry-International Union of Biochemistry and Molecular Biology, Joint Commission on Biochemical Nomenclature single letter abbreviations corresponding to the sequence of letters in ...&lt;br/&gt;&lt;br/&gt;David Wade (2010)  &lt;i&gt;Wade Research Foundation Reports&lt;/i&gt; 5: 3 1-15&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid65</id>
<updated>2010-07-07T23:53:23Z</updated>
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<title type='html'>Preview*: Temporin-/Vespid chemotactic peptide- (or T/V-) like peptides and their consensus sequences.</title>
<summary type='html'>The Temporin-/Vespid Chemotactic Peptide- (or T/V-) like peptides are a group of small [average of 13 amino acids (AAs)], linear (no Cysteine), hydrophobic (avg. 65% hydrophobic AAs), positively charged (avg. net charge at pH 7 = +2), structurally very similar, peptide amides that have been isolated from the skins of frogs and the venoms of insects during the past 30 years. Recently, the number of...&lt;br/&gt;&lt;br/&gt;David Wade (2010)  &lt;i&gt;Wade Research Foundation Reports&lt;/i&gt; 5: 1 1&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid66</id>
<updated>2010-07-07T23:48:26Z</updated>
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<title type='html'>Four billionaire name peptides that contain the CendR motif.</title>
<summary type='html'>The name-to-peptide concept uses the International Union of Pure and Applied Chemistry-International Union of Biochemistry and Molecular Biology, Joint Commission on Biochemical Nomenclature (IUPAC-IUB, JCBN) system for abbreviating the names of amino acids (AAs) with single letters of the English alphabet, and considers the strings of letters in personal and other names as strings of AAs, or pept...&lt;br/&gt;&lt;br/&gt;David Wade (2010)  &lt;i&gt;Wade Research Foundation Reports&lt;/i&gt; 5: 2 1-23&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid18</id>
<updated>2009-12-09T06:16:29Z</updated>
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<title type='html'>Peptides MICROSOFT, GOOGLE, YAHOO, COCACOLA and PEPSICOLA.</title>
<summary type='html'>Three of the most recognizable corporate names are Microsoft, a manufacturer of computer software, and Google and Yahoo, two internet search providers. Two of the most popular soft drink brand names are Coca-Cola and Pepsi-Cola. This article proposes to use the sequences of English alphabet letters in the names of these companies and products as the basis for creating five new peptides, MICROSOFT,...&lt;br/&gt;&lt;br/&gt;David Wade (2007)  &lt;i&gt;Wade Research Foundation Reports&lt;/i&gt; 4: 1 1-16&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid16</id>
<updated>2009-12-09T06:03:51Z</updated>
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<title type='html'>Determining the energies of names (revised version).</title>
<summary type='html'>This article is a revised version of an article with the same title that was published by the author in 2006, and it corrects errors that are present in the previous version. A method is presented for determining the energy of a name as the acoustical energy of the vocalized name.  The names, Madonna and Esther, as spoken by the author and by a computerized text-to-speech program, were used to tes...&lt;br/&gt;&lt;br/&gt;David Wade (2007)  &lt;i&gt;Wade Research Foundation Reports&lt;/i&gt; 4: 3 1-14&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid17</id>
<updated>2009-12-09T06:09:18Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid17'/>
<title type='html'>The tetragrammaton peptides, YHWH and YHVH.</title>
<summary type='html'>This article describes a theoretical experiment that uses the International Union of Pure and Applied Chemistry’s one letter system for abbreviating the chemical names of amino acids to interpret the letter sequences, YHWH and YHVH, English transliterations of the Hebrew name of God, as representing the amino acid sequences of two tetrapeptides, and proposes the chemical synthesis and biological...&lt;br/&gt;&lt;br/&gt;David Wade (2007)  &lt;i&gt;Wade Research Foundation Reports&lt;/i&gt; 4: 2 1-6&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid13</id>
<updated>2009-12-09T05:44:29Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid13'/>
<title type='html'>Acoustic energy as the basis for given name preferences.</title>
<summary type='html'>What is the basis of the preference for one given, or first, name versus another? This article explores that question by analyzing the acoustic, or sound, energy of vocalized names from the US Social Security Administration’s list of the thousand most popular given names for the period of 2000-2005. The 100 most popular, and 100 least popular, male and female given names were vocalized by a comp...&lt;br/&gt;&lt;br/&gt;David Wade (2007)  &lt;i&gt;Wade Research Foundation Reports&lt;/i&gt; 4: 6 1-29&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid14</id>
<updated>2009-12-09T05:43:37Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid14'/>
<title type='html'>The KAROLINSKA peptide.</title>
<summary type='html'>This article proposes the chemical synthesis and study of a peptide that has an amino acid (AA) sequence with one letter abbreviations that correspond to the name, KAROLINSKA: Lysine (K)-Alanine (A)-Arginine (R)-Ornithine (O)-Leucine (L)-Isoleucine (I)-Asparagine (N)-Serine (S)-Lysine (K)-Alanine (A). In this sequence, nine of the ten AAs are represented by official International Union of Pure and...&lt;br/&gt;&lt;br/&gt;David Wade (2007)  &lt;i&gt;Wade Research Foundation Reports&lt;/i&gt; 4: 5 1-7&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid15</id>
<updated>2009-12-09T05:48:18Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid15'/>
<title type='html'>The PRINCETON peptide.</title>
<summary type='html'>This article proposes the chemical synthesis and study of a peptide that has an amino acid (AA) sequence with one letter abbreviations that correspond to the name, PRINCETON: Proline (P)-Arginine (R)-Isoleucine (I)-Asparagine (N)-Cysteine (C)-Glutamic acid (E)-Threonine (T)- Ornithine (O)-Asparagine (N). In this sequence, eight of the nine AAs are represented by official International Union of Pur...&lt;br/&gt;&lt;br/&gt;David Wade (2007)  &lt;i&gt;Wade Research Foundation Reports&lt;/i&gt; 4: 4 1-8&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid19</id>
<updated>2009-12-09T06:19:58Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid19'/>
<title type='html'>Determining the energies of names.</title>
<summary type='html'>A method is presented for determining the energy of a name as the acoustic energy of the spoken name. The names, Madonna and Esther, as spoken by the author, differed by ~0.5 V of acoustic energy. This evidence may support the hypothesis of a difference in the energies of names.&lt;br/&gt;&lt;br/&gt;David Wade (2006)  &lt;i&gt;Wade Research Foundation Reports&lt;/i&gt; 2: 1-3 &lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid21</id>
<updated>2009-12-09T06:40:04Z</updated>
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<title type='html'>Inhibition of Bacillus anthracis and potential surrogate bacilli growth from spore inocula by nisin and other antimicrobial peptides.</title>
<summary type='html'>The ability of nisin, synthetic temporin analogs, magainins, defensins, and cecropins to inhibit Bacillus anthracis, Bacillus cereus, Bacillus thuringiensis, Bacillus mycoides, and Bacillus subtilis growth from spore inocula was determined using well diffusion assays. Nisin, magainin II amide, and defensins were inhibitory in screening against B. anthracis Sterne or B. cereus ATCC 7004, but only n...&lt;br/&gt;&lt;br/&gt;Thomas J Montville, Tara De Siano, Adam Nock, Sally Padhi, David Wade (2006)  &lt;i&gt;J Food Prot&lt;/i&gt; 69: 10 2529-2533&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid1</id>
<updated>2009-12-09T05:04:37Z</updated>
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<title type='html'>Antimicrobial peptides from amphibian skin potently inhibit human immunodeficiency virus infection and transfer of virus from dendritic cells to T cells.</title>
<summary type='html'>Topical antimicrobicides hold great promise in reducing human immunodeficiency virus (HIV) transmission. Amphibian skin provides a rich source of broad-spectrum antimicrobial peptides including some that have antiviral activity. We tested 14 peptides derived from diverse amphibian species for the capacity to inhibit HIV infection. Three peptides (caerin 1.1, caerin 1.9, and maculatin 1.1) complete...&lt;br/&gt;&lt;br/&gt;Scott E VanCompernolle, R Jeffery Taylor, Kyra Oswald-Richter, Jiyang Jiang, Bryan E Youree, John H Bowie, Michael J Tyler, J Michael Conlon, David Wade, Christopher Aiken, Terence S Dermody, Vineet N KewalRamani, Louise A Rollins-Smith, Derya Unutmaz (2005)  &lt;i&gt;J Virol&lt;/i&gt; 79: 18 11598-11606&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid22</id>
<updated>2009-12-09T06:55:12Z</updated>
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<title type='html'>Inactivation of viruses infecting ectothermic animals by amphibian and piscine antimicrobial peptides.</title>
<summary type='html'>The ability of five purified amphibian antimicrobial peptides (dermaseptin-1, temporin A, magainin I, and II, PGLa), crude peptide fractions isolated from the skin of Rana pipiens and R. catesbeiana, and four antimicrobial peptides (AMPs) from hybrid striped bass (piscidin-1N, -1H, -2, and -3) were examined for their ability to reduce the infectivity of channel catfish virus (CCV) and frog virus 3...&lt;br/&gt;&lt;br/&gt;V G Chinchar, L Bryan, U Silphadaung, E Noga, D Wade, L Rollins-Smith (2004)  &lt;i&gt;Virology&lt;/i&gt; 323: 2 268-275&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid2</id>
<updated>2009-12-09T05:07:46Z</updated>
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<title type='html'>Temporin A and related frog antimicrobial peptides use formyl peptide receptor-like 1 as a receptor to chemoattract phagocytes.</title>
<summary type='html'>Many mammalian antimicrobial peptides (AMPs) have multiple effects on antimicrobial immunity. We found that temporin A (TA), a representative frog-derived AMP, induced the migration of human monocytes, neutrophils, and macrophages with a bell-shaped response curve in a pertussis toxin-sensitive manner, activated p44/42 MAPK, and stimulated Ca(2+) flux in monocytes, suggesting that TA is capable of...&lt;br/&gt;&lt;br/&gt;Qian Chen, David Wade, Kahori Kurosaka, Zhao Yuan Wang, Joost J Oppenheim, De Yang (2004)  &lt;i&gt;J Immunol&lt;/i&gt; 173: 4 2652-2659&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid63</id>
<updated>2009-12-10T09:36:39Z</updated>
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<title type='html'>SAPD: Synthetic Antibiotic Peptides Database</title>
<summary type='html'>D. Wade, J. Englund (2004)  &lt;i&gt;Peptide Revolution: Genomics, Proteomics &amp; Therapeutics&lt;/i&gt; 881-882&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid64</id>
<updated>2009-12-10T09:38:57Z</updated>
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<title type='html'>The temporin/VesCP (T/V)-like family of bioactive peptides.</title>
<summary type='html'>D. Wade (2004)  &lt;i&gt;Peptide Revolution: Genomics, Proteomics &amp; Therapeutics&lt;/i&gt; 949-951&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid20</id>
<updated>2009-12-09T06:27:32Z</updated>
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<title type='html'>Biological and structural properties of COLINPOWELL, a synthetic peptide amide.</title>
<summary type='html'>A peptide was designed so that the one letter abbreviations for its amino acid
sequence corresponded to the joined first and last names of the current United States Secretary of State, Colin Powell. Peptide COLINPOWELL (i.e., Cys-Orn-Leu-Ile-Asn-Pro-Orn-Trp-Glu-Leu-Leu) was synthesized as a C-terminal amide, and found to be inactive against bacteria [methicillin-resistant Staphylococcus aureus (M...&lt;br/&gt;&lt;br/&gt;David Wade, De Yang, Michael A. Lea (2004)  &lt;i&gt;Wade Research Foundation Reports&lt;/i&gt; 1: 2-35 &lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid62</id>
<updated>2009-12-10T09:34:34Z</updated>
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<title type='html'>The name game: use of words composed of letters of the English alphabet as a source of novel bioactive peptides.</title>
<summary type='html'>D. Wade (2004)  &lt;i&gt;Peptide Revolution: Genomics, Proteomics &amp; Therapeutics&lt;/i&gt; 580-581&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid50</id>
<updated>2009-12-09T10:48:12Z</updated>
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<title type='html'>The name game: use of words composed of letters of the English alphabet as a source of novel bioactive peptides.</title>
<summary type='html'>David Wade (2003)  &lt;i&gt;Chemistry Preprint Archive&lt;/i&gt; 1:  159-170&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid3</id>
<updated>2009-12-09T05:10:47Z</updated>
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<title type='html'>Activities of temporin family peptides against the chytrid fungus (Batrachochytrium dendrobatidis) associated with global amphibian declines.</title>
<summary type='html'>Temporin A and structurally related peptides produced in amphibian dermal granular glands and in wasp venom were tested for growth inhibition of Batrachochytrium dendrobatidis, a pathogen associated with global amphibian declines. Two natural amphibian temporins, a wasp temporin, and six synthetic analogs effectively inhibited growth. Differences in potency due to amino acid substitution suggest t...&lt;br/&gt;&lt;br/&gt;Louise A Rollins-Smith, Cynthia Carey, J Michael Conlon, Laura K Reinert, Jennifer K Doersam, Tomas Bergman, Jerzy Silberring, Hilkka Lankinen, David Wade (2003)  &lt;i&gt;Antimicrob Agents Chemother&lt;/i&gt; 47: 3 1157-1160&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid23</id>
<updated>2009-12-09T07:13:37Z</updated>
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<title type='html'>Temporin/VesCP (T/V)-like antibiotic peptides, derived from frogs and wasps, induce migration of human monocytes and neutrophils.</title>
<summary type='html'>Several naturally occurring antimicrobial peptides, from mammals and insects, have previously been shown to be chemotactic for human inflammatory cells. Based on this evidence, ten synthetic analogs of naturally occurring antibiotic peptides from the skin secretions of three species of Ranid frogs and the venom of one species of Vespid wasp (i.e., T/V-like peptides) were tested for their abilities...&lt;br/&gt;&lt;br/&gt;De Yang, Qian Chen, Joost J. Oppenheim, Pentti Kuusela, John W. Taylor and David Wade (2003)  &lt;i&gt;Letters in Peptide Science&lt;/i&gt; 10: 2 99-110&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid24</id>
<updated>2009-12-09T07:28:48Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid24'/>
<title type='html'>Unambiguous consensus sequences for temporin-like peptides</title>
<summary type='html'>A group of 34 peptides, that have been isolated from the skins of frogs and the venom of wasps, are structurally similar to 10 antibiotic peptides, called temporins, isolated from the skin of the European red frog, Rana temporaria. These temporin-like peptides have antibiotic and neutrophil stimulating properties. A preliminary consensus sequence derived from 30 frog skin peptides was a good predi...&lt;br/&gt;&lt;br/&gt;David Wade (2002)  &lt;i&gt;Internet Journal of Chemistry&lt;/i&gt; 5: 5 Article 5&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid49</id>
<updated>2009-12-09T10:43:14Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid49'/>
<title type='html'>Unambiguous consensus sequences for temporin-like peptides.</title>
<summary type='html'>A group of 34 peptides, that have been isolated from the skins of frogs and the venom of wasps, are structurally similar to 10 antibiotic peptides, called temporins, isolated from the skin of the European red frog, Rana  temporaria. These temporin-like peptides have antibiotic and neutrophil stimulating properties. A preliminary consensus sequence derived from 30 frog skin peptides was a good pred...&lt;br/&gt;&lt;br/&gt;David Wade (2002)  &lt;i&gt;Chemistry Preprint Archive&lt;/i&gt; 4:  280-300&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid25</id>
<updated>2009-12-09T07:37:22Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid25'/>
<title type='html'>Synthetic antibiotic peptides database.</title>
<summary type='html'>A computerized database for synthetic antibiotic peptides, the SAPD, has been created and is available on the Internet at web address, http://oma.terkko.helsinki.fi:8080/~SAPD. The SAPD is modelled on two pre-existing computer databases for naturally occurring peptide antibiotics, the Antimicrobial Sequences Database and the Peptaibol Database, and it will contain both chemical and biological info...&lt;br/&gt;&lt;br/&gt;David Wade, Jukka Englund (2002)  &lt;i&gt;Protein Pept Lett&lt;/i&gt; 9: 1 53-57&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid12</id>
<updated>2009-12-09T05:16:18Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid12'/>
<title type='html'>Antibiotic Properties of Novel Synthetic Temporin A Analogs and a Cecropin A-Temporin A Hybrid Peptide </title>
<summary type='html'>Temporin A, 18 analogs, and a cecropin A-temporin A hybrid peptide were tested with antibiotic sensitive and resistant bacteria, fungi, human erythrocytes, and in clotting assays.Several peptides were active in these assays, and some analogs (D-TA, W1-TA, and Con-L4,G10) may be useful lead compounds for further antibiotics development.The activity of temporin A was found to be dependent upon sever...&lt;br/&gt;&lt;br/&gt;David Wade, Jan-Ingmar Flock, Charlotta Edlund, Ingegerd Löfving-Arvholm, Matti Sällberg, Tomas Bergman, Angela Silveira, Cecille Unson, Louise Rollins-Smith, Jerzy Silberring, Malcom Richardson, Pentti Kuusela, Hilkka Lankinen  (2002)  &lt;i&gt;Protein &amp; Peptide Letters&lt;/i&gt; 9: 6 533-543&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid27</id>
<updated>2009-12-09T07:44:51Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid27'/>
<title type='html'>Dynorphin A inhibits nociceptin-converting enzyme from the rat spinal cord.</title>
<summary type='html'>Cysteine proteinase found in the spinal cord of rat, called nociceptin-converting enzyme (NCE), is competitively inhibited by dynorphin A and its fragment des-[Tyr(1)]-DYN A. This proteinase converts orphanin FQ/nociceptin (OFQ/N) to two major fragments: OFQ/N(1-11) and further OFQ/N(1-6) with analgesic properties. Dynorphin A at the concentration of 10 microM increases K(M) from 15.0 to 55.9 micr...&lt;br/&gt;&lt;br/&gt;P Suder, D Wade, A Łegowska, J Kotlińska, K Rolka, J Silberring (2001)  &lt;i&gt;Biochem Biophys Res Commun&lt;/i&gt; 287: 4 927-931&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid26</id>
<updated>2009-12-09T07:42:05Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid26'/>
<title type='html'>Synthesis and characterization of new temporin A analogs and a hybrid peptide.</title>
<summary type='html'>Temporin A is one of a group of 31 structurally similar antibiotic peptides isolated from the skins of anurans, 10 of which were isolated from the European red frog, Rana temporaria. The synthesis and bacteriological study of temporin A and 8 analogs were reported previously, and this article describes the synthesis and analyses of 11 new temporin A analogs, and a cecropin A-temporin A hybrid pept...&lt;br/&gt;&lt;br/&gt;David Wade, Tomas Bergman, Jerzy Silberring, and Hilkka Lankinen (2001)  &lt;i&gt;Protein and Peptide Letters&lt;/i&gt; 8: 6 443-450&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid48</id>
<updated>2009-12-09T10:38:07Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid48'/>
<title type='html'>CAMELs against anthrax.</title>
<summary type='html'>CAMELs are a group of novel synthetic antibiotic peptides that may be effective substitutes for ciprofloxacin in the treatment of anthrax infections.&lt;br/&gt;&lt;br/&gt;D. Wade (2001)  &lt;i&gt;Chemistry Preprint Archive&lt;/i&gt; 11:  86-88&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid28</id>
<updated>2009-12-09T08:08:30Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid28'/>
<title type='html'>Development of new antibiotic peptides.</title>
<summary type='html'>David Wade (2001)  &lt;i&gt;Challenges of Emerging Infections: New Pathogens or New Diseases&lt;/i&gt; 119-124&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid4</id>
<updated>2009-12-09T05:18:28Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid4'/>
<title type='html'>Hematological and antifungal properties of temporin A and a cecropin A-temporin A hybrid.</title>
<summary type='html'>Temporin A (TA) and a cecropin A-temporin A hybrid peptide (CATA) were synthesized and assayed for their hemolytic, anticoagulant, and antifungal properties. CATA retains significant antifungal activity, is less hemolytic than TA, and inhibits blood coagulation. These results recommend further studies of the biological activities of CATA.&lt;br/&gt;&lt;br/&gt;D Wade, A Silveira, L Rollins-Smith, T Bergman, J Silberring, H Lankinen (2001)  &lt;i&gt;Acta Biochim Pol&lt;/i&gt; 48: 4 1185-1189&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid5</id>
<updated>2009-12-09T05:23:43Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid5'/>
<title type='html'>Activities of synthetic hybrid peptides against anaerobic bacteria: aspects of methodology and stability.</title>
<summary type='html'>The increasing problem of antibiotic resistance among pathogenic bacteria requires development of new antimicrobial agents. One line of investigation is the synthesis of antimicrobial hybrid peptides. The aim of the present investigation was to determine the in vitro activities of 16 cecropin-melittin hybrid peptides (CAMEL analogues) against 60 anaerobic bacterial strains, to compare their activi...&lt;br/&gt;&lt;br/&gt;H Oh, M Hedberg, D Wade, C Edlund (2000)  &lt;i&gt;Antimicrob Agents Chemother&lt;/i&gt; 44: 1 68-72&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid11</id>
<updated>2009-12-09T04:29:38Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid11'/>
<title type='html'>Temporin Antibiotic Peptides: A Review and Derivation of a Consensus Sequence.</title>
<summary type='html'>The temporins are a group of small, linear, basic, highly hydrophobic, antibiotic, peptide amides that were originally isolated from the skin of the European red frog, Rana temporaria. During the past decade, 30 temporin or temporin-like peptides have been isolated from the skins of Anurans. This article presents a brief review of the temporin literature, an analysis of the amino acid sequences of...&lt;br/&gt;&lt;br/&gt;D. Wade, A. Silveira, J. Silberring, P. Kuusela, H. Lankinen (2000)  &lt;i&gt;Protein and Peptide Letters&lt;/i&gt; 7: 6 349-357&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid29</id>
<updated>2009-12-09T08:13:54Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid29'/>
<title type='html'>Antibacterial activities of temporin A analogs.</title>
<summary type='html'>Temporin A (TA) is a small, basic, highly hydrophobic, antimicrobial peptide amide (FLPLIGRVLSGIL-NH2) found in the skin of the European red frog, Rana temporaria. It has variable antibiotic activities against a broad spectrum of microorganisms, including clinically important methicillin-sensitive and -resistant Staphylococcus aureus as well as vancomycin-resistant Enterococcus faecium strains. In...&lt;br/&gt;&lt;br/&gt;D Wade, J Silberring, R Soliymani, S Heikkinen, I Kilpeläinen, H Lankinen, P Kuusela (2000)  &lt;i&gt;FEBS Lett&lt;/i&gt; 479: 1-2 6-9&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid30</id>
<updated>2009-12-09T08:40:15Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid30'/>
<title type='html'>Comparison of synthesis and antibacterial activity of temporin A.</title>
<summary type='html'>Temporin A is a small, basic, highly hydrophobic, antibacterial peptide found in the skin of the European red frog, Rana temporaria. It was synthesized twice by the FastMoc solid phase method using amino acids protected at the N(alpha)-position with either 9-fluorenylmethoxycarbonyl or 2-(4-nitrophenylsulfonyl)ethoxycarbonyl. The syntheses of temporin A demonstrates the difference between 2-(4-nit...&lt;br/&gt;&lt;br/&gt;I Harjunpää, P Kuusela, M T Smoluch, J Silberring, H Lankinen, D Wade (1999)  &lt;i&gt;FEBS Lett&lt;/i&gt; 449: 2-3 187-190&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid31</id>
<updated>2009-12-09T08:46:46Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid31'/>
<title type='html'>Deuterium isotope effects on noncovalent interactions between molecules.</title>
<summary type='html'>The topic of deuterium isotope effects is usually concerned with the effects on chemical reactions that are caused by the substitution of deuterium atoms for protium, or hydrogen, atoms in a molecule. These effects include changes in the rate of cleavage of covalent bonds to deuterium, or to an atom located adjacent to deuterium, in a reactant molecule. Deuterium isotope effects on other, noncoval...&lt;br/&gt;&lt;br/&gt;D Wade (1999)  &lt;i&gt;Chem Biol Interact&lt;/i&gt; 117: 3 191-217&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid59</id>
<updated>2009-12-10T09:26:18Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid59'/>
<title type='html'>Predicted three dimensional structure for Fib, a fibrinogen-binding protein of Staphylococcus aureus.</title>
<summary type='html'>D. Wade (1999)  &lt;i&gt;Innovation &amp; Perspectives in Solid Phase Synthesis &amp; Combinatorial Libraries 1998&lt;/i&gt; 181-184&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid61</id>
<updated>2009-12-10T09:32:03Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid61'/>
<title type='html'>Fibrinogen-binding sites of the Staphylococcus aureus Fib protein.</title>
<summary type='html'>D. Wade, M. Sällberg, J. Silberring, J.-I. Flock (1999)  &lt;i&gt;Innovation &amp; Perspectives in Solid Phase Synthesis &amp; Combinatorial Libraries 1998&lt;/i&gt; 413-414&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid60</id>
<updated>2009-12-10T09:29:50Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid60'/>
<title type='html'>Antibiotic activity of a synthetic cecropin-melittin hybrid peptide on anaerobic bacteria.</title>
<summary type='html'>D. Wade, C. Edlund, Å Engström, M. Hedberg, J.-I. Flock (1999)  &lt;i&gt;Innovation &amp; Perspectives in Solid Phase Synthesis &amp; Combinatorial Libraries 1998&lt;/i&gt; 411-412&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid6</id>
<updated>2009-12-09T05:27:28Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid6'/>
<title type='html'>Multiple binding sites in the interaction between an extracellular fibrinogen-binding protein from Staphylococcus aureus and fibrinogen.</title>
<summary type='html'>Efb (previously Fib) is a fibrinogen-binding protein secreted by Staphylococcus aureus. It has previously been shown that it plays a role in a wound infection model in the rat and that antibodies against Efb reduce the number of recovered bacteria from the mammary glands in a mouse mastitis model. Efb binds to the alpha-chain of fibrinogen and does not participate in bacterial adherence to fibrino...&lt;br/&gt;&lt;br/&gt;M Palma, D Wade, M Flock, J I Flock (1998)  &lt;i&gt;J Biol Chem&lt;/i&gt; 273: 21 13177-13181&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid34</id>
<updated>2009-12-09T09:05:43Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid34'/>
<title type='html'>Identification of functional domains in Efb, a fibrinogen binding protein of Staphylococcus aureus.</title>
<summary type='html'>Staphylococcus aureus produces and secretes a protein, Efb, that binds to fibrinogen, seems to be required for virulence, and may benefit the microorganism by delaying wound healing. Interactions of Efb with fibrinogen are influenced by divalent metal cations, including Ca2+. Increasing concentrations of Ca2+ increased the binding of fibrinogen to immobilized Efb, whereas binding of Efb to immobil...&lt;br/&gt;&lt;br/&gt;D Wade, M Palma, I Löfving-Arvholm, M Sällberg, J Silberring, J I Flock (1998)  &lt;i&gt;Biochem Biophys Res Commun&lt;/i&gt; 248: 3 690-695&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid57</id>
<updated>2009-12-10T09:22:29Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid57'/>
<title type='html'>Antibiotic peptides with different potencies against different Staphylococci.</title>
<summary type='html'>D. Wade, R.B. Merrifield (1998)  &lt;i&gt;Peptides 1996&lt;/i&gt; 887-888&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid32</id>
<updated>2009-12-09T08:55:21Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid32'/>
<title type='html'>Antianaerobic activity of a cecropin-melittin peptide.</title>
<summary type='html'>OBJECTIVE: Several small, 15-residue peptides that contain portions of the amino acid sequences of both cecropin A and melittin have previously been shown to have broad-spectrum antibacterial activities against aerobic microorganisms, with no undesirable hemolytic properties. It would also be useful to know what effect these hybrid peptides have on anaerobic bacteria. METHODS: The minimum inhibito...&lt;br/&gt;&lt;br/&gt; C.Edlund,  M. Hedberg,  Å. Engström,  J.-I. Flock, D. Wade (1998)  &lt;i&gt;Clin Microbiol Infect&lt;/i&gt; 4: 4 181-185&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid58</id>
<updated>2009-12-10T09:22:00Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid58'/>
<title type='html'>The potential of antibiotic peptides to form coiled-coils.</title>
<summary type='html'>D. Wade (1998)  &lt;i&gt;Peptides 1996&lt;/i&gt; 889-890&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid33</id>
<updated>2009-12-09T09:01:17Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid33'/>
<title type='html'>Structural Analysis of EFB, A Fibrinogen Binding Protein of Staphylococcus aureus.</title>
<summary type='html'>Staphylococcus aureus produces and secretes a small, basic protein, designated Efb, that binds to fibrinogen and seems to be required for virulence of the organism. A 3D model of Efb was developed, and it predicts that the C-terminal half of the protein contains substantial a-helical content. CD analysis of Efb yielded a value of 40-41% a-helix. Calcium and zinc both influence the interactions bet...&lt;br/&gt;&lt;br/&gt;David Wade, Marco Palma, Jan-Ingmar Flock, Kurt D. Berndt, Jerzy Silberring and Stan G. Galaktionov (1998)  &lt;i&gt;Protein and Peptide Letters&lt;/i&gt; 5: 4 199-206&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid56</id>
<updated>2009-12-10T09:23:01Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid56'/>
<title type='html'>Synthetic peptide vaccine for Pseudomonas aeruginosa.</title>
<summary type='html'>D. Wade, P. Semchuk, R.S. Hodges (1996)  &lt;i&gt;Peptides: Chemistry, Structure and Biology&lt;/i&gt; 796-797&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid45</id>
<updated>2009-12-09T10:19:26Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid45'/>
<title type='html'>Channel-forming antibiotic peptides containing all D-amino acids.</title>
<summary type='html'>Antibiotically and/or antimalarially active D-peptides of naturally occurring antibiotics such as cecropin A, B and D, melittin, and Magainin I and II and their addition, deletion and replacement analogs including homologous and heterologous analogs thereof.&lt;br/&gt;&lt;br/&gt;R.B. Merrifield, D. Wade, H.G. Boman (1996)  &lt;i&gt;United State Patent Office (US Patent 5585353)&lt;/i&gt;&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid35</id>
<updated>2009-12-09T09:12:22Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid35'/>
<title type='html'>The potential of naturally occurring antibiotic peptides to form coiled-coils.</title>
<summary type='html'>D. Wade (1996)  &lt;i&gt;Protein and Peptide Letters&lt;/i&gt; 3: 3 169-176&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid55</id>
<updated>2009-12-10T09:12:30Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid55'/>
<title type='html'>Replacement of D-amino acids with L-amino acids in the Cecropin A-Melittin hybrid, all-D CA(1-13)M(1-13)NH2, produces anomalous effects on antibacterial activities.</title>
<summary type='html'>D. Wade, H.G. Boman, S.A. Mitchell, R.B. Merrifield (1994)  &lt;i&gt;Peptides: Chemistry, Structure and Biology&lt;/i&gt; 470-472&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid38</id>
<updated>2009-12-09T09:20:51Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid38'/>
<title type='html'>Structure-immunogenicity relationship of melittin, its transposed analogues, and D-melittin.</title>
<summary type='html'>Melittin, a 26-residue bee venom peptide, is known to induce murine Abs specific for its hydrophilic C-terminus of residues 20-26 and T cell responses specific for its hydrophobic mid-region of residue 11-19. Synthetic melittin analogues with transposed sequences of Ac(21-26) (1-20) and Ac(26-21) (1-20) are found to induce murine Abs specific for the transposed peptide segment and to induce T cell...&lt;br/&gt;&lt;br/&gt;T P King, D Wade, M R Coscia, S Mitchell, L Kochoumian, B Merrifield (1994)  &lt;i&gt;J Immunol&lt;/i&gt; 153: 3 1124-1131&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid36</id>
<updated>2009-12-09T09:15:36Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid36'/>
<title type='html'>Role of nucleases in apoptosis.</title>
<summary type='html'>The last decade has seen the rapid development of research investigating the mechanisms of apoptosis in a variety of experimental systems. Among the multitude of changes observed in apoptotic cells, chromatin cleavage is considered a biochemical hallmark of apoptosis. Chromatin fragmentation is an enzymatic process which depends on the activity of endogenous nuclease(s) and the susceptibility of c...&lt;br/&gt;&lt;br/&gt;B Zhivotovsky, D Wade, P Nicotera, S Orrenius (1994)  &lt;i&gt;Int Arch Allergy Immunol&lt;/i&gt; 105: 4 333-338&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid37</id>
<updated>2009-12-09T09:18:27Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid37'/>
<title type='html'>Formation of 50 kbp chromatin fragments in isolated liver nuclei is mediated by protease and endonuclease activation.</title>
<summary type='html'>Isolated rat liver nuclei were incubated in the presence of divalent cations, and the mechanisms underlying the subsequent chromatin fragmentation were investigated. Either of the two cations, Ca2+ or Mg2+ was sufficient to produce chromatin fragments with sizes between 700 and 300 kbp. The formation of chromatin fragments of 50 kbp as well as the following internucleosomal DNA cleavage--which are...&lt;br/&gt;&lt;br/&gt;B Zhivotovsky, D Wade, A Gahm, S Orrenius, P Nicotera (1994)  &lt;i&gt;FEBS Lett&lt;/i&gt; 351: 2 150-154&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid54</id>
<updated>2009-12-10T09:08:58Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid54'/>
<title type='html'>Synthetic studies on the cecropin antibacterial peptides.</title>
<summary type='html'>R.B. Merrifield, H.G. Boman, D. Andreu, E.L. Merrifield, S. Mitchell, D. Wade (1993)  &lt;i&gt;Peptide Chemistry 1992-Proceedings of the 2nd Japan Symposium on Peptide Chemistry,&lt;/i&gt; 289-292&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid40</id>
<updated>2009-12-09T09:30:25Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid40'/>
<title type='html'>Shortened cecropin A-melittin hybrids. Significant size reduction retains potent antibiotic activity.</title>
<summary type='html'>We have earlier reported two 26-residue antibacterial peptides made up from different segments of cecropin A (CA) and melittin (M). We now report a substantial reduction in size at the C-terminal section of the highly active hybrid CA(1-8)M(1-18), leading to a series of 20-, 18- and 15-residue analogs with antibiotic properties similar to the larger molecule. In particular, the 15-residue hybrids ...&lt;br/&gt;&lt;br/&gt;D Andreu, J Ubach, A Boman, B Wåhlin, D Wade, R B Merrifield, H G Boman (1992)  &lt;i&gt;FEBS Lett&lt;/i&gt; 296: 2 190-194&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid53</id>
<updated>2009-12-10T09:04:36Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid53'/>
<title type='html'>PYLa and a PYLa-melittin hybrid are antibacterial peptides.</title>
<summary type='html'>D. Wade, S.A. Mitchell, H.G. Boman, A. Boman, R.B. Merrifield (1992)  &lt;i&gt;Peptides: Chemistry and Biology&lt;/i&gt; 435-436&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid39</id>
<updated>2009-12-09T09:27:28Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid39'/>
<title type='html'>Antibacterial peptides designed as analogs or hybrids of cecropins and melittin.</title>
<summary type='html'>Eight new analogs of cecropin A, two new analogs of melittin and 30 hybrid peptides containing sequences from cecropins and melittin have been synthesized. The lengths of the peptides have varied from 37 residues (the length of cecropin A) to 18 residues. The peptides have been assayed for lysis of sheep red blood cells and for antibacterial activity against two Gram negative and three Gram positi...&lt;br/&gt;&lt;br/&gt;D Wade, D Andreu, S A Mitchell, A M Silveira, A Boman, H G Boman, R B Merrifield (1992)  &lt;i&gt;Int J Pept Protein Res&lt;/i&gt; 40: 5 429-436&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid52</id>
<updated>2009-12-10T09:00:22Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid52'/>
<title type='html'>The cecropins: an example of the use of peptide synthesis to study a biochemical problem.</title>
<summary type='html'>R.B. Merrifield, H.G. Boman, D. Andreu, Z.-Q. Li, J. Fink, D. Wade (1991)  &lt;i&gt;Peptides 1990&lt;/i&gt; 3-16&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid42</id>
<updated>2009-12-09T09:49:25Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid42'/>
<title type='html'>Peptide antibiotics from the animal kingdom: cecropins and synthetic analogs.</title>
<summary type='html'>The cecropins are a family of small, basic peptides which have been isolated from insects and mammals, and shown to possess broad-spectrum antibacterial activities. This article reviews recent research into the structures and functions of cecropins, and concentrates on work involving the solid-phase synthesis and study of cecropin analogs, model peptides, and hybrids of cecropin and melittin, the ...&lt;br/&gt;&lt;br/&gt;D. Wade, R.B. Merrifield, and H.G. Boman (1991)  &lt;i&gt;Surface Reactive Peptides and Polymers: Discovery and Commercialization&lt;/i&gt; 237-248&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid41</id>
<updated>2009-12-09T09:36:03Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid41'/>
<title type='html'>Deuterium isotope effect in the interaction of N-nitrosodimethylamine, ethanol, and related compounds with cytochrome P-450IIE1.</title>
<summary type='html'>Deuteration of N-nitrosodimethylamine (NDMA) decreases its carcinogenicity and produces an isotope effect on its metabolism. Our previous results showed that deuteration causes a 5-fold increase in the apparent Km, but not the Vmax, for the demethylation and denitrosation of NDMA in microsomes. In the present work, we studied the nature of this deuterium isotope effect with several compounds using...&lt;br/&gt;&lt;br/&gt;C S Yang, H Ishizaki, M J Lee, D Wade, A Fadel (1991)  &lt;i&gt;Chem Res Toxicol&lt;/i&gt; 4: 4 408-413&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid7</id>
<updated>2009-12-09T05:30:48Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid7'/>
<title type='html'>All-D amino acid-containing channel-forming antibiotic peptides.</title>
<summary type='html'>The D enantiomers of three naturally occurring antibiotics--cecropin A, magainin 2 amide, and melittin--were synthesized. In addition, the D enantiomers of two synthetic chimeric cecropin-melittin hybrid peptides were prepared. Each D isomer was shown by circular dichroism to be a mirror image of the corresponding L isomer in several solvent mixtures. In 20% hexafluoro-2-propanol the peptides cont...&lt;br/&gt;&lt;br/&gt;D Wade, A Boman, B Wåhlin, C M Drain, D Andreu, H G Boman, R B Merrifield (1990)  &lt;i&gt;Proc Natl Acad Sci U S A&lt;/i&gt; 87: 12 4761-4765&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid51</id>
<updated>2009-12-10T08:56:04Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid51'/>
<title type='html'>The effects of cecropin analogs and hybrids on pro- and eukaryotic cells.</title>
<summary type='html'>D. Wade, R.B. Merrifield, and H.G. Boman  (1990)  &lt;i&gt;Peptides: Chemistry, Structure and Biology&lt;/i&gt; 120-121&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid43</id>
<updated>2009-12-09T09:54:26Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid43'/>
<title type='html'>Antibacterial and antimalarial properties of peptides that are cecropin-melittin hybrids.</title>
<summary type='html'>Solid phase synthesis was used to produce 5 hybrid peptides containing sequences from the antibacterial peptide, cecropin A, and from the bee venom toxin, melittin. Four of these chimeric peptides showed good antibacterial activity against representative Gram-negative and Gram-positive bacterial species. The best hybrid, cecropin A(1-13)-melittin(1-13) was 100-fold more active than cecropin A agai...&lt;br/&gt;&lt;br/&gt;H G Boman, D Wade, I A Boman, B Wåhlin, R B Merrifield (1989)  &lt;i&gt;FEBS Lett&lt;/i&gt; 259: 1 103-106&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid46</id>
<updated>2009-12-09T10:26:04Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/david.wade#refid46'/>
<title type='html'>Studies of the metabolism of nitrosamines by liver microsomal cytochrome P-450ac.</title>
<summary type='html'>David Wade (1988) &lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid44</id>
<updated>2009-12-09T10:12:38Z</updated>
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<title type='html'>Kinetic isotope effect on the demethylation and denitrosation of N-nitrosodimethylamine in vitro.</title>
<summary type='html'>C.S. Yang, D. Wade, T. Anjo, L.K. Keefer (1987)  &lt;i&gt;Relevance of N-nitroso compounds to human cancer: exposure and mechanisms.&lt;/i&gt; 124-128&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid8</id>
<updated>2009-12-09T05:33:12Z</updated>
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<title type='html'>Nature of N-nitrosodimethylamine demethylase and its inhibitors.</title>
<summary type='html'>The present study was undertaken to examine the nature of the low Km (KmI) form of rat liver microsomal N-nitrosodimethylamine demethylase (NDMAd) and its inhibition by organic compounds which are commonly present in the assay mixture. Using radiometric and colorimetric assay methods with an NADPH-generating system consisting of 0.4 mM NADP, 10 mM glucose-6-phosphate, and glucose-6-phosphate dehyd...&lt;br/&gt;&lt;br/&gt;J S Yoo, R J Cheung, C J Patten, D Wade, C S Yang (1987)  &lt;i&gt;Cancer Res&lt;/i&gt; 47: 13 3378-3383&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid10</id>
<updated>2009-12-09T05:37:01Z</updated>
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<title type='html'>Concurrent generation of methylamine and nitrite during denitrosation of N-nitrosodimethylamine by rat liver microsomes.</title>
<summary type='html'>With the goal of identifying the organic amine product(s) of enzymatic N-nitrosodimethylamine (NDMA) denitrosation, 4 mM NDMA was incubated with liver microsomes from ethanol-treated rats. The concentrations of dimethylamine and methylamine were determined by derivatization with 2,4-dinitrofluorobenzene followed by gas chromatography-mass spectrometry. There was no net increase in the concentratio...&lt;br/&gt;&lt;br/&gt;L K Keefer, T Anjo, D Wade, T Wang, C S Yang (1987)  &lt;i&gt;Cancer Res&lt;/i&gt; 47: 2 447-452&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid9</id>
<updated>2009-12-09T05:35:32Z</updated>
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<title type='html'>Deuterium isotope effect on denitrosation and demethylation of N-nitrosodimethylamine by rat liver microsomes.</title>
<summary type='html'>In an attempt to elucidate the molecular basis for the decrease in rat liver carcinogenicity and DNA-alkylating ability that accompanies deuteration of N-nitrosodimethylamine (NDMA), NDMA and its fully deuterated analogue ([2H6]NDMA) were incubated with acetone-induced rat liver microsomes. Rates for the competing metabolic routes, denitrosation and demethylation, were determined from colorimetric...&lt;br/&gt;&lt;br/&gt;D Wade, C S Yang, C J Metral, J M Roman, J A Hrabie, C W Riggs, T Anjo, L K Keefer, B A Mico (1987)  &lt;i&gt;Cancer Res&lt;/i&gt; 47: 13 3373-3377&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/david.wade/refid47</id>
<updated>2009-12-09T10:28:08Z</updated>
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<title type='html'>Uptake of calcium and phosphate by isolated intestinal cells and interrelations between the uptake processes.</title>
<summary type='html'>David Wade (1982) &lt;br/&gt;</summary>
</entry>
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