Year |
Citation |
Score |
2015 |
Du Vigneaud V, Carpenter FH. The γ-lactam of benzylhomopenicilloic acid and related compounds The Chemistry of Penicillin. 1004-1017. |
0.723 |
|
2015 |
Du Vigneaud V, Carpenter FH, Holley RW, Livermore AH, Rachele JR. Synthetic benzylpenicillin The Chemistry of Penicillin. 1018-1024. |
0.767 |
|
2015 |
Du Vigneaud V, Wood JL, Wright ME. The condensation of oxazolones and d-penicillamine and the resultant antibiotic activity The Chemistry of Penicillin. 892-908. |
0.235 |
|
2015 |
Du Vigneaud V, Melville DB. The thiocyanate derivative of benzylpenicillin methyl ester The Chemistry of Penicillin. 269-309. |
0.277 |
|
2010 |
McKENNIS H, DU VIGNEAUD V. The synthesis of homodesthiobiotin and related compounds. Journal of the American Chemical Society. 68: 832-5. PMID 21024886 DOI: 10.1021/JA01209A036 |
0.317 |
|
2010 |
Banerjee S, Dittmer K, DU Vigneaud V. A MICROBIOLOGICAL AND FLUOROMETRIC TEST FOR MINUTE AMOUNTS OF ALLOXAN. Science (New York, N.Y.). 101: 647-9. PMID 17844093 DOI: 10.1126/Science.101.2634.647 |
0.732 |
|
2010 |
DU Vigneaud V, Dittmer K, Hague E, Long B. THE GROWTH-STIMULATING EFFECT OF BIOTIN FOR THE DIPHTHERIA BACILLUS IN THE ABSENCE OF PIMELIC ACID. Science (New York, N.Y.). 96: 186-7. PMID 17791277 DOI: 10.1126/Science.96.2486.186 |
0.704 |
|
1975 |
Nestor JJ, Ferger MF, du Vigneaud V. [1-Beta-mercapto-beta,beta-pentamethylenepropionic acid]oxytocin, a potent inhibitor of oxytocin. Journal of Medicinal Chemistry. 18: 284-7. PMID 1133819 |
0.284 |
|
1974 |
Dyckes DF, Nestor JJ, Ferger MF, Du Vigneaud V, Chan WY. (1-beta-mercapto-beta,beta-diethylpropionic acid,4-leucine)-8-lysine-vasopressin and (1-beta-mercapto-beta,beta-diethylpropionic acid,4-leucine)oxytocin, compounds possessing antihormonal properties. Journal of Medicinal Chemistry. 17: 969-72. PMID 4855467 |
0.261 |
|
1974 |
Chan WY, Hruby VJ, Du Vigneaud V. Effects of magnesium ion and oxytocin inhibitors on the uterotonic activity of oxytocin and prostaglandins E2 and F2ALPHA. The Journal of Pharmacology and Experimental Therapeutics. 190: 77-87. PMID 4847314 |
0.211 |
|
1974 |
Chan WY, Nestor JJ, Ferger MF, Du Vigneaud V. Inhibition of oxytocic responses to oxytocin in pregnant rats by (1-L-penicillamine)oxytocin and (1-beta-mercapto-beta, beta-diethylpropionic acid)oxytocin. Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 146: 364-6. PMID 4834445 DOI: 10.3181/00379727-146-38105 |
0.27 |
|
1974 |
Dyckes DF, Nestor JJ, Ferger MF, Du Vigneaud V. (1-Beta-mercapto-beta,beta-diethylpropionic acid)-8-lysine-vasopressin, a potent inhibitor of 8-lysine-vasopressin and of oxytocin. Journal of Medicinal Chemistry. 17: 250-2. PMID 4809260 |
0.262 |
|
1974 |
Du Vigneaud V, Cohn M, Chandler JP, Schenck JR, Simmonds S. Nutrition classics from The Journal of Biological Chemistry 140:625-641, 1941. The utilization of the methyl group of methionine in the biological synthesis of choline and creatine. Nutrition Reviews. 32: 144-6. PMID 4597510 DOI: 10.1111/J.1753-4887.1974.Tb06306.X |
0.706 |
|
1974 |
Dyckes DF, Smith CW, Ferger MF, du Vigneaud V. Synthesis and some pharmacological properties of (1-alpha-mercaptoacetic acid)-8-lysine-vasopressin and (1-gamma-mercaptobutyric acid)-8-lysine-vasopressin. Journal of the American Chemical Society. 96: 7549-51. PMID 4427064 |
0.338 |
|
1974 |
Dyckes DF, Nestor JJ, Ferger MF, Du Vigneaud V, Chan WY. [1-β-Mercapto-β,β-diethylpropionic acid,4-leucine]-8-lysine-vasopressin and [1-β-mercapto-β,β-diethylpropionic acid,4-leucine]oxytocin, compounds possessing antihormonal properties Journal of Medicinal Chemistry. 17: 969-972. |
0.219 |
|
1973 |
Jones WC, Nestor JJ, Du Vigneaud V. Synthesis and some pharmacological properties of (1-deamino,9-thioglycine)oxytocin. Journal of the American Chemical Society. 95: 5677-9. PMID 4733810 |
0.357 |
|
1973 |
Dyckes DF, Ferger MF, Du Vigneaud V, Chan WY. Synthesis and some of the pharmacological properties of (4-leucine)-8-lysine-vasopressin and (1-deamino,4-leucine)-8-lysine-vasopressin. Journal of Medicinal Chemistry. 16: 843-7. PMID 4725931 |
0.386 |
|
1973 |
Glass JD, Du Vigneaud V. Solid-phase synthesis and pressor potency of (1-deamino-9-ethylenediamine)-lysine-vasopressin. Journal of Medicinal Chemistry. 16: 160-1. PMID 4683112 |
0.293 |
|
1972 |
Glass JD, du Vigneaud V. Synthesis and certain pharmacological properties of lysine-vasopressinoic acid methylamide and lysine-vasopressinoic acid dimethylamide. Journal of Medicinal Chemistry. 15: 486-8. PMID 5064318 |
0.365 |
|
1972 |
Wille MA, Cahn WY, Du Vigneaud V. Solid phase synthesis of (3,4-dileucine)-oxytocin and a study of some of its pharmacological properties. Journal of Medicinal Chemistry. 15: 11-2. PMID 5061981 |
0.289 |
|
1972 |
Ferger MF, Jones WC, Dyckes DF, Du Vigneaud V. Four cyclic disulfide pentapeptides possessing the ring of vasopressin. Journal of the American Chemical Society. 94: 982-4. PMID 5061145 |
0.252 |
|
1972 |
Hruby VJ, Smith CW, Linn DK, Ferger MF, Du Vigneaud V. The synthesis and some pharmacological properties of tocinoic acid and deaminotocinoic acid. Journal of the American Chemical Society. 94: 5478-80. PMID 5040852 DOI: 10.1021/Ja00770A052 |
0.362 |
|
1972 |
Vavrek RJ, Ferger MF, Allen GA, Rich DH, Blomquist AT, Du Vigneaud V. Synthesis of three oxytocin analogs related to (1-deaminopenicillamine)oxytocin possessing antioxytocic acitvity. Journal of Medicinal Chemistry. 15: 123-6. PMID 5008235 DOI: 10.1021/Jm00272A001 |
0.699 |
|
1972 |
Von Dreele PH, Scheraga HA, Dyckes DF, Ferger MF, Du Vigneaud V. Nuclear magnetic resonance spectrum of deamino-lysine-vasopression in aqueous solution and its structural implications. Proceedings of the National Academy of Sciences of the United States of America. 69: 3322-6. PMID 4508326 DOI: 10.1073/pnas.69.11.3322 |
0.22 |
|
1972 |
Von Dreele PH, Brewster AI, Dadok J, Scheraga HA, Bovey FA, Ferger MF, Du Vigneaud V. Nuclear magnetic resonance spectrum of lysine-vasopressin in aqueous solution and its structural implictions. Proceedings of the National Academy of Sciences of the United States of America. 69: 2169-73. PMID 4506086 DOI: 10.1073/Pnas.69.8.2169 |
0.228 |
|
1972 |
Vavrek RJ, Ferger MF, Allen GA, Rich DH, Blomquist AT, Du Vigneaud V. Synthesis of three oxytocin analogs related to [1-deaminopenicillamine]oxytocin possessing antioxytocic activity Journal of Medicinal Chemistry. 15: 123-126. |
0.626 |
|
1971 |
Von Dreele PH, Brewster AI, Bovey FA, Scheraga HA, Ferger MF, Du Vigneaud V. Nuclear magnetic resonance studies of lysine-vasopressin: structural constraints. Proceedings of the National Academy of Sciences of the United States of America. 68: 3088-91. PMID 5289251 DOI: 10.1073/Pnas.68.12.3088 |
0.227 |
|
1971 |
Von Dreele PH, Brewster AI, Scheraga HA, Ferger MF, Du Vigneaud V. Nuclear magnetic resonance spectrum of lysine-vasopressin and its structural implications. Proceedings of the National Academy of Sciences of the United States of America. 68: 1028-31. PMID 5280520 DOI: 10.1073/Pnas.68.5.1028 |
0.212 |
|
1971 |
Hruby VJ, Ferger MF, Du Vigneaud V. Synthesis and pharmacological properties of deaminotocinamide and a new synthesis of tocinamide. Journal of the American Chemical Society. 93: 5539-42. PMID 5165679 DOI: 10.1021/Ja00750A037 |
0.363 |
|
1971 |
Flouret G, Du Vigneaud V. Deamino-D-oxytocin. Journal of Medicinal Chemistry. 14: 556-7. PMID 5091976 |
0.203 |
|
1971 |
du Vigneaud V, Meador JD, Ferger MF, Allen GA, Blomquist AT. The synthesis and biological properties of [I-deaminopenicillamine]-oxytocin deuterated in the I-position Bioorganic Chemistry. 1: 123-128. DOI: 10.1016/0045-2068(71)90010-1 |
0.609 |
|
1970 |
Takashima H, Hruby VJ, Du Vigneaud V. The synthesis of (1-deamino,4-L-leucine)-oxytocin and (1-deamino,4-L-isoleucine)-oxytocin and some of their pharmacological properties. Journal of the American Chemical Society. 92: 677-80. PMID 5460748 DOI: 10.1021/Ja00706A041 |
0.293 |
|
1970 |
Gillessen D, Du Vigneaud V. Synthesis and pharmacological properties of 4-decarboxamido-8-arginine-vasopressin and its 1-deamino analog. Journal of Medicinal Chemistry. 13: 346-9. PMID 5460500 |
0.378 |
|
1970 |
Chan WY, Du Vigneaud V. Natriuretic, diuretic and anti-arginine-vasopressin (ADH) effects of two analogs of oxytocin: [4-leucine]-oxytocin and [2,4-diisoleucine]-oxytocin. The Journal of Pharmacology and Experimental Therapeutics. 174: 541-9. PMID 5456186 |
0.273 |
|
1970 |
Fraefel W, Du Vigneaud V. The synthesis and pharmacological properties of [1-(delta-mercaptovaleric acid)]-oxytocin, a homolog of deamino-oxytocin containing a twenty-two-membered ring. Journal of the American Chemical Society. 92: 1030-2. PMID 5451008 |
0.373 |
|
1970 |
Takashima H, du Vigneaud V. The synthesis of deamino-oxytocinoic acid and acetone-oxytocinoic acid and their use in the preparation of deamino-oxytocinoylocytocin and oxytocinoyloxytocin. Journal of the American Chemical Society. 92: 2501-4. PMID 5438020 |
0.365 |
|
1970 |
Aanning HL, Yamashiro D, Du Vigneaud V. Synthesis of the parallel dimer of oxytocin Journal of the American Chemical Society. 92: 5214-5216. PMID 5432665 |
0.335 |
|
1970 |
Fraefel W, Du Vigneaud V. (1-(omega-mercaptoundecanoic acid))-oxytocin, a 28-membered ring homolog of deamino-oxytocin. Journal of the American Chemical Society. 92: 4426-7. PMID 5428385 |
0.307 |
|
1970 |
Hruby VJ, Du Vigneaud V, Chan WY. (2,4-Diisoleucine)-oxytocin. An analog of oxytocin with natriuretic and diuretic activities. Journal of Medicinal Chemistry. 13: 185-7. PMID 5418485 |
0.248 |
|
1969 |
Takashima H, Fraefel W, Du Vigneaud V. The synthesis and certain pharmacological properties of deamino-oxytocinoic acid methylamide and deamino-oxytocinoic acid dimethylamide. Journal of the American Chemical Society. 91: 6182-5. PMID 5823190 |
0.362 |
|
1969 |
Hruby VJ, Du Vigneaud V. [Synthesis and some pharmacological activities of [2-L-valine]-oxytocin and [2-L-leucine]-oxytocin. Journal of Medicinal Chemistry. 12: 731-3. PMID 5818088 |
0.292 |
|
1969 |
Hruby VJ, Flouret G, du Vigneaud V. The synthesis and some of the pharmacological properties of [4-L-isoleucine]-oxytocin and [4-L-leucine]-oxytocin. The Journal of Biological Chemistry. 244: 3890-4. PMID 5817165 |
0.293 |
|
1969 |
Havran RT, Du Vigneaud V. The structure of acetone-lysine-vasopressin as established through its synthesis from the acetone derivative of S-benzyl-L-cysteinyl-L-tyrosine. Journal of the American Chemical Society. 91: 2696-8. PMID 5784946 |
0.297 |
|
1969 |
Havran RT, Du Vigneaud V. The synthesis and pharmacological properties of [2-isoleucine]-8-lysine-vasopressin and its 1-deamino analog. Journal of the American Chemical Society. 91: 3626-8. PMID 5784189 |
0.378 |
|
1969 |
Du Vigneaud V. Hormones of the mammalian posterior pituitary gland and their naturally occurring analogues. The Johns Hopkins Medical Journal. 124: 53-65. PMID 5766381 |
0.262 |
|
1969 |
Flouret G, Du Vigneaud V. The synthesis and some pharmacological activities of[4-L-norvaline]-oxytocin and [4-L-norleucine]-oxytocin and their deamino analogs. Journal of Medicinal Chemistry. 12: 1035-8. PMID 5389145 |
0.293 |
|
1969 |
Blomquist AT, Rich DH, Carlson BA, Allen GA, Hruby VJ, Takashima H, Nangeroni LL, Glose P, Du Vigneaud V. Deuterated oxytocins: the synthesis and biological properties of a crystalline analog of deamino-oxytocin deuterated in the 5-asparagine position. Proceedings of the National Academy of Sciences of the United States of America. 64: 263-6. PMID 5263009 DOI: 10.1073/Pnas.64.1.263 |
0.671 |
|
1969 |
Hruby VJ, Du Vigneaud V. The detection of a Schiff base intermediate in the formation of acetone-oxytocin Journal of the American Chemical Society. 91: 3624-3626. |
0.184 |
|
1968 |
Hruby VJ, Yamashiro D, du Vigneaud V. The structure of acetone-oxytocin with studies on the reaction of acetone with various peptides. Journal of the American Chemical Society. 90: 7106-10. PMID 5688360 DOI: 10.1021/Ja01027A040 |
0.24 |
|
1968 |
Chan WY, Hruby VJ, Flouret G, Du Vigneaud V. 4-leucine-oxytocin: Natriuretic, diuretic, and antivasopressin polypeptide Science. 161: 280-281. PMID 5657333 DOI: 10.1126/science.161.3838.280 |
0.221 |
|
1968 |
Yamashiro D, Aanning HL, Branda LA, Cash WD, Murti VV, du Vigneaud V. A synthesis of [1-(N-methyl-hemi-L-cystine)]-oxytocin and a study of its reaction with acetone. Journal of the American Chemical Society. 90: 4141-4. PMID 5655880 |
0.313 |
|
1968 |
Yamashiro D, Hope DB, Du Vigneaud V. Isomeric dimers of oxytocin. Journal of the American Chemical Society. 90: 3857-60. PMID 5653826 |
0.198 |
|
1968 |
Takashima H, Du Vigneaud V, Merrifield RB. The synthesis of deamino-oxytocin by the solid phase method. Journal of the American Chemical Society. 90: 1323-5. PMID 5636536 DOI: 10.1021/ja01007a038 |
0.271 |
|
1968 |
Yamashiro D, Du Vigneaud V. Synthesis of "acetone-oxytocin" from an isopropylidene derivative of S-benzyl-L-cysteinyl-L-tyrosine. Journal of the American Chemical Society. 90: 487-90. PMID 5634625 |
0.294 |
|
1968 |
Blomquist AT, Rich DH, Hruby VJ, Nangeroni LL, Glose P, Du Vigneaud V. Deuterated oxytocins: the synthesis and biological properties of three crystalline analogs of deamino-oxytocin deuterated in the 1-beta-mercaptopropionic acid position. Proceedings of the National Academy of Sciences of the United States of America. 61: 688-92. PMID 5246000 DOI: 10.1073/Pnas.61.2.688 |
0.699 |
|
1967 |
Branda LA, Hruby VJ, Du Vigneaud V. 2-Isoleucine-oxytocin and deamino-2-isoleucine-oxytocin: their synthesis and some of their pharmacologic activities. Molecular Pharmacology. 3: 248-53. PMID 6068341 |
0.359 |
|
1967 |
Jarvis D, Du Vigneaud V. The effect of decreasing the size of the ring present in deamino-oxytocin by one methylene group on its biological properties. The synthesis of 1-mercaptoacetic acid-oxytocin. The Journal of Biological Chemistry. 242: 1768-71. PMID 6067284 |
0.365 |
|
1967 |
Chan WY, Fear R, Du Vigneaud V. Some pharmacologic studies on 1-L-penicillamine-oxytocin and 1-deaminopenicillamine-oxytocin: two potent oxytocin inhibitors. Endocrinology. 81: 1267-77. PMID 6064990 DOI: 10.1210/endo-81-6-1267 |
0.257 |
|
1967 |
Gillessen D, Du Vigneaud V. The synthesis and pharmacological properties of 4-decarboxamido-8-lysine-vasopressin, 5-decarboxamido-8-lysine-vasopressin, and their 1-deamino analogues. The Journal of Biological Chemistry. 242: 4806-12. PMID 6061422 |
0.388 |
|
1967 |
Schulz H, du Vigneaud V. Synthesis and some pharmacological properties of 6-L-penicillamine-oxytocin. Journal of Medicinal Chemistry. 10: 1037-9. PMID 6056028 |
0.327 |
|
1967 |
Yamashiro D, Havran RT, Aanning HL, Du Vigneaud V. Inactivation of lysine-vasopressin by acetone. Proceedings of the National Academy of Sciences of the United States of America. 57: 1058-61. PMID 5231345 |
0.226 |
|
1967 |
Jarvis D, Manning M, Du Vigneaud V. 1-Mercaptoacetic acid-4-β-alanine-oxytocin Biochemistry. 6: 1223-1225. |
0.257 |
|
1966 |
Ferrier BM, Du Vigneaud V. 9-Deamidooxytocin, an analog of the hormone containing a glycine residue in place of the glycinamide residue. Journal of Medicinal Chemistry. 9: 55-7. PMID 6006226 |
0.242 |
|
1966 |
Schulz H, du Vigneaud V. The effect of replacing one of the hydrogens of the beta-carbon of the beta-mercaptopropionic acid residue in deamino-oxytocin by a methyl group on its oxytocic and avian vasodepressor activity. Journal of the American Chemical Society. 88: 5015-8. PMID 5978832 |
0.278 |
|
1966 |
Schulz H, Du Vigneaud V. Synthesis of 1-L-penicillamine-oxytocin, 1-D-penicillamine-oxytocin, and 1-deaminopenicillamine-oxytocin, potent inhibitors of the oxytocic response of oxytocin. Journal of Medicinal Chemistry. 9: 647-50. PMID 5969030 |
0.309 |
|
1966 |
Branda LA, Du Vigneaud V. Deoxy-4-decarboxamido-oxytocin and deamino-deoxy-4-decarboxamido-oxytocin. The Journal of Biological Chemistry. 241: 4051-4. PMID 5950770 |
0.277 |
|
1966 |
Branda LA, Drabarek S, Du Vigneaud V. The synthesis and pharmacological properties of deamino-4-decarboxamido-oxytocin (1-beta-mercaptopropionic acid-1-alpha-aminobutyric acid-oxytocin). The Journal of Biological Chemistry. 241: 2572-5. PMID 5950415 |
0.341 |
|
1966 |
Du Vigneaud V, Flouret G, Walter R. Synthesis and some biological properties of 4-valine-oxytocin and 1-deamino-4-valine-oxytocin. The Journal of Biological Chemistry. 241: 2093-6. PMID 5949929 |
0.373 |
|
1966 |
Ferraro JJ, du Vigneaud V. 7-D-proline-oxytocin and its deamino analog. Diastereoisomers of oxytocin and deamino-oxytocin. Journal of the American Chemical Society. 88: 3847-50. PMID 5916375 |
0.239 |
|
1966 |
Branda LA, Du Vigneaud V. Synthesis and pharmacological properties of 9-decarboxamido-oxytocin. Journal of Medicinal Chemistry. 9: 169-72. PMID 5911792 |
0.357 |
|
1966 |
Yamashiro D, Gillessen D, Du Vigneaud V. Simultaneous synthesis of 1-hemi-D-cystine-oxytocin and oxytocin and separation of the diastereoisomers by partition chromatography on sephadex and by countercurrent distribution. Journal of the American Chemical Society. 88: 1310-3. PMID 5905606 |
0.279 |
|
1966 |
Walter R, Du Vigneaud V. 8-Alanine-oxytocin, 8-alanine-oxypressin, and their deamino analogs. Their synthesis and some of their pharmacological properties Biochemistry. 5: 3720-3727. |
0.376 |
|
1966 |
Yamashiro D, Gillessen D, Du Vigneaud V. Oxytoceine and deamino-oxytoceine Biochemistry. 5: 3711-3720. |
0.208 |
|
1966 |
Walter R, Du Vigneaud V. 1-Deamino-1,6-L-selenocystine-oxytocin, a highly potent isolog of 1-deamino-oxytocin [12] Journal of the American Chemical Society. 88: 1331-1332. |
0.257 |
|
1965 |
Flouret G, Du Vigneaud V. The synthesis of D-oxytocin, the enantiomer of the posterior pituitary hormone, oxytocin [7] Journal of the American Chemical Society. 87: 3775-3776. PMID 14338116 |
0.311 |
|
1965 |
Ferrier BM, Jarvis D, Du Vigneaud V. Deamino-oxytocin. Its isolation by partition chromatography on Sephadex and crystallization from water, and its biological activities. The Journal of Biological Chemistry. 240: 4264-6. PMID 5891826 |
0.205 |
|
1965 |
Walter R, Du Vigneaud V. 6-Hemi-L-selenocystine-oxytocin and 1-deamino-6-hemi-L-selenocystine-oxytocin, highly potent isologs of oxytocin and 1-deamino-oxytocin. Journal of the American Chemical Society. 87: 4192-3. PMID 5845279 DOI: 10.1021/Ja01096A036 |
0.246 |
|
1965 |
Manning M, Du Vigneaud V. 6-Hemi-D-cystine-oxytocin, a diastereoisomer of the posterior pituitary hormone oxytocin. Journal of the American Chemical Society. 87: 3978-82. PMID 5845269 |
0.238 |
|
1965 |
Drabarek S, Du Vigneaud V. 2-D-tyrosine-oxytocin and 2-D-tyrosine-deamino-oxytocin diastereoisomers of oxytocin and deamino-oxytocin. Journal of the American Chemical Society. 87: 3974-8. PMID 5845268 |
0.21 |
|
1965 |
Jarvis D, Ferrier BM, Du Vigneaud V. The effect of increasing the size of the ring present in deamino-oxytocin by one methylene group on its biological properties. The synthesis of 1-gamma-mercaptobutyric acid-oxytocin. The Journal of Biological Chemistry. 240: 3553-7. PMID 5835936 |
0.36 |
|
1965 |
Yamashiro D, Aanning HL, Du Vigneaud V. Inactivation of oxytocin by acetone. Proceedings of the National Academy of Sciences of the United States of America. 54: 166-71. PMID 5216348 |
0.204 |
|
1965 |
Photaki I, Du Vigneaud V. 4-Deamido-oxytocin, an analog of the hormone containing glutamic acid in place of glutamine Journal of the American Chemical Society. 87: 908-913. |
0.299 |
|
1965 |
Manning M, Du Vigneaud V. 4-β-Alanine-oxytocin: An oxytocin analog containing a twenty-one-membered disulfide ring Biochemistry. 4: 1884-1888. |
0.237 |
|
1964 |
Jarvis D, Du Vigneaud V. Crystalline deamino-oxytocin Science. 143: 545-548. PMID 14080324 |
0.22 |
|
1963 |
KIMBROUGH RD, CASH WD, BRANDA LA, CHAN WY, DU VIGNEAUD V. Synthesis and biological properties of 1-desamino-8-lysine-vasopressin. The Journal of Biological Chemistry. 238: 1411-4. PMID 14032722 |
0.373 |
|
1963 |
GOLUBOW J, CHAN WY, DU VIGNEAUD V. Effect of human pregnancy serum on avian depressor activities of oxytocin and desamino-oxytocin. Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 113: 113-5. PMID 13948911 DOI: 10.3181/00379727-113-28293 |
0.205 |
|
1963 |
GOLUBOW J, DU VIGNEAUD V. Comparison of susceptibility of oxytocin and desamino-oxytocin to inactivation by leucine aminopeptidase and alpha-chymotrypsin. Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 112: 218-9. PMID 13948909 |
0.2 |
|
1963 |
Hope DB, Murti VVS, Du Vigneaud V. Synthesis of 1-hemi-D-cystine-oxytocin Journal of the American Chemical Society. 85: 3686-3688. |
0.304 |
|
1962 |
HOPE DB, MURTI VV, DU VIGNEAUD V. A highly potent analogue of oxytocin, desamino-oxytocin. The Journal of Biological Chemistry. 237: 1563-6. PMID 14448781 |
0.321 |
|
1962 |
DILLON TF, DOUGLAS RG, DU VIGNEAUD V. Further observations of transbuccal administration of pitocin for induction and stimulation of labor. Obstetrics and Gynecology. 20: 434-41. PMID 14027906 |
0.203 |
|
1962 |
CHAN WY, DU VIGNEAUD V. Comparison of the pharmacologic properties of oxytocin and its highly potent analogue, desamino-oxytocin. Endocrinology. 71: 977-82. PMID 14019993 DOI: 10.1210/endo-71-6-977 |
0.293 |
|
1962 |
HOPE DB, DU VIGNEAUD V. Synthesis of desamino-desoxyoxytocin, a biologically active analogue of oxytocin. The Journal of Biological Chemistry. 237: 3146-50. PMID 13961656 |
0.365 |
|
1962 |
Schneider CH, Du Vigneaud V. Synthesis of D-leucine-oxytocin, a biologically active diastereoisomer of oxytocin, and demonstration of its separability from oxytocin upon countercurrent distribution Journal of the American Chemical Society. 84: 3005-3008. |
0.305 |
|
1961 |
KIMBROUGH RD, DU VIGNEAUD V. Lysine-vasotocin, a synthetic analogue of the posterior pituitary hormones containing the ring of oxytocin and the side chain of lysine-vasopressin. The Journal of Biological Chemistry. 236: 778-80. PMID 13755994 |
0.289 |
|
1961 |
Jarvis D, Bodanszky M, Du Vigneaud V. The synthesis of 1-(hemi-homocystine)-oxytocin and a study of some of its pharmacological properties Journal of the American Chemical Society. 83: 4780-4784. |
0.355 |
|
1961 |
Meienhofer J, Du Vigneaud V. Synthesis of a biologically active analog of lysine-vasopressin, with phenylalanine replacing tyrosine: 2-Phenylalanine lysine-vasopressin Journal of the American Chemical Society. 82: 6336-6337. |
0.373 |
|
1961 |
Meienhofer J, Du Vigneaud V. Synthesis of a lysine-vasopressin derivative with a methyl substituent on the imino nitrogen of the peptide bond between lysine and glycinamide (9-sarcosine lysine-vasopressin) Journal of the American Chemical Society. 83: 142-145. |
0.315 |
|
1960 |
DILLON TF, DOUGLAS RG, DU VIGNEAUD V, BARBER ML. Transbuccal administration of pitocin for induction and stimulation of labor. Obstetrics and Gynecology. 15: 587-92. PMID 13816785 |
0.206 |
|
1960 |
DU VIGNEAUD V, WINESTOCK G, MURTI VV, HOPE DB, KIMBROUGH RD. Synthesis of 1-beta-mercantopropionic acid oxytocin (desamino-oxytocin), a highly potent analogue of oxytocin. The Journal of Biological Chemistry. 235: PC64-PC66. PMID 13724538 |
0.372 |
|
1960 |
Bodanszky M, Meienhofer J, Du Vigneaud V. Synthesis of lysine-vasopressin by the nitrophenyl ester method Journal of the American Chemical Society. 82: 3195-3198. |
0.359 |
|
1960 |
Meienhofer J, Du Vigneaud V. Preparation of lysine-vasopressin through a crystalline protected nonapeptide intermediate and purification of the hormone by chromatography Journal of the American Chemical Society. 82: 2279-2282. |
0.296 |
|
1960 |
Law HD, Du Vigneaud V. Synthesis of 2-p-methoxyphenylalanine oxytocin (O-methyl-oxytocin) and some observations on its pharmacological behavior Journal of the American Chemical Society. 82: 4579-4581. |
0.259 |
|
1959 |
KATSOYANNIS PG, DU VIGNEAUD V. Arginine vasotocin. Nature. 184: 1465. PMID 14404760 |
0.271 |
|
1959 |
BODANSZKY M, DU VIGNEAUD V. A new crystalline salt of oxytocin. Nature. 184: 981-2. PMID 13801910 DOI: 10.1038/184981a0 |
0.501 |
|
1959 |
LIGHT A, STUDER RO, DU VIGNEAUD V. Isolation of oxytocin and arginine vasopressin by way of a protein complex on a preparative scale. Archives of Biochemistry and Biophysics. 83: 84-7. PMID 13661994 |
0.234 |
|
1959 |
BODANSZKY M, DU VIGNEAUD V. Synthesis of oxytocin by the nitrophenyl ester method. Nature. 183: 1324-5. PMID 13657100 DOI: 10.1038/1831324b0 |
0.585 |
|
1959 |
Katsoyannis PG, Du Vigneaud V. Active principles of the neurohypophysis of cold-blooded vertebrates: Arginine vasotocin Nature. 184: 1465. DOI: 10.1038/1841465a0 |
0.2 |
|
1959 |
Bodanszky M, Du Vigneaud V. Synthesis of a biologically active analog of oxytocin, with phenylalanine replacing tyrosine Journal of the American Chemical Society. 81: 6072-6075. |
0.358 |
|
1959 |
Bodanszky M, Du Vigneaud V. A method of synthesis of long peptide chains using a synthesis of oxytocin as an example Journal of the American Chemical Society. 81: 5688-5691. |
0.317 |
|
1959 |
Bodanszky M, Du Vigneaud V. An improved synthesis of oxytocin Journal of the American Chemical Society. 81: 2504-2507. |
0.339 |
|
1959 |
Lutz WB, Ressler C, Nettleton DE, Du Vigneaud V. Isoasparagine-oxytocin: The isoasparagine isomer of oxytocin Journal of the American Chemical Society. 81: 167-173. |
0.256 |
|
1959 |
Bodanszky M, Du Vigneaud V. Synthesis of a biologically active analog of oxytocin, with phenylalanine replacing tyrosine [6] Journal of the American Chemical Society. 81: 1258-1259. |
0.358 |
|
1958 |
KATSOYANNIS PG, DU VIGNEAUD V. The synthesis of the histidine analog of the vasopressins. Archives of Biochemistry and Biophysics. 78: 555-62. PMID 13618038 |
0.393 |
|
1958 |
KATSOYANNIS PG, DU VIGNEAUD V. Arginine-vasotocin, a synthetic analogue of the posterior pituitary hormones containing the ring of oxytocin and the side chain of vasopressin. The Journal of Biological Chemistry. 233: 1352-4. PMID 13610841 |
0.289 |
|
1958 |
LIGHT A, DU VIGNEAUD V. On the nature of oxytocin and vasopressin from human pituitary. Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 98: 692-6. PMID 13591312 DOI: 10.3181/00379727-98-24154 |
0.217 |
|
1958 |
ACHER R, LIGHT A, DU VIGNEAUD V. Purification of oxytocin and vasopressin by way of a protein complex. The Journal of Biological Chemistry. 233: 116-20. PMID 13563452 |
0.205 |
|
1958 |
DILLON TF, MARBURY BE, BONSNES RW, DOUGLAS RG, DU VIGNEAUD V. Vasopressin as a hemostatic in gynecologic surgery; a preliminary report. Obstetrics and Gynecology. 11: 363-71. PMID 13517741 |
0.174 |
|
1958 |
Du Vigneaud V, Gish DT, Katsoyannis PG, Hess GP. Synthesis of the pressor-antidiuretic hormone, arginine-vasopressin Journal of the American Chemical Society. 80: 3355-3358. |
0.357 |
|
1957 |
LIGHT A, ACHER R, DU VIGNEAUD V. Ion exchange chromatography of purified posterior pituitary preparations. The Journal of Biological Chemistry. 228: 633-41. PMID 13475348 |
0.211 |
|
1957 |
DU VIGNEAUD V, KUCHINSKAS EJ, HORVATH A. L-penicillamine and rat liver transaminase activity. Archives of Biochemistry and Biophysics. 69: 130-7. PMID 13445187 |
0.22 |
|
1957 |
KUCHINSKAS EJ, HORVATH A, DU VIGNEAUD V. An anti-vitamin B6 action of L-penicillamine. Archives of Biochemistry and Biophysics. 68: 69-75. PMID 13435895 |
0.225 |
|
1957 |
DU VIGNEAUD V, KUCHINSKAS EJ. An increased vitamin B6 requirement in the rat on a diet containing L-penicillamine. Archives of Biochemistry and Biophysics. 66: 1-9. PMID 13395520 |
0.22 |
|
1957 |
Du Vigneaud V, Bartlett MF, Jöhl A. The synthesis of lysine-vasopressin Journal of the American Chemical Society. 79: 5572-5575. |
0.395 |
|
1956 |
DU VIGNEAUD V, WARD DN. Studies on the purification of lysine vasopressin from hog pituitary glands. The Journal of Biological Chemistry. 222: 951-8. PMID 13367062 |
0.249 |
|
1956 |
DU VIGNEAUD V. Trail of sulfur research: from insulin to oxytocin. Science (New York, N.Y.). 123: 967-74. PMID 13324123 |
0.175 |
|
1956 |
Katsoyannis PG, Du Vigneaud V. Synthesis of S-benzyl-N-carbobenzoxy-L-cysteinyl-L-tyrosyl-L-phenylalanyl-L-glutaminyl-L- asparagine, a pentapeptide derivative related to vasopressin Journal of the American Chemical Society. 78: 4482-4483. |
0.258 |
|
1956 |
Roeske R, Stewart FHC, Stedman RJ, Du Vigneaud V. Synthesis of a protected tetrapeptide amide containing the carboxyl terminal sequence of lysine-vasopressin Journal of the American Chemical Society. 78: 5883-5887. |
0.313 |
|
1956 |
Bartlett MF, Jöhl A, Roeske R, Stedman RT, Stewart FHC, Ward DN, Du Vigneaud V. Studies on the synthesis of lysine-vasopressin [2] Journal of the American Chemical Society. 78: 2905-2906. |
0.396 |
|
1956 |
Du Vigneaud V, Rachele JR, White AM. A crucial test of transmethylation in vivo by intramolecular isotopic labeling [8] Journal of the American Chemical Society. 78: 5131-5132. |
0.226 |
|
1955 |
DU VIGNEAUD V. Oxytocin, the principal oxytocic hormone of the posterior pituitary gland: its isolation, structure, and synthesis. Experientia. 9-26. PMID 13305558 |
0.305 |
|
1955 |
WOOLLEY DW, MERRIFIELD RB, RESSLER C, DU VIGNEAUD V. Strepogenin activity of synthetic peptides related to oxytocin. Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 89: 669-73. PMID 13254861 DOI: 10.3181/00379727-89-21911 |
0.255 |
|
1955 |
Douglas RG, Bonsnes RW, du Vigneaud VD. Natural and synthetic oxytocin: Preliminary report on the use of both for the induction and stimulation of labor Obstetrics and Gynecology. 6: 254-257. PMID 13254026 |
0.258 |
|
1955 |
RACHELE JR, KUCHINSKAS EJ, KRATZER FH, DU VIGNEAUD V. Hydrogen isotope effect in the oxidation in vivo of methionine labeled in the methyl group. The Journal of Biological Chemistry. 215: 593-601. PMID 13242556 |
0.233 |
|
1954 |
Best CH, Cannan RK, Clarke HT, Cook AS, du Vigneaud V, Kendall EC, King CG, Mason KE, Maynard LA, Pett LB, Sebrell H, Sevringhaus EL, Tainter ML, Youmans JB. Letters to the Editor. American Journal of Public Health and the Nation's Health. 44: 255-6. PMID 18017424 |
0.569 |
|
1954 |
DU VIGNEAUD V. Hormones of the posterior pituitary gland: oxytocin and vasopressin. Harvey Lectures. 50: 1-26. PMID 13306033 |
0.232 |
|
1954 |
LAWLER HC, TAYLOR SP, SWAN AM, DU VIGNEAUD V. Presence of glutamine and asparagine in enzymatic hydrolysates of oxytocin and vasopressin. Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 87: 550-2. PMID 13237303 DOI: 10.3181/00379727-87-21441 |
0.271 |
|
1954 |
RESSLER C, DU VIGNEAUD V. Bromination of performic acid-oxidized oxytocin. The Journal of Biological Chemistry. 211: 809-14. PMID 13221586 |
0.268 |
|
1954 |
NICKERSON K, BONSNESS RW, DOUGLAS RG, CONDLIFFE P, DU VIGNEAUD V. Oxytocin and milk ejection. American Journal of Obstetrics and Gynecology. 67: 1028-34. PMID 13148259 |
0.202 |
|
1954 |
POPENOE EA, DU VIGNEAUD V. A partial sequence of amino acids in performic acid-oxidized vasopressin. The Journal of Biological Chemistry. 206: 353-60. PMID 13130555 |
0.287 |
|
1954 |
Ressler C, Du Vigneaud V. The synthesis of the tetrapeptide amide S-benzyl-L-cysteinyl-L-prolyl-L-leucylglycinamide Journal of the American Chemical Society. 76: 3107-3109. |
0.269 |
|
1954 |
Du Vigneaud V, Ressler C, Swan JM, Roberts CW, Katsoyannis PG. The synthesis of oxytocin Journal of the American Chemical Society. 76: 3115-3121. |
0.383 |
|
1954 |
Katsoyannis PG, Du Vigneaud V. The synthesis of p-toluenesulfonyl-L-isoleucyl-L-glutaminyl-L-asparagine and related peptides Journal of the American Chemical Society. 76: 3113-3115. |
0.27 |
|
1954 |
Du Vigneaud V, Gish DT, Katsoyannis PG. A synthetic preparation possessing biological. Properties associated with arginine-vasopressin [9] Journal of the American Chemical Society. 76: 4751-4752. |
0.312 |
|
1954 |
Swan JM, Du Vigneaud V. The synthesis of L-glutaminyl-L-asparagine, L-glutamine and L-isoglutamine from p-toluenesulfonyl-L-glutamic acid Journal of the American Chemical Society. 76: 3110-3113. |
0.263 |
|
1953 |
GORDON S, DU VIGNEAUD V. Preparation of S,S'-dibenzyloxytocin and its reconversion to oxytocin. Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 84: 723-5. PMID 13134269 |
0.22 |
|
1953 |
DU VIGNEAUD V, RESSLER C, TRIPPETT S. The sequence of amino acids in oxytocin, with a proposal for the structure of oxytocin. The Journal of Biological Chemistry. 205: 949-57. PMID 13129273 |
0.276 |
|
1953 |
LAWLER HC, DU VIGNEAUD V. Enzymatic evidence for intrinsic oxytocic activity of the pressor-antidiuretic hormone. Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 84: 114-6. PMID 13120954 |
0.24 |
|
1953 |
POPENOE EA, DU VIGNEAUD V. Degradative studies on vasopressin and performic acid-oxidized vasopressin. The Journal of Biological Chemistry. 205: 133-43. PMID 13117892 |
0.272 |
|
1953 |
TAYLOR SP, DU VIGNEAUD V, KUNKEL HG. Electrophoretic studies of oxytocin and vasopressin. The Journal of Biological Chemistry. 205: 45-53. PMID 13117882 |
0.23 |
|
1953 |
ROBERTS CW, DU VIGNEAUD V. The synthesis of beta-sulfo-L-Alanyl-L-tyrosine and L-tyrosyl-L-cysteic acid and their dibromotyrosyl analogues. The Journal of Biological Chemistry. 204: 871-5. PMID 13117865 |
0.29 |
|
1953 |
RESSLER C, TRIPPETT S, DU VIGNEAUD V. Free amino groups of performic acid oxidized oxytocin and of its cleavage products formed by treatment with bromine water. The Journal of Biological Chemistry. 204: 861-9. PMID 13117864 |
0.277 |
|
1953 |
MUELLER JM, PIERCE JG, DU VIGNEAUD V. Treatment of performic acid-oxidized oxytocin with bromine water. The Journal of Biological Chemistry. 204: 857-60. PMID 13117863 |
0.244 |
|
1953 |
TAYLOR SP, DU VIGNEAUD V. Electrophoretic properties of oxytocin The Journal of Biological Chemistry. 200: 559-564. PMID 13034814 |
0.219 |
|
1953 |
Du Vigneaud V, Lawler HC, Popenoe EA. Enzymatic cleavage of glycinamide from vasopressin and a proposed structure for this pressor-antidiuretic hormone of the posterior pituitary [23] Journal of the American Chemical Society. 75: 4880-4881. |
0.232 |
|
1953 |
Du Vigneaud V, Ressler C, Swan JM, Roberts CW, Katsoyannis PG, Gordon S. The synthesis of an octapeptide amide with the hormonal activity of oxytocin [22] Journal of the American Chemical Society. 75: 4879-4880. |
0.354 |
|
1953 |
du Vigneaud V, Kinney JM, Wilson JE, Rachele JR. Effect of the presence of labile methyl groups in the diet on labile methyl neogenesis Bba - Biochimica Et Biophysica Acta. 12: 88-91. |
0.243 |
|
1952 |
MACKENZIE CG, DU VIGNEAUD V. Effect of choline and cystine on the oxidation of the methyl group of methionine. The Journal of Biological Chemistry. 195: 487-91. PMID 14946157 |
0.246 |
|
1952 |
POPENOE EA, PIERCE JG, DU VIGNEAUD V, VAN DYKE HB. Oxytocic activity of purified vasopressin Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 81: 506-508. PMID 13027353 DOI: 10.3181/00379727-81-19924 |
0.218 |
|
1952 |
PIERCE JG, GORDON S, DU VIGNEAUD V. Further distribution studies on the oxytocic hormone of the posterior lobe of the pituitary gland and the preparation of an active crystalline flavianate. The Journal of Biological Chemistry. 199: 929-40. PMID 13022701 |
0.238 |
|
1952 |
RESSLER C, RACHELE JR, DU VIGNEAUD V. Studies in vivo on labile methyl synthesis with deuterio-C14-formate The Journal of Biological Chemistry. 197: 1-5. PMID 12981027 |
0.31 |
|
1952 |
VERLY WG, KINNEY JM, DU VIGNEAUD V. Effect of folic acid and leucovorin on synthesis of the labile methyl group from methanol in the rat The Journal of Biological Chemistry. 196: 19-23. PMID 12980938 |
0.348 |
|
1952 |
Popenoe EA, Lawler HC, Du Vigneaud V. Partial purification and amino acid content of vasopressin from hog posterior pituitary glands [13] Journal of the American Chemical Society. 74: 3713. |
0.317 |
|
1952 |
Verly WG, Rachele JR, Du Vigneaud V, Eidinoff ML, Knoll JE. A test of tritium as a labeling device in a biological study Journal of the American Chemical Society. 74: 5941-5943. |
0.202 |
|
1951 |
DAVOLL H, TURNER RA, PIERCE JG, DU VIGNEAUD V. An investigation of the free amino groups on oxytocin and desulfurized oxytocin preparations The Journal of Biological Chemistry. 193: 363-370. PMID 14907724 |
0.301 |
|
1951 |
TURNER RA, PIERCE JG, DU VIGNEAUD V. The desulfurization of oxytocin The Journal of Biological Chemistry. 193: 359-361. PMID 14907723 |
0.228 |
|
1951 |
DU VIGNEAUD V, RESSLER C, RACHELE JR, REYNIERS JA, LUCKEY TD. The synthesis of "biologically labile" methyl groups in the germ-free rat The Journal of Nutrition. 45: 361-376. PMID 14898323 DOI: 10.1093/Jn/45.3.361 |
0.306 |
|
1951 |
MUELLER JM, PIERCE JG, DAVOLL H, du VIGNEAUD V. The oxidation of oxytocin with performic acid. The Journal of Biological Chemistry. 191: 309-13. PMID 14850474 |
0.264 |
|
1951 |
TURNER RA, PIERCE JG, du VIGNEAUD V. The purification and the amino acid content of vasopressin preparations The Journal of Biological Chemistry. 191: 21-28. PMID 14850440 |
0.329 |
|
1951 |
Du Vigneaud V, Verly WGL, Wilson JE, Rachele JR, Ressler C, Kinney JM. One-carbon compounds in the biosynthesis of the "biologically labile" methyl group Journal of the American Chemical Society. 73: 2782-2785. |
0.264 |
|
1950 |
MACKENZIE CG, du VIGNEAUD V. Biochemical stability of the methyl group of creatine and creatinine. The Journal of Biological Chemistry. 185: 185-9. PMID 15436489 |
0.228 |
|
1950 |
FERGER MF, du VIGNEAUD V. Oxidation in vivo of the methyl groups of choline, betaine, dimethylthetin, and dimethyl-beta-propiothetin The Journal of Biological Chemistry. 185: 53-57. PMID 15436475 |
0.262 |
|
1950 |
WILSON JE, du VIGNEAUD V. Inhibition of the growth of the rat by L-penicillamine and its prevention by aminoethanol and related compounds The Journal of Biological Chemistry. 184: 63-70. PMID 15421973 |
0.664 |
|
1950 |
Du Vigneaud V, Ressler C, Rachele JR. The biological synthesis of "labile methyl groups" Science. 112: 267-271. PMID 14781718 |
0.33 |
|
1950 |
RACHELE JR, REED LJ, KIDWAI AR, FERGER MF, du VIGNEAUD V. Conversion of cystathionine labeled with S35 to cystine in vivo. The Journal of Biological Chemistry. 185: 817-26. PMID 14774428 |
0.499 |
|
1950 |
Du Vigneaud V, Verly WG, Wilson JE. Incorporation of the carbon of formaldehyde and formate into the methyl groups of choline [18] Journal of the American Chemical Society. 72: 2819-2820. |
0.24 |
|
1950 |
Du Vigneaud V, Verly WG. Incorporation in vivo of C14 from labeled methanol into the methyl groups of choline [14] Journal of the American Chemical Society. 72: 1049. |
0.251 |
|
1950 |
PIERCE JG, du VIGNEAUD V. Studies on high potency oxytocic material from beef posterior pituitary lobes The Journal of Biological Chemistry. 186: 77-84. |
0.218 |
|
1949 |
BOISSONNAS RA, TURNER RA, DU VIGNEAUD V. Metabolic study of the methyl groups of butter yellow The Journal of Biological Chemistry. 180: 1053-1058. PMID 18139200 |
0.239 |
|
1949 |
REED LJ, KIDWAI AR, DU VIGNEAUD V. Preparation of the optically active isomers of S-benzylhomocysteine by enzymatic resolution. The Journal of Biological Chemistry. 180: 571-4. PMID 18135790 |
0.506 |
|
1949 |
CARROLL WR, STACY GW, DU VIGNEAUD V. alpha-Ketobutyric acid as a product in the enzymatic cleavage of cystathionine The Journal of Biological Chemistry. 180: 375-382. PMID 18133402 |
0.263 |
|
1949 |
LIVERMORE AH, DU VIGNEAUD V. Preparation of high potency oxytocic material by the use of counter-current distribution. The Journal of Biological Chemistry. 180: 365-73. PMID 18133401 |
0.207 |
|
1949 |
FERGER MF, DU VIGNEAUD V. The antiphenylalanine effect of beta-2-thienylalanine for the rat The Journal of Biological Chemistry. 179: 61-65. PMID 18119220 |
0.226 |
|
1949 |
KELLER EB, RACHELE JR, DU VIGNEAUD V. A study of transmethylation with methionine containing deuterium and C14 in the methyl group. The Journal of Biological Chemistry. 177: 733-8. PMID 18110450 |
0.626 |
|
1948 |
MACKENZIE CG, DU VIGNEAUD V. The source of urea carbon. The Journal of Biological Chemistry. 172: 353. PMID 18920800 |
0.179 |
|
1948 |
DU VIGNEAUD V, STEVENS CM. Reactions of mustard-type vesicants with alpha-amino acids. Journal of the American Chemical Society. 70: 1620-4. PMID 18915782 DOI: 10.1021/Ja01184A093 |
0.283 |
|
1948 |
MAW GA, DU VIGNEAUD V. Dimethyl-beta-propiothetin, a new methyl donor The Journal of Biological Chemistry. 174: 381. PMID 18914096 |
0.255 |
|
1948 |
FERGER MF, DU VIGNEAUD V. The microbial growth inhibition produced by optical isomers of beta-2-thienylalanine The Journal of Biological Chemistry. 174: 241-246. PMID 18914080 |
0.244 |
|
1948 |
ARMSTRONG MD, DU VIGNEAUD V. Mercaptals and mercaptoles of cysteine The Journal of Biological Chemistry. 173: 749-751. PMID 18910730 |
0.205 |
|
1948 |
KELLER EB, WOOD JL, DU VIGNEAUD V. An investigation of transmethylation from N1-methylnicotinamide. Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 67: 182-4. PMID 18907623 DOI: 10.3181/00379727-67-16244 |
0.594 |
|
1948 |
DU VIGNEAUD V, STACY GW, TODD D. The synthesis of dl-beta, beta-diethylcysteine and dl-beta ethyl-beta-methylcysteine The Journal of Biological Chemistry. 176: 907-914. PMID 18889945 |
0.244 |
|
1948 |
CARPENTER FH, TURNER RA, DU VIGNEAUD V. Benzylpenicillenic acid as an intermediate in the synthesis of benzylpenicillin. The Journal of Biological Chemistry. 176: 893-906. PMID 18889944 |
0.755 |
|
1948 |
DU VIGNEAUD V. Migration of the methyl group in the body Proceedings of the American Philosophical Society. 92: 127-135. PMID 18873476 |
0.23 |
|
1948 |
DU VIGNEAUD V, MOYER AW, CHANDLER JP. Dimethylthetin as a biological methyl donor The Journal of Biological Chemistry. 174: 477-480. PMID 18865615 |
0.244 |
|
1948 |
DU VIGNEAUD V. An illustration of the power of isotopes in a biochemical problem United States Naval Medical Bulletin. 48: 176-184. PMID 18859240 |
0.173 |
|
1948 |
Holley RW, Carpenter FH, Livermore AH, DU Vigneaud V. A Synthesis of Benzylpenillic Acid. Science (New York, N.Y.). 108: 136-7. PMID 17806860 DOI: 10.1126/Science.108.2797.136 |
0.773 |
|
1948 |
Wilson JE, Du Vigneaud V. L-penicillamine as a metabolic antagonist Science. 107: 653. PMID 17735509 |
0.228 |
|
1948 |
Wood JL, Rachele JR, Stevens CM, Carpenter FH, Du Vigneaud V. The reaction of some radioactive mustard-type vesicants with purified proteins Journal of the American Chemical Society. 70: 2547-2550. |
0.693 |
|
1947 |
CHANDLER JP, GERRARD MW, DU VIGNEAUD V. The utilization for animal growth of tobacco mosaic virus as a sole source of protein in the diet The Journal of Biological Chemistry. 171: 823-828. PMID 20272122 |
0.195 |
|
1947 |
DU VIGNEAUD V, STEVENS CM. Preparation of highly purified mustard gas and its action on yeast. Journal of the American Chemical Society. 69: 1808. PMID 20251425 |
0.209 |
|
1947 |
Du Vigneaud V, Stevens CM. Preparation of highly purified mustard gas and its action on yeast Journal of the American Chemical Society. 69: 1808-1809. |
0.209 |
|
1946 |
Du VIGNEAUD V, CARPENTER FH. Synthetic penicillin. Science (New York, N.Y.). 104: 431-3. PMID 21001954 |
0.743 |
|
1946 |
WOOD JL, Du VIGNEAUD V. A note on the conversion in vivo of the S-benzyl-N-methyl derivatives of cysteine and homocysteine to the N-acetyl-S-benzyl derivatives of cysteine and homocysteine The Journal of Biological Chemistry. 165: 95. PMID 21001189 |
0.253 |
|
1946 |
Du VIGNEAUD V, CHANDLER JP. The rôle of dimethyl- and monomethylaminoethanol in transmethylation reactions in vivo The Journal of Biological Chemistry. 164: 603-613. PMID 21001156 |
0.227 |
|
1946 |
BROWN GB, Du VIGNEAUD V. The thiourea analogue of desthiobiotin The Journal of Biological Chemistry. 163: 761-766. PMID 20985649 |
0.333 |
|
1946 |
Du VIGNEAUD V, SIMMONDS S. A further investigation of the role of betaine in transmethylation reactions in vivo The Journal of Biological Chemistry. 165: 639-648. PMID 20276130 |
0.217 |
|
1946 |
Du VIGNEAUD V, SIMMONDS S, COHN M. A further investigation of the ability of sarcosine to serve as a labile methyl donor. The Journal of Biological Chemistry. 166: 47-52. PMID 20273672 |
0.488 |
|
1946 |
ANSLOW WP, SIMMONDS S, Du VIGNEAUD V. The synthesis of the isomers of cystathionine and a study of their availability in sulfur metabolism The Journal of Biological Chemistry. 166: 35-45. PMID 20273671 |
0.296 |
|
1946 |
du Vigneaud V, Carpenter FH, Holley RW, Livermore AH, Rachele JR. Synthetic Penicillin. Science (New York, N.Y.). 104: 431-50. PMID 17819685 DOI: 10.1126/science.104.2706.431 |
0.764 |
|
1945 |
Wood JL, Du Vigneaud V. The synthesis of optically inactive desthiobiotin Journal of the American Chemical Society. 67: 210-212. |
0.273 |
|
1945 |
Banerjee S, Dittmer K, Du Vigneaud V. A microbiological and fluorometric test for minute amounts of alloxan 1,2 Science. 101: 647-649. |
0.212 |
|
1944 |
Dittmer K, Melville DB, DU Vigneaud V. THE POSSIBLE SYNTHESIS OF BIOTIN FROM DESTHIOBIOTIN BY YEAST AND THE ANTI-BIOTIN EFFECT OF DESTHIOBIOTIN FOR L. CASEI. Science (New York, N.Y.). 99: 203-5. PMID 17783711 DOI: 10.1126/Science.99.2567.203 |
0.714 |
|
1943 |
Irving GW, du Vigneaud V. HORMONES OF THE POSTERIOR LOBE OF THE PITUITARY GLAND Annals of the New York Academy of Sciences. 43: 273-307. DOI: 10.1111/j.1749-6632.1943.tb54084.x |
0.22 |
|
1942 |
DU Vigneaud V, Spangler JM, Burk D, Kensler CJ, Sugiura K, Rhoads CP. THE PROCARCINOGENIC EFFECT OF BIOTIN IN BUTTER YELLOW TUMOR FORMATION. Science (New York, N.Y.). 95: 174-6. PMID 17818886 DOI: 10.1126/science.95.2459.174 |
0.183 |
|
1941 |
Melville DB, Hofmann K, DU Vigneaud V. RESYNTHESIS OF BIOTIN FROM A DEGRADATION PRODUCT. Science (New York, N.Y.). 94: 308-9. PMID 17809737 DOI: 10.1126/Science.94.2439.308 |
0.559 |
|
1940 |
DU Vigneaud V, Melville DB, György P, Rose CS. ON THE IDENTITY OF VITAMIN H WITH BIOTIN. Science (New York, N.Y.). 92: 62-3. PMID 17831766 DOI: 10.1126/Science.92.2377.62 |
0.195 |
|
1940 |
György P, Melville DB, Burk D, DU Vigneaud V. THE POSSIBLE IDENTITY OF VITAMIN H WITH BIOTIN AND COENZYME R. Science (New York, N.Y.). 91: 243-5. PMID 17831182 DOI: 10.1126/Science.91.2358.243 |
0.194 |
|
1940 |
György P, Rose CS, Hofmann K, Melville DB, DU Vigneaud V. A FURTHER NOTE ON THE IDENTITY OF VITAMIN H WITH BIOTIN. Science (New York, N.Y.). 92: 609. PMID 17795447 DOI: 10.1126/Science.92.2400.609 |
0.551 |
|
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