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I L SCHWARTZ

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Articles 156
Citations 942
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Recent Articles
1.
SCHWARTZ I
Tech Rep Brookhaven Natl Lab . 2014 Feb; 685:18. PMID: 24546707
No abstract available.
2.
SCHWARTZ I
Kidney Int . 1996 Jun; 49(6):1530-3. PMID: 8743448
No abstract available.
3.
SCHWARTZ I
Am J Prev Med . 1991 Nov; 7(6):363-73. PMID: 1790044
Sexual assault of women in the United States may have a prevalence rate of 25% or more. Moreover, the majority of survivors of sexual assault know their assailants. Consequences of...
4.
SCHWARTZ I
West J Med . 1990 Jun; 152(6):725-8. PMID: 2353489
Low birth weight is the major determinant of infant mortality. Continuing declines in infant mortality in the United States are due to the use of neonatal intensive care services; less...
5.
Gazis D, Glass J, SCHWARTZ I, Stavropoulos G, Theodoropoulos D
Int J Pept Protein Res . 1989 Nov; 34(5):353-7. PMID: 2613436
Solution methods, using N-hydroxysuccinimide esters, were used to synthesize [Glu(NHNH2)4] oxytocin and [Glu(NHNH2)4, Lys8] vasopressin. In these analogs of neurohypophyseal hormones, the side-chain carboxamide function of a glutamine residue is...
6.
Eggena P, Buku A, Ma C, Wyssbrod H, Gazis D, SCHWARTZ I, et al.
Endocrinology . 1987 Dec; 121(6):2245-50. PMID: 3119316
This study reports the synthesis and biological activities of 1-desamino, 7-lysine-(4-azidobenzoyl), 8-arginine vasotocin (d7-N3-AVT). This compound was found to be biologically active in the rat antidiuretic assay (20 U/mg), to...
7.
Fahrenholz F, Eggena P, Kojro E, Gazis D, SCHWARTZ I
Int J Pept Protein Res . 1987 Nov; 30(5):577-82. PMID: 2830197
The present study describes the synthesis and biological activities of the photoreactive vasotocin analog 1-deamino[8-lysine(N epsilon-4-azidobenzoyl)] vasotocin ([Mpa1, Lys(N epsilon-4-azidobenzoyl)8]vasotocin). The analog was obtained by introducing the photoreactive aryl azido...
8.
Buku A, SCHWARTZ I, Yamin N, Wyssbrod H, Gazis D
J Med Chem . 1987 Aug; 30(8):1509-12. PMID: 3612693
Three arginine-vasopressin (AVP) analogues in which the proline residue in position 7 was substituted with 4-hydroxyproline were synthesized by solid-phase techniques, and their biological activities were evaluated by antidiuretic, pressor,...
9.
Buku A, Eggena P, Wyssbrod H, SCHWARTZ I, Gazis D, Somoza L, et al.
J Med Chem . 1987 Aug; 30(8):1526-9. PMID: 3112398
The chemically reactive groups of [8-arginine]vasotocin (AVT) are the alpha-amino group in position 1, the phenolic hydroxyl group of the tyrosyl residue in position 2, and the side-chain functional group...
10.
Eggena P, Buku A, Ma C, Somoza L, Wyssbrod H, SCHWARTZ I, et al.
Am J Physiol . 1987 Jun; 252(6 Pt 1):C657-62. PMID: 3109249
A photoreactive analogue of vasotocin, [1-desamino,4-lysine(azidobenzoyl),8-arginine]vasotocin (4-N3-AVT), has been examined in the isolated toad urinary bladder for biological activity and binding to hormonal receptors. Although 4-N3-AVT induced only a small...