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Genetics of non-insulin-dependent (type-II) diabetes mellitus.
Kahn CR, Vicent D, Doria A. Kahn CR, et al. Annu Rev Med. 1996;47:509-31. doi: 10.1146/annurev.med.47.1.509. Annu Rev Med. 1996. PMID: 8712800 Review.
Some evidence of involvement has been produced for insulin-receptor substrate-1, glycogen synthase, the glucagon receptor, a ras-related protein (Rad), histocompatibility antigens, PC-1, and fatty acid binding protein, but the contributions of these genes to NIDDM is proba …
Some evidence of involvement has been produced for insulin-receptor substrate-1, glycogen synthase, the glucagon receptor, a ras-rela …
Trinucleotide repeats at the rad locus. Allele distributions in NIDDM and mapping to a 3-cM region on chromosome 16q.
Doria A, Caldwell JS, Ji L, Reynet C, Rich SS, Weremowicz S, Morton CC, Warram JH, Kahn CR, Krolewski AS. Doria A, et al. Diabetes. 1995 Feb;44(2):243-7. doi: 10.2337/diab.44.2.243. Diabetes. 1995. PMID: 7859947
A 10-allele polymorphism was identified in rad (ras associated with diabetes), a gene that is overexpressed in non-insulin-dependent diabetes mellitus (NIDDM) muscle. The polymorphism, designated RAD1, consists of a variable number of trinucleotide repeats (G
A 10-allele polymorphism was identified in rad (ras associated with diabetes), a gene that is overexpressed in non-insulin-dep
Genetic predisposition to diabetic nephropathy. Evidence for a role of the angiotensin I--converting enzyme gene.
Doria A, Warram JH, Krolewski AS. Doria A, et al. Diabetes. 1994 May;43(5):690-5. doi: 10.2337/diab.43.5.690. Diabetes. 1994. PMID: 7909524
DNA from each of these patients was genotyped at the ACE locus by a three-allele restriction fragment-melting polymorphism (RFMP) (Dde I), which we described recently, and a two-allele insertion/deletion recognized as an Xba I restriction fragment-length polymorphis …
DNA from each of these patients was genotyped at the ACE locus by a three-allele restriction fragment-melting polymorphism (RFMP) (Dd …
Angiotensinogen polymorphism M235T, hypertension, and nephropathy in insulin-dependent diabetes.
Doria A, Onuma T, Gearin G, Freire MB, Warram JH, Krolewski AS. Doria A, et al. Hypertension. 1996 May;27(5):1134-9. doi: 10.1161/01.hyp.27.5.1134. Hypertension. 1996. PMID: 8621207
The allele 235T (a threonine in place of a methionine at position 235) of angiotensinogen has been found to be associated with a predisposition to essential hypertension. ...Under a recessive model, allele 235T homozygotes had a 1.6-fold risk of …
The allele 235T (a threonine in place of a methionine at position 235) of angiotensinogen has been found to be associated with …
Codon 972 polymorphism in the insulin receptor substrate-1 gene, obesity, and risk of noninsulin-dependent diabetes mellitus.
Sigal RJ, Doria A, Warram JH, Krolewski AS. Sigal RJ, et al. J Clin Endocrinol Metab. 1996 Apr;81(4):1657-9. doi: 10.1210/jcem.81.4.8636384. J Clin Endocrinol Metab. 1996. PMID: 8636384
Modest associations between NIDDM and a GGG-->AGG single base substitution (corresponding to a glycine-->arginine amino acid substitution) in codon 972 of the gene have been found, but none reached statistical significance. ...In addition, we looked for a
Modest associations between NIDDM and a GGG-->AGG single base substitution (corresponding to a glycine-->arginine amino …
Diabetes susceptibility at IDDM2 cannot be positively mapped to the VNTR locus of the insulin gene.
Doria A, Lee J, Warram JH, Krolewski AS. Doria A, et al. Diabetologia. 1996 May;39(5):594-9. doi: 10.1007/BF00403307. Diabetologia. 1996. PMID: 8739920
Patients and control subjects were genotyped at INS/+ 1140 A/C (a surrogate for the variable number tandem repeat (VNTR) polymorphism in the regulatory part of the INS gene) and a marker 5' of the tyrosine hydroxylase (TH) gene, TH/pINS500-RsaI, making it 10 …
Patients and control subjects were genotyped at INS/+ 1140 A/C (a surrogate for the variable number tandem repeat (VNTR) polym …
Molecular cloning of the human rad gene: gene structure and complete nucleotide sequence.
Caldwell JS, Moyers JS, Doria A, Reynet C, Kahn RC. Caldwell JS, et al. Biochim Biophys Acta. 1996 Aug 23;1316(3):145-8. doi: 10.1016/0925-4439(96)00034-8. Biochim Biophys Acta. 1996. PMID: 8781531
Synergistic effect of angiotensin II type 1 receptor genotype and poor glycaemic control on risk of nephropathy in IDDM.
Doria A, Onuma T, Warram JH, Krolewski AS. Doria A, et al. Diabetologia. 1997 Nov;40(11):1293-9. doi: 10.1007/s001250050823. Diabetologia. 1997. PMID: 9389421
A similar pattern of higher risk of microalbuminuria, specifically among those carriers of allele C1166 who had poor glycaemic control was also found in an independent study of a cross-sectional sample of 551 IDDM individuals, although the effect was smaller in magn
A similar pattern of higher risk of microalbuminuria, specifically among those carriers of allele C1166 who had poor glycaemic contro
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