Raben N - Search Results

1

Molecular scanning for mutations in the insulin receptor substrate-1 (IRS-1) gene in Mexican Americans with Type 2 diabetes mellitus.

Celi FS, Negri C, Tanner K, Raben N, De Pablo F, Rovira A, Pallardo LF, Martin-Vaquero P, Stern MP, Mitchell BD, Shuldiner AR. Celi FS, et al. Among authors: raben n. Diabetes Metab Res Rev. 2000 Sep-Oct;16(5):370-7. doi: 10.1002/1520-7560(2000)9999:9999<::aid-dmrr129>3.0.co;2-b. Diabetes Metab Res Rev. 2000. PMID: 11025561

2

Molecular scanning of the beta-3-adrenergic receptor gene in Pima Indians and Caucasians.

Silver K, Walston J, Yang Y, Pratley R, Ravussin E, Raben N, Shuldiner AR. Silver K, et al. Among authors: raben n. Diabetes Metab Res Rev. 1999 May-Jun;15(3):175-80. doi: 10.1002/(sici)1520-7560(199905/06)15:3<175::aid-dmrr34>3.0.co;2-y. Diabetes Metab Res Rev. 1999. PMID: 10441039 Clinical Trial.

3

Time of onset of non-insulin-dependent diabetes mellitus and genetic variation in the beta 3-adrenergic-receptor gene.

Walston J, Silver K, Bogardus C, Knowler WC, Celi FS, Austin S, Manning B, Strosberg AD, Stern MP, Raben N, et al. Walston J, et al. Among authors: raben n. N Engl J Med. 1995 Aug 10;333(6):343-7. doi: 10.1056/NEJM199508103330603. N Engl J Med. 1995. PMID: 7609750 Free article.

4

Detection of mutations in insulin receptor gene by denaturing gradient gel electrophoresis.

Barbetti F, Gejman PV, Taylor SI, Raben N, Cama A, Bonora E, Pizzo P, Moghetti P, Muggeo M, Roth J. Barbetti F, et al. Among authors: raben n. Diabetes. 1992 Apr;41(4):408-15. doi: 10.2337/diab.41.4.408. Diabetes. 1992. PMID: 1607067

5

Normal coding sequence of insulin gene in Pima Indians and Nauruans, two groups with highest prevalence of type II diabetes.

Raben N, Barbetti F, Cama A, Lesniak MA, Lillioja S, Zimmet P, Serjeantson SW, Taylor SI, Roth J. Raben N, et al. Diabetes. 1991 Jan;40(1):118-22. doi: 10.2337/diab.40.1.118. Diabetes. 1991. PMID: 2015966

6

Barbetti F, Raben N, Kadowaki T, Cama A, Accili D, Gabbay KH, Merenich JA, Taylor SI, Roth J. Barbetti F, et al. Among authors: raben n. J Clin Endocrinol Metab. 1990 Jul;71(1):164-9. doi: 10.1210/jcem-71-1-164. J Clin Endocrinol Metab. 1990. PMID: 2196279

7

Common mutations in the phosphofructokinase-M gene in Ashkenazi Jewish patients with glycogenesis VII--and their population frequency.

Sherman JB, Raben N, Nicastri C, Argov Z, Nakajima H, Adams EM, Eng CM, Cowan TM, Plotz PH. Sherman JB, et al. Among authors: raben n. Am J Hum Genet. 1994 Aug;55(2):305-13. Am J Hum Genet. 1994. PMID: 8037209 Free PMC article.

8

Mutations in muscle phosphofructokinase gene.

Raben N, Sherman JB. Raben N, et al. Hum Mutat. 1995;6(1):1-6. doi: 10.1002/humu.1380060102. Hum Mutat. 1995. PMID: 7550225 Review.

9

A 5' splice junction mutation leading to exon deletion in an Ashkenazic Jewish family with phosphofructokinase deficiency (Tarui disease).

Raben N, Sherman J, Miller F, Mena H, Plotz P. Raben N, et al. J Biol Chem. 1993 Mar 5;268(7):4963-7. J Biol Chem. 1993. PMID: 8444874 Free article.

10

The value of muscle biopsies in Pompe disease: identifying lipofuscin inclusions in juvenile- and adult-onset patients.

Feeney EJ, Austin S, Chien YH, Mandel H, Schoser B, Prater S, Hwu WL, Ralston E, Kishnani PS, Raben N. Feeney EJ, et al. Among authors: raben n. Acta Neuropathol Commun. 2014 Jan 2;2:2. doi: 10.1186/2051-5960-2-2. Acta Neuropathol Commun. 2014. PMID: 24383498 Free PMC article.

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