Shenker A - Search Results

1

Thyroid carcinoma in the McCune-Albright syndrome: contributory role of activating Gs alpha mutations.

Collins MT, Sarlis NJ, Merino MJ, Monroe J, Crawford SE, Krakoff JA, Guthrie LC, Bonat S, Robey PG, Shenker A. Collins MT, et al. Among authors: shenker a. J Clin Endocrinol Metab. 2003 Sep;88(9):4413-7. doi: 10.1210/jc.2002-021642. J Clin Endocrinol Metab. 2003. PMID: 12970318

2

Activating mutations of the stimulatory G protein in the McCune-Albright syndrome.

Weinstein LS, Shenker A, Gejman PV, Merino MJ, Friedman E, Spiegel AM. Weinstein LS, et al. Among authors: shenker a. N Engl J Med. 1991 Dec 12;325(24):1688-95. doi: 10.1056/NEJM199112123252403. N Engl J Med. 1991. PMID: 1944469 Free article.

3

The histopathology of fibrous dysplasia of bone in patients with activating mutations of the Gs alpha gene: site-specific patterns and recurrent histological hallmarks.

Riminucci M, Liu B, Corsi A, Shenker A, Spiegel AM, Robey PG, Bianco P. Riminucci M, et al. Among authors: shenker a. J Pathol. 1999 Jan;187(2):249-58. doi: 10.1002/(SICI)1096-9896(199901)187:2<249::AID-PATH222>3.0.CO;2-J. J Pathol. 1999. PMID: 10365102

4

An activating Gs alpha mutation is present in fibrous dysplasia of bone in the McCune-Albright syndrome.

Shenker A, Weinstein LS, Sweet DE, Spiegel AM. Shenker A, et al. J Clin Endocrinol Metab. 1994 Sep;79(3):750-5. doi: 10.1210/jcem.79.3.8077356. J Clin Endocrinol Metab. 1994. PMID: 8077356

5

Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein GS.

Shenker A, Weinstein LS, Moran A, Pescovitz OH, Charest NJ, Boney CM, Van Wyk JJ, Merino MJ, Feuillan PP, Spiegel AM. Shenker A, et al. J Pediatr. 1993 Oct;123(4):509-18. doi: 10.1016/s0022-3476(05)80943-6. J Pediatr. 1993. PMID: 8410501

6

Screening of candidate oncogenes in human thyrotroph tumors: absence of activating mutations of the G alpha q, G alpha 11, G alpha s, or thyrotropin-releasing hormone receptor genes.

Dong Q, Brucker-Davis F, Weintraub BD, Smallridge RC, Carr FE, Battey J, Spiegel AM, Shenker A. Dong Q, et al. Among authors: shenker a. J Clin Endocrinol Metab. 1996 Mar;81(3):1134-40. doi: 10.1210/jcem.81.3.8772588. J Clin Endocrinol Metab. 1996. PMID: 8772588

7

Fibrous dysplasia of bone in the McCune-Albright syndrome: abnormalities in bone formation.

Riminucci M, Fisher LW, Shenker A, Spiegel AM, Bianco P, Gehron Robey P. Riminucci M, et al. Among authors: shenker a. Am J Pathol. 1997 Dec;151(6):1587-600. Am J Pathol. 1997. PMID: 9403710 Free PMC article.

8

G protein mutations in human disease.

Weinstein LS, Shenker A. Weinstein LS, et al. Among authors: shenker a. Clin Biochem. 1993 Oct;26(5):333-8. doi: 10.1016/0009-9120(93)90109-j. Clin Biochem. 1993. PMID: 8299203 Review.

9

G protein-coupled receptor structure and function: the impact of disease-causing mutations.

Shenker A. Shenker A. Baillieres Clin Endocrinol Metab. 1995 Jul;9(3):427-51. doi: 10.1016/s0950-351x(95)80519-2. Baillieres Clin Endocrinol Metab. 1995. PMID: 7575327 Review.

10

Osteoblastic cells derived from isolated lesions of fibrous dysplasia contain activating somatic mutations of the Gs alpha gene.

Shenker A, Chanson P, Weinstein LS, Chi P, Spiegel AM, Lomri A, Marie PJ. Shenker A, et al. Hum Mol Genet. 1995 Sep;4(9):1675-6. doi: 10.1093/hmg/4.9.1675. Hum Mol Genet. 1995. PMID: 8541861 No abstract available.

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