Levine MA - Search Results

1

Discordance between genetic and epigenetic defects in pseudohypoparathyroidism type 1b revealed by inconsistent loss of maternal imprinting at GNAS1.

Jan de Beur S, Ding C, Germain-Lee E, Cho J, Maret A, Levine MA. Jan de Beur S, et al. Among authors: levine ma. Am J Hum Genet. 2003 Aug;73(2):314-22. doi: 10.1086/377136. Epub 2003 Jul 11. Am J Hum Genet. 2003. PMID: 12858292 Free PMC article.

2

The pseudohypoparathyroidism type lb locus is linked to a region including GNAS1 at 20q13.3.

Jan De Beur SM, O'Connell JR, Peila R, Cho J, Deng Z, Kam S, Levine MA. Jan De Beur SM, et al. Among authors: levine ma. J Bone Miner Res. 2003 Mar;18(3):424-33. doi: 10.1359/jbmr.2003.18.3.424. J Bone Miner Res. 2003. PMID: 12619926 Free article.

3

Growth hormone deficiency in pseudohypoparathyroidism type 1a: another manifestation of multihormone resistance.

Germain-Lee EL, Groman J, Crane JL, Jan de Beur SM, Levine MA. Germain-Lee EL, et al. Among authors: levine ma. J Clin Endocrinol Metab. 2003 Sep;88(9):4059-69. doi: 10.1210/jc.2003-030028. J Clin Endocrinol Metab. 2003. PMID: 12970262

4

High-throughput Molecular Analysis of Pseudohypoparathyroidism 1b Patients Reveals Novel Genetic and Epigenetic Defects.

Danzig J, Li D, Jan de Beur S, Levine MA. Danzig J, et al. Among authors: levine ma. J Clin Endocrinol Metab. 2021 Oct 21;106(11):e4603-e4620. doi: 10.1210/clinem/dgab460. J Clin Endocrinol Metab. 2021. PMID: 34157100 Free PMC article.

5

Paternal imprinting of Galpha(s) in the human thyroid as the basis of TSH resistance in pseudohypoparathyroidism type 1a.

Germain-Lee EL, Ding CL, Deng Z, Crane JL, Saji M, Ringel MD, Levine MA. Germain-Lee EL, et al. Among authors: levine ma. Biochem Biophys Res Commun. 2002 Aug 9;296(1):67-72. doi: 10.1016/s0006-291x(02)00833-1. Biochem Biophys Res Commun. 2002. PMID: 12147228

6

Pseudohypoparathyroidism 1b: exclusion of parathyroid hormone and its receptors as candidate disease genes.

Jan de Beur SM, Ding CL, LaBuda MC, Usdin TB, Levine MA. Jan de Beur SM, et al. Among authors: levine ma. J Clin Endocrinol Metab. 2000 Jun;85(6):2239-46. doi: 10.1210/jcem.85.6.6620. J Clin Endocrinol Metab. 2000. PMID: 10852457

7

Genetic basis for resistance to parathyroid hormone.

Levine MA, Germain-Lee E, Jan de Beur S. Levine MA, et al. Horm Res. 2003;60 Suppl 3:87-95. doi: 10.1159/000074508. Horm Res. 2003. PMID: 14671404 Review.

8

A mouse model of albright hereditary osteodystrophy generated by targeted disruption of exon 1 of the Gnas gene.

Germain-Lee EL, Schwindinger W, Crane JL, Zewdu R, Zweifel LS, Wand G, Huso DL, Saji M, Ringel MD, Levine MA. Germain-Lee EL, et al. Among authors: levine ma. Endocrinology. 2005 Nov;146(11):4697-709. doi: 10.1210/en.2005-0681. Epub 2005 Aug 11. Endocrinology. 2005. PMID: 16099856

9

Body mass index differences in pseudohypoparathyroidism type 1a versus pseudopseudohypoparathyroidism may implicate paternal imprinting of Galpha(s) in the development of human obesity.

Long DN, McGuire S, Levine MA, Weinstein LS, Germain-Lee EL. Long DN, et al. Among authors: levine ma. J Clin Endocrinol Metab. 2007 Mar;92(3):1073-9. doi: 10.1210/jc.2006-1497. Epub 2006 Dec 12. J Clin Endocrinol Metab. 2007. PMID: 17164301

10

Imprinting status of Galpha(s), NESP55, and XLalphas in cell cultures derived from human embryonic germ cells: GNAS imprinting in human embryonic germ cells.

Crane JL, Shamblott MJ, Axelman J, Hsu S, Levine MA, Germain-Lee EL. Crane JL, et al. Among authors: levine ma. Clin Transl Sci. 2009 Oct;2(5):355-60. doi: 10.1111/j.1752-8062.2009.00148.x. Clin Transl Sci. 2009. PMID: 20443919 Free PMC article.

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