Germain-Lee E - 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. 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

Hypocalcemia in nonwhite breast-fed infants. Vitamin D deficiency revisited.

Chang YT, Germain-Lee EL, Doran TF, Migeon CJ, Levine MA, Berkovitz GD. Chang YT, et al. Clin Pediatr (Phila). 1992 Nov;31(11):695-8. doi: 10.1177/000992289203101111. Clin Pediatr (Phila). 1992. PMID: 1424401 No abstract available.

3

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. 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

4

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. J Clin Endocrinol Metab. 2003 Sep;88(9):4059-69. doi: 10.1210/jc.2003-030028. J Clin Endocrinol Metab. 2003. PMID: 12970262

5

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.

6

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. Endocrinology. 2005 Nov;146(11):4697-709. doi: 10.1210/en.2005-0681. Epub 2005 Aug 11. Endocrinology. 2005. PMID: 16099856

7

Short stature, obesity, and growth hormone deficiency in pseudohypoparathyroidism type 1a.

Germain-Lee EL. Germain-Lee EL. Pediatr Endocrinol Rev. 2006 Apr;3 Suppl 2:318-27. Pediatr Endocrinol Rev. 2006. PMID: 16675931 Review.

8

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. 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

9

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. 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.

10

Hypercalcemia in children and adolescents.

Lietman SA, Germain-Lee EL, Levine MA. Lietman SA, et al. Curr Opin Pediatr. 2010 Aug;22(4):508-15. doi: 10.1097/MOP.0b013e32833b7c23. Curr Opin Pediatr. 2010. PMID: 20601885 Free PMC article. Review.

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