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Items: 1 to 20 of 56

1.

Minireview: GNAS: normal and abnormal functions.

Weinstein LS, Liu J, Sakamoto A, Xie T, Chen M.

Endocrinology. 2004 Dec;145(12):5459-64. Epub 2004 Aug 26. Review.

PMID:
15331575
2.

Endocrine manifestations of stimulatory G protein alpha-subunit mutations and the role of genomic imprinting.

Weinstein LS, Yu S, Warner DR, Liu J.

Endocr Rev. 2001 Oct;22(5):675-705. Review.

PMID:
11588148
3.

Gs(alpha) mutations and imprinting defects in human disease.

Weinstein LS, Chen M, Liu J.

Ann N Y Acad Sci. 2002 Jun;968:173-97. Review.

PMID:
12119276
4.

The GNAS locus and pseudohypoparathyroidism.

Bastepe M.

Adv Exp Med Biol. 2008;626:27-40. Review.

PMID:
18372789
5.

[Paternal GNAS mutations: Which phenotypes? What genetic counseling?].

Kottler ML.

Ann Endocrinol (Paris). 2015 May;76(2):105-9. doi: 10.1016/j.ando.2015.03.010. Epub 2015 May 4. Review. French.

PMID:
25952723
6.

Studies of the regulation and function of the Gs alpha gene Gnas using gene targeting technology.

Weinstein LS, Xie T, Zhang QH, Chen M.

Pharmacol Ther. 2007 Aug;115(2):271-91. Epub 2007 Apr 21. Review.

7.

The role of GNAS and other imprinted genes in the development of obesity.

Weinstein LS, Xie T, Qasem A, Wang J, Chen M.

Int J Obes (Lond). 2010 Jan;34(1):6-17. doi: 10.1038/ijo.2009.222. Epub 2009 Oct 20. Review.

8.

[Pseudopseudohypoparathyroidism and genomic imprinting].

Minagawa M.

Clin Calcium. 2007 Aug;17(8):1229-33. Review. Japanese.

PMID:
17660620
9.

GNAS imprinting and pituitary tumors.

Mantovani G, Lania AG, Spada A.

Mol Cell Endocrinol. 2010 Sep 15;326(1-2):15-8. doi: 10.1016/j.mce.2010.04.009. Epub 2010 Apr 14. Review.

PMID:
20398730
10.

GNAS Spectrum of Disorders.

Turan S, Bastepe M.

Curr Osteoporos Rep. 2015 Jun;13(3):146-58. doi: 10.1007/s11914-015-0268-x. Review.

11.

GNAS locus and pseudohypoparathyroidism.

Bastepe M, Jüppner H.

Horm Res. 2005;63(2):65-74. Epub 2005 Feb 9. Review.

PMID:
15711092
12.

[Epigenetics and pseudohypoparathyroidism].

Richard N, Abéguilé G, Coudray N, Kottler ML.

Pathol Biol (Paris). 2010 Oct;58(5):367-71. doi: 10.1016/j.patbio.2009.09.007. Epub 2009 Nov 25. Review. French.

PMID:
19942373
13.

G(s)alpha mutations in fibrous dysplasia and McCune-Albright syndrome.

Weinstein LS.

J Bone Miner Res. 2006 Dec;21 Suppl 2:P120-4. Review.

14.

An update on the clinical and molecular characteristics of pseudohypoparathyroidism.

Levine MA.

Curr Opin Endocrinol Diabetes Obes. 2012 Dec;19(6):443-51. doi: 10.1097/MED.0b013e32835a255c. Review.

15.

Variable imprinting of the heterotrimeric G protein G(s) alpha-subunit within different segments of the nephron.

Weinstein LS, Yu S, Ecelbarger CA.

Am J Physiol Renal Physiol. 2000 Apr;278(4):F507-14. Review.

16.

Recent advances in GNAS epigenetic research of pseudohypoparathyroidism.

Izzi B, Van Geet C, Freson K.

Curr Mol Med. 2012 Jun;12(5):566-73. Review.

PMID:
22300135
17.
18.

Albright's hereditary osteodystrophy and pseudohypoparathyroidism.

Wilson LC, Hall CM.

Semin Musculoskelet Radiol. 2002 Dec;6(4):273-83. Review.

PMID:
12541184
19.

GNAS mutations in Pseudohypoparathyroidism type 1a and related disorders.

Lemos MC, Thakker RV.

Hum Mutat. 2015 Jan;36(1):11-9. doi: 10.1002/humu.22696. Epub 2014 Nov 28. Review.

20.

Pseudohypoparathyroidism type Ia. Albright hereditary osteodystrophy: a model for research on G protein-coupled receptors and genomic imprinting.

Simon A, Koppeschaar HP, Roijers JF, Höppener JW, Lips CJ.

Neth J Med. 2000 Mar;56(3):100-9. Review.

PMID:
10759021

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