296 related articles for article (PubMed ID: 20887824)
1. Potent constitutive cyclic AMP-generating activity of XLαs implicates this imprinted GNAS product in the pathogenesis of McCune-Albright syndrome and fibrous dysplasia of bone.
Mariot V; Wu JY; Aydin C; Mantovani G; Mahon MJ; Linglart A; Bastepe M
Bone; 2011 Feb; 48(2):312-20. PubMed ID: 20887824
[TBL] [Abstract][Full Text] [Related]
2. Coding GNAS mutations leading to hormone resistance impair in vitro agonist- and cholera toxin-induced adenosine cyclic 3',5'-monophosphate formation mediated by human XLalphas.
Linglart A; Mahon MJ; Kerachian MA; Berlach DM; Hendy GN; Jüppner H; Bastepe M
Endocrinology; 2006 May; 147(5):2253-62. PubMed ID: 16484323
[TBL] [Abstract][Full Text] [Related]
3. GNAS mutation detection is related to disease severity in girls with McCune-Albright syndrome and precocious puberty.
Wagoner HA; Steinmetz R; Bethin KE; Eugster EA; Pescovitz OH; Hannon TS
Pediatr Endocrinol Rev; 2007 Aug; 4 Suppl 4():395-400. PubMed ID: 17982386
[TBL] [Abstract][Full Text] [Related]
4. A highly sensitive polymerase chain reaction method detects activating mutations of the GNAS gene in peripheral blood cells in McCune-Albright syndrome or isolated fibrous dysplasia.
Lietman SA; Ding C; Levine MA
J Bone Joint Surg Am; 2005 Nov; 87(11):2489-94. PubMed ID: 16264125
[TBL] [Abstract][Full Text] [Related]
5. Intragenic suppression of a constitutively active allele of Gsα associated with McCune-Albright syndrome.
Tobar-Rubin R; Sultan D; Janevska D; Turcic K; Carroll J; Ooms L; Pals-Rylaarsdam R
J Mol Endocrinol; 2013 Apr; 50(2):193-201. PubMed ID: 23288949
[TBL] [Abstract][Full Text] [Related]
6. Fibrous Dysplasia/McCune-Albright Syndrome: Clinical and Translational Perspectives.
Robinson C; Collins MT; Boyce AM
Curr Osteoporos Rep; 2016 Oct; 14(5):178-86. PubMed ID: 27492469
[TBL] [Abstract][Full Text] [Related]
7. GNAS gene mutations affecting XLαs and bone health: A long neglected relationship.
Xie Y; Chen X; Xie Y; Yu X
Clin Genet; 2023 Sep; 104(3):279-286. PubMed ID: 37249323
[TBL] [Abstract][Full Text] [Related]
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
Endocrinology; 2005 Nov; 146(11):4697-709. PubMed ID: 16099856
[TBL] [Abstract][Full Text] [Related]
9. GNAS transcripts in skeletal progenitors: evidence for random asymmetric allelic expression of Gs alpha.
Michienzi S; Cherman N; Holmbeck K; Funari A; Collins MT; Bianco P; Robey PG; Riminucci M
Hum Mol Genet; 2007 Aug; 16(16):1921-30. PubMed ID: 17566083
[TBL] [Abstract][Full Text] [Related]
10. Extra-long Gαs variant XLαs protein escapes activation-induced subcellular redistribution and is able to provide sustained signaling.
Liu Z; Turan S; Wehbi VL; Vilardaga JP; Bastepe M
J Biol Chem; 2011 Nov; 286(44):38558-38569. PubMed ID: 21890629
[TBL] [Abstract][Full Text] [Related]
11. Minireview: GNAS: normal and abnormal functions.
Weinstein LS; Liu J; Sakamoto A; Xie T; Chen M
Endocrinology; 2004 Dec; 145(12):5459-64. PubMed ID: 15331575
[TBL] [Abstract][Full Text] [Related]
12. Genetic and molecular aspects of McCune-Albright syndrome.
Lietman SA; Schwindinger WF; Levine MA
Pediatr Endocrinol Rev; 2007 Aug; 4 Suppl 4():380-5. PubMed ID: 17982384
[TBL] [Abstract][Full Text] [Related]
13. Maternal
Cui Q; Aksu C; Ay B; Remillard CE; Plagge A; Gardezi M; Dunlap M; Gerstenfeld LC; He Q; Bastepe M
Front Genet; 2021; 12():680537. PubMed ID: 34220953
[No Abstract] [Full Text] [Related]
14. Constitutive stimulatory G protein activity in limb mesenchyme impairs bone growth.
Karaca A; Malladi VR; Zhu Y; Tafaj O; Paltrinieri E; Wu JY; He Q; Bastepe M
Bone; 2018 May; 110():230-237. PubMed ID: 29471062
[TBL] [Abstract][Full Text] [Related]
15. Expression of FGF23 is correlated with serum phosphate level in isolated fibrous dysplasia.
Kobayashi K; Imanishi Y; Koshiyama H; Miyauchi A; Wakasa K; Kawata T; Goto H; Ohashi H; Koyano HM; Mochizuki R; Miki T; Inaba M; Nishizawa Y
Life Sci; 2006 Apr; 78(20):2295-301. PubMed ID: 16337659
[TBL] [Abstract][Full Text] [Related]
16. Activating Gsalpha mutations: analysis of 113 patients with signs of McCune-Albright syndrome--a European Collaborative Study.
Lumbroso S; Paris F; Sultan C;
J Clin Endocrinol Metab; 2004 May; 89(5):2107-13. PubMed ID: 15126527
[TBL] [Abstract][Full Text] [Related]
17. Functional characterization of GNAS mutations found in patients with pseudohypoparathyroidism type Ic defines a new subgroup of pseudohypoparathyroidism affecting selectively Gsα-receptor interaction.
Thiele S; de Sanctis L; Werner R; Grötzinger J; Aydin C; Jüppner H; Bastepe M; Hiort O
Hum Mutat; 2011 Jun; 32(6):653-60. PubMed ID: 21488135
[TBL] [Abstract][Full Text] [Related]
18. Three intragenic suppressors of a GTPase-deficient allele of GNAS associated with McCune-Albright syndrome.
Turcic K; Tobar-Rubin R; Janevska D; Carroll J; Din E; Alvarez R; Haick J; Pals-Rylaarsdam R
J Mol Endocrinol; 2014 Jun; 52(3):321-31. PubMed ID: 24850831
[TBL] [Abstract][Full Text] [Related]
19. A comparative study of fibrous dysplasia and osteofibrous dysplasia with regard to Gsalpha mutation at the Arg201 codon: polymerase chain reaction-restriction fragment length polymorphism analysis of paraffin-embedded tissues.
Sakamoto A; Oda Y; Iwamoto Y; Tsuneyoshi M
J Mol Diagn; 2000 May; 2(2):67-72. PubMed ID: 11272890
[TBL] [Abstract][Full Text] [Related]
20. Transgenic overexpression of the extra-large Gsα variant XLαs enhances Gsα-mediated responses in the mouse renal proximal tubule in vivo.
Liu Z; Segawa H; Aydin C; Reyes M; Erben RG; Weinstein LS; Chen M; Marshansky V; Fröhlich LF; Bastepe M
Endocrinology; 2011 Apr; 152(4):1222-33. PubMed ID: 21303955
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]