200 related articles for article (PubMed ID: 34299200)
1. Somatotroph Tumors and the Epigenetic Status of the
Romanet P; Galluso J; Kamenicky P; Hage M; Theodoropoulou M; Roche C; Graillon T; Etchevers HC; De Murat D; Mougel G; Figarella-Branger D; Dufour H; Cuny T; Assié G; Barlier A
Int J Mol Sci; 2021 Jul; 22(14):. PubMed ID: 34299200
[TBL] [Abstract][Full Text] [Related]
2. GNAS imprinting and pituitary tumors.
Mantovani G; Lania AG; Spada A
Mol Cell Endocrinol; 2010 Sep; 326(1-2):15-8. PubMed ID: 20398730
[TBL] [Abstract][Full Text] [Related]
3. Genetic and Epigenetic Characterization of Growth Hormone-Secreting Pituitary Tumors.
Välimäki N; Schalin-Jäntti C; Karppinen A; Paetau A; Kivipelto L; Aaltonen LA; Karhu A
Mol Cancer Res; 2019 Dec; 17(12):2432-2443. PubMed ID: 31578227
[TBL] [Abstract][Full Text] [Related]
4. Gs alpha overexpression and loss of Gs alpha imprinting in human somatotroph adenomas: association with tumor size and response to pharmacologic treatment.
Picard C; Silvy M; Gerard C; Buffat C; Lavaque E; Figarella-Branger D; Dufour H; Gabert J; Beckers A; Brue T; Enjalbert A; Barlier A
Int J Cancer; 2007 Sep; 121(6):1245-52. PubMed ID: 17514647
[TBL] [Abstract][Full Text] [Related]
5. Impact of gsp oncogene on the expression of genes coding for Gsalpha, Pit-1, Gi2alpha, and somatostatin receptor 2 in human somatotroph adenomas: involvement in octreotide sensitivity.
Barlier A; Pellegrini-Bouiller I; Gunz G; Zamora AJ; Jaquet P; Enjalbert A
J Clin Endocrinol Metab; 1999 Aug; 84(8):2759-65. PubMed ID: 10443675
[TBL] [Abstract][Full Text] [Related]
6. Imprinting of the G(s)alpha gene GNAS1 in the pathogenesis of acromegaly.
Hayward BE; Barlier A; Korbonits M; Grossman AB; Jacquet P; Enjalbert A; Bonthron DT
J Clin Invest; 2001 Mar; 107(6):R31-6. PubMed ID: 11254676
[TBL] [Abstract][Full Text] [Related]
7. Activating genomic alterations in the Gs alpha gene (GNAS) in 274 694 tumors.
Tirosh A; Jin DX; De Marco L; Laitman Y; Friedman E
Genes Chromosomes Cancer; 2020 Sep; 59(9):503-516. PubMed ID: 32337806
[TBL] [Abstract][Full Text] [Related]
8. Methylation and transcripts expression at the imprinted GNAS locus in human embryonic and induced pluripotent stem cells and their derivatives.
Grybek V; Aubry L; Maupetit-Méhouas S; Le Stunff C; Denis C; Girard M; Linglart A; Silve C
Stem Cell Reports; 2014 Sep; 3(3):432-43. PubMed ID: 25241742
[TBL] [Abstract][Full Text] [Related]
9. METTL3-mediated RNA m6A Hypermethylation Promotes Tumorigenesis and GH Secretion of Pituitary Somatotroph Adenomas.
Chang M; Wang Z; Gao J; Yang C; Feng M; Niu Y; Tong WM; Bao X; Wang R
J Clin Endocrinol Metab; 2022 Jan; 107(1):136-149. PubMed ID: 34491359
[TBL] [Abstract][Full Text] [Related]
10. Analysis of Multiple Families With Single Individuals Affected by Pseudohypoparathyroidism Type Ib (PHP1B) Reveals Only One Novel Maternally Inherited GNAS Deletion.
Takatani R; Molinaro A; Grigelioniene G; Tafaj O; Watanabe T; Reyes M; Sharma A; Singhal V; Raymond FL; Linglart A; Jüppner H
J Bone Miner Res; 2016 Apr; 31(4):796-805. PubMed ID: 26479409
[TBL] [Abstract][Full Text] [Related]
11. Analysis of GNAS mutations in 60 growth hormone secreting pituitary tumors: correlation with clinical and pathological characteristics and surgical outcome based on highly sensitive GH and IGF-I criteria for remission.
Freda PU; Chung WK; Matsuoka N; Walsh JE; Kanibir MN; Kleinman G; Wang Y; Bruce JN; Post KD
Pituitary; 2007; 10(3):275-82. PubMed ID: 17594522
[TBL] [Abstract][Full Text] [Related]
12. Detection of hypomethylation syndrome among patients with epigenetic alterations at the GNAS locus.
Perez-Nanclares G; Romanelli V; Mayo S; Garin I; Zazo Seco C; Fernandez-Rebollo E; Martínez F; Lapunzina P; de Nanclares GP;
J Clin Endocrinol Metab; 2012 Jun; 97(6):E1060-7. PubMed ID: 22492776
[TBL] [Abstract][Full Text] [Related]
13. Distinct patterns of abnormal GNAS imprinting in familial and sporadic pseudohypoparathyroidism type IB.
Liu J; Nealon JG; Weinstein LS
Hum Mol Genet; 2005 Jan; 14(1):95-102. PubMed ID: 15537666
[TBL] [Abstract][Full Text] [Related]
14. Imprinting on chromosome 20: tissue-specific imprinting and imprinting mutations in the GNAS locus.
Kelsey G
Am J Med Genet C Semin Med Genet; 2010 Aug; 154C(3):377-86. PubMed ID: 20803660
[TBL] [Abstract][Full Text] [Related]
15. Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects.
Rochtus A; Martin-Trujillo A; Izzi B; Elli F; Garin I; Linglart A; Mantovani G; Perez de Nanclares G; Thiele S; Decallonne B; Van Geet C; Monk D; Freson K
Clin Epigenetics; 2016; 8():10. PubMed ID: 26819647
[TBL] [Abstract][Full Text] [Related]
16. Impact of gsp oncogene on the mRNA content for somatostatin and dopamine receptors in human somatotropinomas.
Taboada GF; Neto LV; Luque RM; Córdoba-Chacón J; de Oliveira Machado E; de Carvalho DP; Kineman RD; Gadelha MR
Neuroendocrinology; 2011; 93(1):40-7. PubMed ID: 21079388
[TBL] [Abstract][Full Text] [Related]
17. Evolution of an aggressive prolactinoma into a growth hormone secreting pituitary tumor coincident with GNAS gene mutation.
Lania AG; Ferrero S; Pivonello R; Mantovani G; Peverelli E; Di Sarno A; Beck-Peccoz P; Spada A; Colao A
J Clin Endocrinol Metab; 2010 Jan; 95(1):13-7. PubMed ID: 19890024
[TBL] [Abstract][Full Text] [Related]
18. Imprinting control within the compact Gnas locus.
Peters J; Holmes R; Monk D; Beechey CV; Moore GE; Williamson CM
Cytogenet Genome Res; 2006; 113(1-4):194-201. PubMed ID: 16575180
[TBL] [Abstract][Full Text] [Related]
19. Simultaneous hyper- and hypomethylation at imprinted loci in a subset of patients with GNAS epimutations underlies a complex and different mechanism of multilocus methylation defect in pseudohypoparathyroidism type 1b.
Maupetit-Méhouas S; Azzi S; Steunou V; Sakakini N; Silve C; Reynes C; Perez de Nanclares G; Keren B; Chantot S; Barlier A; Linglart A; Netchine I
Hum Mutat; 2013 Aug; 34(8):1172-80. PubMed ID: 23649963
[TBL] [Abstract][Full Text] [Related]
20. Identification of a Novel Imprinted Transcript in the Porcine
Ahn J; Wu H; Lee J; Hwang IS; Yu D; Ahn JS; Lee JW; Hwang S; Lee K
Genes (Basel); 2020 Jan; 11(1):. PubMed ID: 31947640
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]