179 related articles for article (PubMed ID: 33536578)
1. Five patients with disorders of calcium metabolism presented with GCM2 gene variants.
García-Castaño A; Madariaga L; Gómez-Conde S; Cordo CLR; López-Iglesias M; Garcia-Fernández Y; Martín A; González P; Goicolea I; de Nanclares GP; De la Hoz AB; Aguayo A; de LaPiscina IM; Martínez R; Saso L; Urrutia I; Velasco O; Castaño L; Gaztambide S
Sci Rep; 2021 Feb; 11(1):2968. PubMed ID: 33536578
[TBL] [Abstract][Full Text] [Related]
2. Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders.
Canaff L; Guarnieri V; Kim Y; Wong BYL; Nolin-Lapalme A; Cole DEC; Minisola S; Eller-Vainicher C; Cetani F; Repaci A; Turchetti D; Corbetta S; Scillitani A; Goltzman D
Eur J Endocrinol; 2022 Feb; 186(3):351-366. PubMed ID: 35038313
[TBL] [Abstract][Full Text] [Related]
3. GCM2-Activating Mutations in Familial Isolated Hyperparathyroidism.
Guan B; Welch JM; Sapp JC; Ling H; Li Y; Johnston JJ; Kebebew E; Biesecker LG; Simonds WF; Marx SJ; Agarwal SK
Am J Hum Genet; 2016 Nov; 99(5):1034-1044. PubMed ID: 27745835
[TBL] [Abstract][Full Text] [Related]
4. Analysis of Activating GCM2 Sequence Variants in Sporadic Parathyroid Adenomas.
Riccardi A; Aspir T; Shen L; Kuo CL; Brown TC; Korah R; Murtha TD; Bellizzi J; Parham K; Carling T; Costa-Guda J; Arnold A
J Clin Endocrinol Metab; 2019 Jun; 104(6):1948-1952. PubMed ID: 30624640
[TBL] [Abstract][Full Text] [Related]
5. Glial cells missing-2 (GCM2) transactivates the calcium-sensing receptor gene: effect of a dominant-negative GCM2 mutant associated with autosomal dominant hypoparathyroidism.
Canaff L; Zhou X; Mosesova I; Cole DE; Hendy GN
Hum Mutat; 2009 Jan; 30(1):85-92. PubMed ID: 18712808
[TBL] [Abstract][Full Text] [Related]
6. Comprehensive next-generation sequencing analyses of hypoparathyroidism: identification of novel GCM2 mutations.
Mitsui T; Narumi S; Inokuchi M; Nagasaki K; Nakazawa M; Sasaki G; Hasegawa T
J Clin Endocrinol Metab; 2014 Nov; 99(11):E2421-8. PubMed ID: 25137426
[TBL] [Abstract][Full Text] [Related]
7. Familial isolated primary hyperparathyroidism associated with germline GCM2 mutations is more aggressive and has a lesser rate of biochemical cure.
El Lakis M; Nockel P; Guan B; Agarwal S; Welch J; Simonds WF; Marx S; Li Y; Nilubol N; Patel D; Yang L; Merkel R; Kebebew E
Surgery; 2018 Jan; 163(1):31-34. PubMed ID: 29108698
[TBL] [Abstract][Full Text] [Related]
8. Presence and significance of a R110W mutation in the DNA-binding domain of GCM2 gene in patients with isolated hypoparathyroidism and their family members.
Tomar N; Bora H; Singh R; Gupta N; Kaur P; Chauhan SS; Sharma YD; Goswami R
Eur J Endocrinol; 2010 Feb; 162(2):407-21. PubMed ID: 19940031
[TBL] [Abstract][Full Text] [Related]
9.
Szalat A; Shpitzen S; Pollack R; Mazeh H; Durst R; Meiner V
Front Endocrinol (Lausanne); 2023; 14():1254156. PubMed ID: 38130397
[TBL] [Abstract][Full Text] [Related]
10. Should the GCM2 gene be tested when screening for familial primary hyperparathyroidism?
Coppin L; Dufosse M; Romanet P; Giraud S; North MO; Cardot Bauters C; Borson-Chazot F; Duchesne L; Métallo M; Lovecchio T; Barlier A; Odou MF
Eur J Endocrinol; 2020 Jan; 182(1):57-65. PubMed ID: 31671402
[TBL] [Abstract][Full Text] [Related]
11. Analysis of the GCM2 gene in isolated hypoparathyroidism: a molecular and biochemical study.
Maret A; Ding C; Kornfield SL; Levine MA
J Clin Endocrinol Metab; 2008 Apr; 93(4):1426-32. PubMed ID: 18182452
[TBL] [Abstract][Full Text] [Related]
12. Gata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2.
Grigorieva IV; Mirczuk S; Gaynor KU; Nesbit MA; Grigorieva EF; Wei Q; Ali A; Fairclough RJ; Stacey JM; Stechman MJ; Mihai R; Kurek D; Fraser WD; Hough T; Condie BG; Manley N; Grosveld F; Thakker RV
J Clin Invest; 2010 Jun; 120(6):2144-55. PubMed ID: 20484821
[TBL] [Abstract][Full Text] [Related]
13. Germline Mutations Related to Primary Hyperparathyroidism Identified by Next-Generation Sequencing.
Park HS; Lee YH; Hong N; Won D; Rhee Y
Front Endocrinol (Lausanne); 2022; 13():853171. PubMed ID: 35586626
[TBL] [Abstract][Full Text] [Related]
14. Germline GCM2 Mutation Screening in Chinese Primary Hyperparathyroidism Patients.
Song A; Yang Y; Wang Y; Liu S; Nie M; Jiang Y; Li M; Xia W; Wang O; Xing X
Endocr Pract; 2020 Oct; 26(10):1093-1104. PubMed ID: 33471711
[TBL] [Abstract][Full Text] [Related]
15. Heterozygous Mutations in TBX1 as a Cause of Isolated Hypoparathyroidism.
Li D; Gordon CT; Oufadem M; Amiel J; Kanwar HS; Bakay M; Wang T; Hakonarson H; Levine MA
J Clin Endocrinol Metab; 2018 Nov; 103(11):4023-4032. PubMed ID: 30137364
[TBL] [Abstract][Full Text] [Related]
16. Gata3 cooperates with Gcm2 and MafB to activate parathyroid hormone gene expression by interacting with SP1.
Han SI; Tsunekage Y; Kataoka K
Mol Cell Endocrinol; 2015 Aug; 411():113-20. PubMed ID: 25917456
[TBL] [Abstract][Full Text] [Related]
17. GCM2 Variants in Familial and Multiglandular Primary Hyperparathyroidism.
Vincze S; Peters NV; Kuo CL; Brown TC; Korah R; Murtha TD; Bellizzi J; Riccardi A; Parham K; Carling T; Costa-Guda J; Arnold A
J Clin Endocrinol Metab; 2022 Apr; 107(5):e2021-e2026. PubMed ID: 34967908
[TBL] [Abstract][Full Text] [Related]
18. Autosomal Dominant PTH Gene Signal Sequence Mutation in a Family With Familial Isolated Hypoparathyroidism.
Cinque L; Sparaneo A; Penta L; Mencarelli A; Rogaia D; Esposito S; Fabrizio FP; Baorda F; Verrotti A; Falorni A; Stangoni G; Hendy GN; Guarnieri V; Prontera P
J Clin Endocrinol Metab; 2017 Nov; 102(11):3961-3969. PubMed ID: 28938448
[TBL] [Abstract][Full Text] [Related]
19. [Progress in diagnosis and therapy: Hypocalcemia due to idiopathic hypoparathyroidism].
Tanaka H
Nihon Naika Gakkai Zasshi; 2007 Apr; 96(4):707-12. PubMed ID: 17506308
[No Abstract] [Full Text] [Related]
20. Genetic Screening in a Large Chinese Cohort of Childhood Onset Hypoparathyroidism by Next-Generation Sequencing Combined with TBX1-MLPA.
Wang Y; Nie M; Wang O; Li Y; Jiang Y; Li M; Xia W; Xing X
J Bone Miner Res; 2019 Dec; 34(12):2254-2263. PubMed ID: 31433868
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]