These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 16322672)

  • 1. [Genes causing parathyroid diseases].
    Ikeda K
    Clin Calcium; 2005 Dec; 15(12):38-44. PubMed ID: 16322672
    [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. The development of the parathyroid gland: from fish to human.
    Zajac JD; Danks JA
    Curr Opin Nephrol Hypertens; 2008 Jul; 17(4):353-6. PubMed ID: 18660669
    [TBL] [Abstract][Full Text] [Related]  

  • 4. GCMB gene, a master regulator of parathyroid gland development, expression, and regulation in hyperparathyroidism.
    Kebebew E; Peng M; Wong MG; Ginzinger D; Duh QY; Clark OH
    Surgery; 2004 Dec; 136(6):1261-6. PubMed ID: 15657585
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic ablation of parathyroid glands reveals another source of parathyroid hormone.
    Günther T; Chen ZF; Kim J; Priemel M; Rueger JM; Amling M; Moseley JM; Martin TJ; Anderson DJ; Karsenty G
    Nature; 2000 Jul; 406(6792):199-203. PubMed ID: 10910362
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. MafB interacts with Gcm2 and regulates parathyroid hormone expression and parathyroid development.
    Kamitani-Kawamoto A; Hamada M; Moriguchi T; Miyai M; Saji F; Hatamura I; Nishikawa K; Takayanagi H; Hitoshi S; Ikenaka K; Hosoya T; Hotta Y; Takahashi S; Kataoka K
    J Bone Miner Res; 2011 Oct; 26(10):2463-72. PubMed ID: 21713993
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Molecular aspects of the etiopathogenesis of the parathyroid gland diseases].
    Lacka K
    Endokrynol Pol; 2005; 56(3):327-33. PubMed ID: 16350727
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Underexpression of Gcm2, a master regulatory gene of parathyroid gland development, in adenomas of primary hyperparathyroidism.
    Correa P; Akerström G; Westin G
    Clin Endocrinol (Oxf); 2002 Oct; 57(4):501-5. PubMed ID: 12354132
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Identification of a novel mutation disrupting the DNA binding activity of GCM2 in autosomal recessive familial isolated hypoparathyroidism.
    Baumber L; Tufarelli C; Patel S; King P; Johnson CA; Maher ER; Trembath RC
    J Med Genet; 2005 May; 42(5):443-8. PubMed ID: 15863676
    [No Abstract]   [Full Text] [Related]  

  • 12. [Hyperparathyroidism-jaw tumor syndrome. A hereditary form of primary hyperparathyroidism with parathyroid carcinoma].
    Raue F; Haag Ch; Frank-Raue K
    Dtsch Med Wochenschr; 2007 Jul; 132(27):1459-62. PubMed ID: 17583828
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutational analysis of the PTH 3'-untranslated region in parathyroid disorders.
    Costa-Guda J; Lauter K; Naveh-Many T; Silver J; Arnold A
    Clin Endocrinol (Oxf); 2006 Dec; 65(6):806-9. PubMed ID: 17121534
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Parafibromin expression, single-gland involvement, and limited parathyroidectomy in familial isolated hyperparathyroidism.
    Iacobone M; Barzon L; Porzionato A; Masi G; Macchi V; Marino F; Viel G; Favia G
    Surgery; 2007 Dec; 142(6):984-91; discussion 984-91. PubMed ID: 18063086
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetics of Hyperparathyroidism, Including Parathyroid Cancer.
    Simonds WF
    Endocrinol Metab Clin North Am; 2017 Jun; 46(2):405-418. PubMed ID: 28476229
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Re: Familial hyperparathyroidism: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations.
    Guarnieri V; Bisceglia M; Bonfitto N; Cetani F; Marcocci C; Minisola S; Battista C; Chiodini I; Cole DE; Scillitani A
    Surgery; 2008 Nov; 144(5):839-40. PubMed ID: 19081034
    [No Abstract]   [Full Text] [Related]  

  • 17. [Idiopathic hypoparathyroidism due to abnormalities in parathyroid organogenesis].
    Tanaka H
    Clin Calcium; 2007 Aug; 17(8):1206-13. PubMed ID: 17660617
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
    Teh BT; Howell VM; Haven CJ; Kahnoski K; Khoo SK; Petillo D; Chen J; Fleuren GJ; Robinson BG; Delbridge LW; Philips J; Nelson AE; Krause U; Hammje K; Dralle H; Hoang-Vu C; Gimm O; Marsh DJ; Morreau H
    Hum Genet; 2004 Jan; 114(2):224. PubMed ID: 15046109
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.