| 1 | GCM2, HRPT4
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| GCM2-Activating Mutations in Familial Isolated Hyperparathyroidism.
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| Guan B, Welch JM, Sapp JC, Ling H, Li Y, Johnston JJ, Kebebew E, Biesecker LG, Simonds WF, Marx SJ, Agarwal SK.
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| Am J Hum Genet 99(5):1034-1044. doi: 10.1016/j.ajhg.2016.08.018.
2016
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| 2 | GATA3, GCM2, MAFB
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| Gata3 cooperates with Gcm2 and MafB to activate parathyroid hormone gene expression by interacting with SP1.
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| Han SI, Tsunekage Y, Kataoka K.
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| Mol Cell Endocrinol 411:113-20. doi: 10.1016/j.mce.2015.04.018.
2015
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| 3 | GCM2
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| Generation of mice encoding a conditional null allele of Gcm2.
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| Yuan Z, Opas EE, Vrikshajanani C, Libutti SK, Levine MA.
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| Transgenic Res 23(4):631-41. doi: 10.1007/s11248-014-9799-7.
2014
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| 4 | GCM2
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| Increased prevalence of the GCM2 polymorphism, Y282D, in primary hyperparathyroidism: analysis of three Italian cohorts.
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| D'Agruma L, Coco M, Guarnieri V, Battista C, Canaff L, Salcuni AS, Corbetta S, Cetani F, Minisola S, Chiodini I, Eller-Vainicher C, Spada A, Marcocci C, Guglielmi G, Zini M, Clemente R, Wong BY, de Martino D, Scillitani A, Hendy GN, Cole DE.
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| J Clin Endocrinol Metab 99(12):E2794-8. doi: 10.1210/jc.2014-2857.
2014
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| 5 | FIHP, GCM2
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| Identification and characterization of C106R, a novel mutation in the DNA-binding domain of GCMB, in a family with autosomal-dominant hypoparathyroidism.
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| Yi HS, Eom YS, Park IeB, Lee S, Hong S, Jüppner H, Mannstadt M, Lee S.
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| Clin Endocrinol (Oxf) 76(5):625-33. doi: 10.1111/j.1365-2265.2011.04256.x.
2012
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| 6 | GCM1, GCM2, HES5
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| Mammalian Gcm genes induce Hes5 expression by active DNA demethylation and induce neural stem cells.
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| Hitoshi S, Ishino Y, Kumar A, Jasmine S, Tanaka KF, Kondo T, Kato S, Hosoya T, Hotta Y, Ikenaka K.
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| Nat Neurosci. 14(8):957-64. 2011
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| 7 | FIHP, GCM2
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| Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism.
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| Bowl MR, Mirczuk SM, Grigorieva IV, Piret SE, Cranston T, Southam L, Allgrove J, Bahl S, Brain C, Loughlin J, Mughal Z, Ryan F, Shaw N, Thakker YV, Tiosano D, Nesbit MA, Thakker RV.
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| Hum Mol Genet 19(10):2028-38. Epub 2010 Feb 27.
2010
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| 8 | CASR, FIHP, GCM2
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| Glial cells missing-2 (GCM2) transactivates the calcium-sensing receptor gene: effect of a dominant-negative GCM2 mutant associated with autosomal dominant hypoparathyroidism.
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| Canaff L, Zhou X, Mosesova I, Cole DE, Hendy GN.
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| Hum Mutat 30(1):85-92.
2009
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| 9 | GCM2
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| Analysis of the GCM2 gene in isolated hypoparathyroidism: a molecular and biochemical study.
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| Maret A, Ding C, Kornfield SL, Levine MA.
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| J Clin Endocrinol Metab 93(4):1426-32. Epub 2008 Jan 8. 2008
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| 10 | FIHP, GCM2
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| Dominant-negative GCMB mutations cause an autosomal dominant form of hypoparathyroidism.
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| Mannstadt M, Bertrand G, Muresan M, Weryha G, Leheup B, Pulusani SR, Grandchamp B, Jüppner H, Silve C.
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| J Clin Endocrinol Metab 93(9):3568-76. Epub 2008 Jun 26.
2008
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| 11 | FIHP, GCM2
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| Identification of a novel mutation disrupting the DNA binding activity of GCM2 in autosomal recessive familial isolated hypoparathyroidism.
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| Baumber L, Tufarelli C, Patel S, King P, Johnson CA, Maher ER, Trembath RC.
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| J Med Genet 42(5):443-8. No abstract available. 2005
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| 12 | FIHP, GCM2
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| GCMB mutation in familial isolated hypoparathyroidism with residual secretion of parathyroid hormone.
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| Thomee C, Schubert SW, Parma J, Le PQ, Hashemolhosseini S, Wegner M, Abramowicz MJ.
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| J Clin Endocrinol Metab 90(5):2487-92. Epub 2005 Feb 22. 2005
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| 13 | GCM1, GCM2
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| Structural requirements for nuclear localization of GCMa/Gcm-1.
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| Hashemolhosseini S, Kilian K, Kardash E, Lischka P, Stamminger T, Wegner M.
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| FEBS Lett 553(3):315-20. 2003
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| 14 | AIRE, GATA3, GCM2
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| Genetic developments in hypoparathyroidism.
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| Thakker RV.
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| Lancet 357(9261):974-6. No abstract available. 2001
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| 15 | FIHP, GCM2
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| Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor GCMB.
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| Ding C, Buckingham B, Levine MA.
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| J Clin Invest 108(8):1215-20. 2001
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| 16 | GCM2
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| Genetic ablation of parathyroid glands reveals another source of parathyroid hormone.
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| Günther T, Chen ZF, Kim J, Priemel M, Rueger JM, Amling M, Moseley JM, Martin TJ, Anderson DJ, Karsenty G.
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| Nature. 406(6792):199-203. 2000
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| 17 | GCM2
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| Isolation and expression analysis of a novel human homologue of the Drosophila glial cells missing (gcm) gene.
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| Kanemura Y, et al.
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| FEBS Lett 442(2-3):151-6. 1999
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| 18 | GCM2
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| GCMB, a second human homolog of the fly glide/gcm gene.
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| Kammerer M, et al.
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| Cytogenet Cell Genet 84(1-2):43-7. 1999
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| 19 | GCM2
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| The regulator of early gliogenesis glial cells missing is a transcription factor with a novel type of DNA-binding domain.
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| Schreiber J, et al.
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| Proc Natl Acad Sci U S A 94(9):4739-44. 1997
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| 20 | GCM1, GCM2
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| The gcm-motif: a novel DNA-binding motif conserved in Drosophila and mammals.
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| Akiyama Y, Hosoya T, Poole AM, Hotta Y.
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| Proc Natl Acad Sci U S A. 93(25):14912-6. 1996
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