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Items: 8

1.
GCM2-Activating Mutations in Familial Isolated Hyperparathyroidism
Bin Guan, James M. Welch, Julie C. Sapp, Hua Ling, Yulong Li, Jennifer J. Johnston, Electron Kebebew, Leslie G. Biesecker, William F. Simonds, Stephen J. Marx, Sunita K. Agarwal
Am J Hum Genet. 2016 Nov 3; 99(5): 1034–1044. Published online 2016 Oct 13. doi: 10.1016/j.ajhg.2016.08.018
PMCID:
PMC5097944
AbstractArticlePDF–900K
2.
Synaptic protein ubiquitination in rat brain revealed by antibody-based ubiquitome analysis
Chan-Hyun Na, Drew R. Jones, Yanling Yang, Xusheng Wang, Yanji Xu, Junmin Peng
J Proteome Res. Author manuscript; available in PMC 2013 Sep 7.
Published in final edited form as: J Proteome Res. 2012 Sep 7; 11(9): 4722–4732. Published online 2012 Aug 15. doi: 10.1021/pr300536k
PMCID:
PMC3443409
AbstractArticlePDF–4.2M
3.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas
Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042
PMCID:
PMC3178059
AbstractArticlePDF–1.0M
4.
Gata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2
Irina V. Grigorieva, Samantha Mirczuk, Katherine U. Gaynor, M. Andrew Nesbit, Elena F. Grigorieva, Qiaozhi Wei, Asif Ali, Rebecca J. Fairclough, Joanna M. Stacey, Michael J. Stechman, Radu Mihai, Dorota Kurek, William D. Fraser, Tertius Hough, Brian G. Condie, Nancy Manley, Frank Grosveld, Rajesh V. Thakker
J Clin Invest. 2010 Jun 1; 120(6): 2144–2155. Published online 2010 May 17. doi: 10.1172/JCI42021
PMCID:
PMC2877956
AbstractArticlePDF–3.4M
5.
Gcm2 is required for the differentiation and survival of parathyroid precursor cells in the parathyroid/thymus primordia
Zhijie Liu, Shannon Yu, Nancy R. Manley
Dev Biol. Author manuscript; available in PMC 2008 May 1.
Published in final edited form as: Dev Biol. 2007 May 1; 305(1): 333–346. Published online 2007 Feb 21. doi: 10.1016/j.ydbio.2007.02.014
PMCID:
PMC1931567
AbstractArticlePDF–3.0M
6.
Identification of a novel mutation disrupting the DNA binding activity of GCM2 in autosomal recessive familial isolated hypoparathyroidism
L Baumber, C Tufarelli, S Patel, P King, C Johnson, E Maher, R Trembath
J Med Genet. 2005 May; 42(5): 443–448. doi: 10.1136/jmg.2004.026898
PMCID:
PMC1736051
SummaryPDF–216K
7.
Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor GCMB
Changlin Ding, Bruce Buckingham, Michael A. Levine
J Clin Invest. 2001 Oct 15; 108(8): 1215–1220. doi: 10.1172/JCI13180
PMCID:
PMC209530
AbstractArticlePDF–577K
8.
Isolation and characterization of mammalian homologs of the Drosophila gene glial cells missing
Jaesang Kim, Bradley W. Jones, Christiane Zock, Zhoufeng Chen, Hai Wang, Corey S. Goodman, David J. Anderson
Proc Natl Acad Sci U S A. 1998 Oct 13; 95(21): 12364–12369. doi: 10.1073/pnas.95.21.12364
PMCID:
PMC22837
AbstractArticlePDF–469K

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