PMC Links for GEO Profiles (Select 33686968) - PMC

Select item 107287201.

The contribution of a novel PHEX gene mutation to X-linked hypophosphatemic rickets: a case report and an analysis of the gene mutation dosage effect in a rat model

Xiaoming Chen, Cijing Cai, Shaocong Lun, Qiuli Ye, Weiyuan Pan, Yushi Chen, Yuexuan Wu, Taoshan Feng, Faming Su, Choudi Ma, Jiaxin Luo, Meilian Liu, Guoda Ma

Front Endocrinol (Lausanne) 2023; 14: 1251718. Published online 2023 Dec 5. doi: 10.3389/fendo.2023.1251718

PMCID:: PMC10728720

Abstract Article PDF–6.3M

Select item 32592422.

The Sclerostin-Bone Protein Interactome

Hemamalini Devarajan-Ketha, Theodore A. Craig, Benjamin J. Madden, H. Robert Bergen, III, Rajiv Kumar

Biochem Biophys Res Commun. Author manuscript; available in PMC 2013 Jan 13.

Published in final edited form as: Biochem Biophys Res Commun. 2012 Jan 13; 417(2): 830–835. Published online 2011 Dec 22. doi: 10.1016/j.bbrc.2011.12.048

PMCID:: PMC3259242

Abstract Article PDF–470K

Select item 31780593.

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

Abstract Article PDF–1.0M

Select item 28591904.

New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice

Bettina Lorenz-Depiereux, Victoria E. Guido, Kenneth R. Johnson, Qing Yin Zheng, Leona H. Gagnon, Joiel D. Bauschatz, Muriel T. Davisson, Linda L. Washburn, Leah Rae Donahue, Tim M. Strom, Eva M. Eicher

Mamm Genome. Author manuscript; available in PMC 2010 Apr 24.

Published in final edited form as: Mamm Genome. 2004 Mar; 15(3): 151–161. doi: 10.1007/s00335-003-2310-z

PMCID:: PMC2859190

Abstract Article PDF–1.9M

Select item 28582215.

A mouse model with postnatal endolymphatic hydrops and hearing loss

Cliff A. Megerian, Maroun T. Semaan, Saba Aftab, Lauren B. Kisley, Qing Yin Zheng, Karen S. Pawlowski, Charles G. Wright, Kumar N. Alagramam

Hear Res. Author manuscript; available in PMC 2010 Apr 21.

Published in final edited form as: Hear Res. 2008 Mar; 237(1-2): 90–105. Published online 2008 Jan 15. doi: 10.1016/j.heares.2008.01.002

PMCID:: PMC2858221

Abstract Article PDF–6.1M

Select item 17124716.

Mutational analysis of the PEX gene in patients with X-linked hypophosphatemic rickets.

I A Holm, X Huang, L M Kunkel

Am J Hum Genet. 1997 Apr; 60(4): 790–797.

PMCID:: PMC1712471

Summary Page Browse PDF–1.3M

Select item 14845027.

Role of Matrix Extracellular Phosphoglycoprotein in the Pathogenesis of X-Linked Hypophosphatemia

Shiguang Liu, Thomas A. Brown, Jianping Zhou, Zhou-Sheng Xiao, Hani Awad, Farshid Guilak, L. Darryl Quarles

J Am Soc Nephrol. Author manuscript; available in PMC 2006 Jul 4.

Published in final edited form as: J Am Soc Nephrol. 2005 Jun; 16(6): 1645–1653. Published online 2005 Apr 20. doi: 10.1681/ASN.2004121060

PMCID:: PMC1484502

Abstract Article PDF–271K

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