Bone Diseases, Developmental research, articles, guidelines & medical evidence database search.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 18 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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Research
Ribosome-mediated specificity in Hox mRNA translation and vertebrate tissue patterning.
Kondrashov Nadya, Pusic Aya, Stumpf Craig R, Shimizu Kunihiko, Hsieh Andrew C ...
Cell Vol 145(3)
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Date 29 Apr 2011
Research
Fibroblast growth factor receptor 3 is a negative regulator of bone growth.
Deng C, Wynshaw-Boris A, Zhou F, Kuo A, Leder P
Cell Vol 84(6)
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Date 22 Mar 1996
Research
Cryo-EM Structure of Chikungunya Virus in Complex with the Mxra8 Receptor.
Basore Katherine, Kim Arthur S, Nelson Christopher A, Zhang Rong, Smith Brittany K ...
Cell Vol 177(7)
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Date 13 Jun 2019
Research
CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta.
Morello Roy, Bertin Terry K, Chen Yuqing, Hicks John, Tonachini Laura ...
Cell Vol 127(2)
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Date 20 Oct 2006
Research
Estrogen prevents bone loss via estrogen receptor alpha and induction of Fas ligand in osteoclasts.
Nakamura Takashi, Imai Yuuki, Matsumoto Takahiro, Sato Shingo, Takeuchi Kazusane ...
Cell Vol 130(5)
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Date 07 Sep 2007
Research
MT1-MMP-deficient mice develop dwarfism, osteopenia, arthritis, and connective tissue disease due to inadequate collagen turnover.
Holmbeck K, Bianco P, Caterina J, Yamada S, Kromer M ...
Cell Vol 99(1)
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Date 01 Oct 1999
Research
An endocytic pathway essential for renal uptake and activation of the steroid 25-(OH) vitamin D3.
Nykjaer A, Dragun D, Walther D, Vorum H, Jacobsen C ...
Cell Vol 96(4)
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Date 19 Feb 1999
Research
Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature.
Briggs Tracy A, Rice Gillian I, Daly Sarah, Urquhart Jill, Gornall Hannah ...
Nature genetics Vol 43(2)
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Date 01 Feb 2011
Research
Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis.
Jenkins Zandra A, van Kogelenberg Margriet, Morgan Tim, Jeffs Aaron, Fukuzawa Ryuji ...
Nature genetics Vol 41(1)
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Date 01 Jan 2009
Research
Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia.
Rock Matthew J, Prenen Jean, Funari Vincent A, Funari Tara L, Merriman Barry ...
Nature genetics Vol 40(8)
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Date 01 Aug 2008
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