Bone Anteversion 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
Generation of superhelical torsion by ATP-dependent chromatin remodeling activities.
Havas K, Flaus A, Phelan M, Kingston R, Wade P A ...
Cell Vol 103(7)
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Date 22 Dec 2000
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
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
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
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
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
Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
Albagha Omar M E, Wani Sachin E, Visconti Micaela R, Alonso Nerea, Goodman Kirsteen ...
Nature genetics Vol 43(7)
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Date 29 May 2011
Research
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein.
Watts Giles D J, Wymer Jill, Kovach Margaret J, Mehta Sarju G, Mumm Steven ...
Nature genetics Vol 36(4)
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Date 01 Apr 2004
Research
Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.
Albagha Omar M E, Visconti Micaela R, Alonso Nerea, Langston Anne L, Cundy Tim ...
Nature genetics Vol 42(6)
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Date 01 Jun 2010
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