Hyperostosis Frontalis Interna 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 19 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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Research
Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus.
Vikkula M, Mariman E C, Lui V C, Zhidkova N I, Tiller G E ...
Cell Vol 80(3)
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Date 10 Feb 1995
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
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
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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
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
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
The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping.
Hästbacka J, de la Chapelle A, Mahtani M M, Clines G, Reeve-Daly M P ...
Cell Vol 78(6)
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Date 23 Sep 1994
Research
Mutations in the RNA component of RNase MRP cause a pleiotropic human disease, cartilage-hair hypoplasia.
Ridanpää M, van Eenennaam H, Pelin K, Chadwick R, Johnson C ...
Cell Vol 104(2)
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Date 26 Jan 2001
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
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