Hallux Limitus 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
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
Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome.
Celli J, Duijf P, Hamel B C, Bamshad M, Kramer B ...
Cell Vol 99(2)
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Date 15 Oct 1999
Research
Spontaneous inflammatory disease in transgenic rats expressing HLA-B27 and human beta 2m: an animal model of HLA-B27-associated human disorders.
Hammer R E, Maika S D, Richardson J A, Tang J P, Taurog J D
Cell Vol 63(5)
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Date 30 Nov 1990
Research
Organ-specific disease provoked by systemic autoimmunity.
Kouskoff V, Korganow A S, Duchatelle V, Degott C, Benoist C ...
Cell Vol 87(5)
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Date 29 Nov 1996
Research
CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
Marcelino J, Carpten J D, Suwairi W M, Gutierrez O M, Schwartz S ...
Nature genetics Vol 23(3)
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Date 01 Nov 1999
Research
Mutations in TRPV4 cause an inherited arthropathy of hands and feet.
Lamandé Shireen R, Yuan Yuan, Gresshoff Irma L, Rowley Lynn, Belluoccio Daniele ...
Nature genetics Vol 43(11)
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Date 02 Oct 2011
Research
Mutation of HOXA13 in hand-foot-genital syndrome.
Mortlock D P, Innis J W
Nature genetics Vol 15(2)
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Date 01 Feb 1997
Research
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data.
Tachmazidou Ioanna, Hatzikotoulas Konstantinos, Southam Lorraine, Esparza-Gordillo Jorge, Haberland Valeriia ...
Nature genetics Vol 51(2)
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Date 01 Feb 2019
Research
CARD15 mutations in Blau syndrome.
Miceli-Richard C, Lesage S, Rybojad M, Prieur A M, Manouvrier-Hanu S ...
Nature genetics Vol 29(1)
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Date 01 Sep 2001
Research
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2.
Jabs E W, Li X, Scott A F, Meyers G, Chen W ...
Nature genetics Vol 8(3)
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Date 01 Nov 1994
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