Ankylosis research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Ankylosis treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
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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
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
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
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
Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia.
Nürnberg P, Thiele H, Chandler D, Höhne W, Cunningham M L ...
Nature genetics Vol 28(1)
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Date 01 May 2001
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
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
Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.
Le Goff Carine, Mahaut Clémentine, Abhyankar Avinash, Le Goff Wilfried, Serre Valérie ...
Nature genetics Vol 44(1)
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Date 11 Dec 2011
Research
Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors.
Snyder R O, Miao C H, Patijn G A, Spratt S K, Danos O ...
Nature genetics Vol 16(3)
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Date 01 Jul 1997
Research
Evidence that a locus for familial psoriasis maps to chromosome 4q.
Matthews D, Fry L, Powles A, Weber J, McCarthy M ...
Nature genetics Vol 14(2)
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Date 01 Oct 1996
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