Joint Instability 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 20 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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7604 Abstracts
Research
A polymorphic genomic duplication on human chromosome 15 is a susceptibility factor for panic and phobic disorders.
Gratacòs M, Nadal M, Martín-Santos R, Pujana M A, Gago J ...
Cell Vol 106(3)
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Date 10 Aug 2001
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
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 genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development.
Cappello Silvia, Gray Mary J, Badouel Caroline, Lange Simona, Einsiedler Melanie ...
Nature genetics Vol 45(11)
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Date 01 Nov 2013
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
Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number.
Lyons Jonathan J, Yu Xiaomin, Hughes Jason D, Le Quang T, Jamil Ali ...
Nature genetics Vol 48(12)
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Date 01 Dec 2016
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
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