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Studies

38654 Unclassified

13440 Research

13047 Reviews

10772 Case Reports

6822 Other Trials

4648 Advanced Trials

2321 Early Trials

432 Meta-Analysis

Guidelines

167 Guidelines

92 Consensuses

86 Cochrane

Congresses

6818 Abstracts

1

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

Institutional score
35.25
Impact
3197.10

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Date 30 Nov 1990

Institutional score
35.25
Impact
3197.10
2

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

Institutional score
0.00
Impact
3197.10

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Date 13 Jun 2019

Institutional score
0.00
Impact
3197.10
3

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

Institutional score
0.00
Impact
3197.10

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Date 29 Nov 1996

Institutional score
0.00
Impact
3197.10
4

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

Institutional score
0.00
Impact
2459.31

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Date 01 May 2001

Institutional score
0.00
Impact
2459.31
5

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

Institutional score
13.14
Impact
2459.31

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Date 01 Nov 1999

Institutional score
13.14
Impact
2459.31
6

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

Institutional score
0.00
Impact
2459.31

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Date 02 Oct 2011

Institutional score
0.00
Impact
2459.31
7

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

Institutional score
0.00
Impact
2459.31

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Date 01 Sep 2001

Institutional score
0.00
Impact
2459.31
8

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

Institutional score
0.00
Impact
2459.31

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Date 11 Dec 2011

Institutional score
0.00
Impact
2459.31
9

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

Institutional score
0.00
Impact
2459.31

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Date 01 Jul 1997

Institutional score
0.00
Impact
2459.31
10

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

Institutional score
0.00
Impact
2459.31

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Date 01 Oct 1996

Institutional score
0.00
Impact
2459.31

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