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Studies

39767 Unclassified

13740 Reviews

13613 Research

11906 Case Reports

6845 Other Trials

4674 Advanced Trials

2319 Early Trials

427 Meta-Analysis

Guidelines

171 Guidelines

91 Consensuses

87 Cochrane

Congresses

7012 Abstracts

1

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
2

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

Institutional score
0.00
Impact
3197.10

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Date 15 Oct 1999

Institutional score
0.00
Impact
3197.10
3

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
4

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
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

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

Institutional score
0.00
Impact
2459.31

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Date 01 Feb 1997

Institutional score
0.00
Impact
2459.31
8

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

Institutional score
56.78
Impact
2459.31

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Date 01 Feb 2019

Institutional score
56.78
Impact
2459.31
9

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
10

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

Institutional score
0.00
Impact
2459.31

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Date 01 Nov 1994

Institutional score
0.00
Impact
2459.31

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