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Studies

63839 Unclassified

29962 Case Reports

22675 Reviews

18137 Research

11356 Other Trials

10699 Early Trials

9368 Advanced Trials

831 Meta-Analysis

Guidelines

262 Guidelines

121 Consensuses

98 Cochrane

Congresses

15253 Abstracts

1

Research

Adrenergic Signaling in Muscularis Macrophages Limits Infection-Induced Neuronal Loss.

Matheis Fanny, Muller Paul A, Graves Christina L, Gabanyi Ilana, Kerner Zachary J ...

Cell Vol 180(1)

Read

Date 09 Jan 2020

Institutional score
39.66
Impact
3860.25

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Date 09 Jan 2020

Institutional score
39.66
Impact
3860.25
2

Research

Pathogenic simian immunodeficiency virus infection is associated with expansion of the enteric virome.

Handley Scott A, Thackray Larissa B, Zhao Guoyan, Presti Rachel, Miller Andrew D ...

Cell Vol 151(2)

Read

Date 12 Oct 2012

Institutional score
0.00
Impact
3197.10

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Date 12 Oct 2012

Institutional score
0.00
Impact
3197.10
3

Research

Immunoglobulin A coating identifies colitogenic bacteria in inflammatory bowel disease.

Palm Noah W, de Zoete Marcel R, Cullen Thomas W, Barry Natasha A, Stefanowski Jonathan ...

Cell Vol 158(5)

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Date 28 Aug 2014

Institutional score
232.44
Impact
3197.10

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Date 28 Aug 2014

Institutional score
232.44
Impact
3197.10
4

Research

Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis.

Sun Lei, Rommens Johanna M, Corvol Harriet, Li Weili, Li Xin ...

Nature genetics Vol 44(5)

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Date 01 May 2012

Institutional score
275.48
Impact
2459.31

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Date 01 May 2012

Institutional score
275.48
Impact
2459.31
5

Research

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3.

Bennett C L, Christie J, Ramsdell F, Brunkow M E, Ferguson P J ...

Nature genetics Vol 27(1)

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Date 01 Jan 2001

Institutional score
297.52
Impact
2459.31

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Date 01 Jan 2001

Institutional score
297.52
Impact
2459.31
6

Research

X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy.

Wildin R S, Ramsdell F, Peake J, Faravelli F, Casanova J L ...

Nature genetics Vol 27(1)

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Date 01 Jan 2001

Institutional score
0.00
Impact
2459.31

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Date 01 Jan 2001

Institutional score
0.00
Impact
2459.31
7

Research

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.

Bitner-Glindzicz M, Lindley K J, Rutland P, Blaydon D, Smith V V ...

Nature genetics Vol 26(1)

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Date 01 Sep 2000

Institutional score
12.87
Impact
2459.31

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Date 01 Sep 2000

Institutional score
12.87
Impact
2459.31
8

Research

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13.

Zielenski J, Corey M, Rozmahel R, Markiewicz D, Aznarez I ...

Nature genetics Vol 22(2)

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Date 01 Jun 1999

Institutional score
0.00
Impact
2459.31

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Date 01 Jun 1999

Institutional score
0.00
Impact
2459.31
9

Research

Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans.

de Pontual Loïc, Yao Evelyn, Callier Patrick, Faivre Laurence, Drouin Valérie ...

Nature genetics Vol 43(10)

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Date 04 Sep 2011

Institutional score
0.00
Impact
2459.31

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Date 04 Sep 2011

Institutional score
0.00
Impact
2459.31
10

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

Institutional score
73.64
Impact
2459.31

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Date 01 Dec 2016

Institutional score
73.64
Impact
2459.31

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