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Studies

72397 Unclassified

29025 Reviews

25338 Case Reports

22780 Research

13151 Advanced Trials

12923 Other Trials

10829 Early Trials

1146 Meta-Analysis

Guidelines

434 Guidelines

215 Consensuses

194 Cochrane

Congresses

17181 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

An Airway Protection Program Revealed by Sweeping Genetic Control of Vagal Afferents.

Prescott Sara L, Umans Benjamin D, Williams Erika K, Brust Rachael D, Liberles Stephen D

Cell Vol 181(3)

Read

Date 30 Apr 2020

Institutional score
219.34
Impact
3860.25

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Date 30 Apr 2020

Institutional score
219.34
Impact
3860.25
3

Research

Residual embryonic cells as precursors of a Barrett's-like metaplasia.

Wang Xia, Ouyang Hong, Yamamoto Yusuke, Kumar Pooja Ashok, Wei Tay Seok ...

Cell Vol 145(7)

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Date 24 Jun 2011

Institutional score
1487.60
Impact
3197.10

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Date 24 Jun 2011

Institutional score
1487.60
Impact
3197.10
4

Research

Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD).

Logan Clare V, Lucke Barbara, Pottinger Caroline, Abdelhamed Zakia A, Parry David A ...

Nature genetics Vol 43(12)

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Date 20 Nov 2011

Institutional score
30.74
Impact
2459.31

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Date 20 Nov 2011

Institutional score
30.74
Impact
2459.31
5

Research

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.

Su Zhan, Gay Laura J, Strange Amy, Palles Claire, Band Gavin ...

Nature genetics Vol 44(10)

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Date 01 Oct 2012

Institutional score
32.20
Impact
2459.31

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Date 01 Oct 2012

Institutional score
32.20
Impact
2459.31
6

Research

Keap1-null mutation leads to postnatal lethality due to constitutive Nrf2 activation.

Wakabayashi Nobunao, Itoh Ken, Wakabayashi Junko, Motohashi Hozumi, Noda Shuhei ...

Nature genetics Vol 35(3)

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Date 01 Nov 2003

Institutional score
16.20
Impact
2459.31

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Date 01 Nov 2003

Institutional score
16.20
Impact
2459.31
7

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
8

Research

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22.

Quaderi N A, Schweiger S, Gaudenz K, Franco B, Rugarli E I ...

Nature genetics Vol 17(3)

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Date 01 Nov 1997

Institutional score
0.00
Impact
2459.31

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Date 01 Nov 1997

Institutional score
0.00
Impact
2459.31
9

Research

Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP.

Xiao S, Yu C, Chou X, Yuan W, Wang Y ...

Nature genetics Vol 27(2)

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Date 01 Feb 2001

Institutional score
7438.00
Impact
2459.31

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Date 01 Feb 2001

Institutional score
7438.00
Impact
2459.31
10

Research

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy.

Brais B, Bouchard J P, Xie Y G, Rochefort D L, Chrétien N ...

Nature genetics Vol 18(2)

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Date 01 Feb 1998

Institutional score
56.78
Impact
2459.31

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Date 01 Feb 1998

Institutional score
56.78
Impact
2459.31

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