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Studies

49090 Unclassified

20690 Reviews

19826 Case Reports

14000 Research

10167 Other Trials

8758 Early Trials

8741 Advanced Trials

731 Meta-Analysis

Guidelines

294 Guidelines

127 Consensuses

116 Cochrane

Congresses

11591 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

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
4

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
5

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
6

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
7

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
8

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
9

Research

Detection of prostatic cancer by solid-phase radioimmunoassay of serum prostatic acid phosphatase.

Foti A G, Cooper J F, Herschman H, Malvaez R R

The New England journal of medicine Vol 297(25)

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Date 22 Dec 1977

Institutional score
0.00
Impact
1998.19

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Date 22 Dec 1977

Institutional score
0.00
Impact
1998.19
10

Research

Psychiatric illness and contraction abnormalities of the esophagus.

Clouse R E, Lustman P J

The New England journal of medicine Vol 309(22)

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Date 01 Dec 1983

Institutional score
0.00
Impact
1998.19

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Date 01 Dec 1983

Institutional score
0.00
Impact
1998.19

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