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Studies

15392 Unclassified

5315 Reviews

3989 Research

3433 Early Trials

3409 Other Trials

2861 Case Reports

2633 Advanced Trials

100 Meta-Analysis

Guidelines

50 Guidelines

46 Cochrane

26 Consensuses

Congresses

2937 Abstracts

1

Research

Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis.

Khajuria Rajiv K, Munschauer Mathias, Ulirsch Jacob C, Fiorini Claudia, Ludwig Leif S ...

Cell Vol 173(1)

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Date 22 Mar 2018

Institutional score
929.75
Impact
3197.10

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Date 22 Mar 2018

Institutional score
929.75
Impact
3197.10
2

Research

Increased myeloid cell responses to M-CSF and RANKL cause bone loss and inflammation in SH3BP2 "cherubism" mice.

Ueki Yasuyoshi, Lin Chin-Yu, Senoo Makoto, Ebihara Takeshi, Agata Naoki ...

Cell Vol 128(1)

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Date 12 Jan 2007

Institutional score
0.00
Impact
3197.10

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Date 12 Jan 2007

Institutional score
0.00
Impact
3197.10
3

Research

Crosstalk between sentinel and helper macrophages permits neutrophil migration into infected uroepithelium.

Schiwon Marzena, Weisheit Christina, Franken Lars, Gutweiler Sebastian, Dixit Akanksha ...

Cell Vol 156(3)

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Date 30 Jan 2014

Institutional score
137.74
Impact
3197.10

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Date 30 Jan 2014

Institutional score
137.74
Impact
3197.10
4

Research

Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein.

Ho M, Chelly J, Carter N, Danek A, Crocker P ...

Cell Vol 77(6)

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Date 17 Jun 1994

Institutional score
0.00
Impact
3197.10

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Date 17 Jun 1994

Institutional score
0.00
Impact
3197.10
5

Research

Physiogenomic resources for rat models of heart, lung and blood disorders.

Malek Renae L, Wang Hong-ying, Kwitek Anne E, Greene Andrew S, Bhagabati Nirmal ...

Nature genetics Vol 38(2)

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Date 01 Feb 2006

Institutional score
0.00
Impact
2459.31

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Date 01 Feb 2006

Institutional score
0.00
Impact
2459.31
6

Research

Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.

Iotchkova Valentina, Huang Jie, Morris John A, Jain Deepti, Barbieri Caterina ...

Nature genetics Vol 48(11)

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Date 01 Nov 2016

Institutional score
391.47
Impact
2459.31

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Date 01 Nov 2016

Institutional score
391.47
Impact
2459.31
7

Research

Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia.

Guernsey Duane L, Jiang Haiyan, Campagna Dean R, Evans Susan C, Ferguson Meghan ...

Nature genetics Vol 41(6)

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Date 01 Jun 2009

Institutional score
16.94
Impact
2459.31

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Date 01 Jun 2009

Institutional score
16.94
Impact
2459.31
8

Research

Genome-wide association study of hematological and biochemical traits in a Japanese population.

Kamatani Yoichiro, Matsuda Koichi, Okada Yukinori, Kubo Michiaki, Hosono Naoya ...

Nature genetics Vol 42(3)

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Date 01 Mar 2010

Institutional score
128.24
Impact
2459.31

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Date 01 Mar 2010

Institutional score
128.24
Impact
2459.31
9

Research

Mutations in SBDS are associated with Shwachman-Diamond syndrome.

Boocock Graeme R B, Morrison Jodi A, Popovic Maja, Richards Nicole, Ellis Lynda ...

Nature genetics Vol 33(1)

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Date 01 Jan 2003

Institutional score
17.30
Impact
2459.31

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Date 01 Jan 2003

Institutional score
17.30
Impact
2459.31
10

Research

The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia.

Draptchinskaia N, Gustavsson P, Andersson B, Pettersson M, Willig T N ...

Nature genetics Vol 21(2)

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Date 01 Feb 1999

Institutional score
37.38
Impact
2459.31

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Date 01 Feb 1999

Institutional score
37.38
Impact
2459.31

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