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Studies

33545 Unclassified

16514 Early Trials

13238 Research

12088 Case Reports

12007 Reviews

9797 Advanced Trials

5737 Other Trials

877 Meta-Analysis

Guidelines

195 Cochrane

189 Guidelines

62 Consensuses

Congresses

7579 Abstracts

1

Research

Increased neutrophil respiratory burst in bcr-null mutants.

Voncken J W, van Schaick H, Kaartinen V, Deemer K, Coates T ...

Cell Vol 80(5)

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Date 10 Mar 1995

Institutional score
0.00
Impact
3197.10

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Date 10 Mar 1995

Institutional score
0.00
Impact
3197.10
2

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
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

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
5

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
6

Research

JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia.

Boztug Kaan, Järvinen Päivi M, Salzer Elisabeth, Racek Tomas, Mönch Sebastian ...

Nature genetics Vol 46(9)

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Date 01 Sep 2014

Institutional score
148.76
Impact
2459.31

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Date 01 Sep 2014

Institutional score
148.76
Impact
2459.31
7

Research

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).

Klein Christoph, Grudzien Magda, Appaswamy Giridharan, Germeshausen Manuela, Sandrock Inga ...

Nature genetics Vol 39(1)

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Date 01 Jan 2007

Institutional score
0.00
Impact
2459.31

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Date 01 Jan 2007

Institutional score
0.00
Impact
2459.31
8

Research

Mutations in proto-oncogene GFI1 cause human neutropenia and target ELA2.

Person Richard E, Li Feng-Qian, Duan Zhijun, Benson Kathleen F, Wechsler Jeremy ...

Nature genetics Vol 34(3)

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Date 01 Jul 2003

Institutional score
297.52
Impact
2459.31

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Date 01 Jul 2003

Institutional score
297.52
Impact
2459.31
9

Research

Mutations associated with neutropenia in dogs and humans disrupt intracellular transport of neutrophil elastase.

Benson Kathleen F, Li Feng-Qian, Person Richard E, Albani Dalila, Duan Zhijun ...

Nature genetics Vol 35(1)

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Date 01 Sep 2003

Institutional score
297.52
Impact
2459.31

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Date 01 Sep 2003

Institutional score
297.52
Impact
2459.31
10

Research

Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia.

Devriendt K, Kim A S, Mathijs G, Frints S G, Schwartz M ...

Nature genetics Vol 27(3)

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Date 01 Mar 2001

Institutional score
0.00
Impact
2459.31

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Date 01 Mar 2001

Institutional score
0.00
Impact
2459.31

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