(Q54390529)

29 May 2018

title

HAX-1 expression in human B lymphoma. (English)

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Bengt Fadeel

object named as

B Fadeel

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A Ottosson-Wadlund

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Rebecca Ceder

object named as

R Ceder

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author name string

A Kwiecinska

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A Ottosson-Wadlund

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R Ceder

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R C Grafström

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E Björck

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A Porwit

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publication date

28 January 2011

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published in

Leukemia

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volume

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issue

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page(s)

868-872

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

cites work

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.321

HAX-1 overexpression, splicing and cellular localization in tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.321

High expression of cyclin B1 predicts a favorable outcome in patients with follicular lymphoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.321

Systematic bioinformatic analysis of expression levels of 17,330 human genes across 9,783 samples from 175 types of healthy and pathological tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.321

A global map of human gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.321

HAX1 deficiency: Impact on lymphopoiesis and B-cell development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.321

HS1-Associated Protein X-1 Regulates Carcinoma Cell Migration and Invasion via Clathrin-Mediated Endocytosis of Integrin αvβ6

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.321

21 January 2018

Identifiers

DOI

10.1038/LEU.2010.321

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