The cellular and molecular mechanisms for neutropenia in Barth syndrome.
about
Successful management of Barth syndrome: a systematic review highlighting the importance of a flexible and multidisciplinary approachThe antimicrobial propeptide hCAP-18 plasma levels in neutropenia of various aetiologies: a prospective study.Exogenous cardiolipin localizes to mitochondria and prevents TAZ knockdown-induced apoptosis in myeloid progenitor cells.New clinical and molecular insights on Barth syndromeAdvances in the understanding of Barth syndrome.Inborn errors of metabolism underlying primary immunodeficiencies.Understanding chronic neutropenia: life is short.The emerging role of immune dysfunction in mitochondrial diseases as a paradigm for understanding immunometabolism.Evaluation of cardiolipin nanodisks as lipidreplacement therapy for Barth syndrome.
P2860
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P2860
The cellular and molecular mechanisms for neutropenia in Barth syndrome.
description
2011 nî lūn-bûn
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2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
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name
The cellular and molecular mechanisms for neutropenia in Barth syndrome.
@en
The cellular and molecular mechanisms for neutropenia in Barth syndrome.
@nl
type
label
The cellular and molecular mechanisms for neutropenia in Barth syndrome.
@en
The cellular and molecular mechanisms for neutropenia in Barth syndrome.
@nl
prefLabel
The cellular and molecular mechanisms for neutropenia in Barth syndrome.
@en
The cellular and molecular mechanisms for neutropenia in Barth syndrome.
@nl
P2093
P2860
P1476
The cellular and molecular mechanisms for neutropenia in Barth syndrome.
@en
P2093
Andrew A Aprikyan
Christopher Allen
David C Dale
Frederic M Vaz
Vahagn Makaryan
Willem Kulik
Yigal Dror
P2860
P304
P356
10.1111/J.1600-0609.2011.01725.X
P577
2011-12-04T00:00:00Z