Advances in the understanding of Barth syndrome
Author:
Affiliation:
1. Institute for Nanotechnology and Stem Cell Biology; Seattle; WA; USA
2. Division of Molecular and Cardiovascular Biology; Cincinnati Children's Research Foundation; Cincinnati; OH; USA
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.12271/fullpdf
Reference87 articles.
1. Comparison of lymphoblast mitochondria from normal subjects and patients with Barth syndrome using electron microscopic tomography;Acehan;Laboratory Investigation,2007
2. Distinct effects of tafazzin deletion in differentiated and undifferentiated mitochondria;Acehan;Mitochondrion,2009
3. Cardiac and skeletal muscle defects in a mouse model of human Barth syndrome;Acehan;Journal of Biological Chemistry,2010
4. Heart transplantation for Barth syndrome;Adwani;Pediatric Cardiology,1997
5. Impaired survival of bone marrow hematopoietic progenitor cells in cyclic neutropenia;Aprikyan;Blood,2001
Cited by 20 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. A Comprehensive Outlook on Dilated Cardiomyopathy (DCM): State-Of-The-Art Developments with Special Emphasis on OMICS-Based Approaches;Journal of Cardiovascular Development and Disease;2022-06-01
2. A new murine model of Barth syndrome neutropenia links TAFAZZIN deficiency to increased ER stress-induced apoptosis;Blood Advances;2022-04-21
3. Hereditary myopathies associated with hematological abnormalities;Muscle & Nerve;2022-01-05
4. Barth syndrome: cardiolipin, cellular pathophysiology, management, and novel therapeutic targets;Molecular and Cellular Biochemistry;2021-01-07
5. TAZ encodes tafazzin, a transacylase essential for cardiolipin formation and central to the etiology of Barth syndrome;Gene;2020-02
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