Complex expression pattern of the Barth syndrome gene product tafazzin in human cell lines and murine tissues

A novel X-linked gene, G4.5. is responsible for Barth syndrome

1996 • 733 citations

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

1983 • 662 citations

Novel Gene Mutations in Patients With Left Ventricular Noncompaction or Barth Syndrome

2001 • 554 citations

Defective Remodeling of Cardiolipin and Phosphatidylglycerol in Barth Syndrome

2000 • 369 citations

X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria

1991 • 270 citations

Analysis of Amino Acid Motifs Diagnostic for the sn-Glycerol-3-phosphate Acyltransferase Reaction

1999 • 261 citations

The X-Linked Gene G4.5 Is Responsible for Different Infantile Dilated Cardiomyopathies

1997 • 229 citations

Remodeling of Cardiolipin by Phospholipid Transacylation

2003 • 203 citations

Aberrant cardiolipin metabolism in the yeast taz1 mutant: a model for Barth syndrome

2003 • 192 citations

Function of Lactococcus lactis Nisin Immunity Genes nisI and nisFEG after Coordinated Expression in the Surrogate Host Bacillus subtilis

2002 • 180 citations

A Conserved Histidine Is Essential for Glycerolipid Acyltransferase Catalysis

1998 • 149 citations

Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28.

1991 • 144 citations

Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome

1997 • 134 citations

Only One Splice Variant of the Human TAZ Gene Encodes a Functional Protein with a Role in Cardiolipin Metabolism

2003 • 132 citations

Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction

2002 • 124 citations

Barth syndrome: Clinical features and confirmation of gene localisation to distal Xq28

1993 • 117 citations

Critical Factors in Basal Cell Adhesion Molecule/Lutheran-mediated Adhesion to Laminin

1999 • 96 citations

Infantile Dilated X-Linked Cardiomyopathy, G4.5 Mutations, Altered Lipids, and Ultrastructural Malformations of Mitochondria in Heart, Liver, and Skeletal Muscle

2002 • 63 citations

Regulation of cytosolic phospholipase A2, cyclooxygenase-1 and -2 expression by PMA, TNFα, LPS and M-CSF in human monocytes and macrophages

2003 • 48 citations

A Conserved Seven Amino Acid Stretch Important for Murine Mitochondrial Glycerol-3-phosphate Acyltransferase Activity

1999 • 44 citations

Dilated cardiomyopathy with neutropenia, short stature, and abnormal carnitine metabolism

1988 • 44 citations

Untitled

2003 • 41 citations

3‐Methylglutaconic aciduria: A marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a ‘new’ type (‘type 4’)

1991 • 33 citations

Functional characteristics of a novel murine estrogen receptor-beta isoform, estrogen receptor-beta 2

2000 • 32 citations

A novel intronic mutation of the TAZ ( G4.5 ) gene in a patient with Barth syndrome: creation of a 5' splice donor site with variant GC consensus and elongation of the upstream exon

2001 • 20 citations

Novel missense mutation (R94S) in the TAZ (G4.5) gene in a Japanese patient with Barth syndrome

2002 • 14 citations