The Human TAZ Gene Complements Mitochondrial Dysfunction in the Yeast taz1Δ Mutant

This publication has 27 references indexed in Scilit:

• Quantification of Free Sialic Acid in Urine by HPLC–Electrospray Tandem Mass Spectrometry: A Tool for the Diagnosis of Sialic Acid Storage Disease
  Clinical Chemistry, 2004
• Only One Splice Variant of the Human TAZ Gene Encodes a Functional Protein with a Role in Cardiolipin Metabolism
  Published by Elsevier ,2003
• Deficiency of tetralinoleoyl‐cardiolipin in Barth syndrome
  Annals of Neurology, 2002
• Defective Remodeling of Cardiolipin and Phosphatidylglycerol in Barth Syndrome
  Biochemical and Biophysical Research Communications, 2000
• The X-Linked Gene G4.5 Is Responsible for Different Infantile Dilated Cardiomyopathies
  American Journal of Human Genetics, 1997
• X‐linked cardioskeletal myopathy and neutropenia (Barth syndrome): Respiratory‐chain abnormalities in cultured fibroblasts
  Journal of Inherited Metabolic Disease, 1996
• Gene disruption with PCR products in Saccharomyces cerevisiae
  Gene, 1995
• 2-Hydroxyphytanic acid oxidase activity in rat and human liver and its deficiency in the Zellweger syndrome
  Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1994
• Barth syndrome: Clinical observations and genetic linkage studies
  American Journal of Medical Genetics, 1994
• The regulation of the matrix volume of mammalian mitochondria in vivo and in vitro and its role in the control of mitochondrial metabolism
  Biochimica et Biophysica Acta (BBA) - Bioenergetics, 1989