TAZ gene

Known as: TAZ1, XAP-2, TAZ 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1991-2017
010203019912017

Papers overview

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Highly Cited
2006
Highly Cited
2006
OBJECTIVE Barth syndrome, an X-linked disorder that is characterized by cardiomyopathy, neutropenia, skeletal myopathy, and… (More)
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2005
2005
Barth syndrome (MIM 302060) is an X-linked condition that includes dilated cardiomyopathy, neutropenia, failure to thrive… (More)
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2004
2004
Barth syndrome is a genetic disorder that is caused by different mutations in the TAZ gene G4.5. The yeast gene TAZ1 is highly… (More)
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Highly Cited
2003
Highly Cited
2003
Mitochondrial cardiolipin (CL) contains unique fatty acid patterns, but it is not known how the characteristic molecular species… (More)
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Highly Cited
2002
Highly Cited
2002
The cellular response to low tissue oxygen concentrations is mediated by the hypoxia-inducible transcription factor HIF-1. Under… (More)
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Highly Cited
2001
Highly Cited
2001
BACKGROUND Mutations in the gene G4.5 result in a wide spectrum of severe infantile cardiomyopathic phenotypes, including… (More)
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Highly Cited
2000
Highly Cited
2000
Cardiolipin (CL) and phosphatidylglycerol (PG) are the major polyglycerophospholipids observed in mammalian tissues. CL is… (More)
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Highly Cited
1997
Highly Cited
1997
Loss-of-function mutations in the G4.5 gene have been shown to cause Barth syndrome (BTHS), an X-linked disorder characterized by… (More)
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Highly Cited
1997
Highly Cited
1997
Barth syndrome (BTHS) is an X-linked disorder characterized clinically by the associated features of cardiac and skeletal… (More)
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Highly Cited
1996
Highly Cited
1996
Barth Syndrome is a severe inherited disorder, often fatal in childhood, characterized by cardiac and skeletal myopathy, short… (More)
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