AGXT gene

Known as: AGXT, AGT1, ALANINE-GLYOXYLATE AMINOTRANSFERASE 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1972-2017
0102019722017

Papers overview

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2013
2013
Halovirus PH1 infects Haloarcula hispanica and was isolated from an Australian salt lake. The burst size in single-step growth… (More)
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Highly Cited
2006
Highly Cited
2006
Primary hyperoxaluria is characterized by severe urolithiasis, nephrocalcinosis, and early renal failure. As treatment options… (More)
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2005
2005
Primary hyperoxaluria (PH1) is a condition caused by a hepatic-based enzyme defect which can lead to renal failure due to oxalate… (More)
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2003
2003
BACKGROUND Combined liver-kidney transplantation is the definitive treatment for end-stage renal disease caused by primary… (More)
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2003
2003
A deficiency of the liver-specific enzyme alanine:glyoxylate aminotransferase (AGT) is responsible for the potentially lethal… (More)
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2001
2001
Primary hyperoxaluria type 1 (PH1) is an autosomal recessive disorder that is caused by a deficiency of alanine: glyoxylate… (More)
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2000
2000
The autosomal recessive disorder primary hyperoxaluria type 1 (PH1) is caused by a deficiency of the liver-specific pyridoxal… (More)
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1997
1997
Primary hyperoxaluria type 1 (PH1) is a severe autosomal recessive inborn error of glyoxylate metabolism caused by deficiency of… (More)
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Highly Cited
1990
Highly Cited
1990
We have previously shown that in some patients with primary hyperoxaluria type 1 (PH1), disease is associated with mistargeting… (More)
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1989
1989
Most patients with the autosomal recessive disease primary hyperoxaluria type 1 (PH1) have a complete deficiency of alanine… (More)
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