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Alpha-Methylacyl-CoA Racemase Deficiency

Known as: AMACR, AMACR DEFICIENCY, AMACRD 
A rare disorder caused by mutation in the AMACR gene. It is characterized by neurological abnormalities that appear in adulthood and include… Expand
National Institutes of Health

Papers overview

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Review
2014
Review
2014
The malignant transformation of cells requires adaptations across multiple metabolic processes to satisfy the energy required for… Expand
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Highly Cited
2011
Highly Cited
2011
Over the past few years several investigators have independently described unique low-grade renal epithelial neoplasms with clear… Expand
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2008
2008
Alpha-methylacyl-CoA racemase (AMACR) deficiency is a rare disorder of fatty acid metabolism which has recently been described in… Expand
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Highly Cited
2008
Highly Cited
2008
GOLPH2 is coding the 73-kDa type II Golgi membrane antigen GOLPH2/GP73. Upregulation of GOLPH2 mRNA has been recently reported in… Expand
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Highly Cited
2005
Highly Cited
2005
α-Methylacyl CoA racemase (AMACR) is overexpressed in prostate cancer relative to benign prostatic tissue. AMACR expression is… Expand
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Highly Cited
2004
Highly Cited
2004
alpha-Methylacyl-CoA racemase (Amacr) deficiency in humans leads to sensory motor neuronal and liver abnormalities. The disorder… Expand
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Highly Cited
2004
Highly Cited
2004
MOTIVATION To understand cancer etiology, it is important to explore molecular changes in cellular processes from normal state to… Expand
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Highly Cited
2004
Highly Cited
2004
Alpha-methylacyl-CoA racemase (AMACR) was first discovered by using cDNA microarray technology as a molecular marker for prostate… Expand
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Review
2004
Review
2004
The diagnosis of limited adenocarcinoma of the prostate is one of the more difficult challenges in surgical pathology. This paper… Expand
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Highly Cited
2003
Highly Cited
2003
Steroid 5α‐reductase 2 (SRD5A2) catalyzes the conversion of testosterone to the more potent androgen, DHT, in the prostate. The… Expand
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