UROD wt Allele

Known as: Uroporphyrinogen III Decarboxylase Gene, UPD, PCT 
Human UROD wild-type allele is located in the vicinity of 1p34 and is approximately 4 kb in length. This allele, which encodes uroporphyrinogen… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1977-2018
0204019772018

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Highly Cited
2010
Highly Cited
2010
Mosaic aneuploidy and uniparental disomy (UPD) arise from mitotic or meiotic events. There are differences between these… (More)
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Highly Cited
2009
Highly Cited
2009
Cytogenetic analysis of acute myeloid leukemia (AML) cells has accelerated the identification of genes important for AML… (More)
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Highly Cited
2008
Highly Cited
2008
Two types of acquired loss of heterozygosity are possible in cancer: deletions and copy-neutral uniparental disomy (UPD… (More)
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Highly Cited
2008
Highly Cited
2008
Pediatric acute lymphoblastic leukemia (ALL) is a malignant disease resulting from accumulation of genetic alterations. A robust… (More)
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Highly Cited
2007
Highly Cited
2007
Loss of heterozygosity (LOH), either with or without accompanying copy-number loss, is a cardinal feature of cancer genomes that… (More)
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Highly Cited
2005
Highly Cited
2005
Genome-wide analysis of single nucleotide polymorphisms in 64 acute myeloid leukemias has revealed that approximately 20… (More)
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Highly Cited
2005
Highly Cited
2005
Beckwith–Wiedemann Syndrome (BWS) results from mutations or epigenetic events involving imprinted genes at 11p15.5. Most BWS… (More)
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Highly Cited
2003
Highly Cited
2003
BACKGROUND Twin studies of bipolar affective disorder (BPD) have either been small or have not used explicit diagnostic criteria… (More)
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Highly Cited
1997
Highly Cited
1997
Angelman syndrome (AS) is a human genetic disorder characterized by mental retardation, seizures, inappropriate laughter… (More)
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Highly Cited
1995
Highly Cited
1995
Maternal uniparental disomy for the entire chromosome 7 has so far been reported in three patients with intrauterine and… (More)
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