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1p36.33

A chromosome band present on 1p
National Institutes of Health

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Chromosome 1 Short ArmChromosomesGLTPD1 wt AlleleGNB1 wt Allele

Papers overview

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2016
2016
1p36 deletion syndrome confirmed by fluorescence in situ hybridization and array-comparative genomic hybridization analysis
Pediatric epilepsy can be caused by various conditions, including specific syndromes. 1p36 deletion syndrome is reported in 1 in… 
2008
2008
Array comparative genomic hybridisation-based identification of two imbalances of chromosome 1p in a 9-year-old girl with a monosomy 1p36 related phenotype and a family history of learning…
IntroductionMonosomy 1p36 is one of the most common terminal deletion syndromes, with an approximate incidence of 1 in every 5000… 
2005
2005
Clinicopathologic significance of loss of heterozygosity on chromosome 1 in cervical cancer.
2004
2004
Methylation status of TP73 in meningiomas.
Highly Cited
2001
Highly Cited
2001
Analysis of p73 gene in meningiomas with deletion at 1p.
2001
2001
P73 EXPRESSION IN NEUROBLASTOMA: A ROLE IN THE BIOLOGY OF ADVANCED TUMORS?
p73, a recently identified gene showing high homology to p53 and mapping to 1p36.33, was presented as a candidate gene for… 
2000
2000
The p73 gene is not mutated in oligodendrogliomas which frequently have a deleted region at chromosome 1p36.3.
An allelic loss of the chromosome 1p36 region is frequently found in oligodendrogliomas, which suggests the presence of putative… 
2000
2000
Molecular alterations of p 73 in human esophageal squamous cell carcinomas : loss of heterozygosity occurs frequently ; loss of imprinting and elevation of p 73 expression may be related to defective…
Yuyang Christine Cai, Guang-yu Yang, Yan Nie, functional similarity to p53. In the SK-N-AS cell line, expresLi-Dong Wang1, Xin… 
1999
1999
Lack of homozygously inactivated p73 in single-copy MYCN primary neuroblastomas and neuroblastoma cell lines.
We examined 18 neuroblastoma cell lines and 32 primary single-copy MYCN tumor specimens to determine whether mutations of p73, a… 
1999
1999
Allelic loss at the p73 locus (1p36.33) is infrequent in malignant melanoma
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