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1p36.3

A chromosome band present on 1p
National Institutes of Health

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5 relations
Chromosome 1 Short ArmChromosomesDFFB wt AlleleTNFRSF18 wt Allele

Papers overview

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2011
2011
Molecular cytogenetic characterization of epithelioid hemangioendothelioma.
2006
2006
Mild craniosynostosis with 1p36.3 trisomy and 1p36.3 deletion syndrome caused by familial translocation t(Y;1)
We report on a 20‐year‐old man and a 16‐year‐old woman with a chromosomal imbalance derived from a balanced translocation, t(Y;1… 
Highly Cited
2004
Highly Cited
2004
Reproducible compartmentalization of individual chromosome domains in human CNS cells revealed by in situ hybridization and three-dimensional reconstruction
Specific chromosome domains in interphase nuclei of neurons and glia were studied by three-dimensional (3-D) reconstruction of… 
Review
2003
Review
2003
Biological and clinical role of p73 in neuroblastoma.
2001
2001
Genetic analysis of p73 localized at chromosome 1p36.3 in primary neuroblastomas.
BACKGROUND Human p73, a novel homolog of p53, has recently been cloned and mapped at chromosome 1p36.3, the locus for putative… 
Highly Cited
2001
Highly Cited
2001
Detailed molecular analysis of 1p36 in neuroblastoma.
BACKGROUND Several lines of evidence es tablish that chromosome band 1p36 is frequently deleted in neuroblastoma primary tumors… 
2000
2000
Fine mapping of the human preprocortistatin gene (CORT) to neuroblastoma consensus deletion region 1p36.3→p36.2, but absence of mutations in primary tumors
The processed product of the human gene preprocortistatin, the peptide cortistatin-17 (hCST-17), bears a strong structural… 
1999
1999
Assignment1 of the gene encoding mannan-binding lectin-associated serine protease 2 (MASP2) to human chromosome 1p36.3→p36.2 by in situ hybridization and somatic cell hybrid analysis
The complement system is an important constituent of the innate immune defense. It can be activated via an immune complex… 
Highly Cited
1997
Highly Cited
1997
Molecular-cytogenetic detection of a deletion of 1p36.3.
We report a deletion of 1p36.3 in a child with microcephaly, mental retardation, broad forehead, deep set eyes, depressed nasal… 
Highly Cited
1995
Highly Cited
1995
Partial monosomy of chromosome 1p36.3: characterization of the critical region and delineation of a syndrome.
We describe 5 patients ranging in age from 3 to 47 years, with karyotypic abnormalities resulting in monosomy for portion of 1p36… 
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