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1p36

A chromosome band present on 1p
National Institutes of Health

Related topics

Related topics

15 relations
CD52 wt AlleleCDK11B wt AlleleCLCN6 wt AlleleChromosome 1 Short Arm

Papers overview

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Highly Cited
2015
Highly Cited
2015
Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
Highly Cited
2009
Highly Cited
2009
A distinctive subtype of t(14;18)-negative nodal follicular non-Hodgkin lymphoma characterized by a predominantly diffuse growth pattern and deletions in the chromosomal region 1p36.
Follicular lymphoma (FL) is a morphologically and genetically well-characterized B-cell non-Hodgkin lymphoma that can show… 
Highly Cited
2003
Highly Cited
2003
Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome.
Monosomy 1p36 is the most common terminal deletion syndrome. This contiguous gene deletion syndrome is presumably caused by… 
Highly Cited
2003
Highly Cited
2003
DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism
Abstract.Four chromosomal loci (PARK2, PARK6, PARK7, and PARK9) associated with autosomal recessive, early onset parkinsonism are… 
Highly Cited
2002
Highly Cited
2002
Asthma and atopy – a total genome scan for susceptibility genes
Background:  Allergic asthma is an increasingly common disease of complex inheritance. Several studies have suggested candidate… 
Highly Cited
1999
Highly Cited
1999
Evidence for a rare prostate cancer-susceptibility locus at chromosome 1p36.
Combining data from a genomic screen in 70 families with a high risk for prostate cancer (PC) with data from candidate-region… 
Highly Cited
1999
Highly Cited
1999
Identification of a new member of the tumor necrosis factor family and its receptor, a human ortholog of mouse GITR
Highly Cited
1997
Highly Cited
1997
Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.
Deletions of the distal short arm of chromosome 1 (1p36) represent a common, newly delineated deletion syndrome, characterized by… 
Review
1995
Review
1995
Tumor necrosis factor ligand superfamily: involvement in the pathology of malignant lymphomas.
The TNF receptor superfamily members are all type I membrane glycoproteins with typical homology in the extracellular domain of… 
Highly Cited
1994
Highly Cited
1994
There may be two tumor suppressor genes on chromosome arm Ip closely associated with biologically distinct subtypes of neuroblastoma
We studied loss of heterozygosity (LOH) on chromosome arm Ip in 108 neuroblastomas using 14 polymorphic DNA markers. One‐hundred… 
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