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1p36.11

A chromosome band present on 1p
National Institutes of Health

Related topics

Related topics

8 relations
CLIC4 wt AlleleCNKSR1 wt AlleleChromosome 1 Short ArmChromosomes
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Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia
Several chronic lymphocytic leukaemia (CLL) susceptibility loci have been reported; however, much of the heritable risk remains… Expand
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2012
2012
Mutations and deletions of ARID1A in breast tumors
Mamo et al. (2011) identified ARID1A as a candidate tumor suppressor gene (TSG) in breast cancer (BC) by an integrated genomic… Expand
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2012
2012
The cannabinoid receptor type 2 Q63R variant increases the risk of celiac disease: implication for a novel molecular biomarker and future therapeutic intervention.
Celiac disease (CD) is a chronic inflammatory disease of the small bowel that occurs with the ingestion of gluten, found in… Expand
2011
2011
CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura
Immune thrombocytopenic purpura is an acquired autoimmune disorder that is the most common cause of thrombocytopenia in children… Expand
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Highly Cited
2011
Highly Cited
2011
A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi Jews.
Retinitis pigmentosa (RP) is a heterogeneous group of inherited retinal degenerations caused by mutations in at least 50 genes… Expand
Highly Cited
2009
Highly Cited
2009
Genomic profiling of plasmablastic lymphoma using array comparative genomic hybridization (aCGH): revealing significant overlapping genomic lesions with diffuse large B-cell lymphoma
BackgroundPlasmablastic lymphoma (PL) is a subtype of diffuse large B-cell lymphoma (DLBCL). Studies have suggested that tumors… Expand
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Highly Cited
2007
Highly Cited
2007
Genomic and functional evidence for an ARID1A tumor suppressor role
ARID1A is located in 1p36.11, a region frequently deleted in human cancers. Using a novel method to screen for tumorigenic cDNA… Expand
2007
2007
Identification of proximal 1p36 deletions using array‐CGH: a possible new syndrome
Monosomy 1p36 is the most common terminal deletion syndrome with an estimated occurrence of 1:5000 live births. Typically, the… Expand
2003
2003
TERE1, a novel gene affecting growth regulation in prostate carcinoma
Recently, we isolated a ubiquitously expressed gene designated TERE1, which has a significant effect on the growth regulation in… Expand
Highly Cited
2000
Highly Cited
2000
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36
Previous cytogenetic/FISH data have demonstrated 1p36 deletions in a relapsing familial clivus chordoma developed by a patient… Expand
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