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1p36.11

A chromosome band present on 1p
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Several chronic lymphocytic leukaemia (CLL) susceptibility loci have been reported; however, much of the heritable risk remains… Expand
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2012
2012
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
Celiac disease (CD) is a chronic inflammatory disease of the small bowel that occurs with the ingestion of gluten, found in… Expand
2011
2011
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
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
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
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
Monosomy 1p36 is the most common terminal deletion syndrome with an estimated occurrence of 1:5000 live births. Typically, the… Expand
2003
2003
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
Previous cytogenetic/FISH data have demonstrated 1p36 deletions in a relapsing familial clivus chordoma developed by a patient… Expand