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19p13

A chromosome band present on 19p
National Institutes of Health

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6 relations
CD209 wt AlleleCDKN2D wt AlleleChromosome 19 Short ArmChromosomes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Association of the genetic markers for myocardial infarction with sudden cardiac death
2007
2007
The P/Q-type voltage-dependent calcium channel as pharmacological target in spinocerebellar ataxia type 6: gabapentin and pregabalin may be of therapeutic benefit.
2005
2005
Genetic variants of Complex I in multiple sclerosis
2003
2003
Heterogeneity of breakpoints in non-LCR-mediated large constitutional deletions of the 17q11.2 NF1 tumour suppressor region
Neurofibromatosis type 1 (NF1) is caused by mutations of the NF1 gene at 17q11.2. The encoded protein, termed neurofibromin… 
2002
2002
Novel der(1)t(1;19) in two patients with myeloid neoplasias.
2001
2001
The 90- and 110-kDa human NFAR proteins are translated from two differentially spliced mRNAs encoded on chromosome 19p13.
The NFAR gene (nuclear factor associated with dsRNA) encodes a putative transcription-associated factor that we have shown is a… 
Review
1995
Review
1995
Genetic changes in ovarian cancer.
The development of cancer is a multistep process involving accumulation of genetic changes which progressively transform normal… 
1993
1993
Molecular Cloning of 19p13 Breakpoint Region in Infantile Leukemia with t(11;19)(q23;p13) Translocation
We studied the breakpoint regions involved in t(11;19)(q23;p13) translocation associated with infantile leukemias. Southern blot… 
1990
1990
Assignment of the erythropoietin receptor (EPOR) gene to mouse chromosome 9 and human chromosome 19.
1985
1985
A folate sensitive heritable fragile site at 19p13
A fragile site at 19pl3 was found in the mother of a newborn girl with Downs syndrome. The fragile site was expressed in medium… 
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