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19p13.1

A chromosome band present on 19p
National Institutes of Health

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9 relations
BRD4 wt AlleleChromosome 19 Short ArmChromosomesELL wt Allele

Papers overview

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2011
2011
Acquisition of mixed lineage leukemia rearrangement in a chronic myeloid leukemia patient while on imatinib
Chronic myeloid leukemia (CML) is a clonal myeloproliferative disorder with a specific genetic abnormality, the Philadelphia… 
Highly Cited
2004
Highly Cited
2004
Detection of the founder effect in Finnish CADASIL families
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited… 
2003
2003
Antisense-mediated loss of calcium homoeostasis endoplasmic reticulum protein (CHERP; ERPROT213-21) impairs Ca2+ mobilization, nuclear factor of activated T-cells (NFAT) activation and cell…
We recently discovered a novel gene on chromosome 19p13.1 and its product, an integral endoplasmic reticulum (ER) membrane… 
2003
2003
Association scan of the novel psoriasis susceptibility region on chromosome 19: evidence for both susceptible and protective loci
Abstract:  To follow up the novel psoriasis susceptibility region on chromosome 19 (PSORS6), we performed an association scan for… 
Highly Cited
2002
Highly Cited
2002
Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel α1 subunit gene, SCN1A
2001
2001
Characterization of t(11;19)(q23;p13.3) by fluorescence in situ hybridization analysis in a pediatric patient with therapy-related acute myelogenous leukemia.
Highly Cited
1999
Highly Cited
1999
The leukemogenic fusion of MLL with ENL creates a novel transcriptional transactivator
Translocations affecting the chromosomal locus 11q23 are hallmarks of infant leukemias. These events disrupt the MLL gene (also… 
1997
1997
Physical mapping of human myosin-IXB (MYO9B), the human orthologue of the rat myosin myr 5, to chromosome 19p13.1.
The gene for human myosin-IXB (MYO9B) was mapped to human chromosome 19p13.1 using fluorescence in situ hybridization. The rat… 
1995
1995
Chromosomal localization of the human prostanoid receptor gene family.
1986
1986
Toward early diagnosis of myotonic dystrophy: construction and characterization of a somatic cell hybrid with a single human der(19) chromosome.
We have constructed a somatic cell hybrid line, designated 908K1, with a single human der(19) chromosome on a Chinese hamster… 
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