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19q13.1

A chromosome band present on 19q
National Institutes of Health

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15 relations
19qAXL wt AlleleCEBPA wt AlleleCLC wt Allele
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Highly Cited
2008
Highly Cited
2008
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer
Genome-wide association (GWA) studies have identified multiple loci at which common variants modestly influence the risk of… Expand
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Highly Cited
2003
Highly Cited
2003
Array-based comparative genomic hybridization for genome-wide screening of DNA copy number in bladder tumors.
Genome-wide copy number profiles were characterized in 41 primary bladder tumors using array-based comparative genomic… Expand
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Highly Cited
2000
Highly Cited
2000
Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL; MIM 221770), also known as Nasu-Hakola… Expand
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Highly Cited
2000
Highly Cited
2000
Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene.
Autosomal recessive Charcot-Marie-Tooth disease (CMT) type 4 (CMT4) is a complex group of demyelinating hereditary motor and… Expand
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Highly Cited
1999
Highly Cited
1999
Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations.
Congenital nephrotic syndrome of the Finnish type (NPHS1) is an autosomal recessive disorder that is caused by mutations in the… Expand
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Highly Cited
1999
Highly Cited
1999
MLL2, the second human homolog of the Drosophila trithorax gene, maps to 19q13.1 and is amplified in solid tumor cell lines
The Mixed Lineage Leukemia (MLL) gene is commonly involved in translocations in infantile leukemia and is amplified in some cases… Expand
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Highly Cited
1998
Highly Cited
1998
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B
Febrile seizures affect approximately 3% of all children under six years of age and are by far the most common seizure disorder… Expand
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Highly Cited
1997
Highly Cited
1997
A cluster of four novel human G protein-coupled receptor genes occurring in close proximity to CD22 gene on chromosome 19q13.1.
In our search for novel human galanin receptor (GALR) subtypes, human genomic DNA was PCR amplified using sets of degenerate… Expand
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Highly Cited
1996
Highly Cited
1996
Isolation of DNA sequences amplified at chromosome 19q13.1-q13.2 including the AKT2 locus in human pancreatic cancer.
In the human pancreatic cancer cell line PANC1, we detected several DNA fragments with abnormally intensified signals by… Expand
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Highly Cited
1991
Highly Cited
1991
A novel putative tyrosine kinase receptor with oncogenic potential.
We have detected transforming activity by a tumorigenicity assay using NIH3T3 cells transfected with DNA from a chronic… Expand
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