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Chromosomes, Human, Pair 19

Known as: 19 chromosome, Chromosome 19 
The designation for each member of the nineteenth largest human autosomal chromosome pair. Chromosome 19 spans more than 63 million base pairs and… 
National Institutes of Health

Related topics

Related topics

18 relations
19q1p/19q CodeletionChromatinChromosome 19 Short Arm

Narrower (1)

Chromosome 19, trisomy 19q

Broader (1)

Chromosomes, Human, 19-20

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2001
Highly Cited
2001
Cotranscription and Intergenic Splicing of HumanP2Y 11 and SSF1 Genes*
The P2Y11 receptor is an ATP receptor positively coupled to the cAMP and phosphoinositide pathways. Ssf1 is a Saccharomyces… 
Highly Cited
1998
Highly Cited
1998
Characterization of gene expression, genomic structure, and chromosomal localization of Hells (Lsh).
Hells (Lsh) is a lymphoid-specific presumptive helicase with highest expression in lymphoid precursor cells. Other members of the… 
Highly Cited
1997
Highly Cited
1997
Localization, by linkage analysis, of the cystinuria type III gene to chromosome 19q13.1.
Cystinuria is an autosomal recessive aminoaciduria in which three urinary phenotypes (I, II, and III) have been described. An… 
Highly Cited
1997
Highly Cited
1997
Molecular analysis of cystinuria in Libyan Jews: exclusion of the SLC3A1 gene and mapping of a new locus on 19q.
Cystinuria is a hereditary disorder of amino acid transport and is manifested by the development of kidney stones. In some… 
Highly Cited
1994
Highly Cited
1994
The pregnancy-specific glycoprotein (PSG) gene cluster on human chromosome 19: fine structure of the 11 PSG genes and identification of 6 new genes forming a third subgroup within the…
The human pregnancy-specific glycoprotein (PSG) genes belong to the carcinoembryonic antigen (CEA) family, which in turn is a… 
Highly Cited
1989
Highly Cited
1989
Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19.
Highly Cited
1988
Highly Cited
1988
A primary map of ten DNA markers and two serological markers for human chromosome 19.
Highly Cited
1983
Highly Cited
1983
Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.
Variations in DNA sequence generate polymorphisms which can be followed through families. A cloned gene specific probe for human… 
Highly Cited
1983
Highly Cited
1983
The mouse genome contains two nonallelic pro-opiomelanocortin genes.
Highly Cited
1982
Highly Cited
1982
Assignment of the structural gene for the third component of human complement to chromosome 19.
The third component of complement (C3) is synthesized and secreted by cultured human primary fibroblasts. A monoclonal antibody… 
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