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Chromosomes, Human, Pair 4

Known as: 4 chromosome, Chromosome 4 
The designation for each member of the fourth largest human autosomal chromosome pair. Chromosome 4 spans more than 186 million base pairs and… 
National Institutes of Health

Related topics

Related topics

15 relations
ChromatinChromosome 4 Short ArmLoss of Chromosome 4Microbiological

Narrower (3)

Chromosome 4 short arm deletionChromosome 4, trisomy 4qRing chromosome 4 syndrome

Broader (1)

Chromosomes, Human, 4-5

Papers overview

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Highly Cited
2005
Highly Cited
2005
Copy number aberrations in mouse breast tumors reveal loci and genes important in tumorigenic receptor tyrosine kinase signaling.
Receptor tyrosine kinase (RTK) signaling plays a key role in the development of breast cancer. Defining the genes and pathways in… 
Highly Cited
2004
Highly Cited
2004
Directed changes in the pattern of Balbiani ring puffing in Chironomus: effects of a sugar treatment
The Balbiani ring situation in larval salivary gland nuclei of Chironomus tentans and of C. pallidivittatus has been… 
Highly Cited
1996
Highly Cited
1996
Mom1 is a semi-dominant modifier of intestinal adenoma size and multiplicity in Min/+ mice.
The intestinal tumor multiplicity in mice heterozygous for ApcMin is strongly modulated by genetic background. On the sensitive… 
Highly Cited
1996
Highly Cited
1996
Mapping of the OB receptor to 1p in a region of nonconserved gene order from mouse and rat to human.
As part of an effort to identify informative molecular markers for genetic analysis of human pedigrees segregating for obesity… 
Highly Cited
1994
Highly Cited
1994
Mapping of a gene for hypergammaglobulinemia to the distal region on chromosome 4 in NZB mice and its contribution to systemic lupus erythematosus in (NZB x NZW)F1 mice.
IgM class hypergammaglobulinemia develops spontaneously in the early life of NZB mice. To determine the chromosomal location of… 
Highly Cited
1993
Highly Cited
1993
Molecular diversity of the SCG10/stathmin gene family in the mouse.
SCG10 is a neuronal growth-associated protein that shares an amino acid sequence similarity with an 18- to 19-kDa phosphoprotein… 
Highly Cited
1992
Highly Cited
1992
Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome.
The parental origin of the de novo deleted chromosome 4 was studied in five cases of Wolf-Hirschhorn syndrome using polymorphic… 
Highly Cited
1989
Highly Cited
1989
Recombinant inbred strain and interspecific backcross analysis of molecular markers flanking the murine agouti coat color locus.
Recombinant inbred strain and interspecific backcross mice were used to create a molecular genetic linkage map of the distal… 
Highly Cited
1988
Highly Cited
1988
Long-range restriction maps of Plasmodium falciparum chromosomes: crossingover and size variation among geographically distant isolates.
Highly Cited
1971
Highly Cited
1971
The 4p- syndrome. A clinically recognizable chromosomal deletion syndrome.
Partial deletion of the short arm of chromosome 4 results in a clinically recognizable and distinct syndrome. Common features… 
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