Mast cell growth factor maps near the steel locus on mouse chromosome 10 and is deleted in a number of steel alleles (Q48251836)

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scientific article published on October 5, 1990

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English	Mast cell growth factor maps near the steel locus on mouse chromosome 10 and is deleted in a number of steel alleles	scientific article published on October 5, 1990

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scholarly article

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Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/1698554

Mast cell growth factor maps near the steel locus on mouse chromosome 10 and is deleted in a number of steel alleles (English)

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10.1016/0092-8674(90)90298-S

https://api.crossref.org/works/10.1016/0092-8674(90)90298-S

1 November 2022

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chromosomal deletion syndrome

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1 November 2022

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Douglas E. Williams

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Williams DE

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Europe PubMed Central

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10 February 2018

http://europepmc.org/abstract/MED/1698554

Stewart D. Lyman

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Lyman SD

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10 February 2018

http://europepmc.org/abstract/MED/1698554

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N. G. Copeland

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D. J. Gilbert

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B. C. Cho

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P. J. Donovan

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N. A. Jenkins

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1 November 2022

D. Cosman

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D. Anderson

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publication date

1 October 1990

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10 February 2018

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5 October 1990

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10.1016/0092-8674(90)90298-S

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1 November 2022

https://api.elsevier.com/content/article/PII:009286749090298S?httpAccept=text/plain

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10.1016/0092-8674(90)90298-S

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Europe PubMed Central

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http://europepmc.org/abstract/MED/1698554

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175-183

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10 February 2018

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Genetic analysis of the mouse using interspecific crosses

1

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10.1016/0092-8674(90)90298-S

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Evidence that Linkage Group IV as well as Linkage Group X of the mouse are in chromosome 10

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The proto-oncogene c-kit encoding a transmembrane tyrosine kinase receptor maps to the mouse W locus

11

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The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene

14

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Mast-cell precursors in the skin of mouse embryos and their deficiency in embryos of Sl/Sld genotype

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Organization, distribution, and stability of endogenous ecotropic murine leukemia virus DNA sequences in chromosomes of Mus musculus

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A molecular genetic linkage map of mouse chromosome 13 anchored by the beige (bg) and satin (sa) loci

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Localization of mouse phenylalanine hydroxylase locus on chromosome 10

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c-kit protein, a transmembrane kinase: identification in tissues and characterization

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A comparison of pigment cell development in albino, steel, and dominant-spotting mutant mouse embryos

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An experimental analysis of the pigment defect caused by mutations at the W and S1 loci in mice

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Spleen-Colony Formation in Anemic Mice of Genotype WW

25

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Studies of the hemopoietic microenvironment. 3. Differences in the splenic microvascular system and stroma between SL-SL d and W-W v anemic mice

27

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Mouse mutants provide new insights into the role of extracellular matrix in cell migration and differentiation

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Association between collagen and glycosaminoglycans is altered in dermal extracellular matrix of fetal Steel (Sld/Sld) mice

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Extracellular matrix from normal but not Steel mutant mice enhances melanogenesis in cultured mouse neural crest cells.

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Hemopoietic cell growth factors and their receptors

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Expression of c-kit gene products in known cellular targets of W mutations in normal and W mutant mice--evidence for an impaired c-kit kinase in mutant mice

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Molecular bases of dominant negative and loss of function mutations at the murine c-kit/white spotting locus: W37, Wv, W41 and W

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Primary structure of c-kit: relationship with the CSF-1/PDGF receptor kinase family--oncogenic activation of v-kit involves deletion of extracellular domain and C terminus.

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W mutant mice with mild or severe developmental defects contain distinct point mutations in the kinase domain of the c-kit receptor

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The Dominant W 42 Spotting Phenotype Results from a Missense Mutation in the c- kit Receptor Kinase

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Identifiers

10.1016/0092-8674(90)90298-S

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/1698554

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/1698554

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