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Article

The tight-skin (Tsk) mutation is closely linked to B2m on mouse chromosome 2.

Mammalian genome : official journal of the International Mammalian Genome Society - 1 Jan 1994

Everett E T, Pablos J L, Harris S E, LeRoy E C, Norris J S

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Identifiers

PMID: 8111131
DOI: 10.1007/BF00360571

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Research trail→

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The tight-skin (Tsk) mutation is closely linked to B2m on mouse chromosome 2.PMID 8111131Read ↗

A high-resolution linkage map of the tight skin 2 (Tsk2) locus: a mouse model for scleroderma (SSc) and other cutaneous fibrotic diseases.Semantic proximity Read ↗

Tight-skin (Tsk) maps on mouse chromosome 2 within the region of linkage homology with human chromosome 15.Semantic proximity Read ↗

The mouse tight skin (Tsk) phenotype is not dependent on the presence of mature T and B lymphocytes.Semantic proximity Read ↗

The tight skin (Tsk) mutation in the mouse, a model for human fibrotic diseases, is tightly linked to the beta 2-microglobulin (B2m) gene on chromosome 2.Semantic proximity Read ↗

Genetic defects in tight skin mice developing a scleroderma-like syndrome.Semantic proximity Read ↗

Mapping of the flaky skin (fsn) mutation on distal mouse chromosome 17.Semantic proximity Read ↗

The tight skin 2 mouse. An animal model of scleroderma displaying cutaneous fibrosis and mononuclear cell infiltration.Semantic proximity Read ↗

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Analysis of the tight skin (Tsk1/+) mouse as a model for testing antifibrotic agents.Semantic proximity Read ↗

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Genetic and physical delineation of the region of the mouse deafness mutation shaker-2.Semantic proximity Read ↗

SOD2 deficiency promotes aging phenotypes in mouse skin.Semantic proximity Read ↗

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