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Literature DB >> 8111131

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

E T Everett¹, J L Pablos, S E Harris, E C LeRoy, J S Norris.

Abstract

Entities: Gene Species

Mesh：

Year: 1994 PMID： 8111131 DOI： 10.1007/bf00360571

Source DB: PubMed Journal: Mamm Genome ISSN： 0938-8990 Impact factor: 2.957

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23 in total

Review 1. Comparative map for mice and humans.

Authors: J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal: Mamm Genome Date: 1992 Impact factor: 2.957

Review 2. Mouse chromosome 2.

Authors: L D Siracusa; C M Abbott
Journal: Mamm Genome Date: 1992 Impact factor: 2.957

3. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene.

Authors: H C Dietz; G R Cutting; R E Pyeritz; C L Maslen; L Y Sakai; G M Corson; E G Puffenberger; A Hamosh; E J Nanthakumar; S M Curristin
Journal: Nature Date: 1991-07-25 Impact factor: 49.962

4. Fibrillin delineates the primary axis of the early avian embryo.

Authors: B C Gallagher; L Y Sakai; C D Little
Journal: Dev Dyn Date: 1993-01 Impact factor: 3.780

5. Marfan phenotype variability in a family segregating a missense mutation in the epidermal growth factor-like motif of the fibrillin gene.

Authors: H C Dietz; R E Pyeritz; E G Puffenberger; R J Kendzior; G M Corson; C L Maslen; L Y Sakai; C A Francomano; G R Cutting
Journal: J Clin Invest Date: 1992-05 Impact factor: 14.808

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

Review 1. Comparative map for mice and humans.

Review 2. Mouse chromosome 2.

3. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene.

4. Fibrillin delineates the primary axis of the early avian embryo.

5. Marfan phenotype variability in a family segregating a missense mutation in the epidermal growth factor-like motif of the fibrillin gene.

6. The tight-skin mouse: physical and biochemical properties of the skin.

7. Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1.

8. Scleroderma-like alterations in collagen metabolism occurring in the TSK (tight skin) mouse.

9. Hereditary emphysema in the tight-skin mouse. Evaluation of pathogenesis.

10. Towards construction of a high resolution map of the mouse genome using PCR-analysed microsatellites.

1. Of mice and Marfan: genetic linkage analyses of the fibrillin genes, Fbn1 and Fbn2, in the mouse genome.