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Literature DB >> 5548211

The glandular aspects of the tabby syndrome in the mouse.

H Grüneberg.

Abstract

Entities: Disease Gene Species

Mesh：

Year: 1971 PMID： 5548211

Source DB: PubMed Journal: J Embryol Exp Morphol ISSN： 0022-0752

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25 in total

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4. A ganglion probably belonging to the N. terminalis system in the nasal mucosa of the mouse.

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The glandular aspects of the tabby syndrome in the mouse.

Review 1. The development of the mammalian outer and middle ear.

2. X chromosome dosage and the response to cerebral ischemia.

3. Modeling recent human evolution in mice by expression of a selected EDAR variant.

4. A ganglion probably belonging to the N. terminalis system in the nasal mucosa of the mouse.

5. p38α MAPK is required for tooth morphogenesis and enamel secretion.

6. X-linked anhidrotic ectodermal dysplasia disruption yields a mouse model for ocular surface disease and resultant blindness.

7. Studies on the pathogenesis of the pseudohermaphroditism in the mouse with testicular feminization.

8. Molecular genetic analysis of the Ta25H deletion: evidence for additional deleted loci.

9. Genotype, phenotype, and karyotype correlation in the XO mouse model of Turner Syndrome.

10. Salivary gland branching morphogenesis: a quantitative systems analysis of the Eda/Edar/NFkappaB paradigm.