Transgenic rescue of the tattered phenotype by using a BAC encoding Ebp

Mammalian Genome

Volumn 12, Issue 4, 2001, Pages 323-325

  Means, Gary D ^a   Boyd, Yvonne ^b   Willis, Cindy R ^a   Derry, Jonathan M J ^a  

^a AMGEN INC   (United States)

^b MRC MAMMALIAN GENETICS UNIT   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EMOPAMIL;

ARTICLE; GENE EXPRESSION; GENE MUTATION; HETEROZYGOSITY; MOUSE; MOUSE STRAIN; NONHUMAN; PHENOTYPE; SEQUENCE HOMOLOGY; TRANSGENIC MOUSE; X CHROMOSOME LINKAGE;

ABNORMALITIES, MULTIPLE; ANIMALS; CARRIER PROTEINS; CHONDRODYSPLASIA PUNCTATA; CHROMOSOMES, ARTIFICIAL, BACTERIAL; FEMALE; HUMANS; MALE; MICE; MICE, TRANSGENIC; PHENOTYPE; SEX CHROMOSOME ABERRATIONS; STEROID ISOMERASES; X CHROMOSOME;

MUS MUSCULUS;

EID: 0035081263     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003350010262     Document Type: Article

References (6)

1. 7-isomerase cause X-linked dominant Conradi-Hünermann syndrome
2. 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata
3. The gene mutated in bare patches and striated mice encodes a novel 3β-hydroxysteroid dehydrogenase
4. A transcript map of a 2-Mb contig in the proximal portion of the mouse X chromosome and regional mapping of the scurfy mutation
5. 7 isomerization
6. The mouse X-linked developmental mutant, tattered, lies between DXMit55 and Xkh and is associated with hyperkeratinization