Analysis of Mid1, Hccs, Arhgap6, and Msl3l1 in X-linked polydactyly (Xpl) and patchy-fur (Paf) mutant mice

Mammalian Genome

Volumn 12, Issue 10, 2001, Pages 796-798

  Cormier, Trena A ^a   Prakash, Siddharth K ^a   Magner, Daniel B ^a   Zoghbi, Huda Y ^a   Van Den Veyver, Ignatia B ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ANIMAL TISSUE; ARTICLE; CHROMOSOME XP; CONTROLLED STUDY; GENE EXPRESSION; GENE MUTATION; GENETIC ANALYSIS; MOUSE MUTANT; NONHUMAN; PHENOTYPE; RAT; SEQUENCE HOMOLOGY; X CHROMOSOME DOMINANT DISORDER; X CHROMOSOME INACTIVATION;

ANIMALS; BLOTTING, NORTHERN; CROSSES, GENETIC; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, DOMINANT; GTPASE-ACTIVATING PROTEINS; LIGASES; LINKAGE (GENETICS); LYASES; MALE; MICE; MICE, MUTANT STRAINS; MICROTUBULE PROTEINS; MOLECULAR SEQUENCE DATA; NUCLEAR PROTEINS; PHENOTYPE; POLYDACTYLY; RNA, MESSENGER; TRANSCRIPTION FACTORS; X CHROMOSOME;

ANIMALIA;

EID: 0034807339     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00335-001-1006-5     Document Type: Article

References (22)

1. PAK3 mutation Q-L) in nonsyndromic X-linked mental retardation
2. Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardation
3. A high frequency of XO offspring from X(Paf)Y* male mice: Evidence that the Paf mutation involves an inversion spanning the X PAR boundary
4. New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome
5. The mouse Mid1 gene: Implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region
6. Mapping of the glycine receptor alpha 2-subunit gene and the GABAA alpha 3-subunit gene on the mouse X chromosome
7. Coupling of heme attachment to import of cytochrome c into yeast mitochondria. Studies with heme lyase-deficient mitochondria and altered apocytochromes c
8. Role of cytochrome c heme lyase in mitochondrial import and accumulation of cytochrome c in Saccharomyces cerevisiae
9. Opitz G/BBB syndrome in Xp22: Mutations in the MID1 gene cluster in the carboxy-terminal domain
10. Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, maps to the pseudoautosomal boundary region
11. Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for rho GTPases, in patients with X-linked mental retardation
12. Patchy fur (Paf), a semidominant X-linked gene associated with a high level of X-Y nondisjunction in male mice
13. Origin and evolution of the regulatory gene male-specific lethal-3
14. A gene spans the pseudoautosomal boundary in mice
15. Characterization of a novel chromo domain gene in Xp22.3 with homology to Drosophila msl-3
16. Functional analysis of ARHGAP6, a novel GTPase-activating protein for RhoA
17. Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22
18. Cloning and characterization of a putative human holocytochrome c-type synthetase gene (HCCS) isolated from the critical region for microphthalmia with linear skin defects (MLS)
19. Cloning and characterization of a novel rho-type GTPase-activating protein gene (ARHGAP6) from the critical region for microphthalmia with linear skin defects
20. X-linked polydactyly (Xpl), a new mutation in the mouse
21. Focal dermal hypoplasia (Goltz syndrome)
22. Characterization and physical mapping in human and mouse of a novel RING finger gene in Xp22