A high-resolution genetic map of mouse Chromosome 19 encompassing the muscle-deficient osteochondrodystrophy (mdf-ocd) region

Mammalian Genome

Volumn 9, Issue 5, 1998, Pages 390-391

  Poirier, Christophe ^a,e   Blot, Stéphane ^b   Fernandes, Marie ^c   Carle, Georges F ^c   Stanescu, Viktor ^d   Stanescu, Ritta ^d   Guénet, Jean Louis ^a  

^a INSTITUT PASTEUR   (France)

^b ECOLE NATIONALE VÉTÉRINAIRE D ALFORT   (France)

^c CNRS   (France)

^d HÔPITAL NECKER ENFANTS MALADES   (France)

^e INST OF PHYS AND CHEMICAL RESEARCH   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CHONDRODYSPLASIA; CHROMOSOME 19; CHROMOSOME MAP; FEMALE; GENE MUTATION; GENETIC LINKAGE; HAPLOTYPE; MALE; MOUSE; NEUROMUSCULAR DISEASE; NEWBORN; NONHUMAN; RECESSIVE INHERITANCE;

ANIMALS; CHROMOSOME MAPPING; CROSSES, GENETIC; DISEASE MODELS, ANIMAL; DWARFISM; FEMALE; GENETIC MARKERS; GENOTYPE; INBREEDING; MALE; MICE; MICE, INBRED C3H; MICE, INBRED C57BL; MOTOR NEURON DISEASE; SPECIES SPECIFICITY;

ANIMALIA; RODENTIA;

EID: 0031834147     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900777     Document Type: Article

References (15)

1. Blot S, Poirier C, Dreyfus P (1995) The mouse mutation muscle deficient (mdf) is characterized by a progressive motoneuron disease. J Neuropathol Exp Neurol 54, 812-825
2. Casteels D, Poirier C, Guénet J-L, Merregaert J (1995) The mouse Fau gene: genomic structure, chromosomal localization and characterization of two retropseudogenes. Genomics 25, 291-294
3. Dietrich W, Miller JC, Steen RG, Merchant M, Damron D, Nahf R, Gross A, Joyce DC, Wessel M, Dredge RD, Marquis A, Stein LD, Goodman N, Page DC, Lander ES (1994) A genetic map of the mouse with 4,006 simple sequence length polymorphisms. Nat Genet 7, 220-245
4. Fernandes M, Poirier C, Lassam NJ, Larsson C, Guénet J-L, Gaudray P, Carle GF (1997) The mouse homologs of RELA and MLK3 are located within a 120 kb fragment on mouse chromosome 19. Mamm Genome 8, 513-515
5. Giovannini M, Romo AJ, Evans GA (1993) Chromosomal localization of the human ciliary neurotrophic factor gene (CNTF) to 11q12 by fluorescence in situ hybridization. Cytogenet Cell Genet 63, 62-63
6. Kas K, Schoenmakers E, van de Ven W, Weber G, Nordenskjöld M, Michiels L, Merregaert J, Larsson C (1993) Assignment of the human FAU gene to subregion of chromosome 11q13. Genomics 17, 387-392
7. Lander ES, Green P, Abrahamson J, Barlow A, Daley M, Lincoln S, Newburg L (1987) MAPMAKER: an interactive computer package for constructing primary genetic linkage maps of experimental and natural populations. Genomics 1, 174-181
8. Mathew S, Murty VV, Dalla FR, Chaganti RS (1993) Chromosomal localization of genes encoding the transcription factors, c-rel, NF-kappa Bp50, NF-kappa Bp65, and lyt-10 by fluorescence in situ hybridization. Oncogene 8, 191-193
9. Orita M, Iwahana H, Kanazawa H, Hayashi K, Sekiya T (1989) Detection of polymorphisms of human DNA by gel electrophoresis as single strand conformational polymorphism. Proc Natl Acad USA 86, 2766-2770
10. Schreiber M, Poirier C, Franchi A, Kurzbauer R, Guénet J-L, Carle GF, Wagner EF (1997) Structure and chromosomal assignment of the mouse fra-1/Fosll (Fos related antigen 1) and exclusion as a candidate gene for osteosclerosis (oc). Oncogene 15, 1171-1178
11. Sendtner M, Schmalbruch H, Stöckli KA, Carroll P, Kreutzberg GW, Thoenen H (1992) Ciliary neurotrophic factor prevents degeneration of motor neurons in mouse mutant progressive motor neuronopathy. Nature 358, 502-504
12. Sinke RJ, Tanigami A, Nakamura Y, Geurts van Kessel A (1993) Reverse mapping of the gene encoding the fos related antigen 1 (fral) within chromosome band 11q13. Genomics 18, 165
13. Sweet HO (1983) Linkage data. Mouse News Lett 68, 72
14. Sweet HO, Bronson RT (1991) Osteochondrodystrophy (ocd): a new autosomal recessive mutation in the mouse. J Hered 82, 140-144
15. Womack JE, MacPike A, Meier H (1980) Muscle deficient, a new mutation in the mouse. J Hered 71, 68