169 related articles for article (PubMed ID: 7613034)
1. Genetic mapping near the myd locus on mouse chromosome 8.
Mills KA; Mathews KD; Scherpbier-Heddema T; Schelper RL; Schmalzel R; Bailey HL; Nadeau JH; Buetow KH; Murray JC
Mamm Genome; 1995 Apr; 6(4):278-80. PubMed ID: 7613034
[TBL] [Abstract][Full Text] [Related]
2. Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q.
Mathews KD; Mills KA; Bailey HL; Schelper RL; Murray JC
Muscle Nerve Suppl; 1995; (2):S98-102. PubMed ID: 23573594
[TBL] [Abstract][Full Text] [Related]
3. Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q.
Mathews KD; Mills KA; Bailey HL; Schelper RL; Murray JC
Muscle Nerve Suppl; 1995; 2():S98-102. PubMed ID: 7739634
[TBL] [Abstract][Full Text] [Related]
4. High-resolution mapping of mouse chromosome 8 identifies an evolutionary chromosomal breakpoint.
Grewal PK; Bolland DJ; Todd LC; Hewitt JE
Mamm Genome; 1998 Aug; 9(8):603-7. PubMed ID: 9680377
[TBL] [Abstract][Full Text] [Related]
5. The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.
Grewal PK; van Deutekom JC; Mills KA; Lemmers RJ; Mathews KD; Frants RR; Hewitt JE
Mamm Genome; 1997 Jun; 8(6):394-8. PubMed ID: 9166581
[TBL] [Abstract][Full Text] [Related]
6. Phenotypic and pathologic evaluation of the myd mouse. A candidate model for facioscapulohumeral dystrophy.
Mathews KD; Rapisarda D; Bailey HL; Murray JC; Schelper RL; Smith R
J Neuropathol Exp Neurol; 1995 Jul; 54(4):601-6. PubMed ID: 7602333
[TBL] [Abstract][Full Text] [Related]
7. Homologs of genes and anonymous loci on human chromosome 13 map to mouse chromosomes 8 and 14.
Koizumi T; Hendel E; Lalley PA; Tchetgen MB; Nadeau JH
Mamm Genome; 1995 Apr; 6(4):263-8. PubMed ID: 7613031
[TBL] [Abstract][Full Text] [Related]
8. The molecular genetics of human facioscapulohumeral muscular dystrophy and the myodystrophy mouse model.
Mathews KD; Mills KA
Curr Opin Neurol; 1996 Oct; 9(5):394-9. PubMed ID: 8894417
[TBL] [Abstract][Full Text] [Related]
9. The protein kinase N (PKN) gene PRKCL1/Prkcl1 maps to human chromosome 19p12-p13.1 and mouse chromosome 8 with close linkage to the myodystrophy (myd) mutation.
Bartsch JW; Mukai H; Takahashi N; Ronsiek M; Fuchs S; Jockusch H; Ono Y
Genomics; 1998 Apr; 49(1):129-32. PubMed ID: 9570957
[TBL] [Abstract][Full Text] [Related]
10. A molecular genetic linkage map of mouse chromosome 7.
Saunders AM; Seldin MF
Genomics; 1990 Nov; 8(3):525-35. PubMed ID: 1981054
[TBL] [Abstract][Full Text] [Related]
11. Localization of the murine cholecystokinin A and B receptor genes.
Samuelson LC; Isakoff MS; Lacourse KA
Mamm Genome; 1995 Apr; 6(4):242-6. PubMed ID: 7613026
[TBL] [Abstract][Full Text] [Related]
12. A molecular genetic linkage map of mouse chromosome 4 including the localization of several proto-oncogenes.
Ceci JD; Siracusa LD; Jenkins NA; Copeland NG
Genomics; 1989 Nov; 5(4):699-709. PubMed ID: 2574141
[TBL] [Abstract][Full Text] [Related]
13. Mapping of PCR-based markers for mouse chromosome 4 on a backcross penetrant for the misty (m) mutation.
Fiedorek FT; Kay ES
Mamm Genome; 1994 Aug; 5(8):479-85. PubMed ID: 7949731
[TBL] [Abstract][Full Text] [Related]
14. Isolation and characterization of a pseudoautosomal region-specific genetic marker in C57BL/6 mice using genomic representational difference analysis.
Kalcheva ID; Matsuda Y; Plass C; Chapman VM
Proc Natl Acad Sci U S A; 1995 Dec; 92(26):12352-6. PubMed ID: 8618899
[TBL] [Abstract][Full Text] [Related]
15. A linkage map of mouse chromosome 19: definition of comparative mapping relationships with human chromosomes 10 and 11 including the MEN1 locus.
Rochelle JM; Watson ML; Oakey RJ; Seldin MF
Genomics; 1992 Sep; 14(1):26-31. PubMed ID: 1358795
[TBL] [Abstract][Full Text] [Related]
16. Linkage of Agt and Actsk-1 to distal mouse chromosome 8 loci: a new conserved linkage.
Abonia JP; Abel KJ; Eddy RL; Elliott RW; Chapman VM; Shows TB; Gross KW
Mamm Genome; 1993; 4(1):25-32. PubMed ID: 8093670
[TBL] [Abstract][Full Text] [Related]
17. Comparative mapping of the Grpr locus on the X chromosomes of man and mouse.
Maslen GL; Boyd Y
Genomics; 1993 Jul; 17(1):106-9. PubMed ID: 8406441
[TBL] [Abstract][Full Text] [Related]
18. An interspecific backcross linkage map of the proximal half of mouse chromosome 14.
Ceci JD; Kingsley DM; Silan CM; Copeland NG; Jenkins NA
Genomics; 1990 Apr; 6(4):673-8. PubMed ID: 1971251
[TBL] [Abstract][Full Text] [Related]
19. Chromosomal localization of the mouse titin gene and its relation to "muscular dystrophy with myositis" and nebulin genes on chromosome 2.
Müller-Seitz M; Kaupmann K; Labeit S; Jockusch H
Genomics; 1993 Dec; 18(3):559-61. PubMed ID: 8307566
[TBL] [Abstract][Full Text] [Related]
20. Maps from two interspecific backcross DNA panels available as a community genetic mapping resource.
Rowe LB; Nadeau JH; Turner R; Frankel WN; Letts VA; Eppig JT; Ko MS; Thurston SJ; Birkenmeier EH
Mamm Genome; 1994 May; 5(5):253-74. PubMed ID: 8075499
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
