146 related articles for article (PubMed ID: 939913)
1. Myodystrophy, a new myopathy on chromosome 8 of the mouse.
Lane PW; Beamer TC; Myers DD
J Hered; 1976; 67(3):135-8. PubMed ID: 939913
[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: 7739634
[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: 23573594
[TBL] [Abstract][Full Text] [Related]
4. Osteosclerosis, a recessive skeletal mutation on chromosome 19 in the mouse.
Marks SC; Seifert MF; Lane PW
J Hered; 1985; 76(3):171-6. PubMed ID: 3998439
[TBL] [Abstract][Full Text] [Related]
5. Muscle protein synthesis in MED myopathy.
Sheff MF; Zacks SI
Lab Invest; 1977 Aug; 37(2):216-22. PubMed ID: 881784
[TBL] [Abstract][Full Text] [Related]
6. Evidence for allelism of leaner and tottering in the mouse.
Tsuji S; Meier H
Genet Res; 1971 Feb; 17(1):83-8. PubMed ID: 4933322
[No Abstract] [Full Text] [Related]
7. Congenital progressive hydronephrosis in mice: a new recessive mutation.
Horton CE; Davisson MT; Jacobs JB; Bernstein GT; Retik AB; Mandell J
J Urol; 1988 Nov; 140(5 Pt 2):1310-5. PubMed ID: 3184310
[TBL] [Abstract][Full Text] [Related]
8. Bradypneic, a new mutation in mice causing slow breathing, runting, and early death.
Green MC; Jahn CL
J Hered; 1977; 68(3):150-6. PubMed ID: 893991
[TBL] [Abstract][Full Text] [Related]
9. Three recessive mutations producing disproportionate dwarfing in mice: achondroplasia, brachymorphic, and stubby.
Lane PW; Dickie MM
J Hered; 1968; 59(5):300-8. PubMed ID: 5713631
[No Abstract] [Full Text] [Related]
10. Two new mutations in linkage group XVI of the house mouse. Flaky tail and varitint-waddler-J.
Lane PW
J Hered; 1972; 63(3):135-40. PubMed ID: 4557539
[No Abstract] [Full Text] [Related]
11. Rachiterata: a new skeletal mutation on chromosome 2 of the mouse.
Varnum DS; Stevens LC
J Hered; 1974; 65(2):91-3. PubMed ID: 4837306
[No Abstract] [Full Text] [Related]
12. Rostral cerebellar malformation, (rcm): a new recessive mutation on chromosome 3 of the mouse.
Lane PW; Bronson RT; Spencer CA
J Hered; 1992; 83(4):315-8. PubMed ID: 1401878
[TBL] [Abstract][Full Text] [Related]
13. Osteopetrosis, a new recessive skeletal mutation on chromosome 12 of the mouse.
Marks SC; Lane PW
J Hered; 1976; 67(1):11-18. PubMed ID: 1262696
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Thin fur, a recessive mutant on chromosome 17 of the mouse.
Key M; Hollander WF
J Hered; 1972; 63(2):97-8. PubMed ID: 5031320
[No Abstract] [Full Text] [Related]
16. aku, a mutation of the mouse homologous to human alkaptonuria, maps to chromosome 16.
Montagutelli X; Lalouette A; Coudé M; Kamoun P; Forest M; Guénet JL
Genomics; 1994 Jan; 19(1):9-11. PubMed ID: 8188247
[TBL] [Abstract][Full Text] [Related]
17. A novel hypothyroid dwarfism due to the missense mutation Arg479Cys of the thyroid peroxidase gene in the mouse.
Takabayashi S; Umeki K; Yamamoto E; Suzuki T; Okayama A; Katoh H
Mol Endocrinol; 2006 Oct; 20(10):2584-90. PubMed ID: 16762971
[TBL] [Abstract][Full Text] [Related]
18. [Distal myopathy with rimmed vacuoles(DMRV)].
Ikeuchi T; Tsuji S
Nihon Rinsho; 1997 Dec; 55(12):3195-9. PubMed ID: 9436435
[TBL] [Abstract][Full Text] [Related]
19. Mocha, a new coat color and behavior mutation on chromosome 10 of the mouse.
Lane PW; Deol MS
J Hered; 1974; 65(6):362-4. PubMed ID: 4448900
[No Abstract] [Full Text] [Related]
20. Cribriform degeneration (cri): a new recessive neurological mutation in the mouse.
Green MC; Sidman RL; Pivetta OH
Science; 1972 May; 176(4036):800-3. PubMed ID: 5031475
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]