High-resolution mapping of the spm (Niemann-pick type C) locus on mouse Chromosome 18

Mammalian Genome

Volumn 8, Issue 5, 1997, Pages 355-356

  Erickson, R P ^a,b   Aviles, R A ^a   Zhang, J ^a,b   Kozloski, M A ^a   Garver, W S ^a   Heidenreich, R A ^a,c  

^a UNIVERSITY OF ARIZONA COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF ARIZONA   (United States)

^c NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; ARTICLE; BAGG ALBINO MOUSE; CHROMOSOME MAP; CLASSIFICATION; COMPARATIVE STUDY; DBA MOUSE; GENETIC MARKER; GENETICS; MOUSE; MOUSE MUTANT; MUTATION; NIEMANN PICK DISEASE;

ANIMALS; CHROMOSOME MAPPING; GENETIC MARKERS; MICE; MICE, INBRED BALB C; MICE, INBRED DBA; MICE, MUTANT STRAINS; MUTATION; NIEMANN-PICK DISEASES;

ANIMALIA;

EID: 0031138488     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900440     Document Type: Article

References (16)

1. Aberdam D, Galliano MF, Mattei M-G, Pisani-Spadafora A, Ortonne JP, Meneguzzi G (1994a) Assignment of mouse nicein genes to Chromosomes 1 and 18. Mamm Genome 5, 229-233
2. Aberdam, D, Aguzzi A, Baudoin C, Galliano M-F, Ortonne J-P, Meneguzzi G (1994b) Developmental expression of nicein adhesion protein (laminin-5) subunits suggests multiple morphogenic roles. Cell Adhesion Comm 2, 115-129
3. Griffith AJ, Burgess DL, Kohrman DC, Yu J, Blaschak J, Blanton SH, Boehnke M, Hecht JT, Ovehauser J, Meisler MH (1996a) Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO. Genomics 34, 299-303
4. Griffith AJ, Radice GL, Burgess DL, Kohrman DC, Hansen GM, Justice MJ, Johnson KR, Davisson MT, Meisler MH (1996b) Location of the 9257 and ataxia mutations on mouse Chromosome 18. Mamm Genome 7, 417-419
5. Higashi A, Murayama S, Pentchev PG, Suzuki K (1993) Cerebellar degeneration in the Niemann-Pick type C mouse. Acta Neuropathol 85, 175-184
6. Johnson KR, Davisson MT (1996) Mouse Chromosome 18. Mamm Genome 6(Suppl), S300-S308
7. Lane PW, Searle AG, Beechey CV, Eicher EM (1981) Chromosome 18 of the house mouse. J Hered 72, 409-412
8. Miyawaki S, Mitsouka S, Sakiyama T, Kitagawa T (1982) Sphingomyelinosis, a new mutation in the mouse. A model of Niemann-Pick disease in humans. J Hered 73, 257-263
9. Miyawaki S, Mitsuoka S, Sakiyama T, Kitaga T (1983) Time course of hepatic lipids accumulation in a strain of mice with an inherited deficiency of sphingomyelinase. J Hered 74, 465-468
10. Miyawaki S, Yoshida H, Mitsuoka S, Enomoto H, Ikehara S (1986) A mouse model for Neimann-Pick disease. Influence of genetic background on disease expression in spm/spm mice. J Hered 77, 379-384
11. Morris MD, Bhuvaneswaran C, Shio H, Fowler S (1982) Lysosome lipid storage in NCTR-BALB/c mice. I. Description of the disease and genetics. Am J Pathol 108, 140-149
12. Pentchev PG, Gal AE, Booth AD, Omodeo-Sale F, Fouks J, Neumeyer BA, Quirk JM, Dawson G, Brady RO (1980) A lysosomal storage disorder in mice characterized by a dual deficiency of sphingomyelinase and glucocerebrosidase. Biochim Biophys Acta 619, 669-679
13. Pentchev PG, Boothe AD, Kruth HS, Weintroub H, Stivers J, Brady RO (1984) A genetic storage disorder in BALB/c mice with a metabolic block in esterification of exogenous cholesterol. J Biol Chem 259, 5784-5791
14. Pentchev PG, Comly ME, Kruth HS, Patel S, Proestel M, Weintroub H (1986) The cholesterol storage disorder of the mutant BALB/c mouse. J Biol Chem 261, 2772-2777
15. Sakai Y, Miyawaki S, Shimizu A, Ohno K, Watanabe T (1991) A molecular genetic linkage map of mouse chromosome 18, including spm, Grl-I, Fim-2/c-fms, and Mbp. Biochem Genet 29, 108-113
16. Silver LM (1995) Mouse Genetics. Concepts and Applications. (New York): Oxford University Press