메뉴 건너뛰기




Volumn 150, Issue 2, 1998, Pages 815-822

Deletion mapping of the head tilt (het) gene in mice: A vestibular mutation causing specific absence of otoliths

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

EID: 0031680234     PISSN: 00166731     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (52)

References (37)
  • 1
    • 0019255127 scopus 로고
    • Development of otoconia
    • ANNIKO, M., 1980 Development of otoconia. Am. J. Otolaryn. 1: 400-410.
    • (1980) Am. J. Otolaryn. , vol.1 , pp. 400-410
    • Anniko, M.1
  • 2
    • 0031541415 scopus 로고    scopus 로고
    • A new spontaneous deletion on chromosome 17 including brachyury
    • BILINSKI, P., J. SCHIMENTI and A. GOSSLER, 1997 A new spontaneous deletion on chromosome 17 including brachyury. Mamm. Genome 12: 932-933.
    • (1997) Mamm. Genome , vol.12 , pp. 932-933
    • Bilinski, P.1    Schimenti, J.2    Gossler, A.3
  • 3
    • 0025218695 scopus 로고
    • Molecular cloning and genetic mapping of the t complex responder candidate gene family
    • BULLARD, D., and J. SCHIMENTI, 1990 Molecular cloning and genetic mapping of the t complex responder candidate gene family. Genetics 124: 957-966.
    • (1990) Genetics , vol.124 , pp. 957-966
    • Bullard, D.1    Schimenti, J.2
  • 4
    • 0000991395 scopus 로고
    • The abnormalities of the inner ear in kreisler mice
    • DEOL, M. S., 1964a The abnormalities of the inner ear in kreisler mice. J. Embryol. Exp. Morphol. 12: 475-490.
    • (1964) J. Embryol. Exp. Morphol. , vol.12 , pp. 475-490
    • Deol, M.S.1
  • 5
    • 0000692668 scopus 로고
    • The origin of the abnormalities of the inner ear in dreher mice
    • DEOL, M. S., 1964b The origin of the abnormalities of the inner ear in dreher mice. J. Embryol. Exp. Morphol. 12: 727-733.
    • (1964) J. Embryol. Exp. Morphol. , vol.12 , pp. 727-733
    • Deol, M.S.1
  • 6
    • 0014292278 scopus 로고
    • Inherited diseases of the inner ear in man in the light of studies on the mouse
    • DEOL, M. S., 1968 Inherited diseases of the inner ear in man in the light of studies on the mouse. J. Med. Genet. 5: 137-158.
    • (1968) J. Med. Genet. , vol.5 , pp. 137-158
    • Deol, M.S.1
  • 7
    • 0013985845 scopus 로고
    • Snell's waltzer, a new mutation affecting behaviour and the inner ear in the mouse
    • DEOL, M. S., and M. C. GREEN, 1966 Snell's waltzer, a new mutation affecting behaviour and the inner ear in the mouse. Genet. Res. 8: 339-345.
    • (1966) Genet. Res. , vol.8 , pp. 339-345
    • Deol, M.S.1    Green, M.C.2
  • 10
    • 0014026380 scopus 로고
    • Neurological defect: Manganese in phenocopy and prevention of a genetic abnormality of inner ear
    • ERWAY, L. C., L. S. HURLEY and A. FRASER, 1966 Neurological defect: manganese in phenocopy and prevention of a genetic abnormality of inner ear. Science 152: 1766-1768.
    • (1966) Science , vol.152 , pp. 1766-1768
    • Erway, L.C.1    Hurley, L.S.2    Fraser, A.3
  • 11
    • 0014987840 scopus 로고
    • Prevention of congenital otolith defect in pallid mutant mice by manganese supplementation
    • ERWAY, L. C., A. S. FRASER and L. S. HURLEY, 1971 Prevention of congenital otolith defect in pallid mutant mice by manganese supplementation. Genetics 67: 97-108.
    • (1971) Genetics , vol.67 , pp. 97-108
    • Erway, L.C.1    Fraser, A.S.2    Hurley, L.S.3
  • 12
    • 0021972372 scopus 로고
    • Molecular probes define different regions of the mouse t complex
    • FOX, H., G. MARTIN, M. F. LYON, B. HERRMAN, A.-M. FRISCHAUF et al., 1985 Molecular probes define different regions of the mouse t complex. Cell 40: 63-69.
    • (1985) Cell , vol.40 , pp. 63-69
    • Fox, H.1    Martin, G.2    Lyon, M.F.3    Herrman, B.4    Frischauf, A.-M.5
  • 13
    • 0028860302 scopus 로고
    • A type VII myosin encoded by the mouse deafness gene shaker-1
    • GIBSON, F., J. WALSH, P. MBURU, A. VARELA, K. A. BROWN et al., 1995 A type VII myosin encoded by the mouse deafness gene shaker-1. Nature 374: 62-64.
    • (1995) Nature , vol.374 , pp. 62-64
    • Gibson, F.1    Walsh, J.2    Mburu, P.3    Varela, A.4    Brown, K.A.5
  • 15
    • 0023652388 scopus 로고
    • A large inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal t complex inversion
    • HERRMANN, B. G., D. P. BARLOW and H. LEHRACH, 1987 A large inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal t complex inversion. Cell 48: 813-825.
    • (1987) Cell , vol.48 , pp. 813-825
    • Herrmann, B.G.1    Barlow, D.P.2    Lehrach, H.3
  • 16
    • 0025062325 scopus 로고
    • Cloning of the T gene required in mesoderm formation in the mouse
    • HERRMANN, B. G., S. LABEIT, A. POUSTKA, T. R. KING and H. LEHRACH, 1990 Cloning of the T gene required in mesoderm formation in the mouse. Nature 343: 617-622.
    • (1990) Nature , vol.343 , pp. 617-622
    • Herrmann, B.G.1    Labeit, S.2    Poustka, A.3    King, T.R.4    Lehrach, H.5
  • 17
    • 0027244281 scopus 로고
    • High-resolution comparative mapping of mouse chromosome 17
    • HIMMELBAUER, H., and L. SILVER, 1993 High-resolution comparative mapping of mouse chromosome 17. Genomics 17: 110-120.
    • (1993) Genomics , vol.17 , pp. 110-120
    • Himmelbauer, H.1    Silver, L.2
  • 18
    • 0027106937 scopus 로고
    • Mouse albino-deletions: From genetics to genes in development
    • HOLDENER-KENNY, B., S. K. SHARAN and T. MAGNUSON, 1992 Mouse albino-deletions: from genetics to genes in development. BioEssays 14: 831-839.
    • (1992) BioEssays , vol.14 , pp. 831-839
    • Holdener-Kenny, B.1    Sharan, S.K.2    Magnuson, T.3
  • 19
    • 0025639183 scopus 로고
    • Genetic and molecular analysis of the proximal region of the mouse t-complex using new molecular probes and partial t-haplotypes
    • HOWARD, C., G. GUMMERE, M. LYON, D. BENNETT and K. ARTZT, 1990 Genetic and molecular analysis of the proximal region of the mouse t-complex using new molecular probes and partial t-haplotypes. Genetics 126: 1103-1114.
    • (1990) Genetics , vol.126 , pp. 1103-1114
    • Howard, C.1    Gummere, G.2    Lyon, M.3    Bennett, D.4    Artzt, K.5
  • 20
    • 0026514917 scopus 로고
    • Deletion of mouse t-complex distorter-1 produces an effect like that of the t-form of the distorter
    • LYON, M., 1992 Deletion of mouse t-complex distorter-1 produces an effect like that of the t-form of the distorter. Genet. Res. Camb. 59: 27-33.
    • (1992) Genet. Res. Camb. , vol.59 , pp. 27-33
    • Lyon, M.1
  • 21
    • 0014587272 scopus 로고
    • Muted, a new mutant affecting coat colour and otoliths of the mouse, and its position in linkage group XIV
    • LYON, M., and R. MEREDITH, 1969 Muted, a new mutant affecting coat colour and otoliths of the mouse, and its position in linkage group XIV. Genet. Res. 14: 163-166.
    • (1969) Genet. Res. , vol.14 , pp. 163-166
    • Lyon, M.1    Meredith, R.2
  • 22
    • 0001445850 scopus 로고
    • Hereditary absence of otoliths in the house mouse
    • LYON, M. F., 1951 Hereditary absence of otoliths in the house mouse. J. Physiol. 114: 410-418.
    • (1951) J. Physiol. , vol.114 , pp. 410-418
    • Lyon, M.F.1
  • 23
    • 0001077455 scopus 로고
    • Absence of otoliths in the mouse: An effect of the pallid mutant
    • LYON, M. F., 1952 Absence of otoliths in the mouse: an effect of the pallid mutant. J. Genet. 51: 638-650.
    • (1952) J. Genet. , vol.51 , pp. 638-650
    • Lyon, M.F.1
  • 24
    • 0344910921 scopus 로고
    • The development of the otoliths of the mouse
    • LYON, M. F., 1955 The development of the otoliths of the mouse. J. Embryol. Exp. Morph. 3: 213-229.
    • (1955) J. Embryol. Exp. Morph. , vol.3 , pp. 213-229
    • Lyon, M.F.1
  • 25
    • 0026648110 scopus 로고
    • Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse
    • LYON, M. F., T. R. KING, Y. GONDO, J. M. GARDNER, Y. NAKATSU et al., 1992 Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse. Proc, Nat. Acad. Sci. USA 89: 6968-6972.
    • (1992) Proc, Nat. Acad. Sci. USA , vol.89 , pp. 6968-6972
    • Lyon, M.F.1    King, T.R.2    Gondo, Y.3    Gardner, J.M.4    Nakatsu, Y.5
  • 27
    • 0029986393 scopus 로고    scopus 로고
    • Complementation mapping of skeletal and central nervous system abnormalities in mice of the piebald deletion complex
    • O'BRIEN, T., D. METALLINOS, H. CHEN, M. SHIN and S. TILGHMAN, 1996 Complementation mapping of skeletal and central nervous system abnormalities in mice of the piebald deletion complex. Genetics 143: 447-461.
    • (1996) Genetics , vol.143 , pp. 447-461
    • O'Brien, T.1    Metallinos, D.2    Chen, H.3    Shin, M.4    Tilghman, S.5
  • 28
    • 0028361936 scopus 로고
    • Molecular genetics of the brown (b)-locus region of mouse chromosome 4: Origin and molecular mapping of radiation and chemical induced lethal brown deletions
    • RINCHIK, E., J. BELL, P. HUNSICKER, J. FRIEDMAN, I. JACKSON et al., 1994 Molecular genetics of the brown (b)-locus region of mouse chromosome 4: origin and molecular mapping of radiation and chemical induced lethal brown deletions. Genetics 137: 845-854.
    • (1994) Genetics , vol.137 , pp. 845-854
    • Rinchik, E.1    Bell, J.2    Hunsicker, P.3    Friedman, J.4    Jackson, I.5
  • 29
    • 0028871957 scopus 로고
    • Complementation analyses for 45 mutations encom- Passing the pink-eyed dilution (p) locus of the mouse
    • RUSSELL, L. B., C. S. MONTGOMERY, N. L. CACHEIRO and D. K. JOHNSON, 1995 Complementation analyses for 45 mutations encom- passing the pink-eyed dilution (p) locus of the mouse. Genetics 141: 1547-1562.
    • (1995) Genetics , vol.141 , pp. 1547-1562
    • Russell, L.B.1    Montgomery, C.S.2    Cacheiro, N.L.3    Johnson, D.K.4
  • 30
    • 0023190490 scopus 로고
    • An unstable family of large DNA elements in the center of mouse t haplotypes
    • SCHIMENTI, J., L. VOLD, D. SOCOLOW and L. M. SILVER, 1987 An unstable family of large DNA elements in the center of mouse t haplotypes. J. Mol. Biol. 194: 583-594.
    • (1987) J. Mol. Biol. , vol.194 , pp. 583-594
    • Schimenti, J.1    Vold, L.2    Socolow, D.3    Silver, L.M.4
  • 31
    • 0031214583 scopus 로고    scopus 로고
    • Characterization of the C3 YAC contig from proximal mouse chromosome 17 and analysis of allelic expression of genes flanking the imprinted Igf2r gene
    • SCHWEIFER, N., P. J. VALK, R. DELWEL, R. COX, F. FRANCIS et al., 1997 Characterization of the C3 YAC contig from proximal mouse chromosome 17 and analysis of allelic expression of genes flanking the imprinted Igf2r gene. Genomics 43: 285-297.
    • (1997) Genomics , vol.43 , pp. 285-297
    • Schweifer, N.1    Valk, P.J.2    Delwel, R.3    Cox, R.4    Francis, F.5
  • 32
    • 0022327611 scopus 로고
    • Mouse t haplotypes
    • SILVER, L. M., 1985 Mouse t haplotypes. Annu. Rev. Genet. 19: 179-208.
    • (1985) Annu. Rev. Genet. , vol.19 , pp. 179-208
    • Silver, L.M.1
  • 33
    • 0029562474 scopus 로고
    • Inherited hearing defects in mice
    • STEEL, K., 1995 Inherited hearing defects in mice. Annu. Rev. Genet. 29: 675-701.
    • (1995) Annu. Rev. Genet. , vol.29 , pp. 675-701
    • Steel, K.1
  • 34
  • 36
    • 0025223305 scopus 로고
    • Inheritance of T-associated sex reversal in mice
    • WASHBURN, L. L., B. K. LEE and E. M. EICHER, 1990 Inheritance of T-associated sex reversal in mice. Genet. Res. 56: 185-191.
    • (1990) Genet. Res. , vol.56 , pp. 185-191
    • Washburn, L.L.1    Lee, B.K.2    Eicher, E.M.3
  • 37
    • 0031018818 scopus 로고    scopus 로고
    • Chromosomal deletion complexes in mice by radiation of embryonic stem cells
    • YOU, Y., R. BERGSTROM, M. KLEMM, B. LEDERMAN, H. NELSON et al., 1997 Chromosomal deletion complexes in mice by radiation of embryonic stem cells. Nature Genet. 15: 285-288.
    • (1997) Nature Genet. , vol.15 , pp. 285-288
    • You, Y.1    Bergstrom, R.2    Klemm, M.3    Lederman, B.4    Nelson, H.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.