메뉴 건너뛰기




Volumn 9, Issue 10, 1998, Pages 835-837

A refined physical and EST map spanning 7.4 Mb of 10q24, a region involved in neurological disorders

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 10Q; CHROMOSOME ANALYSIS; CHROMOSOME MAP; HUMAN; NEUROLOGIC DISEASE; NONHUMAN; YEAST ARTIFICIAL CHROMOSOME;

EID: 0031704920     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900877     Document Type: Article
Times cited : (10)

References (16)
  • 1
    • 0027249595 scopus 로고
    • DbEST-Database for "expressed sequence tags."
    • Boguski MS, Lowe TM, Tolstoshev CM (1993) dbEST-Database for "expressed sequence tags." Nat Genet 4, 332-333
    • (1993) Nat Genet , vol.4 , pp. 332-333
    • Boguski, M.S.1    Lowe, T.M.2    Tolstoshev, C.M.3
  • 3
    • 13344259999 scopus 로고    scopus 로고
    • A comprehensive genetic map of the human genome based on 5,264 microsatellites
    • Dib C, Faure S, Fizames C, Samson D, Drouot N et al. (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380, 152-154
    • (1996) Nature , vol.380 , pp. 152-154
    • Dib, C.1    Faure, S.2    Fizames, C.3    Samson, D.4    Drouot, N.5
  • 4
    • 0031194149 scopus 로고    scopus 로고
    • An integrated physical and genetic map spanning chromosome band 10q24
    • Gray IC, Fallowfield J, Ford S, Nobile C, Volpi EV et al. (1997) An integrated physical and genetic map spanning chromosome band 10q24. Genomics 43, 85-88
    • (1997) Genomics , vol.43 , pp. 85-88
    • Gray, I.C.1    Fallowfield, J.2    Ford, S.3    Nobile, C.4    Volpi, E.V.5
  • 5
    • 0022993652 scopus 로고
    • Mammalian mullidrug resistance gene: Complete cDNA sequence indicates strong homology to bacterial transport protein
    • Gros P, Croop J, Housman D (1986) Mammalian mullidrug resistance gene: complete cDNA sequence indicates strong homology to bacterial transport protein. Cell 74, 371-380
    • (1986) Cell , vol.74 , pp. 371-380
    • Gros, P.1    Croop, J.2    Housman, D.3
  • 6
    • 0028365885 scopus 로고
    • The human cytochrome b561 gene (CYB561) is located at 17q11-qter
    • McBride OW, Yi HF, Srivastava M (1994) The human cytochrome b561 gene (CYB561) is located at 17q11-qter. Genomics 21, 662-663
    • (1994) Genomics , vol.21 , pp. 662-663
    • McBride, O.W.1    Yi, H.F.2    Srivastava, M.3
  • 7
    • 0028844053 scopus 로고
    • Cyclin I: A new cyclin encoded by a gene isolated from human brain
    • Nakamura T, Sonokawa R, Sasaki YF, Ayusawa D, Oishi M et al. (1995) Cyclin I: a new cyclin encoded by a gene isolated from human brain. Exp Cell Res 221, 534-542
    • (1995) Exp Cell Res , vol.221 , pp. 534-542
    • Nakamura, T.1    Sonokawa, R.2    Sasaki, Y.F.3    Ayusawa, D.4    Oishi, M.5
  • 8
    • 0031568287 scopus 로고    scopus 로고
    • Toward cloning of a novel ataxia gene: Refined assignment and physical map of the IOSCa (SCa 8) locus on 10q24
    • Nikali K, Isosomppi J, Lonnqvist T, Mao JI, Suomalainen A et al. (1997) Toward cloning of a novel ataxia gene: refined assignment and physical map of the IOSCA (SCA 8) locus on 10q24. Genomics 39, 185-191
    • (1997) Genomics , vol.39 , pp. 185-191
    • Nikali, K.1    Isosomppi, J.2    Lonnqvist, T.3    Mao, J.I.4    Suomalainen, A.5
  • 9
    • 0028501004 scopus 로고
    • A refined restriction map of YAC clones spanning the entire human dystrophin gene
    • Nobile C, Marchi J (1994) A refined restriction map of YAC clones spanning the entire human dystrophin gene. Mamm Genome 5, 566-571
    • (1994) Mamm Genome , vol.5 , pp. 566-571
    • Nobile, C.1    Marchi, J.2
  • 10
    • 0029059069 scopus 로고
    • Localization of a gene for partial epilepsy to chromosome 10q
    • Ottman R, Risch N, Hauser WA, Pedley TA, Lee JH et al. (1995) Localization of a gene for partial epilepsy to chromosome 10q. Nat Genet 10, 55-60
    • (1995) Nat Genet , vol.10 , pp. 55-60
    • Ottman, R.1    Risch, N.2    Hauser, W.A.3    Pedley, T.A.4    Lee, J.H.5
  • 12
    • 0029126926 scopus 로고
    • Genomic structure and expression of the human gene encoding cytochrome b(561), an integral protein of the chromaffin granule membrane
    • Srivastava M (1995) Genomic structure and expression of the human gene encoding cytochrome b(561), an integral protein of the chromaffin granule membrane. J Biol Chem 270, 22714-22720
    • (1995) J Biol Chem , vol.270 , pp. 22714-22720
    • Srivastava, M.1
  • 13
    • 0027772225 scopus 로고
    • Cloning the partial cDNAs of mu-calpain and m-calpain from porcine skeletal muscle
    • Sun W, Ji SQ, Ebert PJ, Bidwell CA, Hancock DL (1993) Cloning the partial cDNAs of mu-calpain and m-calpain from porcine skeletal muscle. Biochimie 75, 931-936
    • (1993) Biochimie , vol.75 , pp. 931-936
    • Sun, W.1    Ji, S.Q.2    Ebert, P.J.3    Bidwell, C.A.4    Hancock, D.L.5
  • 14
    • 9544233652 scopus 로고    scopus 로고
    • A human canalicular multispecific organic anion transporter (cMOAT) gene is overexpressed in cisplatin-resistant human cancer cell line with decreased drug accumulation
    • Taniguchi K, Wada M, Kohno K, Nakamura T, Kawabe T et al. (1996) A human canalicular multispecific organic anion transporter (cMOAT) gene is overexpressed in cisplatin-resistant human cancer cell line with decreased drug accumulation. Cancer Res 56, 4124-1129
    • (1996) Cancer Res , vol.56 , pp. 4124-11129
    • Taniguchi, K.1    Wada, M.2    Kohno, K.3    Nakamura, T.4    Kawabe, T.5
  • 15
    • 6844250107 scopus 로고    scopus 로고
    • Mutations in the canalicular multispecific organic anion transporter (cMOAT) gene, a novel ABC transporter, in patients with hyperbilirubinemia II/Dubin-Johnson syndrome
    • Wada M, Toh S, Taniguchi K, Nakamura T, Uchiumi T, et al. (1998) Mutations in the canalicular multispecific organic anion transporter (cMOAT) gene, a novel ABC transporter, in patients with hyperbilirubinemia II/Dubin-Johnson syndrome. Hum Mol Genet 7, 203-207
    • (1998) Hum Mol Genet , vol.7 , pp. 203-207
    • Wada, M.1    Toh, S.2    Taniguchi, K.3    Nakamura, T.4    Uchiumi, T.5
  • 16
    • 0030922551 scopus 로고    scopus 로고
    • Homozygosity and linkage disequilibrium mapping of the urofacial (Ochoa) syndrome gene to a 1-cM interval of chromosome 10q23-q24
    • Wang CY, Hawkins-Lee B, Ochoa B, Walker RD, She JX (1997) Homozygosity and linkage disequilibrium mapping of the urofacial (Ochoa) syndrome gene to a 1-cM interval of chromosome 10q23-q24. Am J Hum Genet 60, 1461-1467
    • (1997) Am J Hum Genet , vol.60 , pp. 1461-1467
    • Wang, C.Y.1    Hawkins-Lee, B.2    Ochoa, B.3    Walker, R.D.4    She, J.X.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.