SCOPUS 정보 검색 플랫폼

Clinical Genetics

Volumn 51, Issue 1, 1997, Pages 75-

A new restriction-site polymorphism in the human proteolipid protein gene

(6) Kawanishi, Chiaki a,c Osaka, Hitoshi b Inoue, Ken a Onishi, Hideki a Yamada, Yoshiteru a Kosaka, Kenji a

a YOKOHAMA CITY UNIVERSITY (Japan)

b YOKOHAMA CITY UNIVERSITY HOSPITAL (Japan)

c YOKOHAMA CITY UNIVERSITY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME XQ; DNA POLYMORPHISM; GENE FREQUENCY; GENE LOCUS; GENE MUTATION; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MARKER GENE; PELIZAEUS MERZBACHER DISEASE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; X CHROMOSOME LINKAGE;

EID: 1842295717 PISSN: 00099163 EISSN: None Source Type: Journal
DOI: 10.1111/j.1399-0004.1997.tb02421.x Document Type: Article

Times cited : (2)

References (6)

1
- 0026736001
- Identification of cis-regulatory elements in the myelin proteolipid protein gene
- Berndt JA, Kim JG, Hudson LD. Identification of cis-regulatory elements in the myelin proteolipid protein gene. J Biol Chem 267: 1992: 14730-14737.
- (1992) J Biol Chem , vol.267 , pp. 14730-14737
- Berndt, J.A.¹ Kim, J.G.² Hudson, L.D.³

2
- 0022860245
- Individual exons encode the integral membrane domains of human myelin proteolipid protein
- Diehl H-J, Schaich M, Budzinski R-M, Stoffel W. Individual exons encode the integral membrane domains of human myelin proteolipid protein. Proc Natl Acad Sci USA 83: 1986: 9807-9811.
- (1986) Proc Natl Acad Sci USA , vol.83 , pp. 9807-9811
- Diehl, H.-J.¹ Schaich, M.² Budzinski, R.-M.³ Stoffel, W.⁴

3
- 0027759985
- Genetics of Pelizaeus- Merzbacher disease
- Modes ME, Pratt VM, Dlouhy SR. Genetics of Pelizaeus- Merzbacher disease. Dev Neurosci 15: 1993: 383-394.
- (1993) Dev Neurosci , vol.15 , pp. 383-394
- Modes, M.E.¹ Pratt, V.M.² Dlouhy, S.R.³

4
- 1842390730
- Novel nonsense proteolipid protein gene mutation as a cause of X-linked spastic paraplegia in twin males
- Osaka H, Kawanishi C, Inoue K, Uesugi H, Kurisaki H, Nishiyama K, Yamada Y, Suzuki K, Kimura S, Kosaka K. Novel nonsense proteolipid protein gene mutation as a cause of X-linked spastic paraplegia in twin males. Biochem Biophys Res Commun 170: 1995: 375-382.
- (1995) Biochem Biophys Res Commun , vol.170 , pp. 375-382
- Osaka, H.¹ Kawanishi, C.² Inoue, K.³ Uesugi, H.⁴ Kurisaki, H.⁵ Nishiyama, K.⁶ Yamada, Y.⁷ Suzuki, K.⁸ Kimura, S.⁹ Kosaka, K.¹⁰

5
- 0028239867
- X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus
- Saugier-Veber P, Munnich A, Bonneau D, Rozet J-M, Merrer ML, Gil R, Boespflug-Tanguy O. X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus. Nature Genet 6: 1994: 257-262.
- (1994) Nature Genet , vol.6 , pp. 257-262
- Saugier-Veber, P.¹ Munnich, A.² Bonneau, D.³ Rozet, J.-M.⁴ Merrer, M.L.⁵ Gil, R.⁶ Boespflug-Tanguy, O.⁷

6
- 0026337065
- Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms
- Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper DN, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms. Cytogenet Cell Genet 58: 1991: 1190-1832.
- (1991) Cytogenet Cell Genet , vol.58 , pp. 1190-1832
- Williamson, R.¹ Bowcock, A.² Kidd, K.³ Pearson, P.⁴ Schmidtke, J.⁵ Ceverha, P.⁶ Chipperfield, M.⁷ Cooper, D.N.⁸ Coutelle, C.⁹ Hewitt, J.¹⁰ Klinger, K.¹¹ Langley, K.¹² Beckmann, J.¹³ Tolley, M.¹⁴ Maidak, B.¹⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.