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Volumn 101, Issue 2, 1997, Pages 235-237

Exclusion of PPEF as the gene causing X-linked juvenile reinoschisis

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME XP; CLINICAL ARTICLE; CONTROLLED STUDY; DNA DETERMINATION; DROSOPHILA MELANOGASTER; GENE LOCATION; GENE MUTATION; HUMAN; HUMAN CELL; PRIORITY JOURNAL; RETINOSCHISIS; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SINGLE STRAND CONFORMATION POLYMORPHISM; VITREORETINAL DEGENERATION; X CHROMOSOME LINKAGE;

EID: 0031469312     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050622     Document Type: Article
Times cited : (4)

References (20)
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    • Alitalo T, Francis F, Kere J, Lehrach H, Schlessinger D, Willard HF (1995) A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PICA, GRPR, CALB3 and PHKA2 genes. Genomics 25:691-700
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  • 9
    • 0029980311 scopus 로고    scopus 로고
    • Clinical features in affected males with X-linked retinoschisis
    • George ND, Yates JR, Moore AT (1996) Clinical features in affected males with X-linked retinoschisis. Arch Ophthalmol 114:274-280
    • (1996) Arch Ophthalmol , vol.114 , pp. 274-280
    • George, N.D.1    Yates, J.R.2    Moore, A.T.3
  • 12
    • 8544252382 scopus 로고    scopus 로고
    • A human homolog of the Drosophila retinal degeneration C (rdgc) gene encodes a novel serine- Threonine phosphatase selectively expressed in sensory neurons of neural crest origin
    • Montini E, Rugarli EI, Van de Vosse E, Andolfi G, Puca AA, Den Dunnen JT, Ballabio A, Franco B (1997) A human homolog of the Drosophila retinal degeneration C (rdgc) gene encodes a novel serine- threonine phosphatase selectively expressed in sensory neurons of neural crest origin. Hum Mol Genet 6:1137-1145
    • (1997) Hum Mol Genet , vol.6 , pp. 1137-1145
    • Montini, E.1    Rugarli, E.I.2    Van de Vosse, E.3    Andolfi, G.4    Puca, A.A.5    Den Dunnen, J.T.6    Ballabio, A.7    Franco, B.8
  • 13
    • 0024756969 scopus 로고
    • Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
    • Orita M, Suzuki Y, Sekiya T, Hayashi K (1989) Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. Genomics 5:874-879
    • (1989) Genomics , vol.5 , pp. 874-879
    • Orita, M.1    Suzuki, Y.2    Sekiya, T.3    Hayashi, K.4
  • 16
    • 0024506157 scopus 로고
    • Access to a messenger RNA sequence or its protein product is not limited by tissue or species specificity
    • Sarkar G, Sommer SS (1989) Access to a messenger RNA sequence or its protein product is not limited by tissue or species specificity. Science 244:331-334
    • (1989) Science , vol.244 , pp. 331-334
    • Sarkar, G.1    Sommer, S.S.2
  • 17
    • 0025345760 scopus 로고
    • Rhodopsin activation causes retinal degeneration Drosophila rdgC mutant
    • Steele F, O'Tousa JE (1995) Rhodopsin activation causes retinal degeneration Drosophila rdgC mutant. Neuron 4:883-890
    • (1995) Neuron , vol.4 , pp. 883-890
    • Steele, F.1    O'Tousa, J.E.2
  • 18
    • 0026724733 scopus 로고
    • Drosophila retinal degeneration C (rdgC) encodes a novel serine/threonine protein phosphatase
    • Steele FR, Washburn T, Rieger R, O'Tousa JE (1992) Drosophila retinal degeneration C (rdgC) encodes a novel serine/threonine protein phosphatase. Cell 69:669-676
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  • 20
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    • High resolution mapping by YAC fragmentation of a 2.5 Mb Xp22 region containing the human RS, KFSD and CLS disease genes
    • Van de Vosse E, Van der Bent P, Heus JJ, Van Ommen GJB, Den Dunnen JT (1997) High resolution mapping by YAC fragmentation of a 2.5 Mb Xp22 region containing the human RS, KFSD and CLS disease genes. Mamm Genome 8:497-501
    • (1997) Mamm Genome , vol.8 , pp. 497-501
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.