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Volumn 6, Issue 8, 1996, Pages 742-746

Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical region

Author keywords

[No Author keywords available]

Indexed keywords

DINUCLEOTIDE; SMALL NUCLEAR RIBONUCLEOPROTEIN;

EID: 0029778098     PISSN: 10549803     EISSN: None     Source Type: Journal    
DOI: 10.1101/gr.6.8.742     Document Type: Article
Times cited : (23)

References (18)
  • 1
    • 0028939902 scopus 로고
    • Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15
    • Buiting, K., S. Saitoh, S. Gross, B. Dittrich, S. Schwartz, R.D. Nicholls, and B. Horsthemke. 1995. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nature Genet. 9: 395-400.
    • (1995) Nature Genet , vol.9 , pp. 395-400
    • Buiting, K.1    Saitoh, S.2    Gross, S.3    Dittrich, B.4    Schwartz, S.5    Nicholls, R.D.6    Horsthemke, B.7
  • 2
    • 0025181455 scopus 로고
    • Prader-Willi syndrome: Current understanding of cause and diagnosis
    • Butler, M.G. 1990. Prader-Willi syndrome: Current understanding of cause and diagnosis. Am. J. Med. Genet. 35:319-332.
    • (1990) Am. J. Med. Genet. , vol.35 , pp. 319-332
    • Butler, M.G.1
  • 5
    • 0026595355 scopus 로고
    • Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13
    • Dittrich, B., W.P. Robinson, H. Knoblauch, K. Buiting, K. Schmidt, G. Gillessen-Kaesbach, and B. Horsthemke. 1992. Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13. Hum. Genet. 90: 313-315.
    • (1992) Hum. Genet. , vol.90 , pp. 313-315
    • Dittrich, B.1    Robinson, W.P.2    Knoblauch, H.3    Buiting, K.4    Schmidt, K.5    Gillessen-Kaesbach, G.6    Horsthemke, B.7
  • 8
    • 0030099403 scopus 로고    scopus 로고
    • Imprinted genes have few and small introns
    • Hurst, L.D., G. McVean, and T. Moore. 1996. Imprinted genes have few and small introns. Nature Genet. 12: 234-237.
    • (1996) Nature Genet. , vol.12 , pp. 234-237
    • Hurst, L.D.1    McVean, G.2    Moore, T.3
  • 9
    • 0027018063 scopus 로고
    • Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the Prader-Willi syndrome region
    • Leff, S.E., C.I. Brannan, M.L. Reed, T. Ozcelik, U. Francke, N.G. Copeland, and N.A. Jenkins. 1992. Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the Prader-Willi syndrome region. Nature Genet. 2: 259-264.
    • (1992) Nature Genet. , vol.2 , pp. 259-264
    • Leff, S.E.1    Brannan, C.I.2    Reed, M.L.3    Ozcelik, T.4    Francke, U.5    Copeland, N.G.6    Jenkins, N.A.7
  • 11
    • 0028044579 scopus 로고
    • Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E)
    • Nakao, M., J.S. Sutcliffe, B. Durtschi, A. Mutirangura, D.H. Ledbetter, and A.L. Beaudet. 1994. Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E). Hum. Mol. Genet. 3: 309-315.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 309-315
    • Nakao, M.1    Sutcliffe, J.S.2    Durtschi, B.3    Mutirangura, A.4    Ledbetter, D.H.5    Beaudet, A.L.6
  • 12
    • 0024440608 scopus 로고
    • Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome
    • Nicholls, R.D., J.H.M. Knoll, M.G. Butler, S. Karam, and M. Lalande. 1989. Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome. Nature 342: 281-285.
    • (1989) Nature , vol.342 , pp. 281-285
    • Nicholls, R.D.1    Knoll, J.H.M.2    Butler, M.G.3    Karam, S.4    Lalande, M.5
  • 13
    • 0027026716 scopus 로고
    • Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region
    • Ozcelik, T., S. Leff, W.P. Robinson, T. Donlon, M. Lalande, E. Sanjines, A. Schinzel, and U. Francke. 1992. Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region. Nature Genet. 2: 265-269.
    • (1992) Nature Genet. , vol.2 , pp. 265-269
    • Ozcelik, T.1    Leff, S.2    Robinson, W.P.3    Donlon, T.4    Lalande, M.5    Sanjines, E.6    Schinzel, A.7    Francke, U.8
  • 14
    • 0028289468 scopus 로고
    • Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome
    • Reed, M.L. and S.E. Leff. 1994. Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome. Nature Genet. 6: 163-7.
    • (1994) Nature Genet. , vol.6 , pp. 163-167
    • Reed, M.L.1    Leff, S.E.2
  • 18
    • 0028124726 scopus 로고
    • Identification of a novel paternally expressed gene in the Prader-Willi syndrome region
    • Wevrick, R., J.A. Kerns, and U. Francke. 1994. Identification of a novel paternally expressed gene in the Prader-Willi syndrome region. Hum. Mol. Genet. 3: 1877-1882.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1877-1882
    • Wevrick, R.1    Kerns, J.A.2    Francke, U.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.