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Volumn 45, Issue 2, 2000, Pages 96-97

An NsiI RFLP in the human long QT intronic transcript 1 (LIT1)

Author keywords

11p15.5; Imprinting; LIT1; NsiI RFLP

Indexed keywords

ARTICLE; BECKWITH WIEDEMANN SYNDROME; CANCER; CHROMOSOME 11P; GENE; GENE FREQUENCY; HUMAN; INTRON; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

EID: 0034060262     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380050020     Document Type: Article
Times cited : (3)

References (9)
  • 1
    • 0030027206 scopus 로고    scopus 로고
    • A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5
    • Besnard-Guerin C, Newsham I, Winqvist R, Cavenee WK (1996) A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5. Hum Genet 97:163-170
    • (1996) Hum Genet , vol.97 , pp. 163-170
    • Besnard-Guerin, C.1    Newsham, I.2    Winqvist, R.3    Cavenee, W.K.4
  • 2
    • 0029806141 scopus 로고    scopus 로고
    • Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway
    • Brown KW, Villar AJ, Bickmore W, Clayton-Smith J, Catchpoole D, Maher ER, Reik W (1996) Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway. Hum Mol Genet 5:2027-2032
    • (1996) Hum Mol Genet , vol.5 , pp. 2027-2032
    • Brown, K.W.1    Villar, A.J.2    Bickmore, W.3    Clayton-Smith, J.4    Catchpoole, D.5    Maher, E.R.6    Reik, W.7
  • 5
    • 0031046285 scopus 로고    scopus 로고
    • Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements
    • Lee MP, Hu RJ, Johnson LA, Feinberg AP (1997) Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements. Nature Genet 15:181-185
    • (1997) Nature Genet , vol.15 , pp. 181-185
    • Lee, M.P.1    Hu, R.J.2    Johnson, L.A.3    Feinberg, A.P.4
  • 6
    • 0033609117 scopus 로고    scopus 로고
    • Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting
    • Lee MP, Debaun MR, Mitsuya K, Galonek HL, Brandenburg S, Oshimura M, Feinberg AP (1999) Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting. Proc Natl Acad Sci USA 96:5203-5208
    • (1999) Proc Natl Acad Sci USA , vol.96 , pp. 5203-5208
    • Lee, M.P.1    Debaun, M.R.2    Mitsuya, K.3    Galonek, H.L.4    Brandenburg, S.5    Oshimura, M.6    Feinberg, A.P.7
  • 7
    • 0032813924 scopus 로고    scopus 로고
    • LIT1, an imprinted antisense RNA in the human KVLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids
    • Mitsuya K, Meguro M, Lee MP, Katoh M, Schulz TC, Kugoh H, Yoshida MA, Niikawa N, Feinberg AP, Oshimura M (1999) LIT1, an imprinted antisense RNA in the human KVLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids. Hum Mol Genet 8:1209-1217
    • (1999) Hum Mol Genet , vol.8 , pp. 1209-1217
    • Mitsuya, K.1    Meguro, M.2    Lee, M.P.3    Katoh, M.4    Schulz, T.C.5    Kugoh, H.6    Yoshida, M.A.7    Niikawa, N.8    Feinberg, A.P.9    Oshimura, M.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.