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Volumn 5, Issue 4, 1998, Pages 235-240

A novel gene, ITM, located between p57KIP2 and IPL, is imprinted in mice

Author keywords

Beckwith Wiedemann syndrome; Human chromosome 11p15.5; Imprinting; Maternal expression; Mouse chromosome 7

Indexed keywords

CDKN1C PROTEIN, HUMAN; CDKN1C PROTEIN, MOUSE; COMPLEMENTARY DNA; CYCLIN DEPENDENT KINASE INHIBITOR 1C; NUCLEAR PROTEIN; PROTEIN; TSSC3 PROTEIN;

EID: 0032584803     PISSN: 13402838     EISSN: None     Source Type: Journal    
DOI: 10.1093/dnares/5.4.235     Document Type: Article
Times cited : (14)

References (14)
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  • 2
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  • 5
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    • Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements
    • Lee, M. P., Hu, R. J., Johnson, L. A., and Feinberg, A. P. 1997, Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements, Nat. Genet., 15, 181-185.
    • (1997) Nat. Genet. , vol.15 , pp. 181-185
    • Lee, M.P.1    Hu, R.J.2    Johnson, L.A.3    Feinberg, A.P.4
  • 7
    • 9844265406 scopus 로고    scopus 로고
    • The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis
    • Qian, N., Frank, D., O'Keefe, D. et al. 1997, The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis, Hum. Mol. Genet., 6, 2021-2029.
    • (1997) Hum. Mol. Genet. , vol.6 , pp. 2021-2029
    • Qian, N.1    Frank, D.2    O'Keefe, D.3
  • 8
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    • Ogawa, O., Eccles, M. R., Szeto, J. et al. 1993, Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour, Nature, 362, 749-751.
    • (1993) Nature , vol.362 , pp. 749-751
    • Ogawa, O.1    Eccles, M.R.2    Szeto, J.3
  • 10
    • 0029360421 scopus 로고
    • Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies
    • Paldi, A., Gyapay, G., and Jami, J. 1995, Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies, Curr. Biol., 5, 1030-1035.
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    • Paldi, A.1    Gyapay, G.2    Jami, J.3
  • 11
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    • Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15
    • Buiting, K., Saitoh, S., Gross, S. et al. 1995, Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15, Nat. Genet., 9, 395-400.
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  • 12
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.