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Volumn 1, Issue , 2004, Pages

Genomic imprinting and assisted reproduction

Author keywords

[No Author keywords available]

Indexed keywords

ALBRIGHT SYNDROME; AUTISM; BECKWITH WIEDEMANN SYNDROME; CONGENITAL MALFORMATION; DNA METHYLATION; EMBRYO DEVELOPMENT; EPIGENETICS; FERTILIZATION IN VITRO; GENETIC DISORDER; GENETIC TRANSCRIPTION; GENOME IMPRINTING; HUMAN; INFERTILITY THERAPY; INTRACYTOPLASMIC SPERM INJECTION; MOLECULAR EVOLUTION; NEOPLASM; PATHOPHYSIOLOGY; PLACENTA; PRADER WILLI SYNDROME; REVIEW; RISK ASSESSMENT; SILVER RUSSELL SYNDROME; TRANSCRIPTION REGULATION;

EID: 15444362546     PISSN: 17424755     EISSN: None     Source Type: Journal    
DOI: 10.1186/1742-4755-1-6     Document Type: Review
Times cited : (38)

References (44)
  • 1
    • 0037939678 scopus 로고    scopus 로고
    • Rare congenital disorders, imprinted genes, and assisted reproductive technology
    • Gosden R, Trasler J, Lucifero D, Faddy M: Rare congenital disorders, imprinted genes, and assisted reproductive technology. Lancet 2003, 361:1975-1977.
    • (2003) Lancet , vol.361 , pp. 1975-1977
    • Gosden, R.1    Trasler, J.2    Lucifero, D.3    Faddy, M.4
  • 2
    • 0037372003 scopus 로고    scopus 로고
    • Epigenetic regulation of gene expression: How the genome integrates intrinsic and environmental signals
    • Jaenisch R, Bird A: Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals. Nat Genet 2003, Suppl:245-254.
    • (2003) Nat Genet , Issue.SUPPL. , pp. 245-254
    • Jaenisch, R.1    Bird, A.2
  • 3
    • 0037434652 scopus 로고    scopus 로고
    • Epigenetics and disease: Altered states
    • Dennis C: Epigenetics and disease: Altered states. Nature 2003, 421:686-688.
    • (2003) Nature , vol.421 , pp. 686-688
    • Dennis, C.1
  • 4
    • 0034109336 scopus 로고    scopus 로고
    • Dynamics of DNA methylation pattern
    • Hsieh CL: Dynamics of DNA methylation pattern. Curr Opin Genet Dev 2000, 10:224-228.
    • (2000) Curr Opin Genet Dev , vol.10 , pp. 224-228
    • Hsieh, C.L.1
  • 5
    • 1342306129 scopus 로고    scopus 로고
    • Potential significance of genomic imprinting defects for reproduction and assisted reproductive technology
    • Lucifero D, Chaillet JR, Trasler JM: Potential significance of genomic imprinting defects for reproduction and assisted reproductive technology. Hum Reprod Update 2004, 10:3-18.
    • (2004) Hum Reprod Update , vol.10 , pp. 3-18
    • Lucifero, D.1    Chaillet, J.R.2    Trasler, J.M.3
  • 6
    • 0035234557 scopus 로고    scopus 로고
    • Genomic imprinting: Parental influence on the genome
    • Reik W, Walter J: Genomic imprinting: parental influence on the genome. Nat Rev Genet 2001, 2:21-32.
    • (2001) Nat Rev Genet , vol.2 , pp. 21-32
    • Reik, W.1    Walter, J.2
  • 8
    • 0036333598 scopus 로고    scopus 로고
    • Erasing genomic imprinting memory in mouse clone embryos produced from day 11.5 primordial germ cells
    • Lee J, Inoue K, Ono R, Ogonuki N, Kohda T, Kaneko-Ishino T, Ogura A, Ishino F: Erasing genomic imprinting memory in mouse clone embryos produced from day 11.5 primordial germ cells. Development 2002, 129:1807-1817.
    • (2002) Development , vol.129 , pp. 1807-1817
    • Lee, J.1    Inoue, K.2    Ono, R.3    Ogonuki, N.4    Kohda, T.5    Kaneko-Ishino, T.6    Ogura, A.7    Ishino, F.8
  • 9
    • 0036275755 scopus 로고    scopus 로고
    • Allele-specific expression of imprinted genes in mouse migratory primordial germ cells
    • Szabo PE, Hubner K, Scholer H, Mann JR: Allele-specific expression of imprinted genes in mouse migratory primordial germ cells. Mech Dev 2002, 115:157-160.
    • (2002) Mech Dev , vol.115 , pp. 157-160
    • Szabo, P.E.1    Hubner, K.2    Scholer, H.3    Mann, J.R.4
  • 10
    • 0036797894 scopus 로고    scopus 로고
    • Epigenetic risks related to assisted reproductive technologies: Risk analysis and epigenetic inheritance
    • De Rycke M, Liebaers I, Van Steirteghem A: Epigenetic risks related to assisted reproductive technologies: risk analysis and epigenetic inheritance. Hum Reprod 2002, 17:2487-2494.
    • (2002) Hum Reprod , vol.17 , pp. 2487-2494
    • De Rycke, M.1    Liebaers, I.2    Van Steirteghem, A.3
  • 11
    • 0036836547 scopus 로고    scopus 로고
    • Genomic imprinting and epigenetic reprogramming: Unearthing the garden of forking paths
    • Kierszenbaum AL: Genomic imprinting and epigenetic reprogramming: unearthing the garden of forking paths. Mol Reprod Dev 2002, 63:269-272.
    • (2002) Mol Reprod Dev , vol.63 , pp. 269-272
    • Kierszenbaum, A.L.1
  • 14
    • 0037389185 scopus 로고    scopus 로고
    • Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development
    • Weksberg R, Smith AC, Squire J, Sadowski P: Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development. Hum Mol Genet 2003, 12:61-68.
    • (2003) Hum Mol Genet , vol.12 , pp. 61-68
    • Weksberg, R.1    Smith, A.C.2    Squire, J.3    Sadowski, P.4
  • 15
    • 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: 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 U S A 1999, 96:5203-5208.
    • (1999) Proc Natl Acad Sci U S A , 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
  • 16
    • 0036182963 scopus 로고    scopus 로고
    • Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects
    • DeBaun MR, Niemitz EL, McNeil DE, Brandenburg SA, Lee MP, Feinberg AP: Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects. Am J Hum Genet 2002, 70:604-611.
    • (2002) Am J Hum Genet , vol.70 , pp. 604-611
    • DeBaun, M.R.1    Niemitz, E.L.2    McNeil, D.E.3    Brandenburg, S.A.4    Lee, M.P.5    Feinberg, A.P.6
  • 17
    • 0036846536 scopus 로고    scopus 로고
    • The imprinting mechanism of the Prader-Willi/Angelman regional control center
    • Perk J, Makedonski K, Lande L, Cedar H, Razin A, Shemer R: The imprinting mechanism of the Prader-Willi/Angelman regional control center. EMBO J 2002, 21:5807-5814.
    • (2002) EMBO J , vol.21 , pp. 5807-5814
    • Perk, J.1    Makedonski, K.2    Lande, L.3    Cedar, H.4    Razin, A.5    Shemer, R.6
  • 18
    • 0037304158 scopus 로고    scopus 로고
    • Regulation of imprinting: A multi-tiered process
    • Rand E, Cedar H: Regulation of imprinting: A multi-tiered process. J Cell Biochem 2003, 88:400-407.
    • (2003) J Cell Biochem , vol.88 , pp. 400-407
    • Rand, E.1    Cedar, H.2
  • 19
    • 0033963470 scopus 로고    scopus 로고
    • Imprinting, the X-chromosome, and the male brain: Explaining sex differences in the liability to autism
    • Skuse DH: Imprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autism. Pediat Res 2000, 47:9-16.
    • (2000) Pediat Res , vol.47 , pp. 9-16
    • Skuse, D.H.1
  • 20
    • 0033997450 scopus 로고    scopus 로고
    • The impact of genomic imprinting for neurobehavioral and developmental disorders
    • Nicholls RD: The impact of genomic imprinting for neurobehavioral and developmental disorders. J Clin Invest 2000, 105:413-418.
    • (2000) J Clin Invest , vol.105 , pp. 413-418
    • Nicholls, R.D.1
  • 21
    • 0034827137 scopus 로고    scopus 로고
    • Imprinted genes and mental dysfunction
    • Davies W, Isles AR, Wilkinson LS: Imprinted genes and mental dysfunction. Ann Med 2001, 33:428-436.
    • (2001) Ann Med , vol.33 , pp. 428-436
    • Davies, W.1    Isles, A.R.2    Wilkinson, L.S.3
  • 22
    • 0025863603 scopus 로고
    • Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis
    • Chaillet JR, Vogt TF, Beier DR, Leder P: Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis. Cell 1991, 66:77-83.
    • (1991) Cell , vol.66 , pp. 77-83
    • Chaillet, J.R.1    Vogt, T.F.2    Beier, D.R.3    Leder, P.4
  • 23
    • 0034703865 scopus 로고    scopus 로고
    • The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell development
    • Davis TL, Yang GJ, McCarrey JR, Bartolomei MS: The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell development. Hum Mol Genet 2000, 9:2885-2894.
    • (2000) Hum Mol Genet , vol.9 , pp. 2885-2894
    • Davis, T.L.1    Yang, G.J.2    McCarrey, J.R.3    Bartolomei, M.S.4
  • 24
    • 1642365471 scopus 로고    scopus 로고
    • Analysis of sex differences in EGC imprinting
    • Durcova-Hills G, Burgoyne P, McLaren A: Analysis of sex differences in EGC imprinting. Dev Biol 2004, 268:105-110.
    • (2004) Dev Biol , vol.268 , pp. 105-110
    • Durcova-Hills, G.1    Burgoyne, P.2    McLaren, A.3
  • 26
    • 0037035121 scopus 로고    scopus 로고
    • Low and very low birth weight in infants conceived with use of assisted reproductive technology
    • Schieve LA, Meikle SF, Ferre C, Peterson HB, Jeng G, Wilcox LS: Low and very low birth weight in infants conceived with use of assisted reproductive technology. N Engl J Med 2002, 346:731-737.
    • (2002) N Engl J Med , vol.346 , pp. 731-737
    • Schieve, L.A.1    Meikle, S.F.2    Ferre, C.3    Peterson, H.B.4    Jeng, G.5    Wilcox, L.S.6
  • 27
    • 0037035126 scopus 로고    scopus 로고
    • The risk of major birth defects after intracytoplasmic sperm injection and in vitro fertilization
    • Hansen M, Kurinczuk JJ, Bower C, Webb S: The risk of major birth defects after intracytoplasmic sperm injection and in vitro fertilization. N Engl J Med 2002, 346:725-730.
    • (2002) N Engl J Med , vol.346 , pp. 725-730
    • Hansen, M.1    Kurinczuk, J.J.2    Bower, C.3    Webb, S.4
  • 28
    • 0037222510 scopus 로고    scopus 로고
    • Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19
    • DeBaun MR, Niemitz EL, Feinberg AP: Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19. Am J Hum Genet 2003, 72:156-160.
    • (2003) Am J Hum Genet , vol.72 , pp. 156-160
    • DeBaun, M.R.1    Niemitz, E.L.2    Feinberg, A.P.3
  • 29
    • 0346777377 scopus 로고    scopus 로고
    • Epigenetic risks related to assisted reproductive technologies: Epigenetics, imprinting, ART and icebergs?
    • Maher ER, Afnan M, Barratt CL: Epigenetic risks related to assisted reproductive technologies: epigenetics, imprinting, ART and icebergs? Hum Reprod 2003, 18:2508-2511.
    • (2003) Hum Reprod , vol.18 , pp. 2508-2511
    • Maher, E.R.1    Afnan, M.2    Barratt, C.L.3
  • 32
  • 35
    • 0035052151 scopus 로고    scopus 로고
    • Imprinting analysis in spermatozoa prepared for intracytoplasmic sperm injection (ICSI)
    • Manning M, Lissens W, Liebaers I, Van Steirteghem A, Weidner WI: Imprinting analysis in spermatozoa prepared for intracytoplasmic sperm injection (ICSI). nt J Androl 2001, 24:87-94.
    • (2001) Nt J Androl , vol.24 , pp. 87-94
    • Manning, M.1    Lissens, W.2    Liebaers, I.3    Van Steirteghem, A.4    Weidner, W.I.5
  • 36
    • 0031133236 scopus 로고    scopus 로고
    • Comparison of gonosomal aneuploidy in spermatozoa of normal fertile men and those with severe male factor detected by in-situ hybridization
    • Bernardini L, Martini E, Geraedts JP, Hopman AH, Lanteri S, Conte N, Capitanio GL: Comparison of gonosomal aneuploidy in spermatozoa of normal fertile men and those with severe male factor detected by in-situ hybridization. Mol Hum Reprod 1997, 3:431-438.
    • (1997) Mol Hum Reprod , vol.3 , pp. 431-438
    • Bernardini, L.1    Martini, E.2    Geraedts, J.P.3    Hopman, A.H.4    Lanteri, S.5    Conte, N.6    Capitanio, G.L.7
  • 37
    • 2442686408 scopus 로고    scopus 로고
    • Genomic imprinting in disruptive spermatogenesis
    • Marques CJ, Carvalho F, Sousa M, Barros A: Genomic imprinting in disruptive spermatogenesis. Lancet 2004, 363:1700-1702.
    • (2004) Lancet , vol.363 , pp. 1700-1702
    • Marques, C.J.1    Carvalho, F.2    Sousa, M.3    Barros, A.4
  • 38
    • 0036836602 scopus 로고    scopus 로고
    • Aberrant methylation patterns at the two-cell stage as an indicator of early developmental failure
    • Shi W, Haaf T: Aberrant methylation patterns at the two-cell stage as an indicator of early developmental failure. Mol Reprod Dev 2002, 63:329-334.
    • (2002) Mol Reprod Dev , vol.63 , pp. 329-334
    • Shi, W.1    Haaf, T.2
  • 40
    • 0034112603 scopus 로고    scopus 로고
    • Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo
    • Doherty AS, Mann MR, Tremblay KD, Bartolomei MS, Schultz RM: Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo. Biol Reprod 2000, 62:1526-1535.
    • (2000) Biol Reprod , vol.62 , pp. 1526-1535
    • Doherty, A.S.1    Mann, M.R.2    Tremblay, K.D.3    Bartolomei, M.S.4    Schultz, R.M.5
  • 41
    • 0035116489 scopus 로고    scopus 로고
    • Culture of preimplantation mouse embryos affects fetal development and the expression of imprinted genes
    • Khosla S, Dean W, Brown D, Reik W, Feil R: Culture of preimplantation mouse embryos affects fetal development and the expression of imprinted genes. Biol Reprod 2001, 64:918-926.
    • (2001) Biol Reprod , vol.64 , pp. 918-926
    • Khosla, S.1    Dean, W.2    Brown, D.3    Reik, W.4    Feil, R.5
  • 43
    • 0342572600 scopus 로고    scopus 로고
    • Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19
    • Constancia M, Dean W, Lopes S, Moore T, Kelsey G, Reik W: Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19. Nat Genet 2000, 26:203-206.
    • (2000) Nat Genet , vol.26 , pp. 203-206
    • Constancia, M.1    Dean, W.2    Lopes, S.3    Moore, T.4    Kelsey, G.5    Reik, W.6
  • 44


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.