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Volumn 9, Issue 5, 2004, Pages 371-378

Intrauterine growth restriction - Genetic causes and consequences

Author keywords

Fetal programming; Genomic imprinting; Intrauterine growth restriction; Small for gestational age; Uniparental disomy

Indexed keywords

BECKWITH WIEDEMANN SYNDROME; CHROMOSOME ABERRATION; EMBRYO DEVELOPMENT; ENVIRONMENTAL FACTOR; EXPERIMENTAL MODEL; FETUS DEVELOPMENT; FETUS GROWTH; GENE EXPRESSION; GENE MUTATION; GENOME IMPRINTING; GESTATIONAL AGE; HEREDITY; HUMAN; INTRAUTERINE GROWTH RETARDATION; NONHUMAN; PERINATAL MORTALITY; PHENOTYPE; REVIEW; SILVER RUSSELL SYNDROME; UNIPARENTAL DISOMY;

EID: 12744253343     PISSN: 1744165X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.siny.2004.03.002     Document Type: Article
Times cited : (53)

References (43)
  • 1
    • 12744261475 scopus 로고    scopus 로고
    • http://www.modimes.org/
  • 2
    • 0029082045 scopus 로고
    • The fetal and infant origins of disease
    • Barker D.J. The fetal and infant origins of disease. Eur J Epidemiol. 25:1995;457-463
    • (1995) Eur J Epidemiol , vol.25 , pp. 457-463
    • Barker, D.J.1
  • 3
    • 3042690794 scopus 로고    scopus 로고
    • Fetal growth disorders
    • F.G. Cunningham, N.F. Gant, & K.J. Leveno. New York: Appleton and Lange
    • Cunningham F.G., Gant N.F., Leveno K.J. Fetal growth disorders. Cunningham F.G., Gant N.F., Leveno K.J. Williams obstetrics. 21st ed. :1997;743-764 Appleton and Lange, New York
    • (1997) Williams Obstetrics 21st Ed. , pp. 743-764
    • Cunningham, F.G.1    Gant, N.F.2    Leveno, K.J.3
  • 4
    • 0004219316 scopus 로고    scopus 로고
    • Medicine of the fetus and mother
    • A.E. Reece, & J.C. Hobbins. Philadelphia: Lippincourt-Raven
    • Reece A.E., Hagay Z. Medicine of the fetus and mother. Reece A.E., Hobbins J.C. Prenatal diagnosis of deviant fetal growth. 1999;Lippincourt-Raven, Philadelphia
    • (1999) Prenatal Diagnosis of Deviant Fetal Growth
    • Reece, A.E.1    Hagay, Z.2
  • 5
    • 0041570228 scopus 로고    scopus 로고
    • For debate: Fetal and early postnatal growth restriction lead to diabetes, the metabolic syndrome and renal failure
    • Hales C.N., Ozanne S.E. For debate: fetal and early postnatal growth restriction lead to diabetes, the metabolic syndrome and renal failure. Diabetologia. 46:2003;1013-1019
    • (2003) Diabetologia , vol.46 , pp. 1013-1019
    • Hales, C.N.1    Ozanne, S.E.2
  • 6
    • 0027394822 scopus 로고
    • Fetal growth retardation: Associated malformations and chromosomal abnormalities
    • Snijders R.J., Sherrod C., Gosden C.M., Nicolaides K.H. Fetal growth retardation: associated malformations and chromosomal abnormalities. Am J Obstet Gynecol. 168:1993;547-555
    • (1993) Am J Obstet Gynecol , vol.168 , pp. 547-555
    • Snijders, R.J.1    Sherrod, C.2    Gosden, C.M.3    Nicolaides, K.H.4
  • 7
    • 0021237658 scopus 로고
    • Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis
    • Surani M.A., Barton S.C., Norris M.L. Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis. Nature. 308:1984;548-550
    • (1984) Nature , vol.308 , pp. 548-550
    • Surani, M.A.1    Barton, S.C.2    Norris, M.L.3
  • 8
    • 0021139084 scopus 로고
    • Completion of mouse embryogenesis requires both the maternal and paternal genomes
    • Mcgrath J., Solter D. Completion of mouse embryogenesis requires both the maternal and paternal genomes. Cell. 37:1984;179-183
    • (1984) Cell , vol.37 , pp. 179-183
    • McGrath, J.1    Solter, D.2
  • 10
    • 0022391691 scopus 로고
    • Differential activity of maternally and paternally derived chromosome regions in mice
    • Cattanach B.M., Kirk M. Differential activity of maternally and paternally derived chromosome regions in mice. Nature. 315:1985;496-498
    • (1985) Nature , vol.315 , pp. 496-498
    • Cattanach, B.M.1    Kirk, M.2
  • 11
    • 0025242074 scopus 로고
    • Genome imprinting phenomena on mouse chromosome 7
    • Searle A.G., Beechey C.V. Genome imprinting phenomena on mouse chromosome 7. Genet Res. 56:1990;237-244
    • (1990) Genet Res , vol.56 , pp. 237-244
    • Searle, A.G.1    Beechey, C.V.2
  • 12
    • 12744271875 scopus 로고    scopus 로고
    • http://www.mgu.har.mrc.ac.uk/imprinting/imprinting.html
  • 13
    • 0019153057 scopus 로고
    • A new genetic concept: The uniparental disomy and its potential effect, the isodisomy
    • Engel E. A new genetic concept: the uniparental disomy and its potential effect, the isodisomy. J Genet Hum. 28:1980;11-22
    • (1980) J Genet Hum , vol.28 , pp. 11-22
    • Engel, E.1
  • 14
    • 0034098812 scopus 로고    scopus 로고
    • Mechanisms leading to uniparental disomy and their clinical consequences
    • Robinson W.P. Mechanisms leading to uniparental disomy and their clinical consequences. Bioessays. 22:2000;452-459
    • (2000) Bioessays , vol.22 , pp. 452-459
    • Robinson, W.P.1
  • 15
    • 0031030493 scopus 로고    scopus 로고
    • The incidence of uniparental disomy associated with intrauterine growth retardation in a cohort of thirty-five severely affected babies
    • Moore G.E., Ali Z., Khan R.U., Blunt S., Bennett P.R., Vaughan J.I. The incidence of uniparental disomy associated with intrauterine growth retardation in a cohort of thirty-five severely affected babies. Am J Obstet Gynecol. 176:1997;294-299
    • (1997) Am J Obstet Gynecol , vol.176 , pp. 294-299
    • Moore, G.E.1    Ali, Z.2    Khan, R.U.3    Blunt, S.4    Bennett, P.R.5    Vaughan, J.I.6
  • 20
    • 7344254106 scopus 로고    scopus 로고
    • A catalogue of imprinted genes and parent-of-origin effects in humans and animals
    • Morison I.M., Reeve A.E. A catalogue of imprinted genes and parent-of-origin effects in humans and animals. Hum Mol Genet. 7:1998;1599-1609
    • (1998) Hum Mol Genet , vol.7 , pp. 1599-1609
    • Morison, I.M.1    Reeve, A.E.2
  • 21
    • 0031687985 scopus 로고    scopus 로고
    • Abnormal behaviour and growth retardation associated with loss of the imprinted gene Mest
    • Lefebvre L., Viville S., Barton S.C., Ishino F., Keverne E.B., Surani M.A. Abnormal behaviour and growth retardation associated with loss of the imprinted gene Mest. Nat Genet. 20:1998;163-169
    • (1998) Nat Genet , vol.20 , pp. 163-169
    • Lefebvre, L.1    Viville, S.2    Barton, S.C.3    Ishino, F.4    Keverne, E.B.5    Surani, M.A.6
  • 22
    • 0035140174 scopus 로고    scopus 로고
    • Imprinting of PEG3, the human homologue of a mouse gene involved in nurturing behavior
    • Murphy S.K., Wylie A.A., Jirtle R.L. Imprinting of PEG3, the human homologue of a mouse gene involved in nurturing behavior. Genomics. 71:2001;110-117
    • (2001) Genomics , vol.71 , pp. 110-117
    • Murphy, S.K.1    Wylie, A.A.2    Jirtle, R.L.3
  • 23
    • 0035093826 scopus 로고    scopus 로고
    • Evolution of imprinting mechanisms: The battle of the sexes begins in the zygote
    • Reik W., Walter J. Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote. Nat Genet. 27:2001;255-260
    • (2001) Nat Genet , vol.27 , pp. 255-260
    • Reik, W.1    Walter, J.2
  • 24
    • 0036323502 scopus 로고    scopus 로고
    • Physiological functions of imprinted genes
    • Tycko B., Morison I.M. Physiological functions of imprinted genes. J Cell Physiol. 192:2002;245-258
    • (2002) J Cell Physiol , vol.192 , pp. 245-258
    • Tycko, B.1    Morison, I.M.2
  • 25
    • 0025320906 scopus 로고
    • A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene is disrupted by targeting
    • DeChiara T.M., Efstratiadis A., Robertson E.J. A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene is disrupted by targeting. Nature. 345:1990;78-80
    • (1990) Nature , vol.345 , pp. 78-80
    • Dechiara, T.M.1    Efstratiadis, A.2    Robertson, E.J.3
  • 26
    • 0028575985 scopus 로고
    • Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality
    • Lau M.M., Stewart C.E., Liu Z., Bhatt H., Rotwein P., Stewart C.L. Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality. Genes Dev. 8:1994;2953-2963
    • (1994) Genes Dev , vol.8 , pp. 2953-2963
    • Lau, M.M.1    Stewart, C.E.2    Liu, Z.3    Bhatt, H.4    Rotwein, P.5    Stewart, C.L.6
  • 28
    • 0027270870 scopus 로고
    • Rescue of the T-associated maternal effect in mice carrying null mutations in Igf-2 and Igf2r, two reciprocally imprinted genes
    • Filson A.J., Louvi A., Efstratiadis A., Robertson E.J. Rescue of the T-associated maternal effect in mice carrying null mutations in Igf-2 and Igf2r, two reciprocally imprinted genes. Development. 118:1993;731-736
    • (1993) Development , vol.118 , pp. 731-736
    • Filson, A.J.1    Louvi, A.2    Efstratiadis, A.3    Robertson, E.J.4
  • 29
    • 0025958320 scopus 로고
    • Genomic imprinting in mammalian development: A parental tug of war
    • Moore T., Haig D. Genomic imprinting in mammalian development: a parental tug of war. Trends Genet. 7:1991;45-49
    • (1991) Trends Genet , vol.7 , pp. 45-49
    • Moore, T.1    Haig, D.2
  • 31
    • 0027420362 scopus 로고
    • Disruption of insulin-like growth factor-2 in Beckwith Wiedemann syndrome
    • Weksberg R., Shen D.R., Fei Y.L., Song Q.L., Squire J. Disruption of insulin-like growth factor-2 in Beckwith Wiedemann syndrome. Nat Genet. 5:1993;143-149
    • (1993) Nat Genet , vol.5 , pp. 143-149
    • Weksberg, R.1    Shen, D.R.2    Fei, Y.L.3    Song, Q.L.4    Squire, J.5
  • 34
    • 0033975096 scopus 로고    scopus 로고
    • Beckwith-Wiedemann syndrome: Imprinting in clusters revisited
    • Maher E.R., Reik W. Beckwith-Wiedemann syndrome: imprinting in clusters revisited. J Clin Invest. 105:2000;247-252
    • (2000) J Clin Invest , vol.105 , pp. 247-252
    • Maher, E.R.1    Reik, W.2
  • 35
    • 13344261391 scopus 로고    scopus 로고
    • Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
    • Pilia G., Hughes-Benzie R.M., MacKenzie A., Baybayan P., Chen E.Y., Huber R. Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome. Nat Genet. 12:1996;241-247
    • (1996) Nat Genet , vol.12 , pp. 241-247
    • Pilia, G.1    Hughes-Benzie, R.M.2    MacKenzie, A.3    Baybayan, P.4    Chen, E.Y.5    Huber, R.6
  • 36
    • 0031943536 scopus 로고    scopus 로고
    • Overgrowth syndromes and genomic imprinting: From mouse to man
    • Li M., Squire J.A., Weksberg R. Overgrowth syndromes and genomic imprinting: from mouse to man. Clin Genet. 53:1998;165-170
    • (1998) Clin Genet , vol.53 , pp. 165-170
    • Li, M.1    Squire, J.A.2    Weksberg, R.3
  • 39
    • 0033042181 scopus 로고    scopus 로고
    • An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands
    • Preece M.A., Abu-Amero S.N., Ali Z., Abu-Amero K.K., Wakeling E.L., Stanier P. An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands. J Med Genet. 36:1999;457-460
    • (1999) J Med Genet , vol.36 , pp. 457-460
    • Preece, M.A.1    Abu-Amero, S.N.2    Ali, Z.3    Abu-Amero, K.K.4    Wakeling, E.L.5    Stanier, P.6
  • 40
    • 0036820514 scopus 로고    scopus 로고
    • Chromosome 7p disruptions in Silver-Russell syndrome: Delineating an imprinted candidate gene region
    • Monk D., Bentley L., Hitchins M., Myler R.A., Clayton-Smith J., Ismail S. Chromosome 7p disruptions in Silver-Russell syndrome: delineating an imprinted candidate gene region. Hum Genet. 111:2002;376-387
    • (2002) Hum Genet , vol.111 , pp. 376-387
    • Monk, D.1    Bentley, L.2    Hitchins, M.3    Myler, R.A.4    Clayton-Smith, J.5    Ismail, S.6
  • 41
    • 0035168178 scopus 로고    scopus 로고
    • A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region
    • Hannula K., Lipsanen-Nyman M., Kontiokari T., Kere J. A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region. Am J Hum Genet. 68:2001;247-253
    • (2001) Am J Hum Genet , vol.68 , pp. 247-253
    • Hannula, K.1    Lipsanen-Nyman, M.2    Kontiokari, T.3    Kere, J.4
  • 42
    • 0037440705 scopus 로고    scopus 로고
    • Regulation of supply and demand for maternal nutrients in mammals by imprinted genes
    • Reik W., Constancia M., Fowden A., Anderson N., Dean W., Ferguson-Smith A. Regulation of supply and demand for maternal nutrients in mammals by imprinted genes. J Physiol. 547:2003;35-44
    • (2003) J Physiol , vol.547 , pp. 35-44
    • Reik, W.1    Constancia, M.2    Fowden, A.3    Anderson, N.4    Dean, W.5    Ferguson-Smith, A.6


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