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Volumn 19, Issue 10, 2011, Pages 1026-1031

Mosaics and moles

Author keywords

biparental diploidy; genomic imprinting; hydatidiform mole; mosaicism; persistent trophoblastic disease; triploidy

Indexed keywords

DNA MARKER;

EID: 80053050946     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2011.93     Document Type: Article
Times cited : (38)

References (36)
  • 1
    • 33845543892 scopus 로고    scopus 로고
    • The genetics of hydatidiform moles: New lights on an ancient disease
    • DOI 10.1111/j.1399-0004.2006.00697.x
    • Slim R, Mehio A: The genetics of hydatidiform moles: new lights on an ancient disease. Clin Genet 2007; 71: 25-34. (Pubitemid 44921618)
    • (2007) Clinical Genetics , vol.71 , Issue.1 , pp. 25-34
    • Slim, R.1    Mehio, A.2
  • 2
    • 0019253756 scopus 로고
    • Mechanism of origin of complete hydatidiform moles
    • DOI 10.1038/286714a0
    • Jacobs PA, Wilson CM, Sprenkle JA, et al. Mechanism of origin of complete hydatidiform moles. Nature 1980; 286: 714-716. (Pubitemid 11129825)
    • (1980) Nature , vol.286 , Issue.5774 , pp. 714-716
    • Jacobs, P.A.1    Wilson, C.M.2    Sprenkle, J.A.3
  • 3
    • 0023178950 scopus 로고
    • Hydatidiform mole: Cytogenetically unusual cases and their implications for the present classification
    • Vejerslev LO, Fisher RA, Surti U, et al. Hydatidiform mole: cytogenetically unusual cases and their implications for the present classification. Am J Obstet Gynecol 1987; 157: 180-184. (Pubitemid 17099913)
    • (1987) American Journal of Obstetrics and Gynecology , vol.157 , Issue.1 , pp. 180-184
    • Vejerslev, L.O.1    Fisher, R.A.2    Surti, U.3    Walke, N.4
  • 4
    • 0025964424 scopus 로고
    • Restriction fragment length polymorphism analysis to study the genetic origin of complete hydatidiform mole
    • Ko TM, Hsieh CY, Ho HN, et al. Restriction fragment length polymorphism analysis to study the genetic origin of complete hydatidiform mole. Am J Obstet Gynecol 1991; 164: 901-906.
    • (1991) Am J Obstet Gynecol , vol.164 , pp. 901-906
    • Ko, T.M.1    Hsieh, C.Y.2    Ho, H.N.3
  • 5
    • 0026014488 scopus 로고
    • Molecular genetic analysis of complete hydatidiform moles
    • Kovacs BW, Shahbahrami B, Tast DE, et al. Molecular genetic analysis of complete hydatidiform moles. Cancer Genet Cytogenet 1991; 54: 143-152.
    • (1991) Cancer Genet Cytogenet , vol.54 , pp. 143-152
    • Kovacs, B.W.1    Shahbahrami, B.2    Tast, D.E.3
  • 7
    • 0031018181 scopus 로고    scopus 로고
    • Diploid hydatidiform moles with fetal red blood cells in molar villi. 2 - Genetics
    • DOI 10.1002/(SICI)1096-9896(199702)181:2<189::AID-PATH760>3.0.CO;2- 2
    • Fisher RA, Paradinas FJ, Soteriou BA, et al. Diploid hydatidiform moles with fetal red blood cells in molar villi. 2-Genetics. J Pathol 1997; 181: 189-195. (Pubitemid 27087284)
    • (1997) Journal of Pathology , vol.181 , Issue.2 , pp. 189-195
    • Fisher, R.A.1    Paradinas, F.J.2    Soteriou, B.A.3    Foskett, M.4    Newlands, E.S.5
  • 8
    • 0037041453 scopus 로고    scopus 로고
    • A global disorder of imprinting in the human female germ line
    • DOI 10.1038/416539a
    • Judson H, Hayward BE, Sheridan E, et al. A global disorder of imprinting in the human female germ line. Nature 2002; 416: 539-542. (Pubitemid 34288855)
    • (2002) Nature , vol.416 , Issue.6880 , pp. 539-542
    • Judson, H.1    Hayward, B.E.2    Sheridan, E.3    Bonthron, D.T.4
  • 11
    • 66749144959 scopus 로고    scopus 로고
    • Genetic and epigenetic analysis of recurrent hydatidiform mole
    • Hayward BE, De Vos M, Talati N, et al. Genetic and epigenetic analysis of recurrent hydatidiform mole. Hum Mutat 2009; 30: E629-E639.
    • (2009) Hum Mutat , vol.30
    • Hayward, B.E.1    De Vos, M.2    Talati, N.3
  • 12
    • 0022969706 scopus 로고
    • Diploid complete hydatidiform mole, mosaic for normally fertilized cells and androgenetic homozygous cells. Case report
    • Ford JH, Brown JK, Lew WY, et al. Diploid complete hydatidiform mole, mosaic for normally fertilized cells and androgenetic homozygous cells. Case report. Br J Obstet Gynaecol 1986; 93: 1181-1186. (Pubitemid 17171632)
    • (1986) British Journal of Obstetrics and Gynaecology , vol.93 , Issue.11 , pp. 1181-1186
    • Ford, J.H.1    Brown, J.K.2    Lew, W.Y.C.3    Peters, G.B.4
  • 13
    • 0034098994 scopus 로고    scopus 로고
    • Amniotic tissue in complete hydatidiform moles can be androgenetic
    • DOI 10.1002/(SICI)1096-9896(200005)191:1<67::AID-PATH576>3.0.CO;2-X
    • Weaver DT, Fisher RA, Newlands ES, et al. Amniotic tissue in complete hydatidiform moles can be androgenetic. J Pathol 2000; 191: 67-70. (Pubitemid 30235651)
    • (2000) Journal of Pathology , vol.191 , Issue.1 , pp. 67-70
    • Weaver, D.T.1    Fisher, R.A.2    Newlands, E.S.3    Paradinas, F.J.4
  • 15
    • 0036445384 scopus 로고    scopus 로고
    • Coexisting true hermaphroditism and partial hydatidiform mole developing metastatic gestational trophoblastic tumors. A case report
    • DOI 10.1007/s00428-002-0681-2
    • Shiina H, Oka K, Okane M, et al. Coexisting true hermaphroditism and partial hydatidiform mole developing metastatic gestational trophoblastic tumors. A case report. Virchows Arch 2002; 441: 514-518. (Pubitemid 35430468)
    • (2002) Virchows Archiv , vol.441 , Issue.5 , pp. 514-518
    • Shiina, H.1    Oka, K.2    Okane, M.3    Tanno, W.4    Kawasaki, T.5    Nakayama, M.6
  • 16
    • 36749001048 scopus 로고    scopus 로고
    • KIP2 immunostaining and molecular cytogenetics: combined approach aids in diagnosis of morphologically challenging cases with molar phenotype and in detecting androgenetic cell lines in mosaic/chimeric conceptions
    • DOI 10.1016/j.humpath.2007.05.010, PII S0046817707002638
    • Hoffner L, Dunn J, Esposito N, et al. P57KIP2 immunostaining and molecular cytogenetics: combined approach aids in diagnosis of morphologically challenging cases with molar phenotype and in detecting androgenetic cell lines in mosaic/chimeric conceptions. Hum Pathol 2008; 39: 63-72. (Pubitemid 350216161)
    • (2008) Human Pathology , vol.39 , Issue.1 , pp. 63-72
    • Hoffner, L.1    Dunn, J.2    Esposito, N.3    Macpherson, T.4    Surti, U.5
  • 17
    • 33846364337 scopus 로고    scopus 로고
    • The risk of persistent trophoblastic disease after hydatidiform mole classified by morphology and ploidy
    • DOI 10.1016/j.ygyno.2006.08.025, PII S0090825806006809
    • Niemann I, Hansen ES, Sunde L: The risk of persistent trophoblastic disease after hydatidiform mole classified by morphology and ploidy. Gynecol Oncol 2007; 104: 411-415. (Pubitemid 46135651)
    • (2007) Gynecologic Oncology , vol.104 , Issue.2 , pp. 411-415
    • Niemann, I.1    Hansen, E.S.2    Sunde, L.3
  • 19
    • 0032780885 scopus 로고    scopus 로고
    • A familial case of recurrent hydatidiform molar pregnancies with biparental genomic contribution
    • DOI 10.1007/s004390051071
    • Helwani MN, Seoud M, Zahed L, et al. A familial case of recurrent hydatidiform molar pregnancies with biparental genomic contribution. Hum Genet 1999; 105: 112-115. (Pubitemid 29396972)
    • (1999) Human Genetics , vol.105 , Issue.1-2 , pp. 112-115
    • Helwani, M.N.1    Seoud, M.2    Zahed, L.3    Zaatari, G.4    Khalil, A.5    Slim, R.6
  • 20
    • 0025732872 scopus 로고
    • Hydatidiform mole and fetus with normal karyotype: Support of a separate entity
    • Vejerslev LO, Sunde L, Hansen BF, et al. Hydatidiform mole and fetus with normal karyotype: support of a separate entity. Obstet Gynecol 1991; 77: 868-874.
    • (1991) Obstet Gynecol , vol.77 , pp. 868-874
    • Vejerslev, L.O.1    Sunde, L.2    Hansen, B.F.3
  • 21
    • 0037328947 scopus 로고    scopus 로고
    • Postzygotic diploidization of triploids as a source of unusual cases of mosaicism, chimerism and twinning
    • DOI 10.1093/humrep/deg060
    • Golubovsky MD: Postzygotic diploidization of triploids as a source of unusual cases of mosaicism, chimerism and twinning. Hum Reprod 2003; 18: 236-242. (Pubitemid 36236252)
    • (2003) Human Reproduction , vol.18 , Issue.2 , pp. 236-242
    • Golubovsky, M.D.1
  • 22
    • 54149119394 scopus 로고    scopus 로고
    • Twin pregnancies with diploid hydatidiform mole and co-existing normal fetus may originate from one oocyte
    • Niemann I, Bolund L, Sunde L: Twin pregnancies with diploid hydatidiform mole and co-existing normal fetus may originate from one oocyte. Hum Reprod 2008; 23: 2031-2035.
    • (2008) Hum Reprod , vol.23 , pp. 2031-2035
    • Niemann, I.1    Bolund, L.2    Sunde, L.3
  • 23
    • 28544451675 scopus 로고    scopus 로고
    • Twin pregnancy with a chimeric androgenetic and biparental placenta in one twin displaying placental mesenchymal dysplasia phenotype
    • DOI 10.1002/pd.1255
    • Surti U, Hill LM, Dunn J, et al. Twin pregnancy with a chimeric androgenetic and biparental placenta in one twin displaying placental mesenchymal dysplasia phenotype. Prenat Diagn 2005; 25: 1048-1056. (Pubitemid 41745686)
    • (2005) Prenatal Diagnosis , vol.25 , Issue.11 , pp. 1048-1056
    • Surti, U.1    Hill, L.M.2    Dunn, J.3    Prosen, T.4    Hoffner, L.5
  • 24
    • 34347246694 scopus 로고    scopus 로고
    • Origin and outcome of pregnancies affected by androgenetic/biparental chimerism
    • Robinson WP, Lauzon JL, Innes AM, et al. Origin and outcome of pregnancies affected by androgenetic/biparental chimerism. Hum Reprod 2007; 22: 1114-1122.
    • (2007) Hum Reprod , vol.22 , pp. 1114-1122
    • Robinson, W.P.1    Lauzon, J.L.2    Innes, A.M.3
  • 25
    • 43049109810 scopus 로고    scopus 로고
    • Placental mesenchymal dysplasia with Beckwith- Wiedemann syndrome fetus in the context of biparental and androgenic cell lines
    • Hmida D, Gribaa M, Yacoubi T, et al. Placental mesenchymal dysplasia with Beckwith- Wiedemann syndrome fetus in the context of biparental and androgenic cell lines. Placenta 2008; 29: 454-460.
    • (2008) Placenta , vol.29 , pp. 454-460
    • Hmida, D.1    Gribaa, M.2    Yacoubi, T.3
  • 26
    • 0029030178 scopus 로고
    • Genome-wide loss of maternal alleles in a nephrogenic rest and Wilms tumour from a BWS patient
    • Hoban PR, Heighway J, White GR, et al. Genome-wide loss of maternal alleles in a nephrogenic rest and Wilms tumour from a BWS patient. Hum Genet 1995; 95: 651-656.
    • (1995) Hum Genet , vol.95 , pp. 651-656
    • Hoban, P.R.1    Heighway, J.2    White, G.R.3
  • 27
    • 33645112746 scopus 로고    scopus 로고
    • Congenital hyperinsulinism and mosaic abnormalities of the ploidy
    • Giurgea I, Sanlaville D, Fournet JC, et al. Congenital hyperinsulinism and mosaic abnormalities of the ploidy. J Med Genet 2006; 43: 248-254.
    • (2006) J Med Genet , vol.43 , pp. 248-254
    • Giurgea, I.1    Sanlaville, D.2    Fournet, J.C.3
  • 28
    • 37849033776 scopus 로고    scopus 로고
    • The clinical phenotype of mosaicism for genomewide paternal uniparental disomy: Two new reports
    • Wilson M, Peters G, Bennetts B, et al. The clinical phenotype of mosaicism for genomewide paternal uniparental disomy: two new reports. Am J Med Genet A 2008; 146A: 137-148.
    • (2008) Am J Med Genet A , vol.146 , pp. 137-148
    • Wilson, M.1    Peters, G.2    Bennetts, B.3
  • 29
    • 55849092008 scopus 로고    scopus 로고
    • Androgenetic/biparental mosaicism in an infant with hepatic mesenchymal hamartoma and placental mesenchymal dysplasia
    • Reed RC, Beischel L, Schoof J, et al. Androgenetic/biparental mosaicism in an infant with hepatic mesenchymal hamartoma and placental mesenchymal dysplasia. Pediatr Dev Pathol 2008; 11: 377-383.
    • (2008) Pediatr Dev Pathol , vol.11 , pp. 377-383
    • Reed, R.C.1    Beischel, L.2    Schoof, J.3
  • 30
    • 79951800151 scopus 로고    scopus 로고
    • Constitutional mosaic genome-wide uniparental disomy due to diploidisation: An unusual cancer-predisposing mechanism
    • Romanelli V, Nevado J, Fraga M, et al. Constitutional mosaic genome-wide uniparental disomy due to diploidisation: an unusual cancer-predisposing mechanism. J Med Genet 2011; 48: 212-216.
    • (2011) J Med Genet , vol.48 , pp. 212-216
    • Romanelli, V.1    Nevado, J.2    Fraga, M.3
  • 31
    • 67649126211 scopus 로고    scopus 로고
    • Reproductive consequences of genome-wide paternal uniparental disomy mosaicism: Description of two cases with different mechanisms of origin and pregnancy outcomes
    • Morales C, Soler A, Badenas C, et al. Reproductive consequences of genome-wide paternal uniparental disomy mosaicism: description of two cases with different mechanisms of origin and pregnancy outcomes. Fertil Steril 2009; 92: 393.e5-393.e9.
    • (2009) Fertil Steril , vol.92
    • Morales, C.1    Soler, A.2    Badenas, C.3
  • 32
    • 0028048183 scopus 로고
    • Placental vascular malformation with mesenchymal hyperplasia and a localized chorioangioma - A rarity simulating partial mole
    • Hojberg KE, Aagaard J, Henriques U, et al. Placental vascular malformation with mesenchymal hyperplasia and a localized chorioangioma. A rarity simulating partial mole. Pathol Res Pract 1994; 190: 808-813; discussion 814. (Pubitemid 24302117)
    • (1994) Pathology Research and Practice , vol.190 , Issue.8 , pp. 808-813
    • Hojberg, K.-E.1    Aagaard, J.2    Henriques, U.3    Sunde, L.4
  • 35
    • 69549112757 scopus 로고    scopus 로고
    • Molecular genetic analyses of choriocarcinoma
    • Zhao J, Xiang Y, Wan XR, et al. Molecular genetic analyses of choriocarcinoma. Placenta 2009; 30: 816-820.
    • (2009) Placenta , vol.30 , pp. 816-820
    • Zhao, J.1    Xiang, Y.2    Wan, X.R.3
  • 36
    • 0020530724 scopus 로고
    • A detergent-trypsin method for the preparation of nuclei for flow cytometric DNA analysis
    • Vindelov LL, Christensen IJ, Nissen NI: A detergent-trypsin method for the preparation of nuclei for flow cytometric DNA analysis. Cytometry 1983; 3: 323-327. (Pubitemid 13087609)
    • (1983) Cytometry , vol.3 , Issue.5 , pp. 323-327
    • Vindelov, L.L.1    Christensen, I.J.2    Nissen, N.I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.