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Volumn 5, Issue 5, 2014, Pages 391-395

Chromosome therapy: Correction of large chromosomal aberrations by inducing ring chromosomes in induced Pluripotent Stem Cells (iPSCs)

Author keywords

Chromosome therapy; Compensatory uniparental disomy (UPD); Induced pluripotent stem cells (iPSCs); Miller Dieker Syndrome (MDS); Ring chromosomes

Indexed keywords

AGYRIA; ARTICLE; BIRTH DEFECT; CHROMOSOME 17; CHROMOSOME 21; CHROMOSOME ABERRATION; CHROMOSOME THERAPY; CLINICAL FEATURE; EMBRYO DEVELOPMENT; FIBROBLAST; FLUORESCENCE IN SITU HYBRIDIZATION; GENE SILENCING; GENE THERAPY; GENETIC DISORDER; GENOMIC INSTABILITY; GROWTH RETARDATION; HETEROZYGOSITY LOSS; HUMAN; KARYOTYPE 46, XY; KARYOTYPING; MENTAL DEFICIENCY; MILLER DIEKER SYNDROME; MUTATION; NONHUMAN; PLURIPOTENT STEM CELL; RING CHROMOSOME; STEM CELL TRANSPLANTATION; TARGETED GENE REPAIR; UNIPARENTAL DISOMY; BIOLOGICAL THERAPY; CLASSICAL LISSENCEPHALIES AND SUBCORTICAL BAND HETEROTOPIAS; CYTOLOGY; GENETICS; PROCEDURES;

EID: 84908214218     PISSN: 19491034     EISSN: 19491042     Source Type: Journal    
DOI: 10.4161/nucl.36300     Document Type: Article
Times cited : (16)

References (16)
  • 2
    • 78049276672 scopus 로고    scopus 로고
    • Lissencephaly: Mechanistic insights from animal models and potential therapeutic strategies
    • PMID:20688183
    • Wynshaw-Boris A, Pramparo T, Youn YH, Hirotsune S. Lissencephaly: mechanistic insights from animal models and potential therapeutic strategies. Semin Cell Dev Biol 2010; 21:823-30; PMID:20688183; http://dx.doi.org/10.1016/j.semcdb.2010.07.008
    • (2010) Semin Cell Dev Biol , vol.21 , pp. 823-830
    • Wynshaw-Boris, A.1    Pramparo, T.2    Youn, Y.H.3    Hirotsune, S.4
  • 3
    • 0037385481 scopus 로고    scopus 로고
    • Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3
    • PMID:12621583
    • Cardoso C, Leventer RJ, Ward HL, Toyo-Oka K, Chung J, Gross A, Martin CL, Allanson J, Pilz DT, Olney AH, et al. Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3. Am J Hum Genet 2003; 72:918-30; PMID:12621583; http://dx.doi.org/10.1086/374320
    • (2003) Am J Hum Genet , vol.72 , pp. 918-930
    • Cardoso, C.1    Leventer, R.J.2    Ward, H.L.3    Toyo-Oka, K.4    Chung, J.5    Gross, A.6    Martin, C.L.7    Allanson, J.8    Pilz, D.T.9    Olney, A.H.10
  • 5
    • 0038757833 scopus 로고    scopus 로고
    • 14-3-3epsilon is important for neuronal migration by binding to NUDEL: A molecular explanation for Miller-Dieker syndrome
    • PMID:12796778
    • Toyo-oka K, Shionoya A, Gambello MJ, Cardoso C, Leventer R, Ward HL, Ayala R, Tsai LH, Dobyns W, Ledbetter D, et al. 14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndrome. Nat Genet 2003; 34:274-85; PMID:12796778; http:// dx.doi.org/10.1038/ng1169
    • (2003) Nat Genet , vol.34 , pp. 274-285
    • Toyo-Oka, K.1    Shionoya, A.2    Gambello, M.J.3    Cardoso, C.4    Leventer, R.5    Ward, H.L.6    Ayala, R.7    Tsai, L.H.8    Dobyns, W.9    Ledbetter, D.10
  • 8
    • 0026725258 scopus 로고
    • Uniparental isodisomy due to duplication of chromosome 21 occurring in somatic cells monosomic for chromosome21
    • PMID:1351865
    • Petersen MB, Bartsch O, Adelsberger PA, Mikkelsen M, Schwinger E, Antonarakis SE. Uniparental isodisomy due to duplication of chromosome 21 occurring in somatic cells monosomic for chromosome21. Genomics 1992; 13:269-74; PMID:1351865; http:// dx.doi.org/10.1016/0888-7543(92)90242-K
    • (1992) Genomics , vol.13 , pp. 269-274
    • Petersen, M.B.1    Bartsch, O.2    Adelsberger, P.A.3    Mikkelsen, M.4    Schwinger, E.5    Antonarakis, S.E.6
  • 11
    • 28844461213 scopus 로고    scopus 로고
    • Decatenation checkpoint deficiency in stem and progenitor cells
    • PMID:16338661
    • Damelin M, Sun YE, Sodja VB, Bestor TH. Decatenation checkpoint deficiency in stem and progenitor cells. Cancer Cell 2005; 8:479-84; PMID:16338661; http://dx.doi.org/10.1016/j. ccr.2005.11.004
    • (2005) Cancer Cell , vol.8 , pp. 479-484
    • Damelin, M.1    Sun, Y.E.2    Sodja, V.B.3    Bestor, T.H.4
  • 12
    • 0034098812 scopus 로고    scopus 로고
    • Mechanisms leading to uniparental disomy and their clinical consequences
    • PMID:10797485
    • Robinson WP. Mechanisms leading to uniparental disomy and their clinical consequences. Bioessays 2000; 22:452-9; PMID:10797485; ht t p:// d x. d o i. o r g /10.10 0 2/(S ICI) 1521- 1878(200005)22:5<452::AID-BIES7>3.0.CO;2-K
    • (2000) Bioessays , vol.22 , pp. 452-459
    • Robinson, W.P.1
  • 13
    • 79955998456 scopus 로고    scopus 로고
    • Gene therapy grows into young adulthood: Special review issue
    • PMID:21571785
    • Lee B, Davidson BL. Gene therapy grows into young adulthood: special review issue. Hum Mol Genet 2011; 20(R1):R1; PMID:21571785; http://dx.doi.org/10.1093/hmg/ddr188
    • (2011) Hum Mol Genet , vol.20 , Issue.R1 , pp. R1
    • Lee, B.1    Davidson, B.L.2
  • 14
    • 79955466666 scopus 로고    scopus 로고
    • Disease correction the iPSC way: Advances in iPSC-based therapy
    • PMID:21389982
    • Sancho-Martinez I, Li M, Izpisua Belmonte JC. Disease correction the iPSC way: advances in iPSC-based therapy. Clin Pharmacol Ther 2011; 89:746-9; PMID:21389982; http://dx.doi.org/10.1038/ clpt.2010.341
    • (2011) Clin Pharmacol Ther , vol.89 , pp. 746-749
    • Sancho-Martinez, I.1    Li, M.2    Izpisua Belmonte, J.C.3
  • 15
    • 0141765728 scopus 로고    scopus 로고
    • History of developmental-behavioral pediatrics
    • author reply 216; PMID:12841158
    • Carey WB. History of developmental-behavioral pediatrics. J Dev Behav Pediatr 2003; 24:215, author reply 216; PMID:12841158; http://dx.doi.org/10.1097/00004703-200306000-00035
    • (2003) J Dev Behav Pediatr , vol.24 , pp. 215
    • Carey, W.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.