메뉴 건너뛰기




Volumn 6, Issue , 2013, Pages 15-23

Genetic basis of cohesinopathies

Author keywords

Cohesin; Cohesinopathies; Control; Cornelia de Lange syndrome; Gene expression; Insulators; Roberts syndrome

Indexed keywords

ACYLTRANSFERASE; CELL PROTEIN; COHESIN; ESCO2 PROTEIN; NIPBL PROTEIN; SCC2 PROTEIN; TRANSCRIPTION FACTOR CTCF; UNCLASSIFIED DRUG;

EID: 84877257905     PISSN: 1178704X     EISSN: None     Source Type: Journal    
DOI: 10.2147/TACG.S34457     Document Type: Review
Times cited : (27)

References (49)
  • 1
    • 84861949299 scopus 로고    scopus 로고
    • Cohesin in determining chromosome architecture
    • Haering CH, Jessberger R. Cohesin in determining chromosome architecture. Exp Cell Res. 2012;318:1386-1393.
    • (2012) Exp Cell Res , vol.318 , pp. 1386-1393
    • Haering, C.H.1    Jessberger, R.2
  • 2
    • 77951181571 scopus 로고    scopus 로고
    • Regulators of cohesin network
    • Xiong B, Gerton JL. Regulators of cohesin network. Annu Rev Biochem. 2010;79:131-153.
    • (2010) Annu Rev Biochem , vol.79 , pp. 131-153
    • Xiong, B.1    Gerton, J.L.2
  • 3
    • 10944232673 scopus 로고    scopus 로고
    • Postreplicative recruitment of cohesin to double-strand breaks is required for DNA repair
    • Strom L, Lindroos HB, Shirahige K, Sjogren C. Postreplicative recruitment of cohesin to double-strand breaks is required for DNA repair. Mol Cell. 2004;16:1003-1015.
    • (2004) Mol Cell , vol.16 , pp. 1003-1015
    • Strom, L.1    Lindroos, H.B.2    Shirahige, K.3    Sjogren, C.4
  • 4
    • 77957865812 scopus 로고    scopus 로고
    • Rad21-cohesin haploinsufficiency impedes DNA repair and enhances gastrointestinal radiosensitivity in mice
    • Xu H, Balakrishnan K, Malaterre J, et al. Rad21-cohesin haploinsufficiency impedes DNA repair and enhances gastrointestinal radiosensitivity in mice. PLoS One. 2010;5:e12112.
    • (2010) PLoS One , vol.5
    • Xu, H.1    Balakrishnan, K.2    Malaterre, J.3
  • 5
    • 65549132836 scopus 로고    scopus 로고
    • Distinct targets of the Eco1 acetyltransferase modulate cohesion in S phase and in response to DNA damage
    • Heidinger-Pauli JM, Unal E, Koshland D. Distinct targets of the Eco1 acetyltransferase modulate cohesion in S phase and in response to DNA damage. Mol Cell. 2009;34:311-321.
    • (2009) Mol Cell , vol.34 , pp. 311-321
    • Heidinger-Pauli, J.M.1    Unal, E.2    Koshland, D.3
  • 6
    • 80052821214 scopus 로고    scopus 로고
    • Loading of meiotic cohesin by SCC-2 is required for early processing of DSBs and for the DNA damage checkpoint
    • Lightfoot J, Testori S, Barroso C, Martinez-Perez E. Loading of meiotic cohesin by SCC-2 is required for early processing of DSBs and for the DNA damage checkpoint. Curr Biol. 2011;21:1421-1430.
    • (2011) Curr Biol , vol.21 , pp. 1421-1430
    • Lightfoot, J.1    Testori, S.2    Barroso, C.3    Martinez-Perez, E.4
  • 7
    • 79954601068 scopus 로고    scopus 로고
    • Sister chromatid cohesion control and aneuploidy
    • Barbero JL. Sister chromatid cohesion control and aneuploidy. Cytogenet Genome Res. 2011;133:223-233.
    • (2011) Cytogenet Genome Res , vol.133 , pp. 223-233
    • Barbero, J.L.1
  • 8
    • 2642542322 scopus 로고    scopus 로고
    • Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B
    • Krantz ID, McCallum J, DeScipio C, et al. Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B. Nat Genet. 2004;36:631-635.
    • (2004) Nat Genet , vol.36 , pp. 631-635
    • Krantz, I.D.1    McCallum, J.2    Descipio, C.3
  • 9
    • 2642565901 scopus 로고    scopus 로고
    • NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome
    • Tonkin ET, Wang TJ, Lisgo S, Bamshad MJ, Strachan T. NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome. Nat Genet. 2004;36:636-641.
    • (2004) Nat Genet , vol.36 , pp. 636-641
    • Tonkin, E.T.1    Wang, T.J.2    Lisgo, S.3    Bamshad, M.J.4    Strachan, T.5
  • 10
    • 20944444999 scopus 로고    scopus 로고
    • Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion
    • Vega H, Waisfisz Q, Gordillo M, et al. Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion. Nat Genet. 2005;37: 468-470.
    • (2005) Nat Genet , vol.37 , pp. 468-470
    • Vega, H.1    Waisfisz, Q.2    Gordillo, M.3
  • 11
    • 39449111307 scopus 로고    scopus 로고
    • Cohesins localize with CTCF at the KSHV latency control region and at cellular c-myc and H19/Igf2 insulators
    • Stedman W, Kang H, Lin S, Kissil JL, Bartolomei MS, Lieberman PM. Cohesins localize with CTCF at the KSHV latency control region and at cellular c-myc and H19/Igf2 insulators. EMBO J. 2008;27:654-666.
    • (2008) EMBO J , vol.27 , pp. 654-666
    • Stedman, W.1    Kang, H.2    Lin, S.3    Kissil, J.L.4    Bartolomei, M.S.5    Lieberman, P.M.6
  • 12
    • 39149121436 scopus 로고    scopus 로고
    • Cohesin mediates transcriptional insulation by CCCTC-binding factor
    • Wendt KS, Yoshida K, Itoh T, et al. Cohesin mediates transcriptional insulation by CCCTC-binding factor. Nature. 2008;451:796-801.
    • (2008) Nature , vol.451 , pp. 796-801
    • Wendt, K.S.1    Yoshida, K.2    Itoh, T.3
  • 13
    • 38849121606 scopus 로고    scopus 로고
    • Cohesins functionally associate with CTCF on mammalian chromosome arms
    • Parelho V, Hadjur S, Spivakov M, et al. Cohesins functionally associate with CTCF on mammalian chromosome arms. Cell. 2008;132: 422-433.
    • (2008) Cell , vol.132 , pp. 422-433
    • Parelho, V.1    Hadjur, S.2    Spivakov, M.3
  • 14
    • 70349690201 scopus 로고    scopus 로고
    • Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome
    • Kawauchi S, Calof AL, Santos R, et al. Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome. PLoS Genet. 2009;5:e1000650.
    • (2009) PLoS Genet , vol.5
    • Kawauchi, S.1    Calof, A.L.2    Santos, R.3
  • 15
    • 56649123545 scopus 로고    scopus 로고
    • The cohesin loading factor NIPBL recruits histone deacetylases to mediate local chromatin modifications
    • Jahnke P, Xu W, Wülling M, et al. The cohesin loading factor NIPBL recruits histone deacetylases to mediate local chromatin modifications. Nucleic Acids Res. 2008;36:6450-6458.
    • (2008) Nucleic Acids Res , vol.36 , pp. 6450-6458
    • Jahnke, P.1    Xu, W.2    Wülling, M.3
  • 16
    • 33646379870 scopus 로고    scopus 로고
    • X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations
    • Musio A, Selicorni A, Focarelli ML, et al. X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations. Nat Genet. 2006;38:528-530.
    • (2006) Nat Genet , vol.38 , pp. 528-530
    • Musio, A.1    Selicorni, A.2    Focarelli, M.L.3
  • 17
    • 33847196427 scopus 로고    scopus 로고
    • Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of Cornelia de Lange syndrome with predominant mental retardation
    • Deardorff MA, Kaur M, Yaeger D, et al. Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of Cornelia de Lange syndrome with predominant mental retardation. Am J Hum Genet. 2007;80:485-494.
    • (2007) Am J Hum Genet , vol.80 , pp. 485-494
    • Deardorff, M.A.1    Kaur, M.2    Yaeger, D.3
  • 18
    • 58749104967 scopus 로고    scopus 로고
    • Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA
    • Revenkova E, Focarelli ML, Susani L, et al. Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA. Hum Mol Genet. 2009;18:418-427.
    • (2009) Hum Mol Genet , vol.18 , pp. 418-427
    • Revenkova, E.1    Focarelli, M.L.2    Susani, L.3
  • 19
    • 84862142852 scopus 로고    scopus 로고
    • RAD21 mutations cause a human cohesinopathy
    • Deardorff MA, Wilde JJ, Albrecht M, et al. RAD21 mutations cause a human cohesinopathy. Am J Hum Genet. 2012;90:1014-1027.
    • (2012) Am J Hum Genet , vol.90 , pp. 1014-1027
    • Deardorff, M.A.1    Wilde, J.J.2    Albrecht, M.3
  • 20
    • 0030748778 scopus 로고    scopus 로고
    • SA-1, a nuclear protein encoded by one member of a novel gene family: Molecular cloning and detection in hemopoietic organs
    • Carramolino L, Lee BC, Zaballos A, et al. SA-1, a nuclear protein encoded by one member of a novel gene family: molecular cloning and detection in hemopoietic organs. Gene. 1997;195:151-159.
    • (1997) Gene , vol.195 , pp. 151-159
    • Carramolino, L.1    Lee, B.C.2    Zaballos, A.3
  • 21
    • 0034618070 scopus 로고    scopus 로고
    • Identification and characterization of SA/Scc3 subunits in the Xenopus and human cohesin complexes
    • Losada A, Yokochi T, Kobayashi R, Hirano T. Identification and characterization of SA/Scc3 subunits in the Xenopus and human cohesin complexes. J Cell Biol. 2000;150:405-416.
    • (2000) J Cell Biol , vol.150 , pp. 405-416
    • Losada, A.1    Yokochi, T.2    Kobayashi, R.3    Hirano, T.4
  • 22
    • 0034645067 scopus 로고    scopus 로고
    • Characterization of vertebrate cohesin complexes and their regulation in prophase
    • Sumara I, Vorlaufer E, Gieffers C, Peters BH, Peters JM. Characterization of vertebrate cohesin complexes and their regulation in prophase. J Cell Biol. 2000;151:749-762.
    • (2000) J Cell Biol , vol.151 , pp. 749-762
    • Sumara, I.1    Vorlaufer, E.2    Gieffers, C.3    Peters, B.H.4    Peters, J.M.5
  • 24
    • 21044435063 scopus 로고    scopus 로고
    • Functional contribution of Pds5 to cohesin-mediated cohesion in human cells and Xenopus egg extracts
    • Losada A, Yokochi T, Hirano T. Functional contribution of Pds5 to cohesin-mediated cohesion in human cells and Xenopus egg extracts. J Cell Sci. 2005;118:2133-2141.
    • (2005) J Cell Sci , vol.118 , pp. 2133-2141
    • Losada, A.1    Yokochi, T.2    Hirano, T.3
  • 25
    • 34848911616 scopus 로고    scopus 로고
    • Mice lacking sister chromatid cohesion protein PDS5B exhibit developmental abnormalities reminiscent of Cornelia de Lange syndrome
    • Zhang B, Jain S, Song H, et al. Mice lacking sister chromatid cohesion protein PDS5B exhibit developmental abnormalities reminiscent of Cornelia de Lange syndrome. Development. 2007;134:3191-3201.
    • (2007) Development , vol.134 , pp. 3191-3201
    • Zhang, B.1    Jain, S.2    Song, H.3
  • 26
    • 68849111709 scopus 로고    scopus 로고
    • Dosage effects of cohesin regulatory factor PDS5 on mammalian development: Implications for cohesinopathies
    • Zhang B, Chang J, Fu M, et al. Dosage effects of cohesin regulatory factor PDS5 on mammalian development: implications for cohesinopathies. PLoS One. 2009;4:e5232.
    • (2009) PLoS One , vol.4
    • Zhang, B.1    Chang, J.2    Fu, M.3
  • 27
    • 77951724830 scopus 로고    scopus 로고
    • Cornelia de Lange syndrome: Extending the physical and psychological phenotype
    • Oliver C, Bedeschi MF, Blagowidow N, et al. Cornelia de Lange syndrome: extending the physical and psychological phenotype. Am J Med Genet. 2010;152A:1127-1135.
    • (2010) Am J Med Genet , vol.152 A , pp. 1127-1135
    • Oliver, C.1    Bedeschi, M.F.2    Blagowidow, N.3
  • 28
    • 0027429318 scopus 로고
    • Roberts syndrome: A review of 100 cases and a new rating system for severity
    • Van Den Berg DJ, Francke U. Roberts syndrome: a review of 100 cases and a new rating system for severity. Am J Med Genet. 1993;47: 1104-1123.
    • (1993) Am J Med Genet , vol.47 , pp. 1104-1123
    • Van Den Berg, D.J.1    Francke, U.2
  • 29
    • 46349085795 scopus 로고    scopus 로고
    • The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity
    • Gordillo M, Vega H, Trainer AH, et al. The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity. Hum Mol Genet. 2008;17:2172-2180.
    • (2008) Hum Mol Genet , vol.17 , pp. 2172-2180
    • Gordillo, M.1    Vega, H.2    Trainer, A.H.3
  • 30
    • 79951970629 scopus 로고    scopus 로고
    • Isolated skeletal malformations in a child with a small mosaic ring microduplication of 18 p11.21q11.2: Genotype-phenotype correlations
    • Slavin TP, Kuruvilla K, Curtis CA, Christ LA, Mitchell AL. Isolated skeletal malformations in a child with a small mosaic ring microduplication of 18 p11.21q11.2: genotype-phenotype correlations. Am J Med Genet. 2011;155A:618-621.
    • (2011) Am J Med Genet , vol.155 A , pp. 618-621
    • Slavin, T.P.1    Kuruvilla, K.2    Curtis, C.A.3    Christ, L.A.4    Mitchell, A.L.5
  • 31
    • 84866183822 scopus 로고    scopus 로고
    • HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle
    • Deardorff MA, Bando M, Nakato R, et al. HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle. Nature. 2012;489:313-317.
    • (2012) Nature , vol.489 , pp. 313-317
    • Deardorff, M.A.1    Bando, M.2    Nakato, R.3
  • 32
    • 0033018842 scopus 로고    scopus 로고
    • Nipped-B, a Drosophila homologue of chromosomal adherins, participates in activation by remote enhancers in the cut and Ultrabithorax genes
    • Rollins RA, Morcillo P, Dorsett D. Nipped-B, a Drosophila homologue of chromosomal adherins, participates in activation by remote enhancers in the cut and Ultrabithorax genes. Genetics. 1999;152:577-593.
    • (1999) Genetics , vol.152 , pp. 577-593
    • Rollins, R.A.1    Morcillo, P.2    Dorsett, D.3
  • 33
    • 1842557791 scopus 로고    scopus 로고
    • Drosophila nipped-B protein supports sister chromatid cohesion and opposes the stromalin/Scc3 cohesion factor to facilitate long-range activation of the cut gene
    • Rollins RA, Korom M, Aulner N, Martens A, Dorsett D. Drosophila nipped-B protein supports sister chromatid cohesion and opposes the stromalin/Scc3 cohesion factor to facilitate long-range activation of the cut gene. Mol Cell Biol. 2004;24:3100-3111.
    • (2004) Mol Cell Biol , vol.24 , pp. 3100-3111
    • Rollins, R.A.1    Korom, M.2    Aulner, N.3    Martens, A.4    Dorsett, D.5
  • 34
    • 1342325423 scopus 로고    scopus 로고
    • Evidence of a transcriptional co-activator function of cohesin STAG/SA/Scc3
    • Lara-Pezzi E, Pezzi N, Prieto I, et al. Evidence of a transcriptional co-activator function of cohesin STAG/SA/Scc3. J Biol Chem. 2004;279:6553-6559.
    • (2004) J Biol Chem , vol.279 , pp. 6553-6559
    • Lara-Pezzi, E.1    Pezzi, N.2    Prieto, I.3
  • 35
    • 65649123756 scopus 로고    scopus 로고
    • Architectural roles of multiple chromatin insulators at the human apolipoprotein gene cluster
    • Mishiro T, Ishihara K, Hino S, et al. Architectural roles of multiple chromatin insulators at the human apolipoprotein gene cluster. EMBO J. 2009;28:1234-1245.
    • (2009) EMBO J , vol.28 , pp. 1234-1245
    • Mishiro, T.1    Ishihara, K.2    Hino, S.3
  • 36
    • 59849122478 scopus 로고    scopus 로고
    • Cutting edge: Developmental stage-specific recruitment of cohesin to CTCF sites throughout immunoglobulin loci during B lymphocyte development
    • Degner SC, Wong TP, Jankevicius G, Feeney AJ. Cutting edge: developmental stage-specific recruitment of cohesin to CTCF sites throughout immunoglobulin loci during B lymphocyte development. J Immunol. 2009;182:44-48.
    • (2009) J Immunol , vol.182 , pp. 44-48
    • Degner, S.C.1    Wong, T.P.2    Jankevicius, G.3    Feeney, A.J.4
  • 37
    • 66249144416 scopus 로고    scopus 로고
    • Transcriptional dysregulation in NIPBL and cohesin mutant human cells
    • Liu J, Zhang Z, Bando M, et al. Transcriptional dysregulation in NIPBL and cohesin mutant human cells. PLoS Biol. 2009;7(5):e1000119.
    • (2009) PLoS Biol , vol.7 , Issue.5
    • Liu, J.1    Zhang, Z.2    Bando, M.3
  • 38
    • 84857251182 scopus 로고    scopus 로고
    • CTCF: Insights into insulator function during development
    • Herold M, Bartkuhn M, Renkawitz R. CTCF: insights into insulator function during development. Development. 2012;139:1045-1057.
    • (2012) Development , vol.139 , pp. 1045-1057
    • Herold, M.1    Bartkuhn, M.2    Renkawitz, R.3
  • 39
    • 84876105719 scopus 로고    scopus 로고
    • Chromatin loops, gene positioning, and gene expression
    • Holwerda S, de Laat W. Chromatin loops, gene positioning, and gene expression. Front Genet. 2012;3:217.
    • (2012) Front Genet , vol.3 , pp. 217
    • Holwerda, S.1    de Laat, W.2
  • 40
    • 84885938984 scopus 로고    scopus 로고
    • The intellectual disability of trisomy 21: Differences in gene expression in a case series of patients with lower and higher IQ
    • February 20, [Epub ahead of print.]
    • Mégarbané A, Noguier F, Stora S, et al. The intellectual disability of trisomy 21: differences in gene expression in a case series of patients with lower and higher IQ. Eur J Hum Genet. February 20, 2013. [Epub ahead of print.]
    • (2013) Eur J Hum Genet
    • Mégarbané, A.1    Noguier, F.2    Stora, S.3
  • 41
    • 38849130750 scopus 로고    scopus 로고
    • PiggyBac-based mosaic screen identifies a postmitotic function for cohesin in regulating developmental axon pruning
    • Schuldiner O, Berdnik D, Levy JM, et al. piggyBac-based mosaic screen identifies a postmitotic function for cohesin in regulating developmental axon pruning. Dev Cell. 2008;14:227-238.
    • (2008) Dev Cell , vol.14 , pp. 227-238
    • Schuldiner, O.1    Berdnik, D.2    Levy, J.M.3
  • 42
    • 38849173178 scopus 로고    scopus 로고
    • Cell-type-specific TEV protease cleavage reveals cohesin functions in Drosophila neurons
    • Pauli A, Althoff F, Oliveira RA, et al. Cell-type-specific TEV protease cleavage reveals cohesin functions in Drosophila neurons. Dev Cell. 2008;14:239-251.
    • (2008) Dev Cell , vol.14 , pp. 239-251
    • Pauli, A.1    Althoff, F.2    Oliveira, R.A.3
  • 43
    • 34547762839 scopus 로고    scopus 로고
    • Cohesin-dependent regulation of Runx genes
    • Horsfield JA, Anagnostou SH, Hu JK, et al. Cohesin-dependent regulation of Runx genes. Development. 2007;134:2639-2649.
    • (2007) Development , vol.134 , pp. 2639-2649
    • Horsfield, J.A.1    Anagnostou, S.H.2    Hu, J.K.3
  • 44
    • 77951836691 scopus 로고    scopus 로고
    • A CTCF-independent role for cohesin in tissue-specific transcription
    • Schmidt D, Schwalie PC, Ross-Innes CS, et al. A CTCF-independent role for cohesin in tissue-specific transcription. Genome Res. 2010;20: 578-588.
    • (2010) Genome Res , vol.20 , pp. 578-588
    • Schmidt, D.1    Schwalie, P.C.2    Ross-Innes, C.S.3
  • 45
    • 77954759030 scopus 로고    scopus 로고
    • The human mediator complex: A versatile, genome-wide regulator of transcription
    • Taatjes DJ. The human mediator complex: a versatile, genome-wide regulator of transcription. Trends Biochem Sci. 2010;35: 315-322.
    • (2010) Trends Biochem Sci , vol.35 , pp. 315-322
    • Taatjes, D.J.1
  • 46
    • 77957139539 scopus 로고    scopus 로고
    • Mediator and cohesin connect gene expression and chromatin architecture
    • Kagey MH, Newman JJ, Bilodeau S, et al. Mediator and cohesin connect gene expression and chromatin architecture. Nature. 2011;467: 430-435.
    • (2011) Nature , vol.467 , pp. 430-435
    • Kagey, M.H.1    Newman, J.J.2    Bilodeau, S.3
  • 47
    • 80055027655 scopus 로고    scopus 로고
    • Multifactorial origins of heart and gut defects in nipbl-deficient zebrafish, a model of Cornelia de Lange Syndrome
    • Muto A, Calof AL, Lander AD, Schilling TF. Multifactorial origins of heart and gut defects in nipbl-deficient zebrafish, a model of Cornelia de Lange Syndrome. PLoS Biol. 2011;9:e1001181.
    • (2011) PLoS Biol , vol.9
    • Muto, A.1    Calof, A.L.2    Lander, A.D.3    Schilling, T.F.4
  • 48
    • 79957542842 scopus 로고    scopus 로고
    • A zebrafish model of Roberts syndrome reveals that Esco2 depletion interferes with development by disrupting the cell cycle
    • Mönnich M, Kuriger Z, Print CG, Horsfield JA. A zebrafish model of Roberts syndrome reveals that Esco2 depletion interferes with development by disrupting the cell cycle. PLoS One. 2011;6:e20051.
    • (2011) PLoS One , vol.6
    • Mönnich, M.1    Kuriger, Z.2    Print, C.G.3    Horsfield, J.A.4
  • 49
    • 84862690412 scopus 로고    scopus 로고
    • Establishment and characterization of Roberts syndrome and SC phocomelia model medaka (Oryzias latipes)
    • Morita A, Nakahira K, Hasegawa T, et al. Establishment and characterization of Roberts syndrome and SC phocomelia model medaka (Oryzias latipes). Dev Growth Differ. 2012;54:588-604.
    • (2012) Dev Growth Differ , vol.54 , pp. 588-604
    • Morita, A.1    Nakahira, K.2    Hasegawa, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.