-
1
-
-
84861949299
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
20
-
-
0030748778
-
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
-
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
-
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
-
23
-
-
84860539709
-
A unique role of cohesin-SA1 in gene regulation and development
-
Remeseiro S, Cuadrado A, Gómez-López G, Pisano DG, Losada A. A unique role of cohesin-SA1 in gene regulation and development. EMBO J. 2012;31:2090-2102.
-
(2012)
EMBO J
, vol.31
, pp. 2090-2102
-
-
Remeseiro, S.1
Cuadrado, A.2
Gómez-López, G.3
Pisano, D.G.4
Losada, A.5
-
24
-
-
21044435063
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
44
-
-
77951836691
-
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
-
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
-
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
-
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
-
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
-
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
|