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Items: 1 to 20 of 98

1.

Localisation of the SMC loading complex Nipbl/Mau2 during mammalian meiotic prophase I.

Visnes T, Giordano F, Kuznetsova A, Suja JA, Lander AD, Calof AL, Ström L.

Chromosoma. 2014 Jun;123(3):239-52. doi: 10.1007/s00412-013-0444-7. Epub 2013 Nov 28.

2.

Cohesin loading factor Nipbl localizes to chromosome axes during mammalian meiotic prophase.

Kuleszewicz K, Fu X, Kudo NR.

Cell Div. 2013 Aug 22;8(1):12. doi: 10.1186/1747-1028-8-12.

3.

Neural crest cell-specific inactivation of Nipbl or Mau2 during mouse development results in a late onset of craniofacial defects.

Smith TG, Laval S, Chen F, Rock MJ, Strachan T, Peters H.

Genesis. 2014 Jul;52(7):687-94. doi: 10.1002/dvg.22780. Epub 2014 Apr 21.

PMID:
24700590
4.

Sequential loading of cohesin subunits during the first meiotic prophase of grasshoppers.

Valdeolmillos AM, Viera A, Page J, Prieto I, Santos JL, Parra MT, Heck MM, Martínez-A C, Barbero JL, Suja JA, Rufas JS.

PLoS Genet. 2007 Feb 23;3(2):e28. Epub 2007 Jan 2.

5.

Cohesin component dynamics during meiotic prophase I in mammalian oocytes.

Prieto I, Tease C, Pezzi N, Buesa JM, Ortega S, Kremer L, Martínez A, Martínez-A C, Hultén MA, Barbero JL.

Chromosome Res. 2004;12(3):197-213.

PMID:
15125634
6.

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.

Curr Biol. 2011 Sep 13;21(17):1421-30. doi: 10.1016/j.cub.2011.07.007.

7.

Functional links between Drosophila Nipped-B and cohesin in somatic and meiotic cells.

Gause M, Webber HA, Misulovin Z, Haller G, Rollins RA, Eissenberg JC, Bickel SE, Dorsett D.

Chromosoma. 2008 Feb;117(1):51-66. Epub 2007 Oct 2.

8.

The Smc5-Smc6 complex is required to remove chromosome junctions in meiosis.

Farmer S, San-Segundo PA, Aragón L.

PLoS One. 2011;6(6):e20948. doi: 10.1371/journal.pone.0020948. Epub 2011 Jun 22.

9.

Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction.

Braunholz D, Hullings M, Gil-Rodríguez MC, Fincher CT, Mallozzi MB, Loy E, Albrecht M, Kaur M, Limon J, Rampuria A, Clark D, Kline A, Dalski A, Eckhold J, Tzschach A, Hennekam R, Gillessen-Kaesbach G, Wierzba J, Krantz ID, Deardorff MA, Kaiser FJ.

Eur J Hum Genet. 2012 Mar;20(3):271-6. doi: 10.1038/ejhg.2011.175. Epub 2011 Sep 21. Erratum in: Eur J Hum Genet. 2012 Mar;20(3):366.

10.

Reduction of Nipbl impairs cohesin loading locally and affects transcription but not cohesion-dependent functions in a mouse model of Cornelia de Lange Syndrome.

Remeseiro S, Cuadrado A, Kawauchi S, Calof AL, Lander AD, Losada A.

Biochim Biophys Acta. 2013 Dec;1832(12):2097-102. doi: 10.1016/j.bbadis.2013.07.020. Epub 2013 Aug 3.

11.

A cohesin-independent role for NIPBL at promoters provides insights in CdLS.

Zuin J, Franke V, van Ijcken WF, van der Sloot A, Krantz ID, van der Reijden MI, Nakato R, Lenhard B, Wendt KS.

PLoS Genet. 2014 Feb 13;10(2):e1004153. doi: 10.1371/journal.pgen.1004153. eCollection 2014 Feb.

12.

A novel mammalian HORMA domain-containing protein, HORMAD1, preferentially associates with unsynapsed meiotic chromosomes.

Fukuda T, Daniel K, Wojtasz L, Toth A, Höög C.

Exp Cell Res. 2010 Jan 15;316(2):158-71. doi: 10.1016/j.yexcr.2009.08.007. Epub 2009 Aug 15.

PMID:
19686734
13.

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.

PLoS Biol. 2011 Oct;9(10):e1001181. doi: 10.1371/journal.pbio.1001181. Epub 2011 Oct 25.

14.

Differences in DNA double strand breaks repair in male germ cell types: lessons learned from a differential expression of Mdc1 and 53BP1.

Ahmed EA, van der Vaart A, Barten A, Kal HB, Chen J, Lou Z, Minter-Dykhouse K, Bartkova J, Bartek J, de Boer P, de Rooij DG.

DNA Repair (Amst). 2007 Sep 1;6(9):1243-54. Epub 2007 Mar 21.

PMID:
17376750
15.

Distinct Roles of Meiosis-Specific Cohesin Complexes in Mammalian Spermatogenesis.

Biswas U, Hempel K, Llano E, Pendas A, Jessberger R.

PLoS Genet. 2016 Oct 28;12(10):e1006389. doi: 10.1371/journal.pgen.1006389. eCollection 2016 Oct.

16.

Meiosis-specific cohesin component, Stag3 is essential for maintaining centromere chromatid cohesion, and required for DNA repair and synapsis between homologous chromosomes.

Hopkins J, Hwang G, Jacob J, Sapp N, Bedigian R, Oka K, Overbeek P, Murray S, Jordan PW.

PLoS Genet. 2014 Jul 3;10(7):e1004413. doi: 10.1371/journal.pgen.1004413. eCollection 2014 Jul.

17.

Meiotic cohesin complexes are essential for the formation of the axial element in mice.

Llano E, Herrán Y, García-Tuñón I, Gutiérrez-Caballero C, de Álava E, Barbero JL, Schimenti J, de Rooij DG, Sánchez-Martín M, Pendás AM.

J Cell Biol. 2012 Jun 25;197(7):877-85. doi: 10.1083/jcb.201201100. Epub 2012 Jun 18.

18.

Regional chromatin decompaction in Cornelia de Lange syndrome associated with NIPBL disruption can be uncoupled from cohesin and CTCF.

Nolen LD, Boyle S, Ansari M, Pritchard E, Bickmore WA.

Hum Mol Genet. 2013 Oct 15;22(20):4180-93. doi: 10.1093/hmg/ddt265. Epub 2013 Jun 10.

19.

BRIT1/MCPH1 is essential for mitotic and meiotic recombination DNA repair and maintaining genomic stability in mice.

Liang Y, Gao H, Lin SY, Peng G, Huang X, Zhang P, Goss JA, Brunicardi FC, Multani AS, Chang S, Li K.

PLoS Genet. 2010 Jan 22;6(1):e1000826. doi: 10.1371/journal.pgen.1000826.

20.

Differential association of SMC1alpha and SMC3 proteins with meiotic chromosomes in wild-type and SPO11-deficient male mice.

James RD, Schmiesing JA, Peters AH, Yokomori K, Disteche CM.

Chromosome Res. 2002;10(7):549-60.

PMID:
12498344

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