PMC Links for Protein (Select 49169845) - PMC

Select item 64695771.

BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndrome

Gabrielle Olley, Morad Ansari, Hemant Bengani, Graeme R Grimes, James Rhodes, Alex von Kriegsheim, Ana Blatnik, Fiona J. Stewart, Emma Wakeling, Nicola Carroll, Alison Ross, Soo-Mi Park, DDD study, Wendy A Bickmore, Madapura M Pradeepa, David R FitzPatrick

Nat Genet. Author manuscript; available in PMC 2019 Apr 17.

Published in final edited form as: Nat Genet. 2018 Mar; 50(3): 329–332. Published online 2018 Jan 29. doi: 10.1038/s41588-018-0042-y

Correction in:: Nat Genet. 2018 Feb 12

Correction in:: Nat Genet. 2019 Jun 3

PMCID:: PMC6469577

Abstract Article PDF–871K

Select item 56873032.

Two independent modes of chromatin organization revealed by cohesin removal

Wibke Schwarzer, Nezar Abdennur, Anton Goloborodko, Aleksandra Pekowska, Geoffrey Fudenberg, Yann Loe-Mie, Nuno A Fonseca, Wolfgang Huber, Christian Haering, Leonid Mirny, Francois Spitz

Nature. Author manuscript; available in PMC 2018 Mar 27.

Published in final edited form as: Nature. 2017 Nov 2; 551(7678): 51–56. Published online 2017 Sep 27. doi: 10.1038/nature24281

PMCID:: PMC5687303

Abstract Article PDF–5.8M

Select item 55740933.

The effect of Nipped-B-like (Nipbl) haploinsufficiency on genome-wide cohesin binding and target gene expression: modeling Cornelia de Lange syndrome

Daniel A. Newkirk, Yen-Yun Chen, Richard Chien, Weihua Zeng, Jacob Biesinger, Ebony Flowers, Shimako Kawauchi, Rosaysela Santos, Anne L. Calof, Arthur D. Lander, Xiaohui Xie, Kyoko Yokomori

Clin Epigenetics. 2017; 9: 89. Published online 2017 Aug 25. doi: 10.1186/s13148-017-0391-x

PMCID:: PMC5574093

Abstract Article PDF–3.3M

Select item 52632564.

Nipbl Interacts with Zfp609 and the Integrator Complex to Regulate Cortical Neuron Migration

Debbie L.C. van den Berg, Roberta Azzarelli, Koji Oishi, Ben Martynoga, Noelia Urbán, Dick H.W. Dekkers, Jeroen A. Demmers, François Guillemot

Neuron. 2017 Jan 18; 93(2): 348–361. doi: 10.1016/j.neuron.2016.11.047

PMCID:: PMC5263256

Abstract Article

Select item 50160025.

Conditional Creation and Rescue of Nipbl-Deficiency in Mice Reveals Multiple Determinants of Risk for Congenital Heart Defects

Rosaysela Santos, Shimako Kawauchi, Russell E. Jacobs, Martha E. Lopez-Burks, Hojae Choi, Jamie Wikenheiser, Benedikt Hallgrimsson, Heather A. Jamniczky, Scott E. Fraser, Arthur D. Lander, Anne L. Calof

PLoS Biol. 2016 Sep; 14(9): e2000197. Published online 2016 Sep 8. doi: 10.1371/journal.pbio.2000197

PMCID:: PMC5016002

Abstract Article PDF–20M

Select item 49020176.

Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B

Ian D Krantz, Jennifer McCallum, Cheryl DeScipio, Maninder Kaur, Lynette A Gillis, Dinah Yaeger, Lori Jukofsky, Nora Wasserman, Armand Bottani, Colleen A Morris, Malgorzata J M Nowaczyk, Helga Toriello, Michael J Bamshad, John C Carey, Eric Rappaport, Shimako Kawauchi, Arthur D Lander, Anne L Calof, Hui-hua Li, Marcella Devoto, Laird G Jackson

Nat Genet. Author manuscript; available in PMC 2016 Jun 10.

Published in final edited form as: Nat Genet. 2004 Jun; 36(6): 631–635. Published online 2004 May 16. doi: 10.1038/ng1364

PMCID:: PMC4902017

Abstract Article PDF–1.2M

Select item 27305397.

Multiple Organ System Defects and Transcriptional Dysregulation in the Nipbl^+/− Mouse, a Model of Cornelia de Lange Syndrome

Shimako Kawauchi, Anne L. Calof, Rosaysela Santos, Martha E. Lopez-Burks, Clint M. Young, Michelle P. Hoang, Abigail Chua, Taotao Lao, Mark S. Lechner, Jeremy A. Daniel, Andre Nussenzweig, Leonard Kitzes, Kyoko Yokomori, Benedikt Hallgrimsson, Arthur D. Lander

PLoS Genet. 2009 Sep; 5(9): e1000650. Published online 2009 Sep 18. doi: 10.1371/journal.pgen.1000650

PMCID:: PMC2730539

Abstract Article PDF–1.1M

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