NIPBL (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "NIPBL" in English language version.

Last modified: 11:01:46, 21 August 2026 (UTC)

Ref.Un. Ref.Website

Global rank English rank

2119nih.gov

5^th place

109doi.org

2^nd place

62ensembl.org

630^th place

326^th place

22adsabs.harvard.edu

14^th place

9^th place

11semanticscholar.org

15^th place

8^th place

adsabs.harvard.edu (Global: 14^th place; English: 9^th place)

ui.adsabs.harvard.edu

Kikuchi S, Borek DM, Otwinowski Z, Tomchick DR, Yu H (November 2016). "Crystal structure of the cohesin loader Scc2 and insight into cohesinopathy". Proceedings of the National Academy of Sciences of the United States of America. 113 (44): 12444–12449. Bibcode:2016PNAS..11312444K. doi:10.1073/pnas.1611333113. PMC 5098657. PMID 27791135.
Schwarzer W, Abdennur N, Goloborodko A, Pekowska A, Fudenberg G, Loe-Mie Y, et al. (November 2017). "Two independent modes of chromatin organization revealed by cohesin removal". Nature. 551 (7678): 51–56. Bibcode:2017Natur.551...51S. bioRxiv 10.1101/094185. doi:10.1038/nature24281. PMC 5687303. PMID 29094699.

doi.org (Global: 2^nd place; English: 2^nd place)

Ciosk R, Shirayama M, Shevchenko A, Tanaka T, Toth A, Shevchenko A, et al. (2000). "Cohesin's binding to chromosomes depends on a separate complex consisting of Scc2 and Scc4 proteins". Molecular Cell. 5 (2): 243–254. doi:10.1016/S1097-2765(00)80420-7. PMID 10882066.
Rohatgi S, Clark D, Kline AD, Jackson LG, Pie J, Siu V, et al. (July 2010). "Facial diagnosis of mild and variant CdLS: Insights from a dysmorphologist survey". American Journal of Medical Genetics. Part A. 152A (7): 1641–1653. doi:10.1002/ajmg.a.33441. PMC 4133091. PMID 20583156.
Kikuchi S, Borek DM, Otwinowski Z, Tomchick DR, Yu H (November 2016). "Crystal structure of the cohesin loader Scc2 and insight into cohesinopathy". Proceedings of the National Academy of Sciences of the United States of America. 113 (44): 12444–12449. Bibcode:2016PNAS..11312444K. doi:10.1073/pnas.1611333113. PMC 5098657. PMID 27791135.
Nasmyth K (October 2011). "Cohesin: a catenase with separate entry and exit gates?". Nature Cell Biology. 13 (10): 1170–1177. doi:10.1038/ncb2349. PMID 21968990. S2CID 25382204.
Schwarzer W, Abdennur N, Goloborodko A, Pekowska A, Fudenberg G, Loe-Mie Y, et al. (November 2017). "Two independent modes of chromatin organization revealed by cohesin removal". Nature. 551 (7678): 51–56. Bibcode:2017Natur.551...51S. bioRxiv 10.1101/094185. doi:10.1038/nature24281. PMC 5687303. PMID 29094699.
Rhodes J, Mazza D, Nasmyth K, Uphoff S (2017). "Scc2/Nipbl hops between chromosomal cohesin rings after loading". eLife. 6 e30000. doi:10.7554/eLife.30000. PMC 5621834. PMID 28914604.
Zuin J, Franke V, van Ijcken WF, van der Sloot A, Krantz ID, van der Reijden MI, et al. (February 2014). "A cohesin-independent role for NIPBL at promoters provides insights in CdLS". PLOS Genetics. 10 (2) e1004153. doi:10.1371/journal.pgen.1004153. PMC 3923681. PMID 24550742.
van den Berg DL, Azzarelli R, Oishi K, Martynoga B, Urbán N, Dekkers DH, et al. (January 2017). "Nipbl Interacts with Zfp609 and the Integrator Complex to Regulate Cortical Neuron Migration". Neuron. 93 (2): 348–361. doi:10.1016/j.neuron.2016.11.047. PMC 5263256. PMID 28041881.
Kawauchi S, Calof AL, Santos R, Lopez-Burks ME, Young CM, Hoang MP, et al. (September 2009). "Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome". PLOS Genetics. 5 (9) e1000650. doi:10.1371/journal.pgen.1000650. PMC 2730539. PMID 19763162.

ensembl.org (Global: 630^th place; English: 326^th place)

may2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000164190 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000022141 – Ensembl, May 2017

nih.gov (Global: 5^th place; English: 5^th place)

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: Nipped-B homolog (Drosophila)".
Rohatgi S, Clark D, Kline AD, Jackson LG, Pie J, Siu V, et al. (July 2010). "Facial diagnosis of mild and variant CdLS: Insights from a dysmorphologist survey". American Journal of Medical Genetics. Part A. 152A (7): 1641–1653. doi:10.1002/ajmg.a.33441. PMC 4133091. PMID 20583156.
Kikuchi S, Borek DM, Otwinowski Z, Tomchick DR, Yu H (November 2016). "Crystal structure of the cohesin loader Scc2 and insight into cohesinopathy". Proceedings of the National Academy of Sciences of the United States of America. 113 (44): 12444–12449. Bibcode:2016PNAS..11312444K. doi:10.1073/pnas.1611333113. PMC 5098657. PMID 27791135.
Schwarzer W, Abdennur N, Goloborodko A, Pekowska A, Fudenberg G, Loe-Mie Y, et al. (November 2017). "Two independent modes of chromatin organization revealed by cohesin removal". Nature. 551 (7678): 51–56. Bibcode:2017Natur.551...51S. bioRxiv 10.1101/094185. doi:10.1038/nature24281. PMC 5687303. PMID 29094699.
Rhodes J, Mazza D, Nasmyth K, Uphoff S (2017). "Scc2/Nipbl hops between chromosomal cohesin rings after loading". eLife. 6 e30000. doi:10.7554/eLife.30000. PMC 5621834. PMID 28914604.
Zuin J, Franke V, van Ijcken WF, van der Sloot A, Krantz ID, van der Reijden MI, et al. (February 2014). "A cohesin-independent role for NIPBL at promoters provides insights in CdLS". PLOS Genetics. 10 (2) e1004153. doi:10.1371/journal.pgen.1004153. PMC 3923681. PMID 24550742.
van den Berg DL, Azzarelli R, Oishi K, Martynoga B, Urbán N, Dekkers DH, et al. (January 2017). "Nipbl Interacts with Zfp609 and the Integrator Complex to Regulate Cortical Neuron Migration". Neuron. 93 (2): 348–361. doi:10.1016/j.neuron.2016.11.047. PMC 5263256. PMID 28041881.
Kawauchi S, Calof AL, Santos R, Lopez-Burks ME, Young CM, Hoang MP, et al. (September 2009). "Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome". PLOS Genetics. 5 (9) e1000650. doi:10.1371/journal.pgen.1000650. PMC 2730539. PMID 19763162.

pubmed.ncbi.nlm.nih.gov

Ciosk R, Shirayama M, Shevchenko A, Tanaka T, Toth A, Shevchenko A, et al. (2000). "Cohesin's binding to chromosomes depends on a separate complex consisting of Scc2 and Scc4 proteins". Molecular Cell. 5 (2): 243–254. doi:10.1016/S1097-2765(00)80420-7. PMID 10882066.
Rohatgi S, Clark D, Kline AD, Jackson LG, Pie J, Siu V, et al. (July 2010). "Facial diagnosis of mild and variant CdLS: Insights from a dysmorphologist survey". American Journal of Medical Genetics. Part A. 152A (7): 1641–1653. doi:10.1002/ajmg.a.33441. PMC 4133091. PMID 20583156.
Kikuchi S, Borek DM, Otwinowski Z, Tomchick DR, Yu H (November 2016). "Crystal structure of the cohesin loader Scc2 and insight into cohesinopathy". Proceedings of the National Academy of Sciences of the United States of America. 113 (44): 12444–12449. Bibcode:2016PNAS..11312444K. doi:10.1073/pnas.1611333113. PMC 5098657. PMID 27791135.
Nasmyth K (October 2011). "Cohesin: a catenase with separate entry and exit gates?". Nature Cell Biology. 13 (10): 1170–1177. doi:10.1038/ncb2349. PMID 21968990. S2CID 25382204.
Schwarzer W, Abdennur N, Goloborodko A, Pekowska A, Fudenberg G, Loe-Mie Y, et al. (November 2017). "Two independent modes of chromatin organization revealed by cohesin removal". Nature. 551 (7678): 51–56. Bibcode:2017Natur.551...51S. bioRxiv 10.1101/094185. doi:10.1038/nature24281. PMC 5687303. PMID 29094699.
Rhodes J, Mazza D, Nasmyth K, Uphoff S (2017). "Scc2/Nipbl hops between chromosomal cohesin rings after loading". eLife. 6 e30000. doi:10.7554/eLife.30000. PMC 5621834. PMID 28914604.
Zuin J, Franke V, van Ijcken WF, van der Sloot A, Krantz ID, van der Reijden MI, et al. (February 2014). "A cohesin-independent role for NIPBL at promoters provides insights in CdLS". PLOS Genetics. 10 (2) e1004153. doi:10.1371/journal.pgen.1004153. PMC 3923681. PMID 24550742.
van den Berg DL, Azzarelli R, Oishi K, Martynoga B, Urbán N, Dekkers DH, et al. (January 2017). "Nipbl Interacts with Zfp609 and the Integrator Complex to Regulate Cortical Neuron Migration". Neuron. 93 (2): 348–361. doi:10.1016/j.neuron.2016.11.047. PMC 5263256. PMID 28041881.
Kawauchi S, Calof AL, Santos R, Lopez-Burks ME, Young CM, Hoang MP, et al. (September 2009). "Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome". PLOS Genetics. 5 (9) e1000650. doi:10.1371/journal.pgen.1000650. PMC 2730539. PMID 19763162.

semanticscholar.org (Global: 15^th place; English: 8^th place)

api.semanticscholar.org

Nasmyth K (October 2011). "Cohesin: a catenase with separate entry and exit gates?". Nature Cell Biology. 13 (10): 1170–1177. doi:10.1038/ncb2349. PMID 21968990. S2CID 25382204.

NIPBL (English Wikipedia)

adsabs.harvard.edu (Global: 14th place; English: 9th place)