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NIPBL gene
Known as:
IDN3
, Nipped-B Homolog (Drosophila) Gene
, sister chromatid cohesion 2 homolog (yeast)
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This gene is involved in both limb and cartilage development and may play a role in chromatin cohesion.
National Institutes of Health
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Related topics
Related topics
5 relations
Cell Cycle Control
Limb Development
Nipped-B-Like Protein
chromatin remodeling
Narrower (1)
NIPBL wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Resolving the Genomic Localization of the Kollerin Cohesin-Loader Complex.
K. Wendt
Methods in molecular biology
2017
Corpus ID: 4858668
The kollerin complex, consisting of Scc2/Scc4 in yeast and Nipbl/Mau2 in vertebrates, is crucial for the chromatin-association of…
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2014
2014
Fourier transform microwave/millimeter-wave spectroscopy of the ScC2 (X̃2A1) radical: A model system for endohedral metallofullerenes
J. Min
,
D. Halfen
,
L. Ziurys
2014
Corpus ID: 95068042
2013
2013
Chl1 DNA Helicase Regulates Scc2 Deposition Specifically during DNA-Replication in Saccharomyces cerevisiae
Soumya Rudra
,
R. Skibbens
PLoS ONE
2013
Corpus ID: 5652720
The conserved family of cohesin proteins that mediate sister chromatid cohesion requires Scc2, Scc4 for chromatin-association and…
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2012
2012
Progress in breast cancer research
K. Polyak
,
P. Vogt
Proceedings of the National Academy of Sciences…
2012
Corpus ID: 26665840
Breast cancer is a heterogeneous disease composed of multiple different subtypes with distinct molecular features and clinical…
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2010
2010
Cornelia de Lange syndrome case due to genomic rearrangements including NIPBL.
M. Ratajska
,
J. Wierzba
,
+6 authors
J. Limon
European Journal of Medical Genetics
2010
Corpus ID: 38600969
2007
2007
Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patients
J. Schoumans
,
Josephine Wincent
,
+9 authors
B. Anderlid
European Journal of Human Genetics
2007
Corpus ID: 3180632
Cornelia de Lange syndrome (CdLS; OMIM 122470) is a rare multiple congenital anomaly/mental retardation syndrome characterized by…
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2007
2007
Large genomic rearrangements in NIPBL are infrequent in Cornelia de Lange Syndrome
Z. Bhuiyan
,
H. Stewart
,
E. Redeker
,
M. Mannens
,
R. Hennekam
European Journal of Human Genetics
2007
Corpus ID: 9275592
Cornelia de Lange Syndrome (CdLS) is a multiple congenital anomaly syndrome characterized by a distinctive facial appearance…
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Review
2007
Review
2007
Prenatal/neonatal pathology in two cases of Cornelia de Lange syndrome harboring novel mutations of NIPBL
F. Lalatta
,
S. Russo
,
+8 authors
L. Larizza
Genetics in Medicine
2007
Corpus ID: 3094656
Purpose: This study reviews prenatal findings in two cases with a suspected diagnosis of Cornelia de Lange Syndrome, a…
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Highly Cited
1996
Highly Cited
1996
Gene interaction and single gene effects in colon tumour susceptibility in mice
T. Wezel
,
A. Stassen
,
C. J. Moen
,
A. Hart
,
M. Valk
,
P. Demant
Nature Genetics
1996
Corpus ID: 25649695
To dissect the multigenic control of colon tumour susceptibility in the mouse1 we used the set of 20 CcS/Dem (CcS) recombinant…
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Highly Cited
1996
Highly Cited
1996
Fine mapping of colon tumor susceptibility (Scc) genes in the mouse, different from the genes known to be somatically mutated in colon cancer.
C. J. Moen
,
Peter C. Groot
,
A. Hart
,
M. Snoek
,
Peter Demant
Proceedings of the National Academy of Sciences…
1996
Corpus ID: 2413183
The predisposition to colon cancer is multigenetically controlled in animals and probably also in humans. We have analyzed the…
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