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KIF1BP gene
Known as:
TTC20
, KIAA1279
, kinesin binding protein
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National Institutes of Health
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Related topics
Related topics
1 relation
10q
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Benserazide Perturbs Kif15‐kinesin Binding Protein Interaction with Prolonged Metaphase and Defects in Chromosomal Congression: A Study Based on in silico Modeling and Cell Culture
Jomon Sebastian
,
K. Rathinasamy
Molecular Informatics
2020
Corpus ID: 198911009
The interaction of Kif15 with kinesin binding protein (KBP) is critical for its microtubule localization, bundling of kinetochore…
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Review
2018
Review
2018
Accumulation of potential driver genes with genomic alterations predicts survival of high-risk neuroblastoma patients
C. Suo
,
Wenjiang Deng
,
T. Vu
,
Mingrui Li
,
Leming Shi
,
Y. Pawitan
Biology Direct
2018
Corpus ID: 255981918
Neuroblastoma is the most common pediatric malignancy with heterogeneous clinical behaviors, ranging from spontaneous regression…
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2017
2017
Association of a Novel Nonsense Mutation in KIAA1279 with Goldberg-Shprintzen Syndrome
S. Salehpour
,
Farzad Hashemi-Gorji
,
Z. Soltani
,
S. Ghafouri-Fard
,
M. Miryounesi
Iranian journal of child neurology
2017
Corpus ID: 186705
Goldberg-Shprintzen syndrome (OMIM 609460) (GOSHS) is an autosomal recessive multiple congenital anomaly syndrome distinguished…
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2016
2016
KIAA1279 and Goldberg-Shprintzen Syndrome
A. Brooks
,
R. Hofstra
2016
Corpus ID: 151533585
2010
2010
Polymicrogyria and epilepsy
R. Guerrini
Epilepsia
2010
Corpus ID: 205690510
The term polymicrogyria defines an excessive number of abnormally small, and partly fused, cortical gyri that produce an…
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2009
2009
Characterization of the Stathmin SCG10 and its interactions with Kinesin Binding Protein (KBP) in zebrafish
G. Burzynski
,
M. Alves
,
+5 authors
I. Shepherd
2009
Corpus ID: 78912036
2009
2009
A functional approach to understand the role of the Kinesin Binding Protein (KBP) in Goldberg-Shprintzen syndrome
M. Alves
,
A. Brooks
,
E. Graaff
,
C. Hoogenraad
,
B. Eggen
,
R. Hofstra
2009
Corpus ID: 58379778
2007
2007
304 GOLDBERG-SHPRINTZEN SYNDROME DUE TO A HOMOZYGOUS DELETION IN KIAA1279: CLINICAL FINDINGS AND PRENATAL DIAGNOSIS IN AN AT-RISK FAMILY.
C. Curry
,
M. Tsang
,
M. Friez
,
R. Clark
,
A. Brooks
2007
Corpus ID: 75890681
Goldberg-Shprintzen syndrome (GOSHS) is a rare autosomal recessive disorder characterized by microcephaly with polymicrogyria…
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2004
2004
Haplotype analysis of BRCA1 gene reveals a new gene rearrangement: characterization of a 19.9 KBP deletion
M. Tancredi
,
E. Sensi
,
+6 authors
M. Caligo
European Journal of Human Genetics
2004
Corpus ID: 24108328
Germ-line mutations in the BRCA1 gene cause hereditary predisposition to breast and ovarian cancer. BRCA1 and BRCA2 mutations…
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1992
1992
Structural characterization and expression of a brain specific gene encoding chick kainate binding protein
N. Eshhar
,
C. Hunter
,
R. Wenthold
,
K. Wada
FEBS Letters
1992
Corpus ID: 25697754
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