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TTC28 gene
Known as:
TPRBK
, TTC28
, TETRATRICOPEPTIDE REPEAT DOMAIN-CONTAINING PROTEIN 28
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Targeted Next-Generation Sequencing of 117 Routine Clinical Samples Provides Further Insights into the Molecular Landscape of Uveal Melanoma
S. Thornton
,
S. Coupland
,
+10 authors
H. Kalirai
Cancers
2020
Corpus ID: 216595765
Uveal melanoma (UM) has well-characterised somatic copy number alterations (SCNA) in chromosomes 1, 3, 6 and 8, in addition to…
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2020
2020
Whole genome sequencing analysis identifies recurrent structural alterations in esophageal squamous cell carcinoma
Munmee Dutta
,
H. Nakagawa
,
+12 authors
Masashi Fujita
PeerJ
2020
Corpus ID: 220280820
Esophageal squamous cell carcinoma (ESCC) is the predominant type of esophageal cancer in the Asian region, including Japan. A…
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2018
2018
Atypical Cadherin Dachsous1b Interacts with Ttc28 and Aurora B to Control Microtubule Dynamics in Embryonic Cleavages.
Jiakun Chen
,
Gina D. Castelvecchi
,
+4 authors
L. Solnica-Krezel
Developmental Cell
2018
Corpus ID: 13697550
Highly Cited
2017
Highly Cited
2017
Genomic analysis of oesophageal squamous-cell carcinoma identifies alcohol drinking-related mutation signature and genomic alterations
Jiang Chang
,
W. Tan
,
+24 authors
D. Lin
Nature Communications
2017
Corpus ID: 22091233
Approximately half of the world's 500,000 new oesophageal squamous-cell carcinoma (ESCC) cases each year occur in China. Here, we…
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Highly Cited
2016
Highly Cited
2016
Comprehensive Genetic Landscape of Uveal Melanoma by Whole-Genome Sequencing.
B. Royer-Bertrand
,
Matteo Torsello
,
+15 authors
C. Rivolta
American Journal of Human Genetics
2016
Corpus ID: 11562597
Highly Cited
2015
Highly Cited
2015
Accelerating matchmaking of novel dysmorphology syndromes through clinical and genomic characterization of a large cohort
R. Shaheen
,
N. Patel
,
+22 authors
F. Alkuraya
Genetics in Medicine
2015
Corpus ID: 205143258
Purpose:Dysmorphology syndromes are among the most common referrals to clinical genetics specialists. Inability to match the…
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2014
2014
Frequent L1 retrotranspositions originating from TTC28 in colorectal cancer
E. Pitkänen
,
T. Cajuso
,
+6 authors
O. Kilpivaara
OncoTarget
2014
Corpus ID: 6598522
L1 element retrotranspositions have been found to alter expression of genes neighboring the insertion sites, potentially…
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2012
2012
A novel big protein TPRBK possessing 25 units of TPR motif is essential for the progress of mitosis and cytokinesis.
Tomohiro Izumiyama
,
S. Minoshima
,
Tetsuhiko Yoshida
,
N. Shimizu
Gene
2012
Corpus ID: 579327
Review
2012
Review
2012
Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibromatosis 2 (NF2): a…
T. Davidson
,
P. Sanchez-Lara
,
+5 authors
A. Erdreich-Epstein
BMC Medical Genetics
2012
Corpus ID: 14606895
BackgroundPierre-Robin sequence (PRS) is defined by micro- and/or retrognathia, glossoptosis and cleft soft palate, either caused…
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