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TTC28 gene

Known as: TPRBK, TTC28, TETRATRICOPEPTIDE REPEAT DOMAIN-CONTAINING PROTEIN 28 
 
National Institutes of Health

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
Uveal melanoma (UM) has well-characterised somatic copy number alterations (SCNA) in chromosomes 1, 3, 6 and 8, in addition to… Expand
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2020
2020
Whole genome sequencing analysis identifies recurrent structural alterations in esophageal squamous cell carcinoma
Esophageal squamous cell carcinoma (ESCC) is the predominant type of esophageal cancer in the Asian region, including Japan. A… Expand
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2018
2018
Atypical Cadherin Dachsous1b Interacts with Ttc28 and Aurora B to Control Microtubule Dynamics in Embryonic Cleavages.
Atypical cadherin Dachsous (Dchs) is a conserved regulator of planar cell polarity, morphogenesis, and tissue growth during… Expand
Highly Cited
2017
Highly Cited
2017
Genomic analysis of oesophageal squamous-cell carcinoma identifies alcohol drinking-related mutation signature and genomic alterations
Approximately half of the world's 500,000 new oesophageal squamous-cell carcinoma (ESCC) cases each year occur in China. Here, we… Expand
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Highly Cited
2016
Highly Cited
2016
Comprehensive Genetic Landscape of Uveal Melanoma by Whole-Genome Sequencing.
Uveal melanoma (UM) is a rare intraocular tumor that, similar to cutaneous melanoma, originates from melanocytes. To gain… Expand
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2016
2016
Accelerating matchmaking of novel dysmorphology syndromes through clinical and genomic characterization of a large cohort
Purpose:Dysmorphology syndromes are among the most common referrals to clinical genetics specialists. Inability to match the… Expand
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2014
2014
Frequent L1 retrotranspositions originating from TTC28 in colorectal cancer
L1 element retrotranspositions have been found to alter expression of genes neighboring the insertion sites, potentially… Expand
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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.
Through the comprehensive analysis of the genomic DNA sequence of human chromosome 22, we identified a novel gene of 702 kb… Expand
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Review
2011
Review
2011
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…
BackgroundPierre-Robin sequence (PRS) is defined by micro- and/or retrognathia, glossoptosis and cleft soft palate, either caused… Expand
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