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TTC26 gene

Known as: FLJ12571, IFT56, DYF13 
 
National Institutes of Health

Papers overview

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2019
2019
The clinical consequences of defective primary cilium (ciliopathies) are characterized by marked phenotypic and genetic… Expand
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2018
2018
Aims: The purpose of this study was to propose a pipeline to identify prognostic signature for HCC overall survival (OS… Expand
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2017
2017
ARL13B (a small GTPase) and INPP5E (a phosphoinositide 5-phosphatase) are ciliary proteins encoded by causative genes of Joubert… Expand
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2017
2017
The primary cilium organizes Hedgehog signaling, shapes embryonic development and is the unifying cause of the ciliopathies. We… Expand
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2017
2017
Cilia are key regulators of animal development and depend on intraflagellar transport (IFT) proteins for their formation and… Expand
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2017
2017
Cilia are key regulators of animal development and depend on intraflagellar transport (IFT) proteins to form and function, yet… Expand
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2017
2017
In our previous study, we investigated the regulatory relationship between lncRNAs, miRNA, and mRNAs in an effort to shed light… Expand
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2014
2014
The phenotype of the spontaneous mutant mouse hop-sterile (hop) is characterized by a hopping gait, polydactyly, hydrocephalus… Expand
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2012
2012
In our effort to understand genetic disorders of the photoreceptor cells of the retina, we have focused on intraflagellar… Expand
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2010
2010
DYF-13, originally identified in Caenorhabditis elegans within a collection of dye-filling chemosensory mutants, is one of… Expand
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