TCTN2 gene

Known as: tectonic family member 2, MKS8, TCTN2 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2011-2017
012320112017

Papers overview

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Review
2018
Review
2018
Understanding volcanic paroxysmal explosive activity requires the knowledge of many associated processes. An overview of the… (More)
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2017
2017
Tctn1, Tctn2, and Tctn3 are membrane proteins that localize at the transition zone of primary cilia. Tctn1 and Tctn2 mutations… (More)
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Review
2015
Review
2015
So far very few patients with sequence variants in the closely related tectonic genes TCTN1-3 have been described. By multi-gene… (More)
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2015
2015
The transition zone (TZ) of primary cilia serves as a diffusion barrier to regulate ciliogenesis and receptor localization for… (More)
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2012
2012
Orofaciodigital syndromes (OFDSs) consist of a group of heterogeneous disorders characterized by abnormalities in the oral cavity… (More)
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2012
2012
Joubert syndrome (JS) is an autosomal recessive ciliopathy characterized by hypotonia, ataxia, abnormal eye movements, and… (More)
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2012
2012
We have identified a complex of proteins that form part of the transition zone, a region at the base of the cilium. This complex… (More)
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Highly Cited
2011
Highly Cited
2011
Nephronophthisis (NPHP), Joubert (JBTS), and Meckel-Gruber (MKS) syndromes are autosomal-recessive ciliopathies presenting with… (More)
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2011
2011
Meckel Gruber syndrome (MKS) is an autosomal recessive multisystem disorder that represents a severe form of ciliopathy in humans… (More)
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Highly Cited
2011
Highly Cited
2011
Mutations affecting ciliary components cause ciliopathies. As described here, we investigated Tectonic1 (Tctn1), a regulator of… (More)
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