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WDR35 gene

Known as: KIAA1336, INTRAFLAGELLAR TRANSPORT 121, CHLAMYDOMONAS, HOMOLOG OF, MGC33196 
 
National Institutes of Health

Papers overview

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2018
2018
We describe a patient severely affected with multiple congenital anomalies, including brain malformations and skeletal dysplasia… Expand
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2016
2016
Intraflagellar transport sub-complex A (IFT-A) is known to regulate retrograde IFT in the cilium. To rigorously assess its other… Expand
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2015
2015
Ciliopathies such as cranioectodermal dysplasia, Sensenbrenner syndrome, short-rib polydactyly, and Jeune syndrome are associated… Expand
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2014
2014
AIM To investigate whether naofen is involved in tumor necrosis factor (TNF)-α-mediated apoptosis of hepatocytes induced by… Expand
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2013
2013
To the Editor : Cranioectodermal dysplasia (CED, Sensenbrenner syndrome, OMIM 218330) is a rare autosomal recessive ciliopathy… Expand
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2012
2012
Sensenbrenner syndrome and unclassified short rib-polydactyly conditions are ciliopathies with overlapping phenotypes and genetic… Expand
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Highly Cited
2011
Highly Cited
2011
Defects in cilia formation and function result in a range of human skeletal and visceral abnormalities. Mutations in several… Expand
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Highly Cited
2010
Highly Cited
2010
Sensenbrenner syndrome/cranioectodermal dysplasia (CED) is an autosomal-recessive disease that is characterized by… Expand
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2010
2010
Naofen has recently been identified from the rat brain/spinal cord cDNA library as a substance reactive against an anti… Expand
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1989
1989
Abstract Seedlings of four wheat cultivars were infested with Metopolophium dirhodum nymphs. After aphids had fed for 40 hr on… Expand
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