نتایج جستجو برای: ciliopathy

تعداد نتایج: 423  

2015
Clementine Schouteden Daniel Serwas Mate Palfy Alexander Dammermann

Cilia are cellular projections that perform sensory and motile functions. A key ciliary subdomain is the transition zone, which lies between basal body and axoneme. Previous work in Caenorhabditis elegans identified two ciliopathy-associated protein complexes or modules that direct assembly of transition zone Y-links. Here, we identify C. elegans CEP290 as a component of a third module required...

Journal: :Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 2019

Journal: :AJNR. American journal of neuroradiology 2011
I Harting U Kotzaeridou A Poretti A Seitz J Pietz M Bendszus E Boltshauser

The so-called molar tooth sign is the radiologic hallmark of JSRD. Joubert syndrome is a rare, most often autosomal-recessive disorder with a characteristic malformation of the midhindbrain. We describe 3 patients with JSRD and the additional MR finding of tissue resembling heterotopia in the interpeduncular fossa, which in one patient was combined with a more extensive intramesencephalic heter...

2014
Anas M Alazami Mohammed Zain Seidahmed Fatema Alzahrani Adam O Mohammed Fowzan S Alkuraya

Cranioectodermal dysplasia (CED) is a very rare autosomal recessive disorder characterized by a recognizable craniofacial profile in addition to ectodermal manifestations involving the skin, hair, and teeth. Four genes are known to be mutated in this disorder, all involved in the ciliary intraflagellar transport confirming that CED is a ciliopathy. In a multiplex consanguineous family with typi...

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