نتایج جستجو برای: ciliopathy

تعداد نتایج: 423  

Journal: :Journal of cell science 2011
Carla A M Lopes Suzanna L Prosser Leila Romio Robert A Hirst Chris O'Callaghan Adrian S Woolf Andrew M Fry

Ciliopathies are caused by mutations in genes encoding proteins required for cilia organization or function. We show through colocalization with PCM-1, that OFD1 (the product of the gene mutated in oral-facial-digital syndrome 1) as well as BBS4 and CEP290 (proteins encoded by other ciliopathy genes) are primarily components of centriolar satellites, the particles surrounding centrosomes and ba...

2015
Laura E. Yee Francesc R. Garcia-Gonzalo Rachel V. Bowie Chunmei Li Julie K. Kennedy Kaveh Ashrafi Oliver E. Blacque Michel R. Leroux Jeremy F. Reiter Gregory S. Barsh

Mutations in genes encoding cilia proteins cause human ciliopathies, diverse disorders affecting many tissues. Individual genes can be linked to ciliopathies with dramatically different phenotypes, suggesting that genetic modifiers may participate in their pathogenesis. The ciliary transition zone contains two protein complexes affected in the ciliopathies Meckel syndrome (MKS) and nephronophth...

Journal: :Human molecular genetics 2015
Rivka A Rachel Erin A Yamamoto Mrinal K Dewanjee Helen L May-Simera Yuri V Sergeev Alice N Hackett Katherine Pohida Jeeva Munasinghe Norimoto Gotoh Bill Wickstead Robert N Fariss Lijin Dong Tiansen Li Anand Swaroop

Distinct mutations in the centrosomal-cilia protein CEP290 lead to diverse clinical findings in syndromic ciliopathies. We show that CEP290 localizes to the transition zone in ciliated cells, precisely to the region of Y-linkers between central microtubules and plasma membrane. To create models of CEP290-associated ciliopathy syndromes, we generated Cep290(ko/ko) and Cep290(gt/gt) mice that pro...

2018
Yeon-Joo Kim Daniel Ps Osborn Ji-Young Lee Masatake Araki Kimi Araki Timothy Mohun Johanna Känsäkoski Nina Brandstack Hyun-Taek Kim Francesc Miralles Cheol-Hee Kim Nigel A Brown Hyung-Goo Kim Juan Pedro Martinez-Barbera Paris Ataliotis Taneli Raivio Lawrence C Layman Soo-Hyun Kim

WDR11 has been implicated in congenital hypogonadotropic hypogonadism (CHH) and Kallmann syndrome (KS), human developmental genetic disorders defined by delayed puberty and infertility. However, WDR11's role in development is poorly understood. Here, we report that WDR11 modulates the Hedgehog (Hh) signalling pathway and is essential for ciliogenesis. Disruption of WDR11 expression in mouse and...

2013
Amanda C. Leightner Cynthia J. Hommerding Ying Peng Jeffrey L. Salisbury Vladimir G. Gainullin Peter G. Czarnecki Caroline R. Sussman Peter C. Harris

Meckel syndrome (MKS) is a lethal disorder associated with renal cystic disease, encephalocele, ductal plate malformation, and polydactyly. MKS is genetically heterogeneous and part of a growing list of syndromes called ciliopathies, disorders resulting from defective cilia. TMEM67 mutation (MKS3) is a major cause of MKS and the related ciliopathy Joubert syndrome, although the complete etiolog...

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