نتایج جستجو برای: aipl1

تعداد نتایج: 84  

2015
Juan Hidalgo-de-Quintana Nele Schwarz Ingrid P. Meschede Gabriele Stern-Schneider Michael B. Powner Ewan E. Morrison Clare E. Futter Uwe Wolfrum Michael E. Cheetham Jacqueline van der Spuy

PURPOSE The aim of this study was to investigate the interaction and co-localization of novel interacting proteins with the Leber congenital amaurosis (LCA) associated protein aryl hydrocarbon receptor interacting protein-like 1 (AIPL1). METHODS The CytoTrapXR yeast two-hybrid system was used to screen a bovine retinal cDNA library. A novel interaction between AIPL1 and members of the family ...

Journal: :Human molecular genetics 2011
Cristy A Ku Vince A Chiodo Sanford L Boye Andrew F X Goldberg Tiansen Li William W Hauswirth Visvanathan Ramamurthy

Defects in the photoreceptor-specific gene aryl hydrocarbon receptor interacting protein-like 1 (Aipl1) are associated with Leber congenital amaurosis (LCA), a childhood blinding disease with early-onset retinal degeneration and vision loss. Furthermore, Aipl1 defects are characterized at the most severe end of the LCA spectrum. The rapid photoreceptor degeneration and vision loss observed in t...

Journal: :Investigative ophthalmology & visual science 2011
Francesco Testa Enrico Maria Surace Settimio Rossi Elena Marrocco Annagiusi Gargiulo Valentina Di Iorio Carmela Ziviello Anna Nesti Simona Fecarotta Maria Laura Bacci Massimo Giunti Michele Della Corte Sandro Banfi Alberto Auricchio Francesca Simonelli

PURPOSE To evaluate the suitability of gene delivery-based approaches as potential treatment of Leber congenital amaurosis 4 (LCA4) due to AIPL1 mutations. METHODS Genomic DNA from patients was analyzed using a microarray chip and direct sequencing. A detailed clinical evaluation including fundus autofluorescence (FAF) and optical coherence tomography (OCT) was performed in patients with AIPL...

2012
Mei Hong Tan Donna S. Mackay Jill Cowing Hoai Viet Tran Alexander J. Smith Genevieve A. Wright Arundhati Dev-Borman Robert H. Henderson Phillip Moradi Isabelle Russell-Eggitt Robert E. MacLaren Anthony G. Robson Michael E. Cheetham Dorothy A. Thompson Andrew R. Webster Michel Michaelides Robin R. Ali Anthony T. Moore

Leber Congenital Amaurosis (LCA) and Early Childhood Onset Severe Retinal Dystrophy are clinically and genetically heterogeneous retinal disorders characterised by visual impairment and nystagmus from birth or early infancy. We investigated the prevalence of sequence variants in AIPL1 in a large cohort of such patients (n = 392) and probed the likelihood of disease-causation of the identified v...

2017
Maria Iribarne Yuko Nishiwaki Shohei Nakamura Masato Araragi Eri Oguri Ichiro Masai

Genetic mutations in aryl hydrocarbon receptor interacting protein-like 1 (AIPL1) cause photoreceptor degeneration associated with Leber congenital amaurosis 4 (LCA4) in human patients. Here we report retinal phenotypes of a zebrafish aipl1 mutant, gold rush (gosh). In zebrafish, there are two aipl1 genes, aipl1a and aipl1b, which are expressed mainly in rods and cones, respectively. The gosh m...

Journal: :Biochemical Society transactions 2004
J van der Spuy M E Cheetham

Mutations in the AIPL1 (aryl hydrocarbon receptor interacting protein-like 1) cause the blinding disease Leber's congenital amaurosis. AIPL1 is a homologue of the AIP. AIP functions as part of a chaperone heterocomplex to facilitate signalling by the AhR and plays an important role in regulating the nuclear translocation of the receptor. We review the evidence for the role of AIP in protein tra...

Journal: :Human molecular genetics 2015
Cristy A Ku Vince A Chiodo Sanford L Boye Abigail Hayes Andrew F X Goldberg William W Hauswirth Visvanathan Ramamurthy

Defects in aryl hydrocarbon receptor interacting protein-like1 (AIPL1) are associated with blinding diseases with a wide range of severity in humans. We examined the mechanism behind autosomal dominant cone-rod dystrophy (adCORD) caused by 12 base pair (bp) deletion at proline 351 of hAIPL1 (P351Δ12) mutation in the primate-specific region of human AIPL1. Mutant P351Δ12 human isoform, aryl hydr...

Journal: :Vision Research 2003
Rita S. Sitorus Birgit Lorenz Markus N. Preising

PURPOSE To assess the frequency, the pattern of disease causing mutations, and phenotypic variations in patients with Leber congenital amaurosis (LCA) from Indonesia. PATIENTS AND METHODS Twenty-one unrelated index cases with a clinical diagnosis of LCA were screened for mutations in the coding sequence of RetGC1, RPE65 and AIPL1 gene with single strand conformation polymorphism analysis foll...

Journal: :Molecular vision 2005
Jacqueline van der Spuy Peter M G Munro Philip J Luthert Markus N Preising Toke Bek Steffen Heegaard Michael E Cheetham

PURPOSE An unusual retinal vascular morphology in an enucleated eye from a patient with Leber congenital amaurosis (LCA) has been associated with a mutation in AIPL1. The AIPL1 protein is expressed in the pineal gland and retinal photoreceptors. In the retina, AIPL1 is expressed in both developing cone and rod photoreceptors, but it is restricted to rod photoreceptors in the adult human retina....

Journal: :Archives of ophthalmology 2004
Sharola Dharmaraj Bart P Leroy Melanie M Sohocki Robert K Koenekoop Isabelle Perrault Khalid Anwar Shagufta Khaliq R Summathi Devi David G Birch Elaine De Pool Natalio Izquierdo Lionel Van Maldergem Mohammad Ismail Annette M Payne Graham E Holder Shomi S Bhattacharya Alan C Bird Josseline Kaplan Irene H Maumenee

OBJECTIVES To describe the phenotype of Leber congenital amaurosis (LCA) in 26 probands with mutations in aryl hydrocarbon receptor interacting protein-like 1 protein (AIPL1) and compare it with phenotypes of other LCA-related genes. To describe the electroretinogram (ERG) in heterozygote carriers. METHODS Patients with AIPL1-related LCA were identified in a cohort of 303 patients with LCA by...

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