نتایج جستجو برای: aipl1

تعداد نتایج: 84  

Journal: :Investigative ophthalmology & visual science 2010
Sirichai Pasadhika Gerald A Fishman Edwin M Stone Martin Lindeman Ruth Zelkha Irma Lopez Robert K Koenekoop Mahnaz Shahidi

PURPOSE To evaluate genotypic and macular morphologic correlations in patients with RPE65-, CEP290-, GUCY2D-, or AIPL1-related Leber congenital amaurosis (LCA) using spectral-domain optical coherence tomography (SD-OCT). METHODS SD-OCT macular scans were performed in 21 patients, including 10 with RPE65, 7 with CEP290, 3 with GUCY2D, and 1 with AIPL1 mutations. An image processing software wa...

2014
David Li Chongfei Jin Xiaodong Jiao Lin Li Tahmina Bushra Muhammad Asif Naeem Nadeem H. Butt Tayyab Husnain Paul A. Sieving Sheikh Riazuddin S. Amer Riazuddin J. Fielding Hejtmancik

PURPOSE To localize and identify the gene and mutations causing autosomal recessive retinal dystrophy in two consanguineous Pakistani families. METHODS Consanguineous families from Pakistan were ascertained to be affected with autosomal recessive retinal degeneration. All affected individuals underwent thorough ophthalmologic examinations. Blood samples were collected, and genomic DNA was ext...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه اصفهان - دانشکده زیست شناسی 1392

نابینایی مادرزادی لبر شدیدترین بیماری تحلیل ارثی شبکیه در انسان است. این بیماری به لحاظ ژنتیکی ناهمگن بوده و معمولاً به صورت آتوزومی مغلوب به ارث می رسد. مشخص شده است که انواع جهش ها در ژن aipl1 منجر به ایجاد شدیدترین شکل های این بیماری می شوند. اصولا" تعیین توالی به منظور شناسایی جهش های نقطه ای و دیگر تنوعات توالی موجود در این ژن استفاده می شود که بسیار وقت گیر و پر هزینه میباشد. از این رو روش...

2013
Xin Zhao YanFan Ren Xiaohui Zhang Changxi Chen Bing Dong Yang Li

PURPOSE To describe the clinical and genetic findings in a Chinese family with autosomal dominant cone dystrophy (adCOD). METHODS One family was examined clinically, and genomic DNA was extracted from venous blood of all participants. Genotyping and haplotyping analysis was performed on the known genetic loci for adCOD and autosomal dominant cone-rod dystrophies (adCORD) with a panel of polym...

Journal: :Investigative ophthalmology & visual science 2007
Robert H Henderson Naushin Waseem Rowan Searle Jacqueline van der Spuy Isabelle Russell-Eggitt Shomi S Bhattacharya Dorothy A Thompson Graham E Holder Michael E Cheetham Andrew R Webster Anthony T Moore

PURPOSE Leber congenital amaurosis (LCA) and early-onset severe retinal dystrophy (EOSRD) are genetically heterogeneous, with 11 genes currently implicated. The LCA chip may be used to interrogate many variants in one hybridization reaction. The purpose of this study was to assess the utility of this technology. METHODS One hundred fifty-three patients with LCA and EOSRD were screened using a...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2015
Masaaki Komatsu Heather E Wheeler Suyoun Chung Siew-Kee Low Claudia Wing Shannon M Delaney Lidija K Gorsic Atsushi Takahashi Michiaki Kubo Deanna L Kroetz Wei Zhang Yusuke Nakamura M Eileen Dolan

PURPOSE Paclitaxel is used worldwide in the treatment of breast, lung, ovarian, and other cancers. Sensory peripheral neuropathy is an associated adverse effect that cannot be predicted, prevented, or mitigated. To better understand the contribution of germline genetic variation to paclitaxel-induced peripheral neuropathy, we undertook an integrative approach that combines genome-wide associati...

Journal: :Investigative ophthalmology & visual science 2006
Suzanne Yzer Bart P Leroy Elfride De Baere Thomy J de Ravel Marijke N Zonneveld Krysta Voesenek Ulrich Kellner Jose P Martinez Ciriano Jan-Tjeerd H N de Faber Klaus Rohrschneider Ronald Roepman Anneke I den Hollander Johannes R Cruysberg Françoise Meire Ingele Casteels Norka G van Moll-Ramirez Rando Allikmets L Ingeborgh van den Born Frans P M Cremers

PURPOSE To test the efficiency of a microarray chip as a diagnostic tool in a cohort of northwestern European patients with Leber congenital amaurosis (LCA) and to perform a genotype-phenotype analysis in patients in whom pathologic mutations were identified. METHODS DNAs from 58 patients with LCA were analyzed using a microarray chip containing previously identified disease-associated sequen...

Journal: :Archives of ophthalmology 2010
Martin McKibbin Manir Ali Moin D Mohamed Adam P Booth Fiona Bishop Bishwanath Pal Kelly Springell Yasmin Raashid Hussain Jafri Chris F Inglehearn

OBJECTIVES To report the genetic basis of Leber congenital amaurosis (LCA) in northern Pakistan and to describe the phenotype. METHODS DNA from 14 families was analyzed using single-nucleotide polymorphism and microsatellite genotyping and direct sequencing to determine the genes and mutations involved. The history and examination findings from 64 affected individuals were analyzed to show ge...

2017
Lei-Lei Gao Chun-Xiang Zhou Xiao-Lan Zhang Peng Liu Zhen Jin Gang-Yi Zhu Yang Ma Jing Li Zhi-Xia Yang Dong Zhang

ZP3 is a principal component of the zona pellucida (ZP) of mammalian oocytes and is essential for normal fertility, and knockout of ZP3 causes complete infertility. ZP3 promotes fertilization by recognizing sperm binding and activating the acrosome reaction; however, additional cellular roles for ZP3 in mammalian oocytes have not been yet reported. In the current study, we found that ZP3 was st...

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