نتایج جستجو برای: missense mutation

تعداد نتایج: 293819  

2017
Kai Gao Anel Tankovic Yujia Zhang Hirofumi Kusumoto Jin Zhang Wenjuan Chen Wenshu XiangWei Gil H. Shaulsky Chun Hu Stephen F. Traynelis Hongjie Yuan Yuwu Jiang

OBJECTIVE N-methyl-D-aspartate receptors (NMDAR) subunit GRIN2A/GluN2A mutations have been identified in patients with various neurological diseases, such as epilepsy and intellectual disability / developmental delay (ID/DD). In this study, we investigated the phenotype and underlying molecular mechanism of a GRIN2A missense mutation identified by next generation sequencing on idiopathic focal ...

Journal: :Proceedings of the National Academy of Sciences 2018

حقوقی راد, لاله , دانشپور, مریم سادات , شیخ الاسلامی, سارا , ظریف یگانه, مرجان , هدایتی, مهدی ,

Background: Medullary thyroid carcinoma (MTC) occurs in both sporadic (75%) and hereditary (25%) forms. The missense mutations of the rearranged during transfection (RET) proto-oncogene in MTC development have been well demonstrated. Several studies have been published that indicate the molecular analysis of RET gene may offer early identification of those patients at high risk to develop MTC a...

Fereidoun Azizi Golnoush Dehbashi-Behbahani Laleh Hoghooghi-Rad Marjan Zarif-Yeganeh Mehdi Hedayati Samaneh Farashi Sara Sheikholeslami

Background & Aims: Thyroid cancer is the most common endocrine malignancy. Medullary thyroid carcinoma (MTC) is an aggressive malignant tumor arising from parafollicular cells of the thyroid. MTC occurs in hereditary (25%, hMTC) or sporadic (75%, sMTC) forms. The hMTC form has an autosomal dominant inheritance. RET proto-oncogene mutations, especially the 10, 11, and 16 exones, are associated w...

Journal: :iranian journal of public health 0
samira asgharzade somayeh reiisi mohammad amin tabatabaiefar morteza hashemzadeh chaleshtori

background: hearing loss (hl) is the most frequent neurosensory impairment. hl is highly heterogeneous defect. this disorder affects 1 out of 500 newborns. this study aimed to determine the role of dfnb2 locus and frequency of myo7a gene mutations in a population from west of iran. methods: thirty families investigated in shahrekord university of medical sciences in 2014, genetic linkage analys...

Journal: :International Journal of Pediatric Endocrinology 2016

Journal: :American journal of human genetics 2009
Sean V Tavtigian Peter J Oefner Davit Babikyan Anne Hartmann Sue Healey Florence Le Calvez-Kelm Fabienne Lesueur Graham B Byrnes Shu-Chun Chuang Nathalie Forey Corinna Feuchtinger Lydie Gioia Janet Hall Mia Hashibe Barbara Herte Sandrine McKay-Chopin Alun Thomas Maxime P Vallée Catherine Voegele Penelope M Webb David C Whiteman Suleeporn Sangrajrang John L Hopper Melissa C Southey Irene L Andrulis Esther M John Georgia Chenevix-Trench

The susceptibility gene for ataxia telangiectasia, ATM, is also an intermediate-risk breast-cancer-susceptibility gene. However, the spectrum and frequency distribution of ATM mutations that confer increased risk of breast cancer have been controversial. To assess the contribution of rare variants in this gene to risk of breast cancer, we pooled data from seven published ATM case-control mutati...

2008
Louis S. Pymar Fiona M. Platt Jon M. Askham Ewan E. Morrison Margaret A. Knowles

More than 50% of transitional cell carcinomas of the bladder show loss of heterozygosity of a region spanning the TSC1 locus at 9q34 and mutations of TSC1 have been identified in 14.5% of tumours. These comprise nonsense mutations, splicing mutations, small deletions and missense mutations. Missense mutations are only rarely found in the germline in TSC disease. Therefore, we have examined six ...

Journal: :Japanese journal of clinical oncology 2004
Ying Yuan Yan-qing Huang Shan-rong Cai Yong-mao Song Shu Zheng Su-zhan Zhang

BACKGROUND Hereditary non-polyposis colorectal cancer (HNPCC) is an autosomal dominant disease due to germline mutations of human mismatch repair genes, mainly hMLH1 and hMSH2. The aim of the present study was to identify the point mutations and large genomic deletions of hMLH1 and hMSH2 genes in 14 Chinese HNPCC families. METHODS Fourteen families fulfilling the Chinese HNPCC criteria were i...

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