نتایج جستجو برای: ژن rrna 12s

تعداد نتایج: 45606  

Journal: :Journal of medical genetics 1997
A Pandya X Xia J Radnaabazar J Batsuuri B Dangaansuren N Fischel-Ghodsian W E Nance

Irreversible hearing loss is a catastrophic complication of treatment with aminoglycoside antibiotics such as streptomycin, gentamycin, and kanamycin. Many kindreds showing a matrilineal pattern of inheritance of this trait have been described in China where the widespread use of aminoglycoside antibiotics accounts for approximately 25% of profound deafness in some districts. Because of the cha...

2016
DINGYUAN MA JINGJING ZHANG CHUNYU LUO YING LIN XIUQING JI PING HU ZHENGFENG XU

The aim of the present study was to investigate the genetic etiology of patients with nonsyndromic hearing impairment through gene analysis, and provide accurate genetic counseling and prenatal diagnosis for deaf patients and families with deaf children. Previous molecular etiological studies have demonstrated that the most common molecular changes in Chinese patients with nonsyndromic hearing ...

2016
Yi Xiong Mei Zhong Yi Lin Youliang Yan Xiufeng Lin Xin Li

Non-syndromic hearing loss (NSHL) is a major public health issue and affects a substantial proportion of newborns worldwide. Currently little information is available about the molecular etiology of hearing impairment in the Chinese population. Therefore, this study aimed to perform a comprehensive investigation on the genetic mutation patterns of non-syndromic deafness in Zhongshan City, a cit...

2015
Gaurav Kumar Srivastava Nidhi Rajput Kajal Kumar Jadav Avadh Bihari Shrivastav Himanshu R. Joshi

AIM Partial fragment of D-loop region extending from 35 to 770 were compared with corresponding sequences of 16 wild pigs and 9 domestic pig breeds from different parts of the world for detection of single nucleotide polymorphism (SNP) markers in the region. The paper also reappraises SNP markers from two fragments of cytochrome b gene and a fragment 12S rRNA gene distinguishing the Indian wild...

Journal: :The Laryngoscope 2011
Chen-Chi Wu Tien-Chen Liu Shih-Hao Wang Chuan-Jen Hsu Che-Ming Wu

OBJECTIVES/HYPOTHESIS To explore the genetic characteristics of children with cochlear implants (CIs) and to correlate the auditory performance after implantation to the genetic diagnosis of children with CIs. STUDY DESIGN Prospective cohort study. METHODS Mutations of four common deafness-associated genes, GJB2, SLC26A4, the mitochondrial 12S rRNA gene, and OTOF, were screened in 743 unrel...

Journal: :Brazilian journal of otorhinolaryngology 2011
G Meza N M Torres-Ruíz C Tirado-Gutiérrez P Aguilera

UNLABELLED Streptomycin and aminoglycoside derivatives are commonly used to treat tuberculosis and other stubborn infections; these drugs may alter auditory and/or vestibular function. Mutations in mitochondrial DNA have been associated with hypersensitivity to aminoglycosides; no studies have been conducted in Mexicans, which are very prone to such alterations because aminoglycosides have been...

Journal: :Zoological science 2011
Masato Hirose Matthew H Dick Shunsuke F Mawatari

Morphological characters of statoblasts (including floatoblasts and sessoblasts) in freshwater bryozoans have been important in phylactolaemate systematics and identification in that older phylogenetic hypotheses relied heavily on statoblast morphology. To assess the reliability of statoblast characters in drawing conclusions about phylogeny, we examined the phylogenetic distribution of metric ...

2014
Noor Haslina Masstor Abdullah Samat Shukor Md Nor Badrul Munir Md-Zain

Chiloscyllium, commonly called bamboo shark, can be found inhabiting the waters of the Indo-West Pacific around East Asian countries such as Malaysia, Myanmar, Thailand, Singapore, and Indonesia. The International Union for Conservation of Nature (IUCN) Red List has categorized them as nearly threatened sharks out of their declining population status due to overexploitation. A molecular study w...

2017
Yu Ding Bo-Hou Xia Yao-Shu Teng Guang-Chao Zhuo Jian-Hang Leng

Mutations in mitochondrial genome have been found to be associated with hearing loss. Of these, the mitochondrial 12S rRNA and tRNASer(UCN) are the hot spots for pathogenic mutations associated with deafness. To understand the putative role of mitochondrial DNA (mtDNA) mutations in hearing loss, we recently initiated a mutational screening for the mtDNA mutations in Hangzhou area from Zhejiang ...

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