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早期生长因子1和晶状体蛋白α-A基因多肽与近视的关联性研究
ISSN号:1674-845X
期刊名称:中华眼视光学与视觉科学杂志
时间:0
页码:332-336
语言:中文
相关项目:眼科学
作者:
张清炯|高阳|肖学珊|郭向明|黎仕强|
关于高阳:
介导VLDLR调节Wnt通路—非诺贝特治疗糖尿病视网膜病变的机制研究
关于肖学珊:
NYS7位点CMN新基因克隆与鉴定
新的CMN致病基因的定位与克隆
期刊论文 6
关于郭向明:
Leber遗传性视神经病变诱发因素及发病机制的研究
期刊论文 2
关于张清炯:
颜色视觉多样性的分子基础与锥细胞色觉基因表达模式
期刊论文 4
会议论文 1
著作 1
眼科学
期刊论文 36
高度近视发病的分子与基础研究
高度近视发病的分子与基础研究
家族性高度远视PHH基因定位与克隆
遗传性致盲眼底病的基因突变频谱研究
ARR3基因突变致女性特发性X连锁早发高度近视的分子机制研究
定位于4q的汉族人高度近视基因克隆与表达分析
通过分析蛋白复合体差异研究NYX突变致近视的机制
期刊论文 5
靶向外显子组测序高效实用检测眼遗传病基因突变的研究
期刊论文 14
关于黎仕强:
XLRP新致病基因的定位与克隆
同期刊论文项目
眼科学
期刊论文 36
同项目期刊论文
Common variants in chromosome 4q25 are associated with myopia in Chinese adults
High myopia is not associated with single nucleotide polymorphisms in the COL 2A 1 gene in the Chine
Nonsyndromic High Myopia in a Chinese Family Mapped to MYP1 Linkage Confirmation and Phenotypic Char
Clinical and linkage study on a consanguineous Chinese family with autosomal recessive high myopia
Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A muta
Mutation spectrum and frequency of the RHO gene in 248 Chinese families with retinitis pigmentosa
mtDNA m.3635G > A may be classified as a common primary mutation for Leber hereditary optic neuropat
Mitochondrial DNA haplogroup distribution in Chaoshanese with and without myopia
Mutations in RPGR and RP2 of Chinese Patients with X-Linked Retinitis Pigmentosa
PAX3 mutations and clinical characteristics in Chinese patients with Waardenburg syndrome type 1
Sequence variations of GRM6 in patients with high myopia
An evaluation of OPTC and EPYC as candidate genes for high myopia
Iris Hyperpigmentation in a Chinese Family With Ocular Albinism and the GPR143 Mutation
Investigation of CYP1B1 mutations in Chinese patients with primary congenital glaucoma
Evaluation of MFRP as a candidate gene for high hyperopia
Mitochondrial DNA mutation m.3635G > A may be associated with Leber hereditary optic neuropathy in C
Mutational screening of 10 genes in Chinese patients with microphthalmia and/or coloboma
Association of the single nucleotide polymorphisms in the extracellular matrix metalloprotease-9 gen
Lack of phenotypic effect of triallelic variation in SPATA7 in a family with Leber congenital amauro
KIF21A novel deletion and recurrent mutation in patients with congenital fibrosis of the extraocular
Mutation spectrum of PAX6 in Chinese patients with aniridia
Replication study of significant single nucleotide polymorphisms associated with myopia from two gen
Mutation analysis of 12 genes in Chinese families with congenital cataracts
Replication Study Supports CTNND2 as a Susceptibility Gene for High Myopia
Mutational screening of six genes in Chinese patients with congenital cataract and microcornea
Evaluation of EGR1 as a candidate gene for high myopia
Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular alb
High myopia is not associated with the SNPs in the TGIF, Lumican, TGFB1, and HGF genes
Co-occurrence of A1555G and G11778A in a Chinese family with high penetrance of Leber';s hereditary
Mitochondrial DNA Haplogroups M7b1 '; 2 and M8a Affect Clinical Expression of Leber Hereditary Optic
A recurrent mutation in GUCY2D associated with autosomal dominant cone dystrophy in a China family
Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients with Leber Congenital Amaurosis
Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated p
期刊信息
《中华眼视光学与视觉科学杂志》
中国科技核心期刊
主管单位:中国科学技术协会
主办单位:中华医学会
主编:
地址:浙江省温州市茶山高教园区温州医学院内
邮编:325035
邮箱:zhysgx@126.com
电话:0577-86699366
国际标准刊号:ISSN:1674-845X
国内统一刊号:ISSN:11-5909/R
邮发代号:32-108
获奖情况:
中国学术期刊综合评价数据库来源期刊,浙江省优秀期刊一等奖,中国期刊方阵“双效”期刊
国内外数据库收录:
美国化学文摘(网络版),波兰哥白尼索引,中国中国科技核心期刊
被引量:1786