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国家自然科学基金(30670736)

作品数:9 被引量:13H指数:3
相关作者:刘静宇代小华冯爱平刘木根王擎更多>>
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9 条 记 录,以下是 1-10
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A novel splicing mutation of TIMM8A causes X-linked congenital sensorineural deafness and dystonia syndrome in a Chinese family
The deafness-dystonia syndrome(DDS) is also known as Mohr-Tranebjaerg syndrome (MTS,MIM 304700).It is a rare X...
Cheng Wang1,Yulei Li1,Jun Yu Luo2,Jing Yu Liu(1) 1.College of Life Science and Technology,Huazhong University of Science and Technology,Wuhan,Hubei, 430074,P.R.China 2.Affiliated Secondary School,Huazhong University of Science and Technology,Wuhan,Hubei, 430074,P.R.China
关键词:RT-PCR
文献传递
泛发性发疹型汗管瘤一家系八例被引量:1
2009年
先证者(Ⅲ,)女,41岁。因皮肤多处起棕褐色小丘疹就诊。查体:先证者的面部、额部和眼周、颈部和耳下及上肢遍布棕褐色小丘疹。染色体核型分析正常,诊断为泛发性发疹样汗管瘤。
陈清华冯爱平张向阳蒋苹高勇刘娟杨擎宇刘静宇
关键词:发疹型汗管瘤泛发性染色体核型分析家系先证者丘疹
A novel splicing mutation of TIMM8A causes X-linked congenital sensorineural deafness and dystonia syndrome in a Chinese family
The deafness-dystonia syndrome(DDS) is also known as Mohr-Tranebjaerg syndrome (MTS,MIM 304700).It is a rare X...
王程刘静宇
关键词:RT-PCR
文献传递
先天性眼球震颤伴头震颤及感音性神经性耳聋一大家系
2008年
先证者(Ⅲ19)男,46岁。出生时发现患儿双眼球左右摆动,头不时也左右震颤;目前手有时也震颤,紧张时上述震颤加重。在16~17岁时发现视力下降,有进行性严重趋势;10年前发现听力下降;外观观察无贫血貌,行走正常,劳动能力和生活能力均正常。查体:双下肢肌张力增高,四肢深反射亢进;无感觉异常,双下肢痛觉无异常;跟-膝-胫实验可认为阴性,但比正常人显得较笨拙;
王玉萍姜美子张子波金雄吉盛天昕崔小妞代小华杨康鹃刘静宇
关键词:先天性眼球震颤感音性神经性耳聋大家系下肢肌张力增高视力下降听力下降
9;21相互易位携带者生育多例9p部分三体患者细胞遗传学分析被引量:4
2007年
在河南南阳收集到一个家系4代23人,其中6人患先天性智力障碍,具有轻度的面部和小母指畸形等特点,先证者伴随有癫痫的发生。采用常规的外周血培养染色体G带分析,发现先证者的核型为:46,XY,der(21)t(9;21)(9p22.2;21q22.3)pat,是部分9p三体。对该家系其他成员的染色体进行分析,发现所有患者均为部分9p三体,异常染色体均来自9号与21号染色体平衡易位携带者染色体相互易位的异常分离,因此这是一个部分9p三体综合征家系。而重复区段发生在9号染色体短臂远端一半区域(9pter→9p21)内,该区是关键区,导致智力障碍和面容轻微畸形。
王晓然罗瑞丽代小华刘静宇
Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family被引量:4
2008年
γ -actin (ACTG1) gene is a cytoplasmic nonmuscle actin gene, which encodes a major cytoskeletal protein in the sensory hair cells of the cochlea. Mutations in ACTG1 were found to cause autosomal dominant, progressive, sensorineural hearing loss linked to the DFNA 20/26 locus on chromosome 17q25.3 in European and American families, respectively. In this study, a novel missense mutation (c.364A〉G; p.I122V) co-segregated with the affected individuals in the family and did not exist in the unaffected family members and 150 unrelated normal controls. The alteration of residue Ile122 was predicted to damage its interaction with actin-binding proteins, which may cause disruption of hair cell organization and function. These findings strongly suggested that the I122V mutation in ACTG1 caused autosomal dominant non-syndromic hearing impairment in a Chinese family and expanded the spectrum of ACTG1 mutations causing hearing loss.
Ping LiuHu LiXiang RenHaiyan MaoQihui ZhuZhengfeng ZhuRong YangWenlin YuanJingyu LiuQing WangMugen Liu
关键词:LINKAGE
家族性Fain-病一家系九例
2008年
先证者(Ⅲ17)男,36岁,因酒后头“发闷”就诊。查体:神智正常。心肺(-)。神经系统检查(-)。血生化检查:血清钙、磷及血清铜蓝蛋白测定均在正常范围,血清总三碘甲状腺素原氨酸、血清总甲状腺素、高敏促甲状腺素检测均正常。甲状腺、甲状旁腺、肝脾肾B超未见异常。头颅Ct检查发现,双侧尾状核、豆状核、苍白球、丘脑下部及枕叶等处发现对称性钙化现象。
代小华崔小妞徐海波刘木根王擎刘静宇任翔
关键词:家族性家系头颅CT检查血生化检查总甲状腺素
常染色体显性遗传非综合征性耳聋一家系19例
2011年
先证者(Ⅳ13)男,44岁,汉族。从30岁左右开始出现听力下降,38岁开始使用助听器,偶尔出现耳朵疼痛。纯音测听结果显示其耳聋为混合性耳聋,左耳的听力为75分贝,右耳的听力为74分贝,属于重度耳聋。鼓室导抗测量显示有鼓室积液和中耳粘连。除耳聋之外,不伴随其他症状,临床诊断为非综合征性耳聋。
李雨雷罗君雨徐振平刘静宇
关键词:非综合征性耳聋常染色体显性遗传家系鼓室积液混合性耳聋重度耳聋
家族性特发性震颤一家系25例
2009年
先证者(V7)女,22岁。20岁时发现双手平举时出现细颤,情绪紧张、疲劳、做精细动作时可加重,少量饮酒震颤减轻,但饮酒过多症状加重,甚至累及下肢震颤。写字不变形,日常生活无大影响。查体:发育正常,神清语明,智力正常,步态稳定;十二对脑神经检查未见异常;四肢肌力、肌张力正常,四肢深反射对称;指鼻试验、指指试验、闭目难立征等均阴性;头部CT、MRI未见异常信号影,中线结构无偏移,各部脑室正常,小脑未见萎缩;
杨淑敏张伟华王程高勇张子波金艳花金雄吉刘静宇杨康鹃
关键词:特发性震颤家系情绪紧张少量饮酒饮酒过多神经检查
Visualization and Characterization of High-Order Chromatin Fibers under Light Microscope during Interphase and Mitotic Stages in Plants
2007年
Using genomic in situ hybridization with genomic DNA, high-order chromatin fibers were successfully exhibited under a light microscope through the cell cycle in barley, rice, maize and field bean. From the interphase to prophase and metaphase of mitosis, the fibers were basically similar. Each was estimated to be around 200 nm in diameter, but the strength of signals was not the same along the fiber length. Through the cell cycle a series of dynamic distribution changes occurred in the fibers. In the interphase, they were unraveled. At the early prophase they were arranged with parallel and mirror symmetry. During late-prophase and metaphase, the fibers were bundled and became different visible chromosomes. The parallel coiling and mirror symmetry structures were visible clearly until the metaphase. In anaphase they disappeared. During telophase, in peripheral regions of congregated chromosome group, borderlines of the chromosomes disappeared and the fibers were unraveled. This demonstrated that mitotic chromosomes are assembled and organized by parallel and adjacent coiling of the fibers and the fibers should be the highest order structure for DNA coiling.
Jing-Yu LiuChao-Wen SheZhong-Li HuFen LiYing DiaoLi-Hua LiuYun-Chun Song
关键词:INTERPHASE
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