نتایج جستجو برای: cdkl5

تعداد نتایج: 205  

Journal: :Cell 2016
Ryan N. Doan Byoung-Il Bae Beatriz Cubelos Cindy Chang Amer A. Hossain Samira Al-Saad Nahit M. Mukaddes Ozgur Oner Muna Al-Saffar Soher Balkhy Generoso G. Gascon Marta Nieto Christopher A. Walsh

Comparative analyses have identified genomic regions potentially involved in human evolution but do not directly assess function. Human accelerated regions (HARs) represent conserved genomic loci with elevated divergence in humans. If some HARs regulate human-specific social and behavioral traits, then mutations would likely impact cognitive and social disorders. Strikingly, rare biallelic poin...

2016
Tianyun Wang Hui Guo Bo Xiong Holly A F Stessman Huidan Wu Bradley P Coe Tychele N Turner Yanling Liu Wenjing Zhao Kendra Hoekzema Laura Vives Lu Xia Meina Tang Jianjun Ou Biyuan Chen Yidong Shen Guanglei Xun Min Long Janice Lin Zev N Kronenberg Yu Peng Ting Bai Honghui Li Xiaoyan Ke Zhengmao Hu Jingping Zhao Xiaobing Zou Kun Xia Evan E Eichler

Recurrent de novo (DN) and likely gene-disruptive (LGD) mutations contribute significantly to autism spectrum disorders (ASDs) but have been primarily investigated in European cohorts. Here, we sequence 189 risk genes in 1,543 Chinese ASD probands (1,045 from trios). We report an 11-fold increase in the odds of DN LGD mutations compared with expectation under an exome-wide neutral model of muta...

2013
Lai-Wa Tam Paul T. Ranum Paul A. Lefebvre

The length of Chlamydomonas flagella is tightly regulated. Mutations in four genes-LF1, LF2, LF3, and LF4-cause cells to assemble flagella up to three times wild-type length. LF2 and LF4 encode protein kinases. Here we describe a new gene, LF5, in which null mutations cause cells to assemble flagella of excess length. The LF5 gene encodes a protein kinase very similar in sequence to the protein...

2011
Christian P. Schaaf Aniko Sabo Yasunari Sakai Jacy Crosby Donna Muzny Alicia Hawes Lora Lewis Humeira Akbar Robin Varghese Eric Boerwinkle Richard A. Gibbs Huda Y. Zoghbi

Autism spectrum disorders (ASDs) are a heterogeneous group of neuro-developmental disorders. While significant progress has been made in the identification of genes and copy number variants associated with syndromic autism, little is known to date about the etiology of idiopathic non-syndromic autism. Sanger sequencing of 21 known autism susceptibility genes in 339 individuals with high-functio...

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