Gao K - Search Results

1

A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia.

Gao K, Tankovic A, Zhang Y, Kusumoto H, Zhang J, Chen W, XiangWei W, Shaulsky GH, Hu C, Traynelis SF, Yuan H, Jiang Y. Gao K, et al. PLoS One. 2017 Feb 9;12(2):e0170818. doi: 10.1371/journal.pone.0170818. eCollection 2017. PLoS One. 2017. PMID: 28182669 Free PMC article.

2

SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability.

Kong W, Zhang Y, Gao Y, Liu X, Gao K, Xie H, Wang J, Wu Y, Zhang Y, Wu X, Jiang Y. Kong W, et al. Among authors: gao y, gao k. Epilepsia. 2015 Mar;56(3):431-8. doi: 10.1111/epi.12925. Epub 2015 Feb 26. Epilepsia. 2015. PMID: 25785782 Free article.

3

Different Eukaryotic Initiation Factor 2Bε Mutations Lead to Various Degrees of Intolerance to the Stress of Endoplasmic Reticulum in Oligodendrocytes.

Chen N, Jiang YW, Hao HJ, Ban TT, Gao K, Zhang ZB, Wang JM, Wu Y. Chen N, et al. Among authors: gao k. Chin Med J (Engl). 2015 Jul 5;128(13):1772-7. doi: 10.4103/0366-6999.159353. Chin Med J (Engl). 2015. PMID: 26112719 Free PMC article.

4

De novo KCNMA1 mutations in children with early-onset paroxysmal dyskinesia and developmental delay.

Zhang ZB, Tian MQ, Gao K, Jiang YW, Wu Y. Zhang ZB, et al. Among authors: gao k. Mov Disord. 2015 Aug;30(9):1290-2. doi: 10.1002/mds.26216. Epub 2015 Jul 21. Mov Disord. 2015. PMID: 26195193 No abstract available.

5

Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental Disabilities.

Zhang Y, Kong W, Gao Y, Liu X, Gao K, Xie H, Wu Y, Zhang Y, Wang J, Gao F, Wu X, Jiang Y. Zhang Y, et al. Among authors: gao f, gao y, gao k. PLoS One. 2015 Nov 6;10(11):e0141782. doi: 10.1371/journal.pone.0141782. eCollection 2015. PLoS One. 2015. PMID: 26544041 Free PMC article.

6

Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy.

Ge L, Liu A, Gao K, Du R, Ding J, Mao B, Hua Y, Zhang X, Tan D, Yang H, Fu X, Fan Y, Zhang L, Song S, Wu J, Zhang F, Jiang Y, Wu X, Xiong H. Ge L, et al. Among authors: gao k. Sci Rep. 2018 Oct 9;8(1):14989. doi: 10.1038/s41598-018-33098-3. Sci Rep. 2018. PMID: 30301903 Free PMC article.

7

Large De Novo Microdeletion in Epilepsy with Intellectual and Developmental Disabilities, with a Systems Biology Analysis.

Gao K, Zhang Y, Zhang L, Kong W, Xie H, Wang J, Wu Y, Wu X, Liu X, Zhang Y, Zhang F, Yu AC, Jiang Y. Gao K, et al. Adv Neurobiol. 2018;21:247-266. doi: 10.1007/978-3-319-94593-4_9. Adv Neurobiol. 2018. PMID: 30334225

8

Modeling vanishing white matter disease with patient-derived induced pluripotent stem cells reveals astrocytic dysfunction.

Zhou L, Li P, Chen N, Dai LF, Gao K, Liu YN, Shen L, Wang JM, Jiang YW, Wu Y. Zhou L, et al. Among authors: gao k. CNS Neurosci Ther. 2019 Jun;25(6):759-771. doi: 10.1111/cns.13107. Epub 2019 Feb 5. CNS Neurosci Ther. 2019. PMID: 30720246 Free PMC article.

9

The absence of NIPA2 enhances neural excitability through BK (big potassium) channels.

Liu NN, Xie H, Xiang-Wei WS, Gao K, Wang TS, Jiang YW. Liu NN, et al. Among authors: gao k. CNS Neurosci Ther. 2019 Aug;25(8):865-875. doi: 10.1111/cns.13119. Epub 2019 Mar 20. CNS Neurosci Ther. 2019. PMID: 30895737 Free PMC article.

10

Reanalysis of whole exome sequencing data in patients with epilepsy and intellectual disability/mental retardation.

Li J, Gao K, Yan H, Xiangwei W, Liu N, Wang T, Xu H, Lin Z, Xie H, Wang J, Wu Y, Jiang Y. Li J, et al. Among authors: gao k. Gene. 2019 Jun 5;700:168-175. doi: 10.1016/j.gene.2019.03.037. Epub 2019 Mar 21. Gene. 2019. PMID: 30904718

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