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20篇 您的检索式：作者名="MEISLER M H"

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	题名	作者	年代	出处	被引量
1	Sodium Channel Mutations in Epilepsy and Other Neurological Disorders 显示文摘	MEISLER M H KEARNEY J A	2005	J Clin Invest2005，115，8：	1
2	Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2显示文摘	Spampanato J Escayg A Meisler M H	2001	J Neurosci2001，21，19：	1
3	Insertional mutation of'classical' and novel genes in transgenic mice显示文摘	Meisler M H		0，，10：	1
4	De novo pathogenic SCNSA mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP显示文摘	VEERAMAH K R O'BRIEN J E MEISLER M H et 01	2012	American Journal of Human Ge- netics2012，90，3：	1
5	Sodium channel mutations in epilepsy and other neurological disorders显示文摘	Meisler M H Kearney J A	2005	J Clin Invest2005，115，8：	1
6	Identification of epilepsy genes in human and mouse显示文摘	Meisler M H Kearney J Ottman R	2001	Annu Rev Genet2001，35，1：	1
7	Defective autophagy in neurons and astrocytes from mice deficient in PI(3,5)P2显示文摘	Ferguson C J Lenk G M Meisler M H		0，，24：	1
8	Narrow-strip conjunctival autograft for treatment of pterygium显示文摘	Dupps W J Jeng B H Meisler D M	2007	Ophthalmololcy2007，114，2：	1
9	Narrow-strit conjunctival autograft for treat of pterygium显示文摘	Jr Dupps W J Jeng B H Meisler D M	2007	Ophthalmology2007，114，3：	1
10	Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS +2 显示文摘	Escayg A MacDonald B T Meisler M H	2000	Nat Genet2000，24，4：	1
11	Insertional mutation of classical and novel genes in transgenie mice 显示文摘	MEISLER M H	1992	Trends Genetics1992，8，：	1
12	Narrow-strip conjunctival autograft for treatment of pterygium显示文摘	Dupp9W J Jr Jeng B H Meisler D M	2007	Ophthalmology2007，114，2：	1
13	Evolution and diversity of mammalian sodium channel genes显示文摘	PLUMMER N W MEISLER M H	1999	Genomics1999，57，2：	1
14	Sodium channel mutations in epilepsy and other neurological disorders显示文摘	MEISLER M H KEARNEY J A	2005	J Clin Invest2005，115，8：	1
15	Hypomorphic expression of Dkk1 in the doubleridge mouse: dose dependence and compensatory interactions with Lrp6 显示文摘	Macdonald B T Adamska M Meisler M H	2004	Development2004，131，11：	1
16	Identification of epilepsy genes in human and mouse显示文摘	Meisler M H Kearney J Ottman R	2001	Annu Rev Genet2001，35，3：	1
17	Insertional mutation of classical and novel genes in transgenic mice显示文摘	MEISLER M H	1992	Trends Genetics1992，8，：	1
18	De Novo Pathogenic SCNSA Mutation Identified by Whole-Genome Sequencing of a Family Quartet Af- fected by Infantile Epileptic Encephalopathy and SUDEP显示文摘	VEERAMAH K R OBRIEN J E MEISLER M H	2012	AmJ HumGenet2012，90，：	1
19	Effects of insulin on gene transcription显示文摘	MEISLER M H HOWARD G	1989	Annual Reviews of Physiology1989，51，：	1
20	Mutations of SCNIA, encoding a neuronal sodium channel in two families with GEFS-k 2 显示文摘	Escayg A MacDonald BT Meisler M H	2000	Nat Genet2000，24，4：	1

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