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31篇 您的检索式：作者名="Pulst"

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	题名	作者	年代	出处	被引量
1	Alternative transcripts in the mouse neurofibromatosis type 2 (NF2)gene are conserved and code for schwannomins with distinct C-terminal domains 显示文摘	Huynh DP Nechiporuk T Pulst SM	1994	Hum Mo Genet1994，3，7：	1
2	MoleculaRdefinition of a re-gion of chromosome 21 that causesfeaturesofthe Down syndrome phenotype显示文摘	KAWASHIMAH PULST SM	1990	Am J Hum Genet1990，47，2：	1
3	Neurogenetics:single gene disorders显示文摘		2003	J Neurol Neurosurg Psychiatry2003，74，12：	1
4	Moderate expansion of a nomally biallelic trinucleotide repeat in spinocerebellar ataxia type2 显示文摘	Pulst SM Neehiporuk A Neehiporuk T	1996	Nat Genet1996，14，：	1
5	Moderate expansion of a normary bialletc trinucleotide repeat in spinocerebellar ataxia type 2显示文摘	Pulst SM Nechiporuk A Nechiporuk T	1996	Nat Genet1996，14，：	1
6	Molecular definition of a region of chromo-somal 21 that causes features of the Down syndrome phenotype显示文摘	Korenberg JR Kawashima H Pulst SM	1990	Am J Hum Genet1990，47，：	1
7	Familial multisystem degenera-tion with parkinsonism associated with the 11778 mitochondrial DNAmutation显示文摘	Simon DK Pulst SM Sutton JP	1999	Neurology1999，53，：	1
8	Dystonia-associated forms of torsinA are deficient in ATPase activity显示文摘	Konakova M Pulst SM	2005	J Mol Neurosci2005，25，1：	1
9	Molecular definition of a re-gion of chromosome 21 that causesfeaturesofthe Down syndrome phenotype显示文摘	Korenberg JR KawashimaH Pulst SM	1990	Am J Hum Genet1990，47，2：	1
10	Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2显示文摘	Pulst SM Nechiporuk A Nechiporuk T	1996	Nat Genet1996，14，：	1
11	Generation and characterization of Sca2 (ataxin-2) knockout mice显示文摘	Tim-Rasmus Kiehl Alex Nechiporuk Karla P. Figueroa Mark T. Keating Duong P. Huynh Stefan-M. Pulst	2005	Biochemical and Biophysical Research Communications2005，，1：	1
12	The effect of selective REM- sleep deprivation on the consolidation and affective evaluation of emo- tional memories显示文摘	Wiesner CD Pulst J Krause F	2015	Neurobiol Learn Mere2015，122，：	1
13	Molecular definition of a re-gion of chromosome 21 that causesfeaturesofthe Down syndrome phenotype显示文摘	Korenberg JR KawashimaH Pulst SM		0，，02：	1
14	Proteasome inhibition triggers activity-dependent increase in the size of the recycling vesicle pool in cultured hippocampal neurons 显示文摘	Willeumier K Pulst S M Schweizer F E	2006	J Neurosci2006，26，11：	1
15	Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation显示文摘	Simon DK Pulst SM Sutton JP	1999	Neurology1999，53，8：	1
16	Mloecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype显示文摘	KOR ENBERG JR KAWASHIMAH PULST SM	1990	Am J Hum Genet1990，47，2：	1
17	Effects of NF2 missense mutations on schwannomin interactions显示文摘	Scoles D R Chen M Pulst S M	2002	Biochem Biophys Res Commun2002，290，1：	1
18	Response to ethanol induced ataxia between C57BL/6J and 129X1/SvJ mouse strains using a treadmill based assay 显示文摘	Hansen Stephen T Pulst Stefan M	2012	Pharmacol Biochem Behav2012，103，3：	1
19	Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype显示文摘	Korenberg JR Kawashima H Pulst SM	1990	Am J Hum Genet1990，47，：	1
20	Stablering chromo- some 21 :molecular and clinical definition of thelesion 显示文摘	Falik - Borestein TC Pribyl TM Pulst SM	1992	Am J Med Genet1992，42，1：	1

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