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30篇 您的检索式：作者名="Wollnik"

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	题名	作者	年代	出处	被引量
1	Ion optics in mass spectrometers 显示文摘	WOLLNIK H	1999	Journal of Mass Spectrometry1999，34，：	1
2	Activation and inactivation of homomeric KvLQT1 potassium channels显示文摘	Pusch M Magrassi R Wollnik B	1998	Biophys J1998，75，：	1
3	Homozygous and heterozygous inheritance of PAX3 mutations causes diffeent types of Waardenburg syndrome显示文摘	Wollnik B Tukel T Uyguner O	2003	Am J Med Genet A2003，122，1：	1
4	Time-of-flight mass analyzers显示文摘	WOLLNIK H	1993	Mass Spectrom Rev1993，12，：	1
5	Differential mobility separation of ions using a rectangular asymmetric waveform 显示文摘	Papanastasiou D Wollnik H Rico G	2008	Journal of Physical Chemistry2008，112，16：	1
6	The time-of-flight isochronous (TOFI) spectrometer for direct mass measurements of exotic light nuclei显示文摘	WOUTERS J M WIEIRA D J WOLLNIK H	1987	Nucl Instrum Methods Phys Res1987，26，：	1
7	Differential mobility separation of ions using a rectangular asymmetric waveform显示文摘	PAPANASTASIOU D WOLLNIK H RICO G	2008	Journal of Physical Chemistry:A2008，112，16：	1
8	Differential mobility separation of ions using a rectangular asymmetric waveform 显示文摘	PAPANASTASIOU D WOLLNIK H RICO G	2008	Journal of Physical Chemistry2008，112，16：	1
9	Particle trajectories in a toroidal condenser calculated in a third order approximation显示文摘	Matsuo T Matsuda H Wollnik H	1972	Nuclear Instruments and Methods1972，103，3：	1
10	Timing of torpor bouts during hibernation in Europer hamsters (Cricetus cricetus L) 显示文摘	WABMER T WOLLNIK F	1997	J Comp Phisiol B1997，167，4：	1
11	Homozygous and heterozygous inheritance of P AX3 mutations causes different types of Waardenburg syndrome显示文摘	Wollnik B Tukel T Uyguner 0	2003	Am J Med Genet A2003，122，：	1
12	Differential Mobility Separation of Ions Using a Rectangular Asymmetric Waveform显示文摘	Papanastasiou D Wollnik H Rico G	2008	Journal of Physical Chemistry A2008，112，：	1
13	Activation and in- activation of homomeric KvLQT1 Potassium channels 显示文摘	Pusch M Magrassi R Wollnik B	1998	Biophys J1998，75，2：	1
14	Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta显示文摘	Becker J Semler O Gilissen C Li Y Bolz HJ Giunta C Bergmann C Rohrbach M Koerber F Zimmermann K de Vries P Wirth B Schoenau E Wollnik B Veltman JA Hoischen A Netzer C		0，，：	1
15	A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteo-genesis imperfecta type V with hyperplastic callus显示文摘	Semler O Garbes L Keupp K Swan D Zimmermann K Becker J Iden S Wirth B Eysel P Koerber F Schoenau E Bohlander SK Wollnik B Netzer C		0，，：	1
16	Homozygous and heterozygous inheritance of PAX3 mutations caused different types of waardenburgsyndrome显示文摘	Wollnik B Tukel T Uyguner O	2003	Am J Med Genet A2003，122，：	1
17	Differential mobility separation of ions using a rectangular asymmetric waveform 显示文摘	Papanastasiou D Wollnik H Rico G	2008	J Phys Chem A2008，112，16：	1
18	Effect of three different media on serum free culture of donor corneas and isolated human corneal endothelial cells显示文摘	Bednarz J Doubilei V Wollnik PC	2001	Br J Ophthalmol2001，85，12：	1
19	Activation and inactivation of homomeric KVLQT1 potassium channels 显示文摘	Pusch M Magrassi R Wollnik B	1998	Biophys1998，75，2：	1
20	Pathophysiologieal mech-anisms of dominant and recessive KVLQT1 K^+ channel mutations foundin inherited cardiac arrhythmias显示文摘	Wollnik B Sehroeder BC Kabisch C	1997	Hum Mol Genet1997，6，：	1

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