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18篇 您的检索式：作者名="Pusch CM"

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		题名	作者	年代	出处	被引量
	1	Ten novel ORF15 mutations confirm mutational hot spot in the RPGR gene in European patients with X-linked retinitis pigmentosa显示文摘	Pusch CM Broghammer M Jurklies B Besch D Jacobi FK	2002	Hum Mutat2002，20，5：	1
	2	Cytokineregulation of the trefoil factor family binding proteinGKN2 (GDDR/TFIZl/blottin) in human gastrointestinalepithelial cells显示文摘	Baus-Loncar M Lubka M Pusch CM	2007	Cell Physiol Biochem2007，20，14：	1
	3	The complete form of X- linked congenital stationary night blindness is caused by muta- tions in a gene encoding a leucine-rich repeat protein显示文摘	Pusch CM Zeitz C Brandau O	2000	Na- ture Genetics2000，26，3：	1
	4	Ten novel ORF15 mutations confirm mutational hot spot in the RPGR gene in European patients with X-linked retinitis pigmentosa显示文摘	BROGHAMMER M JURKLIES B	2002	Hum Mutat2002，20，5：	1
	5	Cytokine regulation of the trefoil factor family binding protein GKN2(GDDK/TFIZ1/blottin)in human gastrointestinal epithelial cells显示文摘	Baus-Loncar M Lubka M Pusch CM	2007	Cell Physiol Biochem2007，20，14：	1
	6	Cytokine regulation of the trefoil factor family binding protein GKN2(GDDR/TFIZ1/blottin)in human gastrointestinal epithelial cells显示文摘	Baus-Loncar M Lubka M Pusch CM		0，，：	1
	7	Cytokine regulation of the trefoil factor family binding protein GKN2 (GDDR/TFIZ1/ blottin) in human gastrointestinal epithelial ceils显示文摘	Bans-Loncar M Lubka M Pusch CM	2007	Cell Physiol Biochem2007，20，14：	1
	8	PCR-induced sequence alterations hamper the typing of prehistoric bone samples for diagnostic achondroplasia mutations 显示文摘	Pusch CM Broghammer M Nicholson GJ	2004	Mol Biol Evol2004，21，4：	1
	9	Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene 显示文摘	Scholl HPN Langrova H Pusch CM	2001	Invest Ophthalmol Vis Sci2001，42，：	1
	10	Spiking of contemporary human template DNA with ancient DNA extracts induces mutations under PCR and generates nonauthentic mitochondrial sequences 显示文摘	Pusch CM Bachmann L	2004	Mol Biol Evol2004，21，5：	1
	11	Epigenetic alterations by methylation of RASSFIA and DAPK1 promoter sequences in mammary carcinoma detected in extracellular tumor DNA显示文摘	Ahmed IA Pusch CM Hamad T	2010	Cancer C enet Cytogenet2010，199，2：	1
	12	Ten novel ORF15 mutations confirm mutational hot spot in the RPGR gene in European patients with X-linked retinitis pigmentosa显示文摘	Pusch CM Broghammer M	2002	Hum Mutat2002，20，5：	1
	13	Clinical electrophysiology of two rod pathways:normative values and clinical application显示文摘	Scholl HP Langrova H Pusch CM	2001	Graefe''s Arch Clin Exp Ophthalmol2001，239，2：	1
	14	Slow and fast rod ERG pathway in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene显示文摘	Scholl HP Langrova H Pusch CM	2001	Invest Ophthalmol Vis Sci2001，42，11：	1
	15	The complete form of X-linked congenital stationary night blindness is ca used by mutations in a gene encoding a leucine-rich repeat protein 显示文摘	Pusch CM Zeitz C Brandau O Pesch K Achatz H Feil S Scharfe C Maurer J Jacobi FK Pinckers A Andreasson S Hardcastle A Wissinger B Berger W Meind l A	2000	Nat Genet2000，26，3：	1
	16	Epigenetic alterations by methylation of RASSF1A and DAPK1 promoter sequences in mammary carcinoma detected in extracellular tumor DNA显示文摘	Ahmed IA Pusch CM Hamed T	2010	Cancer Genet Cytogenet2010，199，2：	1
	17	Epigenetic altera- tions by methylation of RASSF1A and DAPK1 promoter sequences in manmary carcinoma detected in extracellular tumor DNA显示文摘	Ahmed IA Pusch CM Hamed T	2010	Cancer Genet Cytogenet2010，199，2：	1
	18	Quantitation of heteroplasmy in mitochondrial DNA mutations by primer extension using VentR (exo-) DNA polymerase and RFLP analysis显示文摘	Jacobi FK Meyer J Pusch CM	2001	Mutation Research2001，478，：	1

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