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17篇 您的检索式：作者名="MENGESHA E"

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		题名	作者	年代	出处	被引量
	1	Upper gastrointestinal endoscopy: a review of 10000 cases 显示文摘	Taye M Kassa E Mengesha B	2004	Ethiop Med J2004，42，2：	1
	2	Upper gastroin_testinal endoscpy:a review of 10 000 cuses显示文摘	Taye M kassa E Mengesha B	2004	E thiop Med2004，42，2：	1
	3	Telomerase shortening and decreased replicative potential,contrasted by continued proliferation of telomerase-positive CD8+CD28(lo)T cells in patients with systemic lupus erythematosus显示文摘	Honda M Mengesha E Albano S Nichols WS Wallace DJ Metzger A	2001	Clin Immunol2001，99，2：	1
	4	Phenotype of non--syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modif- ying enzymes MTO1 and GTPBP3显示文摘	Bykhovskaya Y Mengesha E Wang D	2004	Mol Genet Metab2004，83，：	1
	5	Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation显示文摘	Bykhovskaya Y Mengesha E Wang D	2004	Molecular Genetics and MetaSolism2004，82，1：	1
	6	Missense mutation in pseudouridine synthase 显示文摘	Bykhovskaya Y Casas K Mengesha E	2004	Am J Hum Genet2004，74，6：	1
	7	Telomere shorting and decreased replicativepotential,contrasted by continued proliferation of telomerase-positive CD8+CD28lo T cellsin patients with systemic lupus erythematosus 显示文摘	HONDA M MENGESHA E ALBANO S	2001	Clin Immounol2001，99，2：	1
	8	Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3显示文摘	MENGESHA E WANG D	2004	Mol Genet Metab2004，83，：	1
	9	Human MTFB1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation显示文摘	MENGESHA E WANG D	2004	Mol Genet Metab2004，82，：	1
	10	Human mito- chondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation 显示文摘	Bykhovskaya Y Mengesha E Wang D	2004	Mol Genet Metab2004，82，1：	1
	11	Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modif- ying enzymes MTO1 and GTPBP3 显示文摘	Bykhovskaya Y Mengesha E Wang D	2004	Mol Genet Metab2004，83，3：	1
	12	Telomere shortening and decreassed replicative potentail, contrasted by contimued proliferation of telcomerasepositive CD8+ CD28(lo) T cells in patients with systemic lupus erythematosus显示文摘	Mengesha E Albano S	2001	Clini Immunol2001，99，2：	1
	13	Missense mutation inpseudouridine synthase 1 (PUSl) causes mitochondrial myopathy andsideroblastic anemia (MLASA)显示文摘	Bykhovskaya Y Casas K Mengesha E	2004	AmJ Hum Genet2004，74，6：	1
	14	Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1and GTPBP3显示文摘	Bykhovskaya Y Mengesha E Wang D	2004	Molecular Genetics&Metabolism2004，83，：	1
	15	Human mitochondrial transcription factor B1as a modifler gene for hearing loss associated with the mitochondrial A1555G mutation显示文摘	Bykhovskaya Y Mengesha E Dai W	2004	Molecular Genetics&Metabolism2004，82，：	1
	16	Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deaf-ness-associated mitochondrial 12S ribosomal RNA mutations显示文摘	Guan M-X Yan Q Li X Bykhovskaya Y Gallo-Teran J Hajek P Umeda N Zhao H Garrido G Mengesha E Suzuki T del Castillo I		0，，：	1
	17	Metabolic and cardiovasculargenes in polycystic ovary syndrome:a candidate-wideassociation study(CWAS)显示文摘	Jones M R Chua A K Mengesha E A Taylor K D Chen Y D Li X	2012	Steroids2012，77，：	1

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