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19篇 您的检索式：作者名="Muchir"

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		题名	作者	年代	出处	被引量
	1	Treatment with selumetinib preserves cardiac function and improves survival in cardiomyopathy caused by mutation in the lamin A/C gene 显示文摘	Muchir A Reilly SA Wu W	2012	Cardiovasc Res2012，93，2：	1
	2	Mitogen-activated protein kinase inhibitors improve heart function and prevent fibrosis in cardiomy- opathy caused by mutation in lamin A/C gene 显示文摘	Wu W Muchir A Shan J	2011	Circulation2011，123，1：	1
	3	Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMDIB) 显示文摘	Muchir A Bonne G van der Kooi A J	2000	Hum Mol Genet2000，9，：	1
	4	Mitogen-activated protein kinase inhibitors improve heart function and prevent fibrosis in cardiomyopathy caused by mutation in lamin AIC gene显示文摘	Wu W Muchir A ShanJ	2011	Circulation2011，123，1：	1
	5	Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B) 显示文摘	Muchir A Bonne G van der Kooi A J	2000	Hum Mol Genet2000，9，9：	1
	6	Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb-girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B) 显示文摘	Muchir A Bonne G van der Kooi AJ	2000	Hum Mol Genet2000，9，：	1
	7	Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C 显示文摘	Novelli G Muchir A Sangiuolo F	2002	Am J Hum Genet2002，71，2：	1
	8	Inhibition of extracellular signal- regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins显示文摘	Muchir A Shan J Bonne G	2009	Hum Mol Genet2009，18，2：	1
	9	Clinical and molecular genetic spectrum of autosomal dominant Emery -Dreifuss muscular dystrophy due to mutations of the lamin A/C gene显示文摘	Bonne G Mercuri E Muchir A	2000	Ann Neurol2000，48，：	1
	10	Identification of mutations in the gone encoding lamias A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)显示文摘	Muchir A Bonne G van der Kooi M		0，，9：	1
	11	Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C显示文摘	Novelli G Muchir A Sangiuolo F		0，，：	1
	12	Nuclear envelope alterations in fibroblasts from LGMD1B patients carrying nonsense Y259X heterozygous or homozygous mutation in lamin A/C gene显示文摘	Muchir A van Engelen B G Lammens M	2003	Exp Cell Res2003，291，：	1
	13	Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy显示文摘	Muchir A Pavlidis P Decostre V	2007	J Clin Invest2007，117，5：	1
	14	Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene 显示文摘	Bonne G Mercuri E Muchir A	2000	Ann Neurol2000，48，2：	1
	15	Mitogen-activated protein kinase inhibitor regulation of heart function and fibrosis in cardiomyopathy caused by lamin A/C gene mutation 显示文摘	Muchir A Wu W Worman HJ	2010	Trends Cardiovasc Med2010，20，7：	1
	16	Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C显示文摘	Novelli G Muchir A Sangiuolo F	2002	Am J Hum Genet2002，71，2：	1
	17	Emery-Dreifuss muscular dystrophy 显示文摘	Muchir A Worman J	2007	Curr Neurol Neurosci Rep2007，7，1：	1
	18	纯合子核纤层蛋白A/C基因无义突变的致死表型	Van Engelen B.G.M. Muchir A. Hutchison C.J. 张玉龙	2005	世界核心医学期刊文摘(神经病学分册)2005，0，6：	0
	19	核纤层蛋白A/C基因突变致肌营养不良、心肌病和部分脂代谢异常患者纤维母细胞核膜改变	Muchir A. Medioni J. Laluc M. G. Bonne 邓剑平	2005	世界核心医学期刊文摘(神经病学分册)2005，0，2：	0

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