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20篇 您的检索式：作者名="Meitinger"

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	题名	作者	年代	出处	被引量
1	Genome-wide association studies of atrial fibrillation: past, present, and future 显示文摘	Sinner MF Ellinor PT Meitinger T	2011	Cardiovasc Res2011，89，4：	1
2	Lack of Association Between the MEF2A Gene and Myocardial Infarction显示文摘	Wolfgang Lieb Bj?rn Mayer Inke R. K?nig Iris Borwitzky Anika G?tz Silke Kain Christian Hengstenberg Patrick Linsel-Nitschke Marcus Fischer Angela D?ring H -Erich Wichmann Thomas Meitinger Reinhold Kreutz Andreas Ziegler Heribert Schunkert Jeanette Erdmann	2008	Circulation2008，，2：	1
3	Cellulose extraction from Zoysia japonica pretreated by alumina-doped MgO in AMIMCl显示文摘	Le Liu Meiting Ju Weizun Li Yang Jiang	2014	Carbohydrate Polymers2014，，：	1
4	Developing a new grey dynamic modeling system for evaluation of biology and pollution indicators of the marine environment in coastal areas显示文摘	Xiaogang Tian Meiting Ju Chaofeng Shao Zili Fang	2011	Ocean and Coastal Management2011，，10：	1
5	Associations between calcium and vitamin D supplement use as well as their serum concentrations and subclinical cardiovascular disease phenotypes显示文摘	Inke Thiele Jakob Linseisen Christa Meisinger Sigrid Schwab Cornelia Huth Annette Peters Siegfried Perz Thomas Meitinger Florian Kronenberg Claudia Lamina Joachim Thiery Wolfgang Koenig Wolfgang Rathmann Stefan K??b Cornelia Then Jochen Seissler Barbara T	2015	Atherosclerosis2015，，2：	1
6	Single-channel color image encryption using phase retrieve algorithm in fractional Fourier domain显示文摘	Liansheng Sui Meiting Xin Ailing Tian Haiyan Jin	2013	Optics and Lasers in Engineering2013，，12：	1
7	Pantothenate kinase?associated neurodegeneration显示文摘	Hartig MB Prokisch H Meitinger T	2012	CUff Drug Targets2012，13，9：	1
8	Adolescent growth:genes,hormones and the peer group显示文摘	Hermanussen M Meitinger T Veldhuis JD	2014	Pediatr Endocrinol Rev2014，11，3：	1
9	STAT3 single-nucleotide polymorpbisms and STAT3mutations associated with hyper-IgE syndrome are not responsible for increased serum IgE serum levels in asthma families显示文摘	Wjst M Lichtner P Meitinger T		0，，03：	1
10	Wise Use of Wetlands: Current State of Protection and Utilization of Chinese Wetlands and Recommendations for Improvement显示文摘	Yanxia Wang Yong Yao Meiting Ju	2008	Environmental Management2008，，6：	1
11	Diabetes insipidus,diabetes mellitus,optic atrophy and deafness (DIDMOAD) caused by mu-tations in a novel gene (wolframin) coding for a predicted trans-membrane protein显示文摘	Strom TM Hortnagel K Hofmann S Gekeler F Scharfe C Rabl W Gerbitz KD Meitinger T		0，，：	1
12	Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate显示文摘	Mangold E Ludwig KU Birnbaum S Baluardo C Ferrian M Herms S Reutter H de Assis NA Chawa TA Mattheisen M Steffens M Barth S Kluck N Paul A Becker J Lauster C Schmidt G Braumann B Scheer M Reich RH Hemprich A Potzsch S Blaumeiser B Moebus S Krawczak M Schreiber S Meitinger T Wichmann HE Steegers-Theunissen RP Kramer FJ Cichon S Propping P Wienker TF Knapp M Rubini M Mossey PA Hoffmann P Nothen MM	2010	Nat Genet2010，42，：	1
13	Vitreous-induced modulation of integrins in retinal pigment epithelial cells:Effects of fibroblast growth factor-2显示文摘	Meitinger D Hunt DM Shih DT	2001	Exp Eye Res2001，73，：	1
14	A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures显示文摘	K Schlachter U Gruber-Sedlmayr E Stogmann M Lausecker C Hotzy J Balzar E Schuh C Baumgartner J C. Mueller T Illig H E. Wichmann P Lichtner T Meitinger T M. Strom A Zimprich F Zimprich	2009	Neurology2009，，11：	1
15	An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness 显示文摘	Strom TM Nyakatura G Apfelstedt-Sylla E Hellebrand H Lorenz B Weber BH Wutz K Gutwillinger N Ruther K Drescher B Sauer C Zrenner E Meitinger T R osenthal A Meindl A	1998	Nat Genet1998，19，3：	1
16	Vascular Calcification: An Update on Mechanisms and Challenges in Treatment显示文摘	Meiting Wu Cameron Rementer Cecilia M. Giachelli	2013	Calcified Tissue International2013，，4：	1
17	Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk显示文摘	Rivera A Fisher SA Fritsche LG Keilhauer CN Lichmer P Meitinger T	2005	Hum Mol Genet2005，14，21：	1
18	Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins显示文摘	Meindl A Berger W Meitinger T	1992	Nat Genet1992，2，2：	1
19	A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures显示文摘	K Schlachter U Gruber-Sedlmayr E Stogmann M Lausecker C Hotzy J Balzar E Schuh C Baumgartner J C. Mueller T Illig H E. Wichmann P Lichtner T Meitinger T M. Strom A Zimprich F Zimprich	2009	Neurology2009，，11：	1
20	Age-related macular degeneration and functional promoter and coding variants of the apolipoprotein E gene显示文摘	Fritsche LG Freitag-Wolf S Bettecken T Meitinger T Keilhauer CN Krawczak M		0，，07：	1

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