刘奇迹教授
刘奇迹，男，1970年出生，山东寿光人。山东大学教授，博士研究生导师，医学遗传学系主任，齐鲁医学院副院长，实验畸形学教育部重点实验室副主任, 山东省医学会医学遗传与优生学会主任委员，山东省干细胞学会副会长，山东省遗传学会常务理事，中华医学会医学遗传学分会青年委员，山东省中青年重点科技人才。主要研究方向为遗传病致病基因的发现及分子机制研究。 More+
- [61] 蒋百春 , 刘巧 , 刘奇迹 , 龚瑶琴 and 李曦. X-Linked Intellectual Disability Gene CUL4B Targets Jab1/CSN5 For Degradation and Regulates Bone .... BBA-Molecular Basis of Disease, 1832, 595, 2013.
- [62] 邵常顺 , 李江夏 , 蒋百春 , 刘奇迹 and 龚瑶琴. Whole-exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic.... Hum Mutat, 36, 98, 2015.
- [63] 刘奇迹 , 陈丙玺 , 郭辰虹 , 龚瑶琴 and 邹永新. Characterization of Nuclear Localization Signal in the N Terminus of CUL4B and Its Essential Role.... Journal of biological chemistry, 284, 33320, 2009.
- [64] 龚瑶琴 , 周海滨 , 李曦 , 张锡宇 , 高贵敏 , 郭辰虹 , 陈丙玺 , 刘奇迹 and 邵常顺. Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiatio.... Exp Cell Res., 315, 2953, 2009.
- [65] 孙文杰 , 刘奇迹 , 邵常顺 and 龚瑶琴. Identification and Functional Analysis of a SLC33A1: c.339T>G (p.Ser113Arg) Variant in the Origi.... Hum Mutat, 36, 240, 2015.
- [66] 蒋百春 , 胡慧丽 , 刘奇迹 , 邵常顺 and 龚瑶琴. Zebrafish cul4a, but not cul4b, modulates cardiac and forelimb development by upregulating tbx5a .... Hum Mol Genet., 24, 853, 2015.
- [67] 庞琦 , 刘奇迹 , 姚伟 , 孙金鹏 and 于晓. Biochemical and functional studies of Lymphoid-specific tyrosine phosphatase (Lyp) variants S201F.... Plos one, 7, e43631, 2012.
- [68] 蒋百春 , 王艳 , 刘巧 , 刘奇迹 , 邵常顺 , 龚瑶琴 and 李曦. X-Linked Intellectual Disability Gene CUL4B Targets Jab1/CSN5 For Degradation and Regulates Bone .... Biochimica et Biophysica Acta-Molecular Basis of Disease, 1832, 595, 2013.
- [69] 蒋凡 , 胡慧丽 , 刘奇迹 , 龚瑶琴 and 李曦. MiR-135b-5p and MiR-499a-3p Promote Cell Proliferation and Migration in Atherosclerosis by Direct.... scientific reports, 5, 2015.
- [70] 郭辰虹 , 刘奇迹 , 陈丙玺 , 邵常顺 , 龚瑶琴 and 邹永新. Characterization of Nuclear Localization Signal in the N Terminus of CUL4B and Its Essential Role.... Journal of biological chemistry, 284, 33320, 2009.
- [71] 龚瑶琴 and 张锡宇. A locus for nonspecific X-linked mental retardation mapped to a 22.3 cM region of xp11.3-q22.3. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 129A, 286, 2004.
- [72] 李江夏 and 刘奇迹. Gene-gene interaction of ATG5, ATG7, BLK and BANK1 in systemic lupus erythematosus.. International Journal of Rheumatic Disease, 2016.
- [73] 李江夏 and 刘奇迹. 一个常染色体显性遗传并多指（趾）I型家系HOXD13基因的突变分析. 《中华医学遗传学杂志》, 32, 484, 2015.
- [74] 李江夏 , 胡琴 and 刘奇迹. ORMDL3 contributes to the risk of atherosclerosis in Chinese Han population and mediates oxidized.... scientific reports, 5, 17194, 2015.
- [75] 龚瑶琴 , 李江夏 , 刘招舰 and 刘奇迹. miR-155 Deficiency Ameliorates Autoimmune Inflammation of Systemic Lupus Erythematosus by Targeti.... Journal of Immunology, 194, 5437, 2015.
- [76] 郭辰虹 and 刘奇迹. Association of the ANTXR2 gene polymorphism and ankylosing spondylitis in Chinese Han.. Scand J Rheumatol., 41, 29, 2012.
- [77] 李江夏 , 龚瑶琴 and 刘奇迹. An intronic variant associated with systemic lupus erythematosus changes the binding affinity of .... Genes Immun., 13, 536, 2012.
- [78] 李江夏 , 郭辰虹 , 龚瑶琴 and 刘奇迹. Eight-alanine duplication in homeobox D13 in a Chinese family with synpolydactyly.. Gene, 499, 48, 2012.
- [79] 李江夏 , 龚瑶琴 and 刘奇迹. Pathogenic gene screening and mutation detection in a Chinese family with multiple osteochondroma.... Genet Test Mol Biomarkers., 16, 827, 2012.
- [80] 邵常顺 , 刘奇迹 , 李江夏 , 蒋百春 and 龚瑶琴. Whole-exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic.... Hum Mutat, 36, 98, 2015.