
By Akio Koizumi, Kazuhiro Nagata, Kiyohiro Houkin, Teiji Tominaga, Susumu Miyamoto, Shigeo Kure, Elizabeth Tournier-Lasserve
ISBN-10: 9811027102
ISBN-13: 9789811027109
ISBN-10: 9811027110
ISBN-13: 9789811027116
This booklet provides the most recent findings on organic, epidemiological, and scientific investigations of RNF213, that's considered inquisitive about many organic approaches and performs a key function in cerebro- and heart problems . through discussing the epidemiology and genetic epidemiology of the affliction with a selected specialise in the molecular functionality of RNF213, study utilizing animal versions, prognosis, remedy and medical administration around the globe, this paintings makes a precious contribution to the learn of the disease.Moyamoya disorder Explored via RNF213 is an crucial source for either starting and skilled researchers, pediatricians, neurologists, and neurosurgeons who're looking complete details on grownup and formative years stroke.
Read Online or Download Moyamoya Disease Explored Through RNF213: Genetics, Molecular Pathology, and Clinical Sciences PDF
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Extra resources for Moyamoya Disease Explored Through RNF213: Genetics, Molecular Pathology, and Clinical Sciences
Sample text
Liu Ethnicity (sample size: case/control) Chinese Han (170/507) Chinese Han (96/96) Chinese Han (139 ICASO, 146 non-ICASO/300) Author, year Wu et al. 2012 [24] Wang et al. 2013 [25] Shang et al. 1×10−15). R4810K was a good biomarker for the progression and prognosis of disease 3 Molecular Epidemiology in East Asian Countries and in the World 31 Chinese (255/300) Taiwanese (36/500) Lee et al. 2015 [29] Ethnicity (sample size: case/control) Chinese Guangxi Zhuang (52 MMD, 64 ICASO/80) Zhang et al.
These findings suggest that RNF213 p. 1) [27]. R4810K between Han [26] and Guangxi Zhuang populations with non-MMD ICASO indicates that the genetic background may be different even in different ethnic groups among Chinese population. Further genetic studies are needed to clarify the genetic etiology among different Chinese nationalities. 38 W. Liu Zhang et al. performed a genetic study to identify disease-causing mutations in MMD association genes, including RNF213, ACTA2, BRCC3, and GUCY1A3 in 255 Chinese MMD patients and 300 controls.
2016;91(9):912–7. 24441. The cerebral circulation and metabolism in hyperthyroidism and myxedema. J Clin Invest. 1954;33(11):1434–40. 1172/JCI103021. Serum miRNA signature in Moyamoya disease. PLoS One. 2014;9(8):e102382. 0102382. 49. Elevated Serum MicroRNA Let-7c in Moyamoya disease. J Stroke Cerebrovasc Dis. 2015;24(8):1709–14. 041. Goldberg AD, Allis CD, Bernstein E. Epigenetics: a landscape takes shape. Cell. 2007;128(4):635–8. 006. R4810K in the 17q25-ter region as the most important founder susceptibility gene for MMD among East Asian populations, mainly including Japanese, Korean, and Chinese.