Search Results - "Medical genetics

Individualized medication based on pharmacogenomics and treatment progress in children with IgAV nephritis by Xuerong Yang, Xuerong Yang, Qi Li, Qi Li, Yuanyuan He, Yuanyuan He, Yulian Zhu, Rou Yang, Rou Yang, Xiaoshi Zhu, Xi Zheng, Xi Zheng, Wei Xiong, Yong Yang, Yong Yang

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Chapter 1 Introduction The biolinguistic program: a new beginning by Fujita, Koji

Subjects: “…Genetics (non-medical) bicssc…”
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Chapter 1 Introduction The biolinguistic program: a new beginning by Fujita, Koji

Subjects: “…Genetics (non-medical) bicssc…”
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OAPEN Library: description of the publication

Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: Efficient identification of known microduplications and identification of a nov... by Reichert Jennifer G, Nakamine Alisa, Cohen Ninette, Goldsmith Juliet E, Edelmann Lisa, Cai Guiqing, Hoffman Ellen J, Zurawiecki Danielle M, Silverman Jeremy M, Hollander Eric, Soorya Latha, Anagnostou Evdokia, Betancur Catalina, Buxbaum Joseph D

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Acquired Cold Urticaria vs. Autoinflammatory Diseases, Genetic and Clinical Profile and Differential Diagnosis: Study of a Cohort of Patients in a Tertiary Reference Centre by Gustavo Deza, Anna Mensa-Vilaró, Alvaro March-Rodriguez, Silvia Sánchez, Ramon M. Pujol, Juan I. Aróstegui, Ana M. Giménez-Arnau

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An extension to a statistical approach for family based association studies provides insights into genetic risk factors for multiple sclerosis in the <it>HLA-DRB1 </it>gene by Sadovnick A Dessa, Dyment David A, McMahon Roisin, Ramagopalan Sreeram V, Ebers George C, Wittkowski Knut M

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Genetic associations in community context: a mixed model approach identifies a functional variant in the RBP4 gene associated with HDL-C dyslipidemia by Erfan Aref-Eshghi, Oliver Hurley, Guang Sun, Alvin Simms, Marshall Godwin, Pauline Duke, Mehdee Araee, Masoud Mahdavian, Shabnam Asghari

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Myeloid Leukemia

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The genetically modified human foreskin fibroblast cell line (YhFF#8) stably expressing Cas9 gene: A lab resource report by Farzad Soheilipour, Sohrab Boozarpour, Shiva Aghaei, Ehsan Farashahi Yazd

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Identification of a novel SDHB c.563 T > C mutation responsible for Paraganglioma syndrome and genetic analysis of the SDHB gene in China: a case report by Heye Chen, Wei Yao, Qing He, Xuefang Yu, Bo Bian

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The effect of 'cytochrome P-450 2C9' and 'vitamin K epoxide reductase complex 1' genetic polymorphism upon oral anticoagulation requirements by Hossam Y.K Mohammed, Yousry Z Al-Zohairy, Mahmoud Abd El-Latif Hashish

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Data integration from two microarray platforms identifies bi-allelic genetic inactivation of <it>RIC8A </it>in a breast cancer cell line by Kleivi Kristine, Wolf Maija, Edgren Henrik, Muggerud Aslaug, Dejeux Emelyne, Tost Jörg, Sørlie Therese, Kallioniemi Olli

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Genetic analysis of RNF213 p.R4810K variant in non-moyamoya intracranial artery stenosis/occlusion disease in a Chinese population by Tong Zhang, Congrong Guo, Xin Liao, Jian Xia, XiaoXiao Wang, Jing Deng, Junxia Yan

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Genetic variants in <it>LPL</it>, <it>OASL </it>and <it>TOMM40/APOE-C1-C2-C4 </it>genes are associated with multiple cardiovascular-related traits by Madden Pamela AF, Heath Andrew C, Henders Anjali K, Ferreira Manuel AR, Middelberg Rita PS, Montgomery Grant W, Martin Nicholas G, Whitfield John B

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<it>PNPLA 3</it> I148M genetic variant associates with insulin resistance and baseline viral load in HCV genotype 2 but not in genotype 3 infection by Rembeck Karolina, Maglio Cristina, Lagging Martin, Christensen Peer, Färkkilä Martti, Langeland Nina, Buhl Mads, Pedersen Court, Mørch Kristine, Norkrans Gunnar, Hellstrand Kristoffer, Lindh Magnus, Pirazzi Carlo, Burza Maria, Romeo Stefano, Westin Johan

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Analysis of genetic networks regulating refractive eye development in collaborative cross progenitor strain mice reveals new genes and pathways underlying human myopia by Tatiana V. Tkatchenko, Rupal L. Shah, Takayuki Nagasaki, Andrei V. Tkatchenko

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Genetic and bioinformatic analyses of the expression and function of PI3K regulatory subunit PIK3R3 in an Asian patient gastric cancer library by Zhou Jin, Chen Geng, Tang Yew, Sinha Rohit, Wu Yonghui, Yap Chui, Wang Guihua, Hu Junbo, Xia Xianmin, Tan Patrick, Goh Liang, Yen Paul

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Genetic polymorphisms of GGT1 gene (rs8135987, rs5751901 and rs2017869) are associated with neoadjuvant chemotherapy efficacy and toxicities in breast cancer patients by Lu Sun, Ziping Wu, Yanping Lin, Shuguang Xu, Yumei Ye, Wenjin Yin, Liheng Zhou, Jingsong Lu

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Clinicopathological and genetic characterization of radiotherapy-induced undifferentiated pleomorphic sarcoma following breast cancer: a case series of three tumors and comprehensi... by Ting Lei, Zhiyi Shen, Mengjia Shen, Lingfang Du, Yongqiang Shi, Yan Peng, Zidi Zhou, Wenyue Da, Xi Chen, Qing Li

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Epigenetic loci for blood pressure are associated with hypertensive target organ damage in older African Americans from the genetic epidemiology network of Arteriopathy (GENOA) stu... by Minjung Kho, Wei Zhao, Scott M. Ratliff, Farah Ammous, Thomas H. Mosley, Lulu Shang, Sharon L. R. Kardia, Xiang Zhou, Jennifer A. Smith

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