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Genetic Testing and Molecular Biomarkers|April 12, 2018
Personalized Dosing of Dichloroacetate Using GSTZ1 Clinical Genotyping AssayTaimour Langaee, Richard Wagner, Lloyd P Horne, et al.
Genetic Testing and Molecular Biomarkers|April 12, 2018
Deiodinases, Organic Anion Transporter Polypeptide Polymorphisms, and Thyroid Hormones in Patients with Myocardial InfarctionJulija Brozaitiene, Daina Skiriute, Julius Burkauskas, et al.
Genetic Testing and Molecular Biomarkers|April 12, 2018
Association of RETN and CAP1 SNPs, Expression and Serum Resistin Levels with Breast Cancer in Mexican WomenAlejandrina Muñoz-Palomeque, Miguel Angel Guerrero-Ramirez, Lidia Ariadna Rubio-Chavez, et al.
Genetic Testing and Molecular Biomarkers|January 12, 2010
Easy, rapid, and cost-effective methods for identifying carriers of recurrent GJB2 mutations causing nonsyndromic hearing impairment in the Greek populationHaris Kokotas, Maria Grigoriadou, Angeliki Hatzaki, et al.
Genetic Testing and Molecular Biomarkers|January 12, 2010
A c.1363C>T (p.R455X) nonsense mutation of RB1 gene in a southern Chinese retinoblastoma pedigreeChun-Yue Chen, Chen-Ming Xu, Zhen-Fang Du, et al.
Genetic Testing and Molecular Biomarkers|January 12, 2010
Mutation Analysis and Prenatal Exclusion of Fibrodysplasia Ossificans Progressiva in a Chinese FetusJuan Du, Ling-Li Huang, Yue-Qiu Tan, et al.
Genetic Testing and Molecular Biomarkers|January 16, 2010
Distribution of glutathione S-transferase T1 and M1 genes polymorphisms in North East Indians: a potential reportRegina Devi Thoudam, Dhirendra Singh Yadav, Ashwani Kumar Mishra, et al.
Genetic Testing and Molecular Biomarkers|May 4, 2018
High Expression of PLOD1 Drives Tumorigenesis and Affects Clinical Outcome in Gastrointestinal CarcinomaDazhi Wang, Shuyu Zhang, Fufeng Chen
Genetic Testing and Molecular Biomarkers|May 30, 2018
Knockdown of LncRNA-XIST Suppresses Proliferation and TGF-β1-Induced EMT in NSCLC Through the Notch-1 Pathway by Regulation of miR-137Xi Wang, Guojun Zhang, Zhe Cheng, et al.
Genetic Testing and Molecular Biomarkers|May 29, 2009
A novel mutation (C1425Y) in the FBN2 gene in a father and son with congenital contractural arachnodactylyYing Chen, Yun-Ping Lei, Hong-Xiang Zheng, et al.
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