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Human Genomics|June 9, 2019
Evidence that DNA repair genes, a family of tumor suppressor genes, are associated with evolution rate and size of genomesKonstantinos Voskarides, Harsh Dweep, Charalambos ChrysostomouHuman Genomics|July 11, 2019
Essential genetic findings in neurodevelopmental disordersAna R Cardoso, Mónica Lopes-Marques, Raquel M Silva, et al.Human Genomics|September 17, 2018
Architecture of polymorphisms in the human genome reveals functionally important and positively selected variants in immune response and drug transporter genesYu Jin, Jingbo Wang, Maulana Bachtiar, et al.Human Genomics|July 6, 2019
A novel knowledge-derived data potentizing method revealed unique liver cancer-associated genetic variantsNaznin Sultana, Mijanur Rahman, Sanat Myti, et al.Human Genomics|June 28, 2017
Development and validation of a variant detection workflow for BRCA1 and BRCA2 genes and its clinical application based on the Ion Torrent technologyAna Lígia Buzolin, Caroline Mônaco Moreira, Patricia Rossi Sacramento, et al.Human Genomics|April 24, 2021
Cathelicidin antimicrobial peptide (CAMP) gene promoter methylation induces chondrocyte apoptosisGuoliang Wang, Yanlin Li, Guang Yang, et al.Human Genomics|April 2, 2023
Integrative analysis of a novel super-enhancer-associated lncRNA prognostic signature and identifying LINC00945 in aggravating glioma progressionZhihao Yang, Yinfei Zheng, Haoyuan Wu, et al.Human Genomics|April 2, 2023
Allelic phenotype prediction of phenylketonuria based on the machine learning methodYang Fang, Jinshuang Gao, Yaqing Guo, et al.Human Genomics|March 29, 2023
In silico prioritisation of microRNA-associated common variants in multiple sclerosisIfeolutembi A Fashina, Claire E McCoy, Simon J FurneyHuman Genomics|April 13, 2021
Targeted exome sequencing identifies mutational landscape in a cohort of 1500 Chinese patients with non-small cell lung carcinoma (NSCLC)Ya-Jun Zhou, Wei Zheng, Qing-Hua Zeng, et al.Pageof 111