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Oncology Reports|June 8, 2019
Bile cell‑free DNA as a novel and powerful liquid biopsy for detecting somatic variants in biliary tract cancerNingjia Shen, Dadong Zhang, Lei Yin, et al.Frontiers in Medicine|June 12, 2023
Evaluation of safety and efficacy of inhaled ambroxol in hospitalized adult patients with mucopurulent sputum and expectoration difficultyZeguang Zheng, Kai Yang, Ni Liu, et al.Frontiers in Oncology|June 2, 2020
Co-Occurring Alterations of ERBB2 Exon 20 Insertion in Non-Small Cell Lung Cancer (NSCLC) and the Potential Indicator of Response to AfatinibBo Yuan, Jun Zhao, Chengzhi Zhou, et al.Biorxiv : the Preprint Server for Biology|May 20, 2024
Fast, Accurate, and Versatile Data Analysis Platform for the Quantification of Molecular Spatiotemporal SignalsXuelong Mi, Alex Bo-Yuan Chen, Daniela Duarte, et al.Cancer Genetics|February 22, 2025
Anaplastic meningioma in a 6-year-old with somatic YAP1::MAML2 fusion and multiple endocrine neoplasia type 4 (MEN4) syndromeLauren R Desrosiers-Battu, John H Lee, Izabela Tarasiewicz, et al.Journal of Medical Genetics|September 23, 2022
Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequencesWeimin Bi, Bo Yuan, Pengfei Liu, et al.Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approachArchana Rai, Jonathan Klonowski, Bo Yuan, et al.Proceedings of the National Academy of Sciences of the United States of America|November 15, 2007
Dandruff-associated Malassezia genomes reveal convergent and divergent virulence traits shared with plant and human fungal pathogensJun Xu, Charles W Saunders, Ping Hu, et al.American Journal of Human Genetics|June 21, 2025
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approachArchana Rai, Jonathan Klonowski, Bo Yuan, et al.Nucleic Acids Research|December 17, 2016
Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohortTomasz Gambin, Zeynep C Akdemir, Bo Yuan, et al.Pageof 147