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Human Genomics|May 19, 2023
A heterozygous mutation in UBE2H in a patient with developmental delay leads to an aberrant brain development in zebrafishUnbeom Shin, Yeonsong Choi, Hwa Soo Ko, et al.Human Genomics|February 23, 2023
Analysis of clinical and genomic profiles of therapy-related myeloid neoplasm in KoreaJiwon Yun, Hyojin Song, Sung-Min Kim, et al.Human Genomics|February 16, 2023
Regulon active landscape reveals cell development and functional state changes of human primary osteoblasts in vivoShengran Wang, Yun Gong, Zun Wang, et al.Human Genomics|March 21, 2023
Association of APP gene polymorphisms and promoter methylation with essential hypertension in Guizhou: a case-control studyRuichao Li, Juhui Song, Ansu Zhao, et al.Human Genomics|March 9, 2023
A crowdsourcing database for the copy-number variation of the Spanish populationDaniel López-López, Gema Roldán, Jose L Fernández-Rueda, et al.Human Genomics|February 11, 2023
SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretationJean-Madeleine de Sainte Agathe, Mathilde Filser, Bertrand Isidor, et al.Human Genomics|June 21, 2015
Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approachIoannis Karageorgos, Clint Mizzi, Efstathia Giannopoulou, et al.Human Genomics|June 12, 2020
A potential prognostic prediction model of colon adenocarcinoma with recurrence based on prognostic lncRNA signaturesLipeng Jin, Chenyao Li, Tao Liu, et al.Human Genomics|November 9, 2022
A review on the application of the exposome paradigm to unveil the environmental determinants of age-related diseasesEnmin Ding, Yu Wang, Juan Liu, et al.Human Genomics|August 22, 2021
Abnormal expression profile of plasma-derived exosomal microRNAs in patients with treatment-resistant depressionLian-Di Li, Muhammad Naveed, Zi-Wei Du, et al.Pageof 112