Showing results (241-250 of 266) with videos related to
Sort By:
Pageof 27
Scientific Reports|February 10, 2021
Identification of epigenetic memory candidates associated with gestational age at birth through analysis of methylome and transcriptional dataKohei Kashima, Tomoko Kawai, Riki Nishimura, et al.Genes, Chromosomes & Cancer|June 3, 2022
Quantitative assessment of copy number alterations by liquid biopsy for neuroblastomaRyota Shirai, Tomoo Osumi, Aiko Sato-Otsubo, et al.Pediatric Diabetes|June 10, 2017
Comprehensive screening for monogenic diabetes in 89 Japanese children with insulin-requiring antibody-negative type 1 diabetesKikumi Ushijima, Maki Fukami, Tadayuki Ayabe, et al.Genome Research|January 10, 2014
Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishmentFranck Court, Chiharu Tayama, Valeria Romanelli, et al.Molecular Biology of the Cell|April 4, 2019
The desmosome is a mesoscale lipid raft-like membrane domainJoshua D Lewis, Amber L Caldara, Stephanie E Zimmer, et al.Rheumatology (Oxford, England)|May 9, 2024
Predictive factors and treatment outcomes associated with difficult-to-treat rheumatoid arthritis conditions: the ANSWER cohort studyRyu Watanabe, Kosuke Ebina, Takaho Gon, et al.Communications Biology|October 1, 2020
Comprehensive genetic analysis of pediatric germ cell tumors identifies potential drug targetsYasuo Kubota, Masafumi Seki, Tomoko Kawai, et al.Journal of Medical Genetics|October 13, 2023
Congenital anaemia associated with loss-of-function variants in DNA polymerase epsilon 1Ichiro Takeuchi, Kanako Tanase-Nakao, Ayame Ogawa, et al.Oncogene|November 2, 2022
Identification of the ultrahigh-risk subgroup in neuroblastoma cases through DNA methylation analysis and its treatment exploiting cancer metabolismKentaro Watanabe, Shunsuke Kimura, Masafumi Seki, et al.Genetics in Medicine Open|December 13, 2024
Loss of function in <i>NSD2</i> causes DNA methylation signature similar to that in Wolf-Hirschhorn syndromeTomoko Kawai, Shiori Kinoshita, Yuka Takayama, et al.Pageof 27