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International Journal of Molecular Sciences|June 19, 2024
Comparison of RNA-Sequencing Methods for Degraded RNAHiroki Ura, Yo NiidaElectrophoresis|February 27, 2008
Development of a simple and highly sensitive mutation screening system by enzyme mismatch cleavage with optimized conditions for standard laboratoriesTakanori Tsuji, Yo NiidaNo Shinkei Geka. Neurological Surgery|February 16, 2022
[Subependymal Giant Cell Astrocytoma with Tuberous Sclerosis Complex(TSC-SEGA)]Tomotsugu Ichikawa, Yo NiidaInternational Journal of Molecular Sciences|December 10, 2021
Molecular Bases of Human Malformation Syndromes Involving the SHH Pathway: GLIA/R Balance and Cardinal PhenotypesYo Niida, Sumihito Togi, Hiroki UraScientific Reports|June 22, 2022
Poly(A) capture full length cDNA sequencing improves the accuracy and detection ability of transcript quantification and alternative splicing eventsHiroki Ura, Sumihito Togi, Yo NiidaCureus|January 16, 2024
Streamlining Genetic Diagnosis With Long-Range Polymerase Chain Reaction (PCR)-Based Next-Generation Sequencing for Type I and Type II CollagenopathiesYo Niida, Sumihito Togi, Hiroki UraCurrent Issues in Molecular Biology|August 27, 2021
Application of Combined Long Amplicon Sequencing (CoLAS) for Genetic Analysis of Neurofibromatosis Type 1: A Pilot StudySumihito Togi, Hiroki Ura, Yo NiidaInternational Journal of Molecular Sciences|May 21, 2020
Dual Deep Sequencing Improves the Accuracy of Low-Frequency Somatic Mutation Detection in Cancer Gene Panel TestingHiroki Ura, Sumihito Togi, Yo NiidaBrain & Development|December 7, 2014
Development of a practical NF1 genetic testing method through the pilot analysis of five Japanese families with neurofibromatosis type 1Akiko Okumura, Mamoru Ozaki, Yo NiidaBMC Genomics|April 14, 2022
A comparison of mRNA sequencing (RNA-Seq) library preparation methods for transcriptome analysisHiroki Ura, Sumihito Togi, Yo NiidaPageof 10