His primary areas of study are Genetics, Gene, Molecular biology, Complementary DNA and Genome. His study in Genetics concentrates on Human genome, Transcriptome, Gene expression profiling, Locus and Mitochondrial DNA. His Human genome study incorporates themes from Alternative splicing and Genomics.
His work deals with themes such as Genome evolution, Synteny and Reference genome, which intersect with Genomics. His Molecular biology research incorporates themes from Nucleic acid sequence, DNA, Restriction landmark genomic scanning, Regulation of gene expression and Genomic imprinting. He interconnects Enhancer, Transcription, Computational biology and Sequence analysis in the investigation of issues within Genome.
Yasushi Okazaki mainly investigates Genetics, Gene, Internal medicine, Cell biology and Molecular biology. Genome, Restriction landmark genomic scanning, Mitochondrial DNA, Gene mapping and Human genome are subfields of Genetics in which his conducts study. Yasushi Okazaki studies Genome, namely Genomics.
He has included themes like Gastroenterology, Endocrinology, Oncology and Cardiology in his Internal medicine study. His work deals with themes such as Embryonic stem cell, Induced pluripotent stem cell and Cellular differentiation, which intersect with Cell biology. He has researched Molecular biology in several fields, including DNA and DNA methylation.
Yasushi Okazaki focuses on Internal medicine, Lynch syndrome, Gene, Colorectal cancer and Mitochondrial disease. His Internal medicine study incorporates themes from Gastroenterology, Endocrinology and Oncology. His studies deal with areas such as MSH2 and MSH6 as well as Lynch syndrome.
His Gene research is under the purview of Genetics. His work in the fields of Genetics, such as TOP3A, intersects with other areas such as Bloom syndrome. His study looks at the relationship between Genome and fields such as Cell growth, as well as how they intersect with chemical problems.
His primary areas of investigation include Mitochondrial disease, Genetics, Mitochondrial DNA, MSH6 and Lynch syndrome. His Mitochondrial disease study also includes fields such as
Downregulation and upregulation, Cytochrome c, Molecular biology and MT-ND5 is closely connected to Mitochondrial respiratory chain in his research, which is encompassed under the umbrella topic of Mitochondrial DNA. His MSH6 research includes themes of MLH1, MSH2 and PMS2. His Genome research is multidisciplinary, incorporating elements of Biological pathway and Promoter activity.
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Initial sequencing and comparative analysis of the mouse genome.
Robert H. Waterston;Kerstin Lindblad-Toh;Ewan Birney;Jane Rogers.
The Transcriptional Landscape of the Mammalian Genome
P. Carninci;T. Kasukawa;S. Katayama;J. Gough.
Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs
Y. Okazaki;M. Furuno;T. Kasukawa;J. Adachi.
A promoter-level mammalian expression atlas
Alistair R.R. Forrest;Hideya Kawaji;Michael Rehli;J. Kenneth Baillie.
Functional annotation of a full-length mouse cDNA collection
J. Kawai;A. Shinagawa;K. Shibata;M. Yoshino.
The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line
Harukazu Suzuki;Alistair R.R. Forrest;Erik Van Nimwegen;Carsten O. Daub.
Nature Genetics (2009)
Integrative Annotation of 21,037 Human Genes Validated by Full-Length cDNA Clones
Tadashi Imanishi;Takeshi Itoh;Yutaka Suzuki;Claire O'Donovan.
PLOS Biology (2004)
High-Efficiency Full-Length cDNA Cloning by Biotinylated CAP Trapper
Piero Carninci;Catrine Kvam;Catrine Kvam;Akiko Kitamura;Tomoya Ohsumi.
Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cells
Erik Arner;Carsten O. Daub;Kristoffer Vitting-Seerup;Robin Andersson.
Normalization and subtraction of cap-trapper-selected cDNAs to prepare full-length cDNA libraries for rapid discovery of new genes.
Piero Carninci;Yuko Shibata;Norihito Hayatsu;Yuichi Sugahara.
Genome Research (2000)
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