The scientist’s investigation covers issues in Molecular biology, Helicase, RecQ helicase, Genetics and Werner syndrome. Yasuhiro Furuichi interconnects RNA, Biochemistry, Gene, Cell division and Chromosome instability in the investigation of issues within Molecular biology. His studies deal with areas such as Messenger RNA and Transcription as well as RNA.
In the field of Gene, his study on E2F and Positional cloning overlaps with subjects such as Premature aging. His research in Werner syndrome intersects with topics in Werner's syndrome, Genome instability and Bloom syndrome. In his study, Helicase Gene and Genetic disorder is strongly linked to Compound heterozygosity, which falls under the umbrella field of Rothmund–Thomson syndrome.
His primary areas of investigation include Molecular biology, Genetics, Gene, Werner syndrome and Helicase. His research investigates the link between Molecular biology and topics such as Messenger RNA that cross with problems in Methylation. His Genetics study which covers Cell biology that intersects with Carcinogenesis.
His Werner syndrome research includes elements of Telomere, Cancer research, Werner's syndrome and Genome instability. His study in Helicase is interdisciplinary in nature, drawing from both DNA, DNA damage and Nucleoplasm. His Five-prime cap study, which is part of a larger body of work in RNA, is frequently linked to RNA polymerase II, bridging the gap between disciplines.
His scientific interests lie mostly in Molecular biology, Antibody, Helicase, Phage display and Antigen. His Molecular biology research includes themes of Messenger RNA, Stem cell, HT29 Cells, Colorectal cancer and Gene silencing. As part of one scientific family, Yasuhiro Furuichi deals mainly with the area of Messenger RNA, narrowing it down to issues related to the RNA Helicase A, and often Werner Syndrome Helicase.
Yasuhiro Furuichi has included themes like Recombinant DNA, Toxin, Biochemistry, Microbiology and Affinity chromatography in his Antibody study. His research integrates issues of Cancer research, DNA, DNA damage, DNA repair and Cell biology in his study of Helicase. His Cell biology research includes elements of Telomere, Telomerase and Carcinogenesis.
His primary areas of study are Molecular biology, DNA repair, Pathology, Cell cycle and Cancer research. He performs multidisciplinary study on Molecular biology and RNA polymerase II in his works. His DNA repair research incorporates themes from Serous fluid, Cell growth, Clear cell and Transfection.
The Pathology study combines topics in areas such as Cancer, Ovarian cancer, Adenocarcinoma and In vivo. His work deals with themes such as Mitochondrion and RecQ helicase, DNA damage, Genome instability, which intersect with Cell cycle. He interconnects Cancer cell, Bioinformatics and Helicase in the investigation of issues within Cancer research.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome
Saori Kitao;Akira Shimamoto;Makoto Goto;Robert W. Miller.
Nature Genetics (1999)
Viral and cellular mRNA capping: past and prospects.
Yasuhiro Furuichi;Aaron J Shatkin.
Advances in Virus Research (2000)
Reovirus messenger RNA contains a methylated, blocked 5'-terminal structure: m-7G(5')ppp(5')G-MpCp-
Y Furuichi;M Morgan;S Muthukrishnan;A J Shatkin.
Proceedings of the National Academy of Sciences of the United States of America (1975)
A blocked structure at the 5' terminus of mRNA from cytoplasmic polyhedrosis virus.
Yasuhiro Furuichi;Kin-Ichiro Miura.
Nature (1975)
Bloom’s and Werner’s syndrome genes suppress hyperrecombination in yeast sgs1 mutant: Implication for genomic instability in human diseases
Kazutsune Yamagata;Jun-ichi Kato;Akira Shimamoto;Makoto Goto.
Proceedings of the National Academy of Sciences of the United States of America (1998)
Methylated, blocked 5 termini in HeLa cell mRNA.
Y Furuichi;M Morgan;A J Shatkin;W Jelinek.
Proceedings of the National Academy of Sciences of the United States of America (1975)
Cloning of Two New Human Helicase Genes of the RecQ Family: Biological Significance of Multiple Species in Higher Eukaryotes
Saori Kitao;Itaru Ohsugi;Koji Ichikawa;Makoto Goto.
Genomics (1998)
Characterization and gene cloning of 1,3-beta-D-glucan synthase from Saccharomyces cerevisiae.
Shunsuke B. Inoue;Noriko Takewakt;Tsuyoshi Takasuka;Toshiyuki Mio.
FEBS Journal (1995)
DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus system
Noriyuki Suzuki;Akira Shimamoto;Osamu Imamura;Junro Kuromitsu.
Nucleic Acids Research (1997)
Rothmund-Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome.
Noralane M. Lindor;Yasuhiro Furuichi;Saori Kitao;Akiro Shimamoto.
American Journal of Medical Genetics (2000)
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