Harvard Catalyst Profiles

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Toshiro Kendrick Ohsumi, Ph.D.

Concepts (240)

Concepts are derived automatically from a person's publications.
Concepts are listed by decreasing relevance which is based on many factors, including how many publications the person wrote about that topic, how long ago those publications were written, and how many publications other people have written on that same topic.
Name Number of Publications Most Recent Publication Publications by All Authors Concept Score Why?
Sequence Analysis120122560.400 Why?
Immunologic Deficiency Syndromes420155460.390 Why?
Computational Biology3201335180.200 Why?
Genome4201418030.190 Why?
T-Lymphocytes52016101630.160 Why?
Collagen1200726840.160 Why?
Software1201244340.160 Why?
N-Glycosyl Hydrolases12016680.140 Why?
Oral Ulcer12017960.140 Why?
Skin Ulcer120171180.140 Why?
Gene Rearrangement2201211790.140 Why?
Transcription Factor RelA120172750.140 Why?
RNA, Small Interfering4201435040.130 Why?
Endodeoxyribonucleases120161620.130 Why?
Haploinsufficiency120173290.130 Why?
B-Lymphocytes4201646640.130 Why?
Chromosome Breakage220121730.130 Why?
Biological Therapy120161380.120 Why?
Genes, Dominant120178800.120 Why?
Homeodomain Proteins2201424170.120 Why?
Receptors, Transferrin120152960.120 Why?
Homozygote2201517770.120 Why?
Pedigree6201746460.110 Why?
Sequence Analysis, DNA6201748010.110 Why?
Agammaglobulinemia120141670.110 Why?
Immunoprecipitation220149050.100 Why?
Programming Languages120121340.100 Why?
Mutation62015297170.100 Why?
Calcium Channels120156210.100 Why?
Guanine Nucleotide Exchange Factors120155810.100 Why?
Eukaryota120121000.100 Why?
DEAD-box RNA Helicases120143750.100 Why?
Xenopus220117120.100 Why?
Fibroblasts3201741430.100 Why?
Severe Combined Immunodeficiency120132210.100 Why?
X Chromosome Inactivation120122240.090 Why?
Cytoskeleton1201511850.090 Why?
Protein Multimerization120159710.090 Why?
Genetic Diseases, Inborn120155870.090 Why?
Microfilament Proteins1201511520.090 Why?
Germ Cells120146280.090 Why?
Caspases120139280.090 Why?
Gastrointestinal Tract120168140.090 Why?
Virus Diseases120157100.090 Why?
Secondary Prevention1201615200.090 Why?
DNA Transposable Elements120137480.080 Why?
Clostridium Infections120165480.080 Why?
Microtubule-Associated Proteins2201110860.080 Why?
Antineoplastic Agents, Phytogenic120136230.080 Why?
Chromosomes, Human120114570.080 Why?
Ovum120091890.080 Why?
Killer Cells, Natural2201521330.080 Why?
Sequence Analysis, RNA2201320110.080 Why?
Arginine120129440.080 Why?
DNA Mutational Analysis2201541870.080 Why?
RNA Interference2201428900.080 Why?
Adaptor Proteins, Signal Transducing2201629150.080 Why?
Caenorhabditis elegans Proteins120148490.070 Why?
Lysine1201210080.070 Why?
Child Development Disorders, Pervasive120126150.070 Why?
Mutation, Missense1201525560.070 Why?
Pluripotent Stem Cells120137950.070 Why?
Microtubules1201110900.070 Why?
Paclitaxel1201317070.070 Why?
Chromosome Aberrations1201218110.070 Why?
Microglia1201312610.060 Why?
Antigens, CD1201540240.060 Why?
Caenorhabditis elegans1201414160.060 Why?
Base Sequence52017127970.060 Why?
Finite Element Analysis120074310.060 Why?
Autoimmune Diseases1201621300.060 Why?
Germ-Line Mutation1201217860.060 Why?
DNA, Bacterial1200814650.060 Why?
Genome, Human2201244200.050 Why?
Histones1201225970.050 Why?
Chromatin1201329170.050 Why?
Chromosome Inversion220121270.050 Why?
T-Lymphocytes, Regulatory1201429860.050 Why?
DNA Barcoding, Taxonomic220131360.050 Why?
Chromosomal Instability120211840.050 Why?
Neoplasm Proteins1201336910.050 Why?
RNA1201027470.050 Why?
Animals1520171685610.050 Why?
Neoplasms32021215960.040 Why?
Fatal Outcome2201518490.040 Why?
RNA, Messenger22013130290.040 Why?
Repressor Proteins1201030200.040 Why?
Sequence Alignment2201422570.040 Why?
Diarrhea2201613430.040 Why?
Heart Valve Prosthesis1200714860.040 Why?
Drug Resistance, Neoplasm1201351630.040 Why?
Polymorphism, Genetic1200843280.040 Why?
Xenopus Proteins220114330.040 Why?
Genomic Instability120216950.040 Why?
Genetic Predisposition to Disease22016174000.040 Why?
Autoantibodies2201620360.040 Why?
Databases, Factual1201277160.040 Why?
Dextran Sulfate120172360.040 Why?
Poly I-C120161150.040 Why?
Genomics1201256920.030 Why?
Translocation, Genetic2201214170.030 Why?
Molecular Sequence Data32014181120.030 Why?
Warts12015680.030 Why?
Cells, Cultured32017192230.030 Why?
Cell Degranulation120152870.030 Why?
Fluoroimmunoassay12014330.030 Why?
Mice72016810450.030 Why?
Algorithms22012138530.030 Why?
DNA2202172890.030 Why?
Ion Transport120153200.030 Why?
rac1 GTP-Binding Protein120152360.030 Why?
Tetradecanoylphorbol Acetate120158210.030 Why?
Frameshift Mutation120153990.030 Why?
Oxidoreductases120154240.030 Why?
Consanguinity120154560.030 Why?
Humans1920237420880.030 Why?
Lymphocyte Count120157920.030 Why?
Lymphopenia120152850.030 Why?
Oligonucleotide Array Sequence Analysis2201239200.030 Why?
Macrophages, Peritoneal120132510.030 Why?
Genes, Recessive120156420.030 Why?
Nuclear Proteins2202158510.030 Why?
Mice, Mutant Strains1201518660.030 Why?
Lymphocyte Depletion120146080.030 Why?
Cell Cycle Proteins2201534440.030 Why?
Immunoglobulins120158800.030 Why?
Immune System Diseases120142620.030 Why?
Receptors, Antigen12012530.030 Why?
I-kappa B Kinase120132510.030 Why?
Saccharomyces cerevisiae2201427490.030 Why?
GTPase-Activating Proteins120154970.030 Why?
Mice, Knockout22017145540.030 Why?
Child, Preschool42015409550.030 Why?
Oncogene Proteins120157490.020 Why?
DNA Breaks12011490.020 Why?
Opportunistic Infections120143890.020 Why?
Interspersed Repetitive Sequences12011540.020 Why?
Siblings120158540.020 Why?
Endocytosis120159830.020 Why?
Genetic Diseases, X-Linked120143700.020 Why?
Adaptive Immunity120157120.020 Why?
Male1020173495380.020 Why?
Repetitive Sequences, Nucleic Acid120127990.020 Why?
Mutagenesis, Insertional120136550.020 Why?
HeLa Cells1201631270.020 Why?
Protein Interaction Domains and Motifs120124740.020 Why?
Protein Transport1201519880.020 Why?
Female1020173795920.020 Why?
Chromatin Immunoprecipitation120128920.020 Why?
Early Diagnosis1201411840.020 Why?
Colitis1201711490.020 Why?
Interleukin-101201412000.020 Why?
Methylation1201211070.020 Why?
Karyotyping1201112430.020 Why?
Oogenesis120091310.020 Why?
X Chromosome120128150.020 Why?
Nervous System120125530.020 Why?
NF-kappa B1201725000.020 Why?
Conserved Sequence1201212020.020 Why?
Gene Library1201110760.020 Why?
Gene Expression Profiling2201794100.020 Why?
Carrier Proteins1202150190.020 Why?
Actins1201521200.020 Why?
Tubulin120116950.020 Why?
Databases, Nucleic Acid120082110.020 Why?
Histone-Lysine N-Methyltransferase120126700.020 Why?
Meiosis120093380.020 Why?
Chromosome Deletion1201214000.020 Why?
T-Lymphocyte Subsets1201518370.020 Why?
Transfection1201558920.020 Why?
Animals, Genetically Modified1201215460.020 Why?
Skin Diseases1201510650.020 Why?
Recombination, Genetic1201215860.020 Why?
Mice, Inbred C57BL22015218210.020 Why?
Ligands1201332930.020 Why?
Chromosomal Proteins, Non-Histone120117300.020 Why?
Mitosis1201112080.020 Why?
Mass Spectrometry1201322030.020 Why?
Anemia1201514990.020 Why?
HEK293 Cells1201542000.020 Why?
Child42015774780.020 Why?
Tumor Necrosis Factor-alpha1201744140.020 Why?
Cell Survival1201558720.020 Why?
Blotting, Western1201351800.020 Why?
Oocytes1200911860.020 Why?
DNA-Binding Proteins1202196390.010 Why?
Cell Division1201145640.010 Why?
Hospitalization12023102320.010 Why?
Binding Sites1201261150.010 Why?
DNA Copy Number Variations1201219400.010 Why?
Embryonic Stem Cells1201012940.010 Why?
Cell Cycle1201129640.010 Why?
Adolescent32016856490.010 Why?
Evolution, Molecular1201219370.010 Why?
Flow Cytometry1201359750.010 Why?
Infant22015350700.010 Why?
CD4-Positive T-Lymphocytes1201543790.010 Why?
Autistic Disorder1201211740.010 Why?
Phosphoproteins1201124400.010 Why?
Genome-Wide Association Study22012122200.010 Why?
Genetic Loci1201225720.010 Why?
Saccharomyces cerevisiae Proteins1201218840.010 Why?
Lymphocyte Activation1201355190.010 Why?
Chronic Disease1201791440.010 Why?
Gene Expression1201577900.010 Why?
Protein Biosynthesis1200921260.010 Why?
Drosophila1200914840.010 Why?
RNA-Binding Proteins1201018990.010 Why?
Genetic Testing1201434390.010 Why?
Alleles1201269310.010 Why?
Amino Acid Sequence12013138140.010 Why?
Obesity12023127050.010 Why?
Signal Transduction22015233870.010 Why?
Cohort Studies12023404500.010 Why?
Apoptosis1201697150.010 Why?
Diabetes Mellitus, Type 11201433360.010 Why?
High-Throughput Nucleotide Sequencing1201235850.010 Why?
Cell Proliferation12015104720.010 Why?
Protein Binding1201093870.010 Why?
Cell Line12012159940.010 Why?
Phenotype12015163310.010 Why?
Disease Progression12014132560.010 Why?
Epigenesis, Genetic1201036390.010 Why?
Hematopoietic Stem Cell Transplantation1201554250.010 Why?
Genetic Variation1201265400.010 Why?
Age Factors12013183550.010 Why?
Transcription, Genetic1201077210.010 Why?
Cell Line, Tumor12013166650.010 Why?
Proteins1201060960.010 Why?
Polymorphism, Single Nucleotide12014154940.010 Why?
Retrospective Studies12023770980.010 Why?
Sensitivity and Specificity12008147200.010 Why?
Schizophrenia1201268740.010 Why?
Reproducibility of Results12010198620.010 Why?
Gene Expression Regulation12010120710.010 Why?
Adult220162137120.010 Why?
Aged, 80 and over12016576830.010 Why?
Young Adult12016563500.010 Why?
Aged120161629440.000 Why?
Middle Aged120162131270.000 Why?
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Concepts (240)
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.