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49 results on '"Ohsumi, Toshiro"'

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1. Rethinking Immunological Risk: A Retrospective Cohort Study of Severe SARS-Cov-2 Infections in Individuals With Congenital Immunodeficiencies

2. Loss of the DNA Repair Gene RNase H2 Identifies a Unique Subset of DDR-Deficient Leiomyosarcomas

3. The CIP2A–TOPBP1 axis safeguards chromosome stability and is a synthetic lethal target for BRCA-mutated cancer

5. Integrating circulating T follicular memory cells and autoantibody repertoires for characterization of autoimmune disorders

6. Numerical simulation of thermal noise in Josephson circuits

7. Rethinking immunologic risk: a retrospective cohort study of severe SARS-CoV-2 infections in individuals with congenital immunodeficiencies

11. Deficiency of base excision repair enzyme NEIL3 drives increased predisposition to autoimmunity

13. Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections

15. CIP2A is a prime synthetic-lethal target for BRCA-mutated cancers

22. DOCK2 and a Recessive Immunodeficiency with Early-Onset Invasive Infections

23. A Novel Microbiome Therapeutic Increases Gut Microbial Diversity and Prevents RecurrentClostridium difficileInfection

24. A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency

25. MUT-14 and SMUT-1 DEAD Box RNA Helicases Have Overlapping Roles in Germline RNAi and Endogenous siRNA Formation

27. Genome-wide Chromatin Interactions of the Nanog Locus in Pluripotency, Differentiation, and Reprogramming

31. Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries

32. Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration

33. Histone H3R2 Symmetric Dimethylation and Histone H3K4 Trimethylation Are Tightly Correlated in Eukaryotic Genomes

36. Next-Generation Sequencing Strategies Enable Routine Detection of Balanced Chromosome Rearrangements for Clinical Diagnostics and Genetic Research

42. A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency

44. Transposon activation mutagenesis as a screening tool for identifying resistance to cancer therapeutics.

45. Genome-wide Chromatin Interactions of the NanogLocus in Pluripotency, Differentiation, and Reprogramming

46. Sensitive, specific polymorphism discovery in bacteria using massively parallel sequencing.

48. Sensitive, Specific Polymorphism Discovery in Bacteria Using Massively Parallel Sequencing

49. Integrating circulating T follicular memory cells and autoantibody repertoires for characterization of autoimmune disorders.

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