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Publications by Naomi Kondo

Refractory Chronic Pleurisy Caused by Helicobacter Equorum-Like Bacterium in a Patient With X-Linked Agammaglobulinemia

Journal of Clinical Microbiology

Microbiology

2011

English

Unexpected Cardiopulmonary Arrest Associated With Influenza: Our Experience During the 2009 Pandemic in Japan

Influenza and other Respiratory Viruses

English

Crystal Structure of the Extracellular Signaling Complex of Interleukin-18

Acta Crystallographica Section A: Foundations and Advances

Materials Science

Condensed Matter Physics

Theoretical Chemistry

English

Three Japanese Patients With Beta-Ketothiolase Deficiency Who Share a Mutation, C.431A>C (H144P) in ACAT1

English

Genetic Basis of Peroxisome-Assembly Mutants of Humans, Chinese Hamster Ovary Cells, and Yeast: Identification of a New Complementation Group of Peroxisome-Biogenesis Disorders Apparently Lacking Peroxisomal-Membrane Ghosts

American Journal of Human Genetics

Genetics

1998

English

Temperature-Sensitive Phenotypes of Peroxisome-Assembly Processes Represent the Milder Forms of Human Peroxisome-Biogenesis Disorders

American Journal of Human Genetics

Genetics

1998

English

A PEX6-Defective Peroxisomal Biogenesis Disorder With Severe Phenotype in an Infant, Versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents

American Journal of Human Genetics

Genetics

2002

English

Positioning of Autoimmune TCR-Ob.2F3 and TCR-Ob.3D1 on the MBP85-99/HLA-DR2 Complex

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

2008

English

Mitochondrial Acetoacetyl-CoA Thiolase (T2) Deficiency: T2-Deficient Patients With “Mild” Mutation(s) Were Previously Misinterpreted as Normal by the Coupled Assay With Tiglyl-CoA

English

Temperature-Sensitive Mutation of PEX6 in Peroxisome Biogenesis Disorders in Complementation Group C (CG-C): Comparative Study of PEX6 and PEX1

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Naomi Kondo

Refractory Chronic Pleurisy Caused by Helicobacter Equorum-Like Bacterium in a Patient With X-Linked Agammaglobulinemia

Unexpected Cardiopulmonary Arrest Associated With Influenza: Our Experience During the 2009 Pandemic in Japan

Crystal Structure of the Extracellular Signaling Complex of Interleukin-18

Three Japanese Patients With Beta-Ketothiolase Deficiency Who Share a Mutation, C.431A>C (H144P) in ACAT1

Genetic Basis of Peroxisome-Assembly Mutants of Humans, Chinese Hamster Ovary Cells, and Yeast: Identification of a New Complementation Group of Peroxisome-Biogenesis Disorders Apparently Lacking Peroxisomal-Membrane Ghosts

Temperature-Sensitive Phenotypes of Peroxisome-Assembly Processes Represent the Milder Forms of Human Peroxisome-Biogenesis Disorders

A PEX6-Defective Peroxisomal Biogenesis Disorder With Severe Phenotype in an Infant, Versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents

Positioning of Autoimmune TCR-Ob.2F3 and TCR-Ob.3D1 on the MBP85-99/HLA-DR2 Complex

Mitochondrial Acetoacetyl-CoA Thiolase (T2) Deficiency: T2-Deficient Patients With “Mild” Mutation(s) Were Previously Misinterpreted as Normal by the Coupled Assay With Tiglyl-CoA

Temperature-Sensitive Mutation of PEX6 in Peroxisome Biogenesis Disorders in Complementation Group C (CG-C): Comparative Study of PEX6 and PEX1