Naomi Kondo mostly deals with Genetics, Molecular biology, Immunology, Peroxisomal disorder and Peroxisome. The study incorporates disciplines such as Point mutation, Gene mutation, Complementary DNA, Green fluorescent protein and Nuclear localization sequence in addition to Molecular biology. The Immunology study combines topics in areas such as Peripheral blood mononuclear cell and Pneumonia.
Her research integrates issues of Zellweger syndrome and PEX6 in her study of Peroxisomal disorder. Her biological study spans a wide range of topics, including Complementation and Exon. Her research in Peroxisome intersects with topics in Complementation group, DNA ligase and Chinese hamster ovary cell.
Her main research concerns Immunology, Molecular biology, Genetics, Internal medicine and Gene. As part of her studies on Immunology, Naomi Kondo frequently links adjacent subjects like Peripheral blood mononuclear cell. Her Molecular biology research is multidisciplinary, relying on both Mutation, Mutant, Point mutation, Biochemistry and Complementary DNA.
Her studies in Exon, Allele, Zellweger syndrome, Peroxisomal disorder and Missense mutation are all subfields of Genetics research. Her study looks at the relationship between Internal medicine and fields such as Endocrinology, as well as how they intersect with chemical problems. Her Peroxisome research includes themes of Complementation, Biogenesis and Chinese hamster ovary cell.
Her scientific interests lie mostly in Immunology, Asthma, Internal medicine, Genetics and Molecular biology. Her study in Immunology is interdisciplinary in nature, drawing from both Casein, Complication, Mutation and Desensitization. She has researched Asthma in several fields, including Immunoglobulin E, Pharmacokinetics and Intensive care medicine.
As a part of the same scientific study, she usually deals with the Internal medicine, concentrating on Endocrinology and frequently concerns with Compound heterozygosity and Mutation. Her study in Thiolase and Haploinsufficiency is done as part of Genetics. Her Molecular biology research incorporates themes from Gene, Mutant, Homologous recombination and Exon.
Genetics, Molecular biology, Mutant, Mutation and Guideline are her primary areas of study. Many of her studies involve connections with topics such as Agenesis of the corpus callosum and Genetics. Within one scientific family, Naomi Kondo focuses on topics pertaining to RNA splicing under Molecular biology, and may sometimes address concerns connected to Mutation testing.
She interconnects IRAK4, Blot, HEK 293 cells, Reporter gene and Single-nucleotide polymorphism in the investigation of issues within Mutant. Her Compound heterozygosity research focuses on Enzyme assay and how it connects with Internal medicine. Her Internal medicine study integrates concerns from other disciplines, such as Endocrinology and Pathology.
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.
Human Tyrosine Kinase 2 Deficiency Reveals Its Requisite Roles in Multiple Cytokine Signals Involved in Innate and Acquired Immunity
Yoshiyuki Minegishi;Masako Saito;Tomohiro Morio;Ken Watanabe.
Immunity (2006)
Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly
Yuji Matsuzono;Naohiko Kinoshita;Shigehiko Tamura;Nobuyuki Shimozawa.
Proceedings of the National Academy of Sciences of the United States of America (1999)
Selective utilization of nonhomologous end-joining and homologous recombination DNA repair pathways during nervous system development.
Kenji E. Orii;Youngsoo Lee;Naomi Kondo;Peter J. McKinnon.
Proceedings of the National Academy of Sciences of the United States of America (2006)
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
Masanori Honsho;Shigehiko Tamura;Nobuyuki Shimozawa;Yasuyuki Suzuki.
American Journal of Human Genetics (1998)
MOLECULAR CLONING OF CDNA ENCODING RAT VERY LONG-CHAIN ACYL-COA SYNTHETASE
Atsushi Uchiyama;Toshifumi Aoyama;Keiju Kamijo;Yasushi Uchida.
Journal of Biological Chemistry (1996)
Enzymes of ketone body utilization in human tissues: protein and messenger RNA levels of succinyl-coenzyme A (CoA):3-ketoacid CoA transferase and mitochondrial and cytosolic acetoacetyl-CoA thiolases.
Fukao T;Song Xq;Mitchell Ga;Yamaguchi S.
Pediatric Research (1997)
Cord blood lymphocyte responses to food antigens for the prediction of allergic disorders.
N Kondo;Y Kobayashi;S Shinoda;K Kasahara.
Archives of Disease in Childhood (1992)
d-3-Hydroxyacyl-CoA Dehydratase/d-3-Hydroxyacyl-CoA Dehydrogenase Bifunctional Protein Deficiency: A Newly Identified Peroxisomal Disorder
Yasuyuki Suzuki;Ling Ling Jiang;Masayoshi Souri;Shoko Miyazawa.
American Journal of Human Genetics (1997)
STXBP1 mutations in early infantile epileptic encephalopathy with suppression‐burst pattern
Hirotomo Saitsu;Mitsuhiro Kato;Ippei Okada;Kenji E. Orii.
Epilepsia (2010)
PEX12, the Pathogenic Gene of Group III Zellweger Syndrome: cDNA Cloning by Functional Complementation on a CHO Cell Mutant, Patient Analysis, and Characterization of Pex12p
Kanji Okumoto;Nobuyuki Shimozawa;Atsusi Kawai;Shigehiko Tamura.
Molecular and Cellular Biology (1998)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
Gifu University
Gifu University
Gifu University
Gifu University
Alfred I. duPont Hospital for Children
Kyushu University
Shimane University
University of Hyogo
University of Amsterdam
Shinshu University
University of Regensburg
Kyushu University
Fritz Haber Institute of the Max Planck Society
National Renewable Energy Laboratory
The University of Texas at Austin
Australian National University
University of Leeds
University of Bremen
University of Nicosia
University of California, Berkeley
University of Nottingham
University of Arizona
University of Cambridge
Beth Israel Deaconess Medical Center
Loyola University Chicago
Loyola University Chicago