Nakamura K K - OmicsDI

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CHEBI ID

CHEBI:17822 (15)
CHEBI:26271 (15)
CHEBI:28044 (15)
CHEBI:22653 (15)
CHEBI:18257 (15)
CHEBI:25094 (14)
CHEBI:27570 (14)
CHEBI:15741 (14)
CHEBI:16811 (14)
CHEBI:28300 (14)
CHEBI:18186 (13)
CHEBI:26986 (13)
CHEBI:27897 (13)
CHEBI:17345 (13)
CHEBI:30769 (13)
CHEBI:29016 (13)
CHEBI:16708 (13)
CHEBI:17154 (13)
CHEBI:16335 (13)
CHEBI:18237 (12)
CHEBI:73024 (12)
CHEBI:16704 (12)
CHEBI:7916 (12)
CHEBI:17858 (12)
CHEBI:33508 (12)
CHEBI:24266 (12)
CHEBI:18211 (12)
CHEBI:30915 (12)
CHEBI:17268 (12)
CHEBI:6650 (12)

Metabolite Name

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Aspartate (7)
Valine (7)
NADP+ (7)

Modification

15.994915 (1)
42.010565 (1)
57.021464 (1)

Study type

Transcription profiling by array (87)
ChIP-seq (6)
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Release Date

2022 (759)
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2021 (697)
2025 (675)
2024 (558)
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2000 (9)
1999 (7)
1998 (4)
1997 (3)

Lab affiliation

Department of Cell and Molecular Biology, St. Jude Children’s Research Hospital, Memphis, TN 38105, USA. (2)
MIT (2)
Mie University Graduate School of Medicine (2)
Research Institute for Microbial Diseases (2)
Biomolecular characterization unit, Center for Sustainable Resource Science, RIKEN (1)
Centre for Functional Ecology, University of Coimbra (1)
Children's Hospital of Philadelphia 416B Abramson Pediatric Research Center Philadelphia, PA 19104 Office: 215-590-5320 Lab: 215-590-5319 (1)
Department of Applied Biological Science, Faculty of Science and Technology, Tokyo University of Science, Chiba, Japan. (1)
Department of Cell Biology and Molecular Medicine Nakamura Lab Rutgers New Jersey Medical School Rutgers Biomedical and Health Sciences Rutgers The State University of New Jersey (1)
Department of Cell Biology and Molecular Medicine, Rutgers New Jersey Medical School, Rutgers Biomedical and Health Sciences (1)
Department of Chemistry and Biotechnology, School of Engineering, The University of Tokyo, Tokyo 113-8656, Japan Department of Bioengineering, School of Engineering, The University of Tokyo, Tokyo 113-8656, Japan (1)
Department of Molecular Medicine and Neurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA 92037, USA (1)
Department of Neurology, Nagoya University Graduate School of Medicine (1)
Department of Neurology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan (1)
Division of Plant Environmental Responses, National Institute for Basic Biology, Japan (1)
Genetics and Computational Biology Department, QIMR Berghofer Medical Research Institute, Brisbane, Australia (1)
Institute for Glyco-core Research (iGCORE), Nagoya University, Aichi, Japan (1)
Institute of Functional Epigenetics, Helmholtz Zentrum Muenchen, Germany (1)
Institute of Functional Epigenetics, Helmholtz Zentrum München, Germany (1)
Institute of Functional Epigenetics, Helmholtz Zentrum München, Neuherberg, Germany (1)
Joint Proteomics Facility (1)
Laboratory for Biomarker Development (1)
Ludwig Institute for Cancer Research Department of Oncology, University hospital of Lausanne, Switzerland (1)
Max-Planck Institute for Chemical Ecology, Department of Natural Product Biosynthesis (1)
Member Cell&Molecular Biology Department St.Jude Children's Research Hospital Memphis, TN-38105 (1)
Molecular Pharmacology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY (1)
NIH/NIDCR (1)
Neuroprotection Research Laboratory, Departments of Radiology and Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts, USA (1)
Osaka Univ. (1)
Proteome Research (AG Stühler) Heinrich Heine University Düsseldorf Universitätsstraße 1 40225 Düsseldorf Germany (1)

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A non-canonical vitamin K cycle is a potent ferroptosis suppressor

Raw files corresponding to LC-MS-based relative quantification of oxidized lipids in Pfa1 cells and mouse liver samples subjected to ferroptosis. Data were acquired in parallel reaction monitoring (PRM) MS/MS mode.

ORGANISM(S): Mus Musculus (ncbitaxon:10090)

2022-05-19 | MSV000089489 | MassIVE

Variable characteristics overlooked in human K-562 leukemia cell lines with a common signature.

Not available

S-EPMC11053119 | biostudies-literature

Cyclin K as a direct transcriptional target of the p53 tumor suppressor.

Not available

S-EPMC1531701 | biostudies-literature

Role of the K(Ca)3.1 K+ channel in auricular lymph node CD4+ T-lymphocyte function of the delayed-type hypersensitivity model.

Not available

S-EPMC3696325 | biostudies-literature

Mercurial-resistance determinants in Pseudomonas strain K-62 plasmid pMR68.

Not available

S-EPMC3737084 | biostudies-literature

Evidence in support of a four transmembrane-pore-transmembrane topology model for the Arabidopsis thaliana Na+/K+ translocating AtHKT1 protein, a member of the superfamily of K+ transporters.

Not available

S-EPMC33495 | biostudies-literature

QUEST-MS for plasma biomarkers complementing the specificity of PSA test

To explore plasma biomarkers complementing the specificity of PSA test, we developed a unique proteomic technology QUEST-MS (Quick Enrichment of Small Targets for Mass Spectrometry). The QUEST-MS method based on 96-well formatted sequential reversed phase chromatography allowing efficient enrichment...

ORGANISM(S): Homo sapiens (Human)

2014-01-28 | PXD000383 | Pride