Kuo J J - OmicsDI

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CHEBI ID

CHEBI:16449 (4)
CHEBI:16737 (3)
CHEBI:16919 (3)
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CHEBI:78320 (3)
CHEBI:15318 (2)
CHEBI:15428 (2)
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IsPrivate

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Transcription profiling by array (25)
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Lab affiliation

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Department of Chemistry, Michigan State University, 578 S Shaw Lane, East Lansing, MI 48824, United States. (1)
Department of Molecular, Cellular and Developmental Biology, University of California, Los Angeles (UCLA), Los Angeles, CA 90095, USA (1)
Departments of Medicine (Oncology) and of Chemical and Systems Biology, Stanford School of Medicine, Stanford, CA, USA Stanford Cancer Institute, Stanford, CA, USA (1)
Dr. Jörn Dengjel Department of Biology, University of Fribourg Chemin du Musée 10, 1700 Fribourg, Switzerland T +41 26 300 8631 (1)
Fungal Physiology, CBS-KNAW Fungal Biodiversity Centre Institute of the Royal Netherlands Academy of Arts and Sciences(KNAW) Fungal Molecular Physiology, Utrecht University The Netherlands (1)
Graduate Institute of Pathology and Parasitology, National Defense Medical Center, Taiwan (1)
Gunma University Graduate School of Medicine, Japan (1)
Insitute for Cardiovascular Physiology, Goethe University, Frankfurt, Germany (1)
Institute for Cardiovascular Regeneration, Centre for Molecular Medicine, Goethe University Frankfurt am Main, Germany (1)
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Institute of Chemistry, Academia Sinica, Taiwan (1)
National-local Joint Engineering Laboratory of Breeding and Cultivation of Edible and Medicinal Fungi, Soil and Fertilizer Institute (SFI), Sichuan Academy of Agricultural Sciences (1)
Prof. Dr. Oliver Schilling Heisenberg Professor of Translational Proteomics Institute of Surgical Pathology Faculty of Medicine University of Freiburg Breisacher Strasse 115a D-79106 Freiburg, Germany +49 761 27080610 oliver.schilling@mol-med.uni-freiburg.de (1)
Spanish National Cancer Research Centre (CNIO) Address: Melchor Férnandez Almagro, 3. 28029 Madrid. SPAIN Phone: +34 917 328 000 Ext. 3110 (1)
Translational Genomics Research Institute (1)
Translational Genomics Research Institute (TGen) (1)
UC Santa Barbara (1)
University of Edinburgh (1)

Tags

xref:PubMed:28548038 (1)
xref:PubMed:39048815 (1)
xref:PubMed:17679090 (1)

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Comparisons of Rivaroxaban Following Different Dosage Criteria (ROCKET AF or J-ROCKET AF Trials) in Asian Patients With Atrial Fibrillation.

Not available

S-EPMC6898830 | biostudies-literature

RAG2 PHD finger couples histone H3 lysine 4 trimethylation with V(D)J recombination.

Not available

S-EPMC2988437 | biostudies-literature

Expression data from C57BL/6J and MRL/MpJ hearts following acute myocardial infarction

The Murphy Roth Large (MRL) mouse, a strain capable of regenerating right ventricular myocardium, has a high post-myocardial infarction (MI) survival rate compared with C57BL6/J (C57) mice. The biological processes responsible for this survival advantage are unknown. We compared acute post-MI gene e...

ORGANISM(S): Mus musculus

2010-05-27 | E-GEOD-19322 | biostudies-arrayexpress

The Somatostatin Receptor-4 Agonist J-2156 Alleviates Mechanical Hypersensitivity in a Rat Model of Breast Cancer Induced Bone Pain.

Not available

S-EPMC5962878 | biostudies-literature

Pinnisterols D-J, New 11-Acetoxy-9,11-secosterols with a 1,4-Quinone Moiety from Formosan Gorgonian Coral Pinnigorgia sp. (Gorgoniidae).

Not available

S-EPMC5295231 | biostudies-literature

Tobacco carcinogen 4-[methyl(nitroso)amino]-1-(3-pyridinyl)-1-butanone (NNK) drives metabolic rewiring and epigenetic reprograming in A/J mice lung cancer model and prevention with diallyl sulphide (DAS).

Not available

S-EPMC8947221 | biostudies-literature

Differential regulation of SBF and MBF target genes by genotoxic stress occurs via Rad53-dependent inactivation of the MBF correpressor Nrm1

MBF and SBF transcription factors regulate a large family of coordinately expressed G1/S genes required for early cell cycle functions including DNA replication and repair. SBF is inactivated upon S phase entry by Clb/CDK whereas MBF targets are repressed by the corepressor, Nrm1. Using genome-wide ...

ORGANISM(S): Saccharomyces cerevisiae

2012-02-15 | E-GEOD-33695 | biostudies-arrayexpress

90 min Met4 hyperactivation ChIP-chip

Identification of in vivo binding targets of Met4 and Met32 by conducting chromatin immunoprecipitation studies using genomic tiling arrays (ChIP-on-chip 4X44K whole yeast genome arrays by Agilent) following 90 minutes Met4 hyperactivation.

ORGANISM(S): Saccharomyces cerevisiae

2012-02-21 | E-MEXP-3302 | biostudies-arrayexpress

Small Perturbation Approach Reveals Transcriptomic Steady State

The â??small perturbationâ?? approach is critical in studying the â??steady stateâ?? of a biological system. In our experiments, small perturbations were generated by applying a series of repeating intermittent small doses of ultraviolet radiation to a human keratinocyte cell line, HaCaT. The biolog...

ORGANISM(S): Homo sapiens

2010-06-24 | E-GEOD-7060 | biostudies-arrayexpress

Exoskeletal-assisted walking combined with transcutaneous spinal cord stimulation to improve bone health in persons with spinal cord injury: study protocol for a prospective randomised controlled trial.

Not available

S-EPMC11409316 | biostudies-literature

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