Jordan K K - OmicsDI

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CHEBI ID

CHEBI:16344 (4)
CHEBI:16708 (4)
CHEBI:18107 (4)
CHEBI:15741 (3)
CHEBI:15891 (3)
CHEBI:16335 (3)
CHEBI:16610 (3)
CHEBI:16675 (3)
CHEBI:16704 (3)
CHEBI:16750 (3)
CHEBI:16919 (3)
CHEBI:16927 (3)
CHEBI:17151 (3)
CHEBI:17268 (3)
CHEBI:17562 (3)
CHEBI:17596 (3)
CHEBI:17858 (3)
CHEBI:17924 (3)
CHEBI:18261 (3)
CHEBI:27468 (3)
CHEBI:30769 (3)
CHEBI:32816 (3)
CHEBI:48430 (3)
CHEBI:10072 (2)
CHEBI:133206 (2)
CHEBI:1387 (2)
CHEBI:15318 (2)
CHEBI:15344 (2)
CHEBI:15354 (2)
CHEBI:15414 (2)

Metabolite Name

Adenine (3)
3-methyl-2-oxobutyrate (2)
4-Hydroxybenzoic acid (2)
5-Methyltetrahydrofolic acid (2)
AICAR (2)
Adenosine (2)
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Guanine (2)
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NADH (2)
Nicotinamide adenine dinucleotide (2)
Pantothenic acid (2)
Phosphocreatine (2)
Putrescine (2)
Pyridoxine (2)
Riboflavin (2)
S-Lactoylglutathione (2)
Taurine (2)
Thymidine (2)
Uracil (2)
Uric acid (2)
Xanthine (2)
Xanthosine (2)
(1Z)-N-{(5S)-6-hydroxy-5-[(E)-(1-hydroxybutylidene)amino]hexyl}butanimidic acid (1)
(1Z)-N-{(5S)-6-hydroxy-5-[(E)-(1-hydroxydecylidene)amino]hexyl}decanimidic acid (1)
(1Z)-N-{(5S)-6-hydroxy-5-[(E)-(1-hydroxyhexylidene)amino]hexyl}hexanimidic acid (1)
(1Z,3R)-N-[(5S)-6-(acetyloxy)-5-{(E)-[(3R)-1-hydroxy-3-isocyanobutylidene]amino}hexyl]-3-isocyanobutanimidic acid (1)

IsPrivate

False (2)

First Public Date

2017 (1)

Modification

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

Study type

Transcription profiling by array (55)
RNA-seq of coding RNA (15)
Unknown experiment type (8)
Other (7)
Comparative genomic hybridization by array (5)
ChIP-seq (2)
Methylation profiling by array (2)
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DNA-seq (1)
RNA-seq of non coding RNA (1)

Release Date

2025 (306)
2022 (295)
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2021 (252)
2023 (241)
2020 (173)
2019 (128)
2018 (116)
2014 (90)
2015 (83)
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2012 (42)
2026 (38)
2011 (37)
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2009 (18)
2007 (13)
2008 (12)
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2006 (2)
2003 (2)
2001 (2)
2002 (1)
2000 (1)
1999 (1)

Lab affiliation

Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA USA (2)
CEDOC, NMS, Lisbon, Portugal (1)
Cell Biology Department, Harvard Medical School (1)
Charite Ophthalmology / MDC Cellular Neuroscience (1)
Department for Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology, Hans Knöll Institute Jena, Germany (1)
Department of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, USA (1)
Department of Biomedical Genetics, University of Rochester Medical Center, Rochester, NY 14642, USA Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY 14642, USA (1)
Department of Chemistry, University of Rochester, United States (1)
Department of Chemistry, Wayne State University, United States (1)
Department of Medicine, Weill Cornell Medicine, New York, NY, USA (1)
Department of Pathology, Microbiology, and Immunology;Vanderbilt Institute for Infection, Immunology, and Inflammation. Vanderbilt University Medical Center, Nashville, TN USA (1)
Director of Women’s Health Research Women’s Service Line Inova Health System (1)
Evotec (München) GmbH (1)
Institute of Medical Microbiology, Jena University Hospital, Jena, Germany (1)
Joint Proteomics Facility (1)
Medizinisches Proteom-Center, Medical Faculty, Ruhr-University Bochum, Bochum, Germany, Medical Proteome Analysis, Center for Proteindiagnostics (PRODI), Ruhr-University Bochum, Bochum, Germany (1)
Universität Greifswald Institut für Pharmazie, AG Pharmazeutische Biotechnologie Greifswald, Germany (1)

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Cerebellar gene expression profiles of mouse models for Rett Syndrome reveal MeCP2 targets

Background MeCP2, methyl-CpG-binding protein 2, binds to methylated cytosines at CpG dinucleotides, as well as to unmethylated DNA, and affects chromatin condensation. MECP2 mutations in females lead to Rett syndrome, a neurological disorder characterized by developmental stagnation and regression,...

ORGANISM(S): Mus musculus

2007-08-15 | E-GEOD-8774 | biostudies-arrayexpress

Resistance to aminoglycoside and quinolone drugs among Klebsiella pneumoniae clinical isolates from northern Jordan.

Not available

S-EPMC10757003 | biostudies-literature

Kinase-catalyzed Biotinylation to Map Cell Signaling Pathways (K-BMAPS): Application to Epidermal Growth Factor Signaling

Cell signaling involves a network of protein-protein interactions and post-translational modifications that govern cellular responses to environmental cues. To understand and ultimately modulate these signaling pathways to confront disease, the complex web of proteins that becomes phosphorylated aft...

ORGANISM(S): Homo sapiens (Human)

2021-11-03 | PXD027529 | Pride