Chang Na N - OmicsDI

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UNIPROT ID/AC

A0A024R563 (3)
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A0A087WUD1 (3)
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ENSEMBL ID

ENSG00000147251 (3)
ENSG00000170477 (3)
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CHEBI ID

CHEBI:15354 (3)
CHEBI:15756 (3)
CHEBI:131988 (2)
CHEBI:142219 (2)
CHEBI:15428 (2)
CHEBI:15611 (2)
CHEBI:15698 (2)
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Metabolite Name

Kynurenic acid (2)
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Undecanedioic acid (2)
(3S)-3-hydroxy-3-methylglutaryl-CoA (1)
(7Z,10Z)-hexadecadienoylcarnitine (1)
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1-benzopyrans (1)
1-hydroxy-2-unsubstituted benzenoids (1)
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10-Undecenoic acid (1)
10-formyltetrahydrofuran (1)
11-Octadecanoic acid (Vaccenic acid) (1)
12,13-DHOME;(9Z)-12,13-Dihydroxyoctadec-9-enoic acid (1)
12-aminododecanoic acid (1)
13(S)-HODE;13(S)-Hydroxyoctadeca-9Z,11E-dienoic acid (1)
13-methylmyristic acid (1)
13S-Hydroperoxy-9Z,11E-octadecadienoic acid (1)
13S-Hydroxy-9Z,11E,15Z-octadecatrienoic acid (1)
17-Hydroxylinolenic acid (1)
2'-deoxyadenosine 5'-monophosphate (1)

Study type

Transcription profiling by array (40)
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RNA-seq of coding RNA (15)
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Release Date

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Lab affiliation

Boston University School of Medicine (1)
Center for Infectious Diseases / Parasitology Medical Fakulty Heidelberg University (1)
Center for RNA Research, Institute for Basic Science, Seoul 08826, S. Korea School of Biological Sciences, Seoul National University, Seoul 08826, S. Korea (1)
Department of Biochemistry Center for Biomedical Mass Spectrometry Boston University School of Medicine (1)
Department of Plant Biology, Carnegie Institution for Science, Stanford, California, USA (1)
Institut Pasteur Unité de Dynamique des interactions hôte-pathogène 25, rue du Docteur Roux 75015 Paris, France (1)
Institute of Bioinformatics, Bangalore, Karnataka, India (1)
McKusick-Nathans Institute of Genetic Medicine, Department of Biological Chemistry, Oncology and Pathology, Johns Hopkins University School of Medicine, Baltimore 21205, Maryland, USA (1)
McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, Baltimore, Maryland 21205 USA (1)
The Institute of Cancer Research (1)

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Chang - Frankia sp. CcI3 - Nitrogen limitation

Effect of nitrogen limitation on the gene expression of Frankia sp. CcI3

ORGANISM(S): Frankia sp. Ccl3

2013-10-03 | E-MEXP-3620 | biostudies-arrayexpress

Inhibition of Na+/H+ exchanger (NHE) 7 by 5-(N-ethyl-N-isopropyl)-Amiloride displays anti-cancer activity in non-small cell lung cancer by disrupting cancer stem cell activity and downregulating PD-L1 expression.

Not available

S-EPMC10636675 | biostudies-literature

Adjustment of Immunosuppressants to Facilitate Anti-COVID-19 Antibody Production after mRNA Vaccination in Liver Transplant Recipients.

Not available

S-EPMC10051347 | biostudies-literature

Ezrin regulates NHE3 translocation and activation after Na+-glucose cotransport.

Not available

S-EPMC439003 | biostudies-literature

Epi-reevesioside F inhibits Na+/K+-ATPase, causing cytosolic acidification, Bak activation and apoptosis in glioblastoma.

Not available

S-EPMC4695168 | biostudies-literature

On-Treatment Changes in FIB-4 and 1-Year FIB-4 Values Help Identify Patients with Chronic Hepatitis B Receiving Entecavir Therapy Who Have the Lowest Risk of Hepatocellular Carcinoma.

Not available

S-EPMC7281667 | biostudies-literature

Structure-guided unlocking of Na_X reveals a non-selective tetrodotoxin-sensitive cation channel.

Not available

S-EPMC8931054 | biostudies-literature

Intracellular Na+ overload causes oxidation of CaMKII and leads to Ca2+ mishandling in isolated ventricular myocytes.

Not available

S-EPMC4250389 | biostudies-literature

A substructure-based screening approach to uncover N-nitrosamines in drug substances.

Not available

S-EPMC9931005 | biostudies-literature

Co-Immunoprecipitation of TMEM65

Mitochondrial Ca2+ transport is a critical process in cellular physiology. One pathway for export occurs via Na+/Ca2+exchange (mito-NCX) machinery. TMEM65 has recently been shown to be crucial for mito-NCX activity, but its precise mechanistic role remains unknown. To evaluate whether TMEM65 forms a...

ORGANISM(S): Homo sapiens (Human)

2026-02-09 | PXD064897 | Pride

Co-ip Lc-ms/ms

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630 Results

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