Ma Ni N - OmicsDI

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pride (52)
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CHEBI ID

CHEBI:16737 (3)
CHEBI:16750 (3)
CHEBI:16811 (3)
CHEBI:16919 (3)
CHEBI:17596 (3)
CHEBI:17822 (3)
CHEBI:18186 (3)
CHEBI:18211 (3)
CHEBI:18237 (3)
CHEBI:18257 (3)
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CHEBI:22660 (3)
CHEBI:25094 (3)
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CHEBI:15859 (2)
CHEBI:15978 (2)
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CHEBI:16108 (2)
CHEBI:16235 (2)
CHEBI:16238 (2)

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First Public Date

2017 (2)

Study type

Transcription profiling by array (18)
RNA-seq of coding RNA (3)
Other (2)
ChIP-chip by array (1)
ChIP-seq (1)
RNA-seq of non coding RNA (1)

Release Date

2025 (149)
2022 (129)
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2017 (36)
2013 (30)
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2009 (5)
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2002 (2)
2001 (2)
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2005 (1)

Lab affiliation

Department of Biological Sciences, Seoul National University, Seoul, Republic of Korea (2)
Genecology Research Centre, University of the Sunshine Coast (2)
CSIR- Institute of Microbial Technology, Chandigarh (1)
Caprion Biosciences, 201 President-Kennedy Ave., Montreal, H2X 3Y7, Quebec, Canada (1)
Carnegie Mass Spectrometry Facility at Stanford (1)
Cell Biology and Epigenetics, Department of Biology, Technical University of Darmstadt, Darmstadt, Germany (1)
Chief, Epithelial Signaling and Transport Section NIH, NIDCR, Building 10, Room 1N-112, Bethesda MD 20892. U.S.A. (1)
Chinese Center for Disease Control and Prevention (1)
Dalian Institute of Chemcial and Physics, China (1)
Dalian Institute of Chemical and Physics, Chinese Academy of Sciences (1)
Department of Biochemistry, Purdue University, West Lafayette, IN USA (1)
Department of Biochemistry, University of Oxford, UK (1)
Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA., Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA (1)
Department of Chemistry, Stanford University (1)
Department of Genetics and Evolution, Federal University of São Carlos, São Paulo, Brazil (1)
Department of Pathology, Johns Hopkins Medical School, USA (1)
Dept. of Laboratory Medicine University of California, San Francisco, USA (1)
Director Institute of Molecular Systems Medicine Director Center for Functional Proteomics Goethe University Frankfurt (1)
Director, Duke Molecular Physiology Institute and Sarah W. Stedman Nutrition and Metabolism Center Professor Departments of Medicine (Division of Endocrinology, Metabolism, and Nutrition) and Pharmacology & Cancer Biology Duke University Medical Center (1)
Dr Prof .Gopal Sapkota, MRC PPU, School of Life Sciences University of Dundee (lab head) (1)
Dr Prof. Gopal Sapkota, MRC PPU, School of Life Sciences University of Dundee (1)
Ehime University, JAPAN (1)
Genecology Research Centre, University of the Sunshine Coast, Maroochydore DC, QLD 4558, Australia (1)
Head of Proteomics and Metabolomics Research Program, Basic Research department, Children's Cancer Hospital 57357, Ciro, Egypt. (1)
Head of System Biology Lab. at Lopukhin Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (1)
Institute of Animal Science, Chinese Academy of Agricultural Sciences (1)
Institute of Biochemistry II, Faculty of Medicine, Goethe University, Frankfurt am Main, Germany Frankfurt Cancer Institute, Frankfurt am Main, Germany Cardio-Pulmonary Institute, Frankfurt am Main, Germany (1)
Institute of Botany, CAS Add: No.20 Nanxincun, Xiangshan, Beijing 100093, China (1)
Laboratory Medicine and Pathology Mayo Clinic USA (1)
Laboratory of Medical Proteomics Department of Personalized Medicine Institute of Biomedical Chemistry Moscow (1)

Tags

xref:PubMed:29220486 (2)
xref:EuropePMC:PMC5751042 (2)

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Strong Bonding of Lattice N Activates Metal Ni to Achieve Efficient Water Splitting.

Not available

S-EPMC11789591 | biostudies-literature

Verifying the Rechargeability of Li-CO2 Batteries on Working Cathodes of Ni Nanoparticles Highly Dispersed on N-Doped Graphene.

Not available

S-EPMC5827515 | biostudies-literature

Atomically Dispersed Ni-N-C Catalysts for Electrochemical CO<sub>2</sub> Reduction.

Not available

S-EPMC11899493 | biostudies-literature

Sulfur-Decorated Ni-N-C Catalyst for Electrocatalytic CO₂ Reduction with Near 100 % CO Selectivity.

Not available

S-EPMC9804562 | biostudies-literature

Pairing N-Vacancy and Adjacent Ni-Sites in the Local Microenvironment to Regulate the Urea Oxidation Reaction Pathway With Enhanced Kinetics.

Not available

S-EPMC12272033 | biostudies-literature

Face mask-derived Ni, N-doped graphene sheets for electrocatalytic CO₂-to-CO reduction.

Not available

S-EPMC9988357 | biostudies-literature

Three-dimensional carbon coated and high mass-loaded NiO@Ni foam anode with high specific capacity for lithium ion batteries.

Not available

S-EPMC11664242 | biostudies-literature

Carbon-supported Ni nanoparticles for efficient CO₂ electroreduction.

Not available

S-EPMC6335639 | biostudies-literature

Hyocholic acid species as novel biomarkers for metabolic disorders

Hyocholic acid (HCA) is a major bile acid (BA) species in the BA pool of pigs, a species known for its exceptional resistance to spontaneous development of diabetic phenotypes. HCA and its derivatives are also present in human blood and urine. We investigate whether human HCA profiles can predict th...

2021-10-06 | MTBLS2343 | MetaboLights

RNA binding of mouse retinal ganglion cells (RGCs) in multiple sclerosis and in glaucoma eyes compared to normal controls to identify RNA species bound by deiminated and non-deiminated MA-Brent-1 (bhatt-affy-mouse-581641)

We have identified loss of deiminated MA-Brent-1 (an RNA and export binding protein) in the retinal ganglion cells (RGCs) in multiple sclerosis and in glaucoma eyes compared to normal controls. Deimination refers to posttranslational modification of protein bound arginine (not free arginine) in citr...

ORGANISM(S): Mus musculus

2009-07-01 | E-GEOD-11843 | biostudies-arrayexpress

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