Ang ii - OmicsDI

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Technology Type

Mass Spectrometry (53)
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EI (2)
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Instrument Platform

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Publication Date

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CHEBI ID

CHEBI:28229 (2)
CHEBI:25682 (2)
CHEBI:17929 (2)
CHEBI:16467 (2)
CHEBI:15873 (1)
CHEBI:70958 (1)
CHEBI:17482 (1)
CHEBI:18095 (1)
CHEBI:27971 (1)
CHEBI:18066 (1)
CHEBI:60175 (1)
CHEBI:15611 (1)
CHEBI:15414 (1)
CHEBI:16680 (1)
CHEBI:17287 (1)
CHEBI:15846 (1)
CHEBI:49033 (1)
CHEBI:17858 (1)
CHEBI:16238 (1)
CHEBI:16436 (1)
CHEBI:17126 (1)
CHEBI:18323 (1)
CHEBI:16695 (1)
CHEBI:20607 (1)
CHEBI:16708 (1)
CHEBI:17562 (1)
CHEBI:16283 (1)
CHEBI:16750 (1)
CHEBI:16349 (1)
CHEBI:15729 (1)

Metabolite Name

Guanosine (3)
Lysinoalanine (2)
Phenylalanylserine (2)
Diphenyl phosphate (2)
Prolyl-Arginine (2)
Allylestrenol (2)
LysoPC(20:5(5Z,8Z,11Z,14Z,17Z)/0:0) (2)
4-Vinylcyclohexene (2)
Uridine diphosphate glucose (2)
Dehydrooreadone (2)
Cytidine monophosphate (2)
Biotin sulfone (2)
N-(1-Deoxy-1-fructosyl)leucine (2)
Betaine (2)
Citrulline (2)
Abacavir (2)
Ricinoleic acid (2)
L-Asparagine (2)
L-Threonine (2)
Palmitoleic acid (2)
Taurine (2)
Prostaglandin D2 (2)
2-Methylthioadenosine (2)
Arginine (2)
Lysine (2)
Tyrosine (2)
Serine (2)
Asymmetric dimethylarginine (2)
Threonine (2)
Glutamine (2)

First Public Date

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2020 (9)
2017 (7)
2019 (4)
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Study type

Transcription profiling by array (157)
RNA-seq of coding RNA (25)
ChIP-seq (14)
RNA-seq of non coding RNA (5)
Unknown experiment type (4)
Other (4)
Transcription profiling by SAGE (3)
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Human - One-color microarray (2)
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Comparative genomic hybridization by array (2)
ATAC-seq (2)
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RNA-seq of coding RNA from single cells (2)
Animal - One-color microarray (1)
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Cell line - High-throughput sequencing (1)
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Release Date

2021 (220)
2022 (211)
2023 (158)
2020 (153)
2019 (147)
2025 (134)
2024 (125)
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2005 (15)
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2004 (7)
2002 (2)
1999 (2)
2003 (1)
2001 (1)

Lab affiliation

Department of Plant Science and Technology, Chung-Ang University, Anseong, Republic of Korea (4)
Department of Plant Science and Technology, Chung-Ang University, Anseong 17546, Republic of Korea (3)
Department of Veterinary Biosciences, Melbourne Veterinary School, The University of Melbourne, Parkville, Victoria 3010, Australia (2)
Hangzhou Medical College (2)
Department of Plant Science and Technology, Chung-Ang University, Republic of Korea (2)
Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Australia (1)
Department of Veterinary Biosciences, Melbourne Veterinary School, The University of Melbourne, Australia (1)
Department of Emergency Medicine, Beijing Key Laboratory of Cardiopulmonary Cerebral Resuscitation, Beijing Chaoyang Hospital, Capital Medical University, China (1)
Department of Medicine and Cell Biology Duke University Medical Center, DUMC 102151 (1)
Department of Veterinary Biosciences, The University of Melbourne (1)
University of Melbourne, Florey Institute (1)
Department of Obstetrics Gynaecology and Newborn Health, The University of Melbourne, Australia (1)
Nantong University (1)
Bio21 Mass Spectrometry and Proteomics Facility, The University of Melbourne, Parkville, Victoria 3010, Australia (1)
Department of Medical Biotechnology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Kraków, Poland (1)
Sir Peter MacCallum Department of Oncology, University of Melbourne, Australia; Peter MacCallum Cancer Centre, Melbourne, Australia (1)
Peter MacCallum Cancer Centre, Melbourne, 3000, Victoria, Australia (1)
Bio21 Molecular Science and Biotechnology Institute,Department of Biochemistry and Pharmacology, University of Melbourne (1)
Universidade Federal de Minas Gerais (1)
Department of Plant Science and Technology, Chung-Ang University, Republic of Korea (1)
China-Japan Union Hospital of Jilin University (1)
Jining First People's Hospital Affiliated to Shandong First Medical University (1)
Department of Biochemistry and Chemistry, Research Centre for Extracellular Vesicles, La Trobe Institute for Molecular Science, La Trobe University, Melbourne, VIC 3086, Australia (1)
Melbourne Dental School, Faculty of Medicine, Dentistry & Health Sciences, University of Melbourne, Melbourne, Australia (1)
La Trobe University, Department of Biochemistry and Genetics (1)
Professor, Depts of Physiology, Pharmacology, Nephrology/Medicine, Member, BIO5/Arizona Center on Aging/Sarver Heart Center, University of Arizona College of Medicine (1)
Department of Cardiology, the First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China (1)
Bio21 Mass Spectrometry and Proteomics Facility, The University of Melbourne, Parkville, Victoria 3052, Australia (1)
5Department of Plant Science and Technology, Chung-Ang University, Anseong 17546, Republic of Korea (1)
Dept. Integrative Plant Science, Chuang-Ang University (1)

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High-throughput sequencing of endogenous small RNAs from rat vascular smooth muscle cells with and without Angiotensin II stimulation

Angiotensin II (Ang II)-mediated vascular smooth muscle cells (VSMC) dysfunction plays a critical role in cardiovascular diseases. However, the role of microRNAs (miRNAs) in this process is unclear. We used small RNA deep sequencing to profile Ang II-regulated miRNAs in rat VSMC and evaluated their ...

ORGANISM(S): Rattus norvegicus

2012-03-23 | E-GEOD-35664 | biostudies-arrayexpress

Expression data from mouse tissue Angiotensin II treated for 0,1,3,7days

Angiotensin II (Ang II) mediated signaling plays a key role in the development of hypertension associated target organ damages. However, the gene expression changes regulated by Ang II in the early stage of acute cerebral, cardiac, renal, vascular injury remain unclear. we investigated Ang IIâ??medi...

ORGANISM(S): Mus musculus

2014-07-16 | E-GEOD-59437 | biostudies-arrayexpress

CaMKII inhibition in smooth muscle cells controls Ang-II-induced gene transcription in the aorta

The Ca2+/calmodulin-dependent kinase II is expressed in smooth muscle and believed to mediate intracellular calcium handling and calcium-dependent gene transcription. CaMKII is activated by Angiotensin-II. The multifunctional calcium/calmodulin-dependent kinase II (CaMKII) is activated by Angiotensi...

ORGANISM(S): Mus musculus

2015-07-01 | E-GEOD-64613 | biostudies-arrayexpress

Expression data from Angiotensin II (Ang II)-treated Rat Vascular Smooth Muscle Cells (RVSMC)

Angiotensin II (Ang II)-mediated vascular smooth muscle cells (VSMC) dysfunction plays a critical role in cardiovascular diseases. However, the gene expression in this process is unclear. We used Rat Affymetrix gene array to profile Ang II-regulated gene in RVSMC and evaluated their role in VSMC dys...

ORGANISM(S): Rattus norvegicus

2012-03-23 | E-GEOD-35627 | biostudies-arrayexpress

Impaired Glycolysis-Derived Serine Metabolism as a Key Driver of Podocyte Injury with Senescence

Chronic kidney disease (CKD) is a major health issue, with podocyte injury with senescence playing a central role in glomerulosclerosis. This study investigates the link between glycolysis-derived serine metabolism and podocyte injury with senescence, focusing on the role of phosphoglycerate kina...

2025-08-23 | MTBLS12883 | MetaboLights

Transcriptional network analysis reveals that AT1 and AT2 Angiotensin II receptors are both involved in the regulation of genes essential for glioma progression

Gliomas are aggressive primary brain tumors, presenting surgery limitations due to their highly infiltrative potential. The expression of Angiotensin II (Ang II) receptors in human astrocytomas was previously associated with a poor prognosis. Accordingly, this study was undertaken to reveal the mole...

ORGANISM(S): Rattus norvegicus

2014-12-20 | E-GEOD-47529 | biostudies-arrayexpress

Transcription profiling of human, Bos taurus, and rat adrenocortical cells treated with Angiotensin II

Angiotensin II (Ang-II) regulates adrenal steroid production and gene transcription through several signaling pathways. Changes in gene transcription occur within minutes after Ang-II stimulation, causing an acute increase in aldosterone production and subsequent increase in the overall capacity to ...

ORGANISM(S): Rattus norvegicus

2008-11-06 | E-GEOD-8442 | biostudies-arrayexpress

QTL for renal and cardiac function during Angiotensin II and high-sodium treatment of a backcross between C57BL/6J-to-Balb/CJ-F1 and Balb/CJ

Balb/CJ mice develop heart failure and quickly decompensate during combination treatment with Angiotensin II and high-sodium diet, while C57BL/6J mice do not. Balb/CJ show a predominantly diastolic heart failure, signs of increased pulmonary pressure, relative sodium and fluid retention, peripheral ...

ORGANISM(S): Mus musculus

2019-06-13 | E-MTAB-8047 | biostudies-arrayexpress

Expression data from Ang II induced HUVECs

PRJNA509564 | ENA

Control vs. AngII Infusion: Heart

C57Bl/6J mice received continuous administration of saline or Angiotensin II via implanted minipumps for 7 days, total RNA prepared from homogenized hearts, SAGE library constructed from heart RNA pooled from 6 mice. Keywords: other

ORGANISM(S): Mus musculus

2004-07-22 | E-GEOD-1446 | biostudies-arrayexpress

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