Riley S S - OmicsDI

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Unknown (1807)
Proteomics (59)
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Genomic (2)

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Homo sapiens (61)
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synthetic construct (1)
Xenopus laevis (1)
Escherichia coli str. K-12 substr. MG1655 (1)
288671 (1)
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Aspergillus aculeatus ATCC 16872 (1)
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Aspergillus carbonarius ITEM 5010 (1)
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Saccharomycopsis malanga (1)

Organisms

Escherichia coli str. K-12 substr. MG1655 (1)

Repository

pride (56)
biostudies-arrayexpress (40)
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Disease

Disease free (3)
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Mitochondrial metabolism disease (1)
Type 2 diabetes mellitus (1)

Technology Type

Mass Spectrometry (56)
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Affinity purification coupled with mass spectrometry proteomics (5)
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Instrument Platform

AB SOLiD 4 System (1)
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Publication Date

2025 (18)
2022 (12)
2023 (8)
2013 (7)
2024 (6)
2020 (6)
2026 (6)
2015 (5)
2011 (5)
2010 (5)
2009 (5)
2012 (4)
2021 (4)
2019 (3)
2008 (3)
2018 (2)
2014 (1)
2016 (1)

CHEBI ID

CHEBI:1148 (2)
CHEBI:15366 (2)
CHEBI:15428 (2)
CHEBI:15760 (2)
CHEBI:15887 (2)
CHEBI:15891 (2)
CHEBI:16016 (2)
CHEBI:16024 (2)
CHEBI:16199 (2)
CHEBI:16359 (2)
CHEBI:16530 (2)
CHEBI:16695 (2)
CHEBI:16704 (2)
CHEBI:16708 (2)
CHEBI:16737 (2)
CHEBI:16742 (2)
CHEBI:16750 (2)
CHEBI:16755 (2)
CHEBI:16830 (2)
CHEBI:16958 (2)
CHEBI:17053 (2)
CHEBI:17368 (2)
CHEBI:17418 (2)
CHEBI:17497 (2)
CHEBI:17533 (2)
CHEBI:17568 (2)
CHEBI:17596 (2)
CHEBI:17620 (2)
CHEBI:17754 (2)
CHEBI:17821 (2)

Metabolite Name

6-phosphogluconic acid (2)
Adenine (2)
Chenodeoxycholic acid (2)
Fumarate (2)
Galactose (2)
Glucose-1-phosphate (2)
Glycine (2)
Hypoxanthine (2)
Inosine (2)
Leucine (2)
Methylamine (2)
Phenylacetic acid (2)
Succinate (2)
Taurine (2)
Thymine (2)
Uracil (2)
Xanthine (2)
(4-hydroxy-3-methoxyphenyl)ethanol (1)
(r)-3-hydroxybutyric acid (1)
(s)-3,4-dihydroxybutyric acid (1)
(s)-3-hydroxyisobutyric acid (1)
1,2,3-butanetriol (1)
1,2,3-trihydroxybenzene (1)
1,2,4-benzenetriol (1)
1,2,4-butanetriol (1)
1,2-cyclohexanedione (1)
1,3-diaminopropane (1)
1,3-dihydroxypyridine (1)
1,4-butanediol (1)
1,4-dihydroxy-2,6-dimethoxybenzene (1)

First Public Date

2016 (1)
2014 (1)

Classification

bacteria (1)

Study type

Transcription profiling by array (30)
RNA-seq of coding RNA (5)
MicroRNA profiling by high-throughput sequencing (1)
Comparative genomic hybridization by array (1)
Other (1)
ChIP-seq (1)
DNA-seq (1)

Release Date

2022 (200)
2023 (195)
2025 (180)
2021 (173)
2024 (155)
2020 (140)
2019 (120)
2018 (116)
2017 (102)
2015 (83)
2016 (77)
2013 (63)
2014 (48)
2011 (38)
2012 (33)
2010 (32)
2026 (26)
2009 (21)
2007 (10)
2008 (9)
2006 (9)
2005 (3)
2004 (3)
2001 (3)
2003 (2)
2002 (2)
2000 (1)
1999 (1)
1998 (1)
1997 (1)

Lab affiliation

Principal Investigator Centre for Targeted Protein Degradation, School of Life Sciences (4)
Department of Chemistry, University of Washington, Seattle, WA, USA (3)
Department of Chemistry, Stanford ChEM-H (2)
Department of Chemistry, Stanford University (2)
Principal Investigator Centre for Targeted Protein Degradation (2)
Principal Investigator • Centre for Targeted Protein Degradation (2)
Assistant Professor of Pathology Stanford ChEM-H Institute Scholar Stanford University (1)
CRUK - Beatson Institute for Cancer Research - Switchback Rd, Bearsden, Glasgow G61 1BD - United Kingdom (1)
Canada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver V5Z 1L3, Canada. (1)
College of Life Science, Northwest University, Xi’an, 710069, P. R. China (1)
Dana Farber Cancer Institute (1)
Department of Biology, Brandon University, 3rd Floor, John R. Brodie Science Centre, 270 18th Street, Brandon, MB, Canada, R7A 6A9 (1)
Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA, USA. Department of Cell Biology, Harvard Medical School, Boston, MA, USA. (1)
Department of Chemistry University of Washington, Seattle, WA, USA (1)
Department of Chemistry and Sarafan ChEM-H (1)
Department of Chemistry, Stanford University Howard Hughes Medical Institute, Stanford University (1)
Department of Chemistry, Stanford University Stanford ChEM-H (1)
Department of Chemistry, Stanford University, Stanford, California, USA Howard Hughes Medical Institute, Stanford, California, USA (1)
Department of Chemistry, University of Washington, Seattle, WA (1)
Department of Chemistry, University of Washington, Seattle, Washington 98195, United States (1)
Department of Microbiology and Immunology, Stanford University (1)
Department of Pathology, University of Michigan Medical School (1)
Department of Pediatrics Indiana University School of Medicine Riley Hospital for Children (1)
Department of Pharmaceutical Chemistry, University of California - San Francisco (1)
Department of Pharmacology & Toxicology 1 King’s College Circle Toronto, ON, Canada, M5S 1A8 (1)
Discovery Biology, AstraZeneca Pharmaceuticals (1)
Emory University (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)
Group Systems Biology of Motor Proteins, Department of NMR-based Structural Biology, Max-Planck-Institute for Biophysical Chemistry, Göttingen, Germany (1)
Harry Perkins Institute of Medical Research, QEII Medical Centre, Nedlands, Western Australia 6009, Australia (1)

Tags

xref:PubMed:19767843 (1)
xref:EuropePMC:PMC5225093 (1)
pathogen:bacterium (1)
pathogen (1)

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Expression data from Xenopus anterior gut RFX6 knockdown

Recently a new neonatal diabetes syndrome, Mitchell-Riley syndrome, was discovered. To identify the genetic cause of the syndrome homozygosity mapping was used, several chromosomal regions were linked to Mitchell-Riley syndrome. In situ hybridization of genes from one such region using model organ...

ORGANISM(S): Xenopus laevis

2011-01-24 | E-GEOD-23642 | biostudies-arrayexpress

Voltage-gated potassium channel proteins and stereoselective S-nitroso-l-cysteine signaling.

Not available

S-EPMC7526540 | biostudies-literature

In Vivo Analysis of Tissue S-Nitrosothiols in Pediatric Sepsis.

Not available

S-EPMC10967417 | biostudies-literature

Mitchell-Riley Syndrome: A Novel Mutation in RFX6 Gene.

Not available

S-EPMC4681791 | biostudies-literature

Gut microbiome dysbiosis drives metabolic dysfunction in Familial dysautonomia

Familial dysautonomia (FD) is a rare genetic neurologic disorder caused by impaired neuronal development and progressive degeneration of both the peripheral and central nervous systems. FD is monogenic, with >99.4% of patients sharing an identical point mutation in the elongator acetyltransferase co...

2022-12-06 | MTBLS5138 | MetaboLights

Efficacy of RTS,S/AS01E vaccine against malaria in children 5 to 17 months of age.

Not available

S-EPMC2655100 | biostudies-literature

Safety of the malaria vaccine candidate, RTS,S/AS01E in 5 to 17 month old Kenyan and Tanzanian Children.

Not available

S-EPMC2993932 | biostudies-literature

Crystal structure of phenyl 2,4,5-tri-chloro-benzene-sulfonate.

Not available

S-EPMC4908567 | biostudies-literature

Crystal structure of 3,5-di-methyl-phenyl 2-nitro-benzene-sulfonate.

Not available