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Hyperphosphatemic familial tumoral calcinosis (3)
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Instrument Platform

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2005 (4)
2020 (4)
2022 (2)
2009 (2)
2008 (2)
2007 (2)
2006 (2)
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CHEBI ID

CHEBI:17822 (1)
CHEBI:26271 (1)
CHEBI:25094 (1)
CHEBI:18237 (1)
CHEBI:22660 (1)
CHEBI:27570 (1)
CHEBI:18186 (1)
CHEBI:26986 (1)
CHEBI:16811 (1)
CHEBI:24898 (1)
CHEBI:25017 (1)
CHEBI:15428 (1)
CHEBI:28044 (1)
CHEBI:27266 (1)
CHEBI:16449 (1)
CHEBI:29016 (1)
CHEBI:15366 (1)
CHEBI:78320 (1)
CHEBI:4093 (1)

Metabolite Name

1-Fluoro-25-hydroxy-16-ene-23-yne-26,27-hexadeuterovitamin-D3 (1)
24,24-difluoro-1alpha,25-dihydroxy-24a-homocholecalciferol (1)
1alpha-hydroxy-22-oxacholecalciferol (1)
AC2SGL(18:0/36:0(2Me[S],4Me[S],6Me[S],8Me[S],10Me[S],12Me[R],14Me[R],16Me[R],18Me[R],19OH)) (1)
C25:3 Highly branched isoprenoid A (1)
Hoslundin (1)
Sophoracoumestan A (1)
PIM2(19:0/16:0) (1)
PA(P-16:0/20:5(5Z,8Z,11Z,14Z,17Z)) (1)
PI(22:2(13Z,16Z)/22:1(11Z)) (1)
PI(20:3(8Z,11Z,14Z)/22:2(13Z,16Z)) (1)
PI(17:1(9Z)/20:5(5Z,8Z,11Z,14Z,17Z)) (1)
PG(15:0/22:4(7Z,10Z,13Z,16Z)) (1)
PE-Cer(d16:2(4E,6E)/20:1(11Z)(2OH)) (1)
Isoglobotriglycosylceramide(d18:1/26:0) (1)
PS(P-16:0/19:1(9Z)) (1)
PI(20:2(11Z,14Z)/22:1(11Z)) (1)
PA(P-18:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z)) (1)
CL(1'-[16:0/16:0],3'-[16:0/16:0]) (1)
CL(1'-[16:0/16:0],3'-[18:1(9Z)/16:0]) (1)
Isoglobotriglycosylceramide(d18:1/24:0) (1)
PI(16:1(9Z)/22:1(11Z)) (1)
1,25-Dihydroxycholesterol (1)
CL(1'-[20:4(5Z,8Z,11Z,14Z)/18:2(9Z,12Z)],3'-[20:4(5Z,8Z,11Z,14Z)/20:4(5Z,8Z,11Z,14Z)]) (1)
CL(1'-[16:0/18:0],3'-[18:0/20:0]) (1)
PI(22:4(7Z,10Z,13Z,16Z)/22:1(11Z)) (1)
Isoglobotriglycosylceramide(d18:1/22:0) (1)
Dodecaprenyl phosphate-galacturonic acid (1)
PA(20:4(5Z,8Z,11Z,14Z)/21:0) (1)
MfGL-II (1)

First Public Date

2023 (3)

Study type

Transcription profiling by array (45)
RNA-seq of coding RNA (5)
Comparative genomic hybridization by array (4)
Other (4)
ChIP-seq (4)
RNA-seq of coding RNA from single cells (3)
Genotyping by array (2)
Methylation profiling by array (2)
ChIP-chip by tiling array (1)
Spatial transcriptomics by high-throughput sequencing (1)
Hi-C (1)

Release Date

2023 (159)
2021 (151)
2025 (150)
2022 (140)
2024 (114)
2020 (89)
2019 (83)
2018 (55)
2015 (47)
2016 (45)
2017 (39)
2012 (31)
2026 (30)
2014 (30)
2013 (28)
2010 (21)
2011 (18)
2009 (15)
2008 (6)
2007 (5)
2005 (4)
2006 (3)
2004 (3)
2000 (1)

Lab affiliation

Biological Chemistry Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland, United States (3)
CINVESTAV Unidad Irapuato Km. 9.6 Libramiento Norte Carr. Irapuato-León 36821 Irapuato Gto., México Tel.: +52-462-6239-635 (1)
Center for Alzheimer’s and Related Dementias, National Institutes of Health, Bethesda, MD, USA (1)
Department of Biochemistry and Pharmacology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, VIC, 3010, Australia 2Murdoch Children’s Research Institute, Melbourne, VIC 3052, Australia 3Victorian Clinical Genetics Services, Murdoch Children’s Research Institute, Melbourne, VIC, 3052, Australia (1)
Division Systems Biology of Signal Transduction German Cancer Research Center (DKFZ) Im Neuenheimer Feld 280 69120 Heidelberg, Germany (1)
Functional Proteomics, ICR (1)
Head of Mass Spectrometry and Proteomics STP (lab head) (1)
Institute of Life Sciences (UCL/ISV), Belgium (1)
Marine Chemistry and Geochemistry Woods Hole Oceanographic Institute (1)
NIH/NIDCR (1)
Pronacera Seville, Spain (1)
Proteomics Center, Erasmus MC, Rotterdam (1)
Proteomics Unit. Navarrabiomed. Spain (1)
REQUIMTE-LAQV, Department of Chemistry and Biochemistry, Faculty of Sciences of the University of Porto, 4169-007 Porto, Portugal (1)
UK Dementia Research Institute Imperial College London (1)

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Exploring the Glucose Fluxotype of the E. coli y-ome Using High-Resolution Fluxomics

We have developed a robust workflow to measure high-resolution fluxotypes (metabolic flux phenotypes) for large strain libraries under fully controlled growth conditions. This was achieved by optimizing and automating the whole high-throughput fluxomics process and integrating all relevant software ...

2021-05-13 | MTBLS2188 | MetaboLights

Nucleolin-Sle A Glycoforms as E-Selectin Ligands and Potentially Targetable Biomarkers at the Cell Surface of Gastric Cancer Cells.

Not available

S-EPMC7226152 | biostudies-literature

LaRA 2: parallel and vectorized program for sequence-structure alignment of RNA sequences.

Not available

S-EPMC8734264 | biostudies-literature

O-linked glicoproteomics of gastric cancer cell lines OCUM-1, N87 and KATO-III

Gastric cancer (GC) is the third leading cause of cancer-related death worldwide, continuously requiring innovative target therapies. The sialyl-lewis A (SLeA) antigen offers tremendous potential for precise cancer targeting. This glycan is rarely expressed by healthy tissues and blood cells but is ...

ORGANISM(S): Homo sapiens (Human)

2020-05-11 | PXD016968 | Pride