Ferguson M A MA

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Unknown (650)
Proteomics (37)
Genomics (4)
Transcriptomics (3)
Other (1)
Metabolomics (1)

Organisms

Homo sapiens (36)
Mus musculus (2)
Fusobacterium nucleatum (1)
Trypanosoma brucei (1)
Trypanosoma brucei brucei (1)

Repository

pride (34)
EGA (4)
biostudies-arrayexpress (3)
PAXDB (2)
GPMDB (1)
MassIVE (1)
MetaboLights (1)

Tissue

Cell culture (20)
B cell (3)
Blood (2)
Cell suspension culture (2)
Epithelial cell (2)
Blood cell (1)
Blood serum (1)
Bone marrow (1)
Heart (1)
Liver (1)
Neuron (1)
Neuronal stem cell (1)
Permanent cell line cell (1)
Prostate gland (1)

Disease

Multiple myeloma (3)
Breast cancer (2)
Not Available (1)
Acute leukemia (1)
Brain glioma (1)
Cardiovascular system disease (1)
Frontotemporal dementia (1)
Prostate adenocarcinoma (1)

Technology Type

Mass Spectrometry (34)
Shotgun proteomics (23)
Affinity purification coupled with mass spectrometry proteomics (5)
Bottom-up proteomics (5)
Data-dependent acquisition (2)
Data-independent acquisition (2)
Mass spectrometry (1)

Instrument Platform

HiSeq X Five (1)
Illumina HiSeq 2500 (1)
Instrument (1)
Q Exactive (1)
Liquid Chromatography MS - Alternating (LC-MS (Alternating)) (1)
LTQ-Orbitrap (1)

Publication Date

2021 (16)
2025 (5)
2022 (4)
2018 (2)
2016 (2)
2020 (2)
2013 (2)
2026 (2)
2019 (2)
2011 (1)
2015 (1)
2014 (1)
2009 (1)

UNIPROT ID/AC

5691.AAQ15626 (2)
5691.AAQ15709 (2)
5691.AAQ16021 (2)
5691.AAZ10366 (2)
5691.AAZ10412 (2)
5691.AAZ10463 (2)
5691.AAZ10464 (2)
5691.AAZ10465 (2)
5691.AAZ10466 (2)
5691.AAZ10510 (2)
5691.AAZ10511 (2)
5691.AAZ10512 (2)
5691.AAZ10771 (2)
5691.AAZ10942 (2)
5691.AAZ10991 (2)
5691.AAZ11075 (2)
5691.AAZ11276 (2)
5691.AAZ11337 (2)
5691.AAZ11338 (2)
5691.AAZ11340 (2)
5691.AAZ11529 (2)
5691.AAZ11530 (2)
5691.AAZ11531 (2)
5691.AAZ11532 (2)
5691.AAZ11533 (2)
5691.AAZ11534 (2)
5691.AAZ11535 (2)
5691.AAZ11536 (2)
5691.AAZ11537 (2)
5691.AAZ11660 (2)

CHEBI ID

CHEBI:13389 (1)
CHEBI:15318 (1)
CHEBI:15422 (1)
CHEBI:15603 (1)
CHEBI:16235 (1)
CHEBI:16708 (1)
CHEBI:16828 (1)
CHEBI:16908 (1)
CHEBI:16977 (1)
CHEBI:17050 (1)
CHEBI:17084 (1)
CHEBI:17203 (1)
CHEBI:17239 (1)
CHEBI:17368 (1)
CHEBI:17552 (1)
CHEBI:17568 (1)
CHEBI:17622 (1)
CHEBI:17659 (1)
CHEBI:17895 (1)
CHEBI:18050 (1)
CHEBI:18385 (1)
CHEBI:26806 (1)
CHEBI:29988 (1)
CHEBI:29993 (1)
CHEBI:30769 (1)
CHEBI:37574 (1)
CHEBI:44897 (1)
CHEBI:456215 (1)
CHEBI:57865 (1)
CHEBI:58027 (1)

Metabolite Name

2-Hydroxyglutarate (1)
3-phosphoglycerate (1)
AMP (1)
ATP (1)
Adenine (1)
Arginine phosphate (1)
CDP (1)
CMP (1)
Citrate (1)
GDP (1)
Glyceraldehyde 3-phosphate (1)
Guanine (1)
Hypoxanthine (1)
L-Alanine (1)
L-Aspartate (1)
L-Glutamate (1)
L-Glutamine (1)
L-Leucine (1)
L-Proline (1)
L-Tryptophan (1)
L-Tyrosine (1)
Malate (1)
NAD+ (1)
NADH (1)
Phosphoenolpyruvate (1)
Succinic acid (1)
Thiamin (1)
Thiamin diphosphate (1)
Thiamin monophosphate (1)
UDP (1)

Modification

-17.026549 (1)
0.984016 (1)
15.994915 (1)
203.079373 (1)
31.989829 (1)
42.010565 (1)
57.021464 (1)

Study type

High-throughput sequencing (1)
Transcription profiling by array (1)
RNA-seq of coding RNA (1)

Release Date

2022 (66)
2018 (64)
2020 (64)
2021 (63)
2023 (48)
2024 (47)
2025 (35)
2019 (35)
2017 (31)
2016 (31)
2015 (30)
2013 (26)
2012 (25)
2014 (22)
2011 (20)
2010 (14)
2008 (10)
2026 (8)
2009 (8)
2006 (1)
2005 (1)
2004 (1)
2003 (1)
2000 (1)
1998 (1)

Lab affiliation

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 (16)
Dept. of Laboratory Medicine, University of California, San Francisco, CA (3)
Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA (1)
Centre for Regenerative Medicine, Institute for Regeneration and Repair, University of Edinburgh, Edinburgh EH16 4UU, United Kingdom. Cancer Research UK Edinburgh Centre, University of Edinburgh, Edinburgh EH4 2XR, United Kingdom. (1)
Centre for Gene Regulation and Expression, University of Dundee (1)
Cornell University (1)
Department of Biotechnology and Bioengineering, Technical University of Denmark (1)
Department of Chemistry & Biochemistry Skaggs School of Pharmacy and Pharmaceutical Sciences University of California San Diego 9500 Gillman Drive, La Jolla, CA 92093 (1)
Department of Pharmacology, University of Nevada, Reno School of Medicine (1)
Indiana University School of Medicine, Dept of Pediatrics; Herman B Wells Center for Pediatric Research (1)
Institute for Molecular Biosciences University of Queensland Brisbane Qld 4072 Australia (1)
Lancaster University (1)
OncoProteomics Laboratory, Dept of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands (1)
SChool of Biosciences University of Birminghsam Birminghsm B15 2TT UK (1)
School of Life Sciences (1)
University of Dundee (1)
Victoria University of Wellington, New Zealand (1)

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A Gene of the β3-Glycosyltransferase Family Encodes N-Acetylglucosaminyltransferase II Function in Trypanosoma brucei.

Not available

S-EPMC4919465 | biostudies-literature

Structure of a complex phosphoglycan epitope from gp72 of Trypanosoma cruzi.

Not available

S-EPMC3630849 | biostudies-literature

Fractionation of membrane components from tachyzoite forms of Toxoplasma gondii: differential recognition by immunoglobulin M (IgM) and IgG present in sera from patients with acute or chronic toxoplasmosis.

Not available

S-EPMC86463 | biostudies-literature

A gene catalogue of the euchromatic male-specific region of the horse Y chromosome: comparison with human and other mammals.

Not available

S-EPMC3143126 | biostudies-literature

Reproducibility and Robustness of a Liver Microphysiological System PhysioMimix LC12 under Varying Culture Conditions and Cell Type Combinations.

Not available

S-EPMC10603899 | biostudies-literature

Phase II trial of trastuzumab in combination with cytotoxic chemotherapy for treatment of metastatic osteosarcoma with human epidermal growth factor receptor 2 overexpression: a report from the children's oncology group.

Not available

S-EPMC3397787 | biostudies-literature

ZBTB11 Depletion Targets Metabolic Vulnerabilities in K-Ras Inhibitor Resistant PDAC

Over 95% of pancreatic ductal adenocarcinomas (PDAC) harbor oncogenic mutations in K-Ras. Upon treatment with K-Ras inhibitors, PDAC cancer cells undergo metabolic reprogramming towards an oxidative phosphorylation-dependent, drug-resistant state. However, direct inhibition of complex I is poorly ...

ORGANISM(S): Homo sapiens (Human)

2025-07-15 | PXD052360 | Pride

Zbtb11 pdac k-ras metabolic hipsc