Alzheimers disease

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Unknown (389)
Transcriptomics (202)
Proteomics (163)
Genomics (103)
Metabolomics (34)
Other (9)

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Homo sapiens (142)
Mus musculus (83)
Archaea (39)
Bacteria (39)
Betaherpesvirinae (39)
Borrelia (39)
Botrytis cinerea (39)
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Clostridium perfringens (39)
Cnidaria (39)
Eukaryota (39)
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Fungi (39)
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Human betaherpesvirus 5 (39)
Influenza C virus (39)
Japanese encephalitis virus group (39)
Miscanthus x giganteus (39)
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Rattus norvegicus (11)
Drosophila melanogaster (6)
Saccharomyces cerevisiae (3)
Fusarium sinicum (3)
Caenorhabditis elegans (2)
Punica granatum (1)
Aplysia californica (1)
Mus musculus domesticus (1)
Cricetulus griseus (1)
Microcebus murinus (1)
Escherichia coli (1)

Organisms

Homo sapiens (10)
Mus musculus (7)
feces metagenome (2)
Macaca fascicularis (1)
Drosophila melanogaster (1)
human metagenome (1)
mouse metagenome (1)
mouse gut metagenome (1)
human gut metagenome (1)

Repository

biostudies-arrayexpress (208)
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pride (39)
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ExpressionAtlas (9)
jPOST (9)
PanoramaPublic (9)
geo (6)
GNPS (5)
GPMDB (3)
iProX (3)
PAXDB (3)

Tissue

Brain (29)
Hippocampus (3)
Brain (3)
Blood (3)
Cell culture (3)
Superior frontal gyrus (2)
Entorhinal cortex (2)
Fibroblast cells (2)
Blood plasma (2)
Cerebrospinal fluid (2)
Postcentral gyrus (1)
Posterior cingulate cortex (1)
Temporal cortex (1)
Primary visual cortex (1)
Middle temporal gyrus (1)
Frontal cortex (1)
Neurons (1)
Cerebrospinal fluid (1)
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Liver (1)
Astrocyte (1)
Blood cell (1)
Gray matter (1)
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Pericyte cell (1)
Platelet (1)
Retina (1)
Rheumatoid arthritis disease specific synovial fluid (1)
Stem cell (1)

Disease

Alzheimers disease (21)
Alzheimer's disease (18)
Normal (10)
Not Available (3)
Parkinson's disease (2)
Multiple sclerosis (2)
Alzheimer's disease 1 (2)
Secondary progressive multiple sclerosis (1)
Progressive supranuclear palsy (1)
Essential tremor (1)
Corticobasal degeneration (1)
Mild cognitive impairment (1)
Meningeal tuberculosis (1)
Multiple system atrophy (1)
Neurologically healthy control (1)
Neuroblastoma (1)
Lewy body dementia (1)
Neurodegenerative disease (1)
Tauopathy (1)

Technology Type

Mass Spectrometry (49)
Bottom-up proteomics (15)
Shotgun proteomics (13)
Mass spectrometry (10)
ESI (10)
Mass spectrometry assay (6)
Top-down proteomics (6)
Data-dependent acquisition (5)
ILLUMINA, Illumina MiSeq (2)
NMR (2)
NMR spectroscopy assay (1)
NMR spectroscopy (1)
All-ion fragmentation (1)
Data-independent acquisition (1)
Mass spectrometry imaging (1)
SWATH MS (1)

Instrument Platform

Q Exactive (19)
Orbitrap Fusion Lumos (19)
Orbitrap Exploris 480 (9)
Orbitrap Fusion (8)
Q Exactive HF (7)
Illumina HiSeq 2500 (5)
Illumina NovaSeq 6000 (5)
Orbitrap Eclipse (5)
LTQ Orbitrap Elite (5)
LTQ Orbitrap Velos (5)
Illumina HiSeq 4000 (4)
NextSeq 500 (4)
Q TRAP (4)
Instrument (3)
6495C Triple Quadrupole LC/MS (3)
LTQ FT (3)
BeadBug Benchtop homogenizer (2)
N/A (2)
6410 Triple Quadrupole LC/MS (2)
6545 Q-TOF LC/MS (2)
5-Laser BD FACSAria III (1)
10X Genomics Chromium (1)
None (1)
ScanArray 5000 [PerkinElmer] (1)
Illumina NovaSeq X (1)
NextSeq 2000 (1)
Illumina HiSeq 1000 (1)
NextSeq 550 (1)
Illumina HiSeq 2000 (1)
Illumina HiSeq 3000 (1)

Publication Date

2024 (38)
2025 (34)
2014 (33)
2015 (28)
2013 (25)
2023 (24)
2021 (24)
2022 (21)
2020 (20)
2016 (19)
2010 (19)
2026 (18)
2012 (17)
2011 (14)
2019 (13)
2008 (10)
2007 (10)
2017 (9)
2009 (7)
2018 (6)
2006 (3)
2005 (1)

UNIPROT ID/AC

1433B_HUMAN (3)
1433F_HUMAN (3)
1433G_HUMAN (3)
1433S_HUMAN (3)
1433T_HUMAN (3)
1433Z_HUMAN (3)
2A5A_HUMAN (3)
2A5B_HUMAN (3)
2A5D_HUMAN (3)
2A5E_HUMAN (3)
2A5G_HUMAN (3)
2AAA_HUMAN (3)
2AAB_HUMAN (3)
2ABA_HUMAN (3)
2ABB_HUMAN (3)
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2ABG_HUMAN (3)
3BP1_HUMAN (3)
3BP5L_HUMAN (3)
3HAO_HUMAN (3)
3HIDH_HUMAN (3)
3MG_HUMAN (3)
41_HUMAN (3)
4EBP1_HUMAN (3)
4EBP2_HUMAN (3)
4ET_HUMAN (3)
4F2_HUMAN (3)
5HT1A_HUMAN (3)
5HT1B_HUMAN (3)
5HT2A_HUMAN (3)

CHEBI ID

CHEBI:26271 (4)
CHEBI:27897 (4)
CHEBI:18101 (3)
CHEBI:40521 (3)
CHEBI:91315 (3)
CHEBI:68441 (3)
CHEBI:17768 (3)
CHEBI:27570 (3)
CHEBI:74903 (3)
CHEBI:25858 (3)
CHEBI:28946 (3)
CHEBI:16449 (3)
CHEBI:27266 (3)
CHEBI:24898 (3)
CHEBI:28044 (3)
CHEBI:16811 (3)
CHEBI:17126 (3)
CHEBI:15366 (3)
CHEBI:19289 (3)
CHEBI:16040 (3)
CHEBI:9347 (3)
CHEBI:17802 (3)
CHEBI:29016 (3)
CHEBI:25017 (3)
CHEBI:28484 (3)
CHEBI:82912 (3)
CHEBI:70989 (3)
CHEBI:17012 (3)
CHEBI:46195 (3)
CHEBI:27480 (3)

Metabolite Name

Taurine (4)
Pseudouridine (4)
N4-Acetylsulfamethoxazole (3)
2,4-Dichlorophenol (3)
Geniposidic acid (3)
Gamma-Glutamylcysteine (3)
D-Xylitol (3)
Agnuside (3)
Galacturonic acid (3)
DUMP (3)
Ribitol (3)
Adenosine diphosphate ribose (3)
Epiandrosterone (3)
Leucine (3)
1,3,7-Trimethyluric acid (3)
Rotenone (3)
Salicyluric acid (3)
Dihydrofolic acid (3)
ATP (3)
AMP (3)
4-Nitrophenol (3)
Gingerol (3)
Xanthohumol (3)
6-Hydroxymelatonin (3)
L-Cystine (3)
Androsterone glucuronide (3)
Quercetin (3)
Saccharin (3)
Norfloxacin (3)
Aripiprazole (3)

First Public Date

2024 (18)
2026 (13)
2022 (13)
2025 (10)
2023 (8)
2021 (7)
2020 (3)
2019 (1)
2015 (1)
2014 (1)

Study type

Transcription profiling by array (138)
RNA-seq of coding RNA (24)
Methylation profiling by array (10)
Unknown experiment type (7)
Comparative genomic hybridization by array (4)
Proteomic profiling by array (4)
RNA-seq of total RNA (4)
RNA-seq of non coding RNA (4)
Animal - High-throughput sequencing (2)
MicroRNA profiling by high throughput sequencing (2)
ChIP-seq (2)
ChIP-chip by tiling array (1)
One-color microarray (1)
High-throughput sequencing (1)
Human - One-color microarray (1)
DNA-seq (1)
RNA-seq of coding RNA from single cells (1)
Methylation profiling by high throughput sequencing (1)

Release Date

2014 (59)
2021 (53)
2016 (51)
2015 (50)
2020 (49)
2019 (45)
2013 (43)
2018 (41)
2017 (38)
2012 (25)
2022 (23)
2011 (21)
2010 (21)
2025 (15)
2008 (13)
2024 (12)
2023 (12)
2009 (12)
2007 (9)
2006 (3)
2005 (1)
2026 (1)

Lab affiliation

National Key Laboratory of Medical Molecular Biology & Department of Immunology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences (3)
Lab of Jie Zheng, Neuroscience Research Institute and Department of Neurobiology, School of Basic Medical Sciences, Peking University, Beijing 100083, P.R. China (2)
Aalborg University Laboratory for Medical Massspectrometry (1)
Aarhus University, Denmark (1)
Department of Anatomy and Neurobiolog; Department of Pharmacology, Physiology and Biophysics; Department of Neurology, Boston University Chobanian and Avedisian School of Medicine, Boston, MA, 02118, USA (1)
Department of Chemistry, Vanderbilt University, Nashville, TN, USA (1)
Department of Medical Sciences, Cancer Pharmacology and Computational Medicine, Uppsala University Academic Hospital, Uppsala, Sweden. (1)
Department of Molecular Physiology, Leiden University & Oncode Institute, Leiden 2333 CC, Netherlands (1)
Department of Oncology-Pathology, Karolinska Institutet and Science for Life Laboratory, Stockholm, Sweden (1)
Department of Ophthalmology and Visual Sciences, Case Western reserve University,Cleveland,OH,USA (1)
Department of Pathology (1)
Department of Psychiatry and Human Behavior University of California, Irvine (1)
Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden Department of Molecular Neuroscience, University College London Institute of Neurology, Queen Square, London, UK UK Dementia Research Institute at UCL, London, United Kingdom (1)
Department of immunology, Peking Union Medical College, Beijing, China (1)
Dept Biomedical Sciences, School of Medicine and Health Sciences, Institute of Neurosciences, Universitat de Barcelona, E-08036 Barcelona (1)
Grupo de Neurociencias de Antioquia, SIU, Universidad de Antioquia, Colombia. Instituto de Biología, Facultad de Ciencias Exactas y Naturales, Universidad de Antioquia, Colombia. (1)
King's College London, Dept. of Basic and Clinical Neuroscience, Maurice Wohl Clinical Neuroscience Institute, 5 Cutcombe Road, London, SE5 9NU (1)
Laboratory for Medical Massspectrometry; Aalgorg University (1)
Laboratory for Neuropathology, Department of Imaging and Pathology, KU Leuven (University of Leuven), Leuven, Belgium;Leuven Brain Institute (LBI), KU Leuven (University of Leuven), Leuven, Belgium;Department of Imaging & Pathology, UZ Leuven (University Hospital Leuven), Leuven, Belgium. (1)
Lund University BME (1)
MIRCen, CNRS UMR 9199, Fontenay-aux-Roses, France (1)
Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Germany (1)
Molecular Neuroscience Research Center, Shiga University of Medical Science, Japan (1)
Neuroimmunology and MS Research University Hospital Zurich Frauenklinikstrasse 26 8091 Zurich Switzerland (1)
Neuroplasticity and Neurodegeneration Laboratory, CRIB, Ciudad Real Medical School, University of Castilla-La Mancha, 13071 Ciudad Real, Spain. (1)
Neuroproteomics Lab, Roskamp Institute, Sarasota, FL, USA (1)
Neuroproteomics, Max Delbrueck Center for Molecular Medicine in the Helmholtz Association, Robert-Roessle-Strasse 10, 13125 Berlin, Germany (1)
Professor, Diana Davis Spencer Foundation Chair for Glaucoma Research, The Jackson Laboratory (1)
Research Unit for Molecular Medicine, Department of Clinical Medicine, Aarhus University (1)
Senior Scientific Officer, Centre for Brain Research Indian Institute of Science Campus CV Raman Avenue Bangalore 560012. India. (1)

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Phosphorylated Tau Interactome in the Human Alzheimers Disease Brain

Accumulation of phosphorylated tau is a key pathological feature of Alzheimers disease. Phosphorylated tau accumulation causes synaptic impairment, neuronal dysfunction and formation of neurofibrillary tangles. The pathological actions of phosphorylated tau are mediated by surrounding neuronal prote...

ORGANISM(S): Homo Sapiens (ncbitaxon:9606)

2020-04-17 | MSV000085305 | MassIVE

The interactome of tau phosphorylated at T217 in Alzheimers disease human brain tissue

Tau phosphorylation and aggregation are pathological features of Alzheimers disease. Tau phosphorylated at threonine 217 (pT217) and threonine 231 (pT231) are early fluid biomarkers of Alzheimers disease, suggesting early involvement in disease. However, little is known about the specific actions of...

ORGANISM(S): Homo Sapiens (ncbitaxon:9606)

2024-11-11 | MSV000096377 | MassIVE

Cerebellum Alzheimer's Disease

Ion channel splice array data from cerebellum brain tissue samples collected from Alzheimer's disease patients. Temporal cortex (Alzheimer's disease affected brain tissue structure) and cerebellum (Alzheimer's disease unaffected brain tissue structure) samples from control subjects were compared to ...

ORGANISM(S): Homo sapiens

2010-06-11 | E-GEOD-6777 | biostudies-arrayexpress

Temporal Cortex Alzheimer's Disease

Ion channel splice array data from temporal cortex brain tissue samples collected from Alzheimer's disease patients. Temporal cortex (Alzheimer's disease affected brain tissue structure) and cerebellum (Alzheimer's disease unaffected brain tissue structure) samples from control subjects were compare...

ORGANISM(S): Homo sapiens

2010-06-11 | E-GEOD-6775 | biostudies-arrayexpress

Cerebellum Control (Alzheimer's disease control)

Ion channel splice array data from cerebellum brain tissue samples collected from control (non Alzheimer's disease) subjects. Temporal cortex (Alzheimer's disease affected brain tissue structure) and cerebellum (Alzheimer's disease unaffected brain tissue structure) samples from control subjects wer...

ORGANISM(S): Homo sapiens

2010-06-11 | E-GEOD-6778 | biostudies-arrayexpress

Temporal Cortex Control (Alzheimer's disease control)

Ion channel splice array data from temporal cortex brain tissue samples collected from control subjects (no Alzheimer's disease). Temporal cortex (Alzheimer's disease affected brain tissue structure) and cerebellum (Alzheimer's disease unaffected brain tissue structure) samples from control subjects...

ORGANISM(S): Homo sapiens

2010-06-11 | E-GEOD-6774 | biostudies-arrayexpress

Temporal lobe epilepsy and Alzheimer's disease

This SuperSeries is composed of the following subset Series: GSE6771: Temporal Cortex Control (mesial temporal lobe epilepsy control) GSE6773: Temporal neocortex mesial temporal lobe epilepsy GSE6774: Temporal Cortex Control (Alzheimer's disease control) GSE6775: Temporal Cortex Alzheimer's Disease ...

ORGANISM(S): Homo sapiens

2007-01-23 | E-GEOD-6834 | biostudies-arrayexpress

Corpora amylacea profiling reveals disease stage and brain region-specific alterations in glycogen metabolism in Alzheimer’s disease patient brains (MS (MTBLS))

Increasing evidence indicates that shifts in brain polysaccharide metabolism can influence the progression of multiple neurodegenerative diseases. Here we perform MALDI-MSI analysis of glycogen at different chain lengths in patients at different stages of Alzheimer's Disease. We look at frontal c...

2026-06-12 | MTBLS14754 | MetaboLights

Localized Proteomic Differences in Choroid Plexus of Alzheimers Disease and Epilepsy Patients

Alzheimers disease and epilepsy are reciprocally related. Among sporadic AD patients, seizures occur in 10-22 percent, and subclinical epileptiform abnormalities occur in 22-5 percent. Cognitive deficits, with prominent short-term memory impairments, occur in most epilepsy patients. Common neurophys...

ORGANISM(S): Homo Sapiens (ncbitaxon:9606)

2023-02-27 | MSV000091370 | MassIVE

Transcription profiling of human Alzheimers disease patients to identify genes regulating synaptic function and neuroplasticity in incipient AD

In Alzheimer's disease (AD), early deficits in learning and memory are a consequence of synaptic modification which are likely induced by toxic beta-amyloid oligomers (dAbeta). To identify molecular targets downstream of dAbeta binding we prepared synaptoneurosomes from frontal cortex of control a...

ORGANISM(S): Homo sapiens

2009-01-17 | E-GEOD-12685 | biostudies-arrayexpress

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