Experiments

Searchable full-text extractions: founding hypothesis, core claims, experimental setups, key results and statistics — pulled out of each paper as structure. Search a cell line, an assay or an entity (e.g. HUH7) and find every paper that worked with it. This corpus stands on its own: most entries carry no reproduction assessment (yet).

Publications 1.3k Datasets 392.5k Experiments 4

System / cell line: voxel ✕ Assay: brain ✕ Clear

Of brain and bone: the unusual case of Dr. A.

PMID 20183548 · PMC2997763 · Neurocase · 2009 · 7 claims · 8 setups

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Dr. A's EXT2 mutation may play a role in the pattern of neurodegeneration seen in his FTD, given that Ext1-knockout mice show CNS defects including loss of olfactory bulbs and abnormally small cerebral cortex

structural blood postmortem muscle voxel-based genetic neuropathology
Mapping protein abundance patterns in the brain using voxelation combined with liquid chromatography and mass spectrometry.

PMID 19654045 · PMC2818068 · Methods (San Diego, Calif.) · 2010 · 8 claims · 5 setups

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Voxelation combined with LC-MS enables high-throughput spatial mapping of protein abundance across mouse brain voxels

brain digested voxel amt-tag lc-ms bca
Association of the SerCys DISC1 polymorphism with human hippocampal formation gray matter and function during memory encoding.

PMID 19046394 · PMC2865560 · The European journal of neuroscience · 2008 · 8 claims · 5 setups

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Individuals homozygous for the DISC1 Ser allele show greater HF (parahippocampal) gray matter volume than Cys allele carriers

healthy extracted voxel-based task psychophysiological
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.

PMID 18577546 · PMC2442425 · Brain : a journal of neurology · 2008 · 8 claims · 8 setups

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Co-occurring PED and epilepsy can be caused by autosomal dominant heterozygous mutations in SLC2A1, encoding the glucose transporter GLUT1

family genomic xenopus patients genome-wide pcr glucose

Experiments

Of brain and bone: the unusual case of Dr. A.

Mapping protein abundance patterns in the brain using voxelation combined with liquid chromatography and mass spectrometry.

Association of the SerCys DISC1 polymorphism with human hippocampal formation gray matter and function during memory encoding.

Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.