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ProteomicsLithium-response pathway in hiPSCs implicates the phosphoregulatory set-point for a cytoskeletal
Tobe BTD, Crain AM, Winquist AM, Calabrese B, Makihara H, Zhao W, Lalonde J, Nakamura H, Konopaske G, Sidor M, Pernia C, Yamashita N, Wada M, Inoue Y, Nakamura F, Sheridan SD, Logan R, Brandel M, Wu D, Hunsberger J, Dorsett L, Duerr C, Basa RCB, McCarthy MJ, Udeshi N, Mertins P, Carr SA, Rouleau G, ...
ORGANISM(S): Homo Sapiens (ncbitaxon:9606) 
2017-04-21 | MSV000080975 | MassIVE
UnknownAxonal and periaxonal swelling precede peripheral neurodegeneration in KCC3 knockout mice.
Not available
S-EPMC2242858 | biostudies-literature
UnknownDigital clock drawing test reflects visuospatial ability of older drivers.
Not available
S-EPMC10925675 | biostudies-literature
TranscriptomicsGene expression analysis upon UGT1A_i2 knockdown
Evaluate modulation in gene expression modulation upon UGT1A_i2 knockdown in basal conditions and also under pharmacological treatment (SN-38) 6 samples in duplicate (12 samples total); HT115 colorectal cell line was infected with either UGT1A_i2 shRNA or non-target shRNA and left untreated or treat...
ORGANISM(S): Homo sapiens 
2014-01-08 | E-GEOD-48118 | biostudies-arrayexpress
UnknownA Cell-Surface Membrane Protein Signature for Glioblastoma.
Not available
S-EPMC5512565 | biostudies-literature
UnknownRed blood cell aggregation and dissociation in shear flows simulated by lattice Boltzmann method.
Not available
S-EPMC2254372 | biostudies-literature
UnknownGenetic variability in scaffolding proteins and risk for schizophrenia and autism-spectrum disorders: a systematic review.
Not available
S-EPMC6019351 | biostudies-literature
UnknownGenetics of mirror movements identifies a multifunctional complex required for Netrin-1 guidance and lateralization of motor control.
Not available
S-EPMC10181192 | biostudies-literature
UnknownGBA mutations are associated with Rapid Eye Movement Sleep Behavior Disorder.
Not available
S-EPMC4574811 | biostudies-literature
UnknownThe Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic Resources.
Not available
S-EPMC11160810 | biostudies-literature
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