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TranscriptomicsFVB nerve x SC comparison
wild-type mouse (FVB strain) expression profiles of adult sciatic nerve and of cultured Schwann cell Keywords: other
ORGANISM(S): Mus musculus 
2006-04-15 | E-GEOD-2530 | biostudies-arrayexpress
TranscriptomicsSAGE profiles from cultured keratinocytes and human epidermis
SAGE libraries from cultured, differentiated keratinocytes and human epidermis, both normal and affected by actinic keratosis Keywords = Keratinocyte, Epidermis, Homo sapiens, Actinic Keratosis, TNF alpha
ORGANISM(S): Homo sapiens 
2002-02-21 | E-GEOD-31 | biostudies-arrayexpress
UnknownCopy number variation upstream of PMP22 in Charcot-Marie-Tooth disease.
Not available
S-EPMC2987248 | biostudies-literature
UnknownProof of Pharmacology, Safety, and Pharmacokinetics of the Novel TRPA1 Antagonist BI 1839100: A Randomized, Placebo‐Controlled, Parallel Group, First‐In‐Human Study in Healthy Male Participants
Not available
S-EPMC12292558 | biostudies-literature
UnknownRARS2 Mutations: Is Pontocerebellar Hypoplasia Type 6 a Mitochondrial Encephalopathy?
Not available
S-EPMC5413457 | biostudies-literature
UnknownLetter to the editor on a paper by Kaivola et al. (2020): carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is not associated with amyotrophic lateral sclerosis or frontotemporal dementia.
Not available
S-EPMC9494883 | biostudies-literature
UnknownGenetic testing of common and rare variants in dementia patients from a memory clinic : Dementia-related genetic testing in memory clinic.
Not available
S-EPMC12522692 | biostudies-literature
UnknownHypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneities.
Not available
S-EPMC6240730 | biostudies-literature
UnknownGenome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions.
Not available
S-EPMC8413318 | biostudies-literature
UnknownEXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations.
Not available
S-EPMC3928094 | biostudies-literature
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