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UnknownMechanisms Linking Physical Activity with Psychiatric Symptoms Across the Lifespan: A Systematic Review.
Not available
S-EPMC10587276 | biostudies-literature
UnknownBiomarker Landscape in RASopathies.
Not available
S-EPMC11354534 | biostudies-literature
UnknownInfluence of TFAP2B and KCTD15 genetic variability on personality dimensions in anorexia and bulimia nervosa.
Not available
S-EPMC5607548 | biostudies-literature
UnknownAssociation of OPRD1 Gene Variants with Changes in Body Weight and Psychometric Indicators in Patients with Eating Disorders.
Not available
S-EPMC11396092 | biostudies-literature
UnknownΔ-9-Tetrahydrocannabinol treatment during adolescence and alterations in the inhibitory networks of the adult prefrontal cortex in mice subjected to perinatal NMDA receptor antagonist injection and to postweaning social isolation.
Not available
S-EPMC7266818 | biostudies-literature
GenomicsArchitectural niche organization by LHX2 is linked to hair follicle stem cell function
To identify direct LHX2 target genes in HFSCs, we performed chromatin immunoprecipitation and deep sequencing (ChIP-seq) analysis using FACS-isolated HFSCs. Three independent LHX2 ChIP-seq experiments were conducted.
ORGANISM(S): Mus musculus 
2013-09-05 | E-GEOD-48068 | biostudies-arrayexpress
ModelsSmithAE2002_RanTransport
The model reproduces the compartmental model for Ran transport as depicted in Fig 3 of the paper. Model reproduced using MathSBML. To the extent possible under law, all copyright and related or neighbouring rights to this encoded model have been dedicated to the public domain worldw...
2024-09-02 | BIOMD0000000164 | BioModels
UnknownDiagnostic yield of next-generation sequencing in 87 families with neurodevelopmental disorders.
Not available
S-EPMC8858550 | biostudies-literature
UnknownNovel Compound Heterozygous Mutation in TRAPPC9 Gene: The Relevance of Whole Genome Sequencing.
Not available
S-EPMC8068822 | biostudies-literature
Genomicsena-DATASET-CIPF-CG-30-11-2016-16:37:38:797-425 - samples
The need for a detailed catalogue of local variability for the study of rare diseases within the context of the Medical Genome Project motivated the whole exome sequencing of 267 unrelated individuals, representative of the healthy Spanish population.
EGAD00001003101 | EGA
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