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UnknownEpidemiological evidence for a hereditary contribution to myasthenia gravis: a retrospective cohort study of patients from North America.
Not available
S-EPMC7511637 | biostudies-literature
ProteomicsElp2 mutations perturb the epitranscriptome and lead to a complex neurodevelopmental phenotype
Neurodevelopmental disorders have a variety of aetiologies and most often these are complex genomic traits involving numerous mutations. Intellectual disability (ID) and autism spectrum disorder (ASD) are the most common neurodevelopmental disorders and are characterized by substantial impairment in...
ORGANISM(S): Mus musculus (Mouse) 
2021-01-19 | PXD023653 | Pride
Trna modifications Mouse Brain cortex Elongator complex Epitranscriptome Autism Intellectual disability Elp2 
UnknownWhole-genome resequencing of the wild barley diversity collection: a resource for identifying and exploiting genetic variation for cultivated barley improvement.
Not available
S-EPMC12774595 | biostudies-literature
UnknownSARS-CoV-2 Viral Load in the Nasopharynx at Time of First Infection Among Unvaccinated Individuals: A Secondary Cross-Protocol Analysis of 4 Randomized Trials.
Not available
S-EPMC11117088 | biostudies-literature
UnknownClinical and Demographic Factors Associated With COVID-19, Severe COVID-19, and SARS-CoV-2 Infection in Adults: A Secondary Cross-Protocol Analysis of 4 Randomized Clinical Trials.
Not available
S-EPMC10346130 | biostudies-literature
UnknownRisk of COVID-19 after natural infection or vaccination.
Not available
S-EPMC10518569 | biostudies-literature
UnknownEfficacy and Safety of NVX-CoV2373 in Adults in the United States and Mexico.
Not available
S-EPMC8693692 | biostudies-literature
UnknownStereoacuity in children with anisometropic amblyopia.
Not available
S-EPMC3223370 | biostudies-literature
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