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UnknownCritical Appraisal of Biomedical Literature With a Succinct Journal Club Template: The ROOTs Format.
Not available
S-EPMC5735714 | biostudies-literature
UnknownChange in excitability of a putative decision-making neuron in Aplysia serves as a mechanism in the decision not to feed following food satiation.
Not available
S-EPMC4305457 | biostudies-literature
UnknownRandomized phase II trial of selenomethionine as a modulator of efficacy and toxicity of chemoradiation in squamous cell carcinoma of the head and neck.
Not available
S-EPMC4600191 | biostudies-literature
UnknownLong-term sensitization training in Aplysia decreases the excitability of a decision-making neuron through a sodium-dependent mechanism.
Not available
S-EPMC5435880 | biostudies-literature
UnknownEurythenes atacamensis sp. nov. (Crustacea: Amphipoda) exhibits ontogenetic vertical stratification across abyssal and hadal depths in the Atacama Trench, eastern South Pacific Ocean.
Not available
S-EPMC8120496 | biostudies-literature
UnknownDepression following traumatic brain injury in mice is associated with down-regulation of hippocampal astrocyte glutamate transporters by thrombin.
Not available
S-EPMC6311670 | biostudies-literature
Unknown"It all depends on why it's red": qualitative interviews exploring patient and professional views of a traffic light system for IVF add-ons.
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S-EPMC10305467 | biostudies-literature
ProteomicsDistinct roles of the two Elongator subcomplexes during neurodevelopment
The highly conserved Elongator complex is a translational regulator and a subject of growing interest due to its critical role in neurodevelopment, neurological diseases and brain tumors. Clinically relevant mutations have been reported in the catalytic Elp123 subcomplex, while no mutation in the ac...
ORGANISM(S): Homo sapiens (Human) 
2022-05-17 | PXD032925 | Pride
Developmental delay Intellectual disability Epilepsy Fibroblasts Homo sapiens 
UnknownCaseation of human tuberculosis granulomas correlates with elevated host lipid metabolism.
Not available
S-EPMC2913288 | 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 
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