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Unknown14-3-3ζ deficient mice in the BALB/c background display behavioural and anatomical defects associated with neurodevelopmental disorders.
Not available
S-EPMC4513550 | biostudies-literature
UnknownThe genome and developmental transcriptome of the strongylid nematode Haemonchus contortus.
Not available
S-EPMC4053716 | biostudies-literature
UnknownHuman ultrarare genetic disorders of sulfur metabolism demonstrate redundancies in H2S homeostasis.
Not available
S-EPMC9615310 | biostudies-literature
UnknownA MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis.
Not available
S-EPMC8440635 | biostudies-literature
UnknownA natural history study to track brain and spinal cord changes in individuals with Friedreich's ataxia: TRACK-FA study protocol.
Not available
S-EPMC9678384 | biostudies-literature
UnknownEffect of Fresh vs Standard-issue Red Blood Cell Transfusions on Multiple Organ Dysfunction Syndrome in Critically Ill Pediatric Patients: A Randomized Clinical Trial.
Not available
S-EPMC7081749 | biostudies-literature
UnknownTocilizumab in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial.
Not available
S-EPMC8084355 | biostudies-literature
UnknownHeterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy.
Not available
S-EPMC6556837 | biostudies-literature
UnknownNMDA receptor gene variations as modifiers in Huntington disease: a replication study.
Not available
S-EPMC3186947 | biostudies-literature
UnknownEffects of antiplatelet therapy after stroke due to intracerebral haemorrhage (RESTART): a randomised, open-label trial.
Not available
S-EPMC6617509 | biostudies-literature
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