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UnknownThe Aegilops ventricosa 2NvS segment in bread wheat: cytology, genomics and breeding.
Not available
S-EPMC7843486 | biostudies-literature
UnknownThe Role of PIEZO2 in Human Mechanosensation.
Not available
S-EPMC5911918 | biostudies-literature
UnknownDiversity oriented biosynthesis via accelerated evolution of modular gene clusters.
Not available
S-EPMC5663706 | biostudies-literature
UnknownTAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations.
Not available
S-EPMC4678794 | biostudies-literature
UnknownBiallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy.
Not available
S-EPMC10506156 | biostudies-literature
UnknownDe novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis.
Not available
S-EPMC7895901 | biostudies-literature
UnknownInflammatory Biomarkers of Asymptomatic and Symptomatic Tuberculosis.
Not available
S-EPMC12636496 | biostudies-literature
UnknownExome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria.
Not available
S-EPMC10366952 | biostudies-literature
UnknownDe novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability.
Not available
S-EPMC9241146 | biostudies-literature
UnknownLoss of function mutations in GEMIN5 cause a neurodevelopmental disorder.
Not available
S-EPMC8105379 | biostudies-literature
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