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UnknownA Proteomics Approach to Investigate miR-153-3p and miR-205-5p Targets in Neuroblastoma Cells.
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S-EPMC4669106 | biostudies-literature
UnknownSex-specific disease modifiers in juvenile myoclonic epilepsy.
Not available
S-EPMC8861057 | biostudies-literature
UnknownThe Risk of Breast Cancer According to Mutation Type and Position in Carriers of a Pathogenic Variant in <i>BRCA1</i>.
Not available
S-EPMC12731516 | biostudies-literature
UnknownSLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis.
Not available
S-EPMC10689929 | biostudies-literature
UnknownBRCA1 and BRCA2 genetic testing-pitfalls and recommendations for managing variants of uncertain clinical significance.
Not available
S-EPMC5006185 | biostudies-literature
UnknownMRI Surveillance and Breast Cancer Mortality in Women With BRCA1 and BRCA2 Sequence Variations.
Not available
S-EPMC10905376 | biostudies-literature
UnknownBilateral Oophorectomy and All-Cause Mortality in Women With BRCA1 and BRCA2 Sequence Variations.
Not available
S-EPMC10905374 | biostudies-literature
UnknownGene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies.
Not available
S-EPMC5073625 | biostudies-literature
UnknownDe novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies.
Not available
S-EPMC9166542 | biostudies-literature
UnknownA Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy.
Not available
S-EPMC6556875 | biostudies-literature
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