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UnknownSubstantia nigra related gene polymorphisms associated with antipsychotic-induced acute movement disorders: a genome-wide association study and multi-ancestry validation in schizophrenia.
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S-EPMC12362978 | biostudies-literature
UnknownPredictive role of weight-adjusted waist index in diabetic peripheral neuropathy among patients with type 2 diabetes mellitus.
Not available
S-EPMC12931302 | biostudies-literature
UnknownAnti-cancer effect of danshen and dihydroisotanshinone I on prostate cancer: targeting the crosstalk between macrophages and cancer cells via inhibition of the STAT3/CCL2 signaling pathway.
Not available
S-EPMC5522253 | biostudies-literature
UnknownTargeted fetal NGS panel reveals genetic conditions in sonographically normal fetuses: Insights from a large cohort study.
Not available
S-EPMC12671786 | biostudies-literature
UnknownHearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation.
Not available
S-EPMC7416285 | biostudies-literature
UnknownMPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population.
Not available
S-EPMC10804618 | biostudies-literature
UnknownPhylogenomic analyses highlight innovation and introgression in the continental radiations of Fagaceae across the Northern Hemisphere.
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S-EPMC8921187 | biostudies-literature
UnknownTargeted gene capture and massively parallel sequencing identify TMC1 as the causative gene in a six-generation Chinese family with autosomal dominant hearing loss.
Not available
S-EPMC4567392 | biostudies-literature
UnknownA newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3-4.
Not available
S-EPMC10009913 | biostudies-literature
UnknownMesenchymal stem cell-derived exosomes regulate microglia phenotypes: a promising treatment for acute central nervous system injury.
Not available
S-EPMC10154505 | biostudies-literature
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