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UnknownNext generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects.
Not available
S-EPMC3263993 | biostudies-literature
UnknownHomozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma.
Not available
S-EPMC3169830 | biostudies-literature
UnknownModelling the evolution and spread of HIV immune escape mutants.
Not available
S-EPMC2987822 | biostudies-literature
UnknownPhylogenetic analysis consistent with a clinical history of sexual transmission of HIV-1 from a single donor reveals transmission of highly distinct variants.
Not available
S-EPMC3161944 | biostudies-literature
UnknownDYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration.
Not available
S-EPMC7708302 | biostudies-literature
UnknownSimvastatin in Critically Ill Patients with Covid-19.
Not available
S-EPMC10755839 | biostudies-literature
UnknownAssociations of estimated glomerular filtration rate and albuminuria with mortality and renal failure by sex: a meta-analysis.
Not available
S-EPMC3558410 | biostudies-literature
UnknownEffect of Angiotensin-Converting Enzyme Inhibitor and Angiotensin Receptor Blocker Initiation on Organ Support-Free Days in Patients Hospitalized With COVID-19: A Randomized Clinical Trial.
Not available
S-EPMC10326520 | biostudies-literature
UnknownAge and association of kidney measures with mortality and end-stage renal disease.
Not available
S-EPMC3936348 | biostudies-literature
UnknownGenetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity.
Not available
S-EPMC9951795 | biostudies-literature
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