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A novel pathogenic compound heterozygous variant in C12orf57 gene in a child with Temtamy syndrome p…
Mutations in c12orf57 cause a syndromic form of colobomatous microphthalmia.
Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.
Proteomic Characterization of a Candidate Polygenic Driver of Metabolism in Non-small Cell Lung Canc…
The effect of environmental conditions on expression of Bacteroides fragilis and Bacteroides thetaio…
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Safety and Efficacy of NF135 CPS Immunization
PfSPZ Vaccine: Dose Optimization With Heterologous Challenge in Healthy Malaria-Naïve Adults
Chemoprophylaxis and Plasmodium Falciparum NF54 Sporozoite Immunization Challenged by Heterologous I…
Impact on Morbidity and Mortality of Prophylactic Dosing of Low Molecular Heparin in Child-Pugh B Ci…
Controlled Human Malaria Infection After Bites From Mosquitoes Infected With Two Novel P. Falciparum…
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