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Archives of Microbiology|February 14, 2022
Microbial approaches for sustainable remediation of dye-contaminated wastewater: a reviewDevaraj Bharathi, Jaya Ganesh Thiruvengadam Nandagopal, Rajamani Ranjithkumar, et al.
JPGN Reports|May 17, 2024
Shwachman-Diamond syndrome mimicking mitochondrial hepatopathyOdelya Kaufman, Colleen Donnelly, Emalyn Cork, et al.
Molecular Genetics and Metabolism Reports|February 12, 2020
The N370S/R496H genotype in type 1 Gaucher disease - Natural history and implications for pre symptomatic diagnosis and counselingNatasha Zeid, Chanan Stauffer, Amy Yang, et al.
Pediatric Nephrology (Berlin, Germany)|November 9, 2012
Mitochondrial tRNA(Phe) mutation as a cause of end-stage renal disease in childhoodKristin E D'Aco, Megan Manno, Colleen Clarke, et al.
American Journal of Medical Genetics. Part A|June 3, 2015
Fetal akinesia deformation sequence due to a congenital disorder of glycosylationRebecca Ganetzky, Kosuke Izumi, Andrew Edmondson, et al.
Environmental Research|September 11, 2023
Green synthesis of chitosan/silver nanocomposite using kaempferol for triple negative breast cancer therapy and antibacterial activityDevaraj Bharathi, Rajamani Ranjithkumar, Jaya Ganesh Thiruvengadam Nandagopal, et al.
JACC. Case Reports|October 23, 2023
PPA2 Deficiency in 2 Sisters: A Rare Cause of Sudden Cardiac DeathWill Genthe, Colleen Donnelly, David Ezon, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 2, 2007
Diagnostic challenges in a severely delayed infant with hypersomnolence, failure to thrive and arteriopathy: a unique case of gamma-hydroxybutyric aciduria and Williams syndromeIna Knerr, K Michael Gibson, Jaya Ganesh, et al.
Nature Communications|July 10, 2025
Quantification of transcript isoforms at the single-cell level using SCALPELFranz Ake, Marcel Schilling, Sandra M Fernández-Moya, et al.
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