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JIMD Reports|May 13, 2024
Normal transferrin glycosylation does not rule out severe ALG1 deficiencyInez Bosnyak, Mustafa Sadek, Wasantha Ranatunga, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 9, 2026
Thrombosis at the crossroads of inflammation, coagulation, and vascular biology: Recent advances and emerging therapeutic strategiesMadan Gopal Ramarajan, Abdullah Reda, Sherief Ghozy, et al.
Methods in Enzymology|September 9, 2017
Defining the Architecture of the Core Machinery for the Assembly of Fe-S Clusters in Human MitochondriaOleksandr Gakh, Wasantha Ranatunga, Belinda K Galeano, et al.
European Journal of Medical Genetics|March 3, 2022
Could distal variants in ALG13 lead to atypical clinical presentation?Andrea Accogli, Silvia Radenkovic, Wasantha Ranatunga, et al.
The Journal of Biological Chemistry|August 14, 2016
Architecture of the Human Mitochondrial Iron-Sulfur Cluster Assembly MachineryOleksandr Gakh, Wasantha Ranatunga, Douglas Y Smith, et al.
Molecular Genetics and Metabolism|November 14, 2020
Fetal glycosylation defect due to ALG3 and COG5 variants detected via amniocentesis: Complex glycosylation defect with embryonic lethal phenotypeAlejandro Ferrer, Rodrigo Tzovenos Starosta, Wasantha Ranatunga, et al.
Journal of Inherited Metabolic Disease|September 14, 2022
N-glycoproteomics reveals distinct glycosylation alterations in NGLY1-deficient patient-derived dermal fibroblastsRohit Budhraja, Mayank Saraswat, Diederik De Graef, et al.
Glycobiology|October 3, 2024
N-glycoproteomic and proteomic alterations in SRD5A3-deficient fibroblastsKishore Garapati, Wasantha Ranatunga, Neha Joshi, et al.
Journal of Molecular Biology|May 5, 2004
Structural studies of the Nudix hydrolase DR1025 from Deinococcus radiodurans and its ligand complexesWasantha Ranatunga, Emma E Hill, Jana L Mooster, et al.
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