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Cell|July 11, 1997
Alpha-mannosidase-II deficiency results in dyserythropoiesis and unveils an alternate pathway in oligosaccharide biosynthesisD Chui, M Oh-Eda, Y F Liao, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|August 14, 2001
Real-time optical coherence tomography of the anterior segment at 1310 nmS Radhakrishnan, A M Rollins, J E Roth, et al.The Journal of Clinical Investigation|December 26, 2001
A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)C Kranz, J Denecke, M A Lehrman, et al.Journal of the American Chemical Society|April 9, 2020
Water-Compatible Cycloadditions of Oligonucleotide-Conjugated Strained Allenes for DNA-Encoded Library SynthesisMatthias V Westphal, Liam Hudson, Jeremy W Mason, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|January 22, 2020
Highly Selective, Amine-Derived Cannabinoid Receptor 2 ProbesMatthias V Westphal, Roman C Sarott, Elisabeth A Zirwes, et al.The Journal of Clinical Investigation|April 29, 1998
Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapyR Niehues, M Hasilik, G Alton, et al.Gastrointestinal Endoscopy|July 28, 2001
High-resolution endoscopic imaging of the GI tract: a comparative study of optical coherence tomography versus high-frequency catheter probe EUSA Das, M V Sivak, A Chak, et al.The Journal of Pediatrics|June 4, 1999
Leukocyte adhesion deficiency II syndrome, a generalized defect in fucose metabolismT Marquardt, T Brune, K Lühn, et al.Beneficial Microbes|December 13, 2021
Lacticaseibacillus rhamnosus GG DSM 33156 effects on pathogen defence in the upper respiratory tract: a randomised, double-blind, placebo-controlled paediatric trialA Damholt, M K Keller, K Baranowski, et al.Human Mutation|November 3, 2000
Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)G Matthijs, E Schollen, C Bjursell, et al.Pageof 12