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Frontiers in Physiology|June 15, 2017
A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural AbnormalitiesClaire E L Smith, Jennifer Kirkham, Peter F Day, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1974
Amino-acid sequence of NADP-specific glutamate dehydrogenase of neurospora crassaJ C Wootton, G K Chambers, A A Holder, et al.
Molecular Genetics & Genomic Medicine|March 19, 2023
Targeted nanopore sequencing enables complete characterisation of structural deletions initially identified using exon-based short-read sequencing strategiesBenjamin McClinton, Laura A Crinnion, Martin McKibbin, et al.
Human Molecular Genetics|March 24, 2017
Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stressSteven J Brookes, Martin J Barron, Claire E L Smith, et al.
Archives of Biochemistry and Biophysics|February 1, 1991
Ethanol increases cytochromes P450IIE, IIB1/2, and IIIA in cultured rat hepatocytesJ F Sinclair, J McCaffrey, P R Sinclair, et al.
Clinical Genetics|February 14, 2020
New missense variants in RELT causing hypomineralised amelogenesis imperfectaGeorgios Nikolopoulos, Claire E L Smith, Steven J Brookes, et al.
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