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Preclinical evaluation of AGT mRNA replacement therapy for primary hyperoxaluria type I disease
Science AdvancesPrimary hyperoxaluria type 1 (PH1) is a rare inherited liver disorder caused by alanine glyoxylate aminotransferase (AGT) dysfunction, leading to accumulation of glyoxylate which is then converted into oxalate.
Taihua Yang +22 more
semanticscholar +1 more source
Homoeologous recombination in the presence of Ph1 gene in wheat
Chromosoma, 2016D. Koo, Wenxuan Liu, B. Friebe, B. Gill
semanticscholar +1 more source
Isolation and Genome Sequencing of a Novel Pseudoalteromonas Phage PH1
Current Microbiology, 2016Zhao-yang Liu +7 more
semanticscholar +1 more source
Stones: A novel RNAi therapy for PH1
Nature Reviews Nephrology, 2016Ellen F. Carney
semanticscholar +1 more source
The control of recombination in wheat by Ph1 and its use in breeding.
Methods in molecular biology, 2014G. Moore
semanticscholar +1 more source
Molecular characterization of Ph1 as a major chromosome pairing locus in polyploid wheat
Nature, 2006S. Griffiths +7 more
semanticscholar +1 more source

