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Preclinical evaluation of AGT mRNA replacement therapy for primary hyperoxaluria type I disease

Science Advances
Primary 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

Recombination between homoeologous chromosomes induced in durum wheat by the Aegilops speltoides Su1-Ph1 suppressor

Theoretical and Applied Genetics, 2019
Hao Li   +9 more
semanticscholar   +1 more source

Homoeologous recombination in the presence of Ph1 gene in wheat

Chromosoma, 2016
D. Koo, Wenxuan Liu, B. Friebe, B. Gill
semanticscholar   +1 more source

Isolation and Genome Sequencing of a Novel Pseudoalteromonas Phage PH1

Current Microbiology, 2016
Zhao-yang Liu   +7 more
semanticscholar   +1 more source

Safety, efficacy and survival of patients with primary malignant brain tumours (PMBT) in phase I (Ph1) trials: the 12-year Royal Marsden experience

Journal of Neuro-Oncology, 2018
N. Coleman   +12 more
semanticscholar   +1 more source

Stones: A novel RNAi therapy for PH1

Nature Reviews Nephrology, 2016
Ellen F. Carney
semanticscholar   +1 more source

Molecular characterization of Ph1 as a major chromosome pairing locus in polyploid wheat

Nature, 2006
S. Griffiths   +7 more
semanticscholar   +1 more source

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