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Quoted phrase not found in phrase index: "Glycosylphosphatidylinositol biosynthesis defect 15"
Page 1
Asfotase alfa improved skeletal mineralization and fracture healing in a child with MCAHS.
Kang M, Wu M, Crane JL. Kang M, et al. Bone. 2023 Jul;172:116778. doi: 10.1016/j.bone.2023.116778. Epub 2023 Apr 21. Bone. 2023. PMID: 37088336
Tissue non-specific alkaline phosphatase (TNSALP) is an enzyme that is tethered to the cell membrane by glycosylphosphatidylinositol (GPI) and converts inorganic pyrophosphate to inorganic phosphate. ...Phosphatidylinositol glycan anchor biosynthesis class N (PIGN) …
Tissue non-specific alkaline phosphatase (TNSALP) is an enzyme that is tethered to the cell membrane by glycosylphosphatidylinositol …
Somatic mutations of the PIG-A gene found in Japanese patients with paroxysmal nocturnal hemoglobinuria.
Yamada N, Miyata T, Maeda K, Kitani T, Takeda J, Kinoshita T. Yamada N, et al. Blood. 1995 Feb 15;85(4):885-92. Blood. 1995. PMID: 7531514 Free article.
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal hematologic disorder caused by deficient biosynthesis of the glycosylphosphatidylinositol (GPI) anchor. PIG-A, an X-linked gene that participates in the first step of GPI-anchor synthesis, is responsibl …
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal hematologic disorder caused by deficient biosynthesis of the glyco …