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The Journal of Biological Chemistry|August 21, 2020
PGAP6, a GPI-specific phospholipase A2, has narrow substrate specificity against GPI-anchored proteinsGun-Hee Lee, Morihisa Fujita, Hideki Nakanishi, et al.
Molecular and Biochemical Parasitology|February 8, 2005
Erythrocyte surface glycosylphosphatidyl inositol anchored receptor for the malaria parasiteThanaporn Rungruang, Osamu Kaneko, Yoshiko Murakami, et al.
Genes|February 25, 2023
Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3)Miles D Thompson, Xueying Li, Michele Spencer-Manzon, et al.
The Journal of Biological Chemistry|December 30, 2004
PIG-V involved in transferring the second mannose in glycosylphosphatidylinositolJi Young Kang, Yeongjin Hong, Hisashi Ashida, et al.
British Journal of Haematology|October 25, 2011
Deregulated expression of HMGA2 is implicated in clonal expansion of PIGA deficient cells in paroxysmal nocturnal haemoglobinuriaYoshiko Murakami, Norimitsu Inoue, Tsutomu Shichishima, et al.
Nature Communications|February 15, 2020
Cross-talks of glycosylphosphatidylinositol biosynthesis with glycosphingolipid biosynthesis and ER-associated degradationYicheng Wang, Yusuke Maeda, Yi-Shi Liu, et al.
Molecular Therapy. Advances|May 15, 2026
Optimized AAV vector enables potent therapeutic rescue of inherited glycosylphosphatidylinositol deficiency in miceSaori Umeshita, Kae Imanishi, Shibi Likhite, et al.
Blood Advances|November 20, 2020
Paroxysmal nocturnal hemoglobinuria caused by CN-LOH of constitutional PIGB mutation and 70-kbp microdeletion on 15qSaskia Langemeijer, Charlotte Schaap, Frank Preijers, et al.
Blood|October 24, 2002
Inefficient response of T lymphocytes to glycosylphosphatidylinositol anchor-negative cells: implications for paroxysmal nocturnal hemoglobinuriaYoshiko Murakami, Hiroshi Kosaka, Yusuke Maeda, et al.
The Journal of Biological Chemistry|January 10, 2012
Mechanism for release of alkaline phosphatase caused by glycosylphosphatidylinositol deficiency in patients with hyperphosphatasia mental retardation syndromeYoshiko Murakami, Noriyuki Kanzawa, Kazunobu Saito, et al.
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