Miwa Sohda
Niigata, Japan
Last Updated: 09/26/2026
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Found 12 publications
Glycosylation-deficient mutations in tissue-nonspecific alkaline phosphatase impair its structure and function and are linked to infantile hypophosphatasia.
Journal: The FEBS journal
Published: September 17, 2015
TNFα triggers release of extracellular vesicles containing TNFR1 and TRADD, which can modulate TNFα responses of the parental cells.
Journal: Archives of biochemistry and biophysics
Published: July 30, 2015
Molecular phenotype of tissue-nonspecific alkaline phosphatase with a proline (108) to leucine substitution associated with dominant odontohypophosphatasia.
Journal: Molecular genetics and metabolism
Published: March 11, 2015
GM130 is a parallel tetramer with a flexible rod-like structure and N-terminally open (Y-shaped) and closed (I-shaped) conformations.
Journal: The FEBS journal
Published: November 25, 2014
Trans-Golgi protein p230/golgin-245 is involved in phagophore formation.
Journal: Biochemical and biophysical research communications
Published: November 07, 2014
Tissue-nonspecific alkaline phosphatase and hypophosphatasia
Journal: Clinical calcium
Published: January 30, 2014
A new role for RINT-1 in SNARE complex assembly at the trans-Golgi network in coordination with the COG complex.
Journal: Molecular biology of the cell
Published: July 26, 2013
Identification of a soluble isoform of human IL-17RA generated by alternative splicing.
Journal: Cytokine
Published: June 07, 2013
An asparagine at position 417 of tissue-nonspecific alkaline phosphatase is essential for its structure and function as revealed by analysis of the N417S mutation associated with severe hypophosphatasia.
Journal: Molecular genetics and metabolism
Published: March 13, 2013
Association of nonsense mutation in GABRG2 with abnormal trafficking of GABAA receptors in severe epilepsy.
Journal: Epilepsy research
Published: February 22, 2013
A dimerization defect caused by a glycine substitution at position 420 by serine in tissue-nonspecific alkaline phosphatase associated with perinatal hypophosphatasia.
Journal: The FEBS journal
Published: June 04, 2012
Disulfide bonds are critical for tissue-nonspecific alkaline phosphatase function revealed by analysis of mutant proteins bearing a C(201)-Y or C(489)-S substitution associated with severe hypophosphatasia.
Journal: Biochimica et biophysica acta
Published: November 18, 2011
Showing 1-12 of 12
Last Updated: 09/26/2026