| Molecular modeling predicts structural changes in the A subunit of factor XIII caused by two novel mutations identified in a neonate with severe congenital factor XIII deficiency. Souri M., Yee V.C., Fujii N., Ichinose A.
Thromb. Res. 130:506-510(2012) · Mapped (4) |
| Increase in the plasma levels of protein Z-dependent protease inhibitor in normal pregnancies but not in non-pregnant patients with unexplained recurrent miscarriage. Souri M., Sugiura-Ogasawara M., Saito S., Kemkes-Matthes B., Meijers J.C., Ichinose A.
Thromb. Haemost. 107:507-512(2012) · Mapped (3) |
| Spontaneous regression of the inhibitor against the coagulation factor XIII A subunit in acquired factor XIII deficiency. Ishida F., Okubo K., Ito T., Okumura N., Souri M., Ichinose A.
Thromb. Haemost. 104:1284-1285(2010) · Mapped (4) |
| Impaired clot retraction in factor XIII A subunit-deficient mice. Kasahara K., Souri M., Kaneda M., Miki T., Yamamoto N., Ichinose A.
Blood 115:1277-1279(2010) · Mapped (9) |
| Unique secretion mode of human protein Z: its Gla domain is responsible for inefficient, vitamin K-dependent and warfarin-sensitive secretion. Souri M., Iwata H., Zhang W.G., Ichinose A.
Blood 113:3857-3864(2009) · Mapped (4) |
| Sushi domains in the B subunit of factor XIII responsible for oligomer assembly. Souri M., Kaetsu H., Ichinose A.
Biochemistry 47:8656-8664(2008) · Mapped (1) |
| Factor XIII transglutaminase supports hematogenous tumor cell metastasis through a mechanism dependent on natural killer cell function. Palumbo J.S., Barney K.A., Blevins E.A., Shaw M.A., Mishra A., Flick M.J., Kombrinck K.W., Talmage K.E., Souri M., Ichinose A. et al.
J. Thromb. Haemost. 6:812-819(2008) · Mapped (6) |
| Male-specific cardiac pathologies in mice lacking either the A or B subunit of factor XIII. Souri M., Koseki-Kuno S., Takeda N., Yamakawa M., Takeishi Y., Degen J.L., Ichinose A.
Thromb. Haemost. 99:401-408(2008) · Mapped (9) |
| Regulation of human protein Z gene expression by liver-enriched transcription factor HNF-4alpha and ubiquitous factor Sp1. Sugawara H., Iwata H., Souri M., Ichinose A.
J. Thromb. Haemost. 5:2250-2258(2007) · Mapped (17) |
| A naturally occurring E30Q mutation in the Gla domain of protein Z causes its impaired secretion and subsequent deficiency. Souri M., Koseki-Kuno S., Iwata H., Kemkes-Matthes B., Ichinose A.
Blood 105:3149-3154(2005) · Mapped (1) |
| Truncated mutant B subunit for factor XIII causes its deficiency due to impaired intracellular transportation. Koseki S., Souri M., Koga S., Yamakawa M., Shichishima T., Maruyama Y., Yanai F., Ichinose A.
Blood 97:2667-2672(2001) · UniProtKB (1) |
| Genes for the human mitochondrial trifunctional protein alpha- and beta-subunits are divergently transcribed from a common promoter region. Orii K.E., Orii K.O., Souri M., Orii T., Kondo N., Hashimoto T., Aoyama T.
J. Biol. Chem. 274:8077-8084(1999) · UniProtKB (1) |
| D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder. Suzuki Y., Jiang L.L., Souri M., Miyazawa S., Fukuda S., Zhang Z., Une M., Shimozawa N., Kondo N., Orii T. et al.
Am. J. Hum. Genet. 61:1153-1162(1997) · Mapped (2) |
| Structure of D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein. Jiang L.L., Miyazawa S., Souri M., Hashimoto T.
J. Biochem. 121:364-369(1997) · UniProtKB (1) |
| Genomic DNA organization of human mitochondrial very-long-chain acyl-CoA dehydrogenase and mutation analysis. Orii K.O., Aoyama T., Souri M., Orii K.E., Kondo N., Orii T., Hashimoto T.
Biochem. Biophys. Res. Commun. 217:987-992(1995) · UniProtKB (1) |
| Mutation analysis of very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency: identification and characterization of mutant VLCAD cDNAs from four patients. Souri M., Aoyama T., Orii K., Yamaguchi S., Hashimoto T.
Am. J. Hum. Genet. 58:97-106(1996) · UniProtKB (1) |
| Molecular cloning and functional expression of a human peroxisomal acyl-coenzyme A oxidase. Aoyama T., Tsushima K., Souri M., Kamijo T., Suzuki Y., Shimozawa N., Orii T., Hashimoto T.
Biochem. Biophys. Res. Commun. 198:1113-1118(1994) · UniProtKB (1) |
| Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients. Aoyama T., Souri M., Ushikubo S., Kamijo T., Yamaguchi S., Kelley R.I., Rhead W.J., Uetake K., Tanaka K., Hashimoto T.
J. Clin. Invest. 95:2465-2473(1995) · UniProtKB (1) · Mapped (3) |
| Cloning of human very-long-chain acyl-coenzyme A dehydrogenase and molecular characterization of its deficiency in two patients. Aoyama T., Souri M., Ueno I., Kamijo T., Yamaguchi S., Rhead W.J., Tanaka K., Hashimoto T.
Am. J. Hum. Genet. 57:273-283(1995) · UniProtKB (1) |
