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M Souri

Showing results (21-30 of 41) with videos related to

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Thrombosis and Haemostasis|August 26, 1998
A founder effect is proposed for factor XIII B subunit deficiency caused by the insertion of triplet AAC in exon III encoding the second Sushi domainM Souri, T Izumi, Y Higashi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 30, 2013
Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelinesM Souri, A Biswas, M Misawa, et al.
The Journal of Biological Chemistry|February 26, 1999
Transcriptional regulation of cell type-specific expression of the TATA-less A subunit gene for human coagulation factor XIIIM Kida, M Souri, M Yamamoto, et al.
Biochemical and Biophysical Research Communications|June 30, 1994
Peroxisomal acyl-coenzyme A oxidase is a rate-limiting enzyme in a very-long-chain fatty acid beta-oxidation systemT Aoyama, M Souri, T Kamijo, et al.
Drug Research|January 22, 2014
Synthesis and antinociception activity of new substituted phenothiazines and ethylenediamines as antihistaminic drugsA Ahmadi, N Naderi, M Souri, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 24, 2012
A case of acquired FXIII deficiency with severe bleeding symptomsT Hayashi, Y Kadohira, E Morishita, et al.
European Journal of Ophthalmology|February 24, 2006
Use of autologous plasmin during vitrectomy for diabetic maculopathyT Sakuma, M Tanaka, J Inoue, et al.
European Journal of Ophthalmology|December 6, 2005
Efficacy of autologous plasmin for idiopathic macular hole surgeryT Sakuma, M Tanaka, M Inoue, et al.
British Journal of Haematology|June 19, 2001
Novel Y283C mutation of the A subunit for coagulation factor XIII: molecular modelling predicts its impaired protein folding and dimer formationM Souri, V C Yee, K Kasai, et al.
Biochemical and Biophysical Research Communications|February 15, 1994
Molecular cloning and functional expression of a human peroxisomal acyl-coenzyme A oxidaseT Aoyama, K Tsushima, M Souri, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Thrombosis and Haemostasis|August 26, 1998
A founder effect is proposed for factor XIII B subunit deficiency caused by the insertion of triplet AAC in exon III encoding the second Sushi domainM Souri, T Izumi, Y Higashi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 30, 2013
Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelinesM Souri, A Biswas, M Misawa, et al.
The Journal of Biological Chemistry|February 26, 1999
Transcriptional regulation of cell type-specific expression of the TATA-less A subunit gene for human coagulation factor XIIIM Kida, M Souri, M Yamamoto, et al.
Biochemical and Biophysical Research Communications|June 30, 1994
Peroxisomal acyl-coenzyme A oxidase is a rate-limiting enzyme in a very-long-chain fatty acid beta-oxidation systemT Aoyama, M Souri, T Kamijo, et al.
Drug Research|January 22, 2014
Synthesis and antinociception activity of new substituted phenothiazines and ethylenediamines as antihistaminic drugsA Ahmadi, N Naderi, M Souri, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 24, 2012
A case of acquired FXIII deficiency with severe bleeding symptomsT Hayashi, Y Kadohira, E Morishita, et al.
European Journal of Ophthalmology|February 24, 2006
Use of autologous plasmin during vitrectomy for diabetic maculopathyT Sakuma, M Tanaka, J Inoue, et al.
European Journal of Ophthalmology|December 6, 2005
Efficacy of autologous plasmin for idiopathic macular hole surgeryT Sakuma, M Tanaka, M Inoue, et al.
British Journal of Haematology|June 19, 2001
Novel Y283C mutation of the A subunit for coagulation factor XIII: molecular modelling predicts its impaired protein folding and dimer formationM Souri, V C Yee, K Kasai, et al.
Biochemical and Biophysical Research Communications|February 15, 1994
Molecular cloning and functional expression of a human peroxisomal acyl-coenzyme A oxidaseT Aoyama, K Tsushima, M Souri, et al.
Pageof 5