Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

G Fornaini

Showing results (51-60 of 59) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 59 results.
Blood|September 1, 1985
Hereditary nonspherocytic hemolytic anemia due to a new hexokinase variant with reduced stabilityM Magnani, V Stocchi, L Cucchiarini, et al.
The Italian Journal of Biochemistry|September 1, 1986
Role of hexokinase in the regulation of glucose metabolism in human erythrocytesG Fornaini, M Dachà, V Stocchi, et al.
Biochimie|September 1, 1984
Human erythrocyte phosphoglucomutase: comparison of the kinetic properties of PGM1 and PGM2 isoenzymesP Ninfali, A Accorsi, F Palma, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1985
Glucose-1,6-P2 synthesis, phosphoglucomutase and phosphoribomutase correlate with glucose-1,6-P2 concentration in mammals red blood cellsA Accorsi, A Fazi, P Ninfali, et al.
Canadian Journal of Biochemistry and Cell Biology = Revue Canadienne De Biochimie Et Biologie Cellulaire|March 1, 1985
Glucose 1,6-bisphosphate decline in human erythrocytes: possible involvement of phosphoglucomutase PGM2 isoenzymesP Ninfali, E Piatti, A Accorsi, et al.
The Italian Journal of Biochemistry|September 1, 1986
The relevance of glucose 1,6-bisphosphate formation and degradation to human red blood cell metabolismG Fornaini, M Bossù, A Fazi, et al.
Biochimica Et Biophysica Acta|October 28, 1988
Improved metabolic properties of hexokinase-overloaded human erythrocytesM Magnani, L Rossi, M Bianchi, et al.
British Journal of Haematology|September 1, 1985
Human erythrocyte hexokinase deficiency: a new variant with abnormal kinetic propertiesM Magnani, V Stocchi, F Canestrari, et al.
Acta Haematologica|January 1, 1986
Redox and energetic state of red blood cells in G6PD deficiency, heterozygous beta-thalassemia and the combination of bothM Magnani, V Stocchi, F Canestrari, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
Blood|September 1, 1985
Hereditary nonspherocytic hemolytic anemia due to a new hexokinase variant with reduced stabilityM Magnani, V Stocchi, L Cucchiarini, et al.
The Italian Journal of Biochemistry|September 1, 1986
Role of hexokinase in the regulation of glucose metabolism in human erythrocytesG Fornaini, M Dachà, V Stocchi, et al.
Biochimie|September 1, 1984
Human erythrocyte phosphoglucomutase: comparison of the kinetic properties of PGM1 and PGM2 isoenzymesP Ninfali, A Accorsi, F Palma, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1985
Glucose-1,6-P2 synthesis, phosphoglucomutase and phosphoribomutase correlate with glucose-1,6-P2 concentration in mammals red blood cellsA Accorsi, A Fazi, P Ninfali, et al.
Canadian Journal of Biochemistry and Cell Biology = Revue Canadienne De Biochimie Et Biologie Cellulaire|March 1, 1985
Glucose 1,6-bisphosphate decline in human erythrocytes: possible involvement of phosphoglucomutase PGM2 isoenzymesP Ninfali, E Piatti, A Accorsi, et al.
The Italian Journal of Biochemistry|September 1, 1986
The relevance of glucose 1,6-bisphosphate formation and degradation to human red blood cell metabolismG Fornaini, M Bossù, A Fazi, et al.
Biochimica Et Biophysica Acta|October 28, 1988
Improved metabolic properties of hexokinase-overloaded human erythrocytesM Magnani, L Rossi, M Bianchi, et al.
British Journal of Haematology|September 1, 1985
Human erythrocyte hexokinase deficiency: a new variant with abnormal kinetic propertiesM Magnani, V Stocchi, F Canestrari, et al.
Acta Haematologica|January 1, 1986
Redox and energetic state of red blood cells in G6PD deficiency, heterozygous beta-thalassemia and the combination of bothM Magnani, V Stocchi, F Canestrari, et al.
Pageof 6