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Prenatal Diagnosis|February 1, 1996
PK Mondor: prenatal diagnosis of a frameshift mutation in the LR pyruvate kinase gene associated with severe hereditary non-spherocytic haemolytic anaemiaH Rouger, E Girodon, M Goossens, et al.Analytical Biochemistry|November 15, 1985
Reaction products formed after strong acid treatment of alpha-amino-delta-hydroxyvaleric acidL Cohen-Solal, Y Blouquit, M Cohen-Solal, et al.Joint Bone Spine|June 30, 2000
New factors controlling bone remodelingP Marie, F Debiais, M Cohen-Solal, et al.British Journal of Haematology|March 1, 1996
Five unknown mutations in the LR pyruvate kinase gene associated with severe hereditary nonspherocytic haemolytic anaemia in FranceH Rouger, C Valentin, C T Craescu, et al.Clinical Nephrology|May 15, 2002
Plasma bone-specific alkaline phosphatase changes in hemodialysis patients treated by alfacalcidolP Ureña, O Bernard-Poenaru, M Cohen-Solal, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1975
Nucleotide sequences of the 3'-terminal untranslated region of messenger RNA for human beta globin chainB G Forget, C A Marotta, S M Weissman, et al.Biochemical and Biophysical Research Communications|October 31, 1988
Molecular cloning and nucleotide sequence of murine 2,3-bisphosphoglycerate mutase cDNAP Le Boulch, V Joulin, M C Garel, et al.Human Mutation|September 23, 1998
A phosphoglycerate kinase mutant (PGK Herlev; D285V) in a Danish patient with isolated chronic hemolytic anemia: mechanism of mutation and structure-function relationshipsC Valentin, H Birgens, C T Craescu, et al.Proceedings of the National Academy of Sciences of the United States of America|February 1, 1981
Expression of herpes simplex virus type I thymidine kinase gene in Escherichia coliA C Garapin, F Colbère-Garapin, M Cohen-Solal, et al.European Journal of Biochemistry|August 1, 1980
The human alpha-globin gene. The protein products of the duplicated genes are identicalJ Földi, M Cohen-Solal, C Valentin, et al.Pageof 8