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Biochimie|May 1, 1990
Human bisphosphoglycerate mutase expressed in E coli: purification, characterization and structure studiesM C Calvin, Y Blouquit, M C Garel, et al.Biomedical & Environmental Mass Spectrometry|October 1, 1988
Identification of some abnormal haemoglobins by fast atom bombardment mass spectrometry and fast atom bombardment tandem mass spectrometryD Prome, J C Prome, F Pratbernou, et al.Biochimica Et Biophysica Acta|August 21, 1980
Hemoglobin Pitie-Salpetriere beta 34 (B16) Val replaced by Phe. A new high oxygen affinity variant associated with familial erythrocytosisY Blouquit, F Braconnier, M Cohen-Solal, et al.American Journal of Hematology|April 1, 1993
Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb Questembert (alpha 131[H14]Ser-->Pro) and Hb Caen (alpha 132[H15]Val-->Gly)H Wajcman, C Vasseur, Y Blouquit, et al.British Journal of Haematology|January 1, 1982
Antenatal diagnosis of haemoglobinopathies by Biorex chromatography of haemoglobinY Blouquit, Y Beuzard, L Varnavides, et al.Prenatal Diagnosis|January 1, 1989
Prenatal diagnosis of haemoglobinopathies by ion exchange HPLC of haemoglobinsP Rouyer-Fessard, F Plassa, Y Blouquit, et al.Hemoglobin|January 1, 1986
Hemoglobin La Desirade alpha A2 beta 2 129 (H7) Ala----Val: a new unstable hemoglobinG Merault, L Keclard, J Garin, et al.Hemoglobin|January 1, 1988
Hb Tunis [alpha 2 beta 2 124 (H2)Pro----Ser], a new beta chain variant identified by HPLCA Mrad, Y Blouquit, C Lacombe, et al.Biochimica Et Biophysica Acta|November 14, 1990
Hemoglobin Calais [beta 76 (E20) Ala----Pro]: a hemoglobin variant with decreased intrinsic oxygen affinityH Wajcman, J Kister, M Marden, et al.FEBS Letters|October 18, 1982
Structural study of hemoglobin Knossos, beta 27 (B9) Ala leads to Ser. A new abnormal hemoglobin present as a silent beta-thalassemiaN Arous, F Galacteros, P Fessas, et al.Pageof 10