Showing results (391-400 of 464) with videos related to

Sort By:
Pageof 47
Physiological Research|October 27, 2016
Lower physical fitness in patients with primary aldosteronism is linked to the severity of hypertension and kalemiaV Tuka, M Matoulek, T Zelinka, et al.
Science (New York, N.Y.)|August 4, 1972
An isomorphous heavy-atom derivative of crystaline formylmethionine transfer RNAR W Schevitz, M A Navia, D A Bantz, et al.
Biomedica Biochimica Acta|January 1, 1990
Natural and artificial mutants of the human 2,3-bisphosphoglycerate as a tool for the evaluation of structure-function relationshipsM C Garel, V Lemarchandel, M O Prehu, et al.
Physiological Research|January 6, 2018
The effect of adrenalectomy on exercise response of the renin-angiotensin-aldosterone system and exercise tolerance in primary aldosteronismV Tuka, M Matoulek, J Rosa, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|December 6, 2008
Downstream processing of human antibodies integrating an extraction capture step and cation exchange chromatographyAna M Azevedo, Paula A J Rosa, I Filipa Ferreira, et al.
Plos Computational Biology|March 20, 2010
Comparing families of dynamic causal modelsWill D Penny, Klaas E Stephan, Jean Daunizeau, et al.
Hemoglobin|January 1, 1985
A new case of hemoglobin Providence (alpha 2 beta 2 82 (EF6) Lys----Asn or Asp) discovered in a French Caucasian family. Structural and functional studiesJ Bardakjian, L Leclerc, Y Blouquit, et al.
European Journal of Biochemistry|April 1, 1993
Amino acid residues involved in the catalytic site of human erythrocyte bisphosphoglycerate mutase. Functional consequences of substitutions of His10, His187 and Arg89M C Garel, V Lemarchandel, M C Calvin, et al.
Human Genetics|January 1, 1981
Genetic regulation of gamma gene expression: study of the interaction of beta-thalassemia with heterocellular HPFHA M Soummer, U Testa, P Dujardin, et al.
Acta Haematologica|January 1, 1982
Lasting Hb F reactivation and Hb A2 reduction induced by the treatment of Hodgkin's disease in a woman heterozygous for beta-thalassemia and the Swiss type of the heterocellular hereditary persistence of Hb FP Cech, U Testa, A Dubart, et al.
Pageof 47