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R A Reithmeier

Showing results (71-80 of 83) with videos related to

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Biochemistry|October 6, 1987
Characterization of cardiac calsequestrinJ R Slupsky, M Ohnishi, M R Carpenter, et al.
Journal of Molecular Biology|February 5, 1993
Non-random distribution of amino acids in the transmembrane segments of human type I single span membrane proteinsC Landolt-Marticorena, K A Williams, C M Deber, et al.
The Journal of Biological Chemistry|December 25, 1989
Molecular cloning of the high affinity calcium-binding protein (calreticulin) of skeletal muscle sarcoplasmic reticulumL Fliegel, K Burns, D H MacLennan, et al.
The American Journal of Physiology|January 1, 1994
Interaction of rat kidney P-glycoprotein with a urinary component and various drugs including cyclosporin AJ H Charuk, T W Loo, D M Clarke, et al.
The Journal of Biological Chemistry|December 23, 1994
Identification of an internal topogenic signal sequence in human Band 3, the erythrocyte anion exchangerL Y Tam, T W Loo, D M Clarke, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|June 3, 1999
Structural and functional consequences of an N-glycosylation mutation (HEMPAS) affecting human erythrocyte membrane glycoproteinsH Kameh, C Landolt-Marticorena, J H Charuk, et al.
Journal of Molecular Biology|January 14, 1994
Transmembrane aromatic amino acid distribution in P-glycoprotein. A functional role in broad substrate specificityA B Pawagi, J Wang, M Silverman, et al.
Society of General Physiologists Series|January 1, 1993
Molecular characterization of the erythrocyte chloride-bicarbonate exchangerR A Reithmeier, C Landolt-Marticorena, J R Casey, et al.
Biochemical and Biophysical Research Communications|July 14, 1989
Identification of P-glycoprotein in renal brush border membranesD M Lieberman, R A Reithmeier, V Ling, et al.
European Journal of Biochemistry|June 1, 1995
Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS)J H Charuk, J Tan, M Bernardini, et al.
Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:
Pageof 9
Biochemistry|October 6, 1987
Characterization of cardiac calsequestrinJ R Slupsky, M Ohnishi, M R Carpenter, et al.
Journal of Molecular Biology|February 5, 1993
Non-random distribution of amino acids in the transmembrane segments of human type I single span membrane proteinsC Landolt-Marticorena, K A Williams, C M Deber, et al.
The Journal of Biological Chemistry|December 25, 1989
Molecular cloning of the high affinity calcium-binding protein (calreticulin) of skeletal muscle sarcoplasmic reticulumL Fliegel, K Burns, D H MacLennan, et al.
The American Journal of Physiology|January 1, 1994
Interaction of rat kidney P-glycoprotein with a urinary component and various drugs including cyclosporin AJ H Charuk, T W Loo, D M Clarke, et al.
The Journal of Biological Chemistry|December 23, 1994
Identification of an internal topogenic signal sequence in human Band 3, the erythrocyte anion exchangerL Y Tam, T W Loo, D M Clarke, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|June 3, 1999
Structural and functional consequences of an N-glycosylation mutation (HEMPAS) affecting human erythrocyte membrane glycoproteinsH Kameh, C Landolt-Marticorena, J H Charuk, et al.
Journal of Molecular Biology|January 14, 1994
Transmembrane aromatic amino acid distribution in P-glycoprotein. A functional role in broad substrate specificityA B Pawagi, J Wang, M Silverman, et al.
Society of General Physiologists Series|January 1, 1993
Molecular characterization of the erythrocyte chloride-bicarbonate exchangerR A Reithmeier, C Landolt-Marticorena, J R Casey, et al.
Biochemical and Biophysical Research Communications|July 14, 1989
Identification of P-glycoprotein in renal brush border membranesD M Lieberman, R A Reithmeier, V Ling, et al.
European Journal of Biochemistry|June 1, 1995
Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS)J H Charuk, J Tan, M Bernardini, et al.
Pageof 9