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Biochemistry
|
October 6, 1987
Characterization of cardiac calsequestrin
J 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 proteins
C 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 reticulum
L 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 A
J 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 exchanger
L 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 glycoproteins
H 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 specificity
A B Pawagi, J Wang, M Silverman, et al.
Society of General Physiologists Series
|
January 1, 1993
Molecular characterization of the erythrocyte chloride-bicarbonate exchanger
R 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 membranes
D 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.
Page
of 9
Search research articles
Search
Showing results (71-80 of 83) with videos related to
Sort By:
Page
of 9
Biochemistry
|
October 6, 1987
Characterization of cardiac calsequestrin
J 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 proteins
C 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 reticulum
L 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 A
J 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 exchanger
L 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 glycoproteins
H 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 specificity
A B Pawagi, J Wang, M Silverman, et al.
Society of General Physiologists Series
|
January 1, 1993
Molecular characterization of the erythrocyte chloride-bicarbonate exchanger
R 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 membranes
D 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.
Page
of 9