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Gordon W Stewart

Showing results (21-30 of 32) with videos related to

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Biochimica Et Biophysica Acta|October 27, 2007
Membrane raft actin deficiency and altered Ca2+-induced vesiculation in stomatin-deficient overhydrated hereditary stomatocytosisD Katie Wilkinson, E Jane Turner, Edward T Parkin, et al.
Blood|May 17, 2003
The "stomatin" gene and protein in overhydrated hereditary stomatocytosisBritta Fricke, Annette C Argent, Margaret C Chetty, et al.
Blood|October 22, 2008
The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoproteinLesley J Bruce, Hélène Guizouarn, Nicholas M Burton, et al.
Blood|August 15, 2002
Absence of CD47 in protein 4.2-deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complexLesley J Bruce, Sandip Ghosh, May Jean King, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2012
An infant with pseudohyperkalemia, hemolysis, and seizures: cation-leaky GLUT1-deficiency syndrome due to a SLC2A1 mutationWaleed M Bawazir, Evelien F Gevers, Joanna F Flatt, et al.
European Journal of Human Genetics : EJHG|October 8, 2004
A second locus mapping to 2q35-36 for familial pseudohyperkalaemiaMassimo Carella, Adamo Pio d'Adamo, Sabine Grootenboer-Mignot, et al.
Transfusion|June 21, 2014
Familial pseudohyperkalemia in blood donors: a novel mutation with implications for transfusion practiceWaleed M Bawazir, Joanna F Flatt, Jonathan P Wallis, et al.
Blood|July 28, 2011
Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndromeJoanna F Flatt, Hélène Guizouarn, Nicholas M Burton, et al.
British Journal of Haematology|June 8, 2004
Four new cases of stomatin-deficient hereditary stomatocytosis syndrome: association of the stomatin-deficient cryohydrocytosis variant with neurological dysfunctionBritta Fricke, Helen G Jarvis, Cecil D L Reid, et al.
Nature Genetics|October 18, 2005
Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1Lesley J Bruce, Hannah C Robinson, Hélène Guizouarn, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Biochimica Et Biophysica Acta|October 27, 2007
Membrane raft actin deficiency and altered Ca2+-induced vesiculation in stomatin-deficient overhydrated hereditary stomatocytosisD Katie Wilkinson, E Jane Turner, Edward T Parkin, et al.
Blood|May 17, 2003
The "stomatin" gene and protein in overhydrated hereditary stomatocytosisBritta Fricke, Annette C Argent, Margaret C Chetty, et al.
Blood|October 22, 2008
The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoproteinLesley J Bruce, Hélène Guizouarn, Nicholas M Burton, et al.
Blood|August 15, 2002
Absence of CD47 in protein 4.2-deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complexLesley J Bruce, Sandip Ghosh, May Jean King, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2012
An infant with pseudohyperkalemia, hemolysis, and seizures: cation-leaky GLUT1-deficiency syndrome due to a SLC2A1 mutationWaleed M Bawazir, Evelien F Gevers, Joanna F Flatt, et al.
European Journal of Human Genetics : EJHG|October 8, 2004
A second locus mapping to 2q35-36 for familial pseudohyperkalaemiaMassimo Carella, Adamo Pio d'Adamo, Sabine Grootenboer-Mignot, et al.
Transfusion|June 21, 2014
Familial pseudohyperkalemia in blood donors: a novel mutation with implications for transfusion practiceWaleed M Bawazir, Joanna F Flatt, Jonathan P Wallis, et al.
Blood|July 28, 2011
Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndromeJoanna F Flatt, Hélène Guizouarn, Nicholas M Burton, et al.
British Journal of Haematology|June 8, 2004
Four new cases of stomatin-deficient hereditary stomatocytosis syndrome: association of the stomatin-deficient cryohydrocytosis variant with neurological dysfunctionBritta Fricke, Helen G Jarvis, Cecil D L Reid, et al.
Nature Genetics|October 18, 2005
Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1Lesley J Bruce, Hannah C Robinson, Hélène Guizouarn, et al.
Pageof 4