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Daniel F Wallace

Showing results (21-30 of 55) with videos related to

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American Journal of Hematology|May 13, 2016
Hematopoietic deletion of transferrin receptor 2 in mice leads to a block in erythroid differentiation during iron-deficient anemiaGautam Rishi, Eriza S Secondes, Daniel F Wallace, et al.
American Journal of Physiology. Cell Physiology|December 21, 2007
Defective trafficking and localization of mutated transferrin receptor 2: implications for type 3 hereditary hemochromatosisDaniel F Wallace, Lesa Summerville, Emily M Crampton, et al.
Journal of Hepatology|March 20, 2004
Autosomal dominant iron overload due to a novel mutation of ferroportin1 associated with parenchymal iron loading and cirrhosisDaniel F Wallace, Roslyn M Clark, Hugh A J Harley, et al.
Journal of Gastroenterology and Hepatology|April 13, 2013
Iron storage disease in Asia-Pacific populations: the importance of non-HFE mutationsCameron J McDonald, Daniel F Wallace, Darrell H G Crawford, et al.
Biometals : an International Journal on the Role of Metal Ions in Biology, Biochemistry, and Medicine|April 29, 2021
In vitro identification and characterisation of iron chelating catechol-containing natural products and derivativesZachary J Hawula, Rohan A Davis, Daniel F Wallace, et al.
Bioscience Reports|June 22, 2021
The effect of the flavonol rutin on serum and liver iron content in a genetic mouse model of iron overloadZachary J Hawula, Eriza S Secondes, Daniel F Wallace, et al.
Genesis (New York, N.Y. : 2000)|May 5, 2004
Inactivation of the murine Transferrin Receptor 2 gene using the Cre recombinase: loxP systemDaniel F Wallace, Ian D Tonks, Anna Zournazi, et al.
American Journal of Hematology|July 7, 2017
The dynamics of hepcidin-ferroportin internalization and consequences of a novel ferroportin disease mutationDaniel F Wallace, Cameron J McDonald, Lesa Ostini, et al.
Journal of Hepatology|November 25, 2010
G80S-linked ferroportin disease: classical ferroportin disease in an Asian family and reclassification of the mutant as iron transport defectiveCameron J McDonald, Daniel F Wallace, Lesa Ostini, et al.
World Journal of Gastroenterology|April 6, 2006
Fatty liver in H63D homozygotes with hyperferritinemiaGiada Sebastiani, Daniel F Wallace, Susan E Davies, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
American Journal of Hematology|May 13, 2016
Hematopoietic deletion of transferrin receptor 2 in mice leads to a block in erythroid differentiation during iron-deficient anemiaGautam Rishi, Eriza S Secondes, Daniel F Wallace, et al.
American Journal of Physiology. Cell Physiology|December 21, 2007
Defective trafficking and localization of mutated transferrin receptor 2: implications for type 3 hereditary hemochromatosisDaniel F Wallace, Lesa Summerville, Emily M Crampton, et al.
Journal of Hepatology|March 20, 2004
Autosomal dominant iron overload due to a novel mutation of ferroportin1 associated with parenchymal iron loading and cirrhosisDaniel F Wallace, Roslyn M Clark, Hugh A J Harley, et al.
Journal of Gastroenterology and Hepatology|April 13, 2013
Iron storage disease in Asia-Pacific populations: the importance of non-HFE mutationsCameron J McDonald, Daniel F Wallace, Darrell H G Crawford, et al.
Biometals : an International Journal on the Role of Metal Ions in Biology, Biochemistry, and Medicine|April 29, 2021
In vitro identification and characterisation of iron chelating catechol-containing natural products and derivativesZachary J Hawula, Rohan A Davis, Daniel F Wallace, et al.
Bioscience Reports|June 22, 2021
The effect of the flavonol rutin on serum and liver iron content in a genetic mouse model of iron overloadZachary J Hawula, Eriza S Secondes, Daniel F Wallace, et al.
Genesis (New York, N.Y. : 2000)|May 5, 2004
Inactivation of the murine Transferrin Receptor 2 gene using the Cre recombinase: loxP systemDaniel F Wallace, Ian D Tonks, Anna Zournazi, et al.
American Journal of Hematology|July 7, 2017
The dynamics of hepcidin-ferroportin internalization and consequences of a novel ferroportin disease mutationDaniel F Wallace, Cameron J McDonald, Lesa Ostini, et al.
Journal of Hepatology|November 25, 2010
G80S-linked ferroportin disease: classical ferroportin disease in an Asian family and reclassification of the mutant as iron transport defectiveCameron J McDonald, Daniel F Wallace, Lesa Ostini, et al.
World Journal of Gastroenterology|April 6, 2006
Fatty liver in H63D homozygotes with hyperferritinemiaGiada Sebastiani, Daniel F Wallace, Susan E Davies, et al.
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