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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 anemia
Gautam 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 hemochromatosis
Daniel 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 cirrhosis
Daniel 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 mutations
Cameron 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 derivatives
Zachary 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 overload
Zachary 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 system
Daniel 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 mutation
Daniel 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 defective
Cameron J McDonald, Daniel F Wallace, Lesa Ostini, et al.
World Journal of Gastroenterology
|
April 6, 2006
Fatty liver in H63D homozygotes with hyperferritinemia
Giada Sebastiani, Daniel F Wallace, Susan E Davies, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 55) with videos related to
Sort By:
Page
of 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 anemia
Gautam 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 hemochromatosis
Daniel 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 cirrhosis
Daniel 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 mutations
Cameron 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 derivatives
Zachary 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 overload
Zachary 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 system
Daniel 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 mutation
Daniel 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 defective
Cameron J McDonald, Daniel F Wallace, Lesa Ostini, et al.
World Journal of Gastroenterology
|
April 6, 2006
Fatty liver in H63D homozygotes with hyperferritinemia
Giada Sebastiani, Daniel F Wallace, Susan E Davies, et al.
Page
of 6