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Proceedings of the National Academy of Sciences of the United States of America
|
April 20, 2001
Naturally variant autosomal and sex-linked loci determine the severity of iron overload in beta 2-microglobulin-deficient mice
T J Sproule, E C Jazwinska, R S Britton, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 16, 1997
Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis
S Parkkila, A Waheed, R S Britton, et al.
Cytogenetics and Cell Genetics
|
January 1, 1997
Genetic linkage mapping of 11 novel DNA markers and the ceruloplasmin (Cp) gene on rat chromosome 2
L A Shepel, R E Fleming, J D Haag, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 19, 2000
Transferrin receptor 2: continued expression in mouse liver in the face of iron overload and in hereditary hemochromatosis
R E Fleming, M C Migas, C C Holden, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 17, 1999
Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum
A Waheed, S Parkkila, J Saarnio, et al.
Haematologica
|
April 11, 2000
Cell surface expression of HFE protein in epithelial cells, macrophages, and monocytes
S Parkkila, A K Parkkila, A Waheed, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 28, 2001
Mouse strain differences determine severity of iron accumulation in Hfe knockout model of hereditary hemochromatosis
R E Fleming, C C Holden, S Tomatsu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 17, 1999
Mechanism of increased iron absorption in murine model of hereditary hemochromatosis: increased duodenal expression of the iron transporter DMT1
R E Fleming, M C Migas, X Zhou, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
August 29, 2006
Iron absorption and hepatic iron uptake are increased in a transferrin receptor 2 (Y245X) mutant mouse model of hemochromatosis type 3
S F Drake, E H Morgan, C E Herbison, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
December 16, 2016
The iron status at birth of neonates with risk factors for developing iron deficiency: a pilot study
B C MacQueen, R D Christensen, D M Ward, et al.
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Search research articles
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Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
Proceedings of the National Academy of Sciences of the United States of America
|
April 20, 2001
Naturally variant autosomal and sex-linked loci determine the severity of iron overload in beta 2-microglobulin-deficient mice
T J Sproule, E C Jazwinska, R S Britton, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 16, 1997
Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis
S Parkkila, A Waheed, R S Britton, et al.
Cytogenetics and Cell Genetics
|
January 1, 1997
Genetic linkage mapping of 11 novel DNA markers and the ceruloplasmin (Cp) gene on rat chromosome 2
L A Shepel, R E Fleming, J D Haag, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 19, 2000
Transferrin receptor 2: continued expression in mouse liver in the face of iron overload and in hereditary hemochromatosis
R E Fleming, M C Migas, C C Holden, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 17, 1999
Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum
A Waheed, S Parkkila, J Saarnio, et al.
Haematologica
|
April 11, 2000
Cell surface expression of HFE protein in epithelial cells, macrophages, and monocytes
S Parkkila, A K Parkkila, A Waheed, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 28, 2001
Mouse strain differences determine severity of iron accumulation in Hfe knockout model of hereditary hemochromatosis
R E Fleming, C C Holden, S Tomatsu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 17, 1999
Mechanism of increased iron absorption in murine model of hereditary hemochromatosis: increased duodenal expression of the iron transporter DMT1
R E Fleming, M C Migas, X Zhou, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
August 29, 2006
Iron absorption and hepatic iron uptake are increased in a transferrin receptor 2 (Y245X) mutant mouse model of hemochromatosis type 3
S F Drake, E H Morgan, C E Herbison, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
December 16, 2016
The iron status at birth of neonates with risk factors for developing iron deficiency: a pilot study
B C MacQueen, R D Christensen, D M Ward, et al.
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of 4