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P G Gallagher

Showing results (81-90 of 94) with videos related to

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Experimental Hematology|July 25, 2000
Gene transfer to ankyrin-deficient bone marrow corrects spherocytosis in vitroG J Dooner, J E Barker, P G Gallagher, et al.
Blood Cells, Molecules & Diseases|September 28, 2011
Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindredB L Houston, T Zelinski, S J Israels, et al.
The Journal of Clinical Investigation|January 15, 1997
Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemiaP G Gallagher, M J Petruzzi, S A Weed, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 9, 2000
Long-term expression of gamma-globin mRNA in mouse erythrocytes from retrovirus vectors containing the human gamma-globin gene fused to the ankyrin-1 promoterD E Sabatino, N E Seidel, G J Aviles-Mendoza, et al.
The Journal of Clinical Investigation|March 1, 1995
Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin geneP G Gallagher, S A Weed, W T Tse, et al.
The Journal of Biological Chemistry|August 31, 2001
Erythrocyte ankyrin promoter mutations associated with recessive hereditary spherocytosis cause significant abnormalities in ankyrin expressionP G Gallagher, D E Sabatino, D S Basseres, et al.
The Journal of Clinical Investigation|March 1, 1992
A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrinP G Gallagher, W T Tse, T Coetzer, et al.
Journal of Medical Genetics|May 23, 1998
Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?J J Jonsson, A Renieri, P G Gallagher, et al.
American Journal of Hematology|March 1, 1997
Amino-acid substitution in alpha-spectrin commonly coinherited with nondominant hereditary spherocytosisW T Tse, P G Gallagher, P B Jenkins, et al.
The Journal of Clinical Investigation|January 15, 1996
A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosisP B Jenkins, G K Abou-Alfa, D Dhermy, et al.
Pageof 10

Showing results (81-90 of 94) with videos related to

Sort By:
Pageof 10
Experimental Hematology|July 25, 2000
Gene transfer to ankyrin-deficient bone marrow corrects spherocytosis in vitroG J Dooner, J E Barker, P G Gallagher, et al.
Blood Cells, Molecules & Diseases|September 28, 2011
Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindredB L Houston, T Zelinski, S J Israels, et al.
The Journal of Clinical Investigation|January 15, 1997
Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemiaP G Gallagher, M J Petruzzi, S A Weed, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 9, 2000
Long-term expression of gamma-globin mRNA in mouse erythrocytes from retrovirus vectors containing the human gamma-globin gene fused to the ankyrin-1 promoterD E Sabatino, N E Seidel, G J Aviles-Mendoza, et al.
The Journal of Clinical Investigation|March 1, 1995
Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin geneP G Gallagher, S A Weed, W T Tse, et al.
The Journal of Biological Chemistry|August 31, 2001
Erythrocyte ankyrin promoter mutations associated with recessive hereditary spherocytosis cause significant abnormalities in ankyrin expressionP G Gallagher, D E Sabatino, D S Basseres, et al.
The Journal of Clinical Investigation|March 1, 1992
A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrinP G Gallagher, W T Tse, T Coetzer, et al.
Journal of Medical Genetics|May 23, 1998
Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?J J Jonsson, A Renieri, P G Gallagher, et al.
American Journal of Hematology|March 1, 1997
Amino-acid substitution in alpha-spectrin commonly coinherited with nondominant hereditary spherocytosisW T Tse, P G Gallagher, P B Jenkins, et al.
The Journal of Clinical Investigation|January 15, 1996
A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosisP B Jenkins, G K Abou-Alfa, D Dhermy, et al.
Pageof 10