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G Forget

Showing results (131-140 of 170) with videos related to

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Hemoglobin|January 1, 1978
Studies of globin chain synthesis and globin mRNA content in a patient homozygous for hemoglobin LeporeB G Forget, C Cavallesco, E J Benz, et al.
The Journal of Clinical Investigation|July 1, 1991
Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutationM Garbarz, W T Tse, P G Gallagher, et al.
Cell|June 1, 1978
Variability in the amount of beta-globin mRNA in beta0 thalassemiaE J Benz, B G Forget, D G Hillman, et al.
Experimental Hematology|February 7, 2006
Hematopoiesis following disruption of the Pitx2 homeodomain geneHui Z Zhang, Barbara A Degar, Svetlana Rogoulina, et al.
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.
Gene|January 1, 1985
Polyadenylation of a human mitochondrial ribosomal RNA transcript detected by molecular cloningS J Baserga, A J Linnenbach, S Malcolm, et al.
Human Genetics|October 1, 1990
Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin alleleD Guetarni, A F Roux, N Alloisio, et al.
Blood|December 1, 1984
Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black populationF S Collins, C D Boehm, P G Waber, et al.
American Journal of Hematology|March 1, 1997
Ankyrin Bugey: a de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosisL Morlé, M Bozon, N Alloisio, et al.
JAMA|April 13, 1979
Prenatal diagnosis of homozygous alpha-thalassemiaA M Dozy, E N Forman, D N Abuelo, et al.
Pageof 17

Showing results (131-140 of 170) with videos related to

Sort By:
Pageof 17
Hemoglobin|January 1, 1978
Studies of globin chain synthesis and globin mRNA content in a patient homozygous for hemoglobin LeporeB G Forget, C Cavallesco, E J Benz, et al.
The Journal of Clinical Investigation|July 1, 1991
Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutationM Garbarz, W T Tse, P G Gallagher, et al.
Cell|June 1, 1978
Variability in the amount of beta-globin mRNA in beta0 thalassemiaE J Benz, B G Forget, D G Hillman, et al.
Experimental Hematology|February 7, 2006
Hematopoiesis following disruption of the Pitx2 homeodomain geneHui Z Zhang, Barbara A Degar, Svetlana Rogoulina, et al.
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.
Gene|January 1, 1985
Polyadenylation of a human mitochondrial ribosomal RNA transcript detected by molecular cloningS J Baserga, A J Linnenbach, S Malcolm, et al.
Human Genetics|October 1, 1990
Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin alleleD Guetarni, A F Roux, N Alloisio, et al.
Blood|December 1, 1984
Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black populationF S Collins, C D Boehm, P G Waber, et al.
American Journal of Hematology|March 1, 1997
Ankyrin Bugey: a de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosisL Morlé, M Bozon, N Alloisio, et al.
JAMA|April 13, 1979
Prenatal diagnosis of homozygous alpha-thalassemiaA M Dozy, E N Forman, D N Abuelo, et al.
Pageof 17