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B G Forget

Showing results (161-170 of 192) with videos related to

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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.
Blood|September 1, 1994
Developmental regulation of human gamma- and beta-globin genes in the absence of the locus control regionJ Starck, R Sarkar, M Romana, et al.
Annals of the New York Academy of Sciences|January 1, 1990
Expression of human globin genes in transgenic mice carrying the beta-globin gene cluster with a mutation causing G gamma beta + hereditary persistence of fetal hemoglobinM Tanaka, J A Nolan, A K Bhargava, et al.
Blood|August 1, 1989
Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domainL Morlé, F Morlé, A F Roux, 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.
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.
Blood|August 1, 1992
Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association siteN Alloisio, R Wilmotte, L Morlé, et al.
The Journal of Biological Chemistry|April 10, 1980
Nucleotide sequence of the coding portion of human alpha globin messenger RNAJ T Wilson, L B Wilson, V B Reddy, et al.
Pageof 20

Showing results (161-170 of 192) with videos related to

Sort By:
Pageof 20
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.
Blood|September 1, 1994
Developmental regulation of human gamma- and beta-globin genes in the absence of the locus control regionJ Starck, R Sarkar, M Romana, et al.
Annals of the New York Academy of Sciences|January 1, 1990
Expression of human globin genes in transgenic mice carrying the beta-globin gene cluster with a mutation causing G gamma beta + hereditary persistence of fetal hemoglobinM Tanaka, J A Nolan, A K Bhargava, et al.
Blood|August 1, 1989
Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domainL Morlé, F Morlé, A F Roux, 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.
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.
Blood|August 1, 1992
Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association siteN Alloisio, R Wilmotte, L Morlé, et al.
The Journal of Biological Chemistry|April 10, 1980
Nucleotide sequence of the coding portion of human alpha globin messenger RNAJ T Wilson, L B Wilson, V B Reddy, et al.
Pageof 20