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B G Forget

Showing results (171-180 of 192) with videos related to

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The New England Journal of Medicine|October 11, 1990
Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrinF F Costa, P Agre, P C Watkins, et al.
The Journal of Clinical Investigation|August 1, 1990
Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe)L Morlé, A F Roux, N Alloisio, et al.
The Journal of Clinical Investigation|October 1, 1989
Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosisK E Sahr, T Tobe, A Scarpa, et al.
Blood|July 1, 1987
A new mutation in IVS-1 of the human beta globin gene causing beta thalassemia due to abnormal splicingG F Atweh, C Wong, R Reed, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1979
RNA polymerase III transcriptional units are interspersed among human non-alpha-globin genesC Duncan, P A Biro, P V Choudary, et al.
Genomics|August 1, 1991
Isolation and chromosomal localization of a novel nonerythroid ankyrin geneW T Tse, J C Menninger, T L Yang-Feng, et al.
Genomics|August 1, 1993
Cloning of a portion of the chromosomal gene and cDNA for human beta-fodrin, the nonerythroid form of beta-spectrinJ G Chang, A Scarpa, R L Eddy, et al.
Transactions of the Association of American Physicians|January 1, 1988
Molecular genetics of the human beta-spectrin geneB G Forget, J G Chang, E Coupal, et al.
Blood|February 1, 1986
Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in GreeksP G Waber, M A Bender, R E Gelinas, et al.
Cell|March 1, 1976
Absence of messenger RNA and gene DNA for beta-globin chains in hereditary persistence of fetal hemoglobinB G Forget, D G Hillman, H Lazarus, et al.
Pageof 20

Showing results (171-180 of 192) with videos related to

Sort By:
Pageof 20
The New England Journal of Medicine|October 11, 1990
Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrinF F Costa, P Agre, P C Watkins, et al.
The Journal of Clinical Investigation|August 1, 1990
Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe)L Morlé, A F Roux, N Alloisio, et al.
The Journal of Clinical Investigation|October 1, 1989
Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosisK E Sahr, T Tobe, A Scarpa, et al.
Blood|July 1, 1987
A new mutation in IVS-1 of the human beta globin gene causing beta thalassemia due to abnormal splicingG F Atweh, C Wong, R Reed, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1979
RNA polymerase III transcriptional units are interspersed among human non-alpha-globin genesC Duncan, P A Biro, P V Choudary, et al.
Genomics|August 1, 1991
Isolation and chromosomal localization of a novel nonerythroid ankyrin geneW T Tse, J C Menninger, T L Yang-Feng, et al.
Genomics|August 1, 1993
Cloning of a portion of the chromosomal gene and cDNA for human beta-fodrin, the nonerythroid form of beta-spectrinJ G Chang, A Scarpa, R L Eddy, et al.
Transactions of the Association of American Physicians|January 1, 1988
Molecular genetics of the human beta-spectrin geneB G Forget, J G Chang, E Coupal, et al.
Blood|February 1, 1986
Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in GreeksP G Waber, M A Bender, R E Gelinas, et al.
Cell|March 1, 1976
Absence of messenger RNA and gene DNA for beta-globin chains in hereditary persistence of fetal hemoglobinB G Forget, D G Hillman, H Lazarus, et al.
Pageof 20