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G Forget

Showing results (101-110 of 170) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|August 1, 1980
Cotransfer of circular and linear prokaryotic and eukaryotic DNA sequences into mouse cellsN Hsiung, H Warrick, J K deRiel, et al.
American Journal of Hematology|August 16, 2008
Ankyrin-linked hereditary spherocytosis in an African-American kindredJose Sangerman, Yelena Maksimova, E Jennifer Edelman, et al.
Molecular and Cellular Biology|April 1, 1997
High levels of human gamma-globin gene expression in adult mice carrying a transgene of deletion-type hereditary persistence of fetal hemoglobinM O Arcasoy, M Romana, M E Fabry, et al.
Nature|January 24, 1985
A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobinF S Collins, J E Metherall, M Yamakawa, et al.
Gene|December 1, 1980
Nucleotide sequence of human G gamma globin messenger RNAC Cavallesco, B G Forget, J K deRiel, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1974
Nucleotide sequences of human globin messenger RNAC A Marotta, B G Forget, S M Weissman, et al.
Molecular and Cellular Biology|August 1, 1987
Expression of the affected A gamma globin gene associated with Greek nondeletion hereditary persistence of fetal hemoglobinC J Stoeckert, J E Metherall, M Yamakawa, et al.
The Journal of Biological Chemistry|August 15, 1991
A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chainP G Gallagher, W T Tse, F Costa, et al.
Annales De Medecine Interne|January 1, 1990
[Expectations and defeat in the treatment of epithelial cancer of the ovary]M Weil, C Borel, G Auclerc, et al.
Blood|October 1, 1993
Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletionP G Gallagher, W E Roberts, L Benoit, et al.
Pageof 17

Showing results (101-110 of 170) with videos related to

Sort By:
Pageof 17
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1980
Cotransfer of circular and linear prokaryotic and eukaryotic DNA sequences into mouse cellsN Hsiung, H Warrick, J K deRiel, et al.
American Journal of Hematology|August 16, 2008
Ankyrin-linked hereditary spherocytosis in an African-American kindredJose Sangerman, Yelena Maksimova, E Jennifer Edelman, et al.
Molecular and Cellular Biology|April 1, 1997
High levels of human gamma-globin gene expression in adult mice carrying a transgene of deletion-type hereditary persistence of fetal hemoglobinM O Arcasoy, M Romana, M E Fabry, et al.
Nature|January 24, 1985
A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobinF S Collins, J E Metherall, M Yamakawa, et al.
Gene|December 1, 1980
Nucleotide sequence of human G gamma globin messenger RNAC Cavallesco, B G Forget, J K deRiel, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1974
Nucleotide sequences of human globin messenger RNAC A Marotta, B G Forget, S M Weissman, et al.
Molecular and Cellular Biology|August 1, 1987
Expression of the affected A gamma globin gene associated with Greek nondeletion hereditary persistence of fetal hemoglobinC J Stoeckert, J E Metherall, M Yamakawa, et al.
The Journal of Biological Chemistry|August 15, 1991
A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chainP G Gallagher, W T Tse, F Costa, et al.
Annales De Medecine Interne|January 1, 1990
[Expectations and defeat in the treatment of epithelial cancer of the ovary]M Weil, C Borel, G Auclerc, et al.
Blood|October 1, 1993
Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletionP G Gallagher, W E Roberts, L Benoit, et al.
Pageof 17