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M Brantly

Showing results (11-20 of 40) with videos related to

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Human Molecular Genetics|July 1, 1993
Characterization of a human alpha 1-antitrypsin null allele involving aberrant mRNA splicingV E Laubach, W J Ryan, M Brantly
American Journal of Human Genetics|June 1, 1991
Characterization of the molecular basis of the alpha 1-antitrypsin F alleleH Okayama, M Brantly, M Holmes, et al.
The American Review of Respiratory Disease|December 1, 1989
Characterization of the intracellular mechanism causing the alpha-1-antitrypsin Nullgranite falls deficiency stateM Holmes, D Curiel, M Brantly, et al.
Human Mutation|January 1, 1993
Genetic diversity from a limited repertoire of mutations on different common allelic backgrounds: alpha 1-antitrypsin deficiency variant PduarteJ Hildesheim, G Kinsley, M Bissell, et al.
The Journal of Clinical Investigation|April 1, 1989
Alpha 1-antitrypsin deficiency caused by the alpha 1-antitrypsin Nullmattawa gene. An insertion mutation rendering the alpha 1-antitrypsin gene incapable of producing alpha 1-antitrypsinD Curiel, M Brantly, E Curiel, et al.
The Journal of Biological Chemistry|September 5, 1987
alpha 1-Antitrypsin nullGranite Falls, a nonexpressing alpha 1-antitrypsin gene associated with a frameshift to stop mutation in a coding exonT Nukiwa, H Takahashi, M Brantly, et al.
Molecular Genetics and Metabolism|June 23, 1998
Alpha 1-antitrypsin nonsense mutation associated with a retained truncated protein and reduced mRNAJ Lee, N Novoradovskaya, B Rundquist, et al.
The Journal of Clinical Investigation|June 24, 1998
Inhibition of intracellular degradation increases secretion of a mutant form of alpha1-antitrypsin associated with profound deficiencyN Novoradovskaya, J Lee, Z X Yu, et al.
Chest|September 16, 2000
Formation and current results of a patient-organized registry for alpha(1)-antitrypsin deficiencyJ K Stoller, M Brantly, L E Fleming, et al.
Human Mutation|January 1, 1995
Heterozygosity for an exon 12 splicing mutation and a W234G missense mutation in an American child with chronic tyrosinemia type 1S H Hahn, D Krasnewich, M Brantly, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
Human Molecular Genetics|July 1, 1993
Characterization of a human alpha 1-antitrypsin null allele involving aberrant mRNA splicingV E Laubach, W J Ryan, M Brantly
American Journal of Human Genetics|June 1, 1991
Characterization of the molecular basis of the alpha 1-antitrypsin F alleleH Okayama, M Brantly, M Holmes, et al.
The American Review of Respiratory Disease|December 1, 1989
Characterization of the intracellular mechanism causing the alpha-1-antitrypsin Nullgranite falls deficiency stateM Holmes, D Curiel, M Brantly, et al.
Human Mutation|January 1, 1993
Genetic diversity from a limited repertoire of mutations on different common allelic backgrounds: alpha 1-antitrypsin deficiency variant PduarteJ Hildesheim, G Kinsley, M Bissell, et al.
The Journal of Clinical Investigation|April 1, 1989
Alpha 1-antitrypsin deficiency caused by the alpha 1-antitrypsin Nullmattawa gene. An insertion mutation rendering the alpha 1-antitrypsin gene incapable of producing alpha 1-antitrypsinD Curiel, M Brantly, E Curiel, et al.
The Journal of Biological Chemistry|September 5, 1987
alpha 1-Antitrypsin nullGranite Falls, a nonexpressing alpha 1-antitrypsin gene associated with a frameshift to stop mutation in a coding exonT Nukiwa, H Takahashi, M Brantly, et al.
Molecular Genetics and Metabolism|June 23, 1998
Alpha 1-antitrypsin nonsense mutation associated with a retained truncated protein and reduced mRNAJ Lee, N Novoradovskaya, B Rundquist, et al.
The Journal of Clinical Investigation|June 24, 1998
Inhibition of intracellular degradation increases secretion of a mutant form of alpha1-antitrypsin associated with profound deficiencyN Novoradovskaya, J Lee, Z X Yu, et al.
Chest|September 16, 2000
Formation and current results of a patient-organized registry for alpha(1)-antitrypsin deficiencyJ K Stoller, M Brantly, L E Fleming, et al.
Human Mutation|January 1, 1995
Heterozygosity for an exon 12 splicing mutation and a W234G missense mutation in an American child with chronic tyrosinemia type 1S H Hahn, D Krasnewich, M Brantly, et al.
Pageof 4