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F S Collins

Showing results (141-150 of 297) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 4, 1997
The ataxia-telangiectasia gene product, a constitutively expressed nuclear protein that is not up-regulated following genome damageK D Brown, Y Ziv, S N Sadanandan, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Molecular analysis of deletion and nondeletion hereditary persistence of fetal hemoglobin and identification of a new mutation causing beta-thalassemiaE A Feingold, F S Collins, J E Metherall, et al.
Nucleic Acids Research|September 25, 1999
Design of modified oligodeoxyribonucleotide probes to detect telomere repeat sequences in FISH assaysJ G Hacia, E A Novotny, R A Mayer, et al.
Nature Genetics|October 1, 1995
The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individualsJ P Struewing, D Abeliovich, T Peretz, et al.
The Journal of General Physiology|January 1, 1996
CFTR: the nucleotide binding folds regulate the accessibility and stability of the activated stateD J Wilkinson, M K Mansoura, P Y Watson, et al.
American Journal of Medical Genetics|January 1, 1988
Two patients with ring chromosome 15 syndromeM G Butler, A B Fogo, D A Fuchs, et al.
Nucleic Acids Research|August 11, 1990
Dinucleotide repeat polymorphisms at the D17S250 and D17S261 lociJ L Weber, A E Kwitek, P E May, et al.
Genomics|December 1, 1993
The CA repeat marker D17S791 is located within 40 kb of the WNT3 gene on chromosome 17qS C Chandrasekharappa, S E King, M L Freedman, et al.
Nature|October 31, 1991
A de novo Alu insertion results in neurofibromatosis type 1M R Wallace, L B Andersen, A M Saulino, et al.
Molecular and Cellular Biology|December 1, 1988
Nuclear proteins that bind the human gamma-globin gene promoter: alterations in binding produced by point mutations associated with hereditary persistence of fetal hemoglobinD L Gumucio, K L Rood, T A Gray, et al.
Pageof 30

Showing results (141-150 of 297) with videos related to

Sort By:
Pageof 30
Proceedings of the National Academy of Sciences of the United States of America|March 4, 1997
The ataxia-telangiectasia gene product, a constitutively expressed nuclear protein that is not up-regulated following genome damageK D Brown, Y Ziv, S N Sadanandan, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Molecular analysis of deletion and nondeletion hereditary persistence of fetal hemoglobin and identification of a new mutation causing beta-thalassemiaE A Feingold, F S Collins, J E Metherall, et al.
Nucleic Acids Research|September 25, 1999
Design of modified oligodeoxyribonucleotide probes to detect telomere repeat sequences in FISH assaysJ G Hacia, E A Novotny, R A Mayer, et al.
Nature Genetics|October 1, 1995
The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individualsJ P Struewing, D Abeliovich, T Peretz, et al.
The Journal of General Physiology|January 1, 1996
CFTR: the nucleotide binding folds regulate the accessibility and stability of the activated stateD J Wilkinson, M K Mansoura, P Y Watson, et al.
American Journal of Medical Genetics|January 1, 1988
Two patients with ring chromosome 15 syndromeM G Butler, A B Fogo, D A Fuchs, et al.
Nucleic Acids Research|August 11, 1990
Dinucleotide repeat polymorphisms at the D17S250 and D17S261 lociJ L Weber, A E Kwitek, P E May, et al.
Genomics|December 1, 1993
The CA repeat marker D17S791 is located within 40 kb of the WNT3 gene on chromosome 17qS C Chandrasekharappa, S E King, M L Freedman, et al.
Nature|October 31, 1991
A de novo Alu insertion results in neurofibromatosis type 1M R Wallace, L B Andersen, A M Saulino, et al.
Molecular and Cellular Biology|December 1, 1988
Nuclear proteins that bind the human gamma-globin gene promoter: alterations in binding produced by point mutations associated with hereditary persistence of fetal hemoglobinD L Gumucio, K L Rood, T A Gray, et al.
Pageof 30