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F S Collins

Showing results (171-180 of 297) with videos related to

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Human Molecular Genetics|April 1, 1993
Dinucleotide repeat polymorphism in the Huntington's disease region at the D4S182 locusD A Tagle, K L Blanchard-McQuate, J Valdes, et al.
Nucleic Acids Research|October 20, 1998
Enhanced high density oligonucleotide array-based sequence analysis using modified nucleoside triphosphatesJ G Hacia, S A Woski, J Fidanza, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 24, 1996
The leukemic core binding factor beta-smooth muscle myosin heavy chain (CBF beta-SMMHC) chimeric protein requires both CBF beta and myosin heavy chain domains for transformation of NIH 3T3 cellsR S Adelstein, F S Collins, A Hajra, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 21, 1998
Menin, the product of the MEN1 gene, is a nuclear proteinS C Guru, P K Goldsmith, A L Burns, et al.
Human Mutation|April 24, 2001
Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancersS M Lipkin, V Wang, D L Stoler, et al.
Clinical Genetics|July 1, 1992
DNA deletion in patients with von Recklinghausen neurofibromatosisT Kamei, Y Fukushima, A Shibata, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 14, 1995
The leukemic core binding factor beta-smooth muscle myosin heavy chain (CBF beta-SMMHC) chimeric protein requires both CBF beta and myosin heavy chain domains for transformation of NIH 3T3 cellsA Hajra, P P Liu, Q Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1988
Chromosome jumping from D4S10 (G8) toward the Huntington disease geneJ E Richards, T C Gilliam, J L Cole, et al.
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.
The American Journal of Physiology|July 1, 1997
CFTR activation: additive effects of stimulatory and inhibitory phosphorylation sites in the R domainD J Wilkinson, T V Strong, M K Mansoura, et al.
Pageof 30

Showing results (171-180 of 297) with videos related to

Sort By:
Pageof 30
Human Molecular Genetics|April 1, 1993
Dinucleotide repeat polymorphism in the Huntington's disease region at the D4S182 locusD A Tagle, K L Blanchard-McQuate, J Valdes, et al.
Nucleic Acids Research|October 20, 1998
Enhanced high density oligonucleotide array-based sequence analysis using modified nucleoside triphosphatesJ G Hacia, S A Woski, J Fidanza, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 24, 1996
The leukemic core binding factor beta-smooth muscle myosin heavy chain (CBF beta-SMMHC) chimeric protein requires both CBF beta and myosin heavy chain domains for transformation of NIH 3T3 cellsR S Adelstein, F S Collins, A Hajra, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 21, 1998
Menin, the product of the MEN1 gene, is a nuclear proteinS C Guru, P K Goldsmith, A L Burns, et al.
Human Mutation|April 24, 2001
Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancersS M Lipkin, V Wang, D L Stoler, et al.
Clinical Genetics|July 1, 1992
DNA deletion in patients with von Recklinghausen neurofibromatosisT Kamei, Y Fukushima, A Shibata, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 14, 1995
The leukemic core binding factor beta-smooth muscle myosin heavy chain (CBF beta-SMMHC) chimeric protein requires both CBF beta and myosin heavy chain domains for transformation of NIH 3T3 cellsA Hajra, P P Liu, Q Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1988
Chromosome jumping from D4S10 (G8) toward the Huntington disease geneJ E Richards, T C Gilliam, J L Cole, et al.
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.
The American Journal of Physiology|July 1, 1997
CFTR activation: additive effects of stimulatory and inhibitory phosphorylation sites in the R domainD J Wilkinson, T V Strong, M K Mansoura, et al.
Pageof 30