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Farnaz Absalan

Showing results (1-10 of 6) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|November 21, 2007
Molecular inversion probe assayFarnaz Absalan, Mostafa Ronaghi
Molecular Cell|August 21, 2012
Regulation of yeast pyruvate kinase by ultrasensitive allostery independent of phosphorylationYi-Fan Xu, Xin Zhao, David S Glass, et al.
Plos One|July 17, 2008
High throughput automated allele frequency estimation by pyrosequencingJulie Doostzadeh, Shadi Shokralla, Farnaz Absalan, et al.
Journal of Bone and Mineral Metabolism|April 21, 2007
Intragenic SNP haplotypes associated with 84dup18 mutation in TNFRSF11A in four FEO pedigrees suggest three independent origins for this mutationElahe Elahi, Yousef Shafaghati, Sareh Asadi, et al.
Molecular Systems Biology|May 15, 2013
Nucleotide degradation and ribose salvage in yeastYi-Fan Xu, Fabien Létisse, Farnaz Absalan, et al.
Human Mutation|October 15, 2008
Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson diseaseBalaji S Srinivasan, Jaleh Doostzadeh, Farnaz Absalan, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Methods in Molecular Biology (Clifton, N.J.)|November 21, 2007
Molecular inversion probe assayFarnaz Absalan, Mostafa Ronaghi
Molecular Cell|August 21, 2012
Regulation of yeast pyruvate kinase by ultrasensitive allostery independent of phosphorylationYi-Fan Xu, Xin Zhao, David S Glass, et al.
Plos One|July 17, 2008
High throughput automated allele frequency estimation by pyrosequencingJulie Doostzadeh, Shadi Shokralla, Farnaz Absalan, et al.
Journal of Bone and Mineral Metabolism|April 21, 2007
Intragenic SNP haplotypes associated with 84dup18 mutation in TNFRSF11A in four FEO pedigrees suggest three independent origins for this mutationElahe Elahi, Yousef Shafaghati, Sareh Asadi, et al.
Molecular Systems Biology|May 15, 2013
Nucleotide degradation and ribose salvage in yeastYi-Fan Xu, Fabien Létisse, Farnaz Absalan, et al.
Human Mutation|October 15, 2008
Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson diseaseBalaji S Srinivasan, Jaleh Doostzadeh, Farnaz Absalan, et al.
Pageof 1