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Reza Kalhor

Showing results (21-30 of 42) with videos related to

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Biorxiv : the Preprint Server for Biology|May 20, 2024
Post-translational digital data encoding into the genomes of mammalian cell populationsAlec Callisto, Jonathan Strutz, Kathleen Leeper, et al.
Cell Journal|February 17, 2015
Enrichment of A Rare Subpopulation of miR-302-Expressing Glioma Cells by Serum DeprivationMahmoud-Reza Rafiee, Afsaneh Malekzadeh Shafaroudi, Sara Rohban, et al.
Biorxiv : the Preprint Server for Biology|August 26, 2024
Identifying a gene signature of metastatic potential by linking pre-metastatic state to ultimate metastatic fateJesse S Handler, Zijie Li, Rachel K Dveirin, et al.
Urology Journal|August 21, 2012
A plausible anti-apoptotic role of up-regulated OCT4B1 in bladder tumorsJamshid Asadzadeh, Malek Hossein Asadi, Nasser Shakhssalim, et al.
Cell|November 24, 2022
Quantitative fate mapping: A general framework for analyzing progenitor state dynamics via retrospective lineage barcodingWeixiang Fang, Claire M Bell, Abel Sapirstein, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 8, 2017
Conserved forkhead dimerization motif controls DNA replication timing and spatial organization of chromosomes in <i>S. cerevisiae</i>A Zachary Ostrow, Reza Kalhor, Yan Gan, et al.
Structure (London, England : 1993)|May 9, 2008
Crystal structure of NFAT bound to the HIV-1 LTR tandem kappaB enhancer elementDarren L Bates, Kristen K B Barthel, Yongqing Wu, et al.
Journal of the American Chemical Society|September 30, 2021
Recording Temporal Signals with Minutes Resolution Using Enzymatic DNA SynthesisNamita Bhan, Alec Callisto, Jonathan Strutz, et al.
American Journal of Human Genetics|June 3, 2008
Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arraysSeyedmehdi Shojaee, Farzad Sina, Setareh Sadat Banihosseini, et al.
The Journal of Investigative Dermatology|May 13, 2006
Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotypeElahe Elahi, Reza Kalhor, Setareh S Banihosseini, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
Biorxiv : the Preprint Server for Biology|May 20, 2024
Post-translational digital data encoding into the genomes of mammalian cell populationsAlec Callisto, Jonathan Strutz, Kathleen Leeper, et al.
Cell Journal|February 17, 2015
Enrichment of A Rare Subpopulation of miR-302-Expressing Glioma Cells by Serum DeprivationMahmoud-Reza Rafiee, Afsaneh Malekzadeh Shafaroudi, Sara Rohban, et al.
Biorxiv : the Preprint Server for Biology|August 26, 2024
Identifying a gene signature of metastatic potential by linking pre-metastatic state to ultimate metastatic fateJesse S Handler, Zijie Li, Rachel K Dveirin, et al.
Urology Journal|August 21, 2012
A plausible anti-apoptotic role of up-regulated OCT4B1 in bladder tumorsJamshid Asadzadeh, Malek Hossein Asadi, Nasser Shakhssalim, et al.
Cell|November 24, 2022
Quantitative fate mapping: A general framework for analyzing progenitor state dynamics via retrospective lineage barcodingWeixiang Fang, Claire M Bell, Abel Sapirstein, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 8, 2017
Conserved forkhead dimerization motif controls DNA replication timing and spatial organization of chromosomes in <i>S. cerevisiae</i>A Zachary Ostrow, Reza Kalhor, Yan Gan, et al.
Structure (London, England : 1993)|May 9, 2008
Crystal structure of NFAT bound to the HIV-1 LTR tandem kappaB enhancer elementDarren L Bates, Kristen K B Barthel, Yongqing Wu, et al.
Journal of the American Chemical Society|September 30, 2021
Recording Temporal Signals with Minutes Resolution Using Enzymatic DNA SynthesisNamita Bhan, Alec Callisto, Jonathan Strutz, et al.
American Journal of Human Genetics|June 3, 2008
Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arraysSeyedmehdi Shojaee, Farzad Sina, Setareh Sadat Banihosseini, et al.
The Journal of Investigative Dermatology|May 13, 2006
Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotypeElahe Elahi, Reza Kalhor, Setareh S Banihosseini, et al.
Pageof 5