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Showing results (1031-1040 of 1,192) with videos related to

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Molecular & Cellular Proteomics : MCP|March 1, 2015
Quantitative proteomics reveals protein-protein interactions with fibroblast growth factor 12 as a component of the voltage-gated sodium channel 1.2 (nav1.2) macromolecular complex in Mammalian brainNorelle C Wildburger, Syed R Ali, Wei-Chun J Hsu, et al.
Journal of Vision|November 26, 2015
Spectral sensitivity measurements reveal partial success in restoring missing rod function with gene therapyCaterina Ripamonti, G Bruce Henning, Scott J Robbie, et al.
Molecular Therapy Oncolytics|March 14, 2023
Multivalent <i>in vivo</i> delivery of DNA-encoded bispecific T cell engagers effectively controls heterogeneous GBM tumors and mitigates immune escapeDaniel H Park, Kevin Liaw, Pratik Bhojnagarwala, et al.
International Journal of Oncology|July 17, 2013
Neuroblastoma cells injected into experimental mature teratoma reveal a tropism for embryonic loose mesenchymeS Jamil, J Cedervall, I Hultman, et al.
Human Molecular Genetics|August 23, 2014
The severity of retinal pathology in homozygous Crb1rd8/rd8 mice is dependent on additional genetic factorsUlrich F O Luhmann, Livia S Carvalho, Sophia-Martha Kleine Holthaus, et al.
Open Biology|February 6, 2020
Neoleukin-2 enhances anti-tumour immunity downstream of peptide vaccination targeted by an anti-MHC class II VHHStephanie J Crowley, Patrick T Bruck, Md Aladdin Bhuiyan, et al.
Human Molecular Genetics|December 23, 2020
RPGR isoform imbalance causes ciliary defects due to exon ORF15 mutations in X-linked retinitis pigmentosa (XLRP)Laura Moreno-Leon, Emma L West, Michelle O'Hara-Wright, et al.
Epigenetics & Chromatin|February 3, 2019
Epigenomic signatures in liver and blood of Wilson disease patients include hypermethylation of liver-specific enhancersCharles E Mordaunt, Dorothy A Kieffer, Noreene M Shibata, et al.
Human Molecular Genetics|July 17, 2018
Epigenetic changes of the thioredoxin system in the tx-j mouse model and in patients with Wilson diseaseCharles E Mordaunt, Noreene M Shibata, Dorothy A Kieffer, et al.
Oncogene|March 23, 2011
Genomic evolution in Barrett's adenocarcinoma cells: critical roles of elevated hsRAD51, homologous recombination and Alu sequences in the genomeJ Pal, R Bertheau, L Buon, et al.
Pageof 120

Showing results (1031-1040 of 1,192) with videos related to

Sort By:
Pageof 120
Molecular & Cellular Proteomics : MCP|March 1, 2015
Quantitative proteomics reveals protein-protein interactions with fibroblast growth factor 12 as a component of the voltage-gated sodium channel 1.2 (nav1.2) macromolecular complex in Mammalian brainNorelle C Wildburger, Syed R Ali, Wei-Chun J Hsu, et al.
Journal of Vision|November 26, 2015
Spectral sensitivity measurements reveal partial success in restoring missing rod function with gene therapyCaterina Ripamonti, G Bruce Henning, Scott J Robbie, et al.
Molecular Therapy Oncolytics|March 14, 2023
Multivalent <i>in vivo</i> delivery of DNA-encoded bispecific T cell engagers effectively controls heterogeneous GBM tumors and mitigates immune escapeDaniel H Park, Kevin Liaw, Pratik Bhojnagarwala, et al.
International Journal of Oncology|July 17, 2013
Neuroblastoma cells injected into experimental mature teratoma reveal a tropism for embryonic loose mesenchymeS Jamil, J Cedervall, I Hultman, et al.
Human Molecular Genetics|August 23, 2014
The severity of retinal pathology in homozygous Crb1rd8/rd8 mice is dependent on additional genetic factorsUlrich F O Luhmann, Livia S Carvalho, Sophia-Martha Kleine Holthaus, et al.
Open Biology|February 6, 2020
Neoleukin-2 enhances anti-tumour immunity downstream of peptide vaccination targeted by an anti-MHC class II VHHStephanie J Crowley, Patrick T Bruck, Md Aladdin Bhuiyan, et al.
Human Molecular Genetics|December 23, 2020
RPGR isoform imbalance causes ciliary defects due to exon ORF15 mutations in X-linked retinitis pigmentosa (XLRP)Laura Moreno-Leon, Emma L West, Michelle O'Hara-Wright, et al.
Epigenetics & Chromatin|February 3, 2019
Epigenomic signatures in liver and blood of Wilson disease patients include hypermethylation of liver-specific enhancersCharles E Mordaunt, Dorothy A Kieffer, Noreene M Shibata, et al.
Human Molecular Genetics|July 17, 2018
Epigenetic changes of the thioredoxin system in the tx-j mouse model and in patients with Wilson diseaseCharles E Mordaunt, Noreene M Shibata, Dorothy A Kieffer, et al.
Oncogene|March 23, 2011
Genomic evolution in Barrett's adenocarcinoma cells: critical roles of elevated hsRAD51, homologous recombination and Alu sequences in the genomeJ Pal, R Bertheau, L Buon, et al.
Pageof 120