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Alan J Warren

Showing results (11-20 of 58) with videos related to

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Biorxiv : the Preprint Server for Biology|March 13, 2023
The chemical landscape of the human ribosome at 1.67 Å resolutionAlexandre Faille, Kyle C Dent, Simone Pellegrino, et al.
Blood|August 2, 2011
Defective ribosome assembly in Shwachman-Diamond syndromeChi C Wong, David Traynor, Nicolas Basse, et al.
The Journal of Biological Chemistry|May 31, 2008
Structural consequences of nucleophosmin mutations in acute myeloid leukemiaCharles G Grummitt, Fiona M Townsley, Christopher M Johnson, et al.
Nucleic Acids Research|January 15, 2016
Shwachman-Bodian-Diamond syndrome (SBDS) protein deficiency impairs translation re-initiation from C/EBPα and C/EBPβ mRNAsKyungmin In, Mohamad A Zaini, Christine Müller, et al.
The EMBO Journal|February 17, 2006
The mechanism of repression of the myeloid-specific c-fms gene by Pax5 during B lineage restrictionHiromi Tagoh, Richard Ingram, Nicola Wilson, et al.
British Journal of Haematology|November 2, 2021
Severe congenital neutropenia with elastase, neutrophil expressed (ELANE) gene mutation in a Tanzanian childAika Shoo, Peter Swai, Christine Kindole, et al.
Cell Cycle (Georgetown, Tex.)|October 29, 2010
New insights into 5q- syndrome as a ribosomopathyJillian L Barlow, Lesley F Drynan, Nicola L Trim, et al.
Nucleic Acids Research|September 11, 2009
Characterization of RNA aptamers that disrupt the RUNX1-CBFbeta/DNA complexJenny L Barton, David H J Bunka, Stuart E Knowling, et al.
The Journal of Biological Chemistry|June 17, 2003
Energetic contribution of residues in the Runx1 Runt domain to DNA bindingZhe Li, Jiangli Yan, Christina J Matheny, et al.
Current Biology : CB|January 21, 2020
Pre-emptive Quality Control of a Misfolded Membrane Protein by Ribosome-Driven EffectsRamya Lakshminarayan, Ben P Phillips, Imogen L Binnian, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
Biorxiv : the Preprint Server for Biology|March 13, 2023
The chemical landscape of the human ribosome at 1.67 Å resolutionAlexandre Faille, Kyle C Dent, Simone Pellegrino, et al.
Blood|August 2, 2011
Defective ribosome assembly in Shwachman-Diamond syndromeChi C Wong, David Traynor, Nicolas Basse, et al.
The Journal of Biological Chemistry|May 31, 2008
Structural consequences of nucleophosmin mutations in acute myeloid leukemiaCharles G Grummitt, Fiona M Townsley, Christopher M Johnson, et al.
Nucleic Acids Research|January 15, 2016
Shwachman-Bodian-Diamond syndrome (SBDS) protein deficiency impairs translation re-initiation from C/EBPα and C/EBPβ mRNAsKyungmin In, Mohamad A Zaini, Christine Müller, et al.
The EMBO Journal|February 17, 2006
The mechanism of repression of the myeloid-specific c-fms gene by Pax5 during B lineage restrictionHiromi Tagoh, Richard Ingram, Nicola Wilson, et al.
British Journal of Haematology|November 2, 2021
Severe congenital neutropenia with elastase, neutrophil expressed (ELANE) gene mutation in a Tanzanian childAika Shoo, Peter Swai, Christine Kindole, et al.
Cell Cycle (Georgetown, Tex.)|October 29, 2010
New insights into 5q- syndrome as a ribosomopathyJillian L Barlow, Lesley F Drynan, Nicola L Trim, et al.
Nucleic Acids Research|September 11, 2009
Characterization of RNA aptamers that disrupt the RUNX1-CBFbeta/DNA complexJenny L Barton, David H J Bunka, Stuart E Knowling, et al.
The Journal of Biological Chemistry|June 17, 2003
Energetic contribution of residues in the Runx1 Runt domain to DNA bindingZhe Li, Jiangli Yan, Christina J Matheny, et al.
Current Biology : CB|January 21, 2020
Pre-emptive Quality Control of a Misfolded Membrane Protein by Ribosome-Driven EffectsRamya Lakshminarayan, Ben P Phillips, Imogen L Binnian, et al.
Pageof 6