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Andrew J Simmonds

Showing results (21-30 of 31) with videos related to

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Genetics|May 6, 2004
Molecular and functional analysis of scalloped recessive lethal alleles in Drosophila melanogasterAjay Srivastava, Andrew J Simmonds, Ankush Garg, et al.
Developmental Biology|October 4, 2015
Loss of the Drosophila melanogaster DEAD box protein Ddx1 leads to reduced size and aberrant gametogenesisDevon R Germain, Lei Li, Matthew R Hildebrandt, et al.
Developmental Biology|March 22, 2017
The activity of the Drosophila Vestigial protein is modified by Scalloped-dependent phosphorylationVirginia L Pimmett, Hua Deng, Julie A Haskins, et al.
Traffic (Copenhagen, Denmark)|June 1, 2006
RNA interference effector proteins localize to mobile cytoplasmic puncta in Schizosaccharomyces pombeJon B Carmichael, Cezar Stoica, Henry Parker, et al.
Disease Models & Mechanisms|June 15, 2011
A Drosophila model for the Zellweger spectrum of peroxisome biogenesis disordersFred D Mast, Jing Li, Maninder K Virk, et al.
RNA (New York, N.Y.)|September 22, 2010
Functional characterization of the Drosophila MRP (mitochondrial RNA processing) RNA geneMary D Schneider, Anupinder K Bains, T K Rajendra, et al.
Nature Communications|June 12, 2020
Impaired peroxisomal import in Drosophila oenocytes causes cardiac dysfunction by inducing upd3 as a peroxikineKerui Huang, Ting Miao, Kai Chang, et al.
The Journal of Biological Chemistry|September 25, 2007
A multiprotein complex that mediates translational enhancement in DrosophilaMeryl R Nelson, Hua Luo, Heli K Vari, et al.
The Journal of Cell Biology|August 2, 2006
Gawky is a component of cytoplasmic mRNA processing bodies required for early Drosophila developmentMary D Schneider, Nima Najand, Sana Chaker, et al.
Frontiers in Cell and Developmental Biology|August 26, 2021
The Nitric Oxide Donor, <i>S</i>-Nitrosoglutathione, Rescues Peroxisome Number and Activity Defects in <i>PEX1G843D</i> Mild Zellweger Syndrome FibroblastsYidi Liu, Ceileigh M Weaver, Yarina Sen, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Genetics|May 6, 2004
Molecular and functional analysis of scalloped recessive lethal alleles in Drosophila melanogasterAjay Srivastava, Andrew J Simmonds, Ankush Garg, et al.
Developmental Biology|October 4, 2015
Loss of the Drosophila melanogaster DEAD box protein Ddx1 leads to reduced size and aberrant gametogenesisDevon R Germain, Lei Li, Matthew R Hildebrandt, et al.
Developmental Biology|March 22, 2017
The activity of the Drosophila Vestigial protein is modified by Scalloped-dependent phosphorylationVirginia L Pimmett, Hua Deng, Julie A Haskins, et al.
Traffic (Copenhagen, Denmark)|June 1, 2006
RNA interference effector proteins localize to mobile cytoplasmic puncta in Schizosaccharomyces pombeJon B Carmichael, Cezar Stoica, Henry Parker, et al.
Disease Models & Mechanisms|June 15, 2011
A Drosophila model for the Zellweger spectrum of peroxisome biogenesis disordersFred D Mast, Jing Li, Maninder K Virk, et al.
RNA (New York, N.Y.)|September 22, 2010
Functional characterization of the Drosophila MRP (mitochondrial RNA processing) RNA geneMary D Schneider, Anupinder K Bains, T K Rajendra, et al.
Nature Communications|June 12, 2020
Impaired peroxisomal import in Drosophila oenocytes causes cardiac dysfunction by inducing upd3 as a peroxikineKerui Huang, Ting Miao, Kai Chang, et al.
The Journal of Biological Chemistry|September 25, 2007
A multiprotein complex that mediates translational enhancement in DrosophilaMeryl R Nelson, Hua Luo, Heli K Vari, et al.
The Journal of Cell Biology|August 2, 2006
Gawky is a component of cytoplasmic mRNA processing bodies required for early Drosophila developmentMary D Schneider, Nima Najand, Sana Chaker, et al.
Frontiers in Cell and Developmental Biology|August 26, 2021
The Nitric Oxide Donor, <i>S</i>-Nitrosoglutathione, Rescues Peroxisome Number and Activity Defects in <i>PEX1G843D</i> Mild Zellweger Syndrome FibroblastsYidi Liu, Ceileigh M Weaver, Yarina Sen, et al.
Pageof 4