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Daniela C Zarnescu

Showing results (21-30 of 46) with videos related to

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Circulation Research|June 11, 2011
Desmoplakin and talin2 are novel mRNA targets of fragile X-related protein-1 in cardiac muscleSamantha A Whitman, Cathleen Cover, Lily Yu, et al.
Metabolites|February 25, 2022
TDP-43 Proteinopathy Causes Broad Metabolic Alterations including TCA Cycle Intermediates and Dopamine Levels in Drosophila Models of ALSSuvithanandhini Loganathan, Bryce A Wilson, Sara B Carey, et al.
Nature Chemical Biology|March 11, 2008
Identification of small molecules rescuing fragile X syndrome phenotypes in DrosophilaShuang Chang, Steven M Bray, Zigang Li, et al.
Human Molecular Genetics|November 30, 2014
PPAR gamma activation is neuroprotective in a Drosophila model of ALS based on TDP-43Archi Joardar, Judith Menzl, Taylor C Podolsky, et al.
Nature Communications|December 14, 2017
Endocytosis regulates TDP-43 toxicity and turnoverGuangbo Liu, Alyssa N Coyne, Fen Pei, et al.
Frontiers in Molecular Neuroscience|June 16, 2018
Medium-Chain Fatty Acids, Beta-Hydroxybutyric Acid and Genetic Modulation of the Carnitine Shuttle Are Protective in a <i>Drosophila</i> Model of ALS Based on TDP-43Ernesto Manzo, Abigail G O'Conner, Jordan M Barrows, et al.
Neuron|September 2, 2003
RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in DrosophilaPeng Jin, Daniela C Zarnescu, Fuping Zhang, et al.
Disease Models & Mechanisms|March 9, 2013
Motor neurons and glia exhibit specific individualized responses to TDP-43 expression in a Drosophila model of amyotrophic lateral sclerosisPatricia S Estes, Scott G Daniel, Abigail P McCallum, et al.
Nature Neuroscience|January 3, 2004
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathwayPeng Jin, Daniela C Zarnescu, Stephanie Ceman, et al.
Human Molecular Genetics|July 2, 2015
PABPN1 suppresses TDP-43 toxicity in ALS disease modelsChing-Chieh Chou, Olga M Alexeeva, Shizuka Yamada, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
Circulation Research|June 11, 2011
Desmoplakin and talin2 are novel mRNA targets of fragile X-related protein-1 in cardiac muscleSamantha A Whitman, Cathleen Cover, Lily Yu, et al.
Metabolites|February 25, 2022
TDP-43 Proteinopathy Causes Broad Metabolic Alterations including TCA Cycle Intermediates and Dopamine Levels in Drosophila Models of ALSSuvithanandhini Loganathan, Bryce A Wilson, Sara B Carey, et al.
Nature Chemical Biology|March 11, 2008
Identification of small molecules rescuing fragile X syndrome phenotypes in DrosophilaShuang Chang, Steven M Bray, Zigang Li, et al.
Human Molecular Genetics|November 30, 2014
PPAR gamma activation is neuroprotective in a Drosophila model of ALS based on TDP-43Archi Joardar, Judith Menzl, Taylor C Podolsky, et al.
Nature Communications|December 14, 2017
Endocytosis regulates TDP-43 toxicity and turnoverGuangbo Liu, Alyssa N Coyne, Fen Pei, et al.
Frontiers in Molecular Neuroscience|June 16, 2018
Medium-Chain Fatty Acids, Beta-Hydroxybutyric Acid and Genetic Modulation of the Carnitine Shuttle Are Protective in a <i>Drosophila</i> Model of ALS Based on TDP-43Ernesto Manzo, Abigail G O'Conner, Jordan M Barrows, et al.
Neuron|September 2, 2003
RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in DrosophilaPeng Jin, Daniela C Zarnescu, Fuping Zhang, et al.
Disease Models & Mechanisms|March 9, 2013
Motor neurons and glia exhibit specific individualized responses to TDP-43 expression in a Drosophila model of amyotrophic lateral sclerosisPatricia S Estes, Scott G Daniel, Abigail P McCallum, et al.
Nature Neuroscience|January 3, 2004
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathwayPeng Jin, Daniela C Zarnescu, Stephanie Ceman, et al.
Human Molecular Genetics|July 2, 2015
PABPN1 suppresses TDP-43 toxicity in ALS disease modelsChing-Chieh Chou, Olga M Alexeeva, Shizuka Yamada, et al.
Pageof 5