List of works - William Duddy

<i>Arabidopsis</i> Coexpression Tool: a tool for gene coexpression analysis in <i>Arabidopsis thaliana</i>

scientific article published on 10 July 2021

A Systematic Review of Genotype-Phenotype Correlation across Cohorts Having Causal Mutations of Different Genes in ALS

scientific article published on 29 June 2020

A Systematic Review of Suggested Molecular Strata, Biomarkers and Their Tissue Sources in ALS

scientific article published on 14 May 2019

Activation of Notch Signaling During Ex Vivo Expansion Maintains Donor Muscle Cell Engraftment ⬇️

scientific article published on October 1, 2012

Age-Associated Methylation Suppresses SPRY1, Leading to a Failure of Re-quiescence and Loss of the Reserve Stem Cell Pool in Elderly Muscle

scientific article published on 27 October 2015

Annexin A2 links poor myofiber repair with inflammation and adipogenic replacement of the injured muscle

scientific article published on 21 February 2017

Antisense PMO cocktails effectively skip dystrophin exons 45-55 in myotubes transdifferentiated from DMD patient fibroblasts.

scientific article published on 17 May 2018

Atmospheric oxygen tension slows myoblast proliferation via mitochondrial activation

scientific article

CellWhere: graphical display of interaction networks organized on subcellular localizations

scientific article published on 16 April 2015

Changes in Communication between Muscle Stem Cells and their Environment with Aging.

scientific article published on September 2015

Direct Reprogramming of Human DMD Fibroblasts into Myotubes for In Vitro Evaluation of Antisense-Mediated Exon Skipping and Exons 45-55 Skipping Accompanied by Rescue of Dystrophin Expression.

scientific article published in January 2018

Dystrophin deficiency leads to disturbance of LAMP1-vesicle-associated protein secretion

scientific article published on 24 January 2013

Exon skipping for nonsense mutations in Duchenne muscular dystrophy: too many mutations, too few patients?

scientific article published on June 2012

Exons 45-55 Skipping Using Mutation-Tailored Cocktails of Antisense Morpholinos in the DMD Gene

scientific article published on 26 July 2019

Identification of Novel Antisense-Mediated Exon Skipping Targets in DYSF for Therapeutic Treatment of Dysferlinopathy

scholarly article by Joshua J A Lee et al published 11 October 2018 in Molecular therapy. Nucleic acids

In silico screening based on predictive algorithms as a design tool for exon skipping oligonucleotides in Duchenne muscular dystrophy

scientific article published on 27 March 2015

Mimicry by asx- and ST-turns of the four main types of beta-turn in proteins.

scientific article

Molecular and Cellular Mechanisms Affected in ALS

scientific article published on 25 August 2020

Muscle Gene Sets: a versatile methodological aid to functional genomics in the neuromuscular field

article

Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles

scientific article published on 22 February 2022

Muscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasia.

scientific article published on May 2015

MyoMiner: explore gene co-expression in normal and pathological muscle

scientific article published on 11 May 2020

Personalized Medicine and Molecular Interaction Networks in Amyotrophic Lateral Sclerosis (ALS): Current Knowledge

scientific article published on 13 December 2018

Potential of oligonucleotide-mediated exon-skipping therapy for Duchenne muscular dystrophy.

scientific article

Quantitative Antisense Screening and Optimization for Exon 51 Skipping in Duchenne Muscular Dystrophy.

scientific article published on 28 July 2017

RIPK3-mediated cell death is involved in DUX4-mediated toxicity in facioscapulohumeral dystrophy

scientific article published on 22 October 2021

Recurring main-chain anion-binding motifs in short polypeptides: nests.

scientific article

Skeletal muscle characteristics are preserved in hTERT/cdk4 human myogenic cell lines

scientific article published on 08 December 2016

The isolated muscle fibre as a model of disuse atrophy: characterization using PhAct, a method to quantify f-actin.

scientific article

What Can Machine Learning Approaches in Genomics Tell Us about the Molecular Basis of Amyotrophic Lateral Sclerosis?

scientific article published on 26 November 2020

List of works by William Duddy

<i>Arabidopsis</i> Coexpression Tool: a tool for gene coexpression analysis in <i>Arabidopsis thaliana</i>

A Systematic Review of Genotype-Phenotype Correlation across Cohorts Having Causal Mutations of Different Genes in ALS

A Systematic Review of Suggested Molecular Strata, Biomarkers and Their Tissue Sources in ALS

Activation of Notch Signaling During Ex Vivo Expansion Maintains Donor Muscle Cell Engraftment ⬇️

Age-Associated Methylation Suppresses SPRY1, Leading to a Failure of Re-quiescence and Loss of the Reserve Stem Cell Pool in Elderly Muscle

Annexin A2 links poor myofiber repair with inflammation and adipogenic replacement of the injured muscle

Antisense PMO cocktails effectively skip dystrophin exons 45-55 in myotubes transdifferentiated from DMD patient fibroblasts.

Atmospheric oxygen tension slows myoblast proliferation via mitochondrial activation

CellWhere: graphical display of interaction networks organized on subcellular localizations

Changes in Communication between Muscle Stem Cells and their Environment with Aging.

Direct Reprogramming of Human DMD Fibroblasts into Myotubes for In Vitro Evaluation of Antisense-Mediated Exon Skipping and Exons 45-55 Skipping Accompanied by Rescue of Dystrophin Expression.

Dystrophin deficiency leads to disturbance of LAMP1-vesicle-associated protein secretion

Exon skipping for nonsense mutations in Duchenne muscular dystrophy: too many mutations, too few patients?

Exons 45-55 Skipping Using Mutation-Tailored Cocktails of Antisense Morpholinos in the DMD Gene

Identification of Novel Antisense-Mediated Exon Skipping Targets in DYSF for Therapeutic Treatment of Dysferlinopathy

In silico screening based on predictive algorithms as a design tool for exon skipping oligonucleotides in Duchenne muscular dystrophy

Mimicry by asx- and ST-turns of the four main types of beta-turn in proteins.

Molecular and Cellular Mechanisms Affected in ALS

Muscle Gene Sets: a versatile methodological aid to functional genomics in the neuromuscular field

Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles

Muscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasia.

MyoMiner: explore gene co-expression in normal and pathological muscle

Personalized Medicine and Molecular Interaction Networks in Amyotrophic Lateral Sclerosis (ALS): Current Knowledge

Potential of oligonucleotide-mediated exon-skipping therapy for Duchenne muscular dystrophy.

Quantitative Antisense Screening and Optimization for Exon 51 Skipping in Duchenne Muscular Dystrophy.

RIPK3-mediated cell death is involved in DUX4-mediated toxicity in facioscapulohumeral dystrophy

Recurring main-chain anion-binding motifs in short polypeptides: nests.

Skeletal muscle characteristics are preserved in hTERT/cdk4 human myogenic cell lines

The isolated muscle fibre as a model of disuse atrophy: characterization using PhAct, a method to quantify f-actin.

What Can Machine Learning Approaches in Genomics Tell Us about the Molecular Basis of Amyotrophic Lateral Sclerosis?