Lista de obras - William Duddy - Dominio Público Uruguay

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

artículo científico publicado en 2021

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

artículo científico publicado en 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 ⬇️

artículo científico publicado el 1 de octubre de 2012

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

artículo científico publicado en 2015

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

artículo científico publicado en 2017

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

artículo científico publicado en 2018

Atmospheric oxygen tension slows myoblast proliferation via mitochondrial activation

artículo científico publicado en 2012

CellWhere: graphical display of interaction networks organized on subcellular localizations

artículo científico publicado en 2015

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

artículo científico publicado en 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.

artículo científico publicado en 2018

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

artículo científico publicado en 2013

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

artículo científico publicado en 2012

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

artículo científico publicado en 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

artículo científico publicado en 2015

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

artículo científico publicado en 2004

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

artículo científico publicado en 2022

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

artículo científico publicado en 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.

artículo científico publicado en 2007

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

artículo científico publicado en 2017

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

artículo científico publicado en 2021

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

artículo científico publicado en 2004

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

artículo científico publicado en 2016

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

artículo científico publicado en 2011

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

scientific article published on 26 November 2020

Lista de obras de 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?