Lista de obras - Yvan Torrente - Dominio Público Uruguay

24 month longitudinal data in ambulant boys with Duchenne muscular dystrophy

artículo científico publicado en 2013

AAV6-mediated systemic shRNA delivery reverses disease in a mouse model of facioscapulohumeral muscular dystrophy

artículo científico publicado en 2011

Absence of T and B lymphocytes modulates dystrophic features in dysferlin deficient animal model.

artículo científico publicado en 2012

Alpha sarcoglycan is required for FGF-dependent myogenic progenitor cell proliferation in vitro and in vivo

artículo científico publicado en 2011

Beta-enolase deficiency, a new metabolic myopathy of distal glycolysis

artículo científico publicado en 2001

Blockade of IGF2R improves muscle regeneration and ameliorates Duchenne muscular dystrophy

scientific article published on 02 December 2019

CD133(+) cells isolated from various sources and their role in future clinical perspectives

artículo científico publicado en 2010

CD20-related signaling pathway is differently activated in normal and dystrophic circulating CD133+ stem cells

artículo científico publicado en 2009

Cell Therapy of -Sarcoglycan Null Dystrophic Mice Through Intra-Arterial Delivery of Mesoangioblasts

artículo científico publicado en 2003

Cell based therapy for Duchenne muscular dystrophy

artículo científico publicado en 2009

Combining stem cells and exon skipping strategy to treat muscular dystrophy

artículo científico publicado en 2008

Complete repair of dystrophic skeletal muscle by mesoangioblasts with enhanced migration ability

artículo científico publicado en 2006

Correction 174, p. 231

Correlation of circulating CD133+ progenitor subclasses with a mild phenotype in Duchenne muscular dystrophy patients

artículo científico publicado en 2008

Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs.

artículo científico publicado en 2013

Effect of human skin-derived stem cells on vessel architecture, tumor growth, and tumor invasion in brain tumor animal models

artículo científico publicado en 2007

Effective high-throughput isolation of enriched platelets and circulating pro-angiogenic cells to accelerate skin-wound healing

artículo científico publicado en 2022

Effects of rituximab in two patients with dysferlin-deficient muscular dystrophy

artículo científico publicado en 2010

Ex vivo expansion of human circulating myogenic progenitors on cluster-assembled nanostructured TiO2.

artículo científico publicado en 2010

Expression of CD20 reveals a new store-operated calcium entry modulator in skeletal muscle

artículo científico publicado en 2012

Expression of parathyroid-specific genes in vascular endothelial progenitors of normal and tumoral parathyroid glands

artículo científico publicado en 2009

Full-length dysferlin expression driven by engineered human dystrophic blood derived CD133+ stem cells

artículo científico publicado en 2013

Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study.

artículo científico publicado en 2011

Galectin-1 induces skeletal muscle differentiation in human fetal mesenchymal stem cells and increases muscle regeneration

artículo científico publicado en 2006

Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up

artículo científico publicado en 2011

High-efficiency gene transfer into adult fish: A new tool to study fin regeneration

article

High-resolution X-ray microtomography for three-dimensional visualization of human stem cell muscle homing.

artículo científico publicado en 2006

Hmgb3 is regulated by microRNA-206 during muscle regeneration

artículo científico publicado en 2012

Human circulating AC133+ stem cells restore dystrophin expression and ameliorate function in dystrophic skeletal muscle

Human skin-derived stem cells migrate throughout forebrain and differentiate into astrocytes after injection into adult mouse brain

scientific article published on 01 August 2004

Identification of a putative pathway for the muscle homing of stem cells in a muscular dystrophy model

artículo científico publicado en 2003

Identification of different genomic deletions and one duplication in the dysferlin gene using multiplex ligation-dependent probe amplification and genomic quantitative PCR.

artículo científico publicado en 2009

Immortalized Skin Fibroblasts Expressing Conditional MyoD as a Renewable and Reliable Source of Converted Human Muscle Cells to Assess Therapeutic Strategies for Muscular Dystrophies: Validation of an Exon-Skipping Approach to Restore Dystrophin in D

scholarly article by Soraya Chaouch published in July 2009

Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy

artículo científico publicado en 2012

In vivo biolistic technique in control and mdx dystrophic mice

artículo científico publicado en 1996

In vivo migration of transplanted myoblasts requires matrix metalloproteinase activity.

artículo científico publicado en 2000

In vivo myogenic potential of human CD133+ muscle-derived stem cells: a quantitative study

artículo científico publicado en 2009

In vivo tracking of stem cell by nanotechnologies: future prospects for mouse to human translation

artículo científico publicado en 2010

Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation

artículo científico publicado en 2007

Intraarterial injection of muscle-derived CD34(+)Sca-1(+) stem cells restores dystrophin in mdx mice.

artículo científico publicado en 2001

Intracellular Delivery of a Tat-eGFP Fusion Protein into Muscle Cells

artículo científico publicado en 2001

Magic-factor 1, a partial agonist of Met, induces muscle hypertrophy by protecting myogenic progenitors from apoptosis

artículo científico publicado en 2008

Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs

artículo científico publicado en 2006

Novel insight into stem cell trafficking in dystrophic muscles.

artículo científico publicado en 2012

Organization of extracellular matrix fibers within polyglycolic acid-polylactic acid scaffolds analyzed using X-ray synchrotron-radiation phase-contrast micro computed tomography

artículo científico publicado en 2009

Partial dysferlin reconstitution by adult murine mesoangioblasts is sufficient for full functional recovery in a murine model of dysferlinopathy.

artículo científico publicado en 2010

Pericytes of human skeletal muscle are myogenic precursors distinct from satellite cells

artículo científico publicado en 2007

Perspectives of stem cell therapy in Duchenne muscular dystrophy

artículo científico publicado en 2013

Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measures

artículo científico publicado en 2012

Restoration of human dystrophin following transplantation of exon-skipping-engineered DMD patient stem cells into dystrophic mice

artículo científico publicado en 2007

Skin-derived stem cells transplanted into resorbable guides provide functional nerve regeneration after sciatic nerve resection.

artículo científico publicado en 2007

Stem and progenitor cells in skeletal muscle development, maintenance, and therapy

artículo científico publicado en 2007

Stem cell therapies to treat muscular dystrophy: progress to date

artículo científico publicado en 2010

Stem cell tracking by nanotechnologies

artículo científico publicado en 2010

Stem cell-mediated transfer of a human artificial chromosome ameliorates muscular dystrophy.

artículo científico publicado en 2011

The new challenge of stem cell: brain tumour therapy.

artículo científico publicado en 2008

The role of interleukin-6 (IL-6) in the proliferation and differentiation of human neural stem cells

The role of stem cells in muscular dystrophies

artículo científico

The urokinase plasminogen activator: an interesting way to improve myoblast migration following their transplantation.

artículo científico publicado en 2002

Transplantation of genetically corrected human iPSC-derived progenitors in mice with limb-girdle muscular dystrophy.

artículo científico publicado en 2012

VCAM-1 expression on dystrophic muscle vessels has a critical role in the recruitment of human blood-derived CD133+ stem cells after intra-arterial transplantation

artículo científico publicado en 2006

Lista de obras de Yvan Torrente

24 month longitudinal data in ambulant boys with Duchenne muscular dystrophy

AAV6-mediated systemic shRNA delivery reverses disease in a mouse model of facioscapulohumeral muscular dystrophy

Absence of T and B lymphocytes modulates dystrophic features in dysferlin deficient animal model.

Alpha sarcoglycan is required for FGF-dependent myogenic progenitor cell proliferation in vitro and in vivo

Beta-enolase deficiency, a new metabolic myopathy of distal glycolysis

Blockade of IGF2R improves muscle regeneration and ameliorates Duchenne muscular dystrophy

CD133(+) cells isolated from various sources and their role in future clinical perspectives

CD20-related signaling pathway is differently activated in normal and dystrophic circulating CD133+ stem cells

Cell Therapy of -Sarcoglycan Null Dystrophic Mice Through Intra-Arterial Delivery of Mesoangioblasts

Cell based therapy for Duchenne muscular dystrophy

Combining stem cells and exon skipping strategy to treat muscular dystrophy

Complete repair of dystrophic skeletal muscle by mesoangioblasts with enhanced migration ability

Correction 174, p. 231

Correction 174, p. 231

Correlation of circulating CD133+ progenitor subclasses with a mild phenotype in Duchenne muscular dystrophy patients

Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs.

Effect of human skin-derived stem cells on vessel architecture, tumor growth, and tumor invasion in brain tumor animal models

Effective high-throughput isolation of enriched platelets and circulating pro-angiogenic cells to accelerate skin-wound healing

Effects of rituximab in two patients with dysferlin-deficient muscular dystrophy

Ex vivo expansion of human circulating myogenic progenitors on cluster-assembled nanostructured TiO2.

Expression of CD20 reveals a new store-operated calcium entry modulator in skeletal muscle

Expression of parathyroid-specific genes in vascular endothelial progenitors of normal and tumoral parathyroid glands

Full-length dysferlin expression driven by engineered human dystrophic blood derived CD133+ stem cells

Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study.

Galectin-1 induces skeletal muscle differentiation in human fetal mesenchymal stem cells and increases muscle regeneration

Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up

High-efficiency gene transfer into adult fish: A new tool to study fin regeneration

High-resolution X-ray microtomography for three-dimensional visualization of human stem cell muscle homing.

Hmgb3 is regulated by microRNA-206 during muscle regeneration

Human circulating AC133+ stem cells restore dystrophin expression and ameliorate function in dystrophic skeletal muscle

Human skin-derived stem cells migrate throughout forebrain and differentiate into astrocytes after injection into adult mouse brain

Identification of a putative pathway for the muscle homing of stem cells in a muscular dystrophy model

Identification of different genomic deletions and one duplication in the dysferlin gene using multiplex ligation-dependent probe amplification and genomic quantitative PCR.

Immortalized Skin Fibroblasts Expressing Conditional MyoD as a Renewable and Reliable Source of Converted Human Muscle Cells to Assess Therapeutic Strategies for Muscular Dystrophies: Validation of an Exon-Skipping Approach to Restore Dystrophin in D

Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy

In vivo biolistic technique in control and mdx dystrophic mice

In vivo migration of transplanted myoblasts requires matrix metalloproteinase activity.

In vivo myogenic potential of human CD133+ muscle-derived stem cells: a quantitative study

In vivo tracking of stem cell by nanotechnologies: future prospects for mouse to human translation

Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation

Intraarterial injection of muscle-derived CD34(+)Sca-1(+) stem cells restores dystrophin in mdx mice.

Intracellular Delivery of a Tat-eGFP Fusion Protein into Muscle Cells

Magic-factor 1, a partial agonist of Met, induces muscle hypertrophy by protecting myogenic progenitors from apoptosis

Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs

Novel insight into stem cell trafficking in dystrophic muscles.

Organization of extracellular matrix fibers within polyglycolic acid-polylactic acid scaffolds analyzed using X-ray synchrotron-radiation phase-contrast micro computed tomography

Partial dysferlin reconstitution by adult murine mesoangioblasts is sufficient for full functional recovery in a murine model of dysferlinopathy.

Pericytes of human skeletal muscle are myogenic precursors distinct from satellite cells

Perspectives of stem cell therapy in Duchenne muscular dystrophy

Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measures

Restoration of human dystrophin following transplantation of exon-skipping-engineered DMD patient stem cells into dystrophic mice

Skin-derived stem cells transplanted into resorbable guides provide functional nerve regeneration after sciatic nerve resection.

Stem and progenitor cells in skeletal muscle development, maintenance, and therapy

Stem cell therapies to treat muscular dystrophy: progress to date

Stem cell tracking by nanotechnologies

Stem cell-mediated transfer of a human artificial chromosome ameliorates muscular dystrophy.

The new challenge of stem cell: brain tumour therapy.

The role of interleukin-6 (IL-6) in the proliferation and differentiation of human neural stem cells

The role of stem cells in muscular dystrophies

The urokinase plasminogen activator: an interesting way to improve myoblast migration following their transplantation.

Transplantation of genetically corrected human iPSC-derived progenitors in mice with limb-girdle muscular dystrophy.

VCAM-1 expression on dystrophic muscle vessels has a critical role in the recruitment of human blood-derived CD133+ stem cells after intra-arterial transplantation