Lista de obras - Davide Gabellini - Dominio Público Uruguay

A Human Pluripotent Stem Cell Model of Facioscapulohumeral Muscular Dystrophy-Affected Skeletal Muscles.

artículo científico publicado en 2016

A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy

artículo científico publicado en 2012

A novel L1CAM isoform with angiogenic activity generated by NOVA2-mediated alternative splicing

artículo científico publicado en 2019

A novel molecular mechanism in human genetic disease: a DNA repeat-derived lncRNA.

artículo científico publicado en 2012

A repetitive elements perspective in Polycomb epigenetics

artículo científico publicado en 2012

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

artículo científico publicado en 2011

Alternative splicing and muscular dystrophy.

artículo científico publicado en 2010

Amino acid deprivation triggers a novel GCN2-independent response leading to the transcriptional reactivation of non-native DNA sequences

artículo científico publicado en 2018

Amino acid starvation induces reactivation of silenced transgenes and latent HIV-1 provirus via down-regulation of histone deacetylase 4 (HDAC4)

artículo científico publicado en 2012

DNA methylation analysis of the macrosatellite repeat associated with FSHD muscular dystrophy at single nucleotide level

artículo científico publicado en 2014

Direct interplay between two candidate genes in FSHD muscular dystrophy.

artículo científico publicado en 2014

Diversification of the muscle proteome through alternative splicing

artículo científico publicado en 2018

Early mitotic degradation of the homeoprotein HOXC10 is potentially linked to cell cycle progression

artículo científico publicado en 2003

FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis.

artículo científico publicado en 2013

Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1

artículo científico publicado en 2006

Hmgb3 is regulated by microRNA-206 during muscle regeneration

artículo científico publicado en 2012

In junk we trust: repetitive DNA, epigenetics and facioscapulohumeral muscular dystrophy.

artículo científico publicado en 2010

Inappropriate Gene Activation in FSHD

artículo científico publicado en 2002

Long noncoding RNAs, emerging players in muscle differentiation and disease.

artículo científico publicado en 2014

Molecular basis of facioscapulohumeral muscular dystrophy

artículo científico publicado en 2004

Noncoding RNA Interplay with the Genome

artículo científico publicado en 2016

Overexpression of facioscapulohumeral muscular dystrophy region gene 1 causes primary defects in myogenic stem cells

artículo científico publicado en 2013

Polycomb repressive complex 1 provides a molecular explanation for repeat copy number dependency in FSHD muscular dystrophy.

artículo científico publicado en 2016

Rbfox proteins regulate tissue-specific alternative splicing of Mef2D required for muscle differentiation.

artículo científico publicado en 2015

Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD)

scientific journal article

Report and Abstracts of the 14th Meeting of IIM, the Interuniversity Institute of Myology, - Assisi (Italy), October 12-15, 2017

article

Report on Abstracts of the 15th Meeting of IIM, the Interuniversity Institute of Myology - Assisi (Italy), October 11-14, 2018

article

Streptomyces peucetius daunorubicin biosynthesis gene, dnrF: sequence and heterologous expression

artículo científico publicado en 1995

The Suv420h histone methyltransferases regulate PPAR-γ and energy expenditure in response to environmental stimuli

artículo científico publicado en 2019

The Trithorax protein Ash1L promotes myoblast fusion by activating Cdon expression

artículo científico publicado en 2018

The cell biology of disease: FSHD: copy number variations on the theme of muscular dystrophy ⬇️

artículo científico publicado en 2010

Transcriptional derepression as a cause of genetic diseases

artículo científico publicado en 2003

When enough is enough: genetic diseases associated with transcriptional derepression

artículo científico publicado en 2004

Lista de obras de Davide Gabellini

A Human Pluripotent Stem Cell Model of Facioscapulohumeral Muscular Dystrophy-Affected Skeletal Muscles.

A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy

A novel L1CAM isoform with angiogenic activity generated by NOVA2-mediated alternative splicing

A novel molecular mechanism in human genetic disease: a DNA repeat-derived lncRNA.

A repetitive elements perspective in Polycomb epigenetics

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

Alternative splicing and muscular dystrophy.

Amino acid deprivation triggers a novel GCN2-independent response leading to the transcriptional reactivation of non-native DNA sequences

Amino acid starvation induces reactivation of silenced transgenes and latent HIV-1 provirus via down-regulation of histone deacetylase 4 (HDAC4)

DNA methylation analysis of the macrosatellite repeat associated with FSHD muscular dystrophy at single nucleotide level

Direct interplay between two candidate genes in FSHD muscular dystrophy.

Diversification of the muscle proteome through alternative splicing

Early mitotic degradation of the homeoprotein HOXC10 is potentially linked to cell cycle progression

FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis.

Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1

Hmgb3 is regulated by microRNA-206 during muscle regeneration

In junk we trust: repetitive DNA, epigenetics and facioscapulohumeral muscular dystrophy.

Inappropriate Gene Activation in FSHD

Long noncoding RNAs, emerging players in muscle differentiation and disease.

Molecular basis of facioscapulohumeral muscular dystrophy

Noncoding RNA Interplay with the Genome

Overexpression of facioscapulohumeral muscular dystrophy region gene 1 causes primary defects in myogenic stem cells

Polycomb repressive complex 1 provides a molecular explanation for repeat copy number dependency in FSHD muscular dystrophy.

Rbfox proteins regulate tissue-specific alternative splicing of Mef2D required for muscle differentiation.

Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD)

Report and Abstracts of the 14th Meeting of IIM, the Interuniversity Institute of Myology, - Assisi (Italy), October 12-15, 2017

Report on Abstracts of the 15th Meeting of IIM, the Interuniversity Institute of Myology - Assisi (Italy), October 11-14, 2018

Streptomyces peucetius daunorubicin biosynthesis gene, dnrF: sequence and heterologous expression

The Suv420h histone methyltransferases regulate PPAR-γ and energy expenditure in response to environmental stimuli

The Trithorax protein Ash1L promotes myoblast fusion by activating Cdon expression

The cell biology of disease: FSHD: copy number variations on the theme of muscular dystrophy ⬇️

Transcriptional derepression as a cause of genetic diseases

When enough is enough: genetic diseases associated with transcriptional derepression