Lista de obras - Boris Rogelj - Dominio Público Uruguay

A feedback loop between dipeptide-repeat protein, TDP-43 and karyopherin-α mediates C9orf72-related neurodegeneration

artículo científico publicado en 2018

ALS mutant FUS disrupts nuclear localization and sequesters wild-type FUS within cytoplasmic stress granules

artículo científico publicado en 2013

Allele-specific knockdown of ALS-associated mutant TDP-43 in neural stem cells derived from induced pluripotent stem cells

artículo científico publicado en 2014

An MND/ALS phenotype associated with C9orf72 repeat expansion: abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline.

artículo científico publicado en 2011

Analysis of alternative splicing associated with aging and neurodegeneration in the human brain.

artículo científico publicado en 2011

Astrocytes with TDP-43 inclusions exhibit reduced noradrenergic cAMP and Ca2+ signaling and dysregulated cell metabolism

artículo científico publicado en 2020

Biology and applications of small nucleolar RNAs.

artículo científico publicado en 2011

Brain-specific small nucleolar RNAs.

artículo científico publicado en 2006

C9orf72 poly GA RAN-translated protein plays a key role in amyotrophic lateral sclerosis via aggregation and toxicity

artículo científico publicado en 2017

C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts

scientific article published on 17 September 2020

Characterization of DNA G-quadruplex species forming from C9ORF72 G4C2-expanded repeats associated with amyotrophic lateral sclerosis and frontotemporal lobar degeneration

artículo científico publicado en 2014

Characterizing the RNA targets and position-dependent splicing regulation by TDP-43.

artículo científico publicado en 2011

Clitocypin, a new type of cysteine proteinase inhibitor from fruit bodies of mushroom clitocybe nebularis.

artículo científico publicado en 2000

Cold atmospheric plasma induces stress granule formation via an eIF2α-dependent pathway

scientific article published on 15 September 2020

Cross-Regulation between TDP-43 and Paraspeckles Promotes Pluripotency-Differentiation Transition.

artículo científico publicado en 2019

Differential Expression of Several miRNAs and the Host Genes AATK and DNM2 in Leukocytes of Sporadic ALS Patients.

artículo científico publicado en 2018

Differential expression of microRNAs and other small RNAs in muscle tissue of patients with ALS and healthy age-matched controls.

artículo científico publicado en 2018

Differential roles of the ubiquitin proteasome system and autophagy in the clearance of soluble and aggregated TDP-43 species

artículo científico publicado en 2014

Equistatin, a protease inhibitor from the sea anemone actinia equina, is composed of three structural and functional domains

artículo científico publicado en 2000

Evasin-displaying lactic acid bacteria bind different chemokines and neutralize CXCL8 production in Caco-2 cells

artículo científico publicado en 2017

Exon Specific U1 snRNAs improve ELP1 exon 20 definition and rescue ELP1 protein expression in a Familial Dysautonomia mouse model.

artículo científico publicado en 2018

Expression changes in human skeletal muscle miRNAs following 10 days of bed rest in young healthy males.

artículo científico publicado en 2014

Expression of sea anemone equistatin in potato. Effects of plant proteases on heterologous protein production.

artículo científico publicado en 2003

Expression, purification, and characterization of equistatin in Pichia pastoris

artículo científico publicado en 2000

Functional diversity of small nucleolar RNAs

scientific article published on 01 February 2020

Genetic analysis of amyotrophic lateral sclerosis in the Slovenian population

artículo científico publicado en 2014

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

artículo científico publicado en 2016

Heterogeneous Nuclear Ribonucleoprotein E2 (hnRNP E2) Is a Component of TDP-43 Aggregates Specifically in the A and C Pathological Subtypes of Frontotemporal Lobar Degeneration

scientific article published on 04 June 2019

Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxic

artículo científico publicado en 2013

Interactome screening of C9orf72 dipeptide repeats reveals VCP sequestration and functional impairment by polyGA

artículo científico publicado en 2022

MicroRNA in skeletal muscle development, growth, atrophy, and disease

artículo científico

Modelling FUS Mislocalisation in an In Vitro Model of Innervated Human Muscle.

artículo científico

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

artículo científico publicado en 2009

Neuronal differentiation induces SNORD115 expression and is accompanied by post-transcriptional changes of serotonin receptor 2c mRNA.

artículo científico publicado en 2018

Nuclear RNA foci from C9ORF72 expansion mutation form paraspeckle-like bodies

artículo científico publicado en 2019

Nuclear trafficking in amyotrophic lateral sclerosis and frontotemporal lobar degeneration.

artículo científico publicado en 2016

Optineurin in amyotrophic lateral sclerosis: Multifunctional adaptor protein at the crossroads of different neuroprotective mechanisms

artículo científico publicado en 2017

Optineurin inclusions occur in a minority of TDP-43 positive ALS and FTLD-TDP cases and are rarely observed in other neurodegenerative disorders

artículo científico publicado en 2011

Proteomic analyses reveal that loss of TDP-43 affects RNA processing and intracellular transport

scientific journal article

TDP-43 aggregation mirrors TDP-43 knockdown, affecting the expression levels of a common set of proteins

artículo científico publicado en 2016

The Effect of Different Types of Nanoparticles on FUS and TDP-43 Solubility and Subcellular Localization.

artículo científico publicado en 2017

The Neuronal Adaptor Protein X11β Reduces Amyloid β-Protein Levels and Amyloid Plaque Formation in the Brains of Transgenic Mice

scientific article published on 03 September 2004

The X11 proteins, Abeta production and Alzheimer's disease.

artículo científico publicado en 2006

The X11/Mint family of adaptor proteins.

artículo científico publicado en 2006

The many faces of small nucleolar RNAs.

artículo científico

Transportin 1 colocalization with Fused in Sarcoma (FUS) inclusions is not characteristic for amyotrophic lateral sclerosis-FUS confirming disrupted nuclear import of mutant FUS and distinguishing it from frontotemporal lobar degeneration with FUS i

artículo científico publicado en 2013

Unconventional features of C9ORF72 expanded repeat in amyotrophic lateral sclerosis and frontotemporal lobar degeneration

artículo científico

p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS

scientific article published on 19 November 2011

Lista de obras de Boris Rogelj

A feedback loop between dipeptide-repeat protein, TDP-43 and karyopherin-α mediates C9orf72-related neurodegeneration

ALS mutant FUS disrupts nuclear localization and sequesters wild-type FUS within cytoplasmic stress granules

Allele-specific knockdown of ALS-associated mutant TDP-43 in neural stem cells derived from induced pluripotent stem cells

An MND/ALS phenotype associated with C9orf72 repeat expansion: abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline.

Analysis of alternative splicing associated with aging and neurodegeneration in the human brain.

Astrocytes with TDP-43 inclusions exhibit reduced noradrenergic cAMP and Ca2+ signaling and dysregulated cell metabolism

Biology and applications of small nucleolar RNAs.

Brain-specific small nucleolar RNAs.

C9orf72 poly GA RAN-translated protein plays a key role in amyotrophic lateral sclerosis via aggregation and toxicity

C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts

Characterization of DNA G-quadruplex species forming from C9ORF72 G4C2-expanded repeats associated with amyotrophic lateral sclerosis and frontotemporal lobar degeneration

Characterizing the RNA targets and position-dependent splicing regulation by TDP-43.

Clitocypin, a new type of cysteine proteinase inhibitor from fruit bodies of mushroom clitocybe nebularis.

Cold atmospheric plasma induces stress granule formation via an eIF2α-dependent pathway

Cross-Regulation between TDP-43 and Paraspeckles Promotes Pluripotency-Differentiation Transition.

Differential Expression of Several miRNAs and the Host Genes AATK and DNM2 in Leukocytes of Sporadic ALS Patients.

Differential expression of microRNAs and other small RNAs in muscle tissue of patients with ALS and healthy age-matched controls.

Differential roles of the ubiquitin proteasome system and autophagy in the clearance of soluble and aggregated TDP-43 species

Equistatin, a protease inhibitor from the sea anemone actinia equina, is composed of three structural and functional domains

Evasin-displaying lactic acid bacteria bind different chemokines and neutralize CXCL8 production in Caco-2 cells

Exon Specific U1 snRNAs improve ELP1 exon 20 definition and rescue ELP1 protein expression in a Familial Dysautonomia mouse model.

Expression changes in human skeletal muscle miRNAs following 10 days of bed rest in young healthy males.

Expression of sea anemone equistatin in potato. Effects of plant proteases on heterologous protein production.

Expression, purification, and characterization of equistatin in Pichia pastoris

Functional diversity of small nucleolar RNAs

Genetic analysis of amyotrophic lateral sclerosis in the Slovenian population

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

Heterogeneous Nuclear Ribonucleoprotein E2 (hnRNP E2) Is a Component of TDP-43 Aggregates Specifically in the A and C Pathological Subtypes of Frontotemporal Lobar Degeneration

Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxic

Interactome screening of C9orf72 dipeptide repeats reveals VCP sequestration and functional impairment by polyGA

MicroRNA in skeletal muscle development, growth, atrophy, and disease

Modelling FUS Mislocalisation in an In Vitro Model of Innervated Human Muscle.

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

Neuronal differentiation induces SNORD115 expression and is accompanied by post-transcriptional changes of serotonin receptor 2c mRNA.

Nuclear RNA foci from C9ORF72 expansion mutation form paraspeckle-like bodies

Nuclear trafficking in amyotrophic lateral sclerosis and frontotemporal lobar degeneration.

Optineurin in amyotrophic lateral sclerosis: Multifunctional adaptor protein at the crossroads of different neuroprotective mechanisms

Optineurin inclusions occur in a minority of TDP-43 positive ALS and FTLD-TDP cases and are rarely observed in other neurodegenerative disorders

Proteomic analyses reveal that loss of TDP-43 affects RNA processing and intracellular transport

TDP-43 aggregation mirrors TDP-43 knockdown, affecting the expression levels of a common set of proteins

The Effect of Different Types of Nanoparticles on FUS and TDP-43 Solubility and Subcellular Localization.

The Neuronal Adaptor Protein X11β Reduces Amyloid β-Protein Levels and Amyloid Plaque Formation in the Brains of Transgenic Mice

The X11 proteins, Abeta production and Alzheimer's disease.

The X11/Mint family of adaptor proteins.

The many faces of small nucleolar RNAs.

Transportin 1 colocalization with Fused in Sarcoma (FUS) inclusions is not characteristic for amyotrophic lateral sclerosis-FUS confirming disrupted nuclear import of mutant FUS and distinguishing it from frontotemporal lobar degeneration with FUS i

Unconventional features of C9ORF72 expanded repeat in amyotrophic lateral sclerosis and frontotemporal lobar degeneration

p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS