Lista de obras - Sven Thoms - Dominio Público Uruguay

Cdc48 can distinguish between native and non-native proteins in the absence of cofactors.

artículo científico publicado en 2002

Characterization of two common 5' polymorphisms in PEX1 and correlation to survival in PEX1 peroxisome biogenesis disorder patients ⬇️

artículo científico publicado el 16 de agosto de 2011

Conserved targeting information in mammalian and fungal peroxisomal tail-anchored proteins

artículo científico publicado en 2015

Dual Reporter Systems for the Analysis of Translational Readthrough in Mammals.

artículo científico publicado en 2017

Dysferlin mediates membrane tubulation and links T-tubule biogenesis to muscular dystrophy.

artículo científico publicado en 2017

Farnesylation of pex19p is required for its structural integrity and function in peroxisome biogenesis

artículo científico publicado en 2009

First PEX11β patient extends spectrum of peroxisomal biogenesis disorder phenotypes.

artículo científico publicado en 2012

Functional Translational Readthrough: A Systems Biology Perspective

artículo científico publicado en 2016

Functions of Vertebrate Ferlins

scientific article published on 25 February 2020

Identification of New Fungal Peroxisomal Matrix Proteins and Revision of the PTS1 Consensus

artículo científico publicado en 2016

Import of proteins into peroxisomes: piggybacking to a new home away from home

artículo científico publicado en 2015

Involvement of the Saccharomyces cerevisiae Hydrolase Ldh1p in Lipid Homeostasis ⬇️

artículo científico publicado el 8 de abril de 2011

Lpx1p is a peroxisomal lipase required for normal peroxisome morphology.

artículo científico publicado en 2008

Overexpression of peroxisomal testis-specific 1 protein induces germ cell apoptosis and leads to infertility in male mice

scientific journal article

Peroxisomal lactate dehydrogenase is generated by translational readthrough in mammals

artículo científico publicado en 2014

Peroxisomal matrix protein receptor ubiquitination and recycling.

artículo científico publicado en 2006

Peroxisome formation requires the endoplasmic reticulum channel protein Sec61

scientific article published on 17 January 2012

Pex19p contributes to peroxisome inheritance in the association of peroxisomes to Myo2p

artículo científico publicado en 2012

Pex35 is a regulator of peroxisome abundance

artículo científico publicado en 2017

RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection.

artículo científico publicado en 2009

Role of the ubiquitin-selective CDC48(UFD1/NPL4 )chaperone (segregase) in ERAD of OLE1 and other substrates

artículo científico publicado en 2002

Secretion of soluble VEGF receptor 2 by microvascular endothelial cells derived by human benign prostatic hyperplasia.

artículo científico publicado en 2009

Stop Codon Context-Specific Induction of Translational Readthrough

artículo científico publicado en 2021

Super-resolution imaging reveals the sub-diffraction phenotype of Zellweger Syndrome ghosts and wild-type peroxisomes.

artículo científico publicado en 2018

Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorder

artículo científico publicado en 2017

The Putative Saccharomyces cerevisiae Hydrolase Ldh1p Is Localized to Lipid Droplets ⬇️

artículo científico publicado el 8 de abril de 2011

The Use of Glycosylation Tags as Reporters for Protein Entry into the Endoplasmic Reticulum in Yeast and Mammalian Cells.

artículo científico publicado en 2017

The functional readthrough extension of malate dehydrogenase reveals a modification of the genetic code.

artículo científico publicado en 2016

The unusual extended C-terminal helix of the peroxisomal α/β-hydrolase Lpx1 is involved in dimer contacts but dispensable for dimerization ⬇️

artículo científico publicado el 29 de junio de 2011

Ubp15p, a ubiquitin hydrolase associated with the peroxisomal export machinery

artículo científico publicado en 2011

Lista de obras de Sven Thoms

Cdc48 can distinguish between native and non-native proteins in the absence of cofactors.

Characterization of two common 5' polymorphisms in PEX1 and correlation to survival in PEX1 peroxisome biogenesis disorder patients ⬇️

Conserved targeting information in mammalian and fungal peroxisomal tail-anchored proteins

Dual Reporter Systems for the Analysis of Translational Readthrough in Mammals.

Dysferlin mediates membrane tubulation and links T-tubule biogenesis to muscular dystrophy.

Farnesylation of pex19p is required for its structural integrity and function in peroxisome biogenesis

First PEX11β patient extends spectrum of peroxisomal biogenesis disorder phenotypes.

Functional Translational Readthrough: A Systems Biology Perspective

Functions of Vertebrate Ferlins

Identification of New Fungal Peroxisomal Matrix Proteins and Revision of the PTS1 Consensus

Import of proteins into peroxisomes: piggybacking to a new home away from home

Involvement of the Saccharomyces cerevisiae Hydrolase Ldh1p in Lipid Homeostasis ⬇️

Lpx1p is a peroxisomal lipase required for normal peroxisome morphology.

Overexpression of peroxisomal testis-specific 1 protein induces germ cell apoptosis and leads to infertility in male mice

Peroxisomal lactate dehydrogenase is generated by translational readthrough in mammals

Peroxisomal matrix protein receptor ubiquitination and recycling.

Peroxisome formation requires the endoplasmic reticulum channel protein Sec61

Pex19p contributes to peroxisome inheritance in the association of peroxisomes to Myo2p

Pex35 is a regulator of peroxisome abundance

RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection.

Role of the ubiquitin-selective CDC48(UFD1/NPL4 )chaperone (segregase) in ERAD of OLE1 and other substrates

Secretion of soluble VEGF receptor 2 by microvascular endothelial cells derived by human benign prostatic hyperplasia.

Stop Codon Context-Specific Induction of Translational Readthrough

Super-resolution imaging reveals the sub-diffraction phenotype of Zellweger Syndrome ghosts and wild-type peroxisomes.

Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorder

The Putative Saccharomyces cerevisiae Hydrolase Ldh1p Is Localized to Lipid Droplets ⬇️

The Use of Glycosylation Tags as Reporters for Protein Entry into the Endoplasmic Reticulum in Yeast and Mammalian Cells.

The functional readthrough extension of malate dehydrogenase reveals a modification of the genetic code.

The unusual extended C-terminal helix of the peroxisomal α/β-hydrolase Lpx1 is involved in dimer contacts but dispensable for dimerization ⬇️

Ubp15p, a ubiquitin hydrolase associated with the peroxisomal export machinery