Lista de obras - Emmanuel A Asante - Dominio Público Uruguay

A naturally occurring variant of the human prion protein completely prevents prion disease.

artículo científico publicado en 2015

Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins

artículo científico publicado en 2009

Atypical scrapie prions from sheep and lack of disease in transgenic mice overexpressing human prion protein.

artículo científico publicado en 2013

BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein

artículo científico publicado en 2002

Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein

artículo científico publicado en 2010

Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous mice

artículo científico publicado en 2006

Effect of fixation on brain and lymphoreticular vCJD prions and bioassay of key positive specimens from a retrospective vCJD prevalence study

scientific article published on 10 December 2010

Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy ⬇️

artículo científico publicado el 1 de agosto de 1995

Frontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathology

artículo científico publicado en 2015

Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein.

artículo científico publicado en 2013

Interaction between prion protein and toxic amyloid β assemblies can be therapeutically targeted at multiple sites

artículo científico publicado en 2011

Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice

artículo científico publicado en 2008

Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice

artículo científico publicado en 2012

Pathogenic human prion protein rescues PrP null phenotype in transgenic mice.

artículo científico publicado en 2004

Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein.

artículo científico publicado en 2006

Prion infectivity in variant Creutzfeldt-Jakob disease rectum.

artículo científico publicado en 2006

Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic mice

artículo científico publicado en 2012

Protective Effect of Val129-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease.

artículo científico publicado en 2017

Review. The origin of the prion agent of kuru: molecular and biological strain typing.

artículo científico publicado en 2008

Review: contribution of transgenic models to understanding human prion disease.

artículo científico publicado en 2010

Rskα-actin/hIGF-1 transgenic mice with increased IGF-I in skeletal muscle and blood: Impact on regeneration, denervation and muscular dystrophy

artículo científico publicado en 2006

Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS

artículo científico publicado en 2020

Threshold for epileptiform activity is elevated in prion knockout mice

artículo científico publicado en 2011

Tissue specific expression of an alpha-skeletal actin-lacZ fusion gene during development in transgenic mice

artículo científico publicado en 1994

Transgenic studies of the influence of the PrP structure on TSE diseases.

artículo científico publicado en 2001

Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS.

artículo científico publicado en 2015

Unaltered susceptibility to BSE in transgenic mice expressing human prion protein.

artículo científico publicado en 1995

Lista de obras de Emmanuel A Asante

A naturally occurring variant of the human prion protein completely prevents prion disease.

Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins

Atypical scrapie prions from sheep and lack of disease in transgenic mice overexpressing human prion protein.

BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein

Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein

Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous mice

Effect of fixation on brain and lymphoreticular vCJD prions and bioassay of key positive specimens from a retrospective vCJD prevalence study

Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy ⬇️

Frontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathology

Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein.

Interaction between prion protein and toxic amyloid β assemblies can be therapeutically targeted at multiple sites

Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice

Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice

Pathogenic human prion protein rescues PrP null phenotype in transgenic mice.

Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein.

Prion infectivity in variant Creutzfeldt-Jakob disease rectum.

Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic mice

Protective Effect of Val129-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease.

Review. The origin of the prion agent of kuru: molecular and biological strain typing.

Review: contribution of transgenic models to understanding human prion disease.

Rskα-actin/hIGF-1 transgenic mice with increased IGF-I in skeletal muscle and blood: Impact on regeneration, denervation and muscular dystrophy

Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS

Threshold for epileptiform activity is elevated in prion knockout mice

Tissue specific expression of an alpha-skeletal actin-lacZ fusion gene during development in transgenic mice

Transgenic studies of the influence of the PrP structure on TSE diseases.

Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS.

Unaltered susceptibility to BSE in transgenic mice expressing human prion protein.