Filtros de búsqueda

Lista de obras de Rodney Samaco

A framework for the investigation of rare genetic disorders in neuropsychiatry

scientific article published on 23 September 2019

A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome

artículo científico publicado en 2008

Adult neural function requires MeCP2.

artículo científico publicado en 2011

Complexities of Rett Syndrome and MeCP2: Figure 1 ⬇️

artículo científico publicado el 1 de junio de 2011

Crh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndrome

artículo científico publicado en 2012

Current Perspectives in Autism Spectrum Disorder: From Genes to Therapy

artículo científico publicado en 2016

Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress.

artículo científico publicado en 2008

Duplication of Atxn1l suppresses SCA1 neuropathology by decreasing incorporation of polyglutamine-expanded ataxin-1 into native complexes

artículo científico publicado en 2007

Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes

artículo científico publicado en 2010

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

artículo científico publicado en 2004

Evaluating Two Common Strategies for Research Participant Recruitment Into Autism Studies: Observational Study

scientific article published on 24 September 2020

Expression of FoxP2 during zebrafish development and in the adult brain

artículo científico publicado en 2006

Female Mecp2(+/-) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies

artículo científico publicado en 2012

Forniceal deep brain stimulation rescues hippocampal memory in Rett syndrome mice

artículo científico publicado en 2015

Genetic rodent models of brain disorders: Perspectives on experimental approaches and therapeutic strategies

artículo científico publicado en 2017

Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen

artículo científico publicado en 2021

Loss of MeCP2 Causes Urological Dysfunction and Contributes to Death by Kidney Failure in Mouse Models of Rett Syndrome

artículo científico publicado en 2016

Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities

artículo científico publicado en 2009

Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome.

artículo científico publicado en 2016

MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.

artículo científico publicado en 2002

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

artículo científico publicado en 2004

Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome

artículo científico publicado en 2018

Preclinical research in Rett syndrome: setting the foundation for translational success.

artículo científico publicado en 2012

Rigor and Reproducibility in Rodent Behavioral Research.

artículo científico publicado en 2018

X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.

artículo científico publicado en 2004

miR-19, miR-101 and miR-130 co-regulate ATXN1 levels to potentially modulate SCA1 pathogenesis

artículo científico publicado en 2008

Dominio Público Uruguay está sostenido por:

Acerca de Dominio Público Uruguay

Ayuda