Publications by authors named "Alexandra Cabral"

Claim this Profile
A
A dual-inducible control system for multistep biosynthetic pathways.
Andrés Felipe Carrillo Rincón, Alexandra J Cabral, Andras Gyorgy, Natalie G Farny

J Biol Eng· November 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
How does participation in Global Value Chains affect embodied carbon emissions in international trade? New insights from cross-country panel data analysis.
Camila do Carmo Hermida, Alexandra Maria Rios Cabral, Juliana Costa Ribeiro Prates, Thierry Molnar Prates, Francielly de Fátima Almeida

Environ Sci Pollut Res Int· September 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The enigma of ultraviolet radiation stress granules: Research challenges and new perspectives.
Alexandra J Cabral, Danielle C Costello, Natalie G Farny

Front Mol Biosci· December 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rett syndrome with and without detected MECP2 mutations: an attempt to redefine phenotypes.
Teresa Temudo, Mónica Santos, Elisabete Ramos, Karin Dias, José Pedro Vieira, Alexandra Cabral, Pedro Cabral

Brain Dev· January 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel synonymous substitution in POMGNT1 promotes exon skipping in a patient with congenital muscular dystrophy.
Jorge Oliveira, Isabel Soares-Silva, Ivo Fokkema, Ana Gonçalves, Alexandra Cabral

J Hum Genet· August 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Movement disorders in Rett syndrome: an analysis of 60 patients with detected MECP2 mutation and correlation with mutation type.
Teresa Temudo, Elisabete Ramos, Karin Dias, Clara Barbot, Jose P Vieira, Alexandra Cabral, Pedro Cabral

Mov Disord· July 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Haploinsufficiency of TCF4 causes syndromal mental retardation with intermittent hyperventilation (Pitt-Hopkins syndrome).
Christiane Zweier, Maarit M Peippo, Juliane Hoyer, Sergio Sousa, Armand Bottani, Alexandra Cabral

Am J Hum Genet· May 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis