Advanced search    
Sort by: ▼ relevance publication date title journal

Search: authors:"Laia Pedrola"

6 papers found.
Use AND, OR, NOT, +word, -word, "long phrase", (parentheses) to fine-tune your search.

Non-invasive prediction of NAFLD severity: a comprehensive, independent validation of previously postulated serum microRNA biomarkers

• PubMed • Google Scholar Search for Isabel Conde in:Nature Research journals • PubMed • Google Scholar Search for Guillermo Quintas in:Nature Research journals • PubMed • Google Scholar Search for Laia ... Pedrola in:Nature Research journals • PubMed • Google Scholar Search for Ángela Zaragoza in:Nature Research journals • PubMed • Google Scholar Search for Judith Perez-Rojas in:Nature Research journals

High-Throughput Sequencing of RNA Silencing-Associated Small RNAs in Olive (Olea europaea L.)

Small RNAs (sRNAs) of 20 to 25 nucleotides (nt) in length maintain genome integrity and control gene expression in a multitude of developmental and physiological processes. Despite RNA silencing has been primarily studied in model plants, the advent of high-throughput sequencing technologies has enabled profiling of the sRNA component of more than 40 plant species. Here, we used...

Microbial Diversity in the Midguts of Field and Lab-Reared Populations of the European Corn Borer Ostrinia nubilalis

, data collection and analysis, decision to publish, or preparation of the manuscript. Competing Interests: Daniel Ramo n, Juan F. Martnez and Laia Pedrola are employed by a commercial company

The Transcriptome Analysis of Strongyloides stercoralis L3i Larvae Reveals Targets for Intervention in a Neglected Disease

Background Strongyloidiasis is one of the most neglected diseases distributed worldwide with endemic areas in developed countries, where chronic infections are life threatening. Despite its impact, very little is known about the molecular biology of the parasite involved and its interplay with its hosts. Next generation sequencing technologies now provide unique opportunities to...

Evolutionary and Structural Analyses of GDAP1, Involved in Charcot-Marie-Tooth Disease, Characterize a Novel Class of Glutathione Transferase-Related Genes

Antonio Marco 0 Ana Cuesta Laia Pedrola Francesc Palau Ignacio Marn 0 0 Departamento de Gene tica, Universidad de Valencia , Valencia , Spain; and Laboratory of Genetics and Molecular Medicine

GDAP1, the protein causing Charcot–Marie–Tooth disease type 4A, is expressed in neurons and is associated with mitochondria

Mutations in GDAP1, the ganglioside-induced differentiation-associated protein 1 gene, cause Charcot–Marie–Tooth (CMT) type 4A, a severe autosomal recessive form of neuropathy associated with either demyelinating or axonal phenotypes. Here, we demonstrate that GDAP1 has far greater expression in neurons than in myelinating Schwann cells. We investigated cell localization of GDAP1...