Francisco J Rodriguez-Alvarez
Overview
Explore the profile of Francisco J Rodriguez-Alvarez including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
278
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0
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Recent Articles
1.
Del Pozo-Yauner L, Herrera G, Perez Carreon J, Turbat-Herrera E, Rodriguez-Alvarez F, Ruiz Zamora R
Front Immunol
. 2023 Jul;
14:1203425.
PMID: 37520549
The adaptive immune system of jawed vertebrates generates a highly diverse repertoire of antibodies to meet the antigenic challenges of a constantly evolving biological ecosystem. Most of the diversity is...
2.
Lecoq L, Wiegand T, Rodriguez-Alvarez F, Cadalbert R, Herrera G, Del Pozo-Yauner L, et al.
Chembiochem
. 2018 Dec;
20(8):1027-1031.
PMID: 30565364
Amyloid light-chain (AL) amyloidosis is a rare disease in which plasma-cell-produced monoclonal immunoglobulin light chains misfold and become deposited as fibrils in the extracellular matrix. λ6 subgroup light chains are...
3.
Calucho M, Bernal S, Alias L, March F, Vencesla A, Rodriguez-Alvarez F, et al.
Neuromuscul Disord
. 2018 Feb;
28(3):208-215.
PMID: 29433793
Spinal muscular atrophy (SMA) is a neuromuscular disorder caused by loss or mutations in SMN1. According to age of onset, achieved motor abilities, and life span, SMA patients are classified...
4.
Rodriguez-Alvarez F, Jimenez-Mora E, Caballero M, Gallego B, Chiloeches A, Toro M
Mol Cell Biochem
. 2015 Oct;
411(1-2):253-60.
PMID: 26472731
Somatostatin (SST) is one of the main regulators of thyroid function. It acts by binding to its receptors, which lead to the dissociation of G proteins into Gαi and Gβγ...
5.
Gandia M, Del Castillo F, Rodriguez-Alvarez F, Garrido G, Villamar M, Calderon M, et al.
PLoS One
. 2013 Sep;
8(9):e73566.
PMID: 24039984
The DFNB1 subtype of autosomal recessive, nonsyndromic hearing impairment, caused by mutations affecting the GJB2 (connexin-26) [corrected] gene, is highly prevalent in most populations worldwide. DFNB1 hearing impairment is mostly...
6.
Alias L, Bernal S, Barcelo M, Also-Rallo E, Martinez-Hernandez R, Rodriguez-Alvarez F, et al.
Genet Test Mol Biomarkers
. 2011 May;
15(9):587-94.
PMID: 21548796
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder caused by absence of or mutations in the survival motor neuron1 gene (SMN1). All SMA patients have a highly homologous...
7.
Alias L, Bernal S, Fuentes-Prior P, Barcelo M, Also E, Martinez-Hernandez R, et al.
Hum Genet
. 2008 Dec;
125(1):29-39.
PMID: 19050931
Spinal muscular atrophy (SMA) is caused by mutations in the SMN1 gene. We have studied the molecular pathology of SMA in 745 unrelated Spanish patients using PCR-RFLP, SMN gene dosage...
8.
Calleros L, Lasa M, Rodriguez-Alvarez F, Toro M, Chiloeches A
Apoptosis
. 2006 May;
11(7):1161-73.
PMID: 16699960
Cholesterol is essential for cell viability, and homeostasis of cellular cholesterol is crucial to various cell functions. Here we examined the effect of cholesterol depletion on apoptosis and the mechanisms...