Rogelio Palomino‐Morales

ORCID: 0000-0003-3507-343X
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About
Contact & Profiles
Research Areas
  • Sperm and Testicular Function
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Vasculitis and related conditions
  • Cell Adhesion Molecules Research
  • Systemic Lupus Erythematosus Research
  • Bioactive Compounds and Antitumor Agents
  • Reproductive Biology and Fertility
  • Pancreatic and Hepatic Oncology Research
  • Genomics, phytochemicals, and oxidative stress
  • Cytokine Signaling Pathways and Interactions
  • Inflammasome and immune disorders
  • Cholesterol and Lipid Metabolism
  • ATP Synthase and ATPases Research
  • Cancer, Hypoxia, and Metabolism
  • Rheumatoid Arthritis Research and Therapies
  • Immunodeficiency and Autoimmune Disorders
  • Atherosclerosis and Cardiovascular Diseases
  • Inflammatory Bowel Disease
  • Systemic Sclerosis and Related Diseases
  • Sexual Differentiation and Disorders
  • Cancer, Lipids, and Metabolism
  • Peroxisome Proliferator-Activated Receptors
  • Fatty Acid Research and Health
  • Endoplasmic Reticulum Stress and Disease
  • Galectins and Cancer Biology

Universidad de Granada
2015-2025

Instituto de Investigación Biosanitaria de Granada
2018-2025

Instituto de Parasitología y Biomedicina "López - Neyra"
2008-2011

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
2011

Consejo Superior de Investigaciones Científicas
2008-2010

Parque Tecnológico de la Salud
2010

Corporación para Investigaciones Biológicas
2010

Universidad del Rosario
2010

Medizinische Hochschule Hannover
2010

Junta de Andalucía
2010

We determined the contribution of methylene tetrahydrofolate reductase (MTHFR) 677 C>T and 1298 A>C gene polymorphisms to susceptibility rheumatoid arthritis (RA). also assessed whether these two MTHFR may be implicated in development cardiovascular (CV) events subclinical atherosclerosis manifested by presence endothelial dysfunction, a series Spanish patients with RA. Six hundred twelve fulfilling 1987 American College Rheumatology classification criteria for RA, seen at rheumatology...

10.1186/ar2989 article EN cc-by Arthritis Research & Therapy 2010-01-01

Pancreatic ductal adenocarcinoma is a deadly disease because of late diagnosis and chemoresistance. We aimed to find panel serum cytokines representing diagnostic predictive biomarkers for pancreatic cancer.A cytokine antibody array was performed simultaneously identify 507 in sera patients with cancer healthy controls. The nonparametric Mann-Whitney U test used pairwise compare the controls, pretreated patients, posttreated patients. Fold changes greater than or equal 1.5 less 1/1.5 were...

10.1097/mpa.0000000000000155 article EN Pancreas 2014-06-29

Abstract Protein dynamics is essential to understand protein function and stability, even though rarely investigated as the origin of loss-of-function due genetic variations. Here, we use biochemical, biophysical, cell computational biology tools study two cancer-associated polymorphisms (p.R139W p.P187S) in human NAD(P)H quinone oxidoreductase 1 (NQO1), a FAD-dependent enzyme which activates cancer pro-drugs stabilizes several oncosuppressors. We show that p.P187S strongly destabilizes NQO1...

10.1038/srep20331 article EN cc-by Scientific Reports 2016-02-03

Abstract STUDY QUESTION Do the genetic determinants of idiopathic severe spermatogenic failure (SPGF) differ between generations? SUMMARY ANSWER Our data support that component SPGF is impacted by dynamic changes in environmental exposures over decades. WHAT IS KNOWN ALREADY The form has a multifactorial etiology wherein an interaction genetic, epigenetic, and factors leads to disease onset progression. At level, genome-wide association studies (GWASs) allow analysis millions variants across...

10.1093/humrep/deae007 article EN Human Reproduction 2024-02-01

OBJECTIVES: Genome-wide association studies have reported the role of interleukin (IL)2-IL21chromosomal region at 4q27 in several autoimmune conditions. Mice deficient IL-2 develop a disease with clinical and histological similarity to ulcerative colitis (UC) humans. Modest evidence linkage UC was tentatively proposed for theIL2gene more than decade ago. Therefore, we decide investigate polymorphisms axis (IL2,IL2RA,andIL2RBgenes) inflammatory bowel diseases (IBDs). METHODS: Seven hundred...

10.1038/ajg.2009.224 article EN The American Journal of Gastroenterology 2009-05-26

Interleukin-18 (IL-18) is a proinflammatory cytokine that plays an important role in chronic inflammation and autoimmune disorders. In this study, we aimed to determine the potential of IL18 gene SLE. To define genetic association SLE, have genotyped nine SNPs independent set Spanish cases controls. The polymorphisms were by PCR, using predeveloped TaqMan allele discrimination assay. Two still significant after fine mapping gene. SNP (rs360719) surviving correction for multiple tests was two...

10.1093/hmg/ddp301 article EN Human Molecular Genetics 2009-07-07

Abstract Disease associated genetic variations often cause intracellular enzyme inactivation, dysregulation and instability. However, allosteric communication of mutational effects to distant functional sites leading loss-of-function remains poorly understood. We characterize here interdomain site-to-site by which a common cancer-associated single nucleotide polymorphism (c.C609T/p.P187S) reduces the activity stability in vivo NAD(P)H:quinone oxidoreductase 1 (NQO1). NQO1 is FAD-dependent,...

10.1038/srep44532 article EN cc-by Scientific Reports 2017-03-14

Human proteins are vulnerable towards disease-associated single amino acid replacements affecting protein stability and function. Interestingly, a few studies have shown that consensus acids from mammals or vertebrates can enhance when incorporated into human proteins. Here, we investigate yet unexplored relationships between the high vulnerability of inactivation recent evolutionary site-specific divergence stabilizing acids. Using phylogenetic, structural experimental analyses, show at...

10.1093/hmg/ddx238 article EN Human Molecular Genetics 2017-07-05

The multifunctional nature of human flavoproteins is critically linked to their ability populate multiple conformational states. Ligand binding, post-translational modifications and disease-associated mutations can reshape this functional landscape, although the structure-function relationships these effects are not well understood. Herein, we characterized structural consequences two (the cancer-associated P187S phosphomimetic S82D) on different ligation states which relevant flavin...

10.1016/j.redox.2021.102112 article EN cc-by Redox Biology 2021-08-18

Objective. Dendritic cells localized at the adventitia-media border of normal medium-sized arteries play a pivotal role in initiation giant cell arteritis (GCA). These express singular surface receptor profile, including series Toll-like receptors (TLR). Ligands TLR-4 promote activation and differentiation adventitial dendritic are directly implicated pathogenesis GCA. We aimed to assess potential implication TLR4-(+896 A/G) gene polymorphism susceptibility Methods. A total 210 patients...

10.3899/jrheum.081286 article EN The Journal of Rheumatology 2009-06-16

Allosterism is a common phenomenon in protein biochemistry that allows rapid regulation of stability; dynamics and function. However, the mechanisms by which allosterism occurs (by mutations or post-translational modifications (PTMs)) may be complex, particularly due to long-range propagation perturbation across structures. In this work, we have investigated allosteric communication multifunctional, cancer-related antioxidant NQO1 mutating several fully buried leucine residues (L7, L10 L30)...

10.3390/antiox11061110 article EN cc-by Antioxidants 2022-06-02

Abstract Introduction The objective was to investigate the potential implication of IL18 gene promoter polymorphisms in susceptibility giant-cell arteritis (GCA). Methods In total, 212 patients diagnosed with biopsy-proven GCA were included this study. DNA from and matched controls obtained peripheral blood. Samples genotyped for -137 G>C (rs187238), -607 C>A (rs1946518), -1297 T>C (rs360719) polymerase chain reaction, by using a predesigned TaqMan allele discrimination assay....

10.1186/ar2962 article EN cc-by Arthritis Research & Therapy 2010-03-23

Objective. To examine the influence of STAT4 rs7574865 gene polymorphism on patients with primary Sjögren’s syndrome (SS). Methods. Two different cohorts were studied: 69 SS and 296 controls from Colombia 108 227 Germany. Samples genotyped for single-nucleotide a predesigned TaqMan genotyping assay. We carried out metaanalysis our results combined data published to date. Results. Although no significant differences observed in allele frequencies between Colombians (p = 0.28, OR 1.24, 95% CI...

10.3899/jrheum.091007 article EN The Journal of Rheumatology 2010-04-01

The overall survival of patients with pancreatic ductal adenocarcinoma is extremely low. Although gemcitabine the standard used chemotherapy for this disease, clinical outcomes do not reflect significant improvements, even when combined adjuvant treatments. There an urgent need prognosis markers to be found. aim study was analyze potential value serum cytokines find a profile that can predict outcome in cancer and establish practical index significantly predicts patients' outcomes. We have...

10.1155/2015/518284 article EN cc-by BioMed Research International 2015-01-01

Testes of seasonally breeding species experience a severe functional regression before the non-breeding period, which implies substantial mass reduction due to massive germ-cell depletion. Two alternative mechanisms seasonal depletion have been described in mammals, apoptosis and desquamation (sloughing), but their prevalence has not determined yet reduced number studied. We performed morphological, hormonal, molecular study mechanism testicular males Egyptian long eared-hedgehog...

10.1371/journal.pone.0204851 article EN cc-by PLoS ONE 2018-10-04
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