E. Salido

E. Salido, E. Arbelo, P. Saavedra, 2003, Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry.

Blood Tests for Early Detection of Colorectal Cancer

E. Salido, E. Quintero, A. Gimeno-García, 2010 .

A new HDV mouse model identifies mitochondrial antiviral signaling protein (MAVS) as a key player in IFN-β induction.

E. Salido, M. Buti, J. Prieto, 2017, Journal of hepatology.

Molecular Recognition of PTS-1 Cargo Proteins by Pex5p: Implications for Protein Mistargeting in Primary Hyperoxaluria

E. Salido, A. Pey, A. Albert, 2015, Biomolecules.

Protein Homeostasis Defects of Alanine-Glyoxylate Aminotransferase: New Therapeutic Strategies in Primary Hyperoxaluria Type I

E. Salido, A. Pey, A. Albert, 2013, BioMed research international.

Primary hyperoxalurias: disorders of glyoxylate detoxification.

E. Salido, A. Pey, V. Lorenzo, 2012, Biochimica et biophysica acta.

Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene

E. Salido, H. Waterham, A. Amoroso, 2009, Human mutation.

The Mouse Alanine:Glyoxylate Aminotransferase Gene (Agxt1): Cloning, Expression, and Mapping to Chromosome 1

E. Salido, L. Shapiro, X. M. Li, 1999, Somatic cell and molecular genetics.

The GLUT-1 XbaI Gene Polymorphism Is Associated with Vascular Calcifications in Nondiabetic Uremic Patients

E. Salido, D. Hernández, M. Rufino, 2008, Nephron Clinical Practice.

ACE gene polymorphism and erythropoietin in endurance athletes at moderate altitude.

E. Salido, A. Torres, D. Hernández, 2006, Medicine and science in sports and exercise.

Insight into the specificity and severity of pathogenic mechanisms associated with missense mutations through experimental and structural perturbation analyses

Athi N. Naganathan, E. Salido, S. Ventura, 2018, Human molecular genetics.

Targeting HIF-1α Function in Cancer through the Chaperone Action of NQO1: Implications of Genetic Diversity of NQO1

E. Salido, D. Timson, M. Medina, 2022, Journal of personalized medicine.

Role of ACE gene polymorphism on cardiovascular complications after renal transplantation.

E. Salido, A. Torres, D. Hernández, 2001, Transplantation proceedings.

The Value of Mouse Models of Rare Diseases: A Spanish Experience

E. Salido, M. Dierssen, B. Ibáñez, 2020, Frontiers in Genetics.

Serum lipids and estrogen receptor gene polymorphisms in male-to-female transsexuals: effects of estrogen treatment.

E. Salido, E. Arbelo, P. Saavedra, 2004, European journal of internal medicine.

Contribution of Cyclooxygenase End Products and Oxidative Stress to Intrahepatic Endothelial Dysfunction in Early Non-Alcoholic Fatty Liver Disease

E. Salido, E. Quintero, M. Hernández‐Guerra, 2016, PloS one.

The ACE/DD genotype is associated with the extent of exercise-induced left ventricular growth in endurance athletes.

E. Salido, A. Torres, D. Hernández, 2003, Journal of the American College of Cardiology.

Patients with primary hyperoxaluria type 2 have significant morbidity and require careful follow-up.

E. Salido, B. Hoppe, J. Groothoff, 2019, Kidney international.

Cancer modifier alleles inhibiting lung tumorigenesis are common in inbred mouse strains

E. Salido, T. Dragani, G. Manenti, 2002, International journal of cancer.

ARID2 deficiency promotes tumor progression and is associated with higher sensitivity to PARP inhibition in lung cancer

E. Salido, I. Varela, P. Crespo, 2020, bioRxiv.

Primary hyperoxaluria type 1 in the Canary Islands: A conformational disease due to I244T mutation in the P11L-containing alanine:glyoxylate aminotransferase

E. Salido, L. Shapiro, A. Torres, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Plasma matrix metalloproteinase 9 as an early surrogate biomarker of advanced colorectal neoplasia.

E. Salido, D. Nicolás-Pérez, E. Quintero, 2016, Gastroenterologia y hepatologia.

The distribution of two different vitamin D receptor polymorphisms (BsmI and start codon) in primary hyperparathyroidism

E. Salido, A. Torres, M. Sosa, 2000, Journal of internal medicine.

Randomized Controlled Trial Assessing the Impact of Tacrolimus Versus Cyclosporine on the Incidence of Posttransplant Diabetes Mellitus

E. Salido, E. Porrini, A. Torres, 2018, Kidney international reports.

Bone Marrow-Derived Cells Promote Liver Regeneration in Mice With Erythropoietic Protoporphyria

E. Salido, J. Segovia, J. Bueren, 2009, Transplantation.

Alanine–glyoxylate aminotransferase-deficient mice, a model for primary hyperoxaluria that responds to adenoviral gene transfer

E. Salido, L. Shapiro, A. Torres, 2006, Proceedings of the National Academy of Sciences.

Dietary fish oil does not influence acute rejection rate and graft survival after renal transplantation: a randomized placebo-controlled study.

E. Salido, A. Torres, D. Hernández, 2002, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Influence of genetic polymorphisms of CYP3A5 and ABCB1 on sirolimus pharmacokinetics, patient and graft survival and other clinical outcomes in renal transplant

E. Salido, Armando Torres, M. García-Sáiz, 2017, Drug metabolism and personalized therapy.

Artery Wall Assessment Helps Predict Kidney Transplant Outcome

E. Salido, S. Pitti, A. Torres, 2015, PloS one.

Calcium metabolism and skeletal problems after transplantation.

E. Salido, A. Torres, V. Lorenzo, 2002, Journal of the American Society of Nephrology : JASN.

Systemic Alanine Glyoxylate Aminotransferase mRNA Improves Glyoxylate Metabolism in a Mouse Model of Primary Hyperoxaluria Type 1.

Christian W. Cobaugh, E. Salido, R. Subramanian, 2019, Nucleic acid therapeutics.

HLA-DR class II and ICAM-1 expression on tubular cells taken by fine-needle aspiration biopsy in renal allograft dysfunction.

E. Salido, A. Torres, D. Hernández, 1996, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Collagen type 1 (COL1A1) Sp1 binding site polymorphism is associated with osteoporotic fractures but not with bone density in post-menopausal women from the Canary Islands: a preliminary study

E. Salido, P. Saavedra, M. Sosa, 2007, Aging clinical and experimental research.

Oral Treatment With an Engineered Uricase, ALLN-346, Reduces Hyperuricemia, and Uricosuria in Urate Oxidase-Deficient Mice

E. Salido, R. Terkeltaub, S. Pierzynowski, 2020, Frontiers in Medicine.

Identification and structural and functional characterization of human enamelysin (MMP-20).

E. Salido, C. López-Otín, E. Llano, 1997, Biochemistry.

Molecular therapy of primary hyperoxaluria

E. Salido, Armando Torres, Cristina Martin-Higueras, 2017, Journal of Inherited Metabolic Disease.

Treatment with intermittent calcitriol and calcium reduces bone loss after renal transplantation.

E. Salido, A. Torres, D. Hernández, 2004, Kidney international.

Circulating urokinase receptor as a cause of focal segmental glomerulosclerosis

E. Salido, M. Sarwal, M. Rastaldi, 2011, Nature Medicine.

Naturally-Occurring Rare Mutations Cause Mild to Catastrophic Effects in the Multifunctional and Cancer-Associated NQO1 Protein

E. Salido, A. Pey, Angel L. Pey, 2020, Journal of personalized medicine.

Salicylic Acid Derivatives Inhibit Oxalate Production in Mouse Hepatocytes with Primary Hyperoxaluria Type 1.

E. Salido, J. A. Gómez-Vidal, M. Díaz-Gavilán, 2018, Journal of medicinal chemistry.

Deleted in azoospermia associated protein 1 shuttles between nucleus and cytoplasm during normal germ cell maturation.

E. Salido, P. Yen, R. Swerdloff, 2002, Journal of andrology.

Parathyroid gland calcium receptor gene expression is not regulated by increased dietary phosphorus in normal and renal failure rats.

E. Salido, A. Torres, Armando Torres, 1996, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Characterization of the mouse Dazap1 gene encoding an RNA-binding protein that interacts with infertility factors DAZ and DAZL

E. Salido, P. Yen, T. Dai, 2001, BMC Genomics.

Specific Inhibition of Hepatic Lactate Dehydrogenase Reduces Oxalate Production in Mouse Models of Primary Hyperoxaluria

E. Salido, W. Zhou, H. Dudek, 2018, Molecular therapy : the journal of the American Society of Gene Therapy.

siRNA Therapeutics to Treat Liver Disorders

E. Salido, Cristina Martin-Higueras, Chengjung Lai, 2017 .

Phenotypic correction of a mouse model for primary hyperoxaluria with adeno-associated virus gene transfer.

E. Salido, H. Petry, S. Beattie, 2011, Molecular therapy : the journal of the American Society of Gene Therapy.

Enteric oxalate elimination is induced and oxalate is normalized in a mouse model of primary hyperoxaluria following intestinal colonization with Oxalobacter.

E. Salido, Altin Gjymishka, M. J. Allison, 2011, American journal of physiology. Gastrointestinal and liver physiology.

Allosteric Communication in the Multifunctional and Redox NQO1 Protein Studied by Cavity-Making Mutations

Athi N. Naganathan, E. Salido, P. Man, 2022, Antioxidants.

A Dynamic Core in Human NQO1 Controls the Functional and Stability Effects of Ligand Binding and Their Communication across the Enzyme Dimer

E. Salido, D. Timson, P. Man, 2019, Biomolecules.

Hydroxyproline metabolism in mouse models of primary hyperoxaluria.

E. Salido, S. Cramer, R. Holmes, 2012, American journal of physiology. Renal physiology.

Differential expression of liver and kidney proteins in a mouse model for primary hyperoxaluria type I

E. Salido, J. Hernandez-Fernaud, 2010, The FEBS journal.

The PlA2 polymorphism of the platelet glycoprotein IIIA gene as a risk factor for acute renal allograft rejection.

E. Salido, A. Torres, D. Hernández, 1999, Journal of the American Society of Nephrology : JASN.

Lactate dehydrogenase A inhibitors with a 2,8-dioxabicyclo[3.3.1]nonane scaffold: A contribution to molecular therapies for primary hyperoxalurias.

E. Salido, M. Díaz-Gavilán, A. Alejo-Armijo, 2022, Bioorganic chemistry.

MiceMin / + Apc Intestinal Adenomas in Hematopoietic Prostaglandin D Synthase Suppresses

Henry J. Lin, E. Salido, Y. Urade, 2007 .

Vitamin B6-dependent enzymes and disease

E. Salido, I. Bellezza, B. Cellini, 2020 .

Hyperoxaluria Is Reduced and Nephrocalcinosis Prevented with an Oxalate-Degrading Enzyme in Mice with Hyperoxaluria

E. Salido, A. Margolin, C. Langman, 2008, American Journal of Nephrology.

Iohexol plasma clearance, a simple and reliable method to measure renal function in conscious mice

E. Salido, F. Gaspari, E. Porrini, 2016, Pflügers Archiv - European Journal of Physiology.

High phosphorus diet increases preproPTH mRNA independent of calcium and calcitriol in normal rats.

E. Salido, A. Torres, Armando Torres, 1996, Kidney international.

The Pl A2 Polymorphism of the Platelet Glycoprotein IIIA Gene as a Risk Factor for Acute Renal Allograft Rejection

E. Salido, D. Hernández, Armando Torres, 1999 .

Measurement of glomerular filtration rate: internal and external validations of the iohexol plasma clearance technique by HPLC.

E. Salido, F. Gaspari, E. Porrini, 2014, Clinica chimica acta; international journal of clinical chemistry.

Effect of naturally-occurring mutations on the stability and function of cancer-associated NQO1: Comparison of experiments and computation

E. Salido, K. Lindorff-Larsen, A. Pey, 2022, bioRxiv.

Expression of steroid sulfatase during embryogenesis.

E. Salido, L. Shapiro, S. Mellon, 1997, Endocrinology.

Voltage‐dependent anion channel as a resident protein of lipid rafts: post‐transductional regulation by estrogens and involvement in neuronal preservation against Alzheimer’s disease

E. Salido, J. Hernandez-Fernaud, M. Díaz, 2011, Journal of neurochemistry.

Different phenotypic outcome due to site-specific phosphorylation in the cancer-associated NQO1 enzyme studied by phosphomimetic mutations.

E. Salido, P. Man, M. Medina, 2022, Archives of biochemistry and biophysics.

TNFbeta+250 polymorphism and hyperdynamic state in cardiac surgery with extracorporeal circulation.

E. Salido, J. L. Iribarren, M. Mora, 2008, Interactive cardiovascular and thoracic surgery.

Institutional report - Cardiopulmonary bypass TNFbq250 polymorphism and hyperdynamic state in cardiac surgery with extracorporeal circulation

E. Salido, M. Brouard, 2008 .

Amelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta.

E. Salido, L. Shapiro, U. Landegren, 1995, Genomics.

The human enamel protein gene amelogenin is expressed from both the X and the Y chromosomes.

E. Salido, P. Yen, L. Shapiro, 1992, American journal of human genetics.

Assessment of Urine Proteomics in Type 1 Primary Hyperoxaluria

E. Salido, B. Hoppe, D. Milliner, 2016, American Journal of Nephrology.

Correction of Hyperoxaluria by Liver Repopulation With Hepatocytes in a Mouse Model of Primary Hyperoxaluria Type-1

E. Salido, Jinlan Jiang, C. Guha, 2008, Transplantation.

Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies

E. Salido, G. Nürnberg, M. Wolf, 2012, European Journal of Human Genetics.

Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment.

E. Salido, M. Daudon, N. Jamieson, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Glucose homeostasis changes and pancreatic β-cell proliferation after switching to cyclosporin in tacrolimus-induced diabetes mellitus.

E. Salido, E. Porrini, A. E. Rodríguez-Rodríguez, 2015, Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia.

Small Molecule-Based Enzyme Inhibitors in the Treatment of Primary Hyperoxalurias

E. Salido, J. A. Gómez-Vidal, M. Díaz-Gavilán, 2021, Journal of personalized medicine.

Caenorhabditis elegans AGXT-1 is a mitochondrial and temperature-adapted ortholog of peroxisomal human AGT1: New insights into between-species divergence in glyoxylate metabolism.

E. Salido, A. Miranda-Vizuete, A. Pey, 2016, Biochimica et biophysica acta.

The human autosomal gene DAZLA: testis specificity and a candidate for male infertility.

E. Salido, P. Yen, N. Chai, 1996, Human molecular genetics.

Identification of two novel proteins that interact with germ-cell-specific RNA-binding proteins DAZ and DAZL1.

E. Salido, P. Yen, W. Schempp, 2000, Genomics.

The human DAZ genes, a putative male infertility factor on the Y Chromosome, are highly polymorphic in the DAZ repeat regions

E. Salido, P. Yen, N. Chai, 1997, Mammalian Genome.

Restricted expression of the human DAZ protein in premeiotic germ cells.

E. Salido, P. Yen, K. Eilber, 2008, Human reproduction.

Multiple functional copies of the RBM gene family, a spermatogenesis candidate on the human Y chromosome.

E. Salido, P. Yen, N. Chai, 1997, Genomics.

Steroid sulfatase expression in human placenta: immunocytochemistry and in situ hybridization study.

E. Salido, P. Yen, L. Shapiro, 1990, The Journal of clinical endocrinology and metabolism.

Hematopoietic prostaglandin D synthase suppresses intestinal adenomas in ApcMin/+ mice.

Henry J. Lin, Yoshihiro Urade, E. Salido, 2007, Cancer research.

Expression of the X–inactivation–associated gene XIST during spermatogenesis

E. Salido, P. Yen, T. Mohandas, 1992, Nature Genetics.

Testis-specific transcripts of rat farnesyl pyrophosphate synthetase are developmentally regulated and localized to haploid germ cells.

E. Salido, P. Edwards, C. Clarke, 1991, Biology of reproduction.

Developmentally Regulated and Localized to Haploid Germ Cells1

E. Salido, P. Edwards, C. Clarke, 1991 .

Cloning of the rat steroid sulfatase gene (Sts), a non-pseudoautosomal X-linked gene that undergoes X inactivation

E. Salido, P. Yen, L. Shapiro, 1996, Mammalian Genome.

Cloning and expression of the mouse pseudoautosomal steroid sulphatase gene (Sts)

E. Salido, P. Yen, T. Mohandas, 1996, Nature Genetics.

Colocalization of tyrosine hydroxylase and GAD65 mRNA in mesostriatal neurons

E. Salido, Manuel Rodriguez, T. González-Hernández, 2001, The European journal of neuroscience.

Generation of sequence-tagged sites from Xp22.3 by isolating commonAlu-PCR products of radiation hybrids retaining overlapping human X chromosome fragments

E. Salido, P. Yen, T. Mohandas, 1996, Human Genetics.

Structure of GroEL in Complex with an Early Folding Intermediate of Alanine Glyoxylate Aminotransferase*

E. Salido, J. Valpuesta, J. Martín-Benito, 2010, The Journal of Biological Chemistry.

Natural (and Unnatural) Small Molecules as Pharmacological Chaperones and Inhibitors in Cancer.

E. Salido, D. Timson, A. Pey, 2018, Handbook of experimental pharmacology.

High frequency de novo alterations in the long–range genomic structure of the mouse pseudoautosomal region

E. Salido, L. Shapiro, D. Kipling, 1996, Nature Genetics.

Isolation of a new gene GS2 (DXS1283E) from a CpG island between STS and KAL1 on Xp22.3.

E. Salido, P. Yen, W. C. Lee, 1994, Genomics.

Isolation of a new gene from the distal short arm of the human X chromosome that escapes X-inactivation.

E. Salido, P. Yen, T. Mohandas, 1992, Human molecular genetics.

A new locus for resistance to γ-radiation-induced thymic lymphoma identified using inter-specific consomic and inter-specific recombinant congenic strains of mice

E. Salido, J. Guénet, P. López, 2002, Oncogene.

Structural and functional insights on the roles of molecular chaperones in the mistargeting and aggregation phenotypes associated with primary hyperoxaluria type I.

E. Salido, A. Muga, A. Pey, 2019, Advances in protein chemistry and structural biology.

Single molecule real time sequencing in ADTKD-MUC1 allows complete assembly of the VNTR and exact positioning of causative mutations

E. Salido, R. Reinhardt, A. Ekici, 2018, Scientific Reports.

Liver cell transplantation in severe infantile oxalosis--a potential bridging procedure to orthotopic liver transplantation?

E. Salido, D. Stippel, H. Goebel, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Localization and gestation‐dependent pattern of corticotrophin‐releasing factor receptor subtypes in ovine fetal distal colon

E. Salido, M. Ross, J. Lakshmanan, 2008, Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society.

Targeting HIF-1α Function in Cancer through the Chaperone Action of NQO1

E. Salido, D. Timson, A. Pey, 2020 .

Role of gap junctions modulating hepatic vascular tone in cirrhosis

E. Salido, J. Bosch, E. Quintero, 2014, Liver international : official journal of the International Association for the Study of the Liver.

Mouse p73 gene maps to the distal part of chromosome 4 and might be involved in the progression of gamma-radiation-induced T-cell lymphomas.

E. Salido, M. Serrano, M. Herranz, 1999, Cancer research.

An evaluation of the inactive mouse X chromosome in somatic cell hybrids

E. Salido, P. Yen, T. Mohandas, 1993, Somatic cell and molecular genetics.

A Founder Mutation in Artemis, an SNM1-Like Protein, Causes SCID in Athabascan-Speaking Native Americans1

E. Salido, Yungui Zhou, D. Moshous, 2002, The Journal of Immunology.

Athabascan-Speaking Native Americans SNM 1-Like Protein , Causes SCID in A Founder Mutation in Artemis , an Villartay and

E. Salido, Yungui Zhou, D. Moshous, 2002 .

The combined effect of pre-transplant triglyceride levels and the type of calcineurin inhibitor in predicting the risk of new onset diabetes after renal transplantation.

E. Salido, E. Porrini, A. Torres, 2007, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Targeted Disruption of the Artemis Murine Counterpart Results in SCID and Defective V(D)J Recombination That Is Partially Corrected with Bone Marrow Transplantation1

A. Feeney, E. Salido, S. Bhattacharyya, 2005, The Journal of Immunology.

Regression of left ventricular hypertrophy by lisinopril after renal transplantation: role of ACE gene polymorphism.

E. Salido, A. Torres, D. Hernández, 2000, Kidney international.

Enhanced vulnerability of human proteins towards disease-associated inactivation through divergent evolution

Julian E. Fuchs, E. Salido, D. Timson, 2017, Human molecular genetics.

Transient Expression of Transgenic IL-12 in Mouse Liver Triggers Unremitting Inflammation Mimicking Human Autoimmune Hepatitis

E. Salido, J. Prieto, G. González-Aseguinolaza, 2016, The Journal of Immunology.

Intestinal tumor suppression in ApcMin/+ mice by prostaglandin D2 receptor PTGDR

Henry J. Lin, E. Salido, L. Kudo, 2014, Cancer medicine.

Epigenomic and transcriptional profiling identifies impaired glyoxylate detoxification in NAFLD as a risk factor for hyperoxaluria.

E. Salido, P. Boor, A. Schriewer, 2021, Cell reports.

Characterization of the promoter region of human steriod sulfatase: A gene which escapes X inactivation

E. Salido, P. Yen, L. Shapiro, 1996, Somatic cell and molecular genetics.

Presentation and role of transplantation in adult patients with type 1 primary hyperoxaluria and the I244T AGXT mutation: Single-center experience.

E. Salido, A. Torres, V. Torregrosa, 2006, Kidney international.

Improved Outcome of Infantile Oxalosis Over Time in Europe: Data From the OxalEurope Registry

E. Salido, J. Bacchetta, B. Hoppe, 2022, Kidney international reports.

Inhibition of Glycolate Oxidase With Dicer-substrate siRNA Reduces Calcium Oxalate Deposition in a Mouse Model of Primary Hyperoxaluria Type 1

E. Salido, H. Dudek, B. Holmes, 2016, Molecular therapy : the journal of the American Society of Gene Therapy.

New salicylic acid derivatives, double inhibitors of glycolate oxidase and lactate dehydrogenase, as effective agents decreasing oxalate production.

E. Salido, A. Pey, M. Díaz-Gavilán, 2022, European journal of medicinal chemistry.

CRISPR/Cas9-mediated glycolate oxidase disruption is an efficacious and safe treatment for primary hyperoxaluria type I

E. Salido, F. Prósper, G. González-Aseguinolaza, 2018, Nature Communications.

Glycolate Oxidase Is a Safe and Efficient Target for Substrate Reduction Therapy in a Mouse Model of Primary Hyperoxaluria Type I.

E. Salido, Sergio Luis-Lima, Cristina Martin-Higueras, 2016, Molecular therapy : the journal of the American Society of Gene Therapy.

Digenic Inheritance in Cystinuria Mouse Model

E. Salido, M. Palacín, V. Nunes, 2015, PloS one.

Evolutionary Divergent Suppressor Mutations in Conformational Diseases

E. Salido, A. Pey, Elisa Oppici, 2018, Genes.

In vivo CRISPR-Cas9 inhibition of hepatic LDH as treatment of primary hyperoxaluria

E. Salido, F. Prósper, M. E. Calleja-Cervantes, 2022, Molecular therapy. Methods & clinical development.

Association of Helicobacter pylori‐related Distal Gastric Cancer with the HLA Class II Gene DQB1*0602 and cagA+ Strains in a Southern European Population

E. Salido, J. Gisbert, Á. Lanas, 2005, Helicobacter.

Exploiting the passenger ACO1-deficiency arising from 9p21 deletions to kill T-cell lymphoblastic neoplasia cells.

E. Salido, K. Stamatakis, J. Fernández-Piqueras, 2019, Carcinogenesis.

ARID2 deficiency promotes tumor progression and is associated with higher sensitivity to chemotherapy in lung cancer

E. Salido, I. Varela, P. Crespo, 2021, Oncogene.

Role of low native state kinetic stability and interaction of partially unfolded states with molecular chaperones in the mitochondrial protein mistargeting associated with primary hyperoxaluria

E. Salido, J. M. Sanchez-Ruiz, A. Pey, 2011, Amino Acids.

Estimated Glomerular Filtration Rate in Renal Transplantation: The Nephrologist in the Mist

E. Salido, F. Gaspari, E. Porrini, 2015, Transplantation.

PrimPol, an Archaic Primase/Polymerase Operating in Human Cells

E. Salido, A. Reyes, L. Blanco, 2013, Molecular cell.

The Nucleocapsid protein triggers the main humoral immune response in COVID-19 patients

E. Salido, D. Gillespie, V. Smits, 2021, Biochemical and Biophysical Research Communications.

The PlA 2 Polymorphism of the Platelet Glycoprotein IIIA Gene as a Risk Factor for Acute Renal Allograft Rejection

E. Salido, A. Torres, D. Hernández, 1999 .

Cloning of the mouse steroid sulfatase (Sts) gene

E. Salido, L. Shapiro, X. M. Li, 1994 .

A missense mutation in Tbce causes progressive motor neuronopathy in mice

E. Salido, J. Jaubert, J. Guénet, 2002, Nature Genetics.

Vascular Damage and Kidney Transplant Outcomes: An Unfriendly and Harmful Link

E. Salido, A. Torres, J. Alonso-Titos, 2017, The American journal of the medical sciences.

Deciphering Tacrolimus‐Induced Toxicity in Pancreatic β Cells

E. Salido, E. Porrini, A. E. Rodríguez-Rodríguez, 2017, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Primary hyperoxaluria type 1

E. Salido, R. Wanders, M. Durán, 2020, Definitions.

The Role of Protein Denaturation Energetics and Molecular Chaperones in the Aggregation and Mistargeting of Mutants Causing Primary Hyperoxaluria Type I

E. Salido, A. Pey, D. Riverol, 2013, PloS one.

The consensus-based approach for gene/enzyme replacement therapies and crystallization strategies: the case of human alanine-glyoxylate aminotransferase.

E. Salido, J. M. Sanchez-Ruiz, A. Pey, 2014, The Biochemical journal.

Conformational dynamics is key to understanding loss-of-function of NQO1 cancer-associated polymorphisms and its correction by pharmacological ligands

Julian E. Fuchs, E. Salido, D. Timson, 2016, Scientific Reports.

Type 1 Diabetes Increases the Expression of Proinflammatory Cytokines and Adhesion Molecules in the Artery Wall of Candidate Patients for Kidney Transplantation

E. Salido, A. Torres, D. Hernández, 2012, Diabetes Care.

Prediction of left ventricular mass changes after renal transplantation by polymorphism of the angiotensin-converting-enzyme gene.

E. Salido, A. Torres, D. Hernández, 1997, Kidney international.

Site-to-site interdomain communication may mediate different loss-of-function mechanisms in a cancer-associated NQO1 polymorphism

Julian E. Fuchs, E. Salido, D. Timson, 2017, Scientific Reports.

University of Groningen Single molecule real time sequencing in ADTKD-MUC 1 allows complete assembly of the VNTR and exact positioning of causative mutations

E. Salido, R. Reinhardt, A. Ekici, 2018 .

Renal Disease in Obesity, Metabolic Syndrome and Diabesity

E. Salido, E. Porrini, M. Navarro-Díaz, 2018, Diabetic Nephropathy.

The lower limits for protein stability and foldability in primary hyperoxaluria type I.

E. Salido, A. Pey, Angel L. Pey, 2014, Biochimica et biophysica acta.

Counterintuitive structural and functional effects due to naturally occurring mutations targeting the active site of the disease‐associated NQO1 enzyme *

E. Salido, D. Kavan, P. Man, 2022, The FEBS journal.

Structural basis of the pleiotropic and specific phenotypic consequences of missense mutations in the multifunctional NAD(P)H:quinone oxidoreductase 1 and their pharmacological rescue

Athi N. Naganathan, E. Salido, P. Man, 2021, Redox biology.

Functional and Stability Effects of Ligand Binding

E. Salido, D. Timson, P. Man, 2019 .

Lack of prenatal testosterone surge in fetal rats exposed to alcohol: alterations in testicular morphology and physiology.

E. Salido, R. McGivern, E. Redei, 1988, Alcoholism, clinical and experimental research.

Iohexol plasma clearance, a simple and reliable method to measure renal function in conscious mice

E. Salido, F. Gaspari, E. Porrini, 2016, Pflügers Archiv - European Journal of Physiology.

Influence of vitamin D receptor genotype on bone mass changes after renal transplantation.

E. Salido, A. Torres, D. Hernández, 1996, Kidney international.

CRISPR/Cas9-mediated glycolate oxidase disruption is an efficacious and safe treatment for primary hyperoxaluria type I

E. Salido, F. Prósper, G. González-Aseguinolaza, 2018, Nature Communications.

Impact of metabolic syndrome on graft function and survival after cadaveric renal transplantation.

E. Salido, E. Porrini, A. Torres, 2006, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Vitamin D Receptor Gene Polymorphisms, Bone Mass, Bone Loss and Prevalence of Vertebral Fracture: Differences in Postmenopausal Women and Men

E. Salido, A. Torres, Armando Torres, 1999, Osteoporosis International.

Role of apolipoprotein E epsilon 4 allele on chronic allograft nephropathy after renal transplantation.

E. Salido, A. Torres, B. Marin, 2004, Transplantation proceedings.

Renal Failure Affects the Enzymatic Activities of the Three First Steps in Hepatic Heme Biosynthesis in the Acute Intermittent Porphyria Mouse

E. Salido, P. Harper, A. Fontanellas, 2012, PloS one.

Generation and characterization of human iPSC lines derived from a Primary Hyperoxaluria Type I patient with p.I244T mutation.

E. Salido, F. Prósper, G. González-Aseguinolaza, 2016, Stem cell research.

Generation of an induced pluripotent stem cell line (CIMAi001-A) from a compound heterozygous Primary Hyperoxaluria Type I (PH1) patient carrying p.G170R and p.R122* mutations in the AGXT gene.

E. Salido, F. Prósper, B. Beck, 2019, Stem Cell Research.

Circulating urokinase receptor as a cause of focal segmental glomerulosclerosis

E. Salido, M. Sarwal, M. Rastaldi, 2011, Nature Medicine.

Correction of Hyperoxaluria by Liver Repopulation With Hepatocytes in a Mouse Model of Primary Hyperoxaluria Type-1

E. Salido, Jinlan Jiang, C. Guha, 2008, Transplantation.

Plasma matrix metalloproteinase 9 as an early surrogate biomarker of advanced colorectal neoplasia.

E. Salido, D. Nicolás-Pérez, E. Quintero, 2016, Gastroenterologia y hepatologia.

Expression of DNA Damage Checkpoint Protein Hus1 in Epithelial Ovarian Tumors Correlates With Prognostic Markers

E. Salido, F. Rojo, J. De La Torre, 2008, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

Phosphorylation of Thr9 Affects the Folding Landscape of the N-Terminal Segment of Human AGT Enhancing Protein Aggregation of Disease-Causing Mutants

Athi N. Naganathan, E. Salido, J. Neira, 2022, Molecules.

Primary hyperoxaluria in a compound heterozygote infant

E. Salido, J. Mayordomo-Colunga, F. Santos, 2011, World journal of pediatrics : WJP.

Primary hyperoxaluria in an infant C ase report

E. Salido, J. Mayordomo-Colunga, F. Santos, 2011 .

Erratum to "A new HDV mouse model identifies mitochondrial antiviral signaling protein (MAVS) as a key player in IFN-β induction" [J Hepatol 67 (2017) 669-679].

E. Salido, M. Buti, G. González-Aseguinolaza, 2018, Journal of hepatology.