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Targeting HIF-1α Function in Cancer through the Chaperone Action of NQO1: Implications of Genetic Diversity of NQO1.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 5, p. 747, doi. 10.3390/jpm12050747
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- Publication type:
- Article
Small Molecule-Based Enzyme Inhibitors in the Treatment of Primary Hyperoxalurias.
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- Journal of Personalized Medicine, 2021, v. 11, n. 2, p. 74, doi. 10.3390/jpm11020074
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- Publication type:
- Article
Naturally-Occurring Rare Mutations Cause Mild to Catastrophic Effects in the Multifunctional and Cancer-Associated NQO1 Protein.
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- Journal of Personalized Medicine, 2020, v. 10, n. 4, p. 207, doi. 10.3390/jpm10040207
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- Publication type:
- Article
The Value of Mouse Models of Rare Diseases: A Spanish Experience.
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- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.583932
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- Publication type:
- Article
Treatment of early borderline lesions in low immunological risk kidney transplant patients: a Spanish multicenter, randomized, controlled parallel-group study protocol: the TRAINING study.
- Published in:
- 2022
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- Publication type:
- journal article
Role of gap junctions modulating hepatic vascular tone in cirrhosis.
- Published in:
- Liver International, 2014, v. 34, n. 6, p. 859, doi. 10.1111/liv.12446
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- Publication type:
- Article
The consensus-based approach for gene/enzyme replacement therapies and crystallization strategies: the case of human alanine-glyoxylate aminotransferase.
- Published in:
- Biochemical Journal, 2014, v. 462, n. 3, p. 453, doi. 10.1042/BJ20140250
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- Publication type:
- Article
Case Report: α-Spectrin Mutation Associated with αLELY Polymorphism Responsible for Hereditary Pyropoikilocytosis.
- Published in:
- 2022
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- Publication type:
- Case Study
Circulating urokinase receptor as a cause of focal segmental glomerulosclerosis.
- Published in:
- Nature Medicine, 2011, v. 17, n. 8, p. 952, doi. 10.1038/nm.2411
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- Publication type:
- Article
Low‐affinity immunoglobulin gamma Fc region receptor III‐B (FcγRIIIB, CD16B) deficiency in patients with blood and immune system disorders.
- Published in:
- British Journal of Haematology, 2021, v. 195, n. 5, p. 743, doi. 10.1111/bjh.17828
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- Publication type:
- Article
Transcriptomic rationale for synthetic lethality‐targeting ERCC1 and CDKN1A in chronic myelomonocytic leukaemia.
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- British Journal of Haematology, 2018, v. 182, n. 3, p. 373, doi. 10.1111/bjh.15408
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- Publication type:
- Article
Synergistic effect between chronic estrogen treatment and dha-enriched diet on Aβ burden in APPswe/PSEN1δe9 mice.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P365, doi. 10.1016/j.jalz.2015.06.268
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- Publication type:
- Article
A missense mutation in Tbce causes progressive motor neuronopathy in mice.
- Published in:
- Nature Genetics, 2002, v. 32, n. 3, p. 443, doi. 10.1038/ng1016
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- Publication type:
- Article
Splenic rupture in a plasma cell leukemia, mobilized with G-CSF for autologous stem cell transplant.
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- Journal of Clinical Apheresis, 2010, v. 25, n. 4, p. 223, doi. 10.1002/jca.20233
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- Publication type:
- Article
Large-volume-apheresis facilitates autologous transplantation of hematopoietic progenitors in poor mobilizer patients.
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- Journal of Clinical Apheresis, 2009, v. 24, n. 1, p. 12, doi. 10.1002/jca.20191
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- Publication type:
- Article
Apocrine carcinoma of the anogenital region. A case report including immunohistochemical and molecular study, discussion of differential diagnosis and a review of the literature.
- Published in:
- 2008
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- Publication type:
- Letter
Beta human papillomavirus as a facilitator in the initial phase but not a perpetuator of skin carcinogenesis.
- Published in:
- JEADV Clinical Practice, 2023, v. 2, n. 4, p. 958, doi. 10.1002/jvc2.221
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- Publication type:
- Article
Site-to-site interdomain communication may mediate different loss-of-function mechanisms in a cancer-associated NQO1 polymorphism.
- Published in:
- Scientific Reports, 2017, p. 44532, doi. 10.1038/srep44532
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- Publication type:
- Article
Erratum: Conformational dynamics is key to understanding loss-of-function of NQO1 cancer-associated polymorphisms and its correction by pharmacological ligands.
- Published in:
- Scientific Reports, 2016, p. 21939, doi. 10.1038/srep21939
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- Publication type:
- Article
Conformational dynamics is key to understanding loss-of-function of NQO1 cancer-associated polymorphisms and its correction by pharmacological ligands.
- Published in:
- Scientific Reports, 2016, p. 20331, doi. 10.1038/srep20331
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- Publication type:
- Article
Primary hyperoxaluria in a compound heterozygote infant.
- Published in:
- World Journal of Pediatrics, 2011, v. 7, n. 2, p. 173, doi. 10.1007/s12519-010-0214-z
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- Publication type:
- Article
Digenic Inheritance in Cystinuria Mouse Model.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0137277
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- Publication type:
- Article
Artery Wall Assessment Helps Predict Kidney Transplant Outcome.
- Published in:
- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0129083
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- Publication type:
- Article
The Role of Protein Denaturation Energetics and Molecular Chaperones in the Aggregation and Mistargeting of Mutants Causing Primary Hyperoxaluria Type I.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0071963
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- Publication type:
- Article
Renal Failure Affects the Enzymatic Activities of the Three First Steps in Hepatic Heme Biosynthesis in the Acute Intermittent Porphyria Mouse.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0032978
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- Publication type:
- Article
IMPLEMENTACIÓN DE LA PCR DIGITAL PARA EL DIAGNÓSTICO PRENATAL NO INVASIVO DE LA ENFERMEDAD DE CÉLULAS FALCIFORMES. ESTUDIO PILOTO.
- Published in:
- Anales de la Real Academia Nacional de Medicina, 2024, v. 141, n. 1, p. 21, doi. 10.32440/ar.2024.141.01.rev02
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- Publication type:
- Article
Primary hyperoxaluria.
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- Nefrologia, 2014, v. 34, n. 3, p. 398, doi. 10.3265/Nefrologia.pre2014.Jan.12335
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- Publication type:
- Article
Tissue profiling by nanogold-mediated mass spectrometry and artificial neural networks in the mouse model of human primary hyperoxaluria 1.
- Published in:
- Journal of Applied Biomedicine, 2014, v. 12, n. 2, p. 119, doi. 10.1016/j.jab.2013.12.001
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- Publication type:
- Article
Correction to: Spanish registry of hemoglobinopathies and rare anemias (REHem- AR): demographics, complications, and management of patients with β-thalassemia.
- Published in:
- 2024
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- Publication type:
- Correction Notice
Spanish registry of hemoglobinopathies and rare anemias (REHem-AR): demographics, complications, and management of patients with β-thalassemia.
- Published in:
- Annals of Hematology, 2024, v. 103, n. 5, p. 1525, doi. 10.1007/s00277-024-05694-z
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- Publication type:
- Article
Clinical, biological, and prognostic implications of SF3B1 co-occurrence mutations in very low/low- and intermediate-risk MDS patients.
- Published in:
- Annals of Hematology, 2021, v. 100, n. 8, p. 1995, doi. 10.1007/s00277-020-04360-4
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- Publication type:
- Article
Simultaneous analysis of the expression of 14 genes with individual prognostic value in myelodysplastic syndrome patients at diagnosis: WT1 detection in peripheral blood adversely affects survival.
- Published in:
- Annals of Hematology, 2012, v. 91, n. 12, p. 1887, doi. 10.1007/s00277-012-1538-7
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- Publication type:
- Article
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.
- Published in:
- Amino Acids, 2011, v. 41, n. 5, p. 1233, doi. 10.1007/s00726-010-0801-2
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- Publication type:
- Article
A Dynamic Core in Human NQO1 Controls the Functional and Stability Effects of Ligand Binding and Their Communication across the Enzyme Dimer.
- Published in:
- Biomolecules (2218-273X), 2019, v. 9, n. 11, p. 728, doi. 10.3390/biom9110728
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- Publication type:
- Article
Molecular Recognition of PTS-1 Cargo Proteins by Pex5p: Implications for Protein Mistargeting in Primary Hyperoxaluria.
- Published in:
- Biomolecules (2218-273X), 2015, v. 5, n. 1, p. 121, doi. 10.3390/biom5010121
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- Publication type:
- Article
Association ofHelicobacter pylori-related Distal Gastric Cancer with the HLA Class II Gene DQB1<sup>*</sup>0602 andcagA<sup>+</sup> Strains in a Southern European Population.
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- Helicobacter, 2005, v. 10, n. 1, p. 12, doi. 10.1111/j.1523-5378.2005.00287.x
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- Publication type:
- Article
A new locus for resistance to y-radiation-induces thymic lymphoma identified using inter-specific consomic and inter-specific recombinant congenic strains of mice.
- Published in:
- Oncogene, 2002, v. 21, n. 43, p. 6680, doi. 10.1038/sj.onc.1205846
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- Publication type:
- Article
CRISPR/Cas9-mediated glycolate oxidase disruption is an efficacious and safe treatment for primary hyperoxaluria type I.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07827-1
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- Publication type:
- Article
Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 2, p. 162, doi. 10.1038/ejhg.2012.139
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- Publication type:
- Article
The 372 T/C genetic polymorphism of TIMP-1 is associated with serum levels of TIMP-1 and survival in patients with severe sepsis.
- Published in:
- Critical Care, 2013, v. 17, n. 3, p. 1, doi. 10.1186/cc12739
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- Publication type:
- Article
The 372 T/C genetic polymorphism of TIMP-1 is associated with serum levels of TIMP-1 and survival in patients with severe sepsis.
- Published in:
- 2013
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- Publication type:
- journal article
Insights into the pathogenesis of primary hyperoxaluria type I from the structural dynamics of alanine:glyoxylate aminotransferase variants.
- Published in:
- FEBS Letters, 2024, v. 598, n. 4, p. 485, doi. 10.1002/1873-3468.14800
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- Publication type:
- Article
Characterization of the mouse Dazap1 gene encoding an RNAbinding protein that interacts with infertility factors DAZ and DAZL.
- Published in:
- BMC Genomics, 2001, v. 2, p. 1
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- Publication type:
- Article
Counterintuitive structural and functional effects due to naturally occurring mutations targeting the active site of the disease‐associated NQO1 enzyme.
- Published in:
- FEBS Journal, 2023, v. 290, n. 7, p. 1855, doi. 10.1111/febs.16677
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- Publication type:
- Article
Iohexol plasma clearance, a simple and reliable method to measure renal function in conscious mice.
- Published in:
- Pflügers Archiv: European Journal of Physiology, 2016, v. 468, n. 9, p. 1587, doi. 10.1007/s00424-016-1843-4
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- Publication type:
- Article
Impact of the MTHFR C677T polymorphism on colorectal cancer in a population with low genetic variability.
- Published in:
- International Journal of Colorectal Disease, 2013, v. 28, n. 9, p. 1187, doi. 10.1007/s00384-013-1644-6
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- Publication type:
- Article
Phosphorylation of Thr9 Affects the Folding Landscape of the N-Terminal Segment of Human AGT Enhancing Protein Aggregation of Disease-Causing Mutants.
- Published in:
- Molecules, 2022, v. 27, n. 24, p. 8762, doi. 10.3390/molecules27248762
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- Publication type:
- Article
Intestinal tumor suppression in Apc<sup>Min/+</sup> mice by prostaglandin D<sub>2</sub> receptor PTGDR.
- Published in:
- Cancer Medicine, 2014, v. 3, n. 4, p. 1041, doi. 10.1002/cam4.251
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- Publication type:
- Article
Differential expression of liver and kidney proteins in a mouse model for primary hyperoxaluria type I J. R. Hernández-Fernaud and E. Salido Proteome changes in primary hyperoxaluria.
- Published in:
- FEBS Journal, 2010, v. 277, n. 22, p. 4766, doi. 10.1111/j.1742-4658.2010.07882.x
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- Publication type:
- Article
Exploiting the passenger ACO1-deficiency arising from 9p21 deletions to kill T-cell lymphoblastic neoplasia cells.
- Published in:
- Carcinogenesis, 2020, v. 41, n. 8, p. 1113, doi. 10.1093/carcin/bgz185
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- Publication type:
- Article