Search Results - "GONZALEZ, Fernando A"

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  1. 1

    Soluble antigen arrays provide increased efficacy and safety over free peptides for tolerogenic immunotherapy by Firdessa-Fite, Rebuma, Johnson, Stephanie N, Bechi Genzano, Camillo, Leon, Martin A, Ku, Amy, Ocampo Gonzalez, Fernando A, Milner, Joshua D, Sestak, Joshua O, Berkland, Cory, Creusot, Remi J

    Published in Frontiers in immunology (12-06-2024)
    “…Autoantigen-specific immunotherapy using peptides offers a more targeted approach to treat autoimmune diseases, but clinical implementation has been…”
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  2. 2

    Well-differentiated liposarcoma primary from thymic stroma: Case report and literature review by Furlan, Karina, Miller, Ira, Rohra, Prih, Mir, Fatima, Ocampo Gonzalez, Fernando A., Gattuso, Paolo

    Published in Experimental and molecular pathology (01-10-2020)
    “…Primary liposarcoma of thymic stroma is an exceptionally rare tumor. Histological findings are often definitive for diagnosis, however due to the variability…”
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    Effect of the Paris system for reporting urinary cytology with histologic follow‐up by Rohra, Prih, Ocampo Gonzalez, Fernando A., Yan, Lei, Mir, Fatima, Furlan, Karina, Basu, Sanjib, Barua, Animesh, Cheng, Lin, Park, Ji‐Weon

    Published in Diagnostic cytopathology (01-06-2021)
    “…Background The Paris system (TPS) for Reporting Urinary Cytology provides a standardized reporting system whose main focus is the diagnosis of high‐grade…”
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    Characterization of deletional and non-deletional alpha globin variants in a large cohort from Spain between 2009 and 2014 by de la Fuente-Gonzalo, Félix, Nieto, Jorge M., Villegas, Ana, González, Fernando A., Martínez, Rafael, Ropero, Paloma

    Published in Annals of hematology (01-07-2019)
    “…The hemoglobinopathies are a group of disorders passed down through families (inherited) in which there is abnormal production or structure of the hemoglobin…”
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  5. 5

    Nondeletional α-Thalassemia: Two New Mutations on the α2 Gene by Ropero, Paloma, Arbeteta, Jaime, Nieto, Jorge M., González, Fernando A., González, Beatriz, Villegas, Ana, Benavente, Celina

    Published in Hemoglobin (02-01-2020)
    “…About 10.0% of α-thalassemia (α-thal) cases are due to point mutations, small deletions, or insertions of one or more bases on the α genes that can alter mRNA…”
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    Hb Cervantes, Hb Marañón, Hb La Mancha and Hb Goya: Description of 4 new haemoglobinopathies by de la Fuente-Gonzalo, Félix, Nieto, Jorge M., Ricard, Pilar, Anguita, Javier, Martínez, Rosalina, Cervera, Aurea, Villegas, Ana, González, Fernando A., Ropero, Paloma

    Published in Clinical biochemistry (01-07-2015)
    “…α-thalassemias are caused by a deficiency in or absence of synthesis of the α-chain of haemoglobin (Hb). In contrast, structural haemoglobinopathies are due to…”
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    Hemoglobin Le Lamentin in the province of Albacete, Spain: Discovery of 32 cases by Martínez-López, Rosalina, Ropero, Paloma, Ballesteros Gallar, Cristina, Romero Román, Carlos, de la Fuente-Gonzalo, Félix, M. Nieto, Jorge, Navarro Casado, Laura, González, Fernando A.

    Published in Clinical biochemistry (01-03-2017)
    “…Hemoglobin Le Lamentin (α20(B1)His→Gln) is a ubiquitous variant that has been previously described in a small number of isolated patients. We report the…”
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    Hb Cibeles [α2 CD25(B6) (Gly → Asp)]: a novel alpha chain variant causing alpha-thalassemia by de la Fuente-Gonzalo, Félix, Nieto, Jorge M., Vinuesa, Lara, Sevilla, Julián, Díaz-Mediavilla, Joaquín, Villegas, Ana, González, Fernando A., Ropero, Paloma

    Published in International journal of hematology (01-12-2014)
    “…Thalassemias are the most frequent monogenic disorders around the world and are a serious health problem in areas with a high incidence. Thalassemias are…”
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    Different forms of Hb Le Lamentin. An unexpected finding in Hba1c quantification by Martínez-López, Rosalina, de la Fuente-Gonzalo, Félix, Nieto, Jorge M., Gallar, Cristina Ballesteros, Román, Carlos Romero, Villegas, Ana, González, Fernando A., Martínez, Rafael, Casado, Laura Navarro, Ropero, Paloma

    Published in Clinical biochemistry (01-01-2016)
    “…Glycated hemoglobin (HbA1c) is accepted as the most trusted marker for monitoring patients with diabetes mellitus. Ion-exchange high-performance liquid…”
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  12. 12

    Plasmablastic Lymphoma Associated with Adjacent Mature Plasma Cell Population Exhibiting Opposite Light Chain Restriction by Ocampo Gonzalez, Fernando A., Mahon, Brett, Miller, Ira, Furlan, Karina, Ward, Nicholas

    Published in Case reports in pathology (28-12-2020)
    “…Plasmablastic lymphoma (PBL) is an aggressive high-grade B cell lymphoma, considered a variant of diffuse large B cell lymphoma with approximately 75%…”
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  13. 13

    P2X7 nucleotide receptor activation enhances IFNγ‐induced type II nitric oxide synthase activity in BV‐2 microglial cells by Gendron, Fernand‐Pierre, Chalimoniuk, Malgorzata, Strosznajder, Joanna, Shen, Siming, González, Fernando A., Weisman, Gary A., Sun, Grace Y.

    Published in Journal of neurochemistry (01-10-2003)
    “…Under normal and pathological conditions, brain cells release nucleotides that regulate a wide range of cellular responses due to activation of P2 nucleotide…”
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    P2Y2 receptors activate neuroprotective mechanisms in astrocytic cells by Chorna, Nataliya E., Santiago‐Pérez, Laura I., Erb, Laurie, Seye, Cheikh I., Neary, Joseph T., Sun, Grace Y., Weisman, Gary A., González, Fernando A.

    Published in Journal of neurochemistry (01-10-2004)
    “…Mechanical or ischemic trauma to the CNS causes the release of nucleotides and other neurotransmitters into the extracellular space. Nucleotides can activate…”
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    Association between hemoglobin Groene Hart and hemoglobin J-Paris-I: First case in Spain by de la Fuente-Gonzalo, Félix, Ropero, Paloma, Martínez-Nieto, Jorge, Villegas, Ana, González, Fernando A., Díaz-Mediavilla, Joaquín

    Published in Medicina clinica (09-03-2015)
    “…Thalassemias are the most frequent monogenic disorder around the world. α-Thalassemias are due to a deficiency of synthesis in the alpha-globin chain of the…”
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    Heterozygosity for deletion of hypersensitive site 3 in the human locus control region has an unexpected minor effect on red cell phenotype by Nieto, Jorge M, Villegas, Ana, De La Fuente-Gonzalo, Felix, González, Fernando A, Ropero, Paloma

    Published in Journal of human genetics (01-10-2014)
    “…The locus control region (LCR) is a genetic region that regulates the expression of the β-globin locus (HBB locus). This region is composed of several DNase I…”
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    Functional P2Y2 nucleotide receptors mediate uridine 5'-triphosphate-induced intimal hyperplasia in collared rabbit carotid arteries by SEYE, Cheikh I, QIONGMAN KONG, ERB, Laurie, GARRAD, Richard C, KRUGH, Brent, MEIFANG WANG, TURNER, John T, STUREK, Michael, GONZALEZ, Fernando A, WEISMAN, Gary A

    Published in Circulation (New York, N.Y.) (19-11-2002)
    “…Extracellular uridine 5'-triphosphate (UTP) induces mitogenic activation of smooth muscle cells (SMCs) through binding to P2Y2 nucleotide receptors. P2Y2…”
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    Mechanisms of P2X7 receptor-mediated ERK1/2 phosphorylation in human astrocytoma cells by Gendron, Fernand-Pierre, Neary, Joseph T, Theiss, Patty M, Sun, Grace Y, Gonzalez, Fernando A, Weisman, Gary A

    “…Astrocytes are involved in normal and pathological brain functions, where they become activated and undergo reactive gliosis. Astrocytes have been shown to…”
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    Role of the Nitro Functionality in the DNA Binding of 3-Nitro-10-methylbenzothiazolo[3,2-a]quinolinium Chloride by Colón, Iris Gisela, González, Fernando A, Cordero, Marisol, Zayas, Beatriz, Velez, Christian, Cox, Osvaldo, Kumar, Ajay, Alegría, Antonio E

    Published in Chemical research in toxicology (01-09-2008)
    “…Interest in DNA binding drugs has increased in recent years due to their importance in the treatment of genome-related diseases, like cancer. A new family of…”
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