Search Results - "Mori, MA"

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  1. 1

    Does radiomics play a role in the diagnosis, staging and re-staging of gastroesophageal junction adenocarcinoma? by Mori, Martina, Palumbo, Diego, De Cobelli, Francesco, Fiorino, Claudio

    Published in Updates in surgery (01-02-2023)
    “…Radiomics is an emerging field of investigation in medicine consisting in the extraction of quantitative features from conventional medical images and…”
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    Adipose tissue mitochondrial dysfunction triggers a lipodystrophic syndrome with insulin resistance, hepatosteatosis, and cardiovascular complications by Vernochet, Cecile, Damilano, Federico, Mourier, Arnaud, Bezy, Olivier, Mori, Marcelo A., Smyth, Graham, Rosenzweig, Anthony, Larsson, Nils‐Göran, Kahn, C. Ronald

    Published in The FASEB journal (01-10-2014)
    “…Mitochondrial dysfunction in adipose tissue occurs in obesity, type 2 diabetes, and some forms of lipodystrophy, but whether this dysfunction contributes to or…”
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    Anthelmintic effects of a cationic toxin from a South American rattlesnake venom by Dal Mas, C., Moreira, J.T., Pinto, S., Monte, G.G., Nering, M.B., Oliveira, E.B., Gazarini, M.L., Mori, M.A., Hayashi, M.A.F.

    Published in Toxicon (Oxford) (15-06-2016)
    “…Despite the unquestionable importance of the highly cationic feature of several small polypeptides with high content of positively charged amino acids for…”
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    Reduced Nerve Injury-Induced Neuropathic Pain in Kinin B1 Receptor Knock-Out Mice by Ferreira, Juliano, Beirith, Alessandra, Mori, Marcelo A. S, Araujo, Ronaldo C, Bader, Michael, Pesquero, Joao B, Calixto, Joao B

    Published in The Journal of neuroscience (02-03-2005)
    “…Injury to peripheral nerves often results in a persistent neuropathic pain condition that is characterized by spontaneous pain, allodynia, and hyperalgesia…”
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    Long-term treatment with fish oil prevents memory impairments but not hippocampal damage in rats subjected to transient, global cerebral ischemia by Fernandes, Juliana S, Mori, Marco A, Ekuni, Roberta, Oliveira, Rúbia Maria W, Milani, Humberto

    Published in Nutrition research (New York, N.Y.) (01-11-2008)
    “…Abstract Cerebral ischemia leads to neurodegeneration and cognitive impairment. Fish oil (FO) constitutes a rich dietary source of ω -3 polyunsaturated fatty…”
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    Comparative study of three diagnostic approaches (FISH, STRs and MLPA) in 30 patients with 22q11.2 deletion syndrome by Fernández, L, Lapunzina, P, Arjona, D, López Pajares, I, García-Guereta, L, Elorza, D, Burgueros, M, De Torres, ML, Mori, MA, Palomares, M, García-Alix, A, Delicado, A

    Published in Clinical genetics (01-10-2005)
    “…The 22q11.2 deletion syndrome is commonly diagnosed using fluorescence in situ hybridization (FISH) with commercial probes. The chromosomal breakpoints and…”
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  12. 12

    Kinin B1 and B2 receptor deficiency protects against obesity induced by a high-fat diet and improves glucose tolerance in mice by Morais, Rafael L, Silva, Elton D, Sales, Vicência M, Filippelli-Silva, Rafael, Mori, Marcelo A, Bader, Michael, Pesquero, João B

    Published in Diabetes, metabolic syndrome and obesity (01-01-2015)
    “…The kallikrein-kinin system is well known for its role in pain and inflammation, and has been shown recently by our group to have a role also in the regulation…”
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  13. 13

    Macrocephaly-cutis marmorata telangiectatica congenita: Report of six new patients and a review by Lapunzina, Pablo, Gairí, Alba, Delicado, Alicia, Mori, M. Angeles, Torres, M. Luisa de, Goma, Anton, Navia, Marcelo, Pajares, Isidora López

    “…We report on six additional patients with macrocephaly‐cutis marmorata telangiectatica congenita (M‐CMTC; MIM 602501) and review the literature. This syndrome…”
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    A prenatally diagnosed patient with full monosomy 21: Ultrasound, cytogenetic, clinical, molecular, and necropsy findings by Mori, María A., Lapunzina, Pablo, Delicado, Alicia, Núñez, Guillermo, Rodríguez, José I., de Torres, María L., Herrero, Francisco, Valverde, Eva, López‐Pajares, Isidora

    “…We report on a patient with a full monosomy 21 (FM21) prenatally diagnosed in cord fetal blood, and subsequently confirmed in other tissues. Subtle chromosomal…”
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    Activation of microsomal epoxide hydrolase by interaction with cytochromes P450: kinetic analysis of the association and substrate-specific activation of epoxide hydrolase function by Taura, Ken-ichiro, Yamada, Hideyuki, Naito, Eri, Ariyoshi, Noritaka, Mori, Masa-aki, Oguri, Kazuta

    Published in Archives of biochemistry and biophysics (15-06-2002)
    “…The kinetics of the association between cytochrome P450 (P450) and microsomal epoxide hydrolase (mEH) was studied by means of resonant mirror based on the…”
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    Euchromatic variant 16p+. Implications in prenatal diagnosis by López Pajares, I., Villa, O., Salido, M., Mori, M. A., Gonzalez, A., Lapunzina, P., De Torres, M. L., Vallcorba, I., Palomares, M., Fernández, L., Delicado, A.

    Published in Prenatal diagnosis (01-06-2006)
    “…Background Euchromatic imbalances at the cytogenetic level are usually associated with phenotypic consequences. Among the exceptions are euchromatic variants…”
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    Short Report: Comparative study of three diagnostic approaches (FISH, STRs and MLPA) in 30 patients with 22q11.2 deletion syndrome by Fernández, L, Lapunzina, P, Arjona, D, I López Pajares, García-Guereta, L, Elorza, D, Burgueros, M, ML De Torres, Mori, MA, Palomares, M, García-Alix, A, Delicado, A

    Published in Clinical genetics (01-10-2005)
    “…The 22q11.2 deletion syndrome is commonly diagnosed using fluorescence in situ hybridization (FISH) with commercial probes. The chromosomal breakpoints and…”
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    Journal Article
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    Prevalencia y distribución geográfica del síndrome de Wolf-Hirschhorn en España by Málaga-Diéguez, I, Lapunzina, P, Graña Barreiro, Natalia, Bel Fenellos, María Cristina, Mori, Xana da Silva, Mori, María de los Ángeles, Blanco Lago, Raquel, Nevado Blanco, Julián

    “…BACKGROUND // Wolf-Hirschhorn syndrome is a rare disease of genetic origin caused by the deletion of the distal end of chromosome 4, including at least the…”
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