Search Results - "Mori, MA"
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Does radiomics play a role in the diagnosis, staging and re-staging of gastroesophageal junction adenocarcinoma?
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
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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A case report--intrahepatic arterial infusion with CDDP and S-1 administration can elicit long-term survival for the patient with recurrenced intrahepatic cholangiocarcinoma after resection
Published in Gan to kagaku ryoho (01-11-2010)“…To cure intrahepatic cholangiocarcinoma (ICC), only a surgical resection is the potential treatment at present. However, recurrence tumors in residual liver…”
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Comparing Performances of Predictive Models of Toxicity after Radiotherapy for Breast Cancer Using Different Machine Learning Approaches
Published in Cancers (25-02-2024)“…Different ML models were compared to predict toxicity in RT on a large cohort (n = 1314). The endpoint was RTOG G2/G3 acute toxicity, resulting in 204/1314…”
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Dynamic changes in DICER levels in adipose tissue control metabolic adaptations to exercise
Published in Proceedings of the National Academy of Sciences - PNAS (22-09-2020)“…DICER is a key enzyme in microRNA (miRNA) biogenesis. Here we show that aerobic exercise training up-regulates DICER in adipose tissue of mice and humans. This…”
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Activation of kinin receptor B1 limits encephalitogenic T lymphocyte recruitment to the central nervous system
Published in Nature medicine (01-07-2009)“…Previous proteomic and transcriptional analyses of multiple sclerosis lesions revealed modulation of the renin-angiotensin and the opposing kallikrein-kinin…”
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Anthelmintic effects of a cationic toxin from a South American rattlesnake venom
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
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
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
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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Kinin B1 and B2 receptor deficiency protects against obesity induced by a high-fat diet and improves glucose tolerance in mice
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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Macrocephaly-cutis marmorata telangiectatica congenita: Report of six new patients and a review
Published in American journal of medical genetics. Part A (15-09-2004)“…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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Cytochrome P450 1A1 (CYP1A1) Inhibitor α-Naphthoflavone Interferes with UDP-Glucuronosyltransferase (UGT) Activity in Intact but Not in Permeabilized Hepatic Microsomes from 3-Methylcholanthrene-Treated Rats: Possible Involvement of UGT–P450 Interactions
Published in Biological & pharmaceutical bulletin (2004)“…The effects of cytochrome P450 (P450, CYP) ligands and permeabilization of microsomes on 3-hydroxybenzo(a)pyrene [3-OH-B(a)P] glucuronidation mediated by rat…”
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A prenatally diagnosed patient with full monosomy 21: Ultrasound, cytogenetic, clinical, molecular, and necropsy findings
Published in American journal of medical genetics. Part A (15-05-2004)“…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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Kinin B1 Receptor Deficiency Leads to Leptin Hypersensitivity and Resistance to Obesity
Published in Diabetes (New York, N.Y.) (01-06-2008)“…Kinin B 1 Receptor Deficiency Leads to Leptin Hypersensitivity and Resistance to Obesity Marcelo A. Mori 1 , Ronaldo C. Araújo 1 2 , Felipe C.G. Reis 1 ,…”
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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
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
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
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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Prevalencia y distribución geográfica del síndrome de Wolf-Hirschhorn en España
Published in Revista española de salud pública (2022)“…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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