Zobrazeno 1 - 10 of 16 pro vyhledávání: '"Batlle, Alcira Maria del C."'
1
Study of the relationship between variants of cyp2c9 enzyme and acute intermittent porphyria manifestation
Autor: Abou Assali, Lubna, Gordillo, Diego Miguel, Cerbino, Gabriela Nora, Varela, Laura Sabina, Batlle, Alcira Maria del C., Parera, Victoria Estela, Rossetti, Maria Victoria
Publikováno v: CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Objective: The manifestation of Acute Intermittent Porphyria (AIP) requires many factors. In situations of high demand of heme, initial enzyme of the pathway in parallel to P450 cytochrome genes (CYPs) is induced in response to drugs. It was suggeste
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3056::ace4ee356c07144c336e4fbae6412f8d
https://www.mnkjournals.com/journal/ijlrst/pdf/Volume_8_3_2019/10973.pdf
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3
Scavengers Protection of Cells Against ALA-based Photodynamic Therapy-induced Damage
Autor: Perotti, Carlos Hernan, Fukuda, Haydee, Casas, Adriana Gabriela, Batlle, Alcira Maria del C.
Publikováno v: CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
The exogenously stimulated formation of intracellularly generated protoporphyrin IX, a precursor of haem, is becoming one of the fastest developing areas in the field of photodynamic therapy (PDT). We tested the action of several free radical scaveng
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::678e3db4b3ccee9c15e5c5324fa8a413
https://doi.org/10.1007/s101030200033
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4
Porphyria Cutanea Tarda and HFE Gene Mutations in Argentina
Autor: Colombo, Federico Pablo, Martinez, Javier, Varela, Laura Sabina, Gerez, Esther Noemi, Mendez, Manuel, Batlle, Alcira Maria del C., Rossetti, Maria Victoria, Parera, Victoria Estela
Publikováno v: CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Aims: Porphyria Cutanea Tarda (PCT), the most common of porphyrias is triggered by several factors, including iron overload. Type I Hereditary Hemochromatosis is inherited as an autosomal recessive trait of the mutation p.C282Y or as a compound heter
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::13642777f5623cc8dd44be448ee68d8a
http://www.sciencedomain.org/abstract/2851
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5
Heme metabolism, oxidative and nitrosative markers in a mouse model of Hemochromatosis: Effect of Isoflurane, ethanol and 5-aminolevulinic acid
Autor: Buzaleh, Ana Maria, Moreno Carraledo, Maria, Mendez, Manuel, Batlle, Alcira Maria del C., Enriquez de Salamanca, Rafael, Moran Jimenez, Maria Jose
Publikováno v: CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Hereditary hemochromatosis (HH) is characterized by iron homeostasis alterations. Association between HH and Porphyria Cutanea Tarda has been reported. The aim was to characterize oxidative and nitrosative stress status and its relationship with heme
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e5495b56d994cbace2ac867677151468
http://www.bioinfopublication.org/viewhtml.php?artid=BIA0002063
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6
An odd case of heteroallelic Acute Intermittent Porphyria in the Argentinean Population
Autor: Piñeiro Pauwels, M. B., Gerez, Esther Noemi, Martinez, M. C., Melito, Viviana Alicia, Parera, Victoria Estela, Batlle, Alcira Maria del C., Rossetti, Maria Victoria
AIP is an acute liver disorder caused by a deficiency of porphobilinogen deaminase (PBGD) characterized by neuroabdominal symptoms. It is an autosomal dominant disease. However, homozygous dominant AIP (HD-AIP) have been described. In some cases eryt
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3498::22015fdc9b57eac732aa332040ebfad4
http://cellmolbiol.com/resume_online_papers.php?Id_Article=12719&Annee=2013
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7
Acute Intermittent Porphyria in a Man with Dual Enzyme Deficiencies
Autor: Victoria Estela Parera, L Tomassi, Alcira Batlle, Gabriela Nora Cerbino, Maria Victoria Rossetti, L Abou Assali, Laura Sabina Varela
Publikováno v: Case Reports in Genetics, Vol 2020 (2020)
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Case Reports in Genetics
Porphyrias are a heterogeneous group of metabolic disorders that result from the altered activity of specific enzymes of the hemebiosynthetic pathway and are characterized by accumulation of pathway intermediates. Porphyria cutanea tarda (PCT) is the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6794107689bd3b7240f20bf7580e646c
https://doi.org/10.1155/2020/8873219
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8
HAPLOTYPE ANALYSIS OF SINGLE NUCLEOTIDE POLYMORPHISMS OF CYP1A1 AND CYP1A2 AND ITS RELATIONSHIP WITH THE DEVELOPMENT OF PORPHYRIA CUTANEA TARDA
Autor: Lubna Abou Assali, Diego Miguel Gordillo, Alcira M. Del C. Batlle, Victoria Estela Parera, Laura Sabina Varela, María Victoria Rossett, Gabriela Nora Cerbino
Publikováno v: CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Objective: Porphyria Cutanea Tarda results from decrease hepatic uroporphyrinogen decarboxylase activity. There are twoprincipal types: sporadic or acquired and familial or hereditary Porphyria Cutanea Tarda. Hereditary Porphyria Cutanea Tarda is obs
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce8b0468dffc4251a4d3cdac57c906b6
https://doi.org/10.29111/ijlrst-2018-10961
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9
Effects of volatile anaesthetics on heme metabolism in a murine genetic model of Acute Intermittent Porphyria: A comparative study with other porphyrinogenic drugs
Autor: Johanna Romina Zuccoli, Leda Oliveri, Jimena Verónica Lavandera, María del Carmen Martínez, Silvina Fernanda Ruspini, Ana Maria Buzaleh, E. Gerez, Alcira Batlle
Publikováno v: CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Background: Acute Intermittent Porphyria (AIP) is an inherited disease produced by a deficiency of Porphobilinogen deaminase (PBG-D). The aim of this work was to evaluate the effects of Isoflurane and Sevoflurane on heme metabolism in a mouse genetic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acc36f0a681940c96ca69119569f5750
https://www.sciencedirect.com/science/article/abs/pii/S0304416518300552
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10
Indole acetic acid is responsible for protection against oxidative stress caused by drought in soybean plants: The role of heme oxygenase induction
Autor: Alcira Batlle, Guillermo O. Noriega, Manuel López Lecube, María L. Tomaro, Diego Mario Santa Cruz, Karina B. Balestrasse
Publikováno v: CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Objectives This study was focused on the role of indole acetic acid (IAA) in the defense against oxidative stress damage caused by drought in soybean plants and to elucidate whether heme oxygenase-1 (HO-1) and nitric oxide (NO) are involved in this m
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b802439c50935fb42dafe046757dd8db
https://doi.org/10.1179/1351000214y.0000000095
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