Výsledky vyhledávání - "Batlle, Alcira Maria del C."

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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Cytochrome P450 expression in mouse brain: specific isoenzymes involved in Phase I metabolizing system of porphyrinogenic agents in both microsomes and mitochondria

Autor: Lavandera, Jimena Veronica, Ruspini, Silvina Fernanda, Batlle, Alcira Maria del C., Buzaleh, Ana Maria

Brain cytochrome P450 (CYP) metabolizes a variety of drugs to produce their pharmacological effects within the brain. We have previously observed that porphyrinogenic agents altered CYP levels in brain. The aim of this work was to further study the i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3498::e0de120f5abfa4cc9ed09d7ff3aa9cc2
http://www.nrcresearchpress.com/doi/abs/10.1139/bcb-2014-0088?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub=pubmed&#.WA5IZfnhCJA

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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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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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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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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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