Search Results - "Del Batlle, A M"
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ALA and ALA hexyl ester in free and liposomal formulations for the photosensitisation of tumour organ cultures
Published in British journal of cancer (04-03-2002)“…In spite of the wide range of tumours successfully treated with 5-aminolevulinic acid mediated photodynamic therapy, the fact that 5-aminolevulinic acid has…”
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2
Functional associations of genetic variants involved in the clinical manifestation of erythropoietic protoporphyria in the Argentinean population
Published in Journal of the European Academy of Dermatology and Venereology (01-06-2013)“…Background Combined inheritance of genetic variants in ferrochelatase gene (FECH) are implicated in clinical manifestation of Erythropoietic Protoporphyria…”
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3
Comparative effect of ALA derivatives on protoporphyrin IX production in human and rat skin organ cultures
Published in British Journal of Cancer (01-07-1999)“…Samples of human and rat skin in short-term organ culture exposed to ALA or a range of hydrophobic derivatives were examined for their effect on the…”
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4
Tissue distribution and kinetics of endogenous porphyrins synthesized after topical application of ALA in different vehicles
Published in British Journal of Cancer (01-09-1999)“…The use of 5-aminolaevulinic acid (ALA) is gaining increasing attention for photosensitization in photodynamic therapy of superficially localized tumours. The…”
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5
The very first description of a patient with hepatoerythropoietic porphyria in Argentina. Biochemical and molecular studies
Published in Cellular and molecular biology (Noisy-le-Grand, France) (16-02-2009)“…Hepatoerythropoietic Porphyria (HEP) is the rare homozygous form of Porphyria Cutanea Tarda (PCT). It is characterized clinically by the early onset of severe…”
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6
Induction of hepatic aminolevulinate acid synthetase activity by isoflurane in a genetic model for erythropoietic protoporphyria
Published in Cellular and molecular biology (Noisy-le-Grand, France) (16-02-2009)“…Erythropoietic Protoporphyria (EPP) is an inherited deficiency of ferrochelatase, the last enzyme of the heme pathway. Under general anaesthesia, some patients…”
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7
Purification and properties of coproporphyrinogenase
Published in Biochemical journal (01-12-1965)“…1. Coproporphyrinogenase has been prepared from rat-liver mitochondria and its properties have been studied. The isoelectric point was found to be around pH5.0…”
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8
beta-Carotene partially prevents the damage induced by 1,4-dimethylaminoazobenzene in mice
Published in European journal of cancer prevention (01-08-1998)“…Hepatocarcinogenesis (HC) induced by various carcinogens such as 1,4-dimethylaminoazobenzene (DAB) is a multistep and complex process. The anticancer efficacy…”
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9
Regulatory role of ALA-S and ALA-D in a haem-deficient mutant of Saccharomyces cerevisiae
Published in Cellular and molecular biology (Noisy-le-Grand, France) (01-06-1998)“…The biochemical characteristics of a haem-deficient mutant strain B231 of Saccharomyces cerevisiae isolated from D273-10B strain are described. B231 strain…”
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10
Porphyrins, porphyrias, cancer and photodynamic therapy--a model for carcinogenesis
Published in Journal of photochemistry and photobiology. B, Biology (01-09-1993)“…Porphyrins are the only and most powerful photosensitizers synthesized internally. To understand better the involvement of porphyrins in photosensitization…”
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11
Familial Porphyria Cutanea Tarda: Characterization of Seven Novel Uroporphyrinogen Decarboxylase Mutations and Frequency of Common Hemochromatosis Alleles
Published in American journal of human genetics (01-11-1998)“…Familial porphyria cutanea tarda (f-PCT) results from the half-normal activity of uroporphyrinogen decarboxylase (URO-D). Heterozygotes for this autosomal…”
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12
Acute intermittent porphyria: Biochemical and clinical analysis in the Argentinean population
Published in Clinica chimica acta (01-10-1999)“…Acute intermittent porphyria (AIP) is the most common type of hepatic acute porphyria. In this work, we have analyzed the biochemical data of all Argentinean…”
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13
Enhancement of aminolevulinic acid based photodynamic therapy by adriamycin
Published in Cancer letters (16-12-1997)“…This paper reports on studies that evaluate the interaction between δ-aminolevulinic acid (ALA)-based photodynamic therapy (PDT) and adriamycin (ADM) in an…”
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14
Identification and characterization of two novel mutations that produce acute intermittent porphyria: A 3-base deletion (841-843delGGA) and a missense mutation (T35M)
Published in Human mutation (01-10-2000)“…A partial deficiency of Porphobilinogen deaminase (PBGD) is responsible for acute intermittent porphyria (AIP). AIP is inherited in an autosomal dominant…”
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Two new mutations (H106P and L178V) in the protoporphyrinogen oxidase gene in Argentinean patients with variegate porphyria
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16
Hepatic enzymatic metabolism alterations and oxidative stress during the onset of carcinogenesis: protective role of alpha-tocopherol
Published in European journal of cancer prevention (01-02-1998)“…Oxidants play a role in several stages of carcinogenesis. A high antioxidant capacity is expected to protect 'initiated' cells from excessive oxidant toxicity…”
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17
Metabolic changes in the heme pathway driven by cyclophosphamide treatment in mice
Published in Cellular and molecular biology (Noisy-le-Grand, France) (01-02-1997)“…In previous work we found a 30% increase in the effectiveness of the photodynamic treatment of cancer when combined with the administration of cyclophosphamide…”
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The role of ALA-S and ALA-D in regulating porphyrin biosynthesis in a normal and a HEM R+ mutant strain of Saccharomyces cerevisiae
Published in Yeast (Chichester, England) (01-02-1993)“…Catabolite repression and derepression on delta-aminolevulinate synthase (ALA-S) and delta-aminolevulinate dehydratase (ALA-D) in a normal yeast strain, D27,…”
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19
STZ-induced diabetes in mice and heme pathway enzymes. Effect of allylisopropylacetamide and α-tocopherol
Published in Chemico-biological interactions (14-04-1995)“…A frequent coexistence of diabetes and porphyria disease has been reported. Under normal conditions, porphyrin biosynthesis is well regulated to only form the…”
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20
Identification and characterization of hydroxymethylbilane synthase mutations causing acute intermittent porphyria: Evidence for an ancestral founder of the common G111R mutation
Published in American journal of medical genetics (08-10-1999)“…Acute intermittent porphyria (AIP), the most common hepatic porphyria, results from the half‐normal activity of hydroxymethylbilane synthase (HMB‐synthase; EC…”
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