Zobrazeno 1 - 10 of 29 pro vyhledávání: '"Omar H. Pivetta"'
1
Suppression of COX-2, IL-1β and TNF-α expression and leukocyte infiltration in inflamed skin by bioactive compounds from Rosmarinus officinalis L
Autor: Marcelo L. Rodriguez-Puebla, Luciano A. Rigano, Adrián Alberto Vojnov, Omar H. Pivetta, Eduardo E. Cafferata, Eleonora S. Mengoni, Silvia R. Galliano, Gabriel Vichera, Sivia Moreno
Publikováno v: Fitoterapia. 82:414-421
In the present study, we evaluated the effects of extracts and purified compounds from fresh leaves of Rosmarinus officinalis L. Pretreatment with the major anti-inflammatory compounds, carnosic acid (CA) and carnosol (CS), inhibited phorbol 12-myris
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c6e1ac98a25506e5120cb53d43a9b1d
https://doi.org/10.1016/j.fitote.2010.11.023
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2
Correlation between synaptogenesis and the PTEN phosphatase expression in dendrites during postnatal brain development
Autor: Valeria Kowaljow, Héctor Carminatti, Martin Radrizzani, Roxana V. Costanzo, Omar H. Pivetta, Claudia Perandones
Publikováno v: Molecular Brain Research. 128:8-19
The PTEN (phosphatase and tensin homolog deleted on chromosome 10) tumor suppressor gene codifies a lipid inositol 3′-phosphatase that negatively regulates cell survival mediated by the phosphatidyl inositol 3′ kinase (PIP3-kinase)–protein kina
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::842f32ebfabd27aeea5a577475d61314
https://doi.org/10.1016/j.molbrainres.2004.05.021
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4
Differential expression of CPD1 during postnatal development in the mouse cerebellum
Autor: Marı́a Clara Di Tella, Héctor Carminatti, Guillermo J. Vila-Ortiz, Claudia Perandones, Eduardo G. Cafferata, Anatilde M. González-Guerrico, Tomás A. Santa-Coloma, Victor P. Idoyaga Vargas, Martin Radrizzani, Omar H. Pivetta
Publikováno v: Brain Research. 907:162-174
Several regulated mRNAs were detected by applying differential display to the mouse cerebellum during postnatal development. One cDNA fragment, referred to as CPD1 (GenBank U89345), was characterized and cloned. Northern blots showed maximum mRNA exp
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53cd87ab1a5b9be028197d6696c4e414
https://doi.org/10.1016/s0006-8993(01)02351-4
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6
Developmental regulation of Thy 1.2 rate of synthesis in the mouse cerebellum
Autor: Omar H. Pivetta, V. P. Idoyaga Vargas, Hector Carminatti, Martin Radrizzani
Publikováno v: Journal of Neuroscience Research. 42:220-227
Thy 1.2 is a well-known major cell surface glycoprotein of the central nervous system (CNS). However, the regulation of the expression of this molecule as well as its function are yet to be determined. To approach these problems we studied the synthe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93606241d7a504af175c39bff6951763
https://doi.org/10.1002/jnr.490420209
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7
CFTR gene analysis in Latin American CF patients: Heterogeneous origin and distribution of mutations across the continent
Autor: Omar H. Pivetta, Genoveva Keyeux, Maria C. Luna, Martín M. Pérez
BACKGROUND: Cystic Fibrosis (CF) is the most prevalent Mendelian disorder in European populations. Despite the fact that many Latin American countries have a predominant population of European-descent, CF has remained an unknown entity until recently
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2efc4825b1084201b2c86532f0e9ba13
https://www.sciencedirect.com/science/article/pii/S1569199306001196
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8
Mutations in CFTR gene and clinical correlation in Argentine patients with congenital bilateral absence of the vas deferens
Autor: Estrella M, Levy, Patricia, Granados, Vanesa, Rawe, Santiago Brugo, Olmedo, Maria C, Luna, Eduardo, Cafferata, Omar H, Pivetta
Publikováno v: Medicina. 64(3)
Congenital bilateral absence of the vas deferens (CBAVD) is a form of male infertility in which mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene have been identified. Here we identify different mutations of CFTR and th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2a611240c7c4177b33c680b1b90ad5cb
https://pubmed.ncbi.nlm.nih.gov/15239534
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9
Tyrosine kinase c-Src constitutes a bridge between cystic fibrosis transmembrane regulator channel failure and MUC1 overexpression in cystic fibrosis
Autor: Martin Radrizzani, Eduardo G. Cafferata, Guillermo C. Gallo, Florencia Marcucci, Omar H. Pivetta, Tomás A. Santa-Coloma, Rubén P. Laguens, Roberto R. Favaloro, Sergio V. Perrone, Anatilde M. González-Guerrico, Dieter C. Gruenert
Publikováno v: The Journal of biological chemistry. 277(19)
Cystic fibrosis (CF), a disease caused by mutations in the cystic fibrosis transmembrane regulator (CFTR) chloride channel, is associated in the respiratory system with the accumulation of mucus and impaired lung function. The role of the CFTR channe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a1d77cff2805e78e45325fd89f626c2
https://pubmed.ncbi.nlm.nih.gov/11872746
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10
NF-κB Activation Is Involved in Regulation of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) by Interleukin-1β
Autor: Eduardo G. Cafferata, Tomás A. Santa-Coloma, Omar H. Pivetta, Anatilde González Guerrico
Publikováno v: CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Interleukin-1 beta (IL-1b) regulates the levels of cystic fibrosis transmembrane conductance regulator (CFTR) mRNA and protein in the T84 human carcinoma cell line. Here, we studied the role of the transcription factor NF-kB in this regulation. Initi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dff2021d647d0dcc6b208cd73f3e93ec
https://www.sciencedirect.com/science/article/pii/S0021925819568466
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