Výsledky vyhledávání - "Tatjana Simonic"

Cloning and analysis of transcripts and genes encoding fish-specific proteins related to PrP

Autor: Bice Strumbo, Severino Ronchi, Jill E. Gready, Lorenzo Sangiorgio, Tatjana Simonic

Publikováno v: Fish Physiology and Biochemistry. 32:339-353

We report cloning and tissue expression of transcripts of a fourth fish-specific gene (SPRNB) encoding a prion protein (PrP)-related protein (Shadoo2) from two species, Cyprinus carpio (carp) and Danio rerio (zebrafish), as well as gene or partial tr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8eba6fa440afd342afd5449bbda3f6d9
https://doi.org/10.1007/s10695-006-9108-3

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Evolution of Vertebrate Genes Related to Prion and Shadoo Proteins—Clues from Comparative Genomic Analysis

Autor: Lars S. Jermiin, Marko Premzl, Tatjana Simonic, Jill E. Gready, Jennifer A. Marshall Graves

Publikováno v: Molecular Biology and Evolution. 21:2210-2231

Recent findings of new genes in fish related to the prion protein (PrP) gene PRNP, including our recent report of SPRN coding for Shadoo (Sho) protein found also in mammals, raise issues of their function and evolution. Here we report additional nove

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daeea2657ca90bb191edb588ab055547
https://doi.org/10.1093/molbev/msh245

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Probing the Active Site of l-Aspartate Oxidase by Site-Directed Mutagenesis: Role of Basic Residues in Fumarate Reduction

Autor: Armando Negri, Gabriella Tedeschi, Chiara Treu, Tatjana Simonic, Severino Ronchi, and Andrea Mattevi

Publikováno v: Biochemistry. 40:4738-4744

L-Aspartate oxidase is a very particular oxidase which behaves as a fumarate reductase in anaerobic conditions. Its primary and tertiary structures present remarkable similarity with the soluble fumarate reductase (FRD) from Shewanella frigidimarina

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec49895cab5904fc8675308438121324
https://doi.org/10.1021/bi002406u

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Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncation

Autor: Maria Luisa Tenchini, Pier Mannuccio Mannucci, Stefano Duga, Rosanna Asselta, Massimo Malcovati, Tatjana Simonic, Elena Santagostino, Paul L. F. Giangrande

Publikováno v: Europe PubMed Central
Scopus-Elsevier

Congenital afibrinogenemia is a rare autosomal recessive disorder characterized by the complete absence of plasma fibrinogen and by a bleeding tendency ranging from mild to moderately severe. Beside a deletion of the almost entire Aα-chain gene, onl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41f6f0ecda17b370ed37da1df79945af
https://doi.org/10.1182/blood.v96.7.2496.h8002496_2496_2500

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Missense mutations in the human β fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion

Autor: Maria Luisa Tenchini, Sirous Zeinali, Rosanna Asselta, Tatjana Simonic, Stefano Duga, Elena Santagostino, Massimo Malcovati, Pier Mannuccio Mannucci

Publikováno v: Blood. 95:1336-1341

Congenital afibrinogenemia is a rare autosomal recessive disorder characterized by bleeding that varies from mild to severe and by complete absence or extremely low levels of plasma and platelet fibrinogen. Although several mutations in the fibrinoge

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::dc74220a65b50d3a969f344edcf1f270
https://doi.org/10.1182/blood.v95.4.1336.004k16_1336_1341

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The intron-containing L3 ribosomal protein gene (RPL3): sequence analysis and identification of U43 and of two novel intronic small nucleolar RNAs

Autor: Stefano Duga, Massimo Malcovati, Rosanna Asselta, Severino Ronchi, Tatjana Simonic, Maria Luisa Tenchini

Publikováno v: Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1490:225-236

Isolation and sequencing of bovine and human intron-containing L3 ribosomal protein genes are here reported. They exhibit very similar organisation, both comprising 10 exons and nine introns. A polymorphic locus, involving a 19-bp deletion, was found

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ea6b1de803e71520464f977bc31339b
https://doi.org/10.1016/s0167-4781(99)00237-7

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Analysis of the 16S rRNA gene sequence of the coryneform bacterium associated with hyperkeratotic dermatitis of athymic nude mice and development of a PCR-based detection assay

Autor: Tatjana Simonic, Eugenio Scanziani, Stefano Duga, Luca Crippa, Maria Luisa Tenchini, A Gobbi, Rosanna Asselta

Publikováno v: Molecular and Cellular Probes. 12:191-199

By 16S rDNA sequencing the authors have characterized the coryneform bacteria associated with hyperkeratotic dermatitis (HD) of athymic nude mice isolated from six different outbreaks of the disease in Northern Italy. This analysis has allowed the au

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d9a866d765f13bf1f02d346ced1e617
https://doi.org/10.1006/mcpr.1998.0168

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cDNA cloning and expression of the flavoprotein d-aspartate oxidase from bovine kidney cortex

Autor: Stefano Duga, Tatjana Simonic, Massimo Malcovati, Armando Negri, Gabriella Tedeschi, Severino Ronchi, Maria Luisa Tenchini

Publikováno v: Scopus-Elsevier
Europe PubMed Central

The isolation and sequencing of the complete cDNA coding for a d-aspartate oxidase, as well as the overexpression of the recombinant active enzyme, are reported for the first time. This 2022 bp cDNA, beside the coding portion, comprises a 5´ untrans

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f10fd5e6e292be7a13a1d8a62b1c128a
https://doi.org/10.1042/bj3220729

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