Výsledky vyhledávání - "M. Gomez Lira"

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

PTCH1 gene haplotype association with basal cell carcinoma after transplantation

Autor: Carlo Rugiu, Alberto Forni, Anna Belloni Fortina, Eliana Gotti, A. Begnini, Giampiero Girolomoni, Stefano Piaserico, Giovanni Malerba, M. Gomez Lira, Luigino Boschiero, Alberto Turco, C. Cascone, A. Brunello, Luigi Naldi, G. Tessari

Publikováno v: British Journal of Dermatology. 163:364-370

Summary Background Basal cell carcinoma (BCC) is 10 times more frequent in organ transplant recipients (OTRs) than in the general population. Factors in OTRs conferring increased susceptibility to BCC include ultraviolet radiation exposure, immunosup

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1ca04762e19a41526980cdc8bdcd3df8
https://doi.org/10.1111/j.1365-2133.2010.09776.x

Zobrazit plný text záznamu

Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation

Autor: Luigino Boschiero, Stefano Piaserico, S. Mazzola, Carlo Rugiu, Alberto Turco, Luigi Naldi, Giampiero Girolomoni, M. Gomez Lira, Gianpaolo Tessari, Giovanni Malerba, M. Ortombina, G. Remuzzi, Alberto Forni

Publikováno v: British Journal of Dermatology. 157:49-57

Summary Background Overexpression of cyclooxygenase-2 (COX-2), resulting in excessive prostaglandin production, has been observed in human epidermal keratinocytes after ultraviolet B injury, in squamous cell skin carcinoma (SCC), in actinic keratoses

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8acb4744f697ca6d61df1e2668167ce
https://doi.org/10.1111/j.1365-2133.2007.07921.x

Zobrazit plný text záznamu

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Prevalence of Dementia and Apolipoprotein E Genotype Distribution in the Elderly of Buttapietra, Verona Province, Italy

Autor: S. Filipponi, Alessandro Salviati, E. Fincati, L. De Togni, M. D. Benedetti, M. Gomez Lira, G. Stenta, M. Manfredi, M. Pampanin, Nicolo' Rizzuto, G. Danti

Publikováno v: Neuroepidemiology. 21:74-80

We investigated the prevalence of dementia and the apolipoprotein E (APOE) genotype distribution in the elderly of Buttapietra, a village near Verona, Italy. All residents over the age of 74 (n = 238), including those who were institutionalized, were

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c2efce01198d2d5d23c366c521a2f22
https://doi.org/10.1159/000048620

Zobrazit plný text záznamu

Substitution of an aspartic acid for glycine 700 in the alpha 2(I) chain of type I collagen in a recurrent lethal type II osteogenesis imperfecta dramatically affects the mineralization of bone

Autor: L Cohen-Solal, M Mottes, M Gomez Lira, L Zylberberg, A Sangalli

Publikováno v: Journal of Biological Chemistry. 269:14751-14758

We describe a new dominant mutation of type I collagen responsible for a recurrent lethal osteogenesis imperfecta. Dermal cultured fibroblasts of the proband produced both normal and overmodified type I collagen chains. Previous results (Cohen-Solal,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::723e8499a091846053e21812ffc1f79f
https://doi.org/10.1016/s0021-9258(17)36689-9

Zobrazit plný text záznamu

Paternal mosaicism for a COL1A1 dominant mutation (α1 Ser-415) causes recurrent osteogenesis imperfecta

Autor: Maurizia Valli, M. Gomez Lira, G. Scarano, Fortunato Lonardo, Pier Franco Pignatti, Giuseppe Cetta, Monica Mottes, Antonella Forlino

Publikováno v: Human Mutation. 2:196-204

We describe a dominant point mutation in the COL1A1 gene causing extremely severe osteogenesis imperfecta (OI type II/III) which was detected in the dermal fibroblasts of a proband, diagnosed by ultrasonography at 24 weeks of gestation. Type I collag

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b33400a53c28a32cf7e1519faaf1f180
https://doi.org/10.1002/humu.1380020308

Zobrazit plný text záznamu

A de novo G to T transversion in a pro-alpha 1 (I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain

Autor: Giuseppe Cetta, A Sangalli, M Gomez Lira, P F Pignatti, F Antoniazzi, Maurizia Valli, Ruggero Tenni, M. Mottes, Antonio Rossi

Publikováno v: Journal of Biological Chemistry. 266:1872-1878

Cultured fibroblasts from a patient affected with a moderate form of osteogenesis imperfecta were defective for the synthesis of type I collagen molecules; about half of the alpha 1(I) chains contained a cysteine residue in the triple helical domain

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::16a7cee0e26a1380beafa6979c09c676
https://doi.org/10.1016/s0021-9258(18)52374-7

Zobrazit plný text záznamu

Two new highly polymorphic markers in the 3' UTR region of the PLA2G7 gene

Autor: Lisa Provezza, M. Gomez Lira, C. Terranova, Nicola Martinelli, Pier Franco Pignatti, Claudia Bozzini

Publikováno v: International journal of immunogenetics. 34(6)

We described two new highly polymorphic markers located 31 bp downstream of the last nucleotide of exon 12 in the 3' UTR region of the gene PLA2G7: 1344 +31TG(n) AG(m). Eight and 14 alleles were observed for the AG and TG repeats, respectively. These

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::447bfa307b45e675ccf41e6e1347fba2
https://pubmed.ncbi.nlm.nih.gov/18001304

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání