Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families

Autor: GRECO L, BABRON MC, CORAZZA GR, PERCOPO S, SICA R, CLOT F, FULCHIGNONI LATAUD MC, ZAVATTARI P, MOMIGLIANO RICHIARDI P, CASARI G, TOSI R., GASPARINI, PAOLO

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dris___01099::84357a05138c306a454b920ef27678d1
https://hdl.handle.net/11368/1695534

Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans

Autor: Games Collaborative Group, Ban, M, Booth, D, Heard, R, Stewart, G, Goris, A, Vandenbroeck, K, Dubois, B, Laaksonen, M, Ilonen,J, Alizadeh, M, Edan, G, Babron, MC, Brassat, D, Clanet, M, Cournu Rebeix, I, Fontaine, B, Semana, G, Goedde, R, Epplen, J, Weber, A, Infante Duarte, C, Zipp, F, Rajda, C, Bencsik, K, Vécsei, L, Heggarty, S, Graham, C, Hawkins, S, Liguori,M, Momigliano Richiardi,P, Caputo, D, Grimaldi, LM, Leone, M, Massacesi, L, Milanese, C, Salvetti, M, Trojano, M, Bielecki, B, Mycko, MP, Selmaj, K, Santos, M, Maciel,P, Pereira,C, Silva,A, Silva,BM, Coraddu,F, Marrosu,MG, Akesson,E, Hillert,J, Datta,P, Oturai, A, Harbo, HF, Spurkland,A, Goertsches,R, Villoslada, P, Eraksoy, M, Hensiek,A, Compston,A, Setakis,E, Gray,J, Yeo,TW, Sawcer, S., SAVETTIERI, Giovanni

By combining all the data available from the Genetic Analysis of Multiple sclerosis in EuropeanS (GAMES) project, we have been able to identify 17 microsatellite markers showing consistent evidence for apparent association. As might be expected five

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3658::28840ec8c3800159b133e4816b2d6ea5
http://hdl.handle.net/10447/55533

CD45 and Multiple Sclerosis: the exon 4 C77G polymorphism and new markers

Autor: Gomez, Maria Macarena, Liguori, M., Magnani, C., Bonamini, D., Salviati, Alessandro, Leone, M., Andreoli, V., Trojano, M., Valentino, P., Savatteri, G., Quattrone, A., Pignatti, Pierfranco, Momigliano Richiardi, P., Giordano, M.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1943::f643d314f99f8d95ff85e6422f495afc
http://hdl.handle.net/11562/301831

Identification of single nucleotide variations in the coding and regulatory regions of the myelin-associated glycoprotein gene and study of their association with multiple sclerosis

Autor: D'Alfonso S, Mellai M, Giordano M, Pastore A, Malferrari G, Naldi P, Repice A, Liguori M, Cannoni S, Milanese C, Caputo D, Savettieri G, Momigliano-Richiardi P, Italian Group for the Study of Multiple Sclerosis Genetics.

Publikováno v: Journal of neuroimmunology
(2002).
info:cnr-pdr/source/autori:D'Alfonso S, Mellai M, Giordano M, Pastore A, Malferrari G, Naldi P, Repice A, Liguori M, Cannoni S, Milanese C, Caputo D, Savettieri G, Momigliano-Richiardi P; Italian Group for the Study of Multiple Sclerosis Genetics./titolo:Identification of single nucleotide variations in the coding and regulatory regions of the myelin-associated glycoprotein gene and study of their association with multiple sclerosis./doi:/rivista:Journal of neuroimmunology (Print)/anno:2002/pagina_da:/pagina_a:/intervallo_pagine:/volume

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::55aa8ccb70dff456fef0f0c0a6559c3c
https://publications.cnr.it/doc/50329

Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families

Autor: Greco L., Babron M.C., Corazza G.R., Percopo S., Sica R., Clot F., Fulchignomi-Lataud M.C., Zavattari P., Momigliano-Richiardi P., Casari G., Gasparini P., Tosi R. Mantovani V., De Virgiliis S., Iacono G., D'Alfonso A., Selinger-Leneman H.

Publikováno v: Annals of human genetics
65 (2001): 35–41.
info:cnr-pdr/source/autori:Greco L., Babron M.C., Corazza G.R., Percopo S., Sica R., Clot F., Fulchignomi-Lataud M.C., Zavattari P., Momigliano-Richiardi P., Casari G., Gasparini P., Tosi R. Mantovani V., De Virgiliis S., Iacono G., D'Alfonso A., Selinger-Leneman H., et al./titolo:Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families./doi:/rivista:Annals of human genetics (Print)/anno:2001/pagina_da:35/pagina_a:41/intervallo_pagine:35–41/volume:65

Coeliac disease (CD) is a malabsorptive disorder of the small intestine resulting from ingestion of gluten. The HLA risk factors involved in CD are well known but do not explain the whole genetic susceptibility. Several regions of potential linkage o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::ae48a5abaa13984a7e238274a28681c3
http://www.cnr.it/prodotto/i/4078