A Simple Extraction Method Useful to Purify DNA from Difficult Biologic Sources

Autor: Ida Biunno, Giuliana Saltini, Laura Biagiotti, Roberta Tagliabue, Maurizio Gramegna, Pasquale De Blasio, Melissa Frequin, Claudio Oliveri, Giulia Malferrari

Publikováno v: Cell Preservation Technology. 4:51-54

Several procedures to isolate DNA from difficult sources have previously been described, but they are often expensive, time consuming, and have limited applications. In this paper we describe a simple and versatile protocol to isolate nucleic acids f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f8918fab11f1ff0ba8ed41c457c64802
https://doi.org/10.1089/cpt.2006.4.51

Identification of two novel frameshift mutations in the KCNJ11 gene in two Italian patients affected by Congenital Hyperinsulinism of Infancy

Autor: Maddalena Bove, Valeria Cerioni, Luca Albarello, Stefano Mora, Ida Biunno, L. Bosio, Paola Sogno Valin, Claudio Doglioni, Laura Biagiotti, Stefano Grassi, Fabio Gervasi, Maria Carla Proverbio, Ermanna Rovida, Giuseppe Chiumello, I. Zamproni

Publikováno v: Experimental and molecular pathology
83 (2007): 59–64. doi:10.1016/j.yexmp.2006.11.006
info:cnr-pdr/source/autori:Biagiotti L, Proverbio MC, Bosio L, Gervasi F, Rovida E, Cerioni V, Bove M, Valin PS, Albarello L, Zamproni I, Grassi S, Doglioni C, Mora S, Chiumello G, Biunno I./titolo:Identification of two novel frameshift mutations in the KCNJ11 gene in two Italian patients affected by Congenital Hyperinsulinism of Infancy./doi:10.1016%2Fj.yexmp.2006.11.006/rivista:Experimental and molecular pathology (Print)/anno:2007/pagina_da:59/pagina_a:64/intervallo_pagine:59–64/volume:83

Congenital Hyperinsulinism of Infancy (CHI) is a genetically heterogeneous disorder characterized by profound hypoglycemia related to inappropriate insulin secretion. Two histopathologically and genetically distinct groups are recognized among patien

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70256aef338d7c559aed222329f40b40
http://www.cnr.it/prodotto/i/55890

Identification of a novel polymorphism in the fibronectin type II domain of the SEL1L gene and possible relation to the persistent hyperinsulinemic hypoglycemia of infancy

Autor: Monica Cattaneo, D. Antonello, P. Boettcher, Giulia Malferrari, G. Chiumello, Ida Biunno, Roberto Dominici, Patrick S. Moore, Giuliana Saltini, Laura Biagiotti, E. Lorenzini, Eugenia Monferini, M. Viscardi, Maria Carla Proverbio, I. Zamproni

Publikováno v: Mutation research. 554(1-2)

SEL1L, a human gene located on chromosome 14q24.3–q31, is highly expressed in adult pancreas. It is proximal to D14S67 (IDDM11) a proposed type I diabetes susceptibility locus. Considering the organ specific expression of SEL1L, a fundamental role

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8908619ac26d58a3b094f20120111236
https://pubmed.ncbi.nlm.nih.gov/15450414