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Scholar Results 1 - 10 of about 101 related to Orilieri: Variations of the perforin gene in patients with type 1 diabetes. (0.10 sec) 

Variations of the perforin gene in patients with type 1 diabetes

- diabetesjournals.org
E Orilieri, G Cappellano, R Clementi, A Cometa, M … - Diabetes, 2008 - Am Diabetes Assoc
RESULTS—In both cohorts, allelic frequency of N252S was significantly higher in patients than
in control subjects (combined cohorts: 1.5 vs. 0.4%; odds ratio 6.68 [95% CI 1.83–7.48]). Sequencing
of the entire coding region detected one novel mutation in one patient, causing a P477A ...
Cited by 3 - Related articles - BL Direct - All 4 versions

Perforin polymorphism A91V and susceptibility to B-precursor childhood acute …


PA Mehta, SM Davies, A Kumar, M Devidas, S Lee, T … - Leukemia, 2006 - nature.com
Perforin plays a key role in the cytotoxicity of natural killer and cytotoxic T cells. Genetic mutations
in the perforin gene (PRF1) give rise to approximately 30% cases of familial hemophagocytic
lymphohistiocytosis. A frequent polymorphism, A91V (C to T transition at position 272), ...
Cited by 7 - Related articles - BL Direct - All 4 versions

A sequence variation in the MOG gene is involved in multiple sclerosis …


S D'Alfonso, E Bolognesi, FR Guerini, N Barizzone, S … - Genes and Immunity, 2007 - nature.com
Several studies suggest that the histocompatibility complex (HLA) class I region harbours genes
modulating multiple sclerosis (MS) susceptibility independently from the effect of class II
alleles. A candidate gene in this region is MOG, encoding the myelin oligodendrocyte ...
Cited by 4 - Related articles - BL Direct - All 3 versions

Evidence for association of chromosome 10 open reading frame (C10orf27) gene …


R Goertsches, SE Baranzini, C Morcillo, C Nos, M … - Multiple …, 2008 - msj.sagepub.com
A recent association study has provided evidence that chromosome 10q22.1 may contain candidate
genes for multiple sclerosis (MS). We analysed two intronic and a non-synonymous single nucleotide
polymorphism (SNP) of the C10orf27 gene in 571 patients with MS (relapsing remitting ...
Cited by 3 - Related articles - BL Direct - All 3 versions

Defective stromal cell function in a mouse model of infusion-induced bone marrow …


J Chen, JS Brandt, FM Ellison, RT Calado, NS … - Experimental hematology, 2005 - Elsevier
Donor lymphocytes infiltrated host BM within 3–7 days and expanded significantly between 7
and 10 days, concurrent with the development of leukopenia, thrombocytopenia, and marrow
hypoplasia. BM cells from mice at 7, 10, and 14 days after B6-LN cell infusion were ...
Cited by 3 - Related articles - All 8 versions

Variations of the perforin gene in patients with multiple sclerosis


G Cappellano, E Orilieri, C Comi, A Chiocchetti, S … - Genes and Immunity, 2008 - nature.com
Perforin is involved in cell-mediated cytotoxicity and mutations of its gene (PRF1) cause familial
hemophagocytic lymphohistiocytosis (FLH2). PRF1 sequencing in 190 patients with multiple
sclerosis and 268 controls detected two FLH2-associated variations (A91V, N252S) in ...
Cited by 3 - Related articles - All 3 versions

Fratricide of CD8 cytotoxic T lymphocytes is dependent on cellular activation and …


MW Su, S Pyarajan, JH Chang, CL Yu, YJ Jin, … - Eur. J. …, 2004 - interscience.wiley.com
CD8 + CTL mediate the destruction of cells displaying foreign peptides in association with class
I MHC molecules. Since CD8 + CTL themselves express class I MHC molecules, a phenomenon
known as fratricide can be elicited by T cells presenting antigens to other CTL. To gain ...
Cited by 9 - Related articles - BL Direct - All 4 versions

Germline mutations of the perforin gene are a frequent occurrence in childhood …


S Cannella, A Santoro, G Bruno, M Pillon, L … - CA A Cancer Journal … - interscience.wiley.com
It is also possible that your web browser is not configured or not able to display style sheets.
In this case, although the visual presentation will be degraded, the site should continue to be
functional. We recommend using the latest version of Microsoft or Mozilla web browser to ...
Cited by 4 - Related articles - BL Direct - All 3 versions

Variations of the perforin gene in patients with autoimmunity/lymphoproliferation …

- bloodjournal.org
R Clementi, A Chiocchetti, G Cappellano, E Cerutti, M … - Blood, 2006 - Am Soc Hematology
From the Pediatric Haematology-Oncology, Istituto di Ricovero e Cura a Carattere Scientifico
(IRCCS) Policlinico San Matteo, University of Pavia, Pavia, Italy; Interdisciplinary Research Center
of Autoimmune Diseases (IRCAD) and Department of Medical Sciences, "A. Avogadro" ...
Cited by 17 - Related articles - BL Direct - All 6 versions

The cytotoxic potential of regulatory T cells: what has been learned from gene …


L Marks, RB Levy - Transplantation, 2004 - journals.lww.com
The mechanisms of T-cell regulation are difficult to elucidate because of their complexity and
the numer- ous subcategories of cell populations. There are two fundamental approaches to
address this conundrum. First, it is possible to use a purified cell population and submit ...
Cited by 6 - Related articles - BL Direct - All 3 versions


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