دانلود مقالات ISI درباره سندرم عمان + ترجمه فارسی

اثربخشی ژن درمانی ژن عامل ژنومی در مدل ژن 2 ژن تجویز سندرم نوترکیب امانن تحت تأثیر التهاب و اختلال در تنظیم ایمنی نیست

Efficacy of lentivirus-mediated gene therapy in an Omenn syndrome recombination-activating gene 2 mouse model is not hindered by inflammation and immune dysregulation

Keywords: سندرم عمان; Gene therapy; Omenn syndrome; autoimmunity; lentiviral vector; Rag genes; AIRE; Autoimmune regulator; BAFF; B cell-activating factor; BM; Bone marrow; GT; Gene therapy; HSCT; Hematopoietic stem cell transplantation; Lin−; Lineage negative; LV; Lentivi

دانلود رایگان متن کامل مقاله ISI 22 صفحه سال انتشار : 2018 سفارش ترجمه

ارتباط مختصر در مورد واکسیناسیون فعال سازی ژنهای 1 و 2 در بیماران مبتلا به اختلالات کمبود ایمنی ترکیبی شدید در مصر

Brief CommunicationMutations in Recombination Activating Gene 1 and 2 in patients with severe combined immunodeficiency disorders in Egypt

Keywords: سندرم عمان; SCID; severe combined immunodeficiency disorders; OS; Omenn syndrome; RAG; Recombination Activating Gene; BMT; bone marrow transplant; CVS; chorionic villous sampling; Severe combined immunodeficiency; Omenn syndrome; RAG; Prenatal diagnosis; Egypt;

دانلود رایگان متن کامل مقاله ISI 7 صفحه سال انتشار : 2015 سفارش ترجمه

بروز ابتلا به کمبود ایمنی

Primary immunodeficiency update

Keywords: سندرم عمان; ADA; adenosine deaminase; AIRE; autoimmune regulator; AML; acute myeloid leukemia; APECED; autoimmune polyendocrinopathy, candidiasis, and ectodermal dysplasia; APLAID; autoinflammation and PLCγ2-associated antibody deficiency and immune dysregulation; A

دانلود رایگان متن کامل مقاله ISI 15 صفحه سال انتشار : 2015 سفارش ترجمه

Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy

Keywords: سندرم عمان; PID; primary immune deficiency; SCID; severe combined immunodeficiency; CVID; common variable immunodeficiency; OS; Omenn syndrome; RAG1; recombination-activating gene 1; RAG2; recombination-activating gene 2; RSSs; recombination signal sequences; DSBs; D

دانلود رایگان متن کامل مقاله ISI 14 صفحه سال انتشار : 2016 سفارش ترجمه

Functional analysis of naturally occurring DCLRE1C mutations and correlation with the clinical phenotype of ARTEMIS deficiency

Keywords: سندرم عمان; V(D)J recombination; nonhomologous end-joining; DNA repair; ARTEMIS deficiency; DCLRE1C mutations; severe combined immunodeficiency; A-MuLV; Abelson murine leukemia virus; ExAC; Exome Aggregation Consortium; GFP; Green fluorescent protein; IR; Ionizing ra

دانلود رایگان متن کامل مقاله ISI 18 صفحه سال انتشار : 2015 سفارش ترجمه

Autoimmune manifestations in SCID due to IL7R mutations: Omenn syndrome and cytopenias

Keywords: سندرم عمان; IL7Rα deficiency; SCID; Omenn syndrome; Autoimmune cytopenias; Eosinophilic myocarditis; Primary immunodeficienciesADA, adenosine deaminase deficiency; OS, Omenn syndrome; RAG, recombination activating genes; SCID, severe combined immunodeficiency

دانلود رایگان متن کامل مقاله ISI 5 صفحه سال انتشار : 2014 سفارش ترجمه

Human syndromes of immunodeficiency and dysregulation are characterized by distinct defects in T-cell receptor repertoire development

Keywords: سندرم عمان; T-cell receptor; recombination activating gene; Omenn syndrome; T-cell receptor sequencing; CDR3; Complementarity-determining region 3; IL2RG; IL-2 receptor γ; OS; Omenn syndrome; RAG; Recombination activating gene; SCID; Severe combined immunodeficiency

دانلود رایگان متن کامل مقاله ISI 21 صفحه سال انتشار : 2014 سفارش ترجمه

A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency

Keywords: سندرم عمان; Recombination-activating gene 1; V(D)J recombination; severe combined immune deficiency; Omenn syndrome; autoimmunity; genotype-phenotype correlation; immune repertoire; A-MuLV; Abelson murine leukemia virus; CDR; Complementarity-determining region; CID-G

دانلود رایگان متن کامل مقاله ISI 22 صفحه سال انتشار : 2014 سفارش ترجمه

Hypomorphic Janus kinase 3 mutations result in a spectrum of immune defects, including partial maternal T-cell engraftment

Keywords: سندرم عمان; Severe combined immunodeficiency; cytokine signaling; maternal engraftment; B-LCL; B-lymphoblast cell line; BMT; Bone marrow transplantation; CD40L; CD40 ligand; CFSE; Carboxyfluorescein diacetate succinimidyl ester; GVHD; Graft-versus-host disease; JAK3;

دانلود رایگان متن کامل مقاله ISI 10 صفحه سال انتشار : 2013 سفارش ترجمه

Omenn syndrome: a case report and review of literature

Keywords: سندرم عمان; Omenn syndrome; Severe combined immunodeficiency

دانلود رایگان متن کامل مقاله ISI 5 صفحه سال انتشار : 2011 سفارش ترجمه

Analysis of mutations and recombination activity in RAG-deficient patients

Keywords: سندرم عمان; RAG deficiency; SCID; Omenn syndrome; TCRγδ+ T cells; V(D)J recombination

دانلود رایگان متن کامل مقاله ISI 6 صفحه سال انتشار : 2011 سفارش ترجمه

Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B- SCID or Omenn syndrome

Keywords: سندرم عمان; SCID; severe combined immunodeficiency; RAG; recombinase activating genes; ADA; adenosine deaminase; OS; Omenn syndrome; IL; interleukin; γc; γ chain; CID; combined immunodeficiency; RSS; recombination signal sequences; T-B- SCID;; Omenn syndrome;; RAG1

دانلود رایگان متن کامل مقاله ISI 7 صفحه سال انتشار : 2011 سفارش ترجمه

Defect of regulatory T cells in patients with Omenn syndrome

Keywords: سندرم عمان; Immunodeficiency; V(D)J recombination; Omenn syndrome; regulatory T cells; FOXP3; anergy and tolerance; thymus and the development of T lymphocytes; AIRE; Autoimmune regulator; FOXP3; Forkhead box protein P3; HD; Healthy donor; OS; Omenn syndrome; RAG; Re

دانلود رایگان متن کامل مقاله ISI 8 صفحه سال انتشار : 2010 سفارش ترجمه

More than just SCID—The phenotypic range of combined immunodeficiencies associated with mutations in the recombinase activating genes (RAG) 1 and 2

Keywords: سندرم عمان; Recombinase activating genes defects; Severe combined immunodeficiency; Omenn syndrome; Granulomas; γδ T-cells

دانلود رایگان متن کامل مقاله ISI 10 صفحه سال انتشار : 2010 سفارش ترجمه

Saving the red baby: Successful allogeneic cord blood transplantation in Omenn syndrome

Keywords: سندرم عمان; Omenn syndrome;; Severe combined immunodeficiency;; Neonatal erythroderma;; Hematopoietic stem cell transplantation;; Cord blood transplantation;; Immune reconstitution

دانلود رایگان متن کامل مقاله ISI 5 صفحه سال انتشار : 2009 سفارش ترجمه

Reduced central tolerance in Omenn syndrome leads to immature self-reactive oligoclonal T cells

Keywords: سندرم عمان; Omenn syndrome; autoimmunity; immunodeficiency; SCID; AIRE; tolerance; Foxp3; Treg; oligoclones; TRECAIRE, Autoimmune regulator; DN, Double-negative; DP, Double-positive; Foxp3, Forkhead box P3; NKT, Natural killer T; OS, Omenn syndrome; RAG, Recombinase-

دانلود رایگان متن کامل مقاله ISI 8 صفحه سال انتشار : 2009 سفارش ترجمه

Omenn syndrome: Inflammation in leaky severe combined immunodeficiency

Keywords: سندرم عمان; Immunodeficiency; Omenn syndrome; mutation; SCIDADA, Adenosine deaminase; AIRE, AutoImmune REgulator; CHARGE, Coloboma of the eye, Heart defects, Atresia of the choanae, Retardation of growth and/or development, Genital and/or urinary abnormalities, and E

دانلود رایگان متن کامل مقاله ISI 5 صفحه سال انتشار : 2008 سفارش ترجمه

Variability of clinical and laboratory features among patients with ribonuclease mitochondrial RNA processing endoribonuclease gene mutations

Keywords: سندرم عمان; Cartilage hair hypoplasia; RNase mitochondrial RNA processing endoribonuclease; severe combined immunodeficiency; Omenn syndrome; CD8 lymphopeniaCHH, Cartilage hair hypoplasia; HCT, Hematopoietic cell transplantation; OS, Omenn syndrome; RMRP, Ribonucleas

دانلود رایگان متن کامل مقاله ISI 7 صفحه سال انتشار : 2008 سفارش ترجمه

Clinical application of DNA microarrays: Molecular diagnosis and HLA matching of an Amish child with severe combined immune deficiency

Keywords: سندرم عمان; Severe combined immune deficiency; Omenn syndrome; Molecular biology; Transplantation; HLA matching

دانلود رایگان متن کامل مقاله ISI 8 صفحه سال انتشار : 2008 سفارش ترجمه

GvHD-associated cytokine polymorphisms do not associate with Omenn syndrome rather than T−B− SCID in patients with defects in RAG genes

Keywords: سندرم عمان; RAG-deficient severe combined immunodeficiency; Omenn syndrome; GvHD-associated cytokine gene polymorphisms

دانلود رایگان متن کامل مقاله ISI 5 صفحه سال انتشار : 2007 سفارش ترجمه

Evolution of a T-B- SCID into an Omenn syndrome phenotype following parainfluenza 3 virus infection

Keywords: سندرم عمان; T-B- SCID; Omenn syndrome; RAG mutation; Genotype-phenotype correlation; T cell rearrangement; Exoantigen; Parainfluenza virus infection;

دانلود رایگان متن کامل مقاله ISI 4 صفحه سال انتشار : 2005 سفارش ترجمه

Omenn's syndrome occurring in patients without mutations in recombination activating genes

Keywords: سندرم عمان; Omenn syndrome; Recombination activating gene; Artemis gene; T cell receptor oligoclonality;

دانلود رایگان متن کامل مقاله ISI 11 صفحه سال انتشار : 2005 سفارش ترجمه