نتایج جستجو برای: rag1

تعداد نتایج: 1083  

2016
Deepthi Raveendran Sathees C. Raghavan

RAG complex consisting of RAG1 and RAG2 is a site-specific endonuclease responsible for the generation of antigen receptor diversity. It cleaves recombination signal sequence (RSS), comprising of conserved heptamer and nonamer. Nonamer binding domain (NBD) of RAG1 plays a central role in the recognition of RSS. To investigate the DNA binding properties of the domain, NBD of murine RAG1 was clon...

Journal: :Conservation Genetics Resources 2021

In most Japanese populations of dojo loach (Misgurnus anguillicaudatus), gonochoristic diploids genetically diversified groups (A and B, further subdivided into B1 B2) are present, whereas unisexual clonal lineages inhabit certain localities in the Hokkaido Ishikawa Prefectures Japan. Through a series genetic studies including DNA markers, loaches were deemed to originate from hybridization eve...

Journal: :Science 1996
S Han B Zheng D G Schatz E Spanopoulou G Kelsoe

The products of the Rag1 and Rag2 genes drive genomic V(D)J rearrangements that assemble functional immunoglobulin and T cell antigen receptor genes. Expression of the Rag genes has been thought to be limited to developmentally immature lymphocyte populations that in normal adult animals are primarily restricted to the bone marrow and thymus. Abundant RAG1 and RAG2 protein and messenger RNA was...

Journal: :The Journal of biological chemistry 2004
Fumikiyo Nagawa Satoshi Hirose Hirofumi Nishizumi Tadashi Nishihara Hitoshi Sakano

In V(D)J joining of antigen receptor genes, two recombination signal sequences (RSSs), 12- and 23-RSSs, form a complex with the protein products of recombination activating genes, RAG1 and RAG2. DNaseI footprinting demonstrates that the interaction of RAG proteins with substrate RSS DNA is not just limited to the signal region but involves the coding sequence as well. Joining mutants of RAG1 an...

2017
Philipp C. Rommel Thiago Y. Oliveira Michel C. Nussenzweig Davide F. Robbiani

The cancer datasets used in this study (dbGaP: phs000341.v2.p1 and phs000340.v3.p1; EBI: EGAS00001000399) were generated with the financial support of the National Cancer Institute, the St. Baldrick’s Foundation, Partners for Cures, the American Lebanese Syrian Associated Charities of St. Jude Children’s Research Hospital as part of the St. Jude/Washington University Pediatric Cancer Genome Pro...

2011
Bruno E. F. Mota Nadia Gallardo-Romero Giliane Trindade M. Shannon Keckler Kevin Karem Darin Carroll Marco A. Campos Leda Q. Vieira Flávio G. da Fonseca Paulo C. P. Ferreira Cláudio A. Bonjardim Inger K. Damon Erna G. Kroon

Adverse events upon smallpox vaccination with fully-replicative strains of Vaccinia virus (VACV) comprise an array of clinical manifestations that occur primarily in immunocompromised patients leading to significant host morbidity/mortality. The expansion of immune-suppressed populations and the possible release of Variola virus as a bioterrorist act have given rise to concerns over vaccination...

2016
H Y Yamada G Kumar Y Zhang E Rubin S Lightfoot W Dai C V Rao

Mitotic error-mediated chromosome instability (CIN) can lead to aneuploidy, chromothripsis, DNA damage and/or whole chromosome gain/loss. CIN may prompt rapid accumulation of mutations and genomic alterations. Thus, CIN can promote carcinogenesis. This CIN process results from a mutation in certain genes or environmental challenge such as smoking, and is highly prevalent in various cancers, inc...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2016
Virginia A Carroll Mark K Lafferty Luigi Marchionni Joseph L Bryant Robert C Gallo Alfredo Garzino-Demo

HIV-1 infection is associated with increased risk for B-cell lymphomas. How HIV infection promotes the development of lymphoma is unclear, but it may involve chronic B-cell activation, inflammation, and/or impaired immunity, possibly leading to a loss of control of oncogenic viruses and reduced tumor immunosurveillance. We hypothesized that HIV structural proteins may contribute to lymphomagene...

2012
Necil Kutukculer Nesrin Gulez Neslihan Edeer Karaca Guzide Aksu Afig Berdeli

BACKGROUND Severe combined immunodeficiency is within a heterogeneous group of inherited defects throughout the development of T- and/or B-lymphocytes. Mutations in recombinase-activating genes 1 or 2 (RAG1/2) represent approximately 10% of all SCID cases. RAG1/2 are essential for V(D)J rearrangement of the B- and T-cell receptors. OBJECTIVES The aim of this study was to review clinical, immu...

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