Inbred Nod
Mostrando 1-8 de 8 artigos, teses e dissertações.
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1. Expression and possible functional role of galectin-3 in the / Expressão e possível papel funcional da galectina-3 no timo de camundongos diabéticos não-obesos (NOD)
Galectin-3 belongs to a family of endogenous lectins which bind to -galactosides presented on the cell surface and extracellular matrix glycoproteins. It is involved in multiple biological functions such as cell growth, adhesion, proliferation and apoptosis. Moreover, galectin-3 is found in several tissues and organs, being highly conserved among animal spec
Publicado em: 2010
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2. Effect of GM1 ganglioside in the sciatic nerves of the NOD (non obse diabetic) / Estudo do efeito do gangliosideo GM1 sobre os nervos perifericos do camundongo NOD (Non Obese Diabetic)
A linhagem de camundongos NOD (non obese diabetic) desenvolve espontaneamente diabetes mellitus tipo 1 (DM-1) com marcante similaridade ao observado em humanos, que se estabelece entre 12ª e 24ª semana de vida. Os gangliosideos são glicoesfingolipídeos de membrana que contém ácido siálico em sua composição e estão presentes na maioria das células
Publicado em: 2007
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3. Evaluation of the diacerhein administration effects on modulationof diabetes mellitus and gene expression IL-1 beta , IFN- gama , IL-12 and TNF- alfa in NOD mice / Avaliação dos efeitos da diacereina na modulação do diabetes mellitus e da expressão de citocinas pro-inflamatorias IL-1 beta , TNF- alfa , IFN- gama e IL-12 em ilhotas beta pancreaticas e celulas esplenicas no camundongo NOD (non obese diabetic)
O camundongo NOD é utilizado como modelo experimental por desenvolver diabetes mellitus tipo 1 (DM-1) espontâneo similar ao diabetes mellitus humano resultando na destruição das ilhotas, orquestrada pelos linfócitos T que induzem a liberação de citocinas, entre elas a IL-1, promovendo o processo inflamatório. A diacereína possui propriedades antiinf
Publicado em: 2007
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4. Beta cell expression of endogenous xenotropic retrovirus distinguishes diabetes-susceptible NOD/Lt from resistant NON/Lt mice.
Endogeneous retroviral expression in beta cells is a feature of prediabetes in nonobese diabetic (NOD) mice. The purpose of this study was to characterize the class-specific pattern of retroviral gene expression in NOD/Lt beta cells versus a related, but diabetes-resistant strain, NON/Lt. Electron microscopic comparison of beta cells from both strains indica
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5. The nonobese diabetic scid mouse: model for spontaneous thymomagenesis associated with immunodeficiency.
Homozygosity for the severe combined immunodeficiency (scid) mutation results in a block in T- and B-lymphocyte development. An unusually high incidence of spontaneous thymic lymphoma development was observed after transfer of this mutation from the C.B-17 congenic strain background onto the diabetes-susceptible nonobese diabetic (NOD) background. Thymomagen
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6. A recombination event in the 5' flanking region of the Ly-6C gene correlates with impaired expression in the NOD, NZB and ST strains of mice.
The murine alloantigen, Ly-6C, is found on 45% of bone marrow cells, 25% of splenocytes and 15% of lymph node cells in all inbred strains of mice tested, with the exception of NOD, NZB and ST. In these three strains, Ly-6C expression can be detected on only 5% of bone marrow cells and not at all on cells from spleen or lymph node. NOD and NZB, which are mode
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7. Early expression of antiinsulin autoantibodies of humans and the NOD mouse: Evidence for early determination of subsequent diabetes
With the development of an insulin autoantibody (IAA) assay performed in 96-well filtration plates, we have evaluated prospectively the development of IAA in NOD mice (from 4 weeks of age) and children (from 7 to 10 months of age) at genetic risk for the development of type 1 diabetes. NOD mice had heterogeneous expression of IAA despite being inbred. IAA re
The National Academy of Sciences.
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8. Polymorphism of murine Fas ligand that affects the biological activity
Fas ligand (FasL) is a member of the tumor necrosis factor family and induces apoptosis in Fas (CD95)-bearing target cells. In this study, we generated several mAbs that react with mouse FasL (mFasL) and characterized their functional properties. One of these mAbs, K10, specifically reacted with mFasL derived from C57BL/6 (B6) mice, but not that from BALB/c
The National Academy of Sciences of the USA.