نتایج جستجو برای: rabbit av nod

تعداد نتایج: 73587  

2013
Alexis Wellwood

Bresnan (1973) posited that more is uniformly analyzed as much-er, whether it appears with adjectives (more intelligent, redder) or nouns (more soup). On the earliest degree-semantic analysis of such constructions, much appears but is semantically inert: it serves to morphologically mark the presence of the degree argument which is introduced by adjectives and nouns (Cresswell 1976). I present ...

Journal: :Molecular biology of the cell 2005
Wei Cui Lisa R Sproul Susan M Gustafson Heinrich J G Matthies Susan P Gilbert R S Hawley

Nod, a nonmotile kinesin-like protein, plays a critical role in segregating achiasmate chromosomes during female meiosis. In addition to localizing to oocyte chromosomes, we show that functional full-length Nod-GFP (Nod(FL)-GFP) localizes to the posterior pole of the oocyte at stages 9-10A, as does kinesin heavy chain (KHC), a plus end-directed motor. This posterior localization is abolished in...

Journal: :The Journal of Experimental Medicine 1988
L S Wicker B J Miller A Chai M Terada Y Mullen

The development of autoimmune diabetes in the nonobese diabetic (NOD) mouse is controlled by at least three recessive loci, including one linked to the MHC. To determine whether any of these genetic loci exert their effects via the immune system, radiation bone marrow chimeras were constructed in which (NOD X B10)F1-irradiated recipients were reconstituted with NOD bone marrow cells. Unmanipula...

Journal: :Diabetes 2005
Ethel J Gordon Linda S Wicker Laurence B Peterson David V Serreze Thomas G Markees Leonard D Shultz Aldo A Rossini Dale L Greiner John P Mordes

Costimulation blockade induces prolonged rat islet and skin xenograft survival in C57BL/6 mice. Nonobese diabetic (NOD) mice, which are used to model human autoimmune diabetes, are resistant to costimulation blockade-induced allograft tolerance. We tested the hypothesis that NOD mice would also be resistant to costimulation blockade-induced rat xenograft tolerance. We report that rat islet xeno...

Journal: :The Journal of Experimental Medicine 1993
P L Podolin A Pressey N H DeLarato P A Fischer L B Peterson L S Wicker

The development of type I diabetes in the nonobese diabetic (NOD) mouse is under the control of multiple genes, one or more of which is linked to the major histocompatibility complex (MHC). The MHC class II region has been implicated in disease development, with expression of an I-E transgene in NOD mice shown to provide protection from insulitis and diabetes. To examine the effect of expressin...

2017
Claire Briet Gwladys Bourdenet Ute C. Rogner Chantal Becourt Isabelle Tardivel Laurent Drouot Christophe Arnoult Jean-Claude do Rego Nicolas Prevot Charbel Massaad Olivier Boyer Christian Boitard

Abrogation of ICOS/ICOS ligand (ICOSL) costimulation prevents the onset of diabetes in the non-obese diabetic (NOD) mouse but, remarkably, yields to the development of a spontaneous autoimmune neuromyopathy. At the pathological level, ICOSL-/- NOD mice show stronger protection from insulitis than their ICOS-/- counterparts. Also, the ICOSL-/- NOD model carries a limited C57BL/6 region containin...

Journal: :The Journal of Experimental Medicine 1998
William M. Ridgway Hiroaki Ito Marcella Fassò Chen Yu C. Garrison Fathman

The current paradigm of major histocompatibility complex (MHC) and disease association suggests that efficient binding of autoantigens by disease-associated MHC molecules leads to a T cell-mediated immune response and resultant autoimmune sequelae. The data presented below offer a different model for this association of MHC with autoimmune diabetes. We used several mouse lines expressing differ...

Journal: :Journal of Korean Medical Science 1997
J. Y. Kim J. K. Chi E. J. Kim S. Y. Park Y. W. Kim S. K. Lee

To know the effects of nicotinamide (NCT) treatment for 5 weeks at the early age on insulitis and development of diabetes in non-obese diabetic (NOD) mice, this experiment was performed. Ten ICR (Institute of Cancer Research) and 15 female NOD mice at 4 weeks of age were used. Mice were assigned to ICR and NOD groups, and NOD mice were randomly divided to control and NCT-treated groups. NCT was...

Journal: :Journal of immunology 2009
Paolo Fiorina Mollie Jurewicz Andrea Augello Andrea Vergani Shirine Dada Stefano La Rosa Martin Selig Jonathan Godwin Kenneth Law Claudia Placidi R Neal Smith Carlo Capella Scott Rodig Chaker N Adra Mark Atkinson Mohamed H Sayegh Reza Abdi

Human clinical trials in type 1 diabetes (T1D) patients using mesenchymal stem cells (MSC) are presently underway without prior validation in a mouse model for the disease. In response to this void, we characterized bone marrow-derived murine MSC for their ability to modulate immune responses in the context of T1D, as represented in NOD mice. In comparison to NOD mice, BALB/c-MSC mice were foun...

Journal: :Endocrinology 1998
Abdelaziz Amrani Sylvie Durant Mark Throsby Josiane Coulaud Mireille Dardenne Franc Oise Homo-Delarche

Because few data were available on glucose homeostasis at the early prediabetic stage in the nonobese diabetic (NOD) mouse, we investigated glycemia, insulinemia, and pancreatic insulin content under basal conditions in both sexes of 4-, 6-, and 8-week-old fed NOD mice, compared with sex- and age-matched fed C57BL/6 mice. We also investigated glucose tolerance in both sexes of fasting 8-week-ol...

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