Sentences with phrase «j mice»

Dissociation between Performances in Water Maze and Spontaneous Alternation in BALB / C versus A / J Mice

Why would B6 / J mice be so vulnerable to the effects of a high - fat diet?

The vulnerability of B6 / J mice to diabetes was even more apparent than their vulnerability to obesity:

It had no effect in A / J mice at all.

Surwit's team published several papers comparing the effects of different diets in B6 / J mice to the effects of the same diet in A / J mice, which are highly vulnerable to hearing loss and cancer but resistant to obesity, diabetes, and atherosclerosis.

We can see that the high - fat diet increased fat mass in B6 / J mice to a much greater degree than it did in A / J mice.

Sugar increased adipose mass even further in B6 / J mice fed high - fat diets, but reduced adipose mass in B6 / J mice fed low - fat diets.

Thus, B6D2F1 / J mice are the offspring of a C57BL / 6J female mated to a DBA / 2J male, and D2B6F1 / J mice are offspring of the reciprocal mating.

ß1 - Adrenergic Receptor Contains Multiple IAk and IEk Binding Epitopes That Induce T Cell Responses with Varying Degrees of Autoimmune Myocarditis in A / J Mice.

Adaptive changes in adipocyte gene expression differ in AKR / J and SWR / J mice during diet - induced obesity.

SM / J mice carry a number of rare polymorphic alleles and are often matched to LG / J (Stock No. 000675), A / J (Stock No. 000646) or NZB / BINJ (Stock No. 000684) for quantitative trait locus analysis.

in A / J mice ABR thresholds at 16 and 32 kHz are elevated by 25 days of age and by 3 months of age the ABR thresholds are more than 50 dB above normal

SM / J mice exhibit a hyperresponsiveness to B cell mitogens.

A / J mice are susceptible to infection by Legionella pneumophilia.

This allele was found only in A / J mice, not in A / WySnJ, A / HeJ, C57BL / 6J, SJL / J, SWR / J or 129 / SvJ mice.

LG / J mice are often compared to SM / J (Stock No. 000687) for quantitative trait locus analysis in the areas of atherosclerosis, obesity, and mandible size.

Adaptive changes in adipocyte gene expression differ in AKR / J and SWR / J mice during diet induced obesity.

Surwit RS, Feinglos MN, Rodin J, Sutherland A, Petro AE, Opara EC, Kuhn CM and Rebuffe - Scrive M. Differential effects of fat and sucrose on the development of obesity and diabetes in C57BL / 6J and A / J mice.

SM / J mice carry a number of rare polymorphic alleles and are often matched to other strains for quantitative trait locus analysis.

Differential Effects of Fat and Sucrose on the Development of Obesity and Diabetes in C57BL / 6J and A / J Mice.

Expression of BAC clones containing the Naip5 gene from resistant strains (C57BL / 6J and 129X1 / SvJ) in A / J mice rendered transgenic mice resistant to infection (J: 81887, J: 129300).

On either chow or high fat diet, A / J mice maintain low glucose and insulin levels.

peritoneal macrophages derived from A / J mice are susceptible to Legionella pneumophilia infection; infected macrophages show a 10-fold increase in bacterial burden after 1 day of infection compared to resistant controls (C57BL / 6J)

C57L / J mice are highly susceptible to experimental allergic encephalomyelitis (EAE) and highly responsive to phytohemagglutinin.

In addition, C57L / J mice are highly susceptible to developing atherosclerotic aortic lesions (4500 to 8000 um2 atherosclerotic aortic lesions / aortic cross-section) following 14 weeks on an atherogenic diet (1.25 % cholesterol, 0.5 % cholic acid and 15 % fat)(Paigen et al. 1990).

On a lithogenic diet, C57L / J mice develop gallstones as a result of abnormal regulation of cholesterol synthesis (Xua et al. 2004).

C57L / J mice were inbred following a mutation in a now extinct substrain of C57BR at F22.

In addition, C57L / J mice are highly susceptible to developing atherosclerotic aortic lesions following 14 weeks on an atherogenic diet.

Dodero, L., Damiano, M., Galbusera, A. Bifone, A., Tsaftsaris, S.A., Scattoni, M.L., Gozzi, A * Neuroimaging Evidence of Major Morpho - Anatomical and Functional Abnormalities in the BTBR T+TF / J Mouse Model of Autism.

Ethanol regulation of serum glucocorticoid kinase 1 expression in DBA2 / J mouse prefrontal cortex.

Long - term Analyses of Innervation and Neuromuscular Integrity in the Trembler - J Mouse Model of Charcot - Marie - Tooth Disease.

When using the A / J mouse strain in a publication, please include JAX stock # 000646 in your Materials and Methods section.

When using the SM / J mouse strain in a publication, please include JAX stock # 000687 in your Materials and Methods section.

When using the B6129S8F1 / J mouse strain in a publication, please cite the originating article (s) and include JAX stock # 012868 in your Materials and Methods section.

Not exact matches

The newly created BBC 6 Music Stage will see live performances from Modert Mouse, Alt - J and Beach House.

Pat J You made a true 4rd tier League Cup looked good.This must bee the best of «Micky Mouse Cup» chance ever, cause many gooners here were excited.

The Brainbow mouse was produced by J. Livet J, T. A. Weissman, H. Kang, R. W. Draft, J. Lu, R. A. Bennis, J. R. Sanes, and J. W. Lichtman; see Nature (2007) 450:56 - 62.

The Brainbow mouse was produced by J. Livet J, T. A. Weissman, H. Kang, R. W. Draft, J. Lu, R. A. Bennis, J. R. S

Male mice from 3 strains of genetically modified mice were used in these studies, with each strain compared with a specific background control strain: IL - 15Rα — KO (n = 20)(27) and B6129SF2 / J (B6129) control (n = 16); IL - 15 — KO (n = 8)(28) and BL / 6NTac control (n = 8); and HSA - IL - 15TG (n = 7)(34) and HSA - IL - 15Con control (n = 7).

The following strains of male mice were purchased from The Jackson Laboratory at 8 weeks of age: IL - 15Rα — KO mice (stock no. 003723; n = 20); B6129SF2 / J background control (101045; n = 16).

Citation: Lee S - J (2007) Quadrupling Muscle Mass in Mice by Targeting TGF - ß Signaling Pathways.

Menalled L, Kudwa A, Miller S, Fitzpatrick J, Watson - Johnson J, Keating N, Ruiz M, Mushlin R, Alosio B, McConnell K, Connor D, Murphy C, Oakeshott S, Kwan M, Beltran J, Ghavami A, Brunner D, C. Park L, Ramboz S and Howland D Comprehensive behavioral and molecular characterization of a new knock - in mouse model of Huntington's disease: zQ175.

Maryanski J, Boon T. Immunogenic variants obtained by mutagenesis of mouse mastocytoma P815.

Oakeshott S, Balci F, Filippov I, Murphy C, Port R, Connor D, Paintdakhi A, Lesauter J, Menalled L, Ramboz S, Kwak S, Howland D, Silver R, Brunner D. Circadian Abnormalities in Motor Activity in a BAC Transgenic Mouse Model of Huntington's Disease.

Balazs AB, Ouyang Y, Hong CM, Chen J, Nguyen SM, Rao DS, An DS, Baltimore D. Vectored ImmunoProphylaxis Protects Humanized Mice from Mucosal HIV Transmission.

Oakeshott S, Port R.G, Cummins S, Watson - Johnson J, Ramboz S, Park L, Howland D, Brunner D. HD mouse models reveal clear deficits in learning to perform a simple instrumental response, PLoS Currents: Huntington Disease.2011 Nov 14.

Obese Mice Losing Weight Due to trans - 10, cis - 12 Conjugated Linoleic Acid Supplementation or Food Restriction Harbor Distinct Gut Microbiota — Laura J den Hartigh — JN The Journal of Nutrition

Pierre P, Turley SJ, Gatti E, Hull M, Meltzer J, Mirza A, Inaba K, Steinman RM, Mellman I. Developmental regulation of MHC class II transport in mouse dendritic cells.

Revelli J.P, Smith D, Allen J, Jeter - Jones S, Shadoan M.K, Desai U, Schneider M, Sligtenhorst I, Kirkpatrick L, Platt K.A, Suwanichkul A, Savelieva K, Gerhardt B, Mitchell J, Syrewicz J, Zambrowicz B, Hamman B.D, Vogel P, Powell D.R. Profound obesity secondary to hyperphagia in mice lacking kinase suppressor of ras 2.

Kanda T, Brown JD, Orasanu G, Vogel S, Gonzalez FJ, Sartoretto J, Michel T, Plutzky J. PPARgamma in the endothelium regulates metabolic responses to high - fat diet in mice.