Common Diseases Found in Inbred Strains of Laboratory Mice

Author(s):  
John Sundberg ◽  
Tsutomu Ichiki
1998 ◽  
Vol 93 (1) ◽  
pp. 121-126 ◽  
Author(s):  
Lucineide Gonçalves ◽  
Roberto Magalhães Pinto ◽  
J Júlio Vicente ◽  
Dely Noronha ◽  
Delir Corrêa Gomes

2004 ◽  
Vol 101 (26) ◽  
pp. 9734-9739 ◽  
Author(s):  
B. Yalcin ◽  
J. Fullerton ◽  
S. Miller ◽  
D. A. Keays ◽  
S. Brady ◽  
...  

1998 ◽  
Vol 9 (8) ◽  
pp. 668-670 ◽  
Author(s):  
Angabin Matin ◽  
Gayle B. Collin ◽  
Yoshinobu Asada ◽  
Don Varnum ◽  
Diana L. Martone ◽  
...  

1987 ◽  
Vol 50 (1) ◽  
pp. 69-72 ◽  
Author(s):  
Yutaka Nishioka

SummaryMice are the most widely used experimental mammals, and many inbred strains are available. However, except for the relatively recent strains derived from known wild populations, the relationships between wild and laboratory mice are not well understood. Based on the Y-chromosomal restriction fragmentlength polymorphism, seventeen inbred strains were classified into two groups: strains with the Mus musculus musculus type Y chromosome and those with the M. m. domesticus type Y chromosome. We extended the survey to an additional twenty-two inbred strains. The M. m. musculus type Y chromosome was found in AEJ/GnLe, AAU/SsJ, BDP/J, BXSB/MpJ, DA/HuSn, HTG/GoSfSn, I/LnJ, LP/J, NZW/LacJ, RIIIS/J, SB/Le, SEA/GnJ, SF/CamEi, SK/CamEi, SM/J, WB/ReJ, WC/ReJ and YBR/Ei, while the M. m. domesticus type Y chromosome was present in BUB/BnJ, MA/MyJ, PL/J and ST/bJ.


PeerJ ◽  
2016 ◽  
Vol 4 ◽  
pp. e2318 ◽  
Author(s):  
Kyle J. Beauchemin ◽  
Julie M. Wells ◽  
Alvin T. Kho ◽  
Vivek M. Philip ◽  
Daniela Kamir ◽  
...  

To characterize temporal patterns of transcriptional activity during normal lung development, we generated genome wide gene expression data for 26 pre- and post-natal time points in three common inbred strains of laboratory mice (C57BL/6J, A/J, and C3H/HeJ). Using Principal Component Analysis and least squares regression modeling, we identified both strain-independent and strain-dependent patterns of gene expression. The 4,683 genes contributing to the strain-independent expression patterns were used to define a murine Developing Lung Characteristic Subtranscriptome (mDLCS). Regression modeling of the Principal Components supported the four canonical stages of mammalian embryonic lung development (embryonic, pseudoglandular, canalicular, saccular) defined previously by morphology and histology. For postnatal alveolar development, the regression model was consistent with four stages of alveolarization characterized by episodic transcriptional activity of genes related to pulmonary vascularization. Genes expressed in a strain-dependent manner were enriched for annotations related to neurogenesis, extracellular matrix organization, and Wnt signaling. Finally, a comparison of mouse and human transcriptomics from pre-natal stages of lung development revealed conservation of pathways associated with cell cycle, axon guidance, immune function, and metabolism as well as organism-specific expression of genes associated with extracellular matrix organization and protein modification. The mouse lung development transcriptome data generated for this study serves as a unique reference set to identify genes and pathways essential for normal mammalian lung development and for investigations into the developmental origins of respiratory disease and cancer. The gene expression data are available from the Gene Expression Omnibus (GEO) archive (GSE74243). Temporal expression patterns of mouse genes can be investigated using a study specific web resource (http://lungdevelopment.jax.org).


2008 ◽  
Vol 6 (1) ◽  
pp. 27-33 ◽  
Author(s):  
Eugene V Daev ◽  
Boris P Surinov ◽  
Anna V Dukelskaya

Quantity of antibody producing cells and changes in bone marrow dividing cells of mouse males were studied after the exposure with chemosignals from intact or stressed donor mouse males. Inbred CBA, BALB/c and C57BL/6 strains were used. It is shown that excreted volatiles decrease quantity of antibody producing cells in spleen and at the same time raise the level of mitotic disturbances in bone marrow cells of recipient mice. Pheromone effect depends on genotype and physiological state of the recipients. For the first time we describe here the influence of mouse female pheromone 2,5-dimethylpyrazine on analyzed features. Biological meaning of the discovered effects is discussed.


1989 ◽  
Vol 9 (9) ◽  
pp. 4074-4078
Author(s):  
C J Wawrzyniak ◽  
P M Gallagher ◽  
M A D'Amore ◽  
J E Carter ◽  
S D Lund ◽  
...  

The murine beta-glucuronidase (GUS) gene complex, [Gus], encompasses the GUS structural element, Gus-s, and a set of regulatory elements which serve to modulate Gus-s expression. Three common GUS haplotypes representing virtually all inbred strains of laboratory mice have been compared with respect to GUS mRNA sequence. Results of such comparisons revealed sequence variations which target the location of one of the GUS regulatory elements to sequences within Gus-s and which account for known electrophoretic and heat stability differences among GUS allozymes of the three common GUS haplotypes.


Development ◽  
1969 ◽  
Vol 21 (1) ◽  
pp. 97-103
Author(s):  
Kathleen M. H. Munro ◽  
S. A. Barnett

The house mouse, Mus musculus L., usually has twenty-six presacral vertebrae: these consist of seven cervical, thirteen thoracic and six lumbar vertebrae (Weber, 1950; Deol, 1958; Berry & Searle, 1963; Berry, 1964). The twenty-sixth vertebra is, however, sometimes abnormal, especially among laboratory mice: on one or both sides it may be fused with the sacrum. There are then five typical lumbar vertebrae, instead of six. The proportion of such abnormalities in a population is influenced by genotype, diet and unidentified maternal factors (reviewed by Grüneberg, 1963). Evidence is given below that a low environmental temperature can also increase the incidence of ‘sacralization of L6’. The mice used included three highly inbred strains: A/Tb, A2G/Tb and C57BL/Tb. A permanent breeding colony of each strain was kept at each of two environmental temperatures, namely, 21 °C and −3 °C. In addition, GFF mice were studied at 21 °C only.


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