Sentence examples for mouse models revealed from inspiring English sources
Recent studies in human as well as in mouse models revealed that podocyte plays a central role in FSGS [5].
An examination of the seminal vesicles (Figure 5A) from both mouse models revealed the presence of inclusions in the glandular epithelial cells.
Most importantly, analysis of brain sections derived from Nestin-Cre conditional mouse models revealed the presence of hydrocephalus with dilation of the third ventricle at day P8 (Figure 6C H, n = 2), which was subsequently followed by the dilation of the lateral ventricles, showing a mild but typical triventricular phenotype by day P10 (Figure 6I J, n = 3).
Previous studies in various humanized mouse models revealed an impaired function of human B cells reflected by poor reconstitution of human IgM serum levels and limited ability to undergo immunoglobulin class switch and to secrete immunoglobulins other than IgM [15], [18], [20] [22].
Knockout mouse models revealed similar essential functions for desmosomes in skin cell cell adhesion.
In contrast to the results obtained from AD postmortem brains, the analysis of AD mouse models revealed inconsistent data.
Sauvageau, M. et al. Multiple knockout mouse models reveal lincRNAs are required for life and brain development.
Genome-edited human pluripotent stem cells and genome-edited mouse models reveal that combinatorial genetic interactions contribute to the complex genetic heritability of human cardiomyopathy.
Genetically engineered mouse models reveal essential functions of the BRCA1 protein in tumor suppression.
Thus, even though the current body of literature suggests that anti-growth effects greatly influence mammary epithelial cells [1], mouse models reveal layers of complexity that make it challenging to understand how negative growth responses protect mammary epithelial cells from aberrant proliferation and ultimately tumorigenesis.
Multiple knockout mouse models reveal lincRNAs are required for life and brain development.
