La Manno, G. et al. Molecular diversity of midbrain development in mouse, human, and stem cells.
Chew, GL, Pauli, A, and Schier, AF. (2016) Conservation of uORF repressiveness and sequence features in mouse, human and zebrafish.
The percentages of identity in the same region in comparison with bovine, porcine, rat, mouse, human and chicken were only 39, 42, 41, 40, 45 and 46%, respectively.
These cells have to digest food, take in nutrients, keep out pathogens, communicate with other organs, and respond swiftly to all sorts of stressors – all of these activities are shared between mouse, human and fruit fly.
By employing a candidate-gene approach based on genes encoding members of the TRP superfamily of ion channels, we cloned cDNAs encoding the vanilloid receptor-related osmotically activated channel (VR-OAC) from the rat, mouse, human, and chicken.
This element was highly conserved in mouse, human and rat BMP4 genes.
Bioinformatic analyses corroborate the existence of these complex splicing patterns and new isoforms and confirm the similarities between mouse, human and rat.
The sequencing primers, MF1, MR1, HF2, HR2, SF2 and SR2 (Table S1), were used for the mouse, human and sheep samples respectively.
Using this software and the HMM parameters described above, we searched the entire mouse, human, and rat genomes for candidate COUP-TF DNA binding sites.
Sequence comparison between mouse, human and rat Asxl2 did not find conserved sequence modules at the site of gene trap integration (Fig. 1B).
The Doxycycline (Dox) controlled tet-on-inducible system has successfully been applied to generate iPSCs from mouse, human and pig somatic cells [19], [23], [32].
