As Rorγ−/− mice show alterations in adipocyte size distribution, we examined the metabolic consequences of altered fat cell size in obese mouse models.
The morphological consequences of altered gene expression can link gene expression to developmental fate.
Mechanisms determining FA distribution among milk lipid components and the consequences of altered milk fat globule membrane lipid composition remained to be elucidated.
The purpose of this study was to evaluate factors associated with, and postnatal consequences of, altered patterns of fetal growth in twins.
Many consequences of altered metabolism including the structure of synapses, body temperature, the production of key receptors, and energy transport within neurons were either corrected or improved.
While an appreciation of actin dysregulation as a potential contributor to neurodegenerative disease is just beginning, this study illustrates the severe consequences of altered actin regulation in combination with other defects.
Clearly, further studies will be required to elucidate functional consequences of altered miRNA levels in the blood of OvCA patients.
The integrated gene expression analysis tools enable scientists to derive hypotheses about potential biological consequences of altered gene expression in an interactive manner.
In addition, the physiological consequences of altered gene expression patterns [ 4, 5, 12] and/or the biochemical consequences of amino acid substitutions are rarely investigated [ 1, 5].
To calculate the consequences of altered CMRO2 by hypercapnia, we first assume different values for ΔCMRO2 during hypercapnia and calculate the corresponding calibration constant A (see equation above) from exemplary published BOLD/CBF data during hypercapnia.
Many studies focusing on the ecological consequences of altered biodiversity within the context of specific drivers of environmental change have concentrated on single variables and few species [ 11, 64, 65, 69].
