This image illustrates concepts in the press release titled «Infradian oscillation of
circadian genes in a mouse model of bipolar disorder».
Not exact matches
In 1997 Joseph Takaha - shi of the Howard Hughes Medical Institute at Northwestern University and his colleagues isolated a
gene they called Clock that when mutated yielded
mice with no discernible
circadian rhythm.
These four
genes and their proteins constitute the heart of the biological clock
in flies, and with some modifications they appear to form a mechanism governing
circadian rhythms throughout the animal kingdom, from fish to frogs,
mice to humans.
In recent years, clock researchers have uncovered some of the gears and springs that keep this circadian timepiece running, largely by identifying a handful of key genes in organisms from bread mold to mic
In recent years, clock researchers have uncovered some of the gears and springs that keep this
circadian timepiece running, largely by identifying a handful of key
genes in organisms from bread mold to mic
in organisms from bread mold to
mice.
Scientists compared urination patterns, both volume and frequency,
in normal
mice and
in mice genetically engineered without two
circadian genes, Cryptochrome - 1 and Cryptochrome - 2, resulting
in dysfunctional
circadian rhythms.
The expression of core clock
genes is altered
in mice lacking the Chrono
gene, and the
mice have longer
circadian cycles.
In mice heterozygous for tau - lacZ targeted to the melanopsin gene locus, β - galactosidase — positive RGC axons projected to the SCN and other brain nuclei involved in circadian photoentrainment or the pupillary light refle
In mice heterozygous for tau - lacZ targeted to the melanopsin
gene locus, β - galactosidase — positive RGC axons projected to the SCN and other brain nuclei involved
in circadian photoentrainment or the pupillary light refle
in circadian photoentrainment or the pupillary light reflex.
The researchers also found that
genes related to
circadian rhythms (the body clock) were changed
in mice exposed to e-cigarettes.
A study
in mice has found that variations
in a
gene that regulates the
circadian clock seem to increase the chances of breast cancer spreading.
Looking at
mice with differing risks of metastasis, Kent Hunter at the National Cancer Institute
in Bethesda, Maryland, and his team found a
circadian rhythm
gene, Arntl2, seemed to be involved.
Circadian genes turned out to be also infradian
genes, whose expressions go up and down with mood - change - like behaviors
in these
mice,» Miyakawa explains.
PER2: Deletion of the PER2
gene in mice, associated with the mechanisms of
circadian rhythm, appears to improve DNA repair
in stem cell populations relevant to the immune system, resulting
in a healhier immune cell population, better immune function
in old age, and a modestly extended life span.
Mice lacking molecular - clock components (Per and Cry), or lacking Per
genes in osteoblasts, display high bone mass, suggesting that bone remodeling may also be subject to
circadian regulation.
In the initial report, mice harboring a mutation in the core circadian gene Clock (termed Clock mutant mice) were fed a high - fat (HF) diet and observed to develop obesity at a young age, as well as a variety of metabolic and endocrine abnormalities consistent with the metabolic syndrome (2
In the initial report,
mice harboring a mutation
in the core circadian gene Clock (termed Clock mutant mice) were fed a high - fat (HF) diet and observed to develop obesity at a young age, as well as a variety of metabolic and endocrine abnormalities consistent with the metabolic syndrome (2
in the core
circadian gene Clock (termed Clock mutant
mice) were fed a high - fat (HF) diet and observed to develop obesity at a young age, as well as a variety of metabolic and endocrine abnormalities consistent with the metabolic syndrome (2).