User profiles for Jonathan G. Murphy
Jonathan G MurphyScientist, St. Jude Children's Research Hospital Verified email at stjude.org Cited by 1108 |
The methylated component of the Neurospora crassa genome
…, NA Tountas, SH Cross, BS Margolin, JG Murphy… - Nature, 2003 - nature.com
Cytosine methylation is common, but not ubiquitous, in eukaryotes. Mammals 1 and the
fungus Neurospora crassa 2 , 3 have about 2–3% of cytosines methylated. In mammals, …
fungus Neurospora crassa 2 , 3 have about 2–3% of cytosines methylated. In mammals, …
Role of the central melanocortin circuitry in adaptive thermogenesis of brown adipose tissue
A Voss-Andreae, JG Murphy, KLJ Ellacott… - …, 2007 - academic.oup.com
The central melanocortin 4 receptor (MC4R) plays a critical role in energy homeostasis,
although little is known regarding its role in the regulation of adaptive thermogenesis of brown …
although little is known regarding its role in the regulation of adaptive thermogenesis of brown …
Balanced interactions of calcineurin with AKAP79 regulate Ca2+–calcineurin–NFAT signaling
H Li, MD Pink, JG Murphy, A Stein… - Nature structural & …, 2012 - nature.com
In hippocampal neurons, the scaffold protein AKAP79 recruits the phosphatase calcineurin
to L-type Ca 2+ channels and couples Ca 2+ influx to activation of calcineurin and of its …
to L-type Ca 2+ channels and couples Ca 2+ influx to activation of calcineurin and of its …
[HTML][HTML] AKAP-anchored PKA maintains neuronal L-type calcium channel activity and NFAT transcriptional signaling
L-type voltage-gated Ca 2+ channels (LTCC) couple neuronal excitation to gene transcription.
LTCC activity is elevated by the cyclic AMP (cAMP)-dependent protein kinase (PKA) and …
LTCC activity is elevated by the cyclic AMP (cAMP)-dependent protein kinase (PKA) and …
Melanocortin-3 receptor regulates the normal fasting response
BJ Renquist, JG Murphy, EA Larson… - Proceedings of the …, 2012 - National Acad Sciences
The melanocortin-3 receptor–deficient (MC3-R −/− ) mouse exhibits mild obesity without
hyperphagia or hypometabolism. MC3-R deletion is reported to increase adiposity, reduce lean …
hyperphagia or hypometabolism. MC3-R deletion is reported to increase adiposity, reduce lean …
AKAP79/150 recruits the transcription factor NFAT to regulate signaling to the nucleus by neuronal L-type Ca2+ channels
In neurons, regulation of activity-dependent transcription by the nuclear factor of activated T-cells
(NFAT) depends upon Ca 2+ influx through voltage-gated L-type calcium channels (…
(NFAT) depends upon Ca 2+ influx through voltage-gated L-type calcium channels (…
Serotonin 5-hydroxytryptamine2C receptor signaling in hypothalamic proopiomelanocortin neurons: role in energy homeostasis in females
Hypothalamic proopiomelanocortin (POMC) neurons play a critical role in the regulation of
energy balance, and there is a convergence of critical synaptic input including GABA and …
energy balance, and there is a convergence of critical synaptic input including GABA and …
Obesity-induced inflammation in white adipose tissue is attenuated by loss of melanocortin-3 receptor signaling
Metabolic syndrome, a complex of highly debilitating disorders that includes insulin resistance,
hypertension, and dyslipidemia, is associated with the development of obesity in humans …
hypertension, and dyslipidemia, is associated with the development of obesity in humans …
[HTML][HTML] DPP6 loss impacts hippocampal synaptic development and induces behavioral impairments in recognition, learning and memory
L Lin, JG Murphy, RM Karlsson, RS Petralia… - Frontiers in cellular …, 2018 - frontiersin.org
DPP6 is well known as an auxiliary subunit of Kv4-containing, A-type K + channels which
regulate dendritic excitability in hippocampal CA1 pyramidal neurons. We have recently …
regulate dendritic excitability in hippocampal CA1 pyramidal neurons. We have recently …
Disruption of GpI mGluR-dependent Cav2. 3 translation in a mouse model of fragile X syndrome
EE Gray, JG Murphy, Y Liu, I Trang… - Journal of …, 2019 - Soc Neuroscience
Fragile X syndrome (FXS) is an inherited intellectual impairment that results from the loss of
fragile X mental retardation protein (FMRP), an mRNA binding protein that regulates mRNA …
fragile X mental retardation protein (FMRP), an mRNA binding protein that regulates mRNA …