Exercise metabolism and adaptation in skeletal muscle
Viewing metabolism through the lens of exercise biology has proven an accessible and
practical strategy to gain new insights into local and systemic metabolic regulation. Recent …
practical strategy to gain new insights into local and systemic metabolic regulation. Recent …
Mechanisms of mechanical overload-induced skeletal muscle hypertrophy: current understanding and future directions
MD Roberts, JJ McCarthy… - Physiological …, 2023 - journals.physiology.org
Mechanisms underlying mechanical overload-induced skeletal muscle hypertrophy have
been extensively researched since the landmark report by Morpurgo (1897) of “work …
been extensively researched since the landmark report by Morpurgo (1897) of “work …
ROS-induced ribosome impairment underlies ZAKα-mediated metabolic decline in obesity and aging
G Snieckute, L Ryder, AC Vind, Z Wu, FS Arendrup… - Science, 2023 - science.org
The ribotoxic stress response (RSR) is a signaling pathway in which the p38-and c-Jun N-
terminal kinase (JNK)–activating mitogen-activated protein kinase kinase kinase (MAP3K) …
terminal kinase (JNK)–activating mitogen-activated protein kinase kinase kinase (MAP3K) …
Ribosome stalling is a signal for metabolic regulation by the ribotoxic stress response
G Snieckute, AV Genzor, AC Vind, L Ryder, M Stoneley… - Cell Metabolism, 2022 - cell.com
Impairment of translation can lead to collisions of ribosomes, which constitute an activation
platform for several ribosomal stress-surveillance pathways. Among these is the ribotoxic …
platform for several ribosomal stress-surveillance pathways. Among these is the ribotoxic …
Nitric oxide-induced ribosome collision activates ribosomal surveillance mechanisms
L Ryder, FS Arendrup, JF Martínez, G Snieckute… - Cell Death & …, 2023 - nature.com
Impairment of protein translation can cause stalling and collision of ribosomes and is a
signal for the activation of ribosomal surveillance and rescue pathways. Despite clear …
signal for the activation of ribosomal surveillance and rescue pathways. Despite clear …
Cytosolic aldose metabolism contributes to progression from cirrhosis to hepatocarcinogenesis
Oxidative stress modulates carcinogenesis in the liver; however, direct evidence for
metabolic control of oxidative stress during pathogenesis, particularly, of progression from …
metabolic control of oxidative stress during pathogenesis, particularly, of progression from …
mTOR-dependent loss of PON1 secretion and antiphospholipid autoantibody production underlie autoimmunity-mediated cirrhosis in transaldolase deficiency
Transaldolase deficiency predisposes to chronic liver disease progressing from cirrhosis to
hepatocellular carcinoma (HCC). Transition from cirrhosis to hepatocarcinogenesis depends …
hepatocellular carcinoma (HCC). Transition from cirrhosis to hepatocarcinogenesis depends …
Mechanotransduction in tissue engineering: Insights into the interaction of stem cells with biomechanical cues
Stem cells in their natural microenvironment are exposed to biochemical and biophysical
cues emerging from the extracellular matrix (ECM) and neighboring cells. In particular …
cues emerging from the extracellular matrix (ECM) and neighboring cells. In particular …
TAK1 protein kinase activity is required for TLR signalling and cytokine production in myeloid cells
M Rodrigues, T Petrova, B Tibbs, JSC Arthur… - Biochemical …, 2022 - portlandpress.com
A conditional knock-in mouse was generated in which the TAK1 catalytic subunit was largely
replaced by the kinase-inactive TAK1 [D175A] mutant in immune cells. The activation of …
replaced by the kinase-inactive TAK1 [D175A] mutant in immune cells. The activation of …
Myofibrillar myopathy hallmarks associated with ZAK deficiency
A Stonadge, AV Genzor, A Russell… - Human Molecular …, 2023 - academic.oup.com
The ZAK gene encodes two functionally distinct kinases, ZAKα and ZAKβ. Homozygous loss
of function mutations affecting both isoforms causes a congenital muscle disease. ZAKβ is …
of function mutations affecting both isoforms causes a congenital muscle disease. ZAKβ is …