[HTML][HTML] The chloride channel cystic fibrosis transmembrane conductance regulator (CFTR) controls cellular quiescence by hyperpolarizing the cell membrane during …
AQ Li, ZP Sun, X Liu, JS Yang, F Jin, L Zhu… - Journal of Biological …, 2019 - ASBMB
Cellular quiescence, a reversible state in which growth, proliferation, and other cellular
activities are arrested, is important for self-renewal, differentiation, development …
activities are arrested, is important for self-renewal, differentiation, development …
Downregulation of a CT10 regulator of kinase (Crk) promotes the formation of diapause embryos in the brine shrimp Artemia
ZJ Yan, WT Wu, LY Xu, N Bi, F Yang, WJ Yang… - Gene, 2023 - Elsevier
To survive under harsh environments, embryonic development of Artemia was arrested at
the gastrula stage and released as the diapause embryo. Cell cycle and metabolism were …
the gastrula stage and released as the diapause embryo. Cell cycle and metabolism were …
[HTML][HTML] Signaling Transduction Pathways and G-Protein-Coupled Receptors in Different Stages of the Embryonic Diapause Termination Process in Artemia
T Hao, Z Song, M Zhang, L Zhang - Current Issues in Molecular Biology, 2024 - mdpi.com
Artemia is a widely distributed small aquatic crustacean, renowned for its ability to enter a
state of embryonic diapause. The embryonic diapause termination (EDT) is closely linked to …
state of embryonic diapause. The embryonic diapause termination (EDT) is closely linked to …
Cftr controls lumen expansion and function of Kupffer's vesicle in zebrafish
A Navis, L Marjoram, M Bagnat - Development, 2013 - journals.biologists.com
Regulated fluid secretion is crucial for the function of most organs. In vertebrates, the
chloride channel cystic fibrosis transmembrane conductance regulator (CFTR) is a master …
chloride channel cystic fibrosis transmembrane conductance regulator (CFTR) is a master …
[PDF][PDF] Cystic fibrosis transmembrane conductance regulator (CFTR): an apical marker protein of ionocytes for identifying hypoosmoregulation in gills of the euryhaline …
CK Kang, SC Tsai, ST Lin, TH Lee, PP Hwang - Zool Stud, 2012 - zoolstud.sinica.edu.tw
(2012) Cystic fibrosis transmembrane conductance regulator (CFTR): an apical marker
protein of ionocytes for identifying hypo-osmoregulation in gills of the euryhaline medaka …
protein of ionocytes for identifying hypo-osmoregulation in gills of the euryhaline medaka …
CFTR Cl– channel functional regulation by phosphorylation of focal adhesion kinase at tyrosine 407 in osmosensitive ion transporting mitochondria rich cells of …
WS Marshall, KD Watters… - Journal of …, 2009 - journals.biologists.com
Cystic fibrosis transmembrane conductance regulator (CFTR) anion channels are the
regulated exit pathway in Cl–secretion by teleost mitochondria rich salt secreting (MR) cells …
regulated exit pathway in Cl–secretion by teleost mitochondria rich salt secreting (MR) cells …
The cystic fibrosis transmembrane conductance regulator attenuates the endogenous Ca2+ activated Cl– conductance of Xenopus oocytes
Oocytes from Xenopus laevis activate a Ca 2+ dependent Cl–conductance when exposed to
the Ca 2+ ionophore ionomycin. This Ca 2+ activated Cl–conductance (CaCC) is strongly …
the Ca 2+ ionophore ionomycin. This Ca 2+ activated Cl–conductance (CaCC) is strongly …
Roscovitine Worsens Mycobacterium abscessus Infection by Reducing DUOX2-mediated Neutrophil Response
V Le Moigne, D Rodriguez Rincon… - American Journal of …, 2022 - atsjournals.org
Persistent neutrophilic inflammation associated with chronic pulmonary infection causes
progressive lung injury and, eventually, death in individuals with cystic fibrosis (CF), a …
progressive lung injury and, eventually, death in individuals with cystic fibrosis (CF), a …
[HTML][HTML] Deletion of cftr Leads to an Excessive Neutrophilic Response and Defective Tissue Repair in a Zebrafish Model of Sterile Inflammation
Inflammation-related progressive lung destruction is the leading causes of premature death
in cystic fibrosis (CF), a genetic disorder caused by a defective cystic fibrosis …
in cystic fibrosis (CF), a genetic disorder caused by a defective cystic fibrosis …
Influence of salinity on the localization and expression of the CFTR chloride channel in the ionocytes of Dicentrarchus labrax during ontogeny
C Bodinier, V Boulo, C Lorin‐Nebel… - Journal of …, 2009 - Wiley Online Library
The expression and localization of the cystic fibrosis transmembrane conductance regulator
(CFTR) were determined in four osmoregulatory tissues during the ontogeny of the sea …
(CFTR) were determined in four osmoregulatory tissues during the ontogeny of the sea …