Official Twitter handle for The Epithelial Transport Group (ETG). Cross-section of the traditional American Physiological Society @APSPhysiology
Joined May 2018
- Tweets 665
- Following 116
- Followers 320
- Likes 130
119 Photos and videos
If you wanna get familiar with the thiazide sensitive Na -Cl− cotransporter check this fresh review of G. Gamba ! Thirty years of the NCC cotransporter: from cloning to physiology and structure | American Journal of Physiology-Renal Physiology journals.physiology.org/doi/…
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Lama Al-Qusairi et al. demonstrated that Dietary Anions Control Potassium Excretion; it is More Than a Poorly Absorbable Anion Effect | American Journal of Physiology-Renal Physiology
journals.physiology.org/doi/…
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Jens Leipziger and his collaborators showed recently that the loss of the Secretin Receptor Impairs Renal Bicarbonate Excretion and Aggravates Metabolic Alkalosis in Mice during Acute Base-Loading : Journal of the American Society of Nephrology journals.lww.com/jasn/Abstra…
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WNK1 promotes water homeostasis by acting as a central osmolality sensor for arginine vasopressin release. Let's have a look !
jci.org/articles/view/164222
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The latest study discovered the crucial role of IRAP (insulin-regulated aminopeptidase) in water excretion and the regulation of aquaporin 2 (AQP2) expression.
pubmed.ncbi.nlm.nih.gov/3699…
#APS #APSETG #Kidney #renaldisease
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Check out this research reveals the role of the YAP pathway in regulating activator protein-1 expression in renal tubular cells, shedding light on the underlying mechanisms of tubular injury, inflammation, and fibrosis.
pubmed.ncbi.nlm.nih.gov/3714…
#APS #APSETG #chronickidneydisease
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Friday is for learning!! Have you used the air-liquid interface cultures in your lab?
pubmed.ncbi.nlm.nih.gov/3719…
#APS #APSETG #drugdelivery
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Which CFTR mutation response well to the "correctors"? Check out this study uses deep mutational scanning and reveals that specific mutations have the greatest sensitivity to the correctors.
pubmed.ncbi.nlm.nih.gov/3725…
#APS #APSETG #cysticfibrosis #genetics
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Friday is for learning! Dive into this fascinating review on cystic fibrosis in JAMA!
pubmed.ncbi.nlm.nih.gov/3727…
#APS #APSETG #cysticfibrosis
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Check out this paper utilizing single cell barcode-based lineage tracing (CellTagging) and organoids to identify and functionally assess a new regionally distinct cell population in human developing lungs!
pnas.org/doi/epdf/10.1073/pn…
#APS #APSETG #singlecell #organoids
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Do you perform tissue fixation in your lab on a daily basis? Check out this new formalin alternative and let us know what you think!
pubmed.ncbi.nlm.nih.gov/3732…
#APS #APSETG #histology
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How is the MCT4 transporter-dependent lactate secretion is involved in immunotherapy resistance in KRAS-mutated lung adenocarcinoma? Dive in this new research!
pubmed.ncbi.nlm.nih.gov/3732…
#APS #APSETG #lungcancer #Lactase #cancerimmunotherapy
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Check out this study uncovering 30 previously unidentified CpG sites significantly linked to baseline eGFR and all previously unidentified eight CpG sites associated with eGFR slope!
tinyurl.com/58fd5hex
#APS #epigenetics #diabetes #KidneyDisease
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Do you use two-photon microscopy for your research?
Check out the recent development of the Synthetic Aperture Radar in Two-Photon Microscopy (SAR-TPM)!
tinyurl.com/3z8wpd72
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APS ETG retweeted
APS ETG members: Call for papers in @AJPRenal on diabetic kidney disease, guest associate editors @SKMallipattu and Dr Kyung Lee journals.physiology.org/ajpr…
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Dive in this beautiful review article about diabetic kidney disease talking about the molecular and genetic studies highlight the critical role of podocytes and endothelial cells in driving albuminuria and early kidney disease in diabetes.
tinyurl.com/yfhnpncz
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Have you been thinking of CRISPR-screen and genetics in complicated diseases?
By leveraging direct variant insertion and single-cell sequencing, the researchers explore the impact of noncoding variants on gene expression and regulatory networks.
tinyurl.com/zb79wwhr
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Heterozygous mutations in the gene encoding RagD GTPase have been identified as the cause of this unique autosomal dominant condition!
shorturl.at/TUVX7
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