Search Results - "Yarlagadda, Sunitha"
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Patient-derived pancreas-on-a-chip to model cystic fibrosis-related disorders
Published in Nature communications (16-07-2019)“…Cystic fibrosis (CF) is a genetic disorder caused by defective CF Transmembrane Conductance Regulator (CFTR) function. Insulin producing pancreatic islets are…”
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Characterizing post-branching nephrogenesis in the neonatal rabbit
Published in Scientific reports (06-11-2023)“…Human nephrogenesis ends prior to birth in term infants (34–36 week gestation), with most (60%) nephrons forming in late gestation in two post-branching…”
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Targeting DNAJB9, a novel ER luminal co-chaperone, to rescue ΔF508-CFTR
Published in Scientific reports (08-07-2019)“…The molecular mechanism of Endoplasmic Reticulum-associated degradation (ERAD) of Cystic fibrosis transmembrane-conductance regulator (CFTR) is largely…”
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Compartmentalization of cyclic nucleotide signaling: a question of when, where, and why?
Published in Pflügers Archiv (01-10-2013)“…Preciseness of cellular behavior depends upon how an extracellular cue mobilizes a correct orchestra of cellular messengers and effector proteins spatially and…”
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Compartmentalized Accumulation of cAMP near Complexes of Multidrug Resistance Protein 4 (MRP4) and Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Contributes to Drug-induced Diarrhea
Published in The Journal of biological chemistry (01-05-2015)“…Diarrhea is one of the most common adverse side effects observed in ∼7% of individuals consuming Food and Drug Administration (FDA)-approved drugs. The…”
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The phospholipase A1 activity of lysophospholipase A-I links platelet activation to LPA production during blood coagulation[S]
Published in Journal of lipid research (01-05-2011)“…Platelet activation initiates an upsurge in polyunsaturated (18:2 and 20:4) lysophosphatidic acid (LPA) production. The biochemical pathway(s) responsible for…”
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Guanylate cyclase 2C agonism corrects CFTR mutants
Published in JCI insight (05-10-2017)“…Cystic fibrosis (CF) is a genetic disorder in which epithelium-generated fluid flow from the lung, intestine, and pancreas is impaired due to mutations…”
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Elexacaftor/Tezacaftor/Ivacaftor Improved Clinical Outcomes in a Patient with N1303K-CFTR Based on In Vitro Experimental Evidence
Published in American journal of respiratory and critical care medicine (15-11-2021)“…Huang et al discuss their study on the use of a new generation of cystic fibrosis transmembrane conductance regulator (CFTR) protein modulator in patients with…”
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586 ER LUMINAL ERAD AS A NOVEL TARGET TO RESCUE MUTANT CFTR IN THE INTESTINE
Published in Gastroenterology (New York, N.Y. 1943) (01-05-2020)Get full text
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A personalized medicine approach to optimize care for a pediatric cystic fibrosis patient with atypical clinical symptoms
Published in Pediatric pulmonology (01-01-2024)Get full text
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Drug-induced secretory diarrhea: A role for CFTR
Published in Pharmacological research (01-12-2015)“…[Display omitted] Many medications induce diarrhea as a side effect, which can be a major obstacle to therapeutic efficacy and also a life-threatening…”
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Human Nephrogenesis can Persist Beyond 40 Postnatal Days in Preterm Infants
Published in Kidney international reports (01-02-2024)“…Human nephrogenesis is typically completed by 36 weeks gestation; however, it is impacted by preterm birth. Early studies suggested that nephrogenesis…”
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Stabilizing Rescued Surface-Localized ΔF508 CFTR by Potentiation of Its Interaction with Na+/H+ Exchanger Regulatory Factor 1
Published in Biochemistry (Easton) (01-07-2014)“…Cystic fibrosis (CF) is a recessive genetic disease caused by mutations in CFTR, a plasma-membrane-localized anion channel. The most common mutation in CFTR,…”
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Personalized medicine in cystic fibrosis: genistein supplementation as a treatment option for patients with a rare S1045Y-CFTR mutation
Published in American journal of physiology. Lung cellular and molecular physiology (01-08-2016)“…Cystic fibrosis (CF) is a life-shortening disease caused by the mutations that generate nonfunctional CF transmembrane conductance regulator (CFTR) protein. A…”
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Förster Resonance Energy Transfer — An approach to visualize the spatiotemporal regulation of macromolecular complex formation and compartmentalized cell signaling
Published in Biochimica et biophysica acta (01-10-2014)“…Signaling messengers and effector proteins provide an orchestrated molecular machinery to relay extracellular signals to the inside of cells and thereby…”
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Multi-drug Resistance Protein 4 (MRP4)-mediated Regulation of Fibroblast Cell Migration Reflects a Dichotomous Role of Intracellular Cyclic Nucleotides
Published in The Journal of biological chemistry (08-02-2013)“…It has long been known that cyclic nucleotides and cyclic nucleotide-dependent signaling molecules control cell migration. However, the concept that it is not…”
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Altered cGMP Dynamics at the Plasma Membrane Contribute to Diarrhea in Ulcerative Colitis
Published in The American journal of pathology (01-10-2015)“…Ulcerative colitis (UC) belongs to inflammatory bowel disorders, a group of gastrointestinal disorders that can produce serious recurring diarrhea in affected…”
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Capturing the Direct Binding of CFTR Correctors to CFTR by Using Click Chemistry
Published in Chembiochem : a European journal of chemical biology (21-09-2015)“…Cystic fibrosis (CF) is a lethal genetic disease caused by the loss or dysfunction of the CF transmembrane conductance regulator (CFTR) channel. F508del is the…”
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PKA and actin play critical roles as downstream effectors in MRP4-mediated regulation of fibroblast migration
Published in Cellular signalling (01-07-2015)“…Multidrug resistance protein 4 (MRP4), a member of the ATP binding cassette transporter family, functions as a plasma membrane exporter of cyclic nucleotides…”
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