Search Results - "Yarlagadda, Sunitha"

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    Patient-derived pancreas-on-a-chip to model cystic fibrosis-related disorders by Shik Mun, Kyu, Arora, Kavisha, Huang, Yunjie, Yang, Fanmuyi, Yarlagadda, Sunitha, Ramananda, Yashaswini, Abu-El-Haija, Maisam, Palermo, Joseph J., Appakalai, Balamurugan N., Nathan, Jaimie D., Naren, Anjaparavanda P.

    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 by Schuh, Meredith P., Yarlagadda, Sunitha, Alkhudairy, Lyan, Preusse, Kristina, Kopan, Raphael

    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 by Huang, Yunjie, Arora, Kavisha, Mun, Kyu Shik, Yang, Fanmuyi, Moon, ChangSuk, Yarlagadda, Sunitha, Jegga, Anil, Weaver, Timothy, Naren, Anjaparavanda P.

    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? by Arora, Kavisha, Sinha, Chandrima, Zhang, Weiqiang, Ren, Aixia, Moon, Chang Suk, Yarlagadda, Sunitha, Naren, Anjaparavanda P.

    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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    Guanylate cyclase 2C agonism corrects CFTR mutants by Arora, Kavisha, Huang, Yunjie, Mun, Kyushik, Yarlagadda, Sunitha, Sundaram, Nambirajan, Kessler, Marco M, Hannig, Gerhard, Kurtz, Caroline B, Silos-Santiago, Inmaculada, Helmrath, Michael, Palermo, Joseph J, Clancy, John P, Steinbrecher, Kris A, Naren, Anjaparavanda P

    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 by Huang, Yunjie, Paul, Grace, Lee, Jesun, Yarlagadda, Sunitha, McCoy, Karen, Naren, Anjaparavanda P

    “…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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    Drug-induced secretory diarrhea: A role for CFTR by Moon, Changsuk, Zhang, Weiqiang, Sundaram, Nambirajan, Yarlagadda, Sunitha, Reddy, Vadde Sudhakar, Arora, Kavisha, Helmrath, Michael A., Naren, Anjaparavanda P.

    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 by Carpenter, James, Yarlagadda, Sunitha, VandenHeuvel, Katherine A, Ding, Lili, Schuh, Meredith P

    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 by Arora, Kavisha, Moon, Changsuk, Zhang, Weiqiang, Yarlagadda, Sunitha, Penmatsa, Himabindu, Ren, Aixia, Sinha, Chandrima, Naren, Anjaparavanda P

    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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    Förster Resonance Energy Transfer — An approach to visualize the spatiotemporal regulation of macromolecular complex formation and compartmentalized cell signaling by Sinha, Chandrima, Arora, Kavisha, Moon, Chang Suk, Yarlagadda, Sunitha, Woodrooffe, Koryse, Naren, Anjaparavanda P.

    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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    Altered cGMP Dynamics at the Plasma Membrane Contribute to Diarrhea in Ulcerative Colitis by Arora, Kavisha, Sinha, Chandrima, Zhang, Weiqiang, Moon, Chang Suk, Ren, Aixia, Yarlagadda, Sunitha, Dostmann, Wolfgang R, Adebiyi, Adebowale, Haberman, Yael, Denson, Lee A, Wang, Xusheng, Naren, Anjaparavanda P

    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 by Sinha, Chandrima, Zhang, Weiqiang, Moon, Chang Suk, Actis, Marcelo, Yarlagadda, Sunitha, Arora, Kavisha, Woodroofe, Koryse, Clancy, John P., Lin, Songbai, Ziady, Assem G., Frizzell, Raymond, Fujii, Naoaki, Naren, Anjaparavanda P.

    “…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 by Sinha, Chandrima, Ren, Aixia, Arora, Kavisha, Moon, Chang Suk, Yarlagadda, Sunitha, Woodrooffe, Koryse, Lin, Songbai, Schuetz, John D, Ziady, Assem G, Naren, Anjaparavanda P

    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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