Found: 26
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Early maternal separation induces alterations of colonic epithelial permeability and morphology.
- Published in:
- Pediatric Surgery International, 2014, v. 30, n. 12, p. 1217, doi. 10.1007/s00383-014-3611-x
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- Publication type:
- Article
Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis.
- Published in:
- Life Science Alliance, 2023, v. 6, n. 6, p. 1, doi. 10.26508/lsa.202201857
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- Publication type:
- Article
Correlation of Electrophysiological and Fluorescence-Based Measurements of Modulator Efficacy in Nasal Epithelial Cultures Derived from People with Cystic Fibrosis.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 8, p. 1174, doi. 10.3390/cells12081174
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- Publication type:
- Article
Intestinal epithelial tight junctions and permeability can be rescued through the regulation of endoplasmic reticulum stress by amniotic fluid stem cells during necrotizing enterocolitis.
- Published in:
- FASEB Journal, 2021, v. 35, n. 1, p. 1, doi. 10.1096/fj.202001426R
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- Publication type:
- Article
Augmentation of Cystic Fibrosis Transmembrane Conductance Regulator Function in Human Bronchial Epithelial Cells via SLC6A14-Dependent Amino Acid Uptake: Implications for Treatment of Cystic Fibrosis.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2019, v. 61, n. 6, p. 755, doi. 10.1165/rcmb.2019-0094OC
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- Publication type:
- Article
Inhibition of Amiloride-Sensitive Epithelial Na<sup>+</sup> Absorption by Extracellular Nucleotides in Human Normal and Cystic Fibrosis Airways.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2000, v. 23, n. 6, p. 755, doi. 10.1165/ajrcmb.23.6.4207
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- Publication type:
- Article
Does Integration of Various Ion Channel Measurements Improve Diagnostic Performance in Cystic Fibrosis?
- Published in:
- Annals of the American Thoracic Society, 2014, v. 11, n. 4, p. 562, doi. 10.1513/AnnalsATS.201311-412OC
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- Publication type:
- Article
Impact of CFTR modulation with Ivacaftor on Gut Microbiota and Intestinal Inflammation.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-36364-6
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- Publication type:
- Article
Weight increase in people with cystic fibrosis on CFTR modulator therapy is mainly due to increase in fat mass.
- Published in:
- Frontiers in Pharmacology, 2023, p. 1, doi. 10.3389/fphar.2023.1157459
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- Publication type:
- Article
Orkambi® and amplifier co-therapy improves function from a rare CFTR mutation in gene-edited cells and patient tissue.
- Published in:
- EMBO Molecular Medicine, 2017, v. 9, n. 9, p. 1224, doi. 10.15252/emmm.201607137
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- Publication type:
- Article
Immunoreactive trypsinogen levels in newborn screened infants with an inconclusive diagnosis of cystic fibrosis.
- Published in:
- 2019
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- Publication type:
- journal article
Severely elevated transaminases in an adolescent male with anorexia nervosa.
- Published in:
- International Journal of Eating Disorders, 2013, v. 46, n. 7, p. 751, doi. 10.1002/eat.22162
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- Publication type:
- Article
Inhibition of corticotropin-releasing hormone receptor 1 and activation of receptor 2 protect against colonic injury and promote epithelium repair.
- Published in:
- Scientific Reports, 2017, p. 46616, doi. 10.1038/srep46616
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- Publication type:
- Article
Clinical Mechanism of the CFTR Potentiator Ivacaftor in G551D-Mediated Cystic Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2014, v. 190, n. 2, p. E1, doi. 10.1164/rccm.201404-0703oc
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- Publication type:
- Article
Clinical Mechanism of the Cystic Fibrosis Transmembrane Conductance Regulator Potentiator Ivacaftor in G551D-mediated Cystic Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2014, v. 190, n. 2, p. 175, doi. 10.1164/rccm.201404-0703OC
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- Publication type:
- Article
β-Adrenergic Sweat Secretion as a Diagnostic Test for Cystic Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2012, v. 186, n. 8, p. 732, doi. 10.1164/rccm.201205-0922OC
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- Publication type:
- Article
SHIFTing goals in cystic fibrosis—managing extrapulmonary disease in the era of CFTR modulator therapy; Proceedings of the International Shaping Initiatives and Future Trends (SHIFT) Symposium.
- Published in:
- Pediatric Pulmonology, 2024, v. 59, n. 6, p. 1661, doi. 10.1002/ppul.26970
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- Publication type:
- Article
β‐adrenergic sweat test in children with inconclusive cystic fibrosis diagnosis: Do we need new reference ranges?
- Published in:
- Pediatric Pulmonology, 2023, v. 58, n. 1, p. 187, doi. 10.1002/ppul.26179
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- Publication type:
- Article
A novel frameshift mutation, c.1870delG, in exon 12 of the CFTR gene.
- Published in:
- Human Mutation, 2000, v. 16, n. 3, p. 277, doi. 10.1002/1098-1004(200009)16:3<277::AID-HUMU26>3.0.CO;2-S
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- Publication type:
- Article
Diadenosine Polyphosphates Activate a Ca<sup>2+</sup>-Dependent K<sup>+</sup>-Conductance in Porcine Aortic Smooth Muscle Cells via P2-Purinoceptors.
- Published in:
- Cellular Physiology & Biochemistry (Karger AG), 2000, v. 10, n. 3, p. 125, doi. 10.1159/000016343
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- Publication type:
- Article
Phenotypic profiling of CFTR modulators in patient-derived respiratory epithelia.
- Published in:
- NPJ Genomic Medicine, 2017, v. 2, n. 1, p. N.PAG, doi. 10.1038/s41525-017-0015-6
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- Publication type:
- Article
Risk Factors Associated With Pediatric Acute Recurrent and Chronic Pancreatitis.
- Published in:
- JAMA Pediatrics, 2016, v. 170, n. 6, p. 562, doi. 10.1001/jamapediatrics.2015.4955
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- Publication type:
- Article
Preclinical Studies of a Rare CF-Causing Mutation in the Second Nucleotide Binding Domain (c.3700A>G) Show Robust Functional Rescue in Primary Nasal Cultures by Novel CFTR Modulators.
- Published in:
- Journal of Personalized Medicine, 2020, v. 10, n. 4, p. 209, doi. 10.3390/jpm10040209
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- Publication type:
- Article
The CFTR Mutation c.3453G > C (D1152H) Confers an Anion Selectivity Defect in Primary Airway Tissue that Can be Rescued by Ivacaftor.
- Published in:
- Journal of Personalized Medicine, 2020, v. 10, n. 2, p. 40, doi. 10.3390/jpm10020040
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- Publication type:
- Article
Cystic fibrosis gene modifier SLC26A9 modulates airway response to CFTR-directed therapeutics.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 20, p. 4590, doi. 10.1093/hmg/ddw290
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- Publication type:
- Article
Na+ -Dependent and -Independent Amino Acid Transport Systems in Immortalized Human Kidney Epithelial Cells Derived from the Proximal Tubule.
- Published in:
- Kidney & Blood Pressure Research, 1998, v. 21, n. 1, p. 50, doi. 10.1159/000025843
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- Publication type:
- Article