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AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestations.
Darrah, Rebecca J; Jacono, Frank J; Joshi, Neha; Mitchell, Anna L; Sattar, Abdus; Campanaro, Cara K; Litman, Paul; Frey, Jennifer; Nethery, David E; Barbato, Eric S; Hodges, Craig A; Corvol, Harriet; Cutting, Garry R; Knowles, Michael R; Strug, Lisa J; Drumm, Mitchell L.
Afiliação
  • Darrah RJ; Frances Payne Bolton School of Nursing, Case Western Reserve University, Cleveland, OH 44106, USA; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH 44106, USA. Electronic address: rjm11@case.edu.
  • Jacono FJ; Department of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA; Department of Medicine, Louis Stokes Cleveland VA Medical Center, Cleveland, OH 44106, USA.
  • Joshi N; Department of Pediatrics, Case Western Reserve University, Cleveland, OH 44106, USA.
  • Mitchell AL; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH 44106, USA.
  • Sattar A; Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, OH 44106, USA.
  • Campanaro CK; Department of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
  • Litman P; Frances Payne Bolton School of Nursing, Case Western Reserve University, Cleveland, OH 44106, USA.
  • Frey J; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH 44106, USA.
  • Nethery DE; Department of Medicine, Louis Stokes Cleveland VA Medical Center, Cleveland, OH 44106, USA.
  • Barbato ES; Frances Payne Bolton School of Nursing, Case Western Reserve University, Cleveland, OH 44106, USA.
  • Hodges CA; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH 44106, USA; Department of Pediatrics, Case Western Reserve University, Cleveland, OH 44106, USA.
  • Corvol H; Sorbonne Universités, UPMC Univ Paris 06, INSERM, Centre de Recherche Saint-Antoine (CRSA), Paris 75012, France; Pneumologie pédiatrique, APHP, Hôpital Trousseau, Paris 75012, France.
  • Cutting GR; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • Knowles MR; Marsico Lung Institute/UNC CF Research Center, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North, Carolina, 27599, USA.
  • Strug LJ; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada M5G 0A4; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada M5T 3M7.
  • Drumm ML; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH 44106, USA; Department of Pediatrics, Case Western Reserve University, Cleveland, OH 44106, USA.
J Cyst Fibros ; 18(1): 127-134, 2019 01.
Article em En | MEDLINE | ID: mdl-29937318
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: DNA / Fibrose Cística / Receptor Tipo 2 de Angiotensina / Pulmão / Pneumopatias / Mutação Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Child / Female / Humans / Male Idioma: En Revista: J Cyst Fibros Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: DNA / Fibrose Cística / Receptor Tipo 2 de Angiotensina / Pulmão / Pneumopatias / Mutação Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Child / Female / Humans / Male Idioma: En Revista: J Cyst Fibros Ano de publicação: 2019 Tipo de documento: Article