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Wyszukujesz frazę ""Frizzell RA"" wg kryterium: Autor


Wyświetlanie 1-18 z 18
Tytuł:
SFPQ rescues F508del-CFTR expression and function in cystic fibrosis bronchial epithelial cells.
Autorzy:
Kumar P; Department of Anatomy, Physiology and Genetics, School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD, 20814, USA.
Soni DK; Department of Anatomy, Physiology and Genetics, School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD, 20814, USA.
Sen C; Department of Anatomy, Physiology and Genetics, School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD, 20814, USA.
Larsen MB; Department of Cell Biology, University of Pittsburgh, School of Medicine, Pittsburgh, PA, 1526, USA.
Mazan-Mamczarz K; Laboratory of Genetics and Genomics, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224-6825, USA.
Piao Y; Laboratory of Genetics and Genomics, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224-6825, USA.
De S; Laboratory of Genetics and Genomics, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224-6825, USA.
Gorospe M; Laboratory of Genetics and Genomics, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224-6825, USA.
Frizzell RA; Department of Cell Biology, University of Pittsburgh, School of Medicine, Pittsburgh, PA, 1526, USA.
Biswas R; Department of Anatomy, Physiology and Genetics, School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD, 20814, USA. .; Department of Anatomy, Physiology and Genetics, School of Medicine, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA. .
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Źródło:
Scientific reports [Sci Rep] 2021 Aug 17; Vol. 11 (1), pp. 16645. Date of Electronic Publication: 2021 Aug 17.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Bronchi/*metabolism
Cystic Fibrosis/*metabolism
Cystic Fibrosis Transmembrane Conductance Regulator/*metabolism
PTB-Associated Splicing Factor/*physiology
Bronchi/pathology ; Cells, Cultured ; Cystic Fibrosis/pathology ; Cystic Fibrosis Transmembrane Conductance Regulator/genetics ; Epithelial Cells/metabolism ; Epithelial Cells/pathology ; Gene Expression Regulation/physiology ; Humans ; Mutation ; Transcriptome
Czasopismo naukowe
Tytuł:
Comparative analyses of long non-coding RNA profiles in vivo in cystic fibrosis lung airway and parenchyma tissues.
Autorzy:
Kumar P; Department of Anatomy, Physiology and Genetics, School of Medicine, Uniformed Services University of the Health Sciences, Room B4024, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA.
Sen C; Department of Anatomy, Physiology and Genetics, School of Medicine, Uniformed Services University of the Health Sciences, Room B4024, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA.
Peters K; Departments of Pediatrics and Cell Biology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Frizzell RA; Departments of Pediatrics and Cell Biology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Biswas R; Department of Anatomy, Physiology and Genetics, School of Medicine, Uniformed Services University of the Health Sciences, Room B4024, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA. .
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Źródło:
Respiratory research [Respir Res] 2019 Dec 16; Vol. 20 (1), pp. 284. Date of Electronic Publication: 2019 Dec 16.
Typ publikacji:
Comparative Study; Journal Article
MeSH Terms:
Gene Expression Profiling*
Transcriptome*
Cystic Fibrosis/*genetics
Epithelial Cells/*metabolism
Lung/*metabolism
Parenchymal Tissue/*metabolism
RNA, Long Noncoding/*genetics
Adolescent ; Adult ; Case-Control Studies ; Cell Line ; Cystic Fibrosis/diagnosis ; Cystic Fibrosis/metabolism ; Female ; Gene Expression Regulation ; Gene Regulatory Networks ; Humans ; Male ; Young Adult
Czasopismo naukowe
Tytuł:
miR-16 rescues F508del-CFTR function in native cystic fibrosis epithelial cells.
Autorzy:
Kumar P; Department of Anatomy, Physiology and Genetics, Uniformed Services University School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.
Bhattacharyya S; Department of Anatomy, Physiology and Genetics, Uniformed Services University School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.
Peters KW; Department of Cell Biology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Glover ML; Department of Cell Biology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Sen A; Department of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.
Cox RT; Department of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.
Kundu S; Department of Anatomy, Physiology and Genetics, Uniformed Services University School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.
Caohuy H; Department of Anatomy, Physiology and Genetics, Uniformed Services University School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.
Frizzell RA; Department of Cell Biology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Pollard HB; Department of Anatomy, Physiology and Genetics, Uniformed Services University School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.
Biswas R; Department of Anatomy, Physiology and Genetics, Uniformed Services University School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.
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Źródło:
Gene therapy [Gene Ther] 2015 Nov; Vol. 22 (11), pp. 908-16. Date of Electronic Publication: 2015 Jul 02.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Cystic Fibrosis/*genetics
Cystic Fibrosis/*therapy
Cystic Fibrosis Transmembrane Conductance Regulator/*genetics
MicroRNAs/*genetics
Cell Line ; Cells, Cultured ; Cystic Fibrosis/metabolism ; Cystic Fibrosis/pathology ; Epithelial Cells/pathology ; Genetic Therapy/methods ; Humans ; MicroRNAs/administration & dosage ; MicroRNAs/biosynthesis ; Mutation ; RNA, Messenger/biosynthesis ; RNA, Messenger/genetics ; Respiratory Mucosa/pathology
Czasopismo naukowe
Tytuł:
Reduced histone deacetylase 7 activity restores function to misfolded CFTR in cystic fibrosis.
Autorzy:
Hutt DM; Department of Cell Biology, The Scripps Research Institute, La Jolla, California, USA.
Herman D
Rodrigues AP
Noel S
Pilewski JM
Matteson J
Hoch B
Kellner W
Kelly JW
Schmidt A
Thomas PJ
Matsumura Y
Skach WR
Gentzsch M
Riordan JR
Sorscher EJ
Okiyoneda T
Yates JR 3rd
Lukacs GL
Frizzell RA
Manning G
Gottesfeld JM
Balch WE
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Źródło:
Nature chemical biology [Nat Chem Biol] 2010 Jan; Vol. 6 (1), pp. 25-33. Date of Electronic Publication: 2009 Dec 06.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Mutation*
Cystic Fibrosis/*metabolism
Cystic Fibrosis Transmembrane Conductance Regulator/*metabolism
Histone Deacetylases/*metabolism
Animals ; Bronchi/metabolism ; Cell Membrane/metabolism ; Cricetinae ; Epithelial Cells/metabolism ; Gene Silencing ; Humans ; Hydroxamic Acids/chemistry ; Protein Denaturation ; Protein Folding ; RNA, Small Interfering/metabolism ; Vorinostat
Czasopismo naukowe
    Wyświetlanie 1-18 z 18

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