Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Pauline T. Ikpa"'
Autor:
Pauline T. Ikpa, Marcela Doktorova, Kelly F. Meijsen, Natascha D.A. Nieuwenhuijze, Henkjan J. Verkade, Johan W. Jonker, Hugo R. de Jonge, Marcel J.C. Bijvelds
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 9, Iss 1, Pp 47-60 (2020)
Background & Aims: The bile acid (BA)-activated farnesoid X receptor (FXR) controls hepatic BA synthesis and cell proliferation via the intestinal hormone fibroblast growth factor 19. Because cystic fibrosis (CF) is associated with intestinal dysbios
Externí odkaz:
https://doaj.org/article/0a415309b75c4917861654a9a812df3d
Autor:
Hugo R. de Jonge, Kelly F. Meijsen, Johan W. Jonker, Pauline T. Ikpa, Marcel J. C. Bijvelds, Natascha D.A. Nieuwenhuijze, Henkjan J. Verkade, Marcela Doktorova
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 9, Iss 1, Pp 47-60 (2020)
Cellular and molecular gastroenterology and hepatology, 9(1), 47-60. HANLEY & BELFUS-ELSEVIER INC
Cellular and Molecular Gastroenterology and Hepatology
Cellular and Molecular Gastroenterology and Hepatology, 9(1), 47-60. Elsevier Inc.
Cellular and molecular gastroenterology and hepatology, 9(1), 47-60. HANLEY & BELFUS-ELSEVIER INC
Cellular and Molecular Gastroenterology and Hepatology
Cellular and Molecular Gastroenterology and Hepatology, 9(1), 47-60. Elsevier Inc.
Background & Aims The bile acid (BA)-activated farnesoid X receptor (FXR) controls hepatic BA synthesis and cell proliferation via the intestinal hormone fibroblast growth factor 19. Because cystic fibrosis (CF) is associated with intestinal dysbiosi
Autor:
Kalyan Dulla, Pauline T. Ikpa, Kelly F. Meijsen, Natascha D.A. Nieuwenhuijze, Marcel J. C. Bijvelds, Hugo R. de Jonge
Publikováno v:
Genomics, 112(2), 1139-1150. Academic Press
Cystic fibrosis (CF) is caused by mutations in the gene encoding the CFTR anion channel. Loss of CFTR function in pancreatic, biliary and intestinal epithelia, severely affects gastrointestinal function. Transcriptome analysis indicated the activatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::268191e0adc8855fc2b2b3e50ee1582f
https://pure.eur.nl/en/publications/c492eab8-921d-4390-928c-7ae2cf643362
https://pure.eur.nl/en/publications/c492eab8-921d-4390-928c-7ae2cf643362
Publikováno v:
International Journal of Biochemistry & Cell Biology, 52, 192-200. Elsevier Ltd.
Cystic fibrosis (CF), the most common, life-threatening monogenetic disease in Caucasians, is caused by mutations in the CFTR gene, encoding a cAMP- and cGMP-regulated epithelial chloride channel. Symptomatic therapies treating end-organ manifestatio
Autor:
Yannicka S N Mardenborough, Michele Cristóvão, Claire Wyman, Herrie H.K. Winterwerp, Charlie Laffeber, Josef Jiricny, Mariela Artola-Borán, Joyce H.G. Lebbink, Pauline T. Ikpa, Peter Friedhoff, Aruna Jaddoe, Roland Kanaar, Nicolaas Hermans
Publikováno v:
Nucleic Acids Research, 44(14), 6770-6786
Nucleic Acids Research
Nucleic Acids Research, 44 (14)
Nucleic acids research
Nucleic Acids Research, 44(14), 6770-6786. Oxford University Press
Nucleic Acids Research
Nucleic Acids Research, 44 (14)
Nucleic acids research
Nucleic Acids Research, 44(14), 6770-6786. Oxford University Press
DNA mismatch repair (MMR) is an evolutionarily-conserved process responsible for the repair of replication errors. In Escherichia coli, MMR is initiated by MutS and MutL, which activate MutH to incise transiently-hemimethylated GATC sites. MMR effici
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c69fd41f3671fef2aea00335d8dfd758
http://hdl.handle.net/1887/45348
http://hdl.handle.net/1887/45348