Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Clara J. Foo"'
Autor:
Erika N Sutanto, Amelia Scaffidi, Luke W Garratt, Kevin Looi, Clara J Foo, Michela A Tessari, Richard A Janssen, David F Fischer, Stephen M Stick, Anthony Kicic, AREST CF
Publikováno v:
PLoS ONE, Vol 13, Iss 1, p e0191618 (2018)
Mutations in the cystic fibrosis transmembrane regulator (CFTR) gene can reduce function of the CFTR ion channel activity and impair cellular chloride secretion. The gold standard method to assess CFTR function of ion transport using the Ussing chamb
Externí odkaz:
https://doaj.org/article/7ccb2803f8194d08862579e128f80894
Autor:
Amelia K. Scaffidi, David F. Fischer, Kevin Looi, Stephen M. Stick, Clara J. Foo, Luke W. Garratt, Erika N. Sutanto, Michela Tessari, Richard A.J. Janssen, Anthony Kicic
Publikováno v:
PLoS ONE, Vol 13, Iss 1, p e0191618 (2018)
PLoS ONE
PLoS ONE
Background Mutations in the cystic fibrosis transmembrane regulator (CFTR) gene can reduce function of the CFTR ion channel activity and impair cellular chloride secretion. The gold standard method to assess CFTR function of ion transport using the U
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d947b6be161ee07990c5ad4bc8339b9e
http://europepmc.org/articles/PMC5779693?pdf=render
http://europepmc.org/articles/PMC5779693?pdf=render
Autor:
Anthony Kicic, Luke W. Garratt, Clara J. Foo, B. Banerjee, Erika N. Sutanto, Stephen M. Stick, Kak-Ming Ling, Kevin Looi
Publikováno v:
Respirology. 16:725-737
Asthma is the commonest medical cause for hospital admission for children in Australia, affects more than 300 million people worldwide, and is incurable, severe in large number and refractory to treatment in many. However, there have been no new sign
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0caae9edc4863b7322a25000201dac7
https://doi.org/10.1111/j.1440-1843.2011.02001.x
https://doi.org/10.1111/j.1440-1843.2011.02001.x
Publikováno v:
Gynecological Endocrinology. 23:535-540
Postmenopausal osteoporosis, caused by estrogen deficiency, is characterized by the structural deterioration of bone accompanied by an increase in bone marrow adipocytes. Transgenic animal models have shown that there is a reciprocal relationship bet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89a3bcfc14913d5b35e33601d65c9b8f
https://doi.org/10.1080/09513590701556483
https://doi.org/10.1080/09513590701556483
Autor:
Kak-Ming Ling, Erika N. Sutanto, K. Martinovich, Thomas Iosifidis, E. Kicic-Starcevich, Francis J. Lannigan, Stephen M. Stick, Kevin Looi, Anthony Kicic, Clara J. Foo, Luke W. Garratt
Publikováno v:
Experimental lung research. 40(9)
The bronchial brushing technique presents an opportunity to establish a gold standard in vitro model of Cystic Fibrosis (CF) airway disease. However, unique obstacles exist when establishing CF airway epithelial cells (pAECCF). We aimed to identify d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8fb371a42cffc71971cc09a52f41098
https://pubmed.ncbi.nlm.nih.gov/25191759
https://pubmed.ncbi.nlm.nih.gov/25191759
Autor:
Kevin, Looi, Erika N, Sutanto, Balarka, Banerjee, Luke, Garratt, Kak-Ming, Ling, Clara J, Foo, Stephen M, Stick, Anthony, Kicic
Publikováno v:
Respirology (Carlton, Vic.). 16(5)
Asthma is the commonest medical cause for hospital admission for children in Australia, affects more than 300 million people worldwide, and is incurable, severe in large number and refractory to treatment in many. However, there have been no new sign
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1cc37885f779f6f760a90983c0871ede
https://pubmed.ncbi.nlm.nih.gov/21624002
https://pubmed.ncbi.nlm.nih.gov/21624002
Publikováno v:
D25. CYSTIC FIBROSIS.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f64672a5754947697e2cf594d08ed5e
https://doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a5727
https://doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a5727
Autor:
Darryl A. Knight, Erika N. Sutanto, Paul T. Stevens, David Mullane, Anthony Kicic, Stephen M. Stick, Clara J. Foo
Publikováno v:
American journal of respiratory cell and molecular biology. 44(6)
There is controversy regarding whether cystic fibrosis (CF) airway epithelial cells (AECs) are intrinsically proinflammatory. The objective of the current study was to characterize the inflammatory profiles of AECs from children with CF compared with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2c16c90bc933ce968622b99d329a8a8
https://pubmed.ncbi.nlm.nih.gov/21653905
https://pubmed.ncbi.nlm.nih.gov/21653905
Publikováno v:
D94. CYSTIC FIBROSIS: FROM CLINIC TO LAB AND BACK.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37325e6fb20503e7d142f1e696728b50
https://doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a6578
https://doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a6578