Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Millie Garg"'
Autor:
Michael J Coffey, Ivan Low, Sacha Stelzer-Braid, Bernd Wemheuer, Millie Garg, Torsten Thomas, Adam Jaffe, William D Rawlinson, Chee Y Ooi
Publikováno v:
PLoS ONE, Vol 15, Iss 5, p e0233557 (2020)
Intestinal bacterial dysbiosis is evident in children with cystic fibrosis (CF) and intestinal viruses may be contributory, given their influence on bacterial species diversity and biochemical cycles. We performed a prospective, case-control study on
Externí odkaz:
https://doaj.org/article/1b4788400dab4b23be75642ad0d102a2
Publikováno v:
Paediatric respiratory reviews. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7ed3dedebaf6e11caf8bbaca076b36b
https://pubmed.ncbi.nlm.nih.gov/32917517
https://pubmed.ncbi.nlm.nih.gov/32917517
Autor:
Ivan Low, Chee Y. Ooi, Sacha Stelzer-Braid, Michael J. Coffey, William D. Rawlinson, Torsten Thomas, Adam Jaffe, Bernd Wemheuer, Millie Garg
Publikováno v:
PLoS ONE, Vol 15, Iss 5, p e0233557 (2020)
PLoS ONE
PLoS ONE
Intestinal bacterial dysbiosis is evident in children with cystic fibrosis (CF) and intestinal viruses may be contributory, given their influence on bacterial species diversity and biochemical cycles. We performed a prospective, case-control study on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfc31ffc8cf9991bbf1f377d67d3ee16
https://doaj.org/article/1b4788400dab4b23be75642ad0d102a2
https://doaj.org/article/1b4788400dab4b23be75642ad0d102a2
Autor:
Adrienne Tham, Chee Y. Ooi, Rebecca Brunner, Chai Wei Tong, Victoria Liu, Justine Quintano, Clare E. Collins, Tamarah Katz, Millie Garg, Rosie Sutherland
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 19(1)
Children with CF have been reported to consume significantly more energy-dense, nutrient-poor foods than controls where there are now concerns of inadequate micronutrient intake. There are no current or comprehensive dietary studies assessing micronu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::723a13c3bcf13eadfbdc8540b55b161d
https://pubmed.ncbi.nlm.nih.gov/31530443
https://pubmed.ncbi.nlm.nih.gov/31530443
Autor:
Chee Y. Ooi, Laura Rossi, Michael G. Surette, Saad A. Syed, Tanja Gonska, Bronwen Needham, Kelsey Young, Julie Avolio, Millie Garg
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-8 (2018)
Scientific Reports
Scientific Reports
Cystic fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Next to progressive airway disease, CF is also associated with intestinal inflammation and dysbiosis. Ivacaftor, a CFTR potentiator, h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dc477277120f29c2965a2bfe312ba78
https://doi.org/10.1038/s41598-018-36364-6
https://doi.org/10.1038/s41598-018-36364-6
Autor:
Torsten Thomas, Adam Jaffe, Michael J. Coffey, Chee Y. Ooi, Bronwen Needham, Shaun Nielsen, Nadeem O. Kaakoush, Russell Pickford, Bernd Wemheuer, Millie Garg
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
Intestinal dysbiosis has been observed in children with cystic fibrosis (CF), yet the functional consequences are poorly understood. We investigated the functional capacity of intestinal microbiota and inflammation in children with CF. Stool samples
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e844b90a691e6eff92ee67e1c3165c01
https://pubmed.ncbi.nlm.nih.gov/31819107
https://pubmed.ncbi.nlm.nih.gov/31819107
Publikováno v:
Cochrane Database Syst Rev
The Cochrane Library
The Cochrane Library
BACKGROUND: Cystic fibrosis (CF) is a multisystem disease and the importance of growth and nutrition has been well established, given its implications for lung function and overall survival. It has been established that intestinal dysbiosis (i.e. mic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9659345bf029f7c319b267a60b77f4bc
https://europepmc.org/articles/PMC6491109/
https://europepmc.org/articles/PMC6491109/
Autor:
Tamarah Katz, Michael J. Coffey, Millie Garg, Roxanne Strachan, Adam Jaffe, Sandra Chuang, Yvonne Belessis, Penelope Field, Andrew S. Day, Chee Y. Ooi, John Widger, Steven T. Leach, Bronwen Needham, Tamara Pang
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 17(1)
Background The pathogenesis of gut inflammation, bacterial dysbiosis and increased rates of malignancy in CF is unclear. Fecal M2-pyruvate kinase (M2-PK) is a biomarker indicative of cellular proliferation that may be raised in intestinal malignancy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ea5d6489ef97843827e3a287717252f
https://pubmed.ncbi.nlm.nih.gov/28754328
https://pubmed.ncbi.nlm.nih.gov/28754328
Autor:
Millie Garg, Chee Y. Ooi
Publikováno v:
Current Gastroenterology Reports. 19
Intestinal inflammation, dysbiosis, and increased gastrointestinal malignancy risks are well-described in patients with cystic fibrosis (CF). However, there is limited understanding of their pathophysiology. This review aims to discuss these issues a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5af8bf06af7b61d7ce5cc28bf3d7dade
https://doi.org/10.1007/s11894-017-0546-0
https://doi.org/10.1007/s11894-017-0546-0
Autor:
A. Tham, Chai Wei Tong, Q. Justine, Chee Y. Ooi, Rosie Sutherland, Rebecca Brunner, Victoria Liu, Tamarah Katz, Millie Garg, Clare E. Collins
Publikováno v:
Journal of Cystic Fibrosis. 18:S150
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f05a495287b0f7296b3b245ed94ad5d0
https://doi.org/10.1016/s1569-1993(19)30620-4
https://doi.org/10.1016/s1569-1993(19)30620-4