Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Katrina L. Ellis"'
Autor:
Kate E. Lomax, Craig E. Taplin, Mary B. Abraham, Grant J. Smith, Aveni Haynes, Ella Zomer, Katrina L. Ellis, Helen Clapin, Sophia Zoungas, Alicia J. Jenkins, Jenny Harrington, Martin I. de Bock, Timothy W. Jones, Elizabeth A. Davis
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundTechnology use, including continuous glucose monitoring (CGM) and insulin pump therapy, is associated with improved outcomes in youth with type 1 diabetes (T1D). In 2017 CGM was universally funded for youth with T1D in Australia. In contras
Externí odkaz:
https://doaj.org/article/ae185cb4458b48389965c815cc5dfba2
Autor:
Anindita Chakraborty, Dick C. Chan, Katrina L. Ellis, Jing Pang, Wendy Barnett, Ann Marie Woodward, Mary Vorster, Richard Norman, Eric K. Moses, Gerald F. Watts
Publikováno v:
American Journal of Preventive Cardiology, Vol 10, Iss , Pp 100343- (2022)
Objective: Elevated lipoprotein(a) [Lp(a)] is a common inherited condition associated with cardiovascular disease. This study investigated whether cascade testing for Lp(a) was effective in detecting new cases of elevated Lp(a) in families. Methods:
Externí odkaz:
https://doaj.org/article/453c91e2b4c54b04ae4f7bd66a823d7b
Autor:
Michael M. Page, Katrina L. Ellis, Dick C. Chan, Jing Pang, Amanda J. Hooper, Damon A. Bell, John R. Burnett, Eric K. Moses, Gerald F. Watts
Publikováno v:
Journal of Clinical Lipidology. 16:525-529
Increased risk of coronary artery disease (CAD) in familial hypercholesterolaemia (FH) is modified by factors beyond defects in the low-density lipoprotein receptor pathway. The rs1250229-T single nucleotide polymorphism (SNP) in the FN1 gene is asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1840f134fbbd75c2413e2ba285e20d1d
https://doi.org/10.1016/j.jacl.2022.05.065
https://doi.org/10.1016/j.jacl.2022.05.065
Autor:
Katrina L. Ellis, Eric K. Moses, Gerald F. Watts, Jing Pang, Damon A. Bell, Dick C. Chan, Anindita Chakraborty, John R. Burnett, Amanda J. Hooper
Publikováno v:
Atherosclerosis. 349
Background and aims Familial hypercholesterolaemia (FH) and elevated plasma lipoprotein(a) [Lp(a)] are inherited conditions independently associated with atherosclerotic cardiovascular disease. This study investigated the detection of new cases of el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1bbfe6cf2b412d24e8cfd41e3d8c098
https://pubmed.ncbi.nlm.nih.gov/34862044
https://pubmed.ncbi.nlm.nih.gov/34862044
Autor:
Leopoldo Pérez de Isla, Gerald F. Watts, Pedro Mata, Rodrigo Alonso, Katrina L. Ellis, Francisco Fuentes
Publikováno v:
Journal of the American College of Cardiology. 73:1029-1039
Background Familial hypercholesterolemia (FH) and elevated lipoprotein(a) [Lp(a)] are inherited disorders associated with premature atherosclerotic cardiovascular disease (ASCVD). Cascade testing is recommended for FH, but there are no similar recomm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::331fc0765623b172cf9842c46bf0bf6c
https://doi.org/10.1016/j.jacc.2018.12.037
https://doi.org/10.1016/j.jacc.2018.12.037
Autor:
Barry R Palmer, Sandy Slow, Katrina L Ellis, Anna P Pilbrow, Lorraine Skelton, Chris M Frampton, Suetonia C Palmer, Richard W Troughton, Tim G Yandle, Rob N Doughty, Gillian A Whalley, Michael Lever, Peter M George, Stephen T Chambers, Chris Ellis, A Mark Richards, Vicky A Cameron
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e89029 (2014)
BACKGROUND AND AIMS: The methylene-tetrahydrofolate dehydrogenase (NADP+ dependent) 1-like (MTHFD1L) gene is involved in mitochondrial tetrahydrofolate metabolism. Polymorphisms in MTHFD1L, including rs6922269, have been implicated in risk for corona
Externí odkaz:
https://doaj.org/article/4c6ead0a20264c5eab102d7e26932b90
Publikováno v:
Heart, lungcirculation. 30(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2a960e8ed9a36e036dbeb0a9c25b9c7
https://pubmed.ncbi.nlm.nih.gov/33121881
https://pubmed.ncbi.nlm.nih.gov/33121881
Autor:
Michael M. Page, Damon A. Bell, Dick C. Chan, Katrina L. Ellis, John R. Burnett, Jing Pang, Amanda J. Hooper, Gerald F. Watts
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 510
The rs3798220 and rs10455872 single nucleotide polymorphisms (SNPs) in LPA are associated with increased plasma concentrations of lipoprotein(a) [Lp(a)] and coronary artery disease (CAD).We investigated the association between rs3798220 and rs1045587
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7aafa436cc2cec1fa141017c56ec221c
https://pubmed.ncbi.nlm.nih.gov/32681934
https://pubmed.ncbi.nlm.nih.gov/32681934
Publikováno v:
Journal of Clinical Lipidology. 12:1019-1026
Elevated lipoprotein(a) (Lp[a]) and low-density lipoprotein (LDL) cholesterol are important inheritable risk factors for premature coronary artery disease (CAD). Lp(a) mediates cardiovascular risk through prothrombotic, proinflammatory, and proathero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91f7c54827b4f0e8772ef64638929647
https://doi.org/10.1016/j.jacl.2018.03.090
https://doi.org/10.1016/j.jacl.2018.03.090
Autor:
Katrina L. Ellis, Gerald F. Watts
Publikováno v:
Cardiology Clinics. 36:287-298
Lipoprotein (a) is a low-density lipoprotein-like particle covalently bound to a glycoprotein called apolipoprotein(a) that is under potent genetic control. Plasma levels of lipoprotein (a) vary by up to 1000-fold among individuals, with 1 in 4 havin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f19cee46f7a2a62d8fd1d331075dc620
https://doi.org/10.1016/j.ccl.2017.12.010
https://doi.org/10.1016/j.ccl.2017.12.010