Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Esther J. H. Boey"'
Autor:
Bianca C Bernardo, Xiao-Ming Gao, Yow Keat Tham, Helen Kiriazis, Catherine E Winbanks, Jenny Y Y Ooi, Esther J H Boey, Susanna Obad, Sakari Kauppinen, Paul Gregorevic, Xiao-Jun Du, Ruby C Y Lin, Julie R McMullen
Publikováno v:
PLoS ONE, Vol 9, Iss 2, p e90337 (2014)
Therapeutic inhibition of the miR-34 family (miR-34a,-b,-c), or miR-34a alone, have emerged as promising strategies for the treatment of cardiac pathology. However, before advancing these approaches further for potential entry into the clinic, a more
Externí odkaz:
https://doaj.org/article/8b902a46757b434fbe7761cf030d6d9f
Autor:
Amrita Srivathsan, Wei Xin Tan, Esther J. H. Boey, Denis Bertrand, Amanda Hui Qi Ng, Jayce Jia Yu Koh, Niranjan Nagarajan, Wendy Y. Wang, Bilgenur Baloğlu, Rudolf Meier
Publikováno v:
Molecular Ecology Resources. 18:1035-1049
DNA barcodes are useful for species discovery and species identification, but obtaining barcodes currently requires a well-equipped molecular laboratory, is time-consuming, and/or expensive. We here address these issues by developing a barcoding pipe
Autor:
Kate L. Weeks, Nelly Cemerlang, Hongwei Qian, Xiao-Jun Du, Helen Kiriazis, Xiao-Ming Gao, Yow Keat Tham, Paul Gregorevic, Thawin Pongsukwechkul, Bianca C. Bernardo, Esther J. H. Boey, Chad Johnson, Julie R. McMullen
Publikováno v:
Clinical science (London, England : 1979). 132(3)
We previously showed that medium chain acyl-coenzyme A dehydrogenase (MCAD, key regulator of fatty acid oxidation) is positively modulated in the heart by the cardioprotective kinase, phosphoinositide 3-kinase (PI3K(p110α)). Disturbances in cardiac
Autor:
Kern Rei Chng, Chenhao Li, Andreas Wilm, Niranjan Nagarajan, Esther J. H. Boey, Amanda Hui Qi Ng
Publikováno v:
GigaScience
Background Nanopore sequencing provides a rapid, cheap and portable real-time sequencing platform with the potential to revolutionize genomics. However, several applications are limited by relatively high single-read error rates (>10 %), including RN
Autor:
Aya Matsumoto, Marie A. Bogoyevitch, Nelly Cemerlang, Xiao-Jun Du, Helen Kiriazis, Xiao-Ming Gao, Elizabeth A. Woodcock, Joon Win Tan, Julie R. McMullen, Thomas F. Franke, Esther J. H. Boey, Paul Gregorevic, Bianca C. Bernardo, Kate L. Weeks, Mark A. Febbraio, Hongwei Qian, Yow Keat Tham
Publikováno v:
Circulation: Heart Failure. 5:523-534
Background— Numerous molecular and biochemical changes have been linked with the cardioprotective effects of exercise, including increases in antioxidant enzymes, heat shock proteins, and regulators of cardiac myocyte proliferation. However, a mast
Autor:
Tomomi Ueyama, Natalie A. Mellet, Aya Matsumoto, Mark A. Febbraio, Lydia Lim, Elizabeth A. Woodcock, Nelly Cemerlang, Helen Kiriazis, Junichi Sadoshima, Xiao-Jun Du, Yow Keat Tham, Lynette Pretorius, Bianca C. Bernardo, Geeta Sapra, Esther J. H. Boey, Peter J. Meikle, Julie R. McMullen, Silvana Marasco, Darren C. Henstridge, Jenny Y. Y. Ooi
Publikováno v:
Nature communications. 5
Heart failure (HF) and atrial fibrillation (AF) share common risk factors, frequently coexist and are associated with high mortality. Treatment of HF with AF represents a major unmet need. Here we show that a small molecule, BGP-15, improves cardiac
Autor:
Esther J. H. Boey, Enzo R. Porrello, Julie R. McMullen, Paul Gregorevic, Sindhu Igoor, Ruby C.Y. Lin, Jenny Ying Ying Ooi, Yow Keat Tham, Bianca C. Bernardo, Catherine E. Winbanks, Xiao-Jun Du, Helen Kiriazis, Xiao-Ming Gao, Colleen J. Thomas, Sally S. Nguyen
Publikováno v:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 28(12)
Expression of microRNA-652 (miR-652) increases in the diseased heart, decreases in a setting of cardioprotection, and is inversely correlated with heart function. The aim of this study was to assess the therapeutic potential of inhibiting miR-652 in
Publikováno v:
Circulation Research. 115
Introduction: MicroRNAs (miRNAs) are altered in heart disease and have emerged as promising therapeutic targets. We recently reported that therapeutic inhibition of the miR-34 family (with an 8 mer antimiR) was effective in attenuation of pathologica
Autor:
Susanna Obad, Paul Gregorevic, Yow Keat Tham, Jenny Ying Ying Ooi, Sakari Kauppinen, Ruby C.Y. Lin, Catherine E. Winbanks, Xiao-Jun Du, Xiao-Ming Gao, Bianca C. Bernardo, Helen Kiriazis, Julie R. McMullen, Esther J. H. Boey
Publikováno v:
Bernardo, B C, Gao, X-M, Tham, Y K, Kiriazis, H, Winbanks, C E, Ooi, J Y Y, Boey, E J H, Obad, S, Kauppinen, S, Gregorevic, P, Du, X-J, Lin, R C Y & McMullen, J R 2014, ' Silencing of miR-34a attenuates cardiac dysfunction in a setting of moderate, but not severe, hypertrophic cardiomyopathy ', P L o S One, vol. 9, no. 2, e90337 . https://doi.org/10.1371/journal.pone.0090337
PLoS ONE
PLoS ONE, Vol 9, Iss 2, p e90337 (2014)
PLoS ONE
PLoS ONE, Vol 9, Iss 2, p e90337 (2014)
Therapeutic inhibition of the miR-34 family (miR-34a,-b,-c), or miR-34a alone, have emerged as promising strategies for the treatment of cardiac pathology. However, before advancing these approaches further for potential entry into the clinic, a more
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbf2c1a83dc880692ff744a8c5150529
https://vbn.aau.dk/da/publications/4fba6df1-8983-4d31-b6dd-40faecfbf2fe
https://vbn.aau.dk/da/publications/4fba6df1-8983-4d31-b6dd-40faecfbf2fe
Autor:
David A. Jans, Ivan Hong Wee Ng, Mark A. Febbraio, Esther J. H. Boey, Darren C. Henstridge, MengJie Hu, Yuekang Xu, Marie A. Bogoyevitch, Simon Crawford
Publikováno v:
Biochemical Journal
p32 [also known as HABP1 (hyaluronan-binding protein 1), gC1qR (receptor for globular head domains complement 1q) or C1qbp (complement 1q-binding protein)] has been shown previously to have both mitochondrial and non-mitochondrial localization and fu