Zobrazeno 1 - 10
of 253
pro vyhledávání: '"C.M. Ong"'
Autor:
Y.Y. Chong, S. Thangalazhy-Gopakumar, H.K. Ng, P.B. Ganesan, S. Gan, L.Y. Lee, V.S.A.R. Manickavel, C.M. Ong, H.S. Al Hinai
Publikováno v:
Chemical Engineering Transactions, Vol 56 (2017)
With a rich biomass resource from palm oil industry, Malaysia has high potential in developing the biofuel industry. Fast pyrolysis of biomass provides bio-oil, which has a wide range of projected applications that are comparable to that of the crude
Externí odkaz:
https://doaj.org/article/b97dd9168cb940ffa299ab8e76cb8876
Autor:
Ronald D. Perrone, Dorothee Oberdhan, John Ouyang, Daniel G. Bichet, Klemens Budde, Arlene B. Chapman, Berenice Y. Gitomer, Shigeo Horie, Albert C.M. Ong, Vicente E. Torres, A. Neil Turner, Holly Krasa
Publikováno v:
Kidney International Reports, Vol 8, Iss 5, Pp 989-1001 (2023)
Introduction: The course of autosomal dominant polycystic kidney disease (ADPKD) varies greatly among affected individuals, necessitating natural history studies to characterize the determinants and effects of disease progression. Therefore, we condu
Externí odkaz:
https://doaj.org/article/6263893d07674a6789c237002dc53cb4
Autor:
Ronald D. Perrone, Ali Hariri, Pascal Minini, Curie Ahn, Arlene B. Chapman, Shigeo Horie, Bertrand Knebelmann, Michal Mrug, Albert C.M. Ong, York P.C. Pei, Vicente E. Torres, Vijay Modur, Ronald T. Gansevoort
Publikováno v:
Kidney Medicine, Vol 4, Iss 10, Pp 100538- (2022)
Rationale & Objective: Venglustat, a glucosylceramide synthase inhibitor, inhibits cyst growth and reduces kidney failure in mouse models of autosomal dominant polycystic kidney disease (ADPKD). STAGED-PKD aims to determine the safety and efficacy of
Externí odkaz:
https://doaj.org/article/66ff3b0e6417477da59ccf6a9cdbba1d
Autor:
Roman-Ulrich Müller, A. Lianne Messchendorp, Henrik Birn, Giovambattista Capasso, Emilie Cornec-Le Gall, Olivier Devuyst, Albertien van Eerde, Patrick Guirchoun, Tess Harris, Ewout J. Hoorn, Nine V.A.M. Knoers, Uwe Korst, Djalila Mekahli, Yannick Le Meur, Tom Nijenhuis, Albert C.M. Ong, John A. Sayer, Franz Schaefer, Aude Servais, Vladimir Tesar, Roser Torra, Stephen B. Walsh and Ron T. Gansevoort
Publikováno v:
Počki, Vol 11, Iss 1, Pp 37-39 (2022)
No abstract
Externí odkaz:
https://doaj.org/article/3f3763f45a78472d9048eb2d6d9503c1
Akademický článek
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Publikováno v:
Clinical Kidney Journal
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited cause of end-stage kidney failure. At present, only one drug, tolvaptan, has been approved for use to slow disease progression, but its use is limited by reduced tolera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::312d7e9703f38fff2a4a3afb9355a2aa
https://doi.org/10.1093/ckj/sfab062
https://doi.org/10.1093/ckj/sfab062
Autor:
Albert C.M. Ong, Ron T. Gansevoort
Publikováno v:
Kidney Int
Kidney International, 100(3), 513-515. ELSEVIER SCIENCE INC
Kidney International, 100(3), 513-515. ELSEVIER SCIENCE INC
Autosomal dominant polycystic kidney disease (ADPKD) is characterized by growth of kidney cysts and glomerular filtration rate (GFR) decline. Metformin was found to impact cystogenesis in preclinical models of polycystic disease, is generally conside
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bee8533643b06bff9b95e40fafd3c1d7
https://doi.org/10.1016/j.kint.2021.07.021
https://doi.org/10.1016/j.kint.2021.07.021
Publikováno v:
Renal Failure
article-version (VoR) Version of Record
Renal Failure, Vol 43, Iss 1, Pp 1-15 (2021)
article-version (VoR) Version of Record
Renal Failure, Vol 43, Iss 1, Pp 1-15 (2021)
Objectives\ud \ud A meta-analysis and systematic review was conducted on kidney-related outcomes of three recent pandemics: SARS, MERS, and COVID-19, which were associated with potentially fatal acute respiratory distress syndrome (ARDS).\ud \ud \ud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4533ea74b9443bd46f6e33b8cdf81ce
https://doi.org/10.1080/0886022x.2020.1847724
https://doi.org/10.1080/0886022x.2020.1847724
Autor:
Albertien M. van Eerde, Miguel Barroso-Gil, Fouad T. Chebib, Yannick Le Meur, Vinh Toan Huynh, Andrew Mallett, Amali Mallawaarachchi, Marc Kribs, Himanshu Goel, Eléonore Ponlot, Chirag Patel, John A. Sayer, Albert C.M. Ong, Marie-Pierre Audrézet, Peter C. Harris, Siriane Lefevre, Sarah R. Senum, Valoris Le Brun, Emilie Cornec-Le Gall, Aurore Després
Publikováno v:
Kidney International
Kidney International, Nature Publishing Group, 2020, 98, pp.476-487. ⟨10.1016/j.kint.2020.02.022⟩
Kidney Int
Kidney International, Nature Publishing Group, 2020, 98, pp.476-487. ⟨10.1016/j.kint.2020.02.022⟩
Kidney Int
Monoallelic mutations of DNAJB11 were recently described in seven pedigrees with atypical clinical presentations of autosomal dominant polycystic kidney disease. DNAJB11 encodes one of the main cofactors of the endoplasmic reticulum chaperon BiP, a h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99cf7bdc1add966d6658790fd922ab3a
https://doi.org/10.1016/j.kint.2020.02.022
https://doi.org/10.1016/j.kint.2020.02.022
Autor:
Huamu Chen, Min Li, Xuefei Gao, Dantong Li, Xiaohong Wu, Miaoyue Hu, Liangzhong Sun, Haiyan Wang, Zhihui Yue, Albert C.M. Ong, Xiaoya Wei, Hongrong Lin
Nephronophthisis (NPH) is the most prevalent monogenetic disorder leading to end-stage renal failure (ESRD) in childhood. Mutations in Nphp1, encoding a cilia-localized protein, account for the majority of NPH cases. Despite its identification many y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f2f1e92a0607c6ac444b064fb785ce5
