Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ronald J. Wanders"'
Publikováno v:
Gynecology Obstetrics & Reproductive Medicine, Vol 19, Iss 1 (2016)
Zellweger syndrome (ZS) (Cerebro-Hepato-Renal syndrome) is a rare autosomal recessive disorder characterized by an absence or marked decrease in peroxisomes, resulting in profound muscular hypotonia and death in the neonatal period. The clinical pres
Externí odkaz:
https://doaj.org/article/a2824bbd3d81432a8511e0b8722d9201
Autor:
Thomas Gronemeyer, Sebastian Wiese, Rob Ofman, Christian Bunse, Magdalena Pawlas, Heiko Hayen, Martin Eisenacher, Christian Stephan, Helmut E. Meyer, Hans R. Waterham, Ralf Erdmann, Ronald J. Wanders, Bettina Warscheid
Publikováno v:
PLoS ONE, Vol 8, Iss 10 (2013)
Externí odkaz:
https://doaj.org/article/f467bf61ab264eafa46129c733b8e3a6
Autor:
Thomas Gronemeyer, Sebastian Wiese, Rob Ofman, Christian Bunse, Magdalena Pawlas, Heiko Hayen, Martin Eisenacher, Christian Stephan, Helmut E. Meyer, Hans R. Waterham, Ralf Erdmann, Ronald J. Wanders, Bettina Warscheid
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 10 (2013)
PLoS ONE, Vol 8, Iss 10 (2013)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc700661fc22ec97ff5d3fb0a42c1017
http://europepmc.org/articles/PMC3812376
http://europepmc.org/articles/PMC3812376
Autor:
Aurore, Vluggens, Pierre, Andreoletti, Navin, Viswakarma, Yuzhi, Jia, Kojiro, Matsumoto, Wim, Kulik, Mushfiquddin, Khan, Jiansheng, Huang, Dongsheng, Guo, Sangtao, Yu, Joy, Sarkar, Inderjit, Singh, M Sambasiva, Rao, Ronald J, Wanders, Janardan K, Reddy, Mustapha, Cherkaoui-Malki
Publikováno v:
Laboratory investigation; a journal of technical methods and pathology. 90(5)
Disruption of the peroxisomal acyl-CoA oxidase 1 (Acox1) gene in the mouse results in the development of severe microvesicular hepatic steatosis and sustained activation of peroxisome proliferator-activated receptor-alpha (PPARalpha). These mice mani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6c4d3ac96cc5919ae41c498da8a75a00
https://pubmed.ncbi.nlm.nih.gov/20195242
https://pubmed.ncbi.nlm.nih.gov/20195242
Autor:
Shan, Zha, Sacha, Ferdinandusse, Simone, Denis, Ronald J, Wanders, Charles M, Ewing, Jun, Luo, Angelo M, De Marzo, William B, Isaacs
Publikováno v:
Cancer research. 63(21)
Alpha-methylacyl-CoA racemase (AMACR) is an enzyme involved in beta-oxidation of branched-chain fatty acids and bile acid intermediates. Recent work has identified AMACR as a new diagnostic marker for prostate cancer (PCa). The data from the present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2ecb36bcc60f0694a451e7fc0ce577f3
https://pubmed.ncbi.nlm.nih.gov/14612535
https://pubmed.ncbi.nlm.nih.gov/14612535
Autor:
Xuebin Zhang, Carine De Marcos Lousa, Nellie Schutte‑Lensink, Rob Ofman, Ronald J. Wanders, Stephen A. Baldwin, Alison Baker, Stephan Kemp, Frederica L. Theodoulou
Publikováno v:
Biochemical Journal; Jun2011, Vol. 436 Issue 3, p547-557, 11p
Autor:
Maarten R. Soeters, Hans P. Sauerwein, Marinus Duran, Ronald J. Wanders, Mariëtte T. Ackermans, Eric Fliers, Sander M. Houten, Mireille J. Serlie
Publikováno v:
Clinical Science; 2009, Vol. 116 Issue 7, p585-592, 8p
Autor:
Shan Zha, Sacha Ferdinandusse, Jessica L. Hicks, Simone Denis, Thomas A. Dunn, Ronald J. Wanders, Jun Luo, Angelo M. De Marzo, William B. Isaacs
Publikováno v:
Prostate; Jun2005, Vol. 63 Issue 4, p316-323, 8p
Autor:
Johanna M Jank, Esther M Maier, Dunja D Reiβ, Martin Haslbeck, Kristina F Kemter, Marietta S Truger, Christian P Sommerhoff, Sacha Ferdinandusse, Ronald J Wanders, Søren W Gersting, Ania C Muntau
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e93852 (2014)
The implementation of expanded newborn screening programs reduced mortality and morbidity in medium-chain acyl-CoA dehydrogenase deficiency (MCADD) caused by mutations in the ACADM gene. However, the disease is still potentially fatal. Missense induc
Externí odkaz:
https://doaj.org/article/56d090c0398d4ebb9e1d79f903d77bbd