Zobrazeno 1 - 5
of 5
pro vyhledávání: '"William J Laxen"'
Autor:
Ankit Sabharwal, Mark D Wishman, Roberto Lopez Cervera, MaKayla R Serres, Jennifer L Anderson, Shannon R Holmberg, Bibekananda Kar, Anthony J Treichel, Noriko Ichino, Weibin Liu, Jingchun Yang, Yonghe Ding, Yun Deng, Jean M Lacey, William J Laxen, Perry R Loken, Devin Oglesbee, Steven A Farber, Karl J Clark, Xiaolei Xu, Stephen C Ekker
Publikováno v:
eLife, Vol 11 (2022)
The clinical and largely unpredictable heterogeneity of phenotypes in patients with mitochondrial disorders demonstrates the ongoing challenges in the understanding of this semi-autonomous organelle in biology and disease. Previously, we used the gen
Externí odkaz:
https://doaj.org/article/c6f4d43f2d7246b09a3bf4b4734cee47
Autor:
Ester Perales‐Clemente, Angela L. Hewitt, April L. Studinski, Jan‐Mendelt Tillema, William J. Laxen, Devin Oglesbee, Arne H. Graff, Piero Rinaldo, Brendan C. Lanpher
Publikováno v:
JIMD Reports, Vol 58, Iss 1, Pp 21-28 (2021)
Abstract Introduction Nonaccidental trauma (NAT) is considered when pediatric patients present with intracranial injuries and a negative history of an accidental injury or concomitant medical diagnosis. The evaluation of NAT should include the consid
Externí odkaz:
https://doaj.org/article/051f413ccae14ef8906e30cecd0550a0
Autor:
Cecile Riviere-Cazaux, Jean M Lacey, Lucas P Carlstrom, William J Laxen, Amanda Munoz-Casabella, Matthew D Hoplin, Samar Ikram, Abdullah Bin Zubair, Katherine M Andersen, Arthur E Warrington, Paul A Decker, Timothy J Kaufmann, Jian L Campian, Jeanette E Eckel-Passow, Sani H Kizilbash, Silvia Tortorelli, Terry C Burns
Publikováno v:
medRxiv
D-2-hydroxyglutarate (D-2-HG) is a well-established oncometabolite of isocitrate dehydrogenase (IDH) mutant gliomas. While prior studies have demonstrated that D-2-HG is elevated in the cerebrospinal fluid (CSF) of patients with IDH-mutant gliomas1,2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fe7c909c14104cb0444e6d8a2ca282f
https://doi.org/10.1093/noajnl/vdad061
https://doi.org/10.1093/noajnl/vdad061
Autor:
Roberto Lopez Cervera, Mark D Wishman, Ankit Sabharwal, MaKayla R Serres, Jennifer L Anderson, Shannon R Holmberg, Bibekananda Kar, Anthony J Treichel, Noriko Ichino, Weibin Liu, Jingchun Yang, Yonghe Ding, Yun Deng, Jean M Lacey, William J Laxen, Perry R Loken, Devin Oglesbee, Steven A Farber, Karl J Clark, Xiaolei Xu, Stephen C Ekker
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64d64a7a2d3c077c466084819f973318
https://doi.org/10.7554/elife.65488.sa2
https://doi.org/10.7554/elife.65488.sa2
Autor:
Roberto Lopez Cervera, Mark D Wishman, Ankit Sabharwal, MaKayla R Serres, Jennifer L Anderson, Shannon R Holmberg, Bibekananda Kar, Anthony J Treichel, Noriko Ichino, Weibin Liu, Jingchun Yang, Yonghe Ding, Yun Deng, Jean M Lacey, William J Laxen, Perry R Loken, Devin Oglesbee, Steven A Farber, Karl J Clark, Xiaolei Xu, Stephen C Ekker
Publikováno v:
eLife. 11
The clinical and largely unpredictable heterogeneity of phenotypes in patients with mitochondrial disorders demonstrates the ongoing challenges in the understanding of this semi-autonomous organelle in biology and disease. Previously, we used the gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::033a47376e08eecc2de14d2d8e035281
https://pubmed.ncbi.nlm.nih.gov/36408801
https://pubmed.ncbi.nlm.nih.gov/36408801