Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Ellen Welch"'
Autor:
Ellen Welch
A history of Britain's healthcare system, from the Victorian era to the post-World War II beginnings of the NHS to the Coronavirus pandemic.The Coronavirus pandemic in 2020 has changed life as we know it and thrust the NHS into the spotlight. A natio
Autor:
Grace Liu, Phil Lipari, Anna Mollin, Stephen Jung, Irina Teplova, Marcia Ma, Wencheng Li, Lanqing Ying, Shirley Yeh, Jana Narasimhan, Panayiota Trifillis, Efthimia Leonardi, Ellen Welch, Gregory Voronin, Elaine Dong, Nicholas Mastrandrea, Jonathan Blaize, Marla Weetall
Publikováno v:
Wednesday, April 26.
Autor:
John Babiak, Nicole Risher, Marla Weetall, Diksha Kaushik, Shirley Yeh, Kylie O'Keefe, Valerie Northcutt, Ronald Kong, Young-Choon Moon, Ellen Welch, Lachlan Molony, Jiyuan Ma
Publikováno v:
Xenobiotica. 52:152-164
Emvododstat was identified as a potent inhibitor of dihydroorotate dehydrogenase and is now in clinical development for the treatment of acute myeloid leukaemia and COVID-19. The objective of this paper is to evaluate the metabolism, pharmacokinetics
Autor:
Nicole Risher, Josephine Sheedy, Hasane Ratni, Zhihua Feng, Xin Zhao, Amal Dakka, Anna Mollin, Catherine Lutz, Karen K. Y. Ling, Ellen Welch, Friedrich Metzger, Marla Weetall, Karen S. Chen, Jana Narasimhan, Nikolai Naryshkin, John D. Baird, Chien-Ping Ko
Publikováno v:
Human Molecular Genetics. 31:82-96
Spinal muscular atrophy (SMA) is caused by the loss of the survival motor neuron 1 (SMN1) gene function. The related SMN2 gene partially compensates but produces insufficient levels of SMN protein due to alternative splicing of exon 7. Evrysdi™ (ri
Publikováno v:
BMJ (Clinical research ed.). 377
Autor:
Phillip G. Zaworski, Rachel Schwartz, Jeffrey Burr, Daniel Skutnik, Anna Mollin, Binit Kumar, Quintus Ngumah, Ellen Welch, Briana Johnson, Jana Narasimhan, Marla Weetall
Publikováno v:
Analytical biochemistry. 656
Paired box protein Pax-6 (oculothrombin) is a transcription factor that plays an important regulatory role in ocular, brain, and pancreatic development. Mutations of the PAX6 gene cause aniridia and Peters anomaly. Reduction in Pax-6 protein is also
Publikováno v:
BMJ (Clinical research ed.). 376
Publikováno v:
BMJ. :o1670
Autor:
Ellen Welch
‘I tried to contact my own GP last week. I counted 19 redials and 20 minutes on hold before I was able to speak to a receptionist… only to be told that all the appointments for the day had gone. My experience echoes a familiar tale told up and do
Autor:
Ronald Kong, Ellen Welch, Elizabeth Goodwin, John Babiak, Marla Weetall, Joseph M. Colacino, Young-Choon Moon, Neil Gregory Almstead, Jiyuan Ma, Seongwoo Hwang
Publikováno v:
Pharmacology Research & Perspectives
Pharmacology Research & Perspectives, Vol 8, Iss 2, Pp n/a-n/a (2020)
Pharmacology Research & Perspectives, Vol 8, Iss 2, Pp n/a-n/a (2020)
Ataluren promotes ribosomal readthrough of premature termination codons in mRNA which result from nonsense mutations. In vitro studies were performed to characterize the metabolism and enzyme kinetics of ataluren and its interaction potential with CY