Zobrazeno 1 - 10
of 141
pro vyhledávání: '"Stuart W Peltz"'
Autor:
Westley J Friesen, Briana Johnson, Jairo Sierra, Jin Zhuo, Priya Vazirani, Xiaojiao Xue, Yuki Tomizawa, Ramil Baiazitov, Christie Morrill, Hongyu Ren, Suresh Babu, Young-Choon Moon, Art Branstrom, Anna Mollin, Jean Hedrick, Josephine Sheedy, Gary Elfring, Marla Weetall, Joseph M Colacino, Ellen M Welch, Stuart W Peltz
Publikováno v:
PLoS ONE, Vol 13, Iss 10, p e0206158 (2018)
Nonsense mutations, resulting in a premature stop codon in the open reading frame of mRNAs are responsible for thousands of inherited diseases. Readthrough of premature stop codons by small molecule drugs has emerged as a promising therapeutic approa
Externí odkaz:
https://doaj.org/article/dce988ac8f214e27afc02d4bfe8cf531
Autor:
Liangxian Cao, Marla Weetall, Jenelle Bombard, Hongyan Qi, Tamil Arasu, William Lennox, Jean Hedrick, Josephine Sheedy, Nicole Risher, Peter C Brooks, Panayiota Trifillis, Christopher Trotta, Young-Choon Moon, John Babiak, Neil G Almstead, Joseph M Colacino, Thomas W Davis, Stuart W Peltz
Publikováno v:
PLoS ONE, Vol 11, Iss 12, p e0168366 (2016)
Current anti-VEGF (Vascular Endothelial Growth Factor A) therapies to treat various cancers indiscriminately block VEGF function in the patient resulting in the global loss of VEGF signaling which has been linked to dose-limiting toxicities as well a
Externí odkaz:
https://doaj.org/article/429e9fa300c64e3997b2fda5fbe6a256
Autor:
Richard S Finkel, Kevin M Flanigan, Brenda Wong, Carsten Bönnemann, Jacinda Sampson, H Lee Sweeney, Allen Reha, Valerie J Northcutt, Gary Elfring, Jay Barth, Stuart W Peltz
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e81302 (2013)
Approximately 13% of boys with Duchenne muscular dystrophy (DMD) have a nonsense mutation in the dystrophin gene, resulting in a premature stop codon in the corresponding mRNA and failure to generate a functional protein. Ataluren (PTC124) enables ri
Externí odkaz:
https://doaj.org/article/4c1bae3ea78f472c888682ca55235a59
Autor:
Stuart W. Peltz, Joseph M. Colacino, Art Branstrom, Neil G. Almstead, Allan Jacobson, Thomas W. Davis, John Babiak, Young-Choon Moon, Janet Petruska, Ronald Kong, William Lennox, Seongwoo Hwang, Tamil Arasu, Hongyan Qi, Shirley Yeh, Nicole Risher, Jean Hedrick, Josephine Sheedy, Joshua Du, Wencheng Li, Jason D. Graci, Charles Romfo, Bansri Furia, Min Jung Kim, Jiyuan Ma, Katherine Cintron, Christopher Trotta, Marla Weetall, Liangxian Cao
PTC299 was identified as an inhibitor of VEGFA mRNA translation in a phenotypic screen and evaluated in the clinic for treatment of solid tumors. To guide precision cancer treatment, we performed extensive biological characterization of the activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b38cf3c29f914ea98d3f3c7be961d2f
https://doi.org/10.1158/1535-7163.c.6539454.v1
https://doi.org/10.1158/1535-7163.c.6539454.v1
Autor:
Stuart W. Peltz, Joseph M. Colacino, Art Branstrom, Neil G. Almstead, Allan Jacobson, Thomas W. Davis, John Babiak, Young-Choon Moon, Janet Petruska, Ronald Kong, William Lennox, Seongwoo Hwang, Tamil Arasu, Hongyan Qi, Shirley Yeh, Nicole Risher, Jean Hedrick, Josephine Sheedy, Joshua Du, Wencheng Li, Jason D. Graci, Charles Romfo, Bansri Furia, Min Jung Kim, Jiyuan Ma, Katherine Cintron, Christopher Trotta, Marla Weetall, Liangxian Cao
Supplementary Figures S1-S7: Supplementary Figure S1 shows chemical Synthesis and biological characterization of PTC299. Supplementary Figure S2 shows generation and characterization of PTC299-resistant HT1080 cells. Supplementary Figure 3 shows that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24ac4776ab8dbd1c4bd81dcd8bb2dab7
https://doi.org/10.1158/1535-7163.22509942
https://doi.org/10.1158/1535-7163.22509942
Autor:
Stuart W. Peltz, Joseph M. Colacino, Art Branstrom, Neil G. Almstead, Allan Jacobson, Thomas W. Davis, John Babiak, Young-Choon Moon, Janet Petruska, Ronald Kong, William Lennox, Seongwoo Hwang, Tamil Arasu, Hongyan Qi, Shirley Yeh, Nicole Risher, Jean Hedrick, Josephine Sheedy, Joshua Du, Wencheng Li, Jason D. Graci, Charles Romfo, Bansri Furia, Min Jung Kim, Jiyuan Ma, Katherine Cintron, Christopher Trotta, Marla Weetall, Liangxian Cao
contains the raw data from the Microarrays study in the PTC299-resistant HT1080 cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20ffd21a73c725157d53ebd64ecdca72
https://doi.org/10.1158/1535-7163.22509948.v1
https://doi.org/10.1158/1535-7163.22509948.v1
Autor:
Anuradha Bhattacharyya, Christopher R. Trotta, Jana Narasimhan, Kari J. Wiedinger, Wencheng Li, Kerstin A. Effenberger, Matthew G. Woll, Minakshi B. Jani, Nicole Risher, Shirley Yeh, Yaofeng Cheng, Nadiya Sydorenko, Young-Choon Moon, Gary M. Karp, Marla Weetall, Amal Dakka, Vijayalakshmi Gabbeta, Nikolai A. Naryshkin, Jason D. Graci, Thomas Tripodi, Amber Southwell, Michael Hayden, Joseph M. Colacino, Stuart W. Peltz
Publikováno v:
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-12 (2021)
Nature Communications, Vol 12, Iss 1, Pp 1-12 (2021)
Huntington’s disease (HD) is a hereditary neurodegenerative disorder caused by expansion of cytosine-adenine-guanine (CAG) trinucleotide repeats in the huntingtin (HTT) gene. Consequently, the mutant protein is ubiquitously expressed and drives pat
Autor:
Perry B Shieh, Gary Elfring, Panayiota Trifillis, Claudio Santos, Stuart W Peltz, Julie A Parsons, Susan Apkon, Basil T Darras, Craig Campbell, Craig M McDonald, Richard J Barohn, Enrico Bertini, Kate Bushby, Brigitte Chabrol, Emma Ciafaloni, Jaume Columer, Giacomi Pietro Comi, Anne Connolly, Richard S Finkel, Kevin M Flanigan, Nathalie Goemans, Michela Guglieri, Susan T Iannaccone, Kristi J Jones, Petra Kaufmann, Janbernd Kirschner, Jean K Mah, Katherine Mathews, Eugenio Mercuri, Francesco Muntoni, Yoram Nevo, Andrés Nascimento Osorio, Yann Péréon, Rosaline Quinlivan, J. Ben Renfroe, Barry Russman, Monique Ryan, Jacinda Sampson, Ulrike Schara, Kathryn Selby, Thomas Sejersen, Douglas M Sproule, H. Lee Sweeney, Már Tulinius, Juan J Vilchez, Giuseppe Vita, Thomas Voit, Stephanie Burns-Wechsler, Brenda Wong, Ted Abresch, Erik K Henricson, Kim Coleman, Michelle Eagle, Julaine Florence, Ed Gappmaier, Craig McDonald, Hoda Z Abdel-Hamid, Clemens Bloetzer, Russell J Butterfield, Jong-Hee Chae, Jahannaz Dastgir, Isabelle Desguerre, Raul G Escobar, Erika Finanger, Peter Heydemann, Imelda Hughes, Anna Kaminska, Peter Karachunski, Martin Kudr, Timothy Lotze, Alexandra Prufer de Queiroz Campos Araujo, Maria Bernadete Dutra de Resende, Gihan Tennekoon, Haluk Topaloglu, Ricardo Erazo Torricelli, Lindsay N Alfano, Meredith K James, Linda Lowes, Anna Mayhew, Elena S Mazzone, Leslie Nelson, Kristy J Rose
Publikováno v:
Paediatrics Publications
Aim: Compare efficacies of deflazacort and prednisone/prednisolone in providing clinically meaningful delays in loss of physical milestones in patients with nonsense mutation Duchenne muscular dystrophy. Materials & methods: Placebo data from Phase I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e773db882a9b68ac18148646fe6a8d7
https://ir.lib.uwo.ca/context/paedpub/article/3206/viewcontent/843.pdf
https://ir.lib.uwo.ca/context/paedpub/article/3206/viewcontent/843.pdf
Autor:
Stuart W. Peltz, Christopher R. Trotta, Joseph M. Colacino, Wencheng Li, Yaofeng Cheng, Jana Narasimhan, Amber L. Southwell, Nicole Risher, Shirley Yeh, Nadiya Sydorenko, Michael R. Hayden, Anuradha Bhattacharyya, Marla Weetall, Woll Matthew G, Jani Minakshi B, Kerstin Effenberger
Publikováno v:
I: Experimental therapeutics – preclinical.
Autor:
Jiyuan Ma, Thomas W. Davis, Young-Choon Moon, Hongyan Qi, Stuart W. Peltz, Janet Petruska, Neil Gregory Almstead, Nicole Risher, Art Branstrom, Jean Hedrick, Seongwoo Hwang, Katherine Cintron, William Joseph Lennox, Charles M. Romfo, Tamil Arasu, Liangxian Cao, Josephine Sheedy, John Babiak, Min Jung Kim, Ronald Kong, Wencheng Li, Jason D. Graci, Allan Jacobson, Shirley Yeh, Christopher R. Trotta, Joshua Du, Joseph M. Colacino, Bansri Furia, Marla Weetall
Publikováno v:
Molecular Cancer Therapeutics. 18:3-16
PTC299 was identified as an inhibitor of VEGFA mRNA translation in a phenotypic screen and evaluated in the clinic for treatment of solid tumors. To guide precision cancer treatment, we performed extensive biological characterization of the activity