Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Austin W. Nenninger"'
Autor:
Eric M. Miller, Cody J. Brazel, Krystina A. Brillos-Monia, Philip W. Crawford, Hannah C. Hufford, Michael R. Loncaric, Monica N. Mruzik, Austin W. Nenninger, Christina M. Ragain
Publikováno v:
Computation, Vol 7, Iss 1, p 6 (2019)
The ability for DFT: B3LYP calculations using the 6-31g and lanl2dz basis sets to predict the electrochemical properties of twenty (20) 3-aryl-quinoxaline-2-carbonitrile 1,4-di-N-oxide derivatives with varying degrees of cytotoxic activity in dimethy
Externí odkaz:
https://doaj.org/article/58a8f0d9c9b94500b0fb04328a240107
Autor:
Eric M. Miller, Qing Xia, Mariah E. Cella, Austin W. Nenninger, Monica N. Mruzik, Krystina A. Brillos-Monia, Yong Zhou Hu, Rong Sheng, Christina M. Ragain, Philip W. Crawford
Publikováno v:
Molecules, Vol 22, Iss 9, p 1442 (2017)
The electrochemical properties of twenty 3-aryl-quinoxaline-2-carbonitrile 1,4-di-N-oxide derivatives with varying degrees of cytotoxic activity were investigated in dimethylformamide (DMF) using cyclic voltammetry and first derivative cyclic voltamm
Externí odkaz:
https://doaj.org/article/bf75389007d14db8b153b79d64e377be
Autor:
Austin W. Nenninger, Matthew Willman, Jonathan Willman, Emma Stewart, Philippe Mesidor, Michelle Novoa, Nicole K Morrill, Luis Alvarez, Aurélie Joly-Amado, Melinda M. Peters, Danielle Gulick, Kevin R. Nash
Publikováno v:
Neurotherapeutics
The rare genetic neurodevelopmental disease Angelman syndrome (AS) is caused by the loss of function of UBE3A, a ubiquitin ligase. The disease results in a lifetime of severe symptoms, including intellectual disability and motor impairments for which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::707f8dc00c80eaad7137ba9489378c26
https://doi.org/10.1007/s13311-022-01239-2
https://doi.org/10.1007/s13311-022-01239-2
Autor:
Kevin Nash, Matthew Willman, Nicole K Morrill, Edwin J. Weeber, Hayden E. Greene, Austin W. Nenninger, Jonathan Willman, Andie Dodge, Kristina Lamens
Publikováno v:
Autism Research. 14:645-655
Disruptions to the maternally inherited allele UBE3A, encoding for an E3 ubiquitin ligase, leads to the manifestation of Angelman Syndrome (AS). While this disorder is rare, the symptoms are severe and lifelong including but not limited to: intractab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b72aabdf1316bcc1bd50a49da53b926
https://doi.org/10.1002/aur.2475
https://doi.org/10.1002/aur.2475
Autor:
Anne E. Anderson, Clifton Dietrick, Stephanie L. Ciarlone, Scott V. Dindot, Melinda M. Peters, Hayden E. Greene, Austin W. Nenninger, Edwin J. Weeber, David J. Segal, Kevin Nash, Elizabeth L. Berg, Andie Dodge, Robert Botelho, Siddharth G. Kamath, Jonathan Willman, Diana Chung, Pavel Houdek, Alena Sumová, Henriette O'Geen, Jill L. Silverman
Publikováno v:
Autism Res
Angelman syndrome (AS) is a rare genetic disorder characterized by severe intellectual disability, seizures, lack of speech, and ataxia. The gene responsible for AS was identified as Ube3a and it encodes for E6AP, an E3 ubiquitin ligase. Currently, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a8aeb0a391885e241f43ea7b96494d0
https://pubmed.ncbi.nlm.nih.gov/31961493
https://pubmed.ncbi.nlm.nih.gov/31961493
Autor:
Qing Xia, Christina M. Ragain, Austin W. Nenninger, Krystina A. Brillos-Monia, Mariah E. Cella, Rong Sheng, Monica N. Mruzik, Philip W. Crawford, Yong Zhou Hu, Eric M. Miller
Publikováno v:
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 22, Iss 9, p 1442 (2017)
Molecules; Volume 22; Issue 9; Pages: 1442
Molecules, Vol 22, Iss 9, p 1442 (2017)
Molecules; Volume 22; Issue 9; Pages: 1442
The electrochemical properties of twenty 3-aryl-quinoxaline-2-carbonitrile 1,4-di-N-oxide derivatives with varying degrees of cytotoxic activity were investigated in dimethylformamide (DMF) using cyclic voltammetry and first derivative cyclic voltamm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::851375dc862949938804b00195fbd749
https://pubmed.ncbi.nlm.nih.gov/28858261
https://pubmed.ncbi.nlm.nih.gov/28858261