Zobrazeno 1 - 10
of 1 866
pro vyhledávání: '"Devin, K."'
Autor:
Jonathan G Van Vranken, Jiaming Li, Julian Mintseris, Ting-Yu Wei, Catherine M Sniezek, Meagan Gadzuk-Shea, Steven P Gygi, Devin K Schweppe
Publikováno v:
eLife, Vol 13 (2024)
In response to an ever-increasing demand of new small molecules therapeutics, numerous chemical and genetic tools have been developed to interrogate compound mechanism of action. Owing to its ability to approximate compound-dependent changes in therm
Externí odkaz:
https://doaj.org/article/8bf3b9c5353e41d7be11802c16d7f60c
Autor:
Timothy M. Locke, Rose Fields, Hayden Gizinski, George M. Otto, Melissa J.S. MacEwen, Domnita-Valeria Rusnac, Peixian He, David M. Shechner, Chris D. McGann, Matthew D. Berg, Judit Villen, Yasemin Sancak, Devin K. Schweppe
Publikováno v:
Cell Reports, Vol 43, Iss 11, Pp 114879- (2024)
Summary: Calcium ions play important roles in nearly every biological process, yet whole-proteome analysis of calcium effectors has been hindered by a lack of high-throughput, unbiased, and quantitative methods to identify protein-calcium engagement.
Externí odkaz:
https://doaj.org/article/83058aefa024485bafa97ed7f25ab95d
Autor:
Katilynne Croom, Jeffrey A. Rumschlag, Gemma Molinaro, Michael A. Erickson, Devin K. Binder, Kimberly M. Huber, Khaleel A. Razak
Publikováno v:
Neurobiology of Disease, Vol 200, Iss , Pp 106628- (2024)
Autism Spectrum Disorders (ASD) encompass a wide array of debilitating symptoms, including severe sensory deficits and abnormal language development. Sensory deficits early in development may lead to broader symptomatology in adolescents and adults.
Externí odkaz:
https://doaj.org/article/c7a8da0102e244f6a73d8652804c6f75
Phenotypic analysis of multielectrode array EEG biomarkers in developing and adult male Fmr1 KO mice
Autor:
Carrie R. Jonak, Samantha A. Assad, Terese A. Garcia, Manbir S. Sandhu, Jeffrey A. Rumschlag, Khaleel A. Razak, Devin K. Binder
Publikováno v:
Neurobiology of Disease, Vol 195, Iss , Pp 106496- (2024)
Fragile X Syndrome (FXS) is a leading known genetic cause of intellectual disability with symptoms that include increased anxiety and social and sensory processing deficits. Recent electroencephalographic (EEG) studies in humans with FXS have identif
Externí odkaz:
https://doaj.org/article/74965ce498f142ec95ab17a9e0756993
Autor:
Locke, Timothy M., Fields, Rose, Gizinski, Hayden, Otto, George M., MacEwen, Melissa J.S., Rusnac, Domnita-Valeria, He, Peixian, Shechner, David M., McGann, Chris D., Berg, Matthew D., Villen, Judit, Sancak, Yasemin, Schweppe, Devin K.
Publikováno v:
In Cell Reports 26 November 2024 43(11)
Autor:
Croom, Katilynne, Rumschlag, Jeffrey A., Molinaro, Gemma, Erickson, Michael A., Binder, Devin K., Huber, Kimberly M., Razak, Khaleel A.
Publikováno v:
In Neurobiology of Disease 1 October 2024 200
Publikováno v:
In Acta Astronautica September 2024 222:81-86