Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Karina A. Kruth"'
Publikováno v:
Molecular Autism, Vol 11, Iss 1, Pp 1-11 (2020)
Abstract Efforts to identify the causes of autism spectrum disorders have highlighted the importance of both genetics and environment, but the lack of human models for many of these disorders limits researchers’ attempts to understand the mechanism
Externí odkaz:
https://doaj.org/article/16e7d985df8849498291ba22d57afbab
Autor:
Deniz A, Madencioglu, Karina A, Kruth, Thomas H, Wassink, Vincent A, Magnotta, John A, Wemmie, Aislinn J, Williams
Publikováno v:
Journal of visualized experiments : JoVE. (187)
The precise and timely development of the cerebellum is crucial not only for accurate motor coordination and balance but also for cognition. In addition, disruption in cerebellar development has been implicated in many neurodevelopmental disorders, i
Autor:
Coralie Poulard, Celine Gagnieux, Michael R. Stallcup, Mimi Fang, Deepa Bhojwani, Miles A. Pufall, Daniel S. Gerke, Martin Kampmann, Yong-Mi Kim, Karina A. Kruth, Hye Na Kim
Publikováno v:
Proceedings of the National Academy of Sciences. 116:3052-3061
Glucocorticoids (GCs) are used in combination chemotherapies as front-line treatment for B cell acute lymphoblastic leukemia (B-ALL). Although effective, many patients relapse and become resistant to chemotherapy and GCs in particular. Why these pati
Publikováno v:
Biophysical Journal. 111:323-332
Point mutations in γ-cytoplasmic actin have been shown to result in autosomal-dominant, nonsyndromic, early-onset deafness. Two mutations at the same site, K118M and K118N, provide a unique opportunity to compare the effects of two dissimilar amino
Autor:
Ossama Abu-Halawa, Karina A. Kruth, Mimi A Fang, Dawne N. Shelton, Sarah K Tasian, Martin Kampmann, Miles A. Pufall
Publikováno v:
The FASEB Journal. 31
Autor:
Peter A. Rubenstein, Karina A. Kruth
Hearing requires proper function of the auditory hair cell, which is critically dependent upon its actin-based cytoskeletal structure. Currently, ten point mutations in nonmuscle γ-actin have been identified as causing progressive autosomal dominant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7651d50f4c241b3368f9ed922ace0825
https://europepmc.org/articles/PMC3411063/
https://europepmc.org/articles/PMC3411063/