Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Deniz A, Madencioglu"'
Autor:
Annette J. Klomp, Ashley Plumb, Jacqueline B. Mehr, Deniz A. Madencioglu, Hsiang Wen, Aislinn J. Williams
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-13 (2022)
Abstract The gene CACNA1C, which encodes the pore forming subunit of the L-type calcium channel CaV1.2, is associated with increased risk for neuropsychiatric disorders including schizophrenia, autism spectrum disorder, major depression, and bipolar
Externí odkaz:
https://doaj.org/article/6dbef073db7d4368a9607e5157ecbb68
Autor:
Deniz A. Madencioglu, Karina Kruth, Mallory Shin, Nancy Andreasen, Thomas Wassink, Aislinn Williams
Publikováno v:
Stem Cell Research, Vol 59, Iss , Pp 102636- (2022)
16p11.2 copy number variations have been associated with neurodevelopmental disorders. Human induced pluripotent stem cells were generated from fibroblasts obtained from a patient diagnosed with schizophrenia with a 16p11.2 deletion. The generated ce
Externí odkaz:
https://doaj.org/article/6661ca983b524ac09066dccbe0336190
Autor:
Deniz A. Madencioglu, Gürsel Çalışkan, Pingan Yuanxiang, Kati Rehberg, Yunus E. Demiray, Emre Kul, Alexander Engler, Hussam Hayani, Jorge R. Bergado-Acosta, Anne Kummer, Iris Müller, Inseon Song, Alexander Dityatev, Thilo Kähne, Michael R. Kreutz, Oliver Stork
Publikováno v:
iScience, Vol 24, Iss 8, Pp 102868- (2021)
Summary: Duplications and deletions of short chromosomal fragments are increasingly recognized as the cause for rare neurodevelopmental conditions and disorders. The NDR2 gene encodes a protein kinase important for neuronal development and is part of
Externí odkaz:
https://doaj.org/article/7ea020f929ab4719a7e1d47223fe7152
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:
Deniz A. Madencioglu, Karina Kruth, Mallory Shin, Nancy Andreasen, Thomas Wassink, Aislinn Williams
Publikováno v:
Stem Cell Research, Vol 59, Iss, Pp 102636-(2022)
16p11.2 copy number variations have been associated with neurodevelopmental disorders. Human induced pluripotent stem cells were generated from fibroblasts obtained from a patient diagnosed with schizophrenia with a 16p11.2 deletion. The generated ce
Autor:
Anne Kummer, Gürsel Çalışkan, Hussam Hayani, Oliver Stork, Kati Rehberg, Inseon Song, Michael R. Kreutz, Jorge R. Bergado-Acosta, PingAn Yuanxiang, Thilo Kähne, Alexander Dityatev, Emre Kul, Iris Müller, Yunus Emre Demiray, Deniz A. Madencioglu, Alexander Engler
Publikováno v:
iScience, Vol 24, Iss 8, Pp 102868-(2021)
iScience
iScience, 24(8):102868
iScience 24(8), 102868 (2021). doi:10.1016/j.isci.2021.102868
iScience
iScience, 24(8):102868
iScience 24(8), 102868 (2021). doi:10.1016/j.isci.2021.102868
Summary Duplications and deletions of short chromosomal fragments are increasingly recognized as the cause for rare neurodevelopmental conditions and disorders. The NDR2 gene encodes a protein kinase important for neuronal development and is part of
The Serine/Threonine Kinase Ndr2 Controls Integrin Trafficking and Integrin-Dependent Neurite Growth
Autor:
Bettina Müller, Marlen Thiere, Stefanie Kliche, Oliver Stork, Eike Budinger, Christian Freund, Deniz A. Madencioglu, Kati Rehberg, Bernhard Meineke
Publikováno v:
The Journal of Neuroscience. 34:5342-5354
Integrins have been implicated in various processes of nervous system development, including proliferation, migration, and differentiation of neuronal cells. In this study, we show that the serine/threonine kinase Ndr2 controls integrin-dependent den