Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Scott Barish"'
Publikováno v:
iScience, Vol 27, Iss 7, Pp 110340- (2024)
Summary: The process of how neuronal identity confers circuit organization is intricately related to the mechanisms underlying neurodegeneration and neuropathologies. Modeling this process, the olfactory circuit builds a functionally organized topogr
Externí odkaz:
https://doaj.org/article/1fa88e966e174c2a9d7b2086952ae28b
Autor:
Jia Wern Pan, Qingyun Li, Scott Barish, Sumie Okuwa, Songhui Zhao, Charles Soeder, Matthew Kanke, Corbin D. Jones, Pelin Cayirlioglu Volkan
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-16 (2017)
Abstract Organisms have evolved strikingly parallel phenotypes in response to similar selection pressures suggesting that there may be shared constraints limiting the possible evolutionary trajectories. For example, the behavioral adaptation of speci
Externí odkaz:
https://doaj.org/article/6172b142a6b741928aaa45ea7266853f
Autor:
Scott Barish, Sarah Nuss, Ilya Strunilin, Suyang Bao, Sayan Mukherjee, Corbin D Jones, Pelin C Volkan
Publikováno v:
PLoS Genetics, Vol 14, Iss 8, p e1007560 (2018)
In Drosophila, 50 classes of olfactory receptor neurons (ORNs) connect to 50 class-specific and uniquely positioned glomeruli in the antennal lobe. Despite the identification of cell surface receptors regulating axon guidance, how ORN axons sort to f
Externí odkaz:
https://doaj.org/article/986eb8e5115346739ec501aec8a30b12
Autor:
Qingyun Li, Scott Barish, Sumie Okuwa, Abigail Maciejewski, Alicia T Brandt, Dominik Reinhold, Corbin D Jones, Pelin Cayirlioglu Volkan
Publikováno v:
PLoS Genetics, Vol 12, Iss 1, p e1005780 (2016)
Sensory neuron diversity is required for organisms to decipher complex environmental cues. In Drosophila, the olfactory environment is detected by 50 different olfactory receptor neuron (ORN) classes that are clustered in combinations within distinct
Externí odkaz:
https://doaj.org/article/7d9afc91d0d148f6a1cb3b4671a07d80
Autor:
Erin Conboy, Catherine Nowak, Karen Stals, Elliot S. Stolerman, Brett Bostwick, Tiana M. Scott, Emma Wakeling, Cyril Mignot, Sian Ellard, Brittany C. Michel, Kayla Treat, Berrak Ugur, Jill A. Rosenfeld, Caroline Nava, Sally Ann Lynch, Victoria M. Pratt, Hugo J. Bellen, Aiko Otsubo, Michael F. Wangler, Jennifer Gass, John Herriges, Jennifer B. Phillips, Gaetan Lesca, Bo Yuan, Shinya Yamamoto, Scott Barish, Marjon van Slegtenhorst, Jessica Douglas, Dihong Zhou, Patrick Edery, David R. Murdock, Jeremy Wegner, Jose Camacho, Marie Faoucher, Boris Keren, Camerun Washington, Elena Perenthaler, Kendra Engleman, Francesco Vetrini, Anita Nikoncuk, Alfredo M. Valencia, Daryl A. Scott, Cigall Kadoch, Isabelle Thiffault, Tahsin Stefan Barakat, Chun-An Chen, Lance H. Rodan, Raymond J. Louie, Hongzheng Dai, Alice S. Brooks, Nazar Mashtalir, Monte Westerfield, Nora Shannon
Publikováno v:
Am J Hum Genet
American Journal of Human Genetics, 107(6), 1096-1112. Cell Press
American Journal of Human Genetics, 107(6), 1096-1112. Cell Press
SWI/SNF-related intellectual disability disorders (SSRIDDs) are rare neurodevelopmental disorders characterized by developmental disability, coarse facial features, and fifth digit/nail hypoplasia that are caused by pathogenic variants in genes that
Autor:
Matthew J. Moulton, Scott Barish, Isha Ralhan, Jinlan Chang, Lindsey D. Goodman, Jake G. Harland, Paul C. Marcogliese, Jan O. Johansson, Maria S. Ioannou, Hugo J. Bellen
Publikováno v:
Proc Natl Acad Sci U S A
A growing list of Alzheimer’s disease (AD) genetic risk factors is being identified, but the contribution of each variant to disease mechanism remains largely unknown. We have previously shown that elevated levels of reactive oxygen species (ROS) i
Autor:
Scott, Barish, Mumine, Senturk, Kelly, Schoch, Amanda L, Minogue, Diego, Lopergolo, Chiara, Fallerini, Jake, Harland, Jacob H, Seemann, Nicholas, Stong, Peter G, Kranz, Sujay, Kansagra, Mohamad A, Mikati, Joan, Jasien, Mays, El-Dairi, Paolo, Galluzzi, Francesca, Ariani, Alessandra, Renieri, Francesca, Mari, Michael F, Wangler, Swathi, Arur, Yong-Hui, Jiang, Shinya, Yamamoto, Vandana, Shashi, Stephan, Zuchner
Publikováno v:
Hum Mol Genet
DROSHA encodes a ribonuclease that is a subunit of the Microprocessor complex and is involved in the first step of microRNA (miRNA) biogenesis. To date, DROSHA has not yet been associated with a Mendelian disease. Here, we describe two individuals wi
Autor:
Hugo J. Bellen, Lindsey D. Goodman, Jake G. Harland, Scott Barish, Jan O. Johansson, Maria S. Ioannou, Matthew J. Moulton, Paul C. Marcogliese, Jinlan Chang, Isha Ralhan
SummaryA growing list of Alzheimer’s disease (AD) genetic risk factors is being identified, but the contribution of these genetic mutations to disease remains largely unknown. Accumulating data support a role of lipid dysregulation and excessive RO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d67f6910aaa7334483726c895a83a6ec
https://doi.org/10.1101/2021.03.03.433580
https://doi.org/10.1101/2021.03.03.433580
Autor:
Jan O. Johansson, Scott Barish, Isha Ralhan, Jake G. Harland, Lindsey D. Goodman, Paul C. Marcogliese, Maria S. Ioannou, Jinlan Chang, Hugo J. Bellen, Matthew J. Moulton
Publikováno v:
SSRN Electronic Journal.
A growing list of Alzheimer’s disease (AD) genetic risk factors is being identified, but the contribution of these genetic mutations to disease remains largely unknown. Accumulating data support a role of lipid dysregulation and excessive ROS in th