Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Nicolas F. Berbari"'
Autor:
Ke Ning, Mohajeet B. Bhuckory, Chien-Hui Lo, Brent E. Sendayen, Tia J. Kowal, Ming Chen, Ruchi Bansal, Kun-Che Chang, Douglas Vollrath, Nicolas F. Berbari, Vinit B. Mahajan, Yang Hu, Yang Sun
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-14 (2023)
Abstract Primary cilia are conserved organelles that integrate extracellular cues into intracellular signals and are critical for diverse processes, including cellular development and repair responses. Deficits in ciliary function cause multisystemic
Externí odkaz:
https://doaj.org/article/e3cde6ac1f29410caad2250851acad47
Autor:
Katlyn K. Brewer, Kathryn M. Brewer, Tiffany T. Terry, Tamara Caspary, Christian Vaisse, Nicolas F. Berbari
Publikováno v:
Cells, Vol 13, Iss 3, p 259 (2024)
Primary cilia are hair-like structures found on nearly all mammalian cell types, including cells in the developing and adult brain. A diverse set of receptors and signaling proteins localize within cilia to regulate many physiological and development
Externí odkaz:
https://doaj.org/article/aa82dc4dc3b945f19ac91a531d8b52fc
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
A subset of genetic disorders termed ciliopathies are associated with obesity. The mechanisms behind cilia dysfunction and altered energy homeostasis in these syndromes are complex and likely involve deficits in both development and adult homeostasis
Externí odkaz:
https://doaj.org/article/3b4f42aa4d27488ba4e6c0c8fd43f750
Autor:
Ke Ning, Emilie Song, Brent E. Sendayen, Philipp P. Prosseda, Kun‐Che Chang, Alireza Ghaffarieh, Jorge A. Alvarado, Biao Wang, Kathryn M. Haider, Nicolas F. Berbari, Yang Hu, Yang Sun
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 1, Pp n/a-n/a (2021)
Abstract Background Senior–Loken syndrome is a rare genetic disorder that presents with nephronophthisis and retinal degeneration, leading to end‐stage renal disease and progressive blindness. The most frequent cause of juvenile nephronophthisis
Externí odkaz:
https://doaj.org/article/1c54e82430da430c97c885e52ff91512
Publikováno v:
Journal of Microbiology & Biology Education, Vol 21, Iss 3 (2020)
This study explores whether integrating multicultural content within a genetics laboratory course affected students’ awareness of diversity and their perceptions of scientists’ identities. Genetics laboratory curricula typically focus on content
Externí odkaz:
https://doaj.org/article/07b5d81850b2402680aa4c18c09be404
Autor:
Ruchi Bansal, Staci E. Engle, Patrick J. Antonellis, Logan S. Whitehouse, Anthony J. Baucum, Theodore R. Cummins, Jeremy F. Reiter, Nicolas F. Berbari
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 13 (2019)
Primary cilia dysfunction has been associated with hyperphagia and obesity in both ciliopathy patients and mouse models of cilia perturbation. Neurons throughout the brain possess these solitary cellular appendages, including in the feeding centers o
Externí odkaz:
https://doaj.org/article/9b25369212b44d63bbaada888fbf027e
Autor:
Tia J. Kowal, Onkar S. Dhande, Biao Wang, Qing Wang, Ke Ning, Wendy Liu, Nicolas F. Berbari, Yang Hu, Yang Sun
Publikováno v:
Journal of Comparative Neurology. 530:2176-2187
Loss of retinal ganglion cells (RGCs) underlies several forms of retinal disease including glaucomatous optic neuropathy, a leading cause of irreversible blindness. Several rare genetic disorders associated with cilia dysfunction have retinal degener
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e91f9011de7982c19e05c31490e6bd2
https://doi.org/10.1002/cne.25326
https://doi.org/10.1002/cne.25326
Publikováno v:
Synapse. 77
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9eb809878cfbd1df3b26a32a51d19de2
https://doi.org/10.1002/syn.22264
https://doi.org/10.1002/syn.22264
Autor:
Kathryn M. Brewer, Staci E. Engle, Ruchi Bansal, Katlyn K. Brewer, Kalene R. Jasso, Jeremy C. McIntyre, Christian Vaisse, Jeremy F. Reiter, Nicolas F. Berbari
Primary cilia are small immotile cellular appendages which mediate diverse types of singling and are found on most mammalian cell types including throughout the central nervous system. Cilia are known to localize certain G protein-coupled receptors (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::deae7bbab0be8143b26ccb71c8bec67c
https://doi.org/10.1101/2022.10.13.512090
https://doi.org/10.1101/2022.10.13.512090
Publikováno v:
Semin Cell Dev Biol
An emerging number of rare genetic disorders termed ciliopathies are associated with pediatric obesity. It is becoming clear that the mechanisms associated with cilia dysfunction and obesity in these syndromes are complex. In addition to ciliopathic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5b879e7e433df6947f5b8679cf5d25c
https://doi.org/10.1016/j.semcdb.2020.05.006
https://doi.org/10.1016/j.semcdb.2020.05.006