Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Andrzej T Foik"'
Autor:
Elliot H. Choi, Susie Suh, Andrzej T. Foik, Henri Leinonen, Gregory A. Newby, Xin D. Gao, Samagya Banskota, Thanh Hoang, Samuel W. Du, Zhiqian Dong, Aditya Raguram, Sajeev Kohli, Seth Blackshaw, David C. Lyon, David R. Liu, Krzysztof Palczewski
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-14 (2022)
Leber congenital amaurosis is caused by mutations in RPE65 and leads to retinal degeneration in children. Here, the authors show that in vivo base editing can prolong the survival of cone photoreceptors and rescue their function in a mouse model of t
Externí odkaz:
https://doaj.org/article/ffc071797e4f4fa694375352a34ae7c4
Autor:
Jan C. Frankowski, Andrzej T. Foik, Alexa Tierno, Jiana R. Machhor, David C. Lyon, Robert F. Hunt
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-12 (2021)
Jan Frankowski and Andrzej Foik et al. characterized neuroanatomical, electrophysiological, and functional deficits in the primary visual cortex of mice after traumatic brain injury (TBI). Their results suggest that TBI produces long-lasting impairme
Externí odkaz:
https://doaj.org/article/d0bb20f93ded46f2934af56ab0de9010
Autor:
Dominik Lewandowski, Andrzej T. Foik, Roman Smidak, Elliot H. Choi, Jianye Zhang, Thanh Hoang, Aleksander Tworak, Susie Suh, Henri Leinonen, Zhiqian Dong, Antonio F.M. Pinto, Emily Tom, Jennings Luu, Joan Lee, Xiuli Ma, Erhard Bieberich, Seth Blackshaw, Alan Saghatelian, David C. Lyon, Dorota Skowronska-Krawczyk, Marcin Tabaka, Krzysztof Palczewski
Publikováno v:
JCI Insight, Vol 7, Iss 4 (2022)
Adiponectin receptor 1 (ADIPOR1) is a lipid and glucose metabolism regulator that possesses intrinsic ceramidase activity. Mutations of the ADIPOR1 gene have been associated with nonsyndromic and syndromic retinitis pigmentosa. Here, we show that the
Externí odkaz:
https://doaj.org/article/d6761896c71d4db8902de4c695125400
Publikováno v:
Frontiers in Systems Neuroscience, Vol 14 (2020)
Repetitive visual stimulation is successfully used in a study on the visual evoked potential (VEP) plasticity in the visual system in mammals. Practicing visual tasks or repeated exposure to sensory stimuli can induce neuronal network changes in the
Externí odkaz:
https://doaj.org/article/0751668bf56648cea97afd4ba04bcc1b
Publikováno v:
Frontiers in Systems Neuroscience, Vol 12 (2018)
Oscillations are ubiquitous features of neuronal activity in sensory systems and are considered as a substrate for the integration of sensory information. Several studies have described oscillatory activity in the geniculate visual pathway, but littl
Externí odkaz:
https://doaj.org/article/37541f5f091b40a19fe1fb1bca63a0c6
Publikováno v:
eNeuro, vol 9, iss 3
Inherited retinal degenerative diseases are a prominent cause of blindness. Even though mutations causing death of photoreceptors are mostly known, the pathophysiology downstream in the inner retina and along the visual pathway is incompletely charac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2f55c7b273d2620a19a2c1f5daf10a1
https://pubmed.ncbi.nlm.nih.gov/35701168
https://pubmed.ncbi.nlm.nih.gov/35701168
Autor:
David R. Liu, Elliot H. Choi, David C. Lyon, Krzysztof Palczewski, Philip D. Kiser, Zhiqian Dong, Gregory A. Newby, Wei-Hsi Yeh, Henri Leinonen, Andrzej T. Foik, Susie Suh
Publikováno v:
Nature Biomedical Engineering. 5:169-178
Cytosine base editors and adenine base editors (ABEs) can correct point mutations predictably and independent of Cas9-induced double-stranded DNA breaks (which causes substantial indel formation) and homology-directed repair (which typically leads to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16c683371459353d10dd9402c00b2c8b
https://doi.org/10.1038/s41551-020-00632-6
https://doi.org/10.1038/s41551-020-00632-6
Autor:
Robert F. Hunt, Alexa Tierno, Jan C. Frankowski, Andrzej T. Foik, Jiana R. Machhor, David C. Lyon
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-12 (2021)
Communications Biology
Communications biology, vol 4, iss 1
Communications Biology
Communications biology, vol 4, iss 1
Primary sensory areas of the mammalian neocortex have a remarkable degree of plasticity, allowing neural circuits to adapt to dynamic environments. However, little is known about the effects of traumatic brain injury on visual circuit function. Here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fe2350d023bfa854dcfb3a85d454a4b
https://doi.org/10.1038/s42003-021-02808-5
https://doi.org/10.1038/s42003-021-02808-5
Autor:
Dominik Lewandowski, Andrzej T. Foik, Roman Smidak, Elliot H. Choi, Jianye Zhang, Thanh Hoang, Aleksander Tworak, Susie Suh, Henri Leinonen, Zhiqian Dong, Antonio F.M. Pinto, Emily Tom, Jennings Luu, Joan Lee, Xiuli Ma, Erhard Bieberich, Seth Blackshaw, Alan Saghatelian, David C. Lyon, Dorota Skowronska-Krawczyk, Marcin Tabaka, Krzysztof Palczewski
Publikováno v:
JCI insight, vol 7, iss 4
Adiponectin receptor 1 (ADIPOR1) is a lipid and glucose metabolism regulator that possesses intrinsic ceramidase activity. Mutations of the ADIPOR1 gene have been associated with nonsyndromic and syndromic retinitis pigmentosa. Here, we show that the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0316abd60945766526c84fec1399d774
https://pubmed.ncbi.nlm.nih.gov/35015730
https://pubmed.ncbi.nlm.nih.gov/35015730
Autor:
Elliot H, Choi, Susie, Suh, Andrzej T, Foik, Henri, Leinonen, Gregory A, Newby, Xin D, Gao, Samagya, Banskota, Thanh, Hoang, Samuel W, Du, Zhiqian, Dong, Aditya, Raguram, Sajeev, Kohli, Seth, Blackshaw, David C, Lyon, David R, Liu, Krzysztof, Palczewski
Publikováno v:
Nature communications. 13(1)
Leber congenital amaurosis (LCA) is the most common cause of inherited retinal degeneration in children. LCA patients with RPE65 mutations show accelerated cone photoreceptor dysfunction and death, resulting in early visual impairment. It is therefor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::026b1a88b93bea4c96eb1dbab887b5f2
https://pubmed.ncbi.nlm.nih.gov/35383196
https://pubmed.ncbi.nlm.nih.gov/35383196