Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Ramesh K. Narayanan"'
Autor:
Ramesh K. Narayanan, Gonzalo Perez-siles, Kamila A. Marzec, Alexandra Boyling, Brent Neumann, Manoj P. Menezes, Marina L. Kennerson
Publikováno v:
Genes and Diseases, Vol 11, Iss 4, Pp 101071- (2024)
Externí odkaz:
https://doaj.org/article/1a0652a16abf43909617a03e75b833d3
Autor:
Masahiro Nishide, Kathleen Le Marquand, Mark R. Davis, Gábor M. Halmágyi, Avi Fellner, Ramesh K. Narayanan, Marina L. Kennerson, Stephen W. Reddel, Lisa Worgan, Peter K. Panegyres, Kishore R. Kumar
Publikováno v:
The Cerebellum.
Autosomal dominant variants in ELOVL4 cause spinocerebellar ataxia type 34 (SCA34; ATX-ELOVL4), classically associated with a skin condition known as erythrokeratoderma. Here, we report a large Italian-Maltese-Australian family with spinocerebellar a
Autor:
Ramesh K. Narayanan, Ajay Panwar, Tim J. Butler, Anthony N. Cutrupi, Marina Kennerson, Steve Vucic, Ashokkumar Balasubramaniem, Marie Mangelsdorf, Robyn H. Wallace
Mutations in TDP-43 are known to cause Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD). TDP-43 binds to and regulates splicing of several RNA includingZmynd11. Zmynd11 is a transcriptional repressor and a potential E3 ubiquitin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92395ea8524b76108167c81d854e298a
https://doi.org/10.1101/2022.12.11.519991
https://doi.org/10.1101/2022.12.11.519991
Autor:
Gonzalo Perez-Siles, Melina Ellis, Andrew Burgess, Megan H. Brewer, Steve Vucic, Ramesh K Narayanan, Garth A. Nicholson, Marina L. Kennerson, Brent Neumann, Carolyn Ly
Publikováno v:
Human Molecular Genetics
Charcot–Marie-Tooth (CMT) is a commonly inherited, non-fatal neurodegenerative disorder that affects sensory and motor neurons in patients. More than 90 genes are known to cause axonal and demyelinating forms of CMT. The p.R158H mutation in the pyr
Autor:
Masahiro Nishide, Kathleen Le Marquand, Mark Davis, Gábor M. Halmágyi, Avi Fellner, Ramesh K. Narayanan, Marina L. Kennerson, Stephen W. Reddel, Lisa Worgan, Kishore R. Kumar
Autosomal dominant disease-causing variants in the ELOVL4 gene (Elongation of Very Long Chain Fatty Acids-like 4) cause spinocerebellar ataxia type 34 (SCA34; ATX-ELOVL4), classically associated with a skin condition known as erythrokeratoderma. Here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49c9a545e2d968c3b273a659f6b67cb2
https://doi.org/10.21203/rs.3.rs-2198569/v1
https://doi.org/10.21203/rs.3.rs-2198569/v1
Autor:
Anthony N. Cutrupi, Ramesh K. Narayanan, Gonzalo Perez-Siles, Bianca R. Grosz, Kaitao Lai, Alexandra Boyling, Melina Ellis, Ruby CY Lin, Brent Neumann, Di Mao, Motonari Uesugi, Garth A. Nicholson, Steve Vucic, Mario A. Saporta, Marina L. Kennerson
Distal hereditary motor neuropathies (dHMNs) are a group of inherited diseases involving the progressive, length-dependent axonal degeneration of the lower motor neurons. There are currently 29 reported causative genes and 4 disease loci implicated i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e9424cf6d32b9af3e9f4ab2ce77f068
https://doi.org/10.1101/2022.08.16.504208
https://doi.org/10.1101/2022.08.16.504208
Autor:
Anthony N Cutrupi, Ramesh K Narayanan, Gonzalo Perez-Siles, Bianca R Grosz, Kaitao Lai, Alexandra Boyling, Melina Ellis, Ruby C Y Lin, Brent Neumann, Di Mao, Motonari Uesugi, Garth A Nicholson, Steve Vucic, Mario A Saporta, Marina L Kennerson
Publikováno v:
Brain : a journal of neurology.
Distal hereditary motor neuropathies (dHMNs) are a group of inherited diseases involving the progressive, length-dependent axonal degeneration of the lower motor neurons. There are currently 29 reported causative genes and four disease loci implicate
Autor:
Zong Hong Zhang, Dhanisha J Jhaveri, Vikki M Marshall, Denis C Bauer, Janette Edson, Ramesh K Narayanan, Gregory J Robinson, Andreas E Lundberg, Perry F Bartlett, Naomi R Wray, Qiong-Yi Zhao
Publikováno v:
PLoS ONE, Vol 9, Iss 8, p e103207 (2014)
Recent advances in next-generation sequencing technology allow high-throughput cDNA sequencing (RNA-Seq) to be widely applied in transcriptomic studies, in particular for detecting differentially expressed genes between groups. Many software packages
Externí odkaz:
https://doaj.org/article/93e22399e43e472783d6cdbce44a4fb3
Autor:
Qiongyi Zhao, Geoffrey W. Osborne, Zong Hong Zhang, Perry F. Bartlett, Virginia Nink, Ramesh K. Narayanan, Dhanisha J. Jhaveri, Naomi R. Wray, Gregory J. Robinson, Imogen O’Keeffe
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience. 35(21)
The activity of neural precursor cells in the adult hippocampus is regulated by various stimuli; however, whether these stimuli regulate the same or different precursor populations remains unknown. Here, we developed a novel cell-sorting protocol tha
Autor:
Angel Roberto Barchuk, Stephanie D. Biergans, Zhengyang Zhao, Ramesh K. Narayanan, Zilá Luz Paulino Simões, Alexandre S. Cristino, Flávia Cristina de Paula Freitas, Charles Claudianos, Judith Reinhard
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Increasing evidence suggests small non-coding RNAs (ncRNAs) such as microRNAs (miRNAs) control levels of mRNA expression during experience-related remodelling of the brain. Here we use an associative olfactory learning paradigm in the honeybee Apis m