Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Noam D. Rudnick"'
Autor:
Huijuan Feng, Xiang-Jun Lu, Suvrajit Maji, Linxi Liu, Dmytro Ustianenko, Noam D. Rudnick, Chaolin Zhang
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-14 (2024)
Abstract UV-crosslinking of protein and RNA in direct contacts has been widely used to study protein-RNA complexes while our understanding of the photo-crosslinking mechanisms remains poor. This knowledge gap is due to the challenge of precisely mapp
Externí odkaz:
https://doaj.org/article/ba91412f3e74451492761b3a20f6e1bd
Publikováno v:
International Ophthalmology Clinics. 62:215-229
Autor:
Noam D Rudnick, Filippos Vingopoulos, Jay C Wang, Itika Garg, Ying Cui, Ying Zhu, Rongrong Le, Raviv Katz, Yifan Lu, Nimesh A Patel, John B Miller
Publikováno v:
British Journal of Ophthalmology. :bjophthalmol-2021
Background/aimsTo characterise the morphology, location and functional significance of both macular and extramacular collateral vessels (CVs) in patients with a history of branch retinal vein occlusion (BRVO) using widefield swept-source optical cohe
Autor:
Noam D. Rudnick, Matthew F. Gardiner
Publikováno v:
Pivotal Trials in Ophthalmology ISBN: 9783030639778
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::839c3fe9a61e012dc83ca4c903bc3b37
https://doi.org/10.1007/978-3-030-63978-5_8
https://doi.org/10.1007/978-3-030-63978-5_8
Autor:
Cathleen M. Lutz, Esther Kaunga, Paolo Guarnieri, Noam D. Rudnick, Tom Maniatis, Sean O'Keeffe, Junqiang Ye, Daniele Canzio, Valeria Gerbino
Publikováno v:
Neuron. 106:789-805.e5
DNA sequence variants in the TBK1 gene associate with or cause sporadic or familial amyotrophic lateral sclerosis (ALS). Here we show that mice bearing human ALS-associated TBK1 missense loss-of-function mutations, or mice in which the Tbk1 gene is s
Autor:
Valeria Gerbino, Paolo Guarnieri, Christopher J. Griffey, Juan Carlos Tapia, Noam D. Rudnick, Tom Maniatis, Mark M. Rich, Xueyong Wang, Jason A. Piersaint
Mutations in autophagy genes can cause familial and sporadic amyotrophic lateral sclerosis (ALS). However, the role of autophagy in ALS pathogenesis is poorly understood, in part due to the lack of cell type-specific manipulations of this pathway in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d9366181a96b7160886064f49305792
https://europepmc.org/articles/PMC5625902/
https://europepmc.org/articles/PMC5625902/
Autor:
Kevin Monahan, Kimberly M. Newberry, Richard M. Myers, Tom Maniatis, Florencia Pauli, Polina D. Kehayova, Noam D. Rudnick
Publikováno v:
Proceedings of the National Academy of Sciences. 109:9125-9130
Extraordinary single-cell diversity is generated in the vertebrate nervous system by the combinatorial expression of the clustered protocadherin genes ( Pcdh α, -β, and -γ). This diversity is generated by a combination of stochastic promoter choic
Autor:
Noam D. Rudnick, Steven J. Siegel, Christopher Jepson, Bruce I. Turetsky, Freda Patterson, Andrew A. Strasser, Caryn Lerman, Jennifer M. Phillips, Joseph M. Frey
Publikováno v:
Nicotine & Tobacco Research. 12:589-597
Background: Nicotine alters auditory event-related potentials (ERPs) in rodents and humans and is an effective treatment for smoking cessation. Less is known about the effects of the partial nicotine agonist varenicline on ERPs. Methods: We measured
Autor:
Nan Ma, Noam D. Rudnick, Samantha L. White, Richard S. Ehrlichman, Holly C. Dow, Arati S. Kreibich, Steven J. Siegel, Edward S. Brodkin, Ted Abel, Steven N. Luminais, Chang-Gyu Hahn
Publikováno v:
Brain Research. 1294:116-127
Neuregulin-1 (NRG1) is one of susceptibility genes for schizophrenia and plays critical roles in glutamatergic, dopaminergic and GABAergic signaling. Using mutant mice heterozygous for Nrg1 (Nrg1(+/-)) we studied the effects of Nrg1 signaling on beha
Publikováno v:
Cell Calcium. 45:310-317
Calcium ions (Ca 2+ ) released from inositol trisphosphate (IP 3 )-sensitive intracellular stores may participate in both the transient and extended regulation of neuronal excitability in neocortical and hippocampal pyramidal neurons. IP 3 receptor (