Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Arpana Arjun"'
Autor:
Georgia Panagiotakos, Christos Haveles, Arpana Arjun, Ralitsa Petrova, Anshul Rana, Thomas Portmann, Sergiu P Paşca, Theo D Palmer, Ricardo E Dolmetsch
Publikováno v:
eLife, Vol 8 (2019)
The syndromic autism spectrum disorder (ASD) Timothy syndrome (TS) is caused by a point mutation in the alternatively spliced exon 8A of the calcium channel Cav1.2. Using mouse brain and human induced pluripotent stem cells (iPSCs), we provide eviden
Externí odkaz:
https://doaj.org/article/1dd70c6ef5624a2a82b753832aeeacc0
Akademický článek
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Autor:
Andrews, Madeline G., Siebert, Clara, Wang, Li, White, Matthew L., Ross, Jayden, Morales, Raul, Donnay, Megan, Bamfonga, Gradi, Mukhtar, Tanzila, McKinney, Arpana Arjun, Gemenes, Kaila, Wang, Shaohui, Bi, Qiuli, Crouch, Elizabeth E., Parikshak, Neelroop, Panagiotakos, Georgia, Huang, Eric, Bhaduri, Aparna, Kriegstein, Arnold R.
Publikováno v:
In Cell Stem Cell 5 October 2023 30(10):1382-1391
Publikováno v:
Development (Cambridge, England). 149(17)
Calcium influx can be stimulated by various intra- and extracellular signals to set coordinated gene expression programs into motion. As such, the precise regulation of intracellular calcium represents a nexus between environmental cues and intrinsic
Akademický článek
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Publikováno v:
Annals of plastic surgery. 86(1)
Individuals with gender dysphoria often seek medical interventions, such as hormone treatment and surgery, to live as their identified gender. Cross-sex hormone therapy typically consists of various estrogen formulations which confer varying risks of
Autor:
Georgia Panagiotakos, Christos S Haveles, Anshul Rana, Thomas Portmann, Theo D. Palmer, Arpana Arjun, Ralitsa Petrova, Ricardo E. Dolmetsch, Sergiu P. Paşca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf11666ea099cf333f975f82b5bcee75
https://doi.org/10.7554/elife.51037.sa2
https://doi.org/10.7554/elife.51037.sa2
Autor:
Sergiu P. Paşca, Georgia Panagiotakos, Christos S Haveles, Thomas Portmann, Ricardo E. Dolmetsch, Anshul Rana, Theo D. Palmer, Arpana Arjun, Ralitsa Petrova
Publikováno v:
eLife, Vol 8 (2019)
eLife
eLife
The syndromic autism spectrum disorder (ASD) Timothy syndrome (TS) is caused by a point mutation in the alternatively spliced exon 8A of the calcium channel Cav1.2. Using mouse brain and human induced pluripotent stem cells (iPSCs), we provide eviden
Autor:
Diane Jung, Carlos E. Cunha, Georgia Panagiotakos, Nils Lovegren, Andreas Mayer, Anne A. Leyrat, Jay A. A. West, Michael L. Gonzales, Arturo Alvarez-Buylla, Lukasz Szpankowski, Tomasz J. Nowakowski, Beatriz Alvarado, Dmitry Velmeshev, Jiadong Chen, Simone Mayer, Ugomma C. Eze, Arnold R. Kriegstein, Emmy Li, Mercedes F. Paredes, Shaohui Wang, Aparna Bhaduri, Arpana Arjun, Alex A. Pollen
Publikováno v:
Neuron, vol 102, iss 1
Neuron
Neuron
In the developing human neocortex, progenitor cells generate diverse cell types prenatally. Progenitor cells and newborn neurons respond to signaling cues, including neurotransmitters. While single-cell RNA sequencing has revealed cellular diversity,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8aa26330944a1e30cfa4ff301709adc6
https://escholarship.org/uc/item/7sg4h391
https://escholarship.org/uc/item/7sg4h391
Autor:
Arpana Arjun, Dagmar Ringe, Eric J. Huang, Gregory A. Petsko, Yuxi Zhang, Steven Finkbeiner, Daniel Peisach, Xingli Li, Anthony Batarse, Haiyan Qiu, Hilary C. Archbold, Elizabeth M. H. Tank, Shulin Ju, Sami J. Barmada
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, vol 112, iss 25
Barmada, SJ; Ju, S; Arjun, A; Batarse, A; Archbold, HC; Peisach, D; et al.(2015). Amelioration of toxicity in neuronal models of amyotrophic lateral sclerosis by hUPF1. Proceedings of the National Academy of Sciences of the United States of America, 112(25), 7821-7826. doi: 10.1073/pnas.1509744112. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/5dn3b2m6
Barmada, SJ; Ju, S; Arjun, A; Batarse, A; Archbold, HC; Peisach, D; et al.(2015). Amelioration of toxicity in neuronal models of amyotrophic lateral sclerosis by hUPF1. Proceedings of the National Academy of Sciences of the United States of America, 112(25), 7821-7826. doi: 10.1073/pnas.1509744112. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/5dn3b2m6
© 2015, National Academy of Sciences. All rights reserved. Over 30% of patients with amyotrophic lateral sclerosis (ALS) exhibit cognitive deficits indicative of frontotemporal dementia (FTD), suggesting a common pathogenesis for both diseases. Cons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b41a215b7bf5513f473f2324ad29053
https://escholarship.org/uc/item/5dn3b2m6
https://escholarship.org/uc/item/5dn3b2m6