Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Toni V."'
Many cellular organelles are membrane-bound structures with complex membrane composition and shape. Their shapes have been observed to depend on the metabolic state of the organelle, and the mechanisms that couple biochemical pathways and membrane sh
Externí odkaz:
http://arxiv.org/abs/2209.15080
Autor:
Earle-Randell, Toni V., Wiggins, Joseph B., Ma, Yingbo, Celepkolu, Mehmet, Bounajim, Dolly, Gao, Zhikai, Ruiz, Julianna Martinez, Boyer, Kristy Elizabeth, Israel, Maya, Lynch, Collin F., Wiebe, Eric
Publikováno v:
In International Journal of Child-Computer Interaction June 2024 40
Autor:
Joseph B. Wiggins, Toni V. Earle-Randell, Dolly Bounajim, Yingbo Ma, Julianna Martinez Ruiz, Ruohan Liu, Mehmet Celepkolu, Maya Israel, Eric Wiebe, Collin F. Lynch, Kristy Elizabeth Boyer
Publikováno v:
Proceedings of the 22nd ACM International Conference on Intelligent Virtual Agents.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b5e08627b4c258beee23534c3279c90
https://doi.org/10.1145/3514197.3549683
https://doi.org/10.1145/3514197.3549683
Professional Correctional Management Operating a Death Row Population: Putting Theory into Practice.
Autor:
Bair, Toni V.1 (AUTHOR)
Publikováno v:
Washington & Lee Law Review. Summer2016, Vol. 73 Issue 3, p1189-1212. 25p.
Autor:
Wong TH, Chiu WZ, Breedveld GJ, Li KW, Verkerk AJ, Hondius D, Hukema RK, Seelaar H, Frick P, Severijnen LA, Lammers GJ, Lebbink JH, van Duinen SG, Kamphorst W, Rozemuller AJ, Bakker EB, Neumann M, Willemsen R, Bonifati V, Smit AB, van Swieten J, Netherlands Brain Bank, International Parkinsonism Genetics Network, Ferreira J, Correia Guedes L, Chien HF, Barbosa ER, Merola A, Zibetti M, Lopiano L, Tassorelli C, Pacchetti C, Nappi G, Riboldazzi G, Bono G, Padovani A, Borroni B, Fincati E, Bertolasi L, Tinazzi M, Bonizzato A, Dalla Libera A, Guidi M, Marini P, Massaro F, Marconi R, Onofrj M, Thomas A, Vanacore N, Meco G, Fabbrini G, Fabrizio E, Manfredi M, Berardelli A, Stocchi F, Vacca L, De Mari M, Dell'Aquila C, Iliceto G, Lamberti P, Toni V, Trianni G, Saddi V, Cossu G, Melis M., CORTELLI, PIETRO, CAPELLARI, SABINA
Publikováno v:
Brain, 137, 1361-1373
Wong, T H, Chiu, W Z, Breedveld, G J, Li, K W, Verkerk, A J, Hondius, D C, Hukema, R K, Seelaar, H, Frick, P, Severijnen, L A, Lammers, G J, Lebbink, J, van Duinen, S G, Kamphorst, W, Rozemuller, A J M, Bakker, E B, Neumann, M, Willemsen, R, Bonifati, V, Smit, A B & van Swieten, J C 2014, ' PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology ', Brain, vol. 137, no. 5, pp. 1361-1373 . https://doi.org/10.1093/brain/awu067
Brain, 137(5), 1361-1373. Oxford University Press
Brain, 137, 1361-1373. Oxford University Press
Brain: a journal of neurology, 137(Pt 5), 1361-73. Oxford University Press
Brain 137(5), 1361-1373 (2014). doi:10.1093/brain/awu067
Wong, T H, Chiu, W Z, Breedveld, G J, Li, K W, Verkerk, A J, Hondius, D C, Hukema, R K, Seelaar, H, Frick, P, Severijnen, L A, Lammers, G J, Lebbink, J, van Duinen, S G, Kamphorst, W, Rozemuller, A J M, Bakker, E B, Neumann, M, Willemsen, R, Bonifati, V, Smit, A B & van Swieten, J C 2014, ' PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology ', Brain, vol. 137, no. 5, pp. 1361-1373 . https://doi.org/10.1093/brain/awu067
Brain, 137(5), 1361-1373. Oxford University Press
Brain, 137, 1361-1373. Oxford University Press
Brain: a journal of neurology, 137(Pt 5), 1361-73. Oxford University Press
Brain 137(5), 1361-1373 (2014). doi:10.1093/brain/awu067
Inclusions of intermediate filaments are found in a number of neurodegenerative diseases. Using whole exome sequencing, linkage analysis and proteomics, Wong and Chiu et al. identify a new familial neurodegenerative disease with intermediate filament
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e75fa646b3cfb07151e5070a075e377f
https://doi.org/10.1093/brain/awu067
https://doi.org/10.1093/brain/awu067
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Autor:
Bonifati V., Rohe C. F., Breedveld G. J., Fabrizio E., De Mari M., Tassorelli C., Tavella A., Marconi R., Nicholl D. J., Chien H. F., Fincati E., Abbruzzese G., Marini P., De Gaetano A., Horstink M. W., Maat Kievit J. A., Sampaio C., Antonini A., Stocchi F., Toni V., Guidi M., Dalla Libera A., Tinazzi M., De Pandis F., Fabbrini G., Goldwurm S., de Klein A., Barbosa E., Lopiano L., Martignoni E., Lamberti P., Vanacore N., Meco G., Oostra B.A., Italian Parkinson Genetics Network, MONTAGNA, PASQUALE
Publikováno v:
Neurology, 65, 87-95
Neurology, 65, 1, pp. 87-95
Neurology, 65(1), 87-95. Lippincott Williams & Wilkins
Neurology, 65, 1, pp. 87-95
Neurology, 65(1), 87-95. Lippincott Williams & Wilkins
Item does not contain fulltext OBJECTIVE: To assess the prevalence, nature, and associated phenotypes of PINK1 gene mutations in a large series of patients with early-onset (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb8a2828c43dbbcbdf7062ec15cf7e25
https://hdl.handle.net/2066/48716
https://hdl.handle.net/2066/48716
Autor:
Reid, William J., Bailey-Dempsey, Cynthia A., Cain, Elizabeth, Cook, Toni V., Burchard, John D.
Publikováno v:
Social Work Research, 1994 Dec 01. 18(4), 227-236.
Externí odkaz:
https://www.jstor.org/stable/42659228
Akademický článek
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