Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Janneth Oleas"'
Autor:
Fumiaki Yokoi, Janneth Oleas, Hong Xing, Yuning Liu, Kelly M. Dexter, Carly Misztal, Melinda Gerard, Iakov Efimenko, Patrick Lynch, Matthew Villanueva, Raul Alsina, Shiv Krishnaswamy, David E. Vaillancourt, Yuqing Li
Publikováno v:
Neurobiology of Disease, Vol 134, Iss , Pp - (2020)
DYT1 early-onset generalized torsion dystonia is a hereditary movement disorder characterized by abnormal postures and repeated movements. It is caused mainly by a heterozygous trinucleotide deletion in DYT1/TOR1A, coding for torsinA. The mutation ma
Externí odkaz:
https://doaj.org/article/8857dc22f5384221b15e263ebcee882d
Autor:
Fumiaki Yokoi, Mai T. Dang, Yuqing Li, Huan-Xin Chen, Janneth Oleas, Kelly M. Dexter, Hong Xing
Publikováno v:
Behav Brain Res
DYT1 dystonia is a movement disorder mainly caused by a trinucleotide deletion (ΔGAG) in DYT1 (TOR1A), coding for torsinA. DYT1 dystonia patients show trends of decreased striatal ligand-binding activities to dopamine receptors 1 (D1R) and 2 (D2R).
Autor:
Kelly M. Dexter, Fumiaki Yokoi, Janneth Oleas, Patrick Lynch, Matthew Villanueva, Carly I. Misztal, Raul Alsina, Hong Xing, Yuning Liu, Yuqing Li, Melinda Gerard, Iakov Efimenko, Shiv Krishnaswamy, David E. Vaillancourt
Publikováno v:
Neurobiology of Disease, Vol 134, Iss, Pp-(2020)
Neurobiol Dis
Neurobiol Dis
DYT1 early-onset generalized torsion dystonia is a hereditary movement disorder characterized by abnormal postures and repeated movements. It is caused mainly by a heterozygous trinucleotide deletion in DYT1/TOR1A, coding for torsinA. The mutation ma
Publikováno v:
Movement Disorders. 28:990-1000
Dystonia is a neurological disorder characterized by abnormal involuntary movements that are prolonged and often cause twisting and turning. Several genetically modified worms, fruit flies, and rodents have been generated as models of genetic dystoni
Publikováno v:
Microbiology
The tight control of autolysis by Streptococcus mutans is critical for proper virulence gene expression and biofilm formation. A pair of dicistronic operons, SMU.575/574 (lrgAB) and SMU.1701/1700 (designated cidAB), encode putative membrane proteins
Dystonia is a neurological disorder characterized by sustained muscle contractions that lead to abnormal movements and postures. Genetic rodent models have been generated for DYT1, DYT11, DYT12, and DYT25 dystonias. Although these models do not displ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4db98671cdcc3141cc65ee60ec26bce0
https://doi.org/10.1016/b978-0-12-405195-9.00028-7
https://doi.org/10.1016/b978-0-12-405195-9.00028-7
Autor:
Rami R. Ajjuri, Yousuf Ali, Giuseppe Arena, Tetsuo Ashizawa, Georg Auburger, Devika P. Bagchi, Barbara Baldo, Sally L. Baxter, Robert F. Berman, Lester I. Binder, Craig Blackstone, Carlo Breda, Jonathan M. Brotchie, Edward A. Burton, Diany Paola Calderon, Guy A. Caldwell, Kim A. Caldwell, M. Angela Cenci, Jianmin Chen, Marie-Francoise Chesselet, Lyndsey E. Collins-Praino, Carlo Colosimo, Benjamin Combs, Mercè Correa, Maria Cristina D’Adamo, Helena Dai, Debkanya Datta, Mark P. DeAndrade, Paula Dietrich, Ioannis Dragatsis, David Eidelberg, Sherif F. El-Khamisy, Craig L. Evinger, Coralie Fassier, Maciej Figiel, Susan H. Fox, Veronica Francardo, Amanda A.H. Freeman, Steven Frucht, John Gardiner, Benoit Giasson, Flaviano Giorgini, Suzana Gispert, Pilar González-Cabo, Viviana Gradinaru, Marleshia Hall, Hiroko Hama, Adrian Handforth, Susan Hayflick, Jamilé Hazan, Peter Hedera, Gary A. Heiman, Karl Herrup, Ellen J. Hess, Patrick Hickey, Diana S. Himmelstein, Pieter J. Hoekstra, Corinne Houart, Michael Ryan Hunsaker, Hanna Iderberg, Vernic Jackson-Lewis, Joseph Jankovic, H.A. Jinnah, Tarja Joensuu, Tom M. Johnston, Keith A. Josephs, Nicholas M. Kanaan, Kamran Khodakhah, Kwang-Soo Kim, F. Klinker, Gurdeep S. Kooner, Outi Kopra, Paul T. Kotzbauer, Elena Kozina, Florian Krismer, Wlodzimierz J. Krzyzosiak, Korah P. Kuruvilla, Daniela Kuzdas, Charalambos P. Kyriacou, Blair R. Leavitt, Mark S. LeDoux, Anna-Elina Lehesjoki, Deranda Lester, Jada Lewis, Jiali Li, D. Liebetanz, Hanna Lindgren, Giovanna R. Mallucci, Amandeep Mann, Russell L. Margolis, Robert P. Mason, Gelareh Mazarei, Michael P. McDonald, Judith Melki, Aurélie Méneret, Mariana Moscovich, Irene Neuner, Janis M. O’Donnell, Janneth Oleas, William G. Ondo, Puneet Opal, Harry T. Orr, Emily F. Ozdowski, Massimo Pandolfo, Peristera Paschou, Juan M. Pascual, Amar Patel, Neepa Patel, João N. Peres, Mauro Pessia, Åsa Petersén, Simona Petrucci, Ronald F. Pfeiffer, Nicolás M. Phielipp, Ilse Sanet Pienaar, Christopher Pittenger, Mark R. Plummer, Samantha Podurgiel, Serge Przedborski, Andreas Puschmann, Lawrence T. Reiter, Yan Ren, Benoît Renvoisé, Samuel J. Rose, Owen A. Ross, Emmanuel Roze, Kai Ruan, Dobrila D. Rudnicki, Naruhiko Sahara, Wataru Sako, John D. Salamone, Subhabrata Sanyal, Thomas L. Saunders, Susanne A. Schneider, Eva C. Schulte, Jared J. Schwartzer, Nina T. Sherwood, Ody Sibon, Richard J. Smeyne, Mark Stacy, Philip Starr, Brian E. Staveley, Nadia Stefanova, S.H. Subramony, Nicole Swann, Pawel M. Switonski, Wojciech J. Szlachcic, Kwok-Keung Tai, Valeria Tiranti, Daniel D. Truong, Henna Tyynismaa, Aziz M. Uluğ, Enza M. Valente, Jay A. Van Gerpen, Rafael P. Vázquez-Manrique, Satya Vemula, Marie Vidailhet, Ruth H. Walker, Sarah M. Ward, Owen S. Wells, Gregor K. Wenning, Kathleen A. Willet, Juliane Winkelmann, Zbigniew K. Wszolek, Jianfeng Xiao, X. William Yang, Emil Ylikallio, Fumiaki Yokoi, Zhenyu Yue, R. Grace Zhai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cb6b796146860f53192cc50e4f17a42
https://doi.org/10.1016/b978-0-12-405195-9.01002-7
https://doi.org/10.1016/b978-0-12-405195-9.01002-7
Dystonia is a neurological disorder characterized by abnormal involuntary movements that are prolonged and often cause twisting and turning. Several genetically modified worms, fruit flies, and rodents have been generated as models of genetic dystoni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8da95b760195f73c268727977b89d664
http://hdl.handle.net/2108/80712
http://hdl.handle.net/2108/80712