Zobrazeno 1 - 7
of 7
pro vyhledávání: '"NiCole Finch"'
Autor:
Imogen J. Swift, Rosa Rademakers, NiCole Finch, Matt Baker, Roberta Ghidoni, Luisa Benussi, Giuliano Binetti, Giacomina Rossi, Matthis Synofzik, Carlo Wilke, David Mengel, Caroline Graff, Leonel T. Takada, Raquel Sánchez-Valle, Anna Antonell, Daniela Galimberti, Chiara Fenoglio, Maria Serpente, Marina Arcaro, Stefanie Schreiber, Stefan Vielhaber, Philipp Arndt, Isabel Santana, Maria Rosario Almeida, Fermín Moreno, Myriam Barandiaran, Alazne Gabilondo, Johannes Stubert, Estrella Gómez-Tortosa, Pablo Agüero, M. José Sainz, Tomohito Gohda, Maki Murakoshi, Nozomu Kamei, Sarah Kittel-Schneider, Andreas Reif, Johannes Weigl, Jinlong Jian, Chuanju Liu, Ginette Serrero, Thomas Greither, Gerit Theil, Ebba Lohmann, Stefano Gazzina, Silvia Bagnoli, Giovanni Coppola, Amalia Bruni, Mirja Quante, Wieland Kiess, Andreas Hiemisch, Anne Jurkutat, Matthew S. Block, Aaron M. Carlson, Geir Bråthen, Sigrid Botne Sando, Gøril Rolfseng Grøntvedt, Camilla Lauridsen, Amanda Heslegrave, Carolin Heller, Emily Abel, Alba Gómez-Núñez, Roger Puey, Andrea Arighi, Enmanuela Rotondo, Lize C. Jiskoot, Lieke H. H. Meeter, João Durães, Marisa Lima, Miguel Tábuas-Pereira, João Lemos, Bradley Boeve, Ronald C. Petersen, Dennis W. Dickson, Neill R. Graff-Radford, Isabelle LeBer, Leila Sellami, Foudil Lamari, Fabienne Clot, Barbara Borroni, Valentina Cantoni, Jasmine Rivolta, Alberto Lleó, Juan Fortea, Daniel Alcolea, Ignacio Illán-Gala, Lucie Andres-Cerezo, Philip Van Damme, Jordi Clarimon, Petra Steinacker, Emily Feneberg, Markus Otto, Emma L. van der Ende, John C. van Swieten, Harro Seelaar, Henrik Zetterberg, Aitana Sogorb-Esteve, Jonathan D. Rohrer
Publikováno v:
Alzheimer’s Research & Therapy, Vol 16, Iss 1, Pp 1-13 (2024)
Abstract Background Pathogenic heterozygous mutations in the progranulin gene (GRN) are a key cause of frontotemporal dementia (FTD), leading to significantly reduced biofluid concentrations of the progranulin protein (PGRN). This has led to a number
Externí odkaz:
https://doaj.org/article/1d7c751ac55c494a90e49ef788756561
Autor:
Jackson, Jazmyne, NiCole Finch, Baker, Matthew, Kachergus, Jennifer, Mariely DeJesus-Hernandez, Pereira, Kimberly, Christopher, Elizabeth, Prudencio, Mercedes, Heckman, Michael, E. Thompson, Dickson, Dennis, Jaimin Shah, BjöRn Oskarsson, Petrucelli, Leonard, Rademakers, Rosa, Marka Van Blitterswijk
Additional file 1 Table S1. Characteristics of overall cohort; Table S2. Characteristics of expression cohort; Figure S1. Comparison blood and brain; Figure S2. Southern blot examples.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::149f0821b102e9a29fec49fb7380075b
Autor:
Dickson, Dennis, Baker, Matthew, Jackson, Jazmyne, Mariely DeJesus-Hernandez, NiCole Finch, Shulan Tian, Heckman, Michael, Pottier, Cyril, Gendron, Tania, Murray, Melissa, Yingxue Ren, Reddy, Joseph, Graff-Radford, Neill, Boeve, Bradley, Petersen, Ronald, Knopman, David, Josephs, Keith, Petrucelli, Leonard, Bjรถrn Oskarsson, Sheppard, John, Asmann, Yan, Rademakers, Rosa, Marka Van Blitterswijk
Figure S1 a Module-trait relationships are presented for patients with an expanded C9orf72 repeat and patients without this repeat (C9Plus vs. C9Minus). b For patients with an expansion and control subjects (C9Plus vs. Control), module-trait relation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e5bb9cca300b193a466f9a9c78a9aea
Autor:
Nicholson, Alexandra, Xiaolai Zhou, Perkerson, Ralph, Tammee Parsons, Chew, Jeannie, Mieu Brooks, Mariely DeJesus-Hernandez, NiCole Finch, Matchett, Billie, Kurti, Aishe, Jansen-West, Karen, Perkerson, Emilie, Daughrity, Lillian, Castanedes-Casey, Monica, Rousseau, Linda, Phillips, Virginia, Fenghua Hu, Gendron, Tania, Murray, Melissa, Dickson, Dennis, Fryer, John, Petrucelli, Leonard, Rademakers, Rosa
Figures S1 through S10. Figure S1. Transcript expression of Tmem106b in Tmem106b deficiency mice at different ages. Figure S2. Tmem106b reduction does not alter the expression of its family members. Figure S3. Tmem106b immunoreactivity in mice with T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1a9924e7a874c48b151ba402e966f4b
Autor:
Michael K. Yoon, Christina Amaral, Eleftherios I. Paschalis, Hang Lee, Matteo Tomasi, Kevin E. Houston, Nicole Finch
Publikováno v:
Translational Vision Science & Technology
Purpose We further optimized and evaluated the safety of the magnetic levator prosthesis (MLP) for temporary management of severe blepharoptosis, and compared efficacy and comfort against the ptosis crutch. Methods The interpalpebral fissure (IPF) of
Autor:
Aleksandra, Wojtas, Kristin A, Heggeli, Nicole, Finch, Matt, Baker, Mariely, Dejesus-Hernandez, Steven G, Younkin, Dennis W, Dickson, Neill R, Graff-Radford, Rosa, Rademakers
Publikováno v:
American journal of neurodegenerative disease. 1(1)
Alzheimer disease (AD) and frontotemporal dementia (FTD) are two frequent forms of primary neurodegenerative dementias with overlapping clinical symptoms. Pathogenic mutations of the amyloid precursor protein (APP) and presenilins 1 and 2 (PSEN1, PSE
Autor:
NiCole Finch, Matt Baker, Richard Crook, Katie Swanson, Karen Kuntz, Rebecca Surtees, Gina Bisceglio, Anne Rovelet-Lecrux, Bradley Boeve, Ronald C. Petersen, Dennis W. Dickson, Steven G. Younkin, Vincent Deramecourt, Julia Crook, Neill R. Graff-Radford, Rosa Rademakers
Publikováno v:
Brain: A Journal of Neurology; Mar2009, Vol. 132 Issue 3, p583-583, 1p