Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Shong, Lau"'
Autor:
Adrian Minson, Emma Verner, Pratyush Giri, Shu Min Wong, Sumita Ratnasingam, Jason Butler, Wojciech Janowski, Matthew Ku, Chan Cheah, Mark Hertzberg, Kirsten Herbert, Nada Hamad, Costas Yannakou, Paul Neeson, Javad Saghebi, Piers Blombery, Molly Robertson, Lei Shong Lau, Jing Xie, John Seymour, Michael Dickinson
Publikováno v:
HemaSphere, Vol 7, p e8608732 (2023)
Externí odkaz:
https://doaj.org/article/de98225c7c534dbabf8bebb769e5a36d
Autor:
Shong Lau, Shani Stern
Publikováno v:
Frontiers in Aging Neuroscience, Vol 15 (2023)
Externí odkaz:
https://doaj.org/article/cb25297d1e7c4f3ea7cd39c92e575e7a
Autor:
Mark van den Hurk, Shong Lau, Maria C. Marchetto, Jerome Mertens, Shani Stern, Olga Corti, Alexis Brice, Beate Winner, Jürgen Winkler, Fred H. Gage, Cedric Bardy
Publikováno v:
npj Parkinson's Disease, Vol 8, Iss 1, Pp 1-18 (2022)
Abstract Complex genetic predispositions accelerate the chronic degeneration of midbrain substantia nigra neurons in Parkinson’s disease (PD). Deciphering the human molecular makeup of PD pathophysiology can guide the discovery of therapeutics to s
Externí odkaz:
https://doaj.org/article/14683e153a4e4a20901fa0656fbb2213
Autor:
Shani Stern, Shong Lau, Andreea Manole, Idan Rosh, Menachem Mendel Percia, Ran Ben Ezer, Maxim N. Shokhirev, Fan Qiu, Simon Schafer, Abed AlFatah Mansour, Kile P. Mangan, Tchelet Stern, Polina Ofer, Yam Stern, Ana Paula Diniz Mendes, Jose Djamus, Lynne Randolph Moore, Ritu Nayak, Sapir Havusha Laufer, Aidan Aicher, Amanda Rhee, Thomas L. Wong, Thao Nguyen, Sara B. Linker, Beate Winner, Beatriz C. Freitas, Eugenia Jones, Irit Sagi, Cedric Bardy, Alexis Brice, Juergen Winkler, Maria C. Marchetto, Fred H. Gage
Publikováno v:
npj Parkinson's Disease, Vol 8, Iss 1, Pp 1-16 (2022)
Abstract Several mutations that cause Parkinson’s disease (PD) have been identified over the past decade. These account for 15–25% of PD cases; the rest of the cases are considered sporadic. Currently, it is accepted that PD is not a single monol
Externí odkaz:
https://doaj.org/article/2fa050a5687248eaa0da9d23e96a5eb4
Australian fertility preservation guidelines for people with cancer 2022: review and recommendations
Autor:
Violet Kieu, Catharyn Stern, Jessica Harris, Yasmin Jayasinghe, Natalie Bradford, Wanyuan Cui, Rebecca Deans, Tamara Hunter, Catherine Allingham, Stefan C Kane, Lei Shong Lau, Shanna Logan, Robert McLachlan, Kristen Neville, Michelle Peate, Marianne Phillips, Carla Saunders, Marianne Tome, Rita Upreti, Kate White, Antoinette Anazodo, Roger J Hart
Publikováno v:
Medical Journal of Australia. 217:564-569
Autor:
Janelle Drouin‐Ouellet, Shong Lau, Per Ludvik Brattås, Daniella Rylander Ottosson, Karolina Pircs, Daniela A Grassi, Lucy M Collins, Romina Vuono, Annika Andersson Sjöland, Gunilla Westergren‐Thorsson, Caroline Graff, Lennart Minthon, Håkan Toresson, Roger A Barker, Johan Jakobsson, Malin Parmar
Publikováno v:
EMBO Molecular Medicine, Vol 9, Iss 8, Pp 1117-1131 (2017)
Abstract Direct conversion of human fibroblasts into mature and functional neurons, termed induced neurons (iNs), was achieved for the first time 6 years ago. This technology offers a promising shortcut for obtaining patient‐ and disease‐specific
Externí odkaz:
https://doaj.org/article/e73f830423c14f13b05bd7371e571788
Autor:
Olof Torper, Daniella Rylander Ottosson, Maria Pereira, Shong Lau, Tiago Cardoso, Shane Grealish, Malin Parmar
Publikováno v:
Cell Reports, Vol 12, Iss 3, Pp 474-481 (2015)
The possibility of directly converting non-neuronal cells into neurons in situ in the brain would open therapeutic avenues aimed at repairing the brain after injury or degenerative disease. We have developed an adeno-associated virus (AAV)-based repo
Externí odkaz:
https://doaj.org/article/939202a546e344ef89edaec724195d81
Publikováno v:
Cell Reports, Vol 9, Iss 5, Pp 1673-1680 (2014)
Summary: Recent findings show that human fibroblasts can be directly programmed into functional neurons without passing via a proliferative stem cell intermediate. These findings open up the possibility of generating subtype-specific neurons of human
Externí odkaz:
https://doaj.org/article/2129d56389e24bbca6885e9da92c3dc2
Autor:
Shani Stern, Shong Lau, Andreea Manole, Idan Rosh, Menahem Percia, Ran Ben Ezer, Maxim N. Shokhirev, Fan Qiu, Simon Schafer, Abed Mansour, Tchelet Stern, Pola Ofer, Yam Stern, Ana Mendes Diniz, Lynne Randolph Moore, Ritu Nayak, Aidan Aicher, Amanda Rhee, Thomas L. Wong, Thao Nguyen, Sara B. Linker, Beate Winner, Beatriz C. Freitas, Eugenia Jones, Cedric Bardy, Alexis Brice, Juergen Winkler, Maria C. Marchetto, Fred H. Gage
Several mutations that cause Parkinson’s disease (PD) have been identified over the past decade. These account for 15-25% of PD cases; the rest of the cases are considered sporadic. Currently, it is accepted that PD is not a single monolithic disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b45c602fcde062bde33415f1c163fa90
https://doi.org/10.1101/2021.12.31.474654
https://doi.org/10.1101/2021.12.31.474654
Autor:
Shong Lau, Shani Stern, Sara Linker, Ioana Da Silva, Nako Nakatsuka, Juliane Tampé, Ana Beltrán-Arranz, Ian Haliburton, Coral Castro Rivera, Nicolas Spiesshofer, Alexis Brice, Beate Winner, Jurgen Winkler, Andreea Manole, Nicholas Wood, Henry Houlden, Fred Gage
Human aging is the main risk factor for Parkinson’s disease (PD). To better understand age-related PD pathogenesis, we modeled PD with directly reprogrammed dopaminergic neurons (iDA) which preserve donor aging signatures. By transcriptome analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a064303df8cb229193daab1937691d08
https://doi.org/10.21203/rs.3.rs-1168396/v1
https://doi.org/10.21203/rs.3.rs-1168396/v1