Zobrazeno 1 - 10
of 155
pro vyhledávání: '"Elisabeth, Singer"'
Autor:
Reed, Jerome, Reed, Olivia
Publikováno v:
American Music Teacher, 1999 Dec 01. 49(3), 64-65.
Externí odkaz:
https://www.jstor.org/stable/43545142
Autor:
Anna Niewiadomska-Cimicka, Lorraine Fievet, Magdalena Surdyka, Ewelina Jesion, Céline Keime, Elisabeth Singer, Aurélie Eisenmann, Zaneta Kalinowska-Poska, Hoa Huu Phuc Nguyen, Agnieszka Fiszer, Maciej Figiel, Yvon Trottier
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 8, p 4354 (2024)
Polyglutamine (polyQ)-encoding CAG repeat expansions represent a common disease-causing mutation responsible for several dominant spinocerebellar ataxias (SCAs). PolyQ-expanded SCA proteins are toxic for cerebellar neurons, with Purkinje cells (PCs)
Externí odkaz:
https://doaj.org/article/4e2d6384325841c7a1537de20931963b
Autor:
Libo Yu-Taeger, Arianna Novati, Jonasz Jeremiasz Weber, Elisabeth Singer-Mikosch, Ann-Sophie Pabst, Fubo Cheng, Carsten Saft, Jennifer Koenig, Gisa Ellrichmann, Taneli Heikkinen, Mahmoud A. Pouladi, Olaf Riess, Huu Phuc Nguyen
Publikováno v:
Cells, Vol 11, Iss 23, p 3779 (2022)
Body weight (BW) loss and reduced body mass index (BMI) are the most common peripheral alterations in Huntington disease (HD) and have been found in HD mutation carriers and HD animal models before the manifestation of neurological symptoms. This sug
Externí odkaz:
https://doaj.org/article/182d9543377f43cc8144fbbfc702c74e
Autor:
Elisabeth Singer-Brehm
Publikováno v:
Aschkenas. 32:429-463
Hidden in the attics of old synagogues in Germany, the very last remnants of former Genizot survived unnoticed not only the NS period, but also the following years of secular use of these buildings. Since the 1950s Genizot have been found mostly in t
Autor:
Elisabeth Singer, Carolin Walter, Jonasz J. Weber, Ann-Christin Krahl, Ulrike A. Mau-Holzmann, Nadine Rischert, Olaf Riess, Laura E. Clemensson, Huu P. Nguyen
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
Abstract Huntington disease is a fatal neurodegenerative disorder caused by a CAG repeat expansion in the gene encoding the huntingtin protein. Expression of the mutant protein disrupts various intracellular pathways and impairs overall cell function
Externí odkaz:
https://doaj.org/article/baca3f0edb594d1fb92d80a01ad67420
Autor:
Fanny George, Catherine Daniel, Muriel Thomas, Elisabeth Singer, Axel Guilbaud, Frédéric J. Tessier, Anne-Marie Revol-Junelles, Frédéric Borges, Benoît Foligné
Publikováno v:
Frontiers in Microbiology, Vol 9 (2018)
Lactic acid bacteria (LAB) are representative members of multiple ecosystems on earth, displaying dynamic interactions within animal and plant kingdoms in respect with other microbes. This highly heterogeneous phylogenetic group has coevolved with pl
Externí odkaz:
https://doaj.org/article/1e5f95ef37824a29a53a3776eeda9a92
Autor:
Elisabeth Singer, Lilit Hunanyan, Magda M. Melkonyan, Jonasz J. Weber, Lusine Danielyan, Huu Phuc Nguyen
Publikováno v:
Pharmaceuticals, Vol 14, Iss 3, p 257 (2021)
Huntington’s disease (HD) is a monogenetic neurodegenerative disorder characterized by the accumulation of polyglutamine-expanded huntingtin (mHTT). There is currently no cure, and therefore disease-slowing remedies are sought to alleviate symptoms
Externí odkaz:
https://doaj.org/article/84cac017ab2c42369e0a0807e2db2a90
Autor:
Magdalena Surdyka, Anna Niewiadomska-Cimicka, Zaneta Kalinowska-Poska, Ewelina Jesion, Elisabeth Singer-Mikosch, Lorraine Fievet, Agnieszka Fiszer, Nicholas S Caron, Michael R Hayden, Huu Phuc Nguyen, Yvon Trottier, Maciej Figiel
Publikováno v:
I: Experimental therapeutics – preclinical.
Autor:
Libo Yu-Taeger, Arianna Novati, Jonasz Jeremiasz Weber, Elisabeth Singer-Mikosch, Ann-Sophie Pabst, Carsten Saft, Jennifer König, Gisa Ellrichmann, Taneli Heikkinen, Mahmoud A Pouladi, Olaf Riess, Huu Phuc Nguyen
Publikováno v:
A: Pathogenic mechanisms.
Autor:
Libo Yu-Taeger, Janice Stricker-Shaver, Katrin Arnold, Patrycja Bambynek-Dziuk, Arianna Novati, Elisabeth Singer, Ali Lourhmati, Claire Fabian, Janine Magg, Olaf Riess, Matthias Schwab, Alexandra Stolzing, Lusine Danielyan, Hoa Huu Phuc Nguyen
Publikováno v:
Cells, Vol 8, Iss 6, p 595 (2019)
Intrastriatal administration of mesenchymal stem cells (MSCs) has shown beneficial effects in rodent models of Huntington disease (HD). However, the invasive nature of surgical procedure and its potential to trigger the host immune response may limit
Externí odkaz:
https://doaj.org/article/a1cc28f483b44180a8ee4c7e39c3904f