Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Saja Gharaba"'
Publikováno v:
Neurobiology of Disease, Vol 201, Iss , Pp 106667- (2024)
Huntington's Disease (HD) is an inheritable neurodegenerative condition caused by an expanded CAG trinucleotide repeat in the HTT gene with a direct correlation between CAG repeats expansion and disease severity with earlier onset-of- disease. Previo
Externí odkaz:
https://doaj.org/article/dfb094b42c054460a5dfa8c2dd253ef3
Autor:
Saja Gharaba, Omri Paz, Lea Feld, Anastasia Abashidze, Maydan Weinrab, Noam Muchtar, Adam Baransi, Aviv Shalem, Uri Sprecher, Lior Wolf, Haguy Wolfenson, Miguel Weil
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 11 (2023)
Primary fibroblasts from patient’s skin biopsies are directly isolated without any alteration in the genome, retaining in culture conditions their endogenous cellular characteristics and biochemical properties. The aim of this study was to identify
Externí odkaz:
https://doaj.org/article/1b3d070e04c445f2bd658d685c0fa744
Autor:
Saja Gharaba, Omri Paz, Lea Feld, Anastasia Abashidze, Maydan Weinrab, Haguy Wolfenson, Miguel Weil
Human primary skin fibroblast cells from patient’s skin biopsies were used previously as a model to study different neurodegenerative diseases, including Huntington’s Disease (HD). These cells are directly isolated from the patient’s tissue wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::341b13e93123034615bd88a1363a7c1d
https://doi.org/10.1101/2022.04.03.486386
https://doi.org/10.1101/2022.04.03.486386