Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tahleel Ali-Nasser"'
Autor:
Joshua M. Hazan, Raziel Amador, Tahleel Ali-Nasser, Tamar Lahav, Stav Roni Shotan, Miryam Steinberg, Ziv Cohen, Dvir Aran, David Meiri, Yehuda G. Assaraf, Roderic Guigó, Assaf C. Bester
Publikováno v:
Journal of Biomedical Science, Vol 31, Iss 1, Pp 1-19 (2024)
Abstract Background Long non-coding RNAs (lncRNAs) are pivotal players in cellular processes, and their unique cell-type specific expression patterns render them attractive biomarkers and therapeutic targets. Yet, the functional roles of most lncRNAs
Externí odkaz:
https://doaj.org/article/0a7a3f91e9a74ebfbf0006c5add69662
Publikováno v:
Molecular vision. 28
To identify the molecular mechanisms of the development of autosomal dominant retinitis pigmentosa (adRP) with incomplete penetrance in an Israeli Muslim Arab family.Two patients with adRP underwent a detailed ophthalmic evaluation, including fundusc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ab866cc11a03ddeb2ef997cf289c1c62
https://pubmed.ncbi.nlm.nih.gov/36338669
https://pubmed.ncbi.nlm.nih.gov/36338669
Publikováno v:
Ophthalmic genetics. 42(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3580b1a9b839a50f0a8df803c1481d68
https://pubmed.ncbi.nlm.nih.gov/33599192
https://pubmed.ncbi.nlm.nih.gov/33599192
Background: TCC21B is a ciliary protein. The most common phenotypic features associated with TCC21B biallelic mutations are nephronophthisis and skeletal abnormalities. To date, retinal dystrophy has been reported in only one patient. Materials and M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b8a212d122fcea5aad46a025105f8fc
