Výsledky vyhledávání - "Steffany Bennett"

Akademický článek

Generation of the human iPSC line AKOSi010-A from fibroblasts of a female FAHN patient, carrying the compound heterozygous mutation p.Gly45Arg/p.His319Arg

Autor: Fatima Efendic, Christin Völkner, Saskia Krohn, Hugo Murua Escobar, Sunita Venkateswaran, Steffany Bennett, Andreas Hermann, Moritz J. Frech

Publikováno v: Stem Cell Research, Vol 63, Iss , Pp 102863- (2022)

Fatty acid hydroxylase-associated neurodegeneration (FAHN) is a rare childhood onset neurodegenerative disease caused by mutations in the FA2H gene. Patients display abnormal myelination, cerebellar atrophy and some have iron deposition in the centra

Externí odkaz: https://doaj.org/article/aab543386ef64e7b8f4316cf757dbd93

Zobrazit plný text záznamu

Akademický článek

The aPKC-CBP Pathway Regulates Adult Hippocampal Neurogenesis in an Age-Dependent Manner

Autor: Ayden Gouveia, Karolynn Hsu, Yosuke Niibori, Matthew Seegobin, Gonzalo I. Cancino, Ling He, Fredric E. Wondisford, Steffany Bennett, Diane Lagace, Paul W. Frankland, Jing Wang

Publikováno v: Stem Cell Reports, Vol 7, Iss 4, Pp 719-734 (2016)

While epigenetic modifications have emerged as attractive substrates to integrate environmental changes into the determination of cell identity and function, specific signals that directly activate these epigenetic modifications remain unknown. Here,

Externí odkaz: https://doaj.org/article/452a88eb944140d79f63eaaa0b556802

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání