Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Alon Daya"'
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
GNE Myopathy is a rare, recessively inherited neuromuscular worldwide disorder, caused by a spectrum of bi-allelic mutations in the human GNE gene. GNE encodes a bi-functional enzyme responsible for the rate-limiting step of sialic acid biosynthesis
Externí odkaz:
https://doaj.org/article/73a3cdaec61e4bfa8d1cb55a92fa614d
Autor:
Nili Ilouz, Avi Harazi, Miriam Guttman, Alon Daya, Shmuel Ruppo, Lena Yakovlev, Stella Mitrani-Rosenbaum
Publikováno v:
Frontiers in Genome Editing, Vol 4 (2022)
GNE myopathy is an adult onset neuromuscular disorder characterized by slowly progressive distal and proximal muscle weakness, caused by missense recessive mutations in the GNE gene. Although the encoded bifunctional enzyme is well known as the limit
Externí odkaz:
https://doaj.org/article/d01d9991c3af4e9fb487a592ffdc49a9
Publikováno v:
Disease Models & Mechanisms, Vol 13, Iss 3 (2020)
Sarcopenia – the accelerated age-related loss of muscle mass and function – is an under-diagnosed condition, and is central to deteriorating mobility, disability and frailty in older age. There is a lack of treatment options for older adults at r
Externí odkaz:
https://doaj.org/article/bd306abe839c427e96bc5414619d8c54
Autor:
Letizia Zullo, Matteo Bozzo, Alon Daya, Alessio Di Clemente, Francesco Paolo Mancini, Aram Megighian, Nir Nesher, Eric Röttinger, Tal Shomrat, Stefano Tiozzo, Alberto Zullo, Simona Candiani
Publikováno v:
Cells, Vol 9, Iss 9, p 1925 (2020)
Cells with contractile functions are present in almost all metazoans, and so are the related processes of muscle homeostasis and regeneration. Regeneration itself is a complex process unevenly spread across metazoans that ranges from full-body regene
Externí odkaz:
https://doaj.org/article/0603c1d4842a43b18b273a1555fe0c03
Autor:
Eric Röttinger, Simona Candiani, Nir Nesher, Alessio Di Clemente, Matteo Bozzo, Francesco Mancini, Alberto Zullo, Aram Megighian, Letizia Zullo, Tal Shomrat, Stefano Tiozzo, Alon Daya
Publikováno v:
Cells
Cells, MDPI, 2020, 9 (9), pp.1925. ⟨10.3390/cells9091925⟩
Cells, Vol 9, Iss 1925, p 1925 (2020)
Cells, MDPI, 2020, 9 (9), pp.1925. ⟨10.3390/cells9091925⟩
Cells, Vol 9, Iss 1925, p 1925 (2020)
International audience; Cells with contractile functions are present in almost all metazoans, and so are the related processes of muscle homeostasis and regeneration. Regeneration itself is a complex process unevenly spread across metazoans that rang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5511a677f8158fa2257820abaa5e5f31
Autor:
Nicolas-George H. Eliades, Angela Mastrogiacomo, Brendan J. Godley, Simon Demetropoulos, Yakup Kaska, Wayne J. Fuller, Yaniv Levy, Andreas Demetropoulos, Phil J. Bradshaw, Yaron Tikochinski, Lucy I. Wright, Robin T. E. Snape, Annette C. Broderick, Alon Daya, Carlos Carreras
The assessment of the composition and dynamics of endangered populations is crucial for management and conservation, and appropriate genetic markers are critical. The genetic structuring of the Mediterranean green turtle (Chelonia mydas) populations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ede7c3a8a711d83de09ee6ff677ae0f
https://doi.org/10.1002/aqc.2908
https://doi.org/10.1002/aqc.2908
Autor:
Uri Roll, Eli Geffen, Yaron Tikochinski, Alon Daya, Inbar Munwes, Adam Friedmann, Sarig Gafny
Publikováno v:
Molecular Ecology. 19:2675-2689
Several hypotheses are available to predict change in genetic diversity when approaching peripheral populations. We used the eastern spadefoot toad in Israel as a model system to examine these hypotheses using population genetics analyses and network
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f77bae948d20025192e459b8eab3024c
https://doi.org/10.1111/j.1365-294x.2010.04712.x
https://doi.org/10.1111/j.1365-294x.2010.04712.x
Autor:
Adam Friedmann, Tzukit Tal-Goldberg, Stella Mitrani-Rosenbaum, Alon Daya, Yoav Gothilf, Michal Becker-Cohen, Shaojun Du, Gad D. Vatine
Publikováno v:
Human molecular genetics. 23(13)
GNE Myopathy is a rare recessively inherited neuromuscular disorder caused by mutations in the GNE gene, which codes for the key enzyme in the metabolic pathway of sialic acid synthesis. The process by which GNE mutations lead to myopathy is not well
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14cf988cf19176175775b607ab3331d7
https://pubmed.ncbi.nlm.nih.gov/24488768
https://pubmed.ncbi.nlm.nih.gov/24488768
Publikováno v:
Marine genomics. 6
The Mediterranean population of the green sea turtle Chelonia mydas is critically endangered. Genetic analysis of this population using the ordinary haplotyping system, based on sequence analysis of a segment of the mitochondrial DNA (mtDNA) D-loop (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0699b40001a7b77903aa624d1ddda322
https://pubmed.ncbi.nlm.nih.gov/22578655
https://pubmed.ncbi.nlm.nih.gov/22578655
Autor:
Inbar, Munwes, Eli, Geffen, Uri, Roll, Adam, Friedmann, Alon, Daya, Yaron, Tikochinski, Sarig, Gafny
Publikováno v:
Molecular ecology. 19(13)
Several hypotheses are available to predict change in genetic diversity when approaching peripheral populations. We used the eastern spadefoot toad in Israel as a model system to examine these hypotheses using population genetics analyses and network
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::68bd7df6f675d79d37ce82ece49be80f
https://pubmed.ncbi.nlm.nih.gov/20561190
https://pubmed.ncbi.nlm.nih.gov/20561190