Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jamie L Elliott"'
Autor:
Daniel J Kelley, Richard J Davidson, Jamie L Elliott, Garet P Lahvis, Jerry C P Yin, Anita Bhattacharyya
Publikováno v:
PLoS ONE, Vol 2, Iss 9, p e931 (2007)
Fragile X syndrome (FX), the most common heritable cause of mental retardation and autism, is a developmental disorder characterized by physical, cognitive, and behavioral deficits. FX results from a trinucleotide expansion mutation in the fmr1 gene
Externí odkaz:
https://doaj.org/article/7bb58cd129b64a66ad3a9cdddfc8848b
Autor:
Jerry Cp Yin, Jamie L. Elliott
Publikováno v:
Future Neurology. 2:389-396
While the search for the genetic foundation of complex diseases receives a great deal of attention in the popular scientific press, it is merely the first step in a very long journey from gene identification to therapeutic options. Unexpectedly, even
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef91f29844f2e66872a9fbbf9636d534
https://doi.org/10.2217/14796708.2.4.389
https://doi.org/10.2217/14796708.2.4.389
Publikováno v:
Journal of Insect Science
Ferritin is a 24-subunit molecule, made up of heavy chain (HC) and light chain (LC) subunits, which stores and controls the release of dietary iron in mammals, plants, and insects. In mosquitoes, dietary iron taken in a bloodmeal is stored inside fer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a298951d54697fec5f41e3e4446e11b8
http://europepmc.org/articles/PMC4535588
http://europepmc.org/articles/PMC4535588
Publikováno v:
The FASEB Journal. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7ad4f4292dd02d7f49b37360ebe3a1d
https://doi.org/10.1096/fasebj.22.1_supplement.1016.2
https://doi.org/10.1096/fasebj.22.1_supplement.1016.2
Autor:
Garet P. Lahvis, Anita Bhattacharyya, Jerry C. P. Yin, Richard J. Davidson, Jamie L. Elliott, Daniel J. Kelley
Publikováno v:
PLoS ONE
PLoS ONE, Vol 2, Iss 9, p e931 (2007)
PLoS ONE, Vol 2, Iss 9, p e931 (2007)
Fragile X syndrome (FX), the most common heritable cause of mental retardation and autism, is a developmental disorder characterized by physical, cognitive, and behavioral deficits. FX results from a trinucleotide expansion mutation in the fmr1 gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c7a121206493e6fe35410a3cc68045d
http://europepmc.org/articles/PMC1976557
http://europepmc.org/articles/PMC1976557