Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nicole A. Gabreski"'
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 10, Iss 1, Pp 1-14 (2018)
Abstract Background Sensory processing deficits are frequently co-morbid with neurodevelopmental disorders. For example, patients with fragile X syndrome (FXS), caused by a silencing of the FMR1 gene, exhibit impairments in visual function specific t
Externí odkaz:
https://doaj.org/article/6612f006674d45c595997af990ac38be
Publikováno v:
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders, Vol 10, Iss 1, Pp 1-14 (2018)
Journal of Neurodevelopmental Disorders, Vol 10, Iss 1, Pp 1-14 (2018)
Background Sensory processing deficits are frequently co-morbid with neurodevelopmental disorders. For example, patients with fragile X syndrome (FXS), caused by a silencing of the FMR1 gene, exhibit impairments in visual function specific to the dor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4d49e45ea7abb4a5ac46ef1e36964fd
https://doi.org/10.1186/s11689-018-9241-1
https://doi.org/10.1186/s11689-018-9241-1
Autor:
Christopher R. Donnelly, Brian A. Pierchala, Monzurul Chowdhury, Nicole A. Gabreski, Esther B. Suh
Publikováno v:
The Journal of Cell Biology
Programmed cell death is a critical process in sculpting the developing nervous system, but the underlying signaling mechanisms remain poorly defined. Donnelly et al. demonstrate a non-canonical function for the neurotrophic factor receptor Ret in p7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62ccec0f713844dd85c8065df2d2eec9
https://pubmed.ncbi.nlm.nih.gov/30018091
https://pubmed.ncbi.nlm.nih.gov/30018091
Autor:
Brian A. Pierchala, Nicole A. Gabreski, Janki K. Vaghasia, Silvia S. Novakova, Neil Q. McDonald
Publikováno v:
The Journal of biological chemistry. 291(31)
Rearranged during transfection (RET), a receptor tyrosine kinase that is activated by the glial cell line-derived neurotrophic factor family ligands (GFLs), plays a crucial role in the development and function of the nervous system and additionally i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba9878c8900e67742714686f7283366d
https://pubmed.ncbi.nlm.nih.gov/27226544
https://pubmed.ncbi.nlm.nih.gov/27226544
Glial cell line-derived neurotrophic factor (GDNF) promotes PNS development and kidney morphogenesis via a receptor complex consisting of the glycerophosphatidylinositol (GPI)-anchored, ligand binding receptor GDNF family receptor α1 (GFRα1) and th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42343cd853dfcca7402d826699a6d42d
https://europepmc.org/articles/PMC4579380/
https://europepmc.org/articles/PMC4579380/
Publikováno v:
Journal of Equine Veterinary Science. 29:321-322
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50488575ff9ac095d6a4e4d5f928cb90
https://doi.org/10.1016/j.jevs.2009.04.029
https://doi.org/10.1016/j.jevs.2009.04.029
Publikováno v:
Animal Genetics. 43:650-650
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb88a897af33531cb852a15c913c4246
https://doi.org/10.1111/j.1365-2052.2011.02305.x
https://doi.org/10.1111/j.1365-2052.2011.02305.x
Autor:
Helen E. Brown, Abra Brisbin, Donald Miller, Douglas F. Antczak, Samantha A. Brooks, Jason G. Mezey, Nicole A. Gabreski, Cassandra Streeter, Deborah Cook
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 6, Iss 4, p e1000909 (2010)
PLoS Genetics, Vol 6, Iss 4, p e1000909 (2010)
Lavender Foal Syndrome (LFS) is a lethal inherited disease of horses with a suspected autosomal recessive mode of inheritance. LFS has been primarily diagnosed in a subgroup of the Arabian breed, the Egyptian Arabian horse. The condition is character
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2aed2466b3be30f0a525f8ea596ee7a
https://doi.org/10.1371/journal.pgen.1000909
https://doi.org/10.1371/journal.pgen.1000909