Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Christopher Stoddard"'
Publikováno v:
Applied Sciences, Vol 11, Iss 21, p 10501 (2021)
On-slope pilot testing of snow tubes was conducted at two ski areas in the United States to examine the effects of deceleration mats. Snow tube and rider kinematics were measured using an instrumented bodysuit and a GPS system worn by the rider. For
Externí odkaz:
https://doaj.org/article/b3ced9653417497f83c738c3a20b2c95
Autor:
Christopher Y Chen, Nickesha C Anderson, Sandy Becker, Martin Schicht, Christopher Stoddard, Lars Bräuer, Friedrich Paulsen, Laura Grabel
Publikováno v:
PLoS ONE, Vol 13, Iss 11, p e0198703 (2018)
The transcription factor NKX2.1, expressed at high levels in the medial ganglionic eminence (MGE), is a master regulator of cortical interneuron progenitor development. To identify gene candidates with expression profiles similar to NKX2.1, previous
Externí odkaz:
https://doaj.org/article/85bd819e3f144649ac08ed52836206e0
Autor:
Marwa Elamin, Aurelie Dumarchey, Christopher Stoddard, Tiwanna M. Robinson, Christopher Cowie, Dea Gorka, Stormy J. Chamberlain, Eric S. Levine
Publikováno v:
Stem Cell Reports. 18:884-898
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6c93b2a60719e264cfe88891fab8db4
https://doi.org/10.1016/j.stemcr.2023.02.002
https://doi.org/10.1016/j.stemcr.2023.02.002
Autor:
Steven J. Mayerl, Simona Bajgai, Allison L. Ludwig, Lindsey D. Jager, Brittany N. Williams, Cole Bacig, Christopher Stoddard, Divya Sinha, Benjamin D. Philpot, David M. Gamm
Publikováno v:
Stem cell reports. 17(11)
Interphotoreceptor matrix proteoglycan 2 (IMPG2) mutations cause a severe form of early-onset retinitis pigmentosa (RP) with macular involvement. IMPG2 is expressed by photoreceptors and incorporated into the matrix that surrounds the inner and outer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dce60f6aa073da695a1a563ecb58928c
https://pubmed.ncbi.nlm.nih.gov/36206764
https://pubmed.ncbi.nlm.nih.gov/36206764
Autor:
Marwa Elamin, Aurelie Dumarchey, Christopher Stoddard, Tiwanna M. Robinson, Christopher Cowie, Dea Gorka, Stormy J. Chamberlain, Eric S. Levine
Chromosome 15q11-q13 duplication syndrome (Dup15q) is a neurodevelopmental disorder caused by maternal duplications of this region. Autism and epilepsy are key features of Dup15q, but affected individuals also exhibit intellectual disability and deve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::397f01756f7e1396f5c28f6d3b21262d
https://doi.org/10.1101/2022.03.11.483963
https://doi.org/10.1101/2022.03.11.483963
Autor:
Noelle D. Germain, Justin Cotney, Christopher Stoddard, Stormy J. Chamberlain, Andrea Wilderman, Jack S. Hsiao, Geno J Villafano, Leighton J. Core, Luke A Wojenski
Publikováno v:
Proceedings of the National Academy of Sciences. 116:2181-2186
Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by the loss of function from the maternal allele of UBE3A , a gene encoding an E3 ubiquitin ligase. UBE3A is only expressed from the maternally inherited allele in mature human neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0711ad5925222d31c1c00317c427ef65
https://doi.org/10.1073/pnas.1815279116
https://doi.org/10.1073/pnas.1815279116
Autor:
Andrea Wilderman, Justin Cotney, Leighton J. Core, Noelle D. Germain, Geno J Villafano, Christopher Stoddard, Stormy J. Chamberlain, Jack S. Hsiao, Luke A Wojenski
Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by the loss of function from the maternal allele of UBE3A, a gene encoding an E3 ubiquitin ligase. UBE3A is only expressed from the maternally-inherited allele in mature human neur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::726b3dc6cd05137f66fb185c585f9355
Autor:
Roger Ackroyd, Nicola Brown, David Vernon, David Roberts, Timothy Stephenson, Stuart Marcus, Christopher Stoddard, Malcolm Reed
Publikováno v:
Photochemistry and Photobiology. 70:656
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd8008cb2540fbdb00a147b425988d1f
https://doi.org/10.1562/0031-8655(1999)070<0656:aapodb>2.3.co
https://doi.org/10.1562/0031-8655(1999)070<0656:aapodb>2.3.co