Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Wesley Banks"'
Publikováno v:
The FASEB Journal. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cef6cdb0f41a1b41cc449ee7c6e17d1
https://doi.org/10.1096/fasebj.2022.36.s1.r3231
https://doi.org/10.1096/fasebj.2022.36.s1.r3231
Autor:
O.P. Kenny, Benjamin Girgenti, Wesley Banks, Mostafa Rahimi Azghadi, Brendan Calvert, James Whinney, Bronson Philippa, Ronald D. White, Jamie Johns, Peter V. Ridd, Jake C. Wood, Alex Olsen, Dmitry A. Konovalov
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-12 (2019)
Scientific Reports
Scientific Reports
Robotic weed control has seen increased research of late with its potential for boosting productivity in agriculture. Majority of works focus on developing robotics for croplands, ignoring the weed management problems facing rangeland stock farmers.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9856fc61192ba1e0e6af22dc9f4692fd
http://link.springer.com/article/10.1038/s41598-018-38343-3
http://link.springer.com/article/10.1038/s41598-018-38343-3
Publikováno v:
Autism Research. 7:459-467
The serotonin 2A receptor gene (HTR2A) harbors two functional single nucleotide polymorphisms (SNPs) that are frequent in populations of African and European descent; rs6311, which affects mRNA expression, and rs6314, which changes the amino acid seq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2f45432369ca15afa20a906b1701ccb
https://doi.org/10.1002/aur.1383
https://doi.org/10.1002/aur.1383
Publikováno v:
American Journal of Medical Genetics Part A. 164:1188-1191
Basan syndrome is an extremely rare ectodermal dysplasia with autosomal dominant inheritance and variable expressivity. The etiology of Basan syndrome remains unknown. To identify the Basan syndrome gene, we sequenced keratin 14 (KRT14) and SMARCAD1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::660403c91f83f3042d135ec24fd7dcd0
https://doi.org/10.1002/ajmg.a.36438
https://doi.org/10.1002/ajmg.a.36438
Publikováno v:
Autism research : official journal of the International Society for Autism Research. 7(4)
The serotonin 2A receptor gene (HTR2A) harbors two functional single nucleotide polymorphisms (SNPs) that are frequent in populations of African and European descent; rs6311, which affects mRNA expression, and rs6314, which changes the amino acid seq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::28734708c6fbcdc7a2dda5407e6fef7e
https://pubmed.ncbi.nlm.nih.gov/24753316
https://pubmed.ncbi.nlm.nih.gov/24753316