Zobrazeno 1 - 10
of 101
pro vyhledávání: '"Webb, Robin"'
Autor:
Yoon, Susan, Ploss, Alexa, Hutzel, Margaret, Webb, Robin, Hatfield, Ally, Lee, Joyce Y., Munshi, Additti, Radney, Angelise, McClellan, Jen
Publikováno v:
In Child Abuse & Neglect March 2024 149
Autor:
Holler, Christopher J., Webb, Robin L., Laux, Ashley L., Beckett, Tina L., Niedowicz, Dana M., Ahmed, Rachel R., Liu, Yinxing, Simmons, Christopher R., Dowling, Amy L.S., Spinelli, Angela, Khurgel, Moshe, Estus, Steven, Head, Elizabeth, Hersh, Louis B., Murphy, M. Paul
Publikováno v:
In The American Journal of Pathology 2012 180(1):337-350
Autor:
Webb, Robin
Between the 20th and 21st of September 2022 Oxford Archaeology East conducted an archaeological evaluation on land to the east of Guilfords, Harlow, Essex (centered on NGR TL 47682 12342) ahead of the construction of a flood alleviation basin and ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1136abc6d38eb2a0f2993419816b1868
Autor:
Webb, Robin
Publikováno v:
Theses and Dissertations--Molecular and Cellular Biochemistry.
The ZNF9 gene on chromosome 3 encodes the cellular nucleic acid binding protein (CNBP), a ubiquitously expressed, 177 amino acid (≈19.5kDa) protein that is highly conserved among vertebrates. The function of the protein is largely unknown, however
Akademický článek
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Autor:
Webb, Robin
Oxford Archaeology East (OA East) undertook a watching brief on land to the south of Station Road, Barnack, Peterborough (NGR TF 08430 05501) ahead of the installation of a new sewage overflow pipe alongside an existing pipe. Works took place over th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5797f28f492af2e314b74f313740459
Autor:
Wiseman, Frances K, Pulford, Laura J, Barkus, Chris, Liao, Fan, Portelius, Erik, Webb, Robin, Chávez-gutiérrez, Lucia, Cleverley, Karen, Noy, Sue, Sheppard, Olivia, Collins, Toby, Powell, Caroline, Sarell, Claire J, Rickman, Matthew, Choong, Xun, Tosh, Justin L, Siganporia, Carlos, Whittaker, Heather T, Stewart, Floy, Szaruga, Maria, Murphy, Michael P, Blennow, Kaj, De Strooper, Bart, Zetterberg, Henrik, Bannerman, David, Holtzman, David M, Tybulewicz, Victor L J, Fisher, Elizabeth M C, Strydom, Andre, Fisher, Elizabeth, Nizetic, Dean, Hardy, John, Tybulewicz, Victor, Karmiloff-smith, Annette
Publikováno v:
Wiseman, F K, Pulford, L J, Barkus, C, Liao, F, Portelius, E, Webb, R, Chávez-gutiérrez, L, Cleverley, K, Noy, S, Sheppard, O, Collins, T, Powell, C, Sarell, C J, Rickman, M, Choong, X, Tosh, J L, Siganporia, C, Whittaker, H T, Stewart, F, Szaruga, M, Murphy, M P, Blennow, K, De Strooper, B, Zetterberg, H, Bannerman, D, Holtzman, D M, Tybulewicz, V L J, Fisher, E M C, Strydom, A, Fisher, E, Nizetic, D, Hardy, J, Tybulewicz, V & Karmiloff-smith, A 2018, ' Trisomy of human chromosome 21 enhances amyloid-β deposition independently of an extra copy of APP ', Brain, vol. 141, no. 8, pp. 2457-2474 . https://doi.org/10.1093/brain/awy159
Down syndrome, caused by trisomy of chromosome 21, is the single most common risk factor for early-onset Alzheimer’s disease. Worldwide approximately 6 million people have Down syndrome, and all these individuals will develop the hallmark amyloid p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2761::797997128991e22f407546041cabc51b
https://kclpure.kcl.ac.uk/ws/files/104625419/Trisomy_of_human_chromosome_WISEMAN_Publishedonline26June2018_GOLD_VoR_CC_BY_.pdf
https://kclpure.kcl.ac.uk/ws/files/104625419/Trisomy_of_human_chromosome_WISEMAN_Publishedonline26June2018_GOLD_VoR_CC_BY_.pdf
Autor:
Wiseman, Frances K, Pulford, Laura J, Barkus, Chris, Liao, Fan, Portelius, Erik, Webb, Robin, Chavez-Gutierrez, Lucia, Cleverley, Karen, Noy, Sue, Sheppard, Olivia, Collins, Toby, Powell, Caroline, Sarell, Claire J, Rickman, Matthew, Choong, Xun, Tosh, Justin L, Siganporia, Carlos, Whittaker, Heather T, Stewart, Floy, Szaruga, Maria, Murphy, Michael P, Blennow, Kaj, de Strooper, Bart, Zetterberg, Henrik, Bannerman, David, Holtzman, David M, Tybulewicz, Victor LJ, Fisher, Elizabeth MC
Down syndrome, caused by trisomy of chromosome 21, is the single most common risk factor for early-onset Alzheimer's disease. Worldwide approximately 6 million people have Down syndrome, and all these individuals will develop the hallmark amyloid pla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1131::aed097e70c8597701ac6995eb6cd7b97
https://lirias.kuleuven.be/handle/123456789/628796
https://lirias.kuleuven.be/handle/123456789/628796
Akademický článek
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