Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Alexis Cooper"'
Autor:
Alexis Cooper, Benedikt Berninger
Publikováno v:
eLife, Vol 11 (2022)
New findings cast doubt on whether suppressing the RNA-binding protein PTBP1 can force astrocytes to become dopaminergic neurons.
Externí odkaz:
https://doaj.org/article/76e7f9be5f5c4f188174dfdc2ad680fb
Autor:
Alexis Cooper, Tamer Butto, Niklas Hammer, Somanath Jagannath, Desiree Lucia Fend-Guella, Junaid Akhtar, Konstantin Radyushkin, Florian Lesage, Jennifer Winter, Susanne Strand, Jochen Roeper, Ulrich Zechner, Susann Schweiger
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
Birk-Barel intellectual disability is an imprinting syndrome due to maternally-only transmitted mutations of KCNK9/TASK3. Here authors are using a heterozygous deletion of the active maternal Kcnk9 allele to model the disease and show phenotypic resc
Externí odkaz:
https://doaj.org/article/fea75db2dad1436d96f90d9e76ec3153
Autor:
Christoph Wilmanns, Alexis Cooper, Leesa Wockner, Sotirios Katsandris, Nadine Glaser, Alexander Meyer, Oliver Bartsch, Harald Binder, Paul Karl Walter, Ulrich Zechner
Publikováno v:
EBioMedicine, Vol 2, Iss 2, Pp 158-164 (2015)
Background: Clinical assessment and prognostic stratification of primary varicose veins have remained controversial and the molecular pathogenesis is unknown. Previous data have suggested a contribution of the MTHFR (methylenetetrahydrofolate reducta
Externí odkaz:
https://doaj.org/article/6993e76304564198ad52cfeebe628a57
Autor:
Antje Motzek, Jelena Knežević, Olivier J Switzeny, Alexis Cooper, Ivo Barić, Robert Beluzić, Kevin A Strauss, Erik G Puffenberger, S Harvey Mudd, Oliver Vugrek, Ulrich Zechner
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0151261 (2016)
S-adenosylhomocysteine hydrolase (AHCY) deficiency is a rare autosomal recessive disorder in methionine metabolism caused by mutations in the AHCY gene. Main characteristics are psychomotor delay including delayed myelination and myopathy (hypotonia,
Externí odkaz:
https://doaj.org/article/6217b3de51a9474eb9d537f71aed4845
Publikováno v:
Langmuir. 39:5579-5590
Publikováno v:
European Conference on e-Learning. 21:79-86
This paper explores machine identification of argumentative moves in asynchronous online student debates. Student debate is a technique for engaging with topics which have no clear answer. Online debates differ from less-structured discussion-board c
Giant unilamellar vesicles (GUVs) are micrometer scale minimal cellular mimics that are useful for synthetic biology and drug delivery. Unlike assembly in low-salt solutions, assembly of GUVs in solutions with ionic concentrations of 100-150 mM Na/KC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f188f25a5d30f9016998947aa3826628
https://doi.org/10.1101/2022.10.08.511425
https://doi.org/10.1101/2022.10.08.511425
Publikováno v:
Biophysical Journal. 122:175a
Autor:
Robert Cole, Jacob Fustos, Brian Hart, Brennan Hill, Susan Wade, Alexis Cooper, Daniel Cardona, Arman Sabbaghi, Carter Bullard
Publikováno v:
Ground System Architecture Workshop (GSAW-2022), Held Virtually, 23 Feb - 3 Mar 22.
Autor:
Susann Schweiger, Junaid Akhtar, Konstantin Radyushkin, Desiree Lucia Fend-Guella, Susanne Strand, Somanath Jagannath, Ulrich Zechner, Jennifer Winter, Florian Lesage, Jochen Roeper, Alexis Cooper, Niklas Hammer, Tamer Butto
Publikováno v:
Nature Communications, 11(1):480
Nature Communications
Nature Communications, Nature Publishing Group, 2020, 11 (1), pp.480. ⟨10.1038/s41467-019-13918-4⟩
Nature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
Nature Communications, 2020, 11 (1), pp.480. ⟨10.1038/s41467-019-13918-4⟩
Nature Communications
Nature Communications, Nature Publishing Group, 2020, 11 (1), pp.480. ⟨10.1038/s41467-019-13918-4⟩
Nature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
Nature Communications, 2020, 11 (1), pp.480. ⟨10.1038/s41467-019-13918-4⟩
Mutations in the actively expressed, maternal allele of the imprinted KCNK9 gene cause Birk-Barel intellectual disability syndrome (BBIDS). Using a BBIDS mouse model, we identify here a partial rescue of the BBIDS-like behavioral and neuronal phenoty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70cd76999641b15dc74479d7e8eb2849
https://repository.publisso.de/resource/frl:6422240
https://repository.publisso.de/resource/frl:6422240