Caenorhabditis elegans levamisole resistance geneslev-1, unc-29, and unc-38 encode functional nicotinic acetylcholine receptor subunits
…, MD Squire, TM Barnes, C Tornoe… - Journal of …, 1997 - Soc Neuroscience
We show that three of the eleven genes of the nematodeCaenorhabditis elegans that
mediate resistance to the nematocide levamisole and to other cholinergic agonists encode …
mediate resistance to the nematocide levamisole and to other cholinergic agonists encode …
Lophotoxin-insensitive nematode nicotinic acetylcholine receptors
C Tornøe, L Holden-Dye, C Garland… - Journal of …, 1996 - journals.biologists.com
Nematode nicotinic acetylcholine receptors (nAChRs) are molecular targets of several
anthelmintic drugs. Studies to date on Caenorhabditis elegans and Ascaris suum have …
anthelmintic drugs. Studies to date on Caenorhabditis elegans and Ascaris suum have …
[BOOK][B] Biological Science: exploring the science of life
A Goodenough, J Scott, G Cameron, D Hawkins… - 2022 - books.google.com
… Dr Jonathan RM Thacker, Senior Lecturer, Biological Sciences, University of the West of
Scotland Dr Camilla Tornoe, School of Life Sciences, University of Sussex Dr Halina Vaughan, …
Scotland Dr Camilla Tornoe, School of Life Sciences, University of Sussex Dr Halina Vaughan, …
Cardiovascular outcomes in patients who experienced a myocardial infarction while treated with liraglutide versus placebo in the LEADER trial
MA Nauck, K Tornøe, S Rasmussen… - Diabetes and …, 2018 - journals.sagepub.com
Objective: Animal studies demonstrated that glucagon-like peptide-1 receptor agonists
reduce myocardial necrosis following regional ischaemia induction. This effect may improve …
reduce myocardial necrosis following regional ischaemia induction. This effect may improve …
[PDF][PDF] Structure and function of the bacterial protein toxin phenomycin
Phenomycin is a bacterial mini-protein of 89 amino acids discovered more than 50 years
ago with toxicity in the nanomolar regime toward mammalian cells. The protein inhibits the …
ago with toxicity in the nanomolar regime toward mammalian cells. The protein inhibits the …
Our tropical home: Danish'empire migrants' in the US Virgin Islands, 1917-1945
P ØSTERGAARD HANSEN - 2017 - cadmus.eui.eu
In 1917 Denmark sold its Caribbean colony to the United States. At a time when other European
empires were promoting social and economic reforms in the colonies, the Danish state …
empires were promoting social and economic reforms in the colonies, the Danish state …
Computational evolution of threonine-rich β-hairpin peptides mimicking specificity and affinity of antibodies
H Hu, C Kofoed, M Li, JPL Gonçalves… - ACS Central …, 2019 - ACS Publications
The development of recognition molecules with antibody-like properties is of great value to
the biotechnological and bioanalytical communities. The recognition molecules presented …
the biotechnological and bioanalytical communities. The recognition molecules presented …
Glycomimetic based approach toward selective carbonic anhydrase inhibitors
The synthesis of selective inhibitors of human carbonic anhydrases (hCAs) is of paramount
importance to avoid side effects derived from undesired interactions with isoforms not …
importance to avoid side effects derived from undesired interactions with isoforms not …
[HTML][HTML] The EndoC-βH1 cell line is a valid model of human beta cells and applicable for screenings to identify novel drug target candidates
VG Tsonkova, FW Sand, XA Wolf, LG Grunnet… - Molecular …, 2018 - Elsevier
Objective To characterize the EndoC-βH1 cell line as a model for human beta cells and
evaluate its beta cell functionality, focusing on insulin secretion, proliferation, apoptosis and ER …
evaluate its beta cell functionality, focusing on insulin secretion, proliferation, apoptosis and ER …
[PDF][PDF] Exploring architectures displaying multimeric presentations of a trihydroxypiperidine iminosugar
C Matassini, S Mirabella, A Goti… - Beilstein Journal of …, 2015 - beilstein-journals.org
The synthesis of new multivalent architectures based on a trihydroxypiperidine α-fucosidase
inhibitor is reported herein. Tetravalent and nonavalent dendrimers were obtained by …
inhibitor is reported herein. Tetravalent and nonavalent dendrimers were obtained by …