Correction to “Isoindolinone-Based PET Tracers for Imaging Mutant Huntingtin Aggregates”
Longbin Liu, Peter Johnson, Matthew R. Mills, Penelope A. Turner et autres
Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.
Longbin Liu, Peter Johnson, Matthew R. Mills, Penelope A. Turner et autres
Longbin Liu, Peter Johnson, Matthew R. Mills, Penelope A. Turner et autres
Huntington’s disease (HD) is caused by the repeat expansion of the CAG trinucleotide in the mutant Huntingtin gene (m HTT ) within the exon1 region, resulting in an expanded polyglutamine-containing mHTT exon1 protein that serves as the source of the hallmark mHTT …
us, gb, de, be, fr, it (code pays fourni par la source)
Longbin Liu, Peter Johnson, Michael E. Prime, Vinod K. Khetarpal et autres
Therapeutic interventions are being developed for Huntington’s disease (HD), a hallmark of which is mutant huntingtin protein (mHTT) aggregates. Following the advancement to human testing of two [ 11 C]-PET ligands for aggregated mHTT, attributes for further optimization were identified. We replaced …
us, gb, it, be, se, de (code pays fourni par la source)
Daniele Bertoglio, Jonathan Bard, Manuela Heßmann, Longbin Liu et autres
Huntington’s disease (HD) is a dominantly inherited neurodegenerative disorder caused by a CAG trinucleotide expansion in the huntingtin ( HTT ) gene that encodes the pathologic mutant HTT (mHTT) protein with an expanded polyglutamine (polyQ) tract. Whereas several therapeutic programs targeting mHTT …
be, us, de, gb (code pays fourni par la source)
Frank Herrmann, Manuela Heßmann, Sabine Schaertl, Karola Berg-Rosseburg et autres
Huntington's disease (HD) is caused by a CAG trinucleotide repeat expansion in the first exon of the huntingtin (HTT) gene coding for the huntingtin (HTT) protein. The misfolding and consequential aggregation of CAG-expanded mutant HTT (mHTT) underpin HD pathology. Our interest in …
de, gb, ch, us (code pays fourni par la source)
Longbin Liu, Peter Johnson, Michael E. Prime, Vinod K. Khetarpal et autres
The expanded polyglutamine-containing mutant huntingtin (mHTT) protein is implicated in neuronal degeneration of medium spiny neurons in Huntington’s disease (HD) for which multiple therapeutic approaches are currently being evaluated to eliminate or reduce mHTT. Development of effective and orthogonal biomarkers will ensure …
us, gb, it, se, de (code pays fourni par la source)
Daniele Bertoglio, Jonathan Bard, Manuela Heßmann, Longbin Liu et autres
Abstract Huntington’s disease (HD) is a dominantly inherited neurodegenerative disorder caused by a CAG trinucleotide expansion in the huntingtin ( HTT ) gene that encodes the pathologic mutant HTT (mHTT) protein with an expanded polyglutamine (PolyQ) tract. While several therapeutic programs targeting …
be, us, de, gb (code pays fourni par la source)
Longbin Liu, Michael E. Prime, Matt R. Lee, Vinod K. Khetarpal et autres
Abstract Mutant huntingtin (mHTT) protein carrying the elongated N-terminal polyglutamine (polyQ) tract misfolds and forms protein aggregates characteristic of Huntington’s disease (HD) pathology. A high-affinity ligand specific for mHTT aggregates could serve as a positron emission tomography (PET) imaging biomarker for HD …
us, gb, se, it, de (code pays fourni par la source)
Erik Schmok, Mahin Abad Dar, Jochen Behrends, Hanna Erdmann et autres
Suppressor of cytokine signaling 3 (SOCS3) is a feedback inhibitor of interleukin (IL)-6 signaling in macrophages. In the absence of this molecule, macrophages become extremely prone to an IL-6-dependent expression of arginase-1 (Arg1) and nitric oxide synthase (NOS)2, the prototype markers for …
de, jp (code pays fourni par la source)
Erik Schmok, Mahin Abad Dar, Jochen Behrends, Hanna Erdmann et autres
Holger Sann, Jasmin von Erichsen, Manuela Heßmann, Andreas Pahl et autres
de (code pays fourni par la source)
Manuela Heßmann, Alexandra Rausch, Dominik Rückerl, Pamela Scott Adams et autres
de, us (code pays fourni par la source)
BNTIC News n’est pas le producteur de ces données. Les publications sont interrogées à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, AfricArXiv, ROR et la Banque mondiale, sans clé d’accès. OpenAlex reste optionnel. Aucun service payant n’est nécessaire et aucune donnée externe n’est enregistrée en base. Consulter les sources et leurs limites.
L'essentiel de l'actu tech du Burkina & d'Afrique, chaque semaine dans votre boîte mail.
Gratuit · sans spam · désinscription en un clic