Ribosome association primes the stringent factor Rel for tRNA-dependent locking in the A-site and activation of (p)ppGpp synthesis.

Autor: Takada H; Department of Molecular Biology, Umeå University, SE-901 87 Umeå, Sweden.; Laboratory for Molecular Infection Medicine Sweden (MIMS), Umeå University, SE-901 87 Umeå, Sweden., Roghanian M; Department of Molecular Biology, Umeå University, SE-901 87 Umeå, Sweden.; Laboratory for Molecular Infection Medicine Sweden (MIMS), Umeå University, SE-901 87 Umeå, Sweden., Caballero-Montes J; Cellular and Molecular Microbiology, Faculté des Sciences, Université Libre de Bruxelles (ULB), Building BC, Room 1C4 203, Boulevard du Triomphe, 1050 Brussels, Belgium., Van Nerom K; Cellular and Molecular Microbiology, Faculté des Sciences, Université Libre de Bruxelles (ULB), Building BC, Room 1C4 203, Boulevard du Triomphe, 1050 Brussels, Belgium., Jimmy S; Department of Molecular Biology, Umeå University, SE-901 87 Umeå, Sweden.; Laboratory for Molecular Infection Medicine Sweden (MIMS), Umeå University, SE-901 87 Umeå, Sweden., Kudrin P; University of Tartu, Institute of Technology, 50411 Tartu, Estonia., Trebini F; Department of Molecular Biology, Umeå University, SE-901 87 Umeå, Sweden., Murayama R; Akita Prefectural Research Center for Public Health and Environment, 6-6 Senshu-Kubotamachi, Akita, 010-0874, Japan., Akanuma G; Department of Life Science, Graduate School of Science, Gakushuin University, Tokyo, Japan., Garcia-Pino A; Cellular and Molecular Microbiology, Faculté des Sciences, Université Libre de Bruxelles (ULB), Building BC, Room 1C4 203, Boulevard du Triomphe, 1050 Brussels, Belgium.; WELBIO, Avenue Hippocrate 75, 1200 Brussels, Belgium., Hauryliuk V; Department of Molecular Biology, Umeå University, SE-901 87 Umeå, Sweden.; Laboratory for Molecular Infection Medicine Sweden (MIMS), Umeå University, SE-901 87 Umeå, Sweden.; University of Tartu, Institute of Technology, 50411 Tartu, Estonia.

Publikováno v: Nucleic acids research [Nucleic Acids Res] 2021 Jan 11; Vol. 49 (1), pp. 444-457.

Vogt-Koyanagi-Harada syndrome: Clinical and instrumental contribution

Autor: D Daniele, R Bacci, Trebini F, Appiotti A, Scarzella G, A Inglezis

Publikováno v: The Italian Journal of Neurological Sciences. 12:479-484

Vogt-Koyanagi-Harada syndrome is a rare disease, which probably has a cell-mediated autoimmune pathogenesis, marked by ocular (anterior and/or posterior uveitis), dermatological (poliosis, canities, vitiligo) and neurological (meningo-encephalitis) d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f60e18c1dd3dfda5e8115905f8584da
https://doi.org/10.1007/bf02335510

A late onset variant of ataxia-telangiectasia with a compound heterozygous genotype, A8030G/7481insA

Autor: Saviozzi, S, Saluto, A, Taylor, A, Last, J, Trebini, F, Paradiso, M, Grosso, E, Funaro, A, Ponzio, G, Migone, N, Brusco, A

A taxia-telangiectasia (A-T) is a multisystem autosomal recessive disorder, with an estimated frequency of 1/40 000-1/100 000 live births.1 The ataxia-telangiectasia mutated gene ( ATM ), located on chromosome 11q22-23,2 encodes a nuclear 370 kDa pho

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1a047b68b9c23474f09a39a2f293440
https://europepmc.org/articles/PMC1734960/

A case of Miller Fisher syndrome: atypical findings and therapeutic considerations

Autor: M. Buonocore, Appiotti A, Trebini F, Scarzella G

Publikováno v: Italian journal of neurological sciences. 13(4)

The Miller Fisher syndrome (MFS) is generally considered to be a disease of the peripheral nervous system. In some cases contemporary involvement of the central nervous system has been described (CNS). We report a case in which it was possible to pro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cebf4c423a0dab66715d3bc435a61c4e
https://pubmed.ncbi.nlm.nih.gov/1318288

A late onset variant of ataxia-telangiectasia with a compound heterozygous genotype, A8030G/7481insA.

Autor: Saviozzi, S., Saluto, A., Taylor, A.M.R., Last, J.I.L., Trebini, F., Paradiso, M.C., Grosso, E., Funaro, A., Ponzio, G., Migone, N., Brusco, A.

Publikováno v: Journal of Medical Genetics; Jan2002, Vol. 39 Issue 1, p57, 5p, 3 Diagrams, 1 Chart, 1 Graph