Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Marko Kroselj"'
Autor:
Doroteja Novak, Barbara Janota, Anton Amadeus Hörmann, Agnieszka Sawicka, Marko Kroselj, Alicja Hubalewska-Dydejczyk, Melpomeni Fani, Renata Mikolajczak, Petra Kolenc, Clemens Decristoforo, Piotr Garnuszek
Publikováno v:
Pharmaceutics, Vol 15, Iss 3, p 885 (2023)
Broad availability and cost-effectiveness of 99Mo/99mTc generators worldwide support the use, and thus the development, of novel 99mTc-labelled radiopharmaceuticals. In recent years, preclinical and clinical developments for neuroendocrine neoplasms
Externí odkaz:
https://doaj.org/article/f1622523023c4c7a8174d282234f634f
Autor:
Alicja Hubalewska-Dydejczyk, Clemens Decristoforo, Petra Kolenc, Renata Mikolajczak, Luka Ležaić, Andrej Suden, Piotr Garnuszek, Urban Simoncic, Irene Virgolini, Malgorzata Trofimiuk-Muldner, Marta Opalinska, Christine Rangger, Boguslaw Glowa, Konrad Skorkiewicz, Melpomeni Fani, Staszczak Anna Sowa, Barbara Janota, Marko Kroselj, Katja Zaletel, Guggenberg Elisabeth Von
Publikováno v:
Endocrine Abstracts.
Autor:
Uroš Javornik, Marko Anderluh, Janez Plavec, Tihomir Tomašič, Petra Kolenc Peitl, Marko Kroselj, Doroteja Novak
Publikováno v:
ChemMedChem. 16:155-163
The cholecystokinin-2/gastrin receptor (CCK2 R) is considered a suitable target for the development of radiolabelled antagonists, due to its overexpression in various tumours, but no such compounds are available in clinical use. Therefore, we designe
Publikováno v:
Reference Module in Biomedical Sciences
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2c79f5d7af4b152ab9113c617f2a618
https://doi.org/10.1016/b978-0-12-822960-6.00041-7
https://doi.org/10.1016/b978-0-12-822960-6.00041-7
Autor:
Tanja Gmeiner, Milos Petrik, Aljaz Socan, Clemens Decristoforo, Christine Rangger, P. Kolenc Peitl, Marko Kroselj, U. Svajger, Zbynek Novy
Publikováno v:
Nuclear Medicine and Biology. 71:23-31
Introduction Indium-111 when formulated as indium-111 oxine remains the gold standard for long term cell tracking, whereas radiometals for improved PET applications still have to be established. We here describe the on-cartridge formation of gallium-
Autor:
Marko Kroselj, Petra Kolenc Peitl, Tanja Gmeiner, Roger Knopp, Thorsten Dreger, Katja Zaletel, Aljaz Socan
Publikováno v:
Nuclear Medicine Communications. 37:207-214
OBJECTIVE With the vast development of theranostics and, recently, (68)Ga-radiolabeled molecules, there is also a need for novel, smaller, flexible, safe, and efficient modular automated synthesis systems in different clinical settings. The aim of ou
Autor:
Irena Mlinarič-Raščan, Tanja Gmeiner, Petra Kolenc Peitl, Marijana Leskovec, Aljaž Sočan, Marko Kroselj
Publikováno v:
Zdravniški Vestnik, Vol 87, Iss 9-10, Pp 439–452-439–452 (2018)
Nuklearna medicina pri obravnavi onkoloških bolnikov omogoča slikovni prikaz oziroma lokalizacijo tumorjev, ciljano zdravljenje ter spremljanje uspešnosti zdravljenja. Visoko specifične radiooznačene peptidne učinkovine lahko izkoristimo za cil
Autor:
Renata Mikolajczak, Laura Ihli, Piotr Garnuszek, Clemens Decristoforo, Theodosia Maina, Leopold Kremser, Alicja Hubalewska-Dydejczyk, Paola Anna Erba, Michał Maurin, Dariusz Pawlak, Marko Kroselj, Petra Kolenc Peitl, Helmut R. Maecke, Christine Rangger
Publikováno v:
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences
Introduction A variety of radiolabelled minigastrin analogues targeting the cholecystokinin 2 (CCK2) receptor were developed and compared in a concerted preclinical testing to select the most promising radiotracer for diagnosis and treatment of medul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4920a5a3f7c45cab0a326c1209d4c3a
https://ruj.uj.edu.pl/xmlui/handle/item/94836
https://ruj.uj.edu.pl/xmlui/handle/item/94836
Autor:
Petra Kolenc Peitl, Rosalba Mansi, Helmut R. Maecke, Marko Kroselj, Marija Sollner Dolenc, Jean Claude Reubi, Maria-Luisa Tamma, Friederike Braun, Beatrice Waser
Publikováno v:
Bioconjugate chemistry. 26(6)
The metabolic instability and high kidney retention of minigastrin (MG) analogues hamper their suitability for use in peptide-receptor radionuclide therapy of CCK2/gastrin receptor-expressing tumors. High kidney retention has been related to N-termin
Autor:
Sergej Hojker, Petra Kolenc Peitl, Petra Tomse, Slavko Pecar, Aljaz Socan, Marko Kroselj, Tanja Gmeiner Stopar
Publikováno v:
Nuclear medicine communications. 30(10)
OBJECTIVE Yttrium-90 (Y)-labelled peptides such as DOTATOC and antibodies such as Zevalin are widely used in radionuclide therapy. Indium-111 (In) is used as a Y surrogate for imaging and dosimetry purposes. We aimed to investigate accuracy, geometry