Zobrazeno 1 - 10
of 5 316
pro vyhledávání: '"Thomas A. Albert"'
Autor:
T. Elise Potthoff, Carolin Walter, Daniela Jeising, Daniel Münter, Archana Verma, Eric Suero Molina, Walter Stummer, Martin Dugas, Wolfgang Hartmann, Matthias Dottermusch, Lea Altendorf, Ulrich Schüller, Sophia Scheuermann, Christian Seitz, Thomas K. Albert, Kornelius Kerl
Publikováno v:
Journal of Translational Medicine, Vol 22, Iss 1, Pp 1-18 (2024)
Abstract Background Pituitary neuroendocrine tumors (PitNET) are among the most common intracranial tumors. Despite a frequent benign course, aggressive behavior can occur. Tumor behavior is known to be under the influence of the tumor microenvironme
Externí odkaz:
https://doaj.org/article/9d87dc91d88548038291cde05a5e76b8
Autor:
Anja Fischer, Thomas K. Albert, Natalia Moreno, Marta Interlandi, Jana Mormann, Selina Glaser, Paurnima Patil, Flavia W. de Faria, Mathis Richter, Archana Verma, Sebastian T. Balbach, Rabea Wagener, Susanne Bens, Sonja Dahlum, Carolin Göbel, Daniel Münter, Clara Inserte, Monika Graf, Eva Kremer, Viktoria Melcher, Gioia Di Stefano, Raffaella Santi, Alexander Chan, Ahmet Dogan, Jonathan Bush, Martin Hasselblatt, Sylvia Cheng, Signe Spetalen, Alexander Fosså, Wolfgang Hartmann, Heidi Herbrüggen, Stella Robert, Florian Oyen, Martin Dugas, Carolin Walter, Sarah Sandmann, Julian Varghese, Claudia Rossig, Ulrich Schüller, Alexandar Tzankov, Martin B. Pedersen, Francesco A. d’Amore, Karin Mellgren, Udo Kontny, Venkatesh Kancherla, Luis Veloza, Edoardo Missiaglia, Virginie Fataccioli, Philippe Gaulard, Birgit Burkhardt, Oliver Soehnlein, Wolfram Klapper, Laurence de Leval, Reiner Siebert, Kornelius Kerl
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-18 (2024)
Abstract Peripheral T-cell lymphoma, not otherwise specified (PTCL-NOS) is a heterogeneous group of malignancies with poor outcome. Here, we identify a subgroup, PTCL-NOS SMARCB1- , which is characterized by the lack of the SMARCB1 protein and occurs
Externí odkaz:
https://doaj.org/article/f9838f5a5f15480799585f8fa2420a7e
Autor:
Owens, Jessie Ann
Publikováno v:
Notes, 2004 Dec 01. 61(2), 551-553.
Externí odkaz:
https://www.jstor.org/stable/4487412
Autor:
Kapriev, Georgi
Publikováno v:
Архив за средновековна философия и култура / Archive for Medieval Philosophy and Culture / Archiv für mittelalterliche Philosophie und Kultur. (07):289-294
Externí odkaz:
https://www.ceeol.com/search/article-detail?id=10687
Autor:
Rockett, William
Publikováno v:
The Sixteenth Century Journal, 1999 Oct 01. 30(3), 845-847.
Externí odkaz:
https://www.jstor.org/stable/2544849
Publikováno v:
The Bulletin of the Cleveland Museum of Art, 1928 Jan 01. 15(1), 7-9.
Externí odkaz:
https://www.jstor.org/stable/25137080
Autor:
Théry, G.
Publikováno v:
Revue des Sciences philosophiques et théologiques, 1921 Jan 01. 10(3), 373-377.
Externí odkaz:
https://www.jstor.org/stable/44411138
Autor:
Morin, Christina
Publikováno v:
Eighteenth-Century Ireland / Iris an dá chultúr, 2013 Jan 01. 28, 204-206.
Externí odkaz:
https://www.jstor.org/stable/24389703
Publikováno v:
Schwäbische Heimat. 68:248
Thomas Held, Albert und Gerhard Raff: Raff. Familiengeschichte(n) aus sieben Jahrhunderten. Degerloch 2016. Fester Einband, 372 Seiten. Fest gebunden € 30,–. (erhältlich bei Dr. Gerhard Raff, Karl- Pfaff-Straße 2, Stuttgart-Degerloch)
Autor:
Melanie Schoof, Shweta Godbole, Thomas K. Albert, Matthias Dottermusch, Carolin Walter, Annika Ballast, Nan Qin, Marlena Baca Olivera, Carolin Göbel, Sina Neyazi, Dörthe Holdhof, Catena Kresbach, Levke-Sophie Peter, Gefion Dorothea Epplen, Vanessa Thaden, Michael Spohn, Mirjam Blattner-Johnson, Franziska Modemann, Martin Mynarek, Stefan Rutkowski, Martin Sill, Julian Varghese, Ann-Kristin Afflerbach, Alicia Eckhardt, Daniel Münter, Archana Verma, Nina Struve, David T. W. Jones, Marc Remke, Julia E. Neumann, Kornelius Kerl, Ulrich Schüller
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-13 (2023)
Abstract Pediatric high-grade gliomas of the subclass MYCN (HGG-MYCN) are highly aggressive tumors frequently carrying MYCN amplifications, TP53 mutations, or both alterations. Due to their rarity, such tumors have only recently been identified as a
Externí odkaz:
https://doaj.org/article/09d9e0ef2e924a438dede74c6b3805ed