Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Julia M A, Pickl"'
Autor:
Ariane Hallermayr, Tobias Wohlfrom, Verena Steinke-Lange, Anna Benet-Pagès, Florentine Scharf, Ellen Heitzer, Ulrich Mansmann, Christopher Haberl, Maike de Wit, Holger Vogelsang, Markus Rentsch, Elke Holinski-Feder, Julia M. A. Pickl
Publikováno v:
Journal of Hematology & Oncology, Vol 15, Iss 1, Pp 1-14 (2022)
Abstract Background Analysis of circulating free DNA (cfDNA) is a promising tool for personalized management of colorectal cancer (CRC) patients. Untargeted cfDNA analysis using whole-genome sequencing (WGS) does not need a priori knowledge of the pa
Externí odkaz:
https://doaj.org/article/0efaedafd6e94b90ae2a7a9642900c92
Autor:
Ariane Hallermayr, Teresa M. Neuhann, Verena Steinke-Lange, Florentine Scharf, Andreas Laner, Roland Ewald, Ben Liesfeld, Elke Holinski-Feder, Julia M. A. Pickl
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
BackgroundLiquid biopsy (LB) is a promising complement to tissue biopsy for detection of clinically relevant genetic variants in cancer and mosaic diseases. A combined workflow to enable parallel tissue and LB analysis is required to maximize diagnos
Externí odkaz:
https://doaj.org/article/8a2c3251a2a24700811c9875987e1cce
Autor:
Vincent Schwenk, Rafaela Magalhaes Leal Silva, Florentine Scharf, Katharina Knaust, Martin Wendlandt, Tanja Häusser, Julia M A Pickl, Verena Steinke-Lange, Andreas Laner, Monika Morak, Elke Holinski-Feder, Dieter A Wolf
Publikováno v:
Journal of medical genetics.
PurposeWhereas most human genes encode multiple mRNA isoforms with distinct function, clinical workflows for assessing this heterogeneity are not readily available. This is a substantial shortcoming, considering that up to 25% of disease-causing gene
Autor:
Florentine, Scharf, Rafaela Magalhaes, Leal Silva, Monika, Morak, Alex, Hastie, Julia M A, Pickl, Kai, Sendelbach, Christian, Gebhard, Melanie, Locher, Andreas, Laner, Verena, Steinke-Lange, Udo, Koehler, Elke, Holinski-Feder, Dieter A, Wolf
Publikováno v:
Journal of medical genetics. 59(10)
Approximately 20% of patients with clinical familial adenomatous polyposis (FAP) remain unsolved after molecular genetic analysis of theWe applied multidimensional genomic analysis employing chromosomal microarray profiling, optical mapping, long-rea
Autor:
Florentine Scharf, Rafaela Magalhaes Leal Silva, Monika Morak, Alex Hastie, Julia M A Pickl, Kai Sendelbach, Christian Gebhard, Melanie Locher, Andreas Laner, Verena Steinke-Lange, Udo Koehler, Elke Holinski-Feder, Dieter A Wolf
PurposeApproximately 20% of patients with clinical familial adenomatous polyposis (FAP) remain unsolved after molecular genetic analysis of the APC and other polyposis genes, suggesting additional pathomechanisms.MethodsWe applied multidimensional ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf8b4295c2d013950175836a8fc03078
https://mediatum.ub.tum.de/doc/1689191/document.pdf
https://mediatum.ub.tum.de/doc/1689191/document.pdf
Publikováno v:
Briefings in Bioinformatics. 19:918-929
The identification of microRNA (miRNA) target genes is crucial for understanding miRNA function. Many methods for the genome-wide miRNA target identification have been developed in recent years; however, they have several limitations including the de
Autor:
Vladimir Kuryshev, Boris Hadaschik, Michael Falkenstein, Diana Tichy, Doreen Heckmann, Yanis Tolstov, Julia Schüler, Stefan Duensing, Wilfried Roth, Agnes Hotz-Wagenblatt, Holger Sültmann, Julia M. A. Pickl, Markus Hohenfellner, Glen Kristiansen, Daniel Reidenbach
Publikováno v:
Oncotarget
// Julia M.A. Pickl 1 , Diana Tichy 2 , Vladimir Y. Kuryshev 1 , Yanis Tolstov 3 , Michael Falkenstein 3 , Julia Schuler 4 , Daniel Reidenbach 1 , Agnes Hotz-Wagenblatt 5 , Glen Kristiansen 6 , Wilfried Roth 7 , Boris Hadaschik 8 , Markus Hohenfellne
Publikováno v:
BioMed Research International, Vol 2014 (2014)
BioMed Research International
BioMed Research International
The availability of ultra-high throughput DNA and RNA sequencing technologies in recent years has led to the identification of numerous novel transcripts, whose functions are unknown as yet. Evidence is accumulating that many of these molecules are d