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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 21
2022
Steinlein, Ortrud K.; Reithmair, Marlene; Syunyaeva, Zulfiya und Sattler, Elke C.
(2022):
Delayed diagnosis of Birt-Hogg-Dube syndrome might be aggravated by gender bias.
In: Eclinicalmedicine, Bd. 51
[PDF, 268kB]
2021
Sattler, Elke C.; Syunyaeva, Zulfiya; Reithmair, Marlene; Dempke, Wolfram und Steinlein, Ortrud K.
(2021):
Colorectal cancer risk in families with Birt-Hogg-Dube syndrome increased.
In: European Journal of Cancer, Bd. 151: S. 168-174
Brandes, Florian; Borrmann, Melanie; Buschmann, Dominik; Meidert, Agnes S.; Reithmair, Marlene; Langkamp, Markus; Pridzun, Lutz; Kirchner, Benedikt; Billaud, Jean-Noel; Amin, Nirav M.; Pearson, Joseph C.; Klein, Matthias; Hauer, Daniela; Zoubalan, Clarissa Gevargez; Lindemann, Anja; Chouker, Alexander; Felbinger, Thomas W.; Steinlein, Ortrud K.; Pfaffl, Michael W.; Kaufmann, Ines und Schelling, Gustav
(2021):
Progranulin signaling in sepsis, community-acquired bacterial pneumonia and COVID-19: a comparative, observational study.
In: Intensive Care Medicine Experimental, Bd. 9, Nr. 1, 43
Brandes, Florian; Borrmann, Melanie; Buschmann, Dominik; Meidert, Agnes S.; Reithmair, Marlene; Langkamp, Markus; Pridzun, Lutz; Kirchner, Benedikt; Billaud, Jean-Noël; Amin, Nirav M.; Pearson, Joseph C.; Klein, Matthias; Hauer, Daniela; Gevargez Zoubalan, Clarissa; Lindemann, Anja; Choukér, Alexander; Felbinger, Thomas W.; Steinlein, Ortrud K.; Pfaffl, Michael W.; Kaufmann, Ines und Schelling, Gustav
(2021):
Progranulin signaling in sepsis, community-acquired bacterial pneumonia and COVID-19: a comparative, observational study.
In: Intensive care medicine experimental, Bd. 9, 43
[PDF, 3MB]
2020
Sattler, Elke C.; Syunyaeva, Zulfiya; Mansmann, Ulrich 
ORCID: https://orcid.org/0000-0002-9955-8906 und Steinlein, Ortrud K.
(2020):
Response.
In: Chest, Bd. 158, Nr. 4: S. 1793-1794
ORCID: https://orcid.org/0000-0002-9955-8906 und Steinlein, Ortrud K.
(2020):
Response.
In: Chest, Bd. 158, Nr. 4: S. 1793-1794
Sattler, Elke C.; Syunyaeva, Zulfiya; Mansmann, Ulrich und Steinlein, Ortrud K.
(2020):
Genetic Risk Factors for Spontaneous Pneumothorax in Birt-Hogg-Dubé Syndrome.
In: Chest, Bd. 157, Nr. 5: S. 1199-1206
2018
Steinlein, Ortrud K.; Ertl-Wagner, Birgit; Ruzicka, Thomas und Sattler, Elke C.
(2018):
Birt-Hogg-Dube syndrome: an underdiagnosed genetic tumor syndrome.
In: Journal der Deutschen Dermatologischen Gesellschaft, Bd. 16, Nr. 3: S. 278-284
Sattler, E. C. und Steinlein, Ortrud K.
(2018):
Delayed diagnosis of Birt-Hogg-Dube syndrome due to marked intrafamilial clinical variability: a case report.
In: BMC Medical Genetics
19:45
[PDF, 652kB]
Sattler, Elke C.; Reithmair, Marlene und Steinlein, Ortrud K.
(2018):
Kidney cancer characteristics and genotype-phenotype-correlations in Birt-Hogg-Dube syndrome.
In: PLOS One 13(12), e0209504 [PDF, 768kB]
In: PLOS One 13(12), e0209504 [PDF, 768kB]
Buschmann, Dominik; Kirchner, Benedikt; Hermann, Stefanie; Maerte, Melanie; Wurmser, Christine; Brandes, Florian; Kotschote, Stefan; Bonin, Michael; Steinlein, Ortrud K.; Pfaffl, Michael W.; Schelling, Gustav und Reithmair, Marlene
(2018):
Evaluation of serum extracellular vesicle isolation methods for profiling miRNAs by next-generation sequencing.
In: Journal of Extracellular Vesicles, Bd. 7, Nr. 1, 1481321
[PDF, 4MB]
2017
Reithmair, Marlene; Buschmann, Dominik; Märte, Melanie; Kirchner, Benedikt; Hagl, Daniel; Kaufmann, Ines; Pfob, Martina; Chouker, Alexander; Steinlein, Ortrud K.; Pfaffl, Michael W. und Schelling, Gustav
(2017):
Cellular and extracellular miRNAs are blood-compartment-specific diagnostic targets in sepsis.
In: Journal of Cellular and Molecular Medicine, Bd. 21, Nr. 10: S. 2403-2411
[PDF, 933kB]
Müller, Stefan; Kutschka, Ilona; Mehräin, Yasmin; Niculescu, Luana; Giehl, Kathrin und Steinlein, Ortrud K.
(2017):
A case of Rothmund-Thomson syndrome without mosaic trisomy 8, but with structural chromosome instability.
11th European Cytogenetics Conference, Florence, Italy, July 01-04, 2017.
Molecular Cytogenetics.
Bd. 10, Nr. Suppl. 3, 1.P82
BioMed Central.
[PDF, 195kB]
Laviolette, Laura A.; Mermoud, Julien; Calvo, Isabel A.; Olson, Nicholas; Boukhali, Myriam; Steinlein, Ortrud K.; Roider, Elisabeth; Sattler, Elke C.; Huang, Dachuan; Teh, Bin Tean; Motamedi, Mo; Haas, Wilhelm und Iliopoulos, Othon
(2017):
Negative regulation of EGFR signalling by the human folliculin tumour suppressor protein.
In: Nature Communications, Bd. 8, 15866
[PDF, 2MB]
2016
Mehraein, Yasmin; Schmid, Irene; Eggert, Marlene; Kohlhase, Jürgen und Steinlein, Ortrud K.
(2016):
DICER1 syndrome can mimic different genetic tumor predispositions.
In: Cancer Letters, Bd. 370, Nr. 2: S. 275-278
Korenke, Georg-Christoph; Eggert, Marlene; Thiele, Holger; Nürnberg, Peter; Sander, Thomas und Steinlein, Ortrud K.
(2016):
Nocturnal frontal lobe epilepsy caused by a mutation in the GATOR1 complex gene NPRL3.
In: Epilepsia, Bd. 57, Nr. 3, E60-E63
2015
Mehraein, Yasmin; Pfob, Martina; Steinlein, Ortrud K.; Aichinger, Eric; Eggert, Marlene; Bubendorff, Valerie; Mannhart, Adelina und Müller, Stefan
(2015):
2q37.3 Deletion Syndrome: Two Cases with Highly Distinctive Facial Phenotype, Discordant Association with Schizophrenic Psychosis, and Shared Deletion Breakpoint Region on 2q37.3.
In: Cytogenetic and Genome Research, Bd. 146, Nr. 1: S. 33-38
[PDF, 405kB]
Eggert, Marlene; Winterer, Georg; Wanischeck, Mario; Hoda, Jean-Charles; Bertrand, Daniel und Steinlein, Ortrud K.
(2015):
The nicotinic acetylcholine receptor alpha 4 subunit contains a functionally relevant SNP Haplotype.
In: BMC Genetics
16:46
[PDF, 540kB]
2014
Schmälter, Ann-Kristin; Kuzyk, Alexandra; Righolt, Christiaan H.; Neusser, Michaela; Steinlein, Ortrud K.; Müller, Stefan und Mai, Sabine
(2014):
Distinct nuclear orientation patterns for mouse chromosome 11 in normal B lymphocytes.
In: BMC Cell Biology
15:22
[PDF, 1MB]
2013
Eggert, Marlene; Pfob, Martina und Steinlein, Ortrud K.
(2013):
Melanocortin-3-receptor promoter polymorphism associated with tuberculosis susceptibility does not influence protein expression.
In: BMC Research Notes
6:99
[PDF, 146kB]
2011
Steinlein, Ortrud K.; Aichinger, Eric; Trucks, Holger und Sander, Thomas
(2011):
Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta.
In: BMC Medical Genetics
12:152
[PDF, 562kB]
2010
Prodinger, Peter M.; Sarbia, Mario; Massann, Joerg; Straka, Christian; Meyer, Guenther und Steinlein, Ortrud K.
(2010):
Gorlin syndrome associated with small bowel carcinoma and mesenchymal proliferation of the gastrointestinal tract: case report and review of literature.
In: BMC Cancer
10:360
[PDF, 772kB]