Ungelenk M - Search Results

1

Splicing factor YBX1 mediates persistence of JAK2-mutated neoplasms.

Jayavelu AK, Schnöder TM, Perner F, Herzog C, Meiler A, Krishnamoorthy G, Huber N, Mohr J, Edelmann-Stephan B, Austin R, Brandt S, Palandri F, Schröder N, Isermann B, Edlich F, Sinha AU, Ungelenk M, Hübner CA, Zeiser R, Rahmig S, Waskow C, Coldham I, Ernst T, Hochhaus A, Jilg S, Jost PJ, Mullally A, Bullinger L, Mertens PR, Lane SW, Mann M, Heidel FH. Jayavelu AK, et al. Among authors: ungelenk m. Nature. 2020 Dec;588(7836):157-163. doi: 10.1038/s41586-020-2968-3. Epub 2020 Nov 25. Nature. 2020. PMID: 33239784

2

Disruption of KCC2 in Parvalbumin-Positive Interneurons Is Associated With a Decreased Seizure Threshold and a Progressive Loss of Parvalbumin-Positive Interneurons.

Herrmann T, Gerth M, Dittmann R, Pensold D, Ungelenk M, Liebmann L, Hübner CA. Herrmann T, et al. Among authors: ungelenk m. Front Mol Neurosci. 2022 Feb 3;14:807090. doi: 10.3389/fnmol.2021.807090. eCollection 2021. Front Mol Neurosci. 2022. PMID: 35185464 Free PMC article.

3

Histone demethylase KDM4C is a functional dependency in JAK2-mutated neoplasms.

Ernst P, Schnöder TM, Huber N, Perner F, Jayavelu AK, Eifert T, Hsu CJ, Tubío-Santamaría N, Crodel CC, Ungelenk M, Hübner CA, Clement JH, Hochhaus A, Heidel FH. Ernst P, et al. Among authors: ungelenk m. Leukemia. 2022 Jul;36(7):1843-1849. doi: 10.1038/s41375-022-01611-3. Epub 2022 Jun 2. Leukemia. 2022. PMID: 35654819 Free PMC article.

4

Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception.

Chiabrando D, Castori M, di Rocco M, Ungelenk M, Gießelmann S, Di Capua M, Madeo A, Grammatico P, Bartsch S, Hübner CA, Altruda F, Silengo L, Tolosano E, Kurth I. Chiabrando D, et al. Among authors: ungelenk m. PLoS Genet. 2016 Dec 6;12(12):e1006461. doi: 10.1371/journal.pgen.1006461. eCollection 2016 Dec. PLoS Genet. 2016. PMID: 27923065 Free PMC article.

5

Sepsis induces long-lasting impairments in CD4+ T-cell responses despite rapid numerical recovery of T-lymphocyte populations.

Ammer-Herrmenau C, Kulkarni U, Andreas N, Ungelenk M, Ravens S, Hübner C, Kather A, Kurth I, Bauer M, Kamradt T. Ammer-Herrmenau C, et al. Among authors: ungelenk m. PLoS One. 2019 Feb 7;14(2):e0211716. doi: 10.1371/journal.pone.0211716. eCollection 2019. PLoS One. 2019. PMID: 30730978 Free PMC article.

6

Associations of common genetic risk variants of the muscarinic acetylcholine receptor M2 with cardiac autonomic dysfunction in patients with schizophrenia.

Refisch A, Komatsuzaki S, Ungelenk M, Chung HY, Schumann A, Schilling SS, Jantzen W, Schröder S, Mühleisen TW, Nöthen MM, Hübner CA, Bär KJ. Refisch A, et al. Among authors: ungelenk m. World J Biol Psychiatry. 2023 Jan;24(1):1-11. doi: 10.1080/15622975.2022.2043561. Epub 2022 Mar 9. World J Biol Psychiatry. 2023. PMID: 35172679

7

Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia.

Refisch A, Komatsuzaki S, Ungelenk M, Schumann A, Chung HY, Schilling SS, Jantzen W, Schröder S, Nöthen MM, Mühleisen TW, Hübner CA, Bär KJ. Refisch A, et al. Among authors: ungelenk m. Genes (Basel). 2022 Nov 16;13(11):2132. doi: 10.3390/genes13112132. Genes (Basel). 2022. PMID: 36421807 Free PMC article.

8

RUNX3 Transcript Variants Have Distinct Roles in Ovarian Carcinoma and Differently Influence Platinum Sensitivity and Angiogenesis.

Heinze K, Hölzer M, Ungelenk M, Gerth M, Thomale J, Heller R, Morden CR, McManus KJ, Mosig AS, Dürst M, Runnebaum IB, Häfner N. Heinze K, et al. Among authors: ungelenk m. Cancers (Basel). 2021 Jan 26;13(3):476. doi: 10.3390/cancers13030476. Cancers (Basel). 2021. PMID: 33530588 Free PMC article.

9

Stroke-like onset of brain stem degeneration presents with unique MRI sign and heterozygous NMNAT2 variant: a case report.

Schulz A, Wagner F, Ungelenk M, Kurth I, Redecker C. Schulz A, et al. Among authors: ungelenk m. Transl Neurodegener. 2016 Dec 27;5:23. doi: 10.1186/s40035-016-0069-x. eCollection 2016. Transl Neurodegener. 2016. PMID: 28035283 Free PMC article.

10

Genetic abnormalities in bicuspid aortic valve root phenotype: preliminary results.

Girdauskas E, Geist L, Disha K, Kazakbaev I, Groß T, Schulz S, Ungelenk M, Kuntze T, Reichenspurner H, Kurth I. Girdauskas E, et al. Among authors: ungelenk m. Eur J Cardiothorac Surg. 2017 Jul 1;52(1):156-162. doi: 10.1093/ejcts/ezx065. Eur J Cardiothorac Surg. 2017. PMID: 28387797

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