Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 52 entries
Sorted by: Best Match Show Resources per page
Progesterone receptor membrane component 1 is phosphorylated upon progestin treatment in breast cancer cells.

Oncotarget

Willibald M, Bayer G, Stahlhut V, Poschmann G, Stühler K, Gierke B, Pawlak M, Seeger H, Mueck AO, Niederacher D, Fehm T, Neubauer H.
PMID: 29069804
Oncotarget. 2017 Aug 02;8(42):72480-72493. doi: 10.18632/oncotarget.19819. eCollection 2017 Sep 22.

Menopausal hormone therapy, using estrogen and synthetic progestins, is associated with an increased risk of developing breast cancer. The effect of progestins on breast cells is complex and not yet fully understood. In previous

Cite
Willibald M, Bayer G, Stahlhut V, et al. Progesterone receptor membrane component 1 is phosphorylated upon progestin treatment in breast cancer cells. Oncotarget. 2017;8(42):72480-72493doi: 10.18632/oncotarget.19819.
Willibald, M., Bayer, G., Stahlhut, V., Poschmann, G., Stühler, K., Gierke, B., Pawlak, M., Seeger, H., Mueck, A. O., Niederacher, D., Fehm, T., & Neubauer, H. (2017). Progesterone receptor membrane component 1 is phosphorylated upon progestin treatment in breast cancer cells. Oncotarget, 8(42), 72480-72493. https://doi.org/10.18632/oncotarget.19819
Willibald, Marina, et al. "Progesterone receptor membrane component 1 is phosphorylated upon progestin treatment in breast cancer cells." Oncotarget vol. 8,42 (2017): 72480-72493. doi: https://doi.org/10.18632/oncotarget.19819
Willibald M, Bayer G, Stahlhut V, Poschmann G, Stühler K, Gierke B, Pawlak M, Seeger H, Mueck AO, Niederacher D, Fehm T, Neubauer H. Progesterone receptor membrane component 1 is phosphorylated upon progestin treatment in breast cancer cells. Oncotarget. 2017 Aug 02;8(42):72480-72493. doi: 10.18632/oncotarget.19819. eCollection 2017 Sep 22. PMID: 29069804; PMCID: PMC5641147.
Copy Download .nbib Format: NLM
[Erratum to: Teleradiological report turnaround times. An internal efficiency and quality control analysis].

Der Radiologe

Seithe T, Busse R, Rief M, Doyscher R, Albrecht L, Rathke H, Jonczyk M, Poschmann R, Tepe H, Hamm B, de Bucourt M.
PMID: 26081675
Radiologe. 2015 Jun;55(6):497. doi: 10.1007/s00117-015-2864-2.

No abstract available.

Cite
Seithe T, Busse R, Rief M, et al. Erratum zu: Teleradiologische Prozess- und Untersuchungszeiten. Eine institutsinterne Effizienz- und Qualitätsanalyse. [Erratum to: Teleradiological report turnaround times. An internal efficiency and quality control analysis]. Radiologe. 2015;55(6):497doi: 10.1007/s00117-015-2864-2.
Seithe, T., Busse, R., Rief, M., Doyscher, R., Albrecht, L., Rathke, H., Jonczyk, M., Poschmann, R., Tepe, H., Hamm, B., & de Bucourt, M. (2015). Erratum zu: Teleradiologische Prozess- und Untersuchungszeiten. Eine institutsinterne Effizienz- und Qualitätsanalyse. [Erratum to: Teleradiological report turnaround times. An internal efficiency and quality control analysis]. Der Radiologe, 55(6), 497. https://doi.org/10.1007/s00117-015-2864-2
Seithe, T, et al. "Erratum zu: Teleradiologische Prozess- und Untersuchungszeiten. Eine institutsinterne Effizienz- und Qualitätsanalyse." [Erratum to: Teleradiological report turnaround times. An internal efficiency and quality control analysis]. Der Radiologe vol. 55,6 (2015): 497. doi: https://doi.org/10.1007/s00117-015-2864-2
Seithe T, Busse R, Rief M, Doyscher R, Albrecht L, Rathke H, Jonczyk M, Poschmann R, Tepe H, Hamm B, de Bucourt M. Erratum zu: Teleradiologische Prozess- und Untersuchungszeiten. Eine institutsinterne Effizienz- und Qualitätsanalyse. [Erratum to: Teleradiological report turnaround times. An internal efficiency and quality control analysis]. Radiologe. 2015 Jun;55(6):497. doi: 10.1007/s00117-015-2864-2. German. PMID: 26081675.
Copy Download .nbib Format: NLM
Thrombocyte activation increases with the degree of carotid artery stenosis.

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association

Stolz E, Oschmann P, Pötzsch B, Kraus J, Kaps M.
PMID: 17903894
J Stroke Cerebrovasc Dis. 2002 Nov-Dec;11(6):324-9. doi: 10.1053/jscd.2002.130126.

Thrombocyte activation and subsequent aggregate formation play a pivotal role in arterio-arterial embolism in high grade carotid artery stenosis. The aim of this study was to test the hypothesis that the amount of activated thrombocytes would differ with the...

Cite
Stolz E, Oschmann P, Pötzsch B, et al. Thrombocyte activation increases with the degree of carotid artery stenosis. J Stroke Cerebrovasc Dis. 2002;11(6):324-9doi: 10.1053/jscd.2002.130126.
Stolz, E., Oschmann, P., Pötzsch, B., Kraus, J., & Kaps, M. (2002). Thrombocyte activation increases with the degree of carotid artery stenosis. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association, 11(6), 324-9. https://doi.org/10.1053/jscd.2002.130126
Stolz, Erwin, et al. "Thrombocyte activation increases with the degree of carotid artery stenosis." Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association vol. 11,6 (2002): 324-9. doi: https://doi.org/10.1053/jscd.2002.130126
Stolz E, Oschmann P, Pötzsch B, Kraus J, Kaps M. Thrombocyte activation increases with the degree of carotid artery stenosis. J Stroke Cerebrovasc Dis. 2002 Nov-Dec;11(6):324-9. doi: 10.1053/jscd.2002.130126. PMID: 17903894.
Copy Download .nbib Format: NLM
Sodium phosphaethynolate as a building block for heterocycles.

Angewandte Chemie (International ed. in English)

Chen X, Alidori S, Puschmann FF, Santiso-Quinones G, Benkő Z, Li Z, Becker G, Grützmacher HF, Grützmacher H.
PMID: 24453139
Angew Chem Int Ed Engl. 2014 Feb 03;53(6):1641-5. doi: 10.1002/anie.201308220. Epub 2014 Jan 22.

Phosphorus-containing heterocycles have evolved from laboratory curiosities to functional components, such as ligands in catalytically active metal complexes or molecular constituents in electronic devices. The straightforward synthesis of functionalized heterocycles on a larger scale remains a challenge. Herein, we...

Cite
Chen X, Alidori S, Puschmann FF, et al. Sodium phosphaethynolate as a building block for heterocycles. Angew Chem Int Ed Engl. 2014;53(6):1641-5doi: 10.1002/anie.201308220.
Chen, X., Alidori, S., Puschmann, F. F., Santiso-Quinones, G., Benkő, Z., Li, Z., Becker, G., Grützmacher, H. F., & Grützmacher, H. (2014). Sodium phosphaethynolate as a building block for heterocycles. Angewandte Chemie (International ed. in English), 53(6), 1641-5. https://doi.org/10.1002/anie.201308220
Chen, Xiaodan, et al. "Sodium phosphaethynolate as a building block for heterocycles." Angewandte Chemie (International ed. in English) vol. 53,6 (2014): 1641-5. doi: https://doi.org/10.1002/anie.201308220
Chen X, Alidori S, Puschmann FF, Santiso-Quinones G, Benkő Z, Li Z, Becker G, Grützmacher HF, Grützmacher H. Sodium phosphaethynolate as a building block for heterocycles. Angew Chem Int Ed Engl. 2014 Feb 03;53(6):1641-5. doi: 10.1002/anie.201308220. Epub 2014 Jan 22. PMID: 24453139.
Copy Download .nbib Format: NLM
Measurement of e+e---> micro+ micro-: A test of electroweak theories.

Physical review letters

Adeva B, Becker U, Becker-Szendy R, Berdugo J, Boehm A, Branson JG, Burger JD, Capell M, Cerrada M, Chang CC, Chang YH, Chen HS, Chen M, Chen ML, Chen MY, Chu YS, Deffur E, Deiters K, Demarteau M, Dong BZ, Duinker P, Fesefeldt HS, Fong D, Fukushima M, Garrido L, Han RD, Harting D, Herten G, Ho MC, Hueser D, Hussain M, Ilyas MM, Jiang DZ, Klein M, Krenz W, Kuijer P, Leiste R, Li QZ, Linnhoefer D, Luckey D, Luit EJ, Mana C, Marquina MA, Martinez M, Massaro GG, Mnich J, Mount R, Nadeem K, Newman H, Nowak WD, Pohl M, Poschmann FP, Rau RR, Rodriguez S, Rohde M, Rubio JA, Rykaczewski H, Sachwitz M, Salicio J, Schreiber HJ, Schroeder U, Schug J, Stone H, Swider GM.
PMID: 10032415
Phys Rev Lett. 1985 Aug 12;55(7):665-668. doi: 10.1103/PhysRevLett.55.665.

No abstract available.

Cite
Adeva B, Becker U, Becker-Szendy R, et al. Measurement of e+e---> micro+ micro-: A test of electroweak theories. Phys Rev Lett. 1985;55(7):665-668doi: 10.1103/PhysRevLett.55.665.
Adeva, B., Becker, U., Becker-Szendy, R., Berdugo, J., Boehm, A., Branson, J. G., Burger, J. D., Capell, M., Cerrada, M., Chang, C. C., Chang, Y. H., Chen, H. S., Chen, M., Chen, M. L., Chen, M. Y., Chu, Y. S., Deffur, E., Deiters, K., Demarteau, M., Dong, B. Z., Duinker, P., Fesefeldt, H. S., Fong, D., Fukushima, M., Garrido, L., Han, R. D., Harting, D., Herten, G., Ho, M. C., Hueser, D., Hussain, M., Ilyas, M. M., Jiang, D. Z., Klein, M., Krenz, W., Kuijer, P., Leiste, R., Li, Q. Z., Linnhoefer, D., Luckey, D., Luit, E. J., Mana, C., Marquina, M. A., Martinez, M., Massaro, G. G., Mnich, J., Mount, R., Nadeem, K., Newman, H., Nowak, W. D., Pohl, M., Poschmann, F. P., Rau, R. R., Rodriguez, S., Rohde, M., Rubio, J. A., Rykaczewski, H., Sachwitz, M., Salicio, J., Schreiber, H. J., Schroeder, U., Schug, J., Stone, H., & Swider, G. M. (1985). Measurement of e+e---> micro+ micro-: A test of electroweak theories. Physical review letters, 55(7), 665-668. https://doi.org/10.1103/PhysRevLett.55.665
Adeva, et al. "Measurement of e+e---> micro+ micro-: A test of electroweak theories." Physical review letters vol. 55,7 (1985): 665-668. doi: https://doi.org/10.1103/PhysRevLett.55.665
Adeva B, Becker U, Becker-Szendy R, Berdugo J, Boehm A, Branson JG, Burger JD, Capell M, Cerrada M, Chang CC, Chang YH, Chen HS, Chen M, Chen ML, Chen MY, Chu YS, Deffur E, Deiters K, Demarteau M, Dong BZ, Duinker P, Fesefeldt HS, Fong D, Fukushima M, Garrido L, Han RD, Harting D, Herten G, Ho MC, Hueser D, Hussain M, Ilyas MM, Jiang DZ, Klein M, Krenz W, Kuijer P, Leiste R, Li QZ, Linnhoefer D, Luckey D, Luit EJ, Mana C, Marquina MA, Martinez M, Massaro GG, Mnich J, Mount R, Nadeem K, Newman H, Nowak WD, Pohl M, Poschmann FP, Rau RR, Rodriguez S, Rohde M, Rubio JA, Rykaczewski H, Sachwitz M, Salicio J, Schreiber HJ, Schroeder U, Schug J, Stone H, Swider GM. Measurement of e+e---> micro+ micro-: A test of electroweak theories. Phys Rev Lett. 1985 Aug 12;55(7):665-668. doi: 10.1103/PhysRevLett.55.665. PMID: 10032415.
Copy Download .nbib Format: NLM
Author Correction: Alveolar macrophages are epigenetically altered after inflammation, leading to long-term lung immunoparalysis.

Nature immunology

Roquilly A, Jacqueline C, Davieau M, Mollé A, Sadek A, Fourgeux C, Rooze P, Broquet A, Misme-Aucouturier B, Chaumette T, Vourc'h M, Cinotti R, Marec N, Gauttier V, McWilliam HEG, Altare F, Poschmann J, Villadangos JA, Asehnoune K.
PMID: 32581370
Nat Immunol. 2020 Aug;21(8):962. doi: 10.1038/s41590-020-0739-9.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Cite
Roquilly A, Jacqueline C, Davieau M, et al. Author Correction: Alveolar macrophages are epigenetically altered after inflammation, leading to long-term lung immunoparalysis. Nat Immunol. 2020;21(8):962doi: 10.1038/s41590-020-0739-9.
Roquilly, A., Jacqueline, C., Davieau, M., Mollé, A., Sadek, A., Fourgeux, C., Rooze, P., Broquet, A., Misme-Aucouturier, B., Chaumette, T., Vourc'h, M., Cinotti, R., Marec, N., Gauttier, V., McWilliam, H. E. G., Altare, F., Poschmann, J., Villadangos, J. A., & Asehnoune, K. (2020). Author Correction: Alveolar macrophages are epigenetically altered after inflammation, leading to long-term lung immunoparalysis. Nature immunology, 21(8), 962. https://doi.org/10.1038/s41590-020-0739-9
Roquilly, Antoine, et al. "Author Correction: Alveolar macrophages are epigenetically altered after inflammation, leading to long-term lung immunoparalysis." Nature immunology vol. 21,8 (2020): 962. doi: https://doi.org/10.1038/s41590-020-0739-9
Roquilly A, Jacqueline C, Davieau M, Mollé A, Sadek A, Fourgeux C, Rooze P, Broquet A, Misme-Aucouturier B, Chaumette T, Vourc'h M, Cinotti R, Marec N, Gauttier V, McWilliam HEG, Altare F, Poschmann J, Villadangos JA, Asehnoune K. Author Correction: Alveolar macrophages are epigenetically altered after inflammation, leading to long-term lung immunoparalysis. Nat Immunol. 2020 Aug;21(8):962. doi: 10.1038/s41590-020-0739-9. PMID: 32581370.
Copy Download .nbib Format: NLM
The Proteomic Landscape of Cysteine Oxidation That Underpins Retinoic Acid-Induced Neuronal Differentiation.

Journal of proteome research

Brenig K, Grube L, Schwarzländer M, Köhrer K, Stühler K, Poschmann G.
PMID: 32202429
J Proteome Res. 2020 May 01;19(5):1923-1940. doi: 10.1021/acs.jproteome.9b00752. Epub 2020 Apr 03.

The initial phases of neuronal differentiation are key to neuronal function. A particularly informative model to study these initial phases are retinoic acid-stimulated SH-SY5Y cells. Although these progressions are associated with redox-sensitive processes, it is largely undefined how the...

Cite
Brenig K, Grube L, Schwarzländer M, et al. The Proteomic Landscape of Cysteine Oxidation That Underpins Retinoic Acid-Induced Neuronal Differentiation. J Proteome Res. 2020;19(5):1923-1940doi: 10.1021/acs.jproteome.9b00752.
Brenig, K., Grube, L., Schwarzländer, M., Köhrer, K., Stühler, K., & Poschmann, G. (2020). The Proteomic Landscape of Cysteine Oxidation That Underpins Retinoic Acid-Induced Neuronal Differentiation. Journal of proteome research, 19(5), 1923-1940. https://doi.org/10.1021/acs.jproteome.9b00752
Brenig, Katrin, et al. "The Proteomic Landscape of Cysteine Oxidation That Underpins Retinoic Acid-Induced Neuronal Differentiation." Journal of proteome research vol. 19,5 (2020): 1923-1940. doi: https://doi.org/10.1021/acs.jproteome.9b00752
Brenig K, Grube L, Schwarzländer M, Köhrer K, Stühler K, Poschmann G. The Proteomic Landscape of Cysteine Oxidation That Underpins Retinoic Acid-Induced Neuronal Differentiation. J Proteome Res. 2020 May 01;19(5):1923-1940. doi: 10.1021/acs.jproteome.9b00752. Epub 2020 Apr 03. PMID: 32202429.
Copy Download .nbib Format: NLM
Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism.

Redox biology

Wilms C, Lepka K, Häberlein F, Edwards S, Felsberg J, Pudelko L, Lindenberg TT, Poschmann G, Qin N, Volbracht K, Prozorovski T, Meuth SG, Kahlert UD, Remke M, Aktas O, Reifenberger G, Bräutigam L, Odermatt B, Berndt C.
PMID: 34952462
Redox Biol. 2021 Dec 21;49:102221. doi: 10.1016/j.redox.2021.102221. Epub 2021 Dec 21.

Redox regulation of specific cysteines via oxidoreductases of the thioredoxin family is increasingly being recognized as an important signaling pathway. Here, we demonstrate that the cytosolic isoform of the vertebrate-specific oxidoreductase Glutaredoxin 2 (Grx2c) regulates the redox state of...

Cite
Wilms C, Lepka K, Häberlein F, et al. Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism. Redox Biol. 2021;49:102221doi: 10.1016/j.redox.2021.102221.
Wilms, C., Lepka, K., Häberlein, F., Edwards, S., Felsberg, J., Pudelko, L., Lindenberg, T. T., Poschmann, G., Qin, N., Volbracht, K., Prozorovski, T., Meuth, S. G., Kahlert, U. D., Remke, M., Aktas, O., Reifenberger, G., Bräutigam, L., Odermatt, B., & Berndt, C. (2021). Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism. Redox biology, 49102221. https://doi.org/10.1016/j.redox.2021.102221
Wilms, Christina, et al. "Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism." Redox biology vol. 49 (2021): 102221. doi: https://doi.org/10.1016/j.redox.2021.102221
Wilms C, Lepka K, Häberlein F, Edwards S, Felsberg J, Pudelko L, Lindenberg TT, Poschmann G, Qin N, Volbracht K, Prozorovski T, Meuth SG, Kahlert UD, Remke M, Aktas O, Reifenberger G, Bräutigam L, Odermatt B, Berndt C. Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism. Redox Biol. 2021 Dec 21;49:102221. doi: 10.1016/j.redox.2021.102221. Epub 2021 Dec 21. PMID: 34952462.
Copy Download .nbib Format: NLM
Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism.

Redox biology

Wilms C, Lepka K, Häberlein F, Edwards S, Felsberg J, Pudelko L, Lindenberg TT, Poschmann G, Qin N, Volbracht K, Prozorovski T, Meuth SG, Kahlert UD, Remke M, Aktas O, Reifenberger G, Bräutigam L, Odermatt B, Berndt C.
PMID: 34952462
Redox Biol. 2021 Dec 21;49:102221. doi: 10.1016/j.redox.2021.102221. Epub 2021 Dec 21.

Redox regulation of specific cysteines via oxidoreductases of the thioredoxin family is increasingly being recognized as an important signaling pathway. Here, we demonstrate that the cytosolic isoform of the vertebrate-specific oxidoreductase Glutaredoxin 2 (Grx2c) regulates the redox state of...

Cite
Wilms C, Lepka K, Häberlein F, et al. Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism. Redox Biol. 2021;49:102221doi: 10.1016/j.redox.2021.102221.
Wilms, C., Lepka, K., Häberlein, F., Edwards, S., Felsberg, J., Pudelko, L., Lindenberg, T. T., Poschmann, G., Qin, N., Volbracht, K., Prozorovski, T., Meuth, S. G., Kahlert, U. D., Remke, M., Aktas, O., Reifenberger, G., Bräutigam, L., Odermatt, B., & Berndt, C. (2021). Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism. Redox biology, 49102221. https://doi.org/10.1016/j.redox.2021.102221
Wilms, Christina, et al. "Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism." Redox biology vol. 49 (2021): 102221. doi: https://doi.org/10.1016/j.redox.2021.102221
Wilms C, Lepka K, Häberlein F, Edwards S, Felsberg J, Pudelko L, Lindenberg TT, Poschmann G, Qin N, Volbracht K, Prozorovski T, Meuth SG, Kahlert UD, Remke M, Aktas O, Reifenberger G, Bräutigam L, Odermatt B, Berndt C. Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism. Redox Biol. 2021 Dec 21;49:102221. doi: 10.1016/j.redox.2021.102221. Epub 2021 Dec 21. PMID: 34952462.
Copy Download .nbib Format: NLM
Alveolar Macrophages: Adaptation to Their Anatomic Niche during and after Inflammation.

Cells

Martin FP, Jacqueline C, Poschmann J, Roquilly A.
PMID: 34685700
Cells. 2021 Oct 12;10(10). doi: 10.3390/cells10102720.

At the early stages of life development, alveoli are colonized by embryonic macrophages, which become resident alveolar macrophages (ResAM) and self-sustain by local division. Genetic and epigenetic signatures and, to some extent, the functions of ResAM are dictated by...

Cite
Martin FP, Jacqueline C, Poschmann J, et al. Alveolar Macrophages: Adaptation to Their Anatomic Niche during and after Inflammation. Cells. 2021;10(10)doi: 10.3390/cells10102720.
Martin, F. P., Jacqueline, C., Poschmann, J., & Roquilly, A. (2021). Alveolar Macrophages: Adaptation to Their Anatomic Niche during and after Inflammation. Cells, 10(10), . https://doi.org/10.3390/cells10102720
Martin, Florian Pierre, et al. "Alveolar Macrophages: Adaptation to Their Anatomic Niche during and after Inflammation." Cells vol. 10,10 (2021). doi: https://doi.org/10.3390/cells10102720
Martin FP, Jacqueline C, Poschmann J, Roquilly A. Alveolar Macrophages: Adaptation to Their Anatomic Niche during and after Inflammation. Cells. 2021 Oct 12;10(10). doi: 10.3390/cells10102720. PMID: 34685700; PMCID: PMC8534884.
Copy Download .nbib Format: NLM
Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism.

Redox biology

Wilms C, Lepka K, Häberlein F, Edwards S, Felsberg J, Pudelko L, Lindenberg TT, Poschmann G, Qin N, Volbracht K, Prozorovski T, Meuth SG, Kahlert UD, Remke M, Aktas O, Reifenberger G, Bräutigam L, Odermatt B, Berndt C.
PMID: 34952462
Redox Biol. 2021 Dec 21;49:102221. doi: 10.1016/j.redox.2021.102221. Epub 2021 Dec 21.

Redox regulation of specific cysteines via oxidoreductases of the thioredoxin family is increasingly being recognized as an important signaling pathway. Here, we demonstrate that the cytosolic isoform of the vertebrate-specific oxidoreductase Glutaredoxin 2 (Grx2c) regulates the redox state of...

Cite
Wilms C, Lepka K, Häberlein F, et al. Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism. Redox Biol. 2021;49:102221doi: 10.1016/j.redox.2021.102221.
Wilms, C., Lepka, K., Häberlein, F., Edwards, S., Felsberg, J., Pudelko, L., Lindenberg, T. T., Poschmann, G., Qin, N., Volbracht, K., Prozorovski, T., Meuth, S. G., Kahlert, U. D., Remke, M., Aktas, O., Reifenberger, G., Bräutigam, L., Odermatt, B., & Berndt, C. (2021). Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism. Redox biology, 49102221. https://doi.org/10.1016/j.redox.2021.102221
Wilms, Christina, et al. "Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism." Redox biology vol. 49 (2021): 102221. doi: https://doi.org/10.1016/j.redox.2021.102221
Wilms C, Lepka K, Häberlein F, Edwards S, Felsberg J, Pudelko L, Lindenberg TT, Poschmann G, Qin N, Volbracht K, Prozorovski T, Meuth SG, Kahlert UD, Remke M, Aktas O, Reifenberger G, Bräutigam L, Odermatt B, Berndt C. Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism. Redox Biol. 2021 Dec 21;49:102221. doi: 10.1016/j.redox.2021.102221. Epub 2021 Dec 21. PMID: 34952462.
Copy Download .nbib Format: NLM
[No title available]

Cancers

Kurz L, Miklyaeva A, Skowron MA, Overbeck N, Poschmann G, Becker T, Eul K, Kurz T, Schönberger S, Calaminus G, Stühler K, Dykhuizen E, Albers P, Nettersheim D.
PMID: 32272809
Cancers (Basel). 2020 Apr 07;12(4). doi: 10.3390/cancers12040905.

Germ cell tumors (GCTs) are the most common solid malignancies found in young men. Although they generally have high cure rates, metastases, resistance to cisplatin-based therapy, and late toxicities still represent a lethal threat, arguing for the need of...

Cite
Kurz L, Miklyaeva A, Skowron MA, et al. . Cancers (Basel). 2020;12(4)doi: 10.3390/cancers12040905.
Kurz, L., Miklyaeva, A., Skowron, M. A., Overbeck, N., Poschmann, G., Becker, T., Eul, K., Kurz, T., Schönberger, S., Calaminus, G., Stühler, K., Dykhuizen, E., Albers, P., & Nettersheim, D. (2020). . Cancers, 12(4), . https://doi.org/10.3390/cancers12040905
Kurz, Lukas, et al. "." Cancers vol. 12,4 (2020). doi: https://doi.org/10.3390/cancers12040905
Kurz L, Miklyaeva A, Skowron MA, Overbeck N, Poschmann G, Becker T, Eul K, Kurz T, Schönberger S, Calaminus G, Stühler K, Dykhuizen E, Albers P, Nettersheim D. . Cancers (Basel). 2020 Apr 07;12(4). doi: 10.3390/cancers12040905. PMID: 32272809; PMCID: PMC7226530.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 52 entries