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First record of Phanuropsis laniger Johnson in Brazil and first record of Phanuropsis semiflaviventris Girault in Amazonas (Hymenoptera: Platygastridae) with notes of their hosts, stink-bugs of cupuaçu.

Biodiversity data journal

Mahlmann T, Oliveira BG.
PMID: 27226758
Biodivers Data J. 2016 Apr 14;(4):e8142. doi: 10.3897/BDJ.4.e8142. eCollection 2016.

BACKGROUND: We report the first record and collection of Phanuropsis laniger Johnson, 1987, for Brazil since its original description. In addition we expand the distribution of Phanuropsis semiflaviventris Girault, 1916, for Amazonas, Brazil and present an updated list of...

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Mahlmann T, Oliveira BG. First record of Phanuropsis laniger Johnson in Brazil and first record of Phanuropsis semiflaviventris Girault in Amazonas (Hymenoptera: Platygastridae) with notes of their hosts, stink-bugs of cupuaçu. Biodivers Data J. 2016;(4):e8142doi: 10.3897/BDJ.4.e8142.
Mahlmann, T., & Oliveira, B. G. (2016). First record of Phanuropsis laniger Johnson in Brazil and first record of Phanuropsis semiflaviventris Girault in Amazonas (Hymenoptera: Platygastridae) with notes of their hosts, stink-bugs of cupuaçu. Biodiversity data journal, (4), e8142. https://doi.org/10.3897/BDJ.4.e8142
Mahlmann, Thiago, and Oliveira, Bruno G. "First record of Phanuropsis laniger Johnson in Brazil and first record of Phanuropsis semiflaviventris Girault in Amazonas (Hymenoptera: Platygastridae) with notes of their hosts, stink-bugs of cupuaçu." Biodiversity data journal vol. ,4 (2016): e8142. doi: https://doi.org/10.3897/BDJ.4.e8142
Mahlmann T, Oliveira BG. First record of Phanuropsis laniger Johnson in Brazil and first record of Phanuropsis semiflaviventris Girault in Amazonas (Hymenoptera: Platygastridae) with notes of their hosts, stink-bugs of cupuaçu. Biodivers Data J. 2016 Apr 14;(4):e8142. doi: 10.3897/BDJ.4.e8142. eCollection 2016. PMID: 27226758; PMCID: PMC4867698.
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MiRTargetLink--miRNAs, Genes and Interaction Networks.

International journal of molecular sciences

Hamberg M, Backes C, Fehlmann T, Hart M, Meder B, Meese E, Keller A.
PMID: 27089332
Int J Mol Sci. 2016 Apr 14;17(4):564. doi: 10.3390/ijms17040564.

Information on miRNA targeting genes is growing rapidly. For high-throughput experiments, but also for targeted analyses of few genes or miRNAs, easy analysis with concise representation of results facilitates the work of life scientists. We developed miRTargetLink, a tool...

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Hamberg M, Backes C, Fehlmann T, et al. MiRTargetLink--miRNAs, Genes and Interaction Networks. Int J Mol Sci. 2016;17(4):564doi: 10.3390/ijms17040564.
Hamberg, M., Backes, C., Fehlmann, T., Hart, M., Meder, B., Meese, E., & Keller, A. (2016). MiRTargetLink--miRNAs, Genes and Interaction Networks. International journal of molecular sciences, 17(4), 564. https://doi.org/10.3390/ijms17040564
Hamberg, Maarten, et al. "MiRTargetLink--miRNAs, Genes and Interaction Networks." International journal of molecular sciences vol. 17,4 (2016): 564. doi: https://doi.org/10.3390/ijms17040564
Hamberg M, Backes C, Fehlmann T, Hart M, Meder B, Meese E, Keller A. MiRTargetLink--miRNAs, Genes and Interaction Networks. Int J Mol Sci. 2016 Apr 14;17(4):564. doi: 10.3390/ijms17040564. PMID: 27089332; PMCID: PMC4849020.
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Functional characterization of the ectopically expressed olfactory receptor 2AT4 in human myelogenous leukemia.

Cell death discovery

Manteniotis S, Wojcik S, Brauhoff P, Möllmann M, Petersen L, Göthert JR, Schmiegel W, Dührsen U, Gisselmann G, Hatt H.
PMID: 27551494
Cell Death Discov. 2016 Jan 25;2:15070. doi: 10.1038/cddiscovery.2015.70. eCollection 2016.

The olfactory receptor (OR) family was found to be expressed mainly in the nasal epithelium. In the last two decades members of the OR family were detected to be functional expressed in different parts of the human body such...

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Manteniotis S, Wojcik S, Brauhoff P, et al. Functional characterization of the ectopically expressed olfactory receptor 2AT4 in human myelogenous leukemia. Cell Death Discov. 2016;2:15070doi: 10.1038/cddiscovery.2015.70.
Manteniotis, S., Wojcik, S., Brauhoff, P., Möllmann, M., Petersen, L., Göthert, J. R., Schmiegel, W., Dührsen, U., Gisselmann, G., & Hatt, H. (2016). Functional characterization of the ectopically expressed olfactory receptor 2AT4 in human myelogenous leukemia. Cell death discovery, 215070. https://doi.org/10.1038/cddiscovery.2015.70
Manteniotis, S, et al. "Functional characterization of the ectopically expressed olfactory receptor 2AT4 in human myelogenous leukemia." Cell death discovery vol. 2 (2016): 15070. doi: https://doi.org/10.1038/cddiscovery.2015.70
Manteniotis S, Wojcik S, Brauhoff P, Möllmann M, Petersen L, Göthert JR, Schmiegel W, Dührsen U, Gisselmann G, Hatt H. Functional characterization of the ectopically expressed olfactory receptor 2AT4 in human myelogenous leukemia. Cell Death Discov. 2016 Jan 25;2:15070. doi: 10.1038/cddiscovery.2015.70. eCollection 2016. PMID: 27551494; PMCID: PMC4979481.
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Simultaneous determination of glucocorticoid alcohols, their succinates and hydrocortisone in plasma.

Journal of pharmaceutical and biomedical analysis

Rohdewald P, Rehder J, Drehsen G, Hochhaus G, Derendorf H, Möllmann H.
PMID: 16867648
J Pharm Biomed Anal. 1985;3(6):566-73. doi: 10.1016/0731-7085(85)80074-1.

A reversed-phase high-performance liquid chromatographic (HPLC) assay is described for the simultaneous determination of methylprednisolone, methylprednisolone-21-hemisuccinate and endogenous hydrocortisone in biological fluids. This assay is also applicable to the determination of prednisolone-21-hemisuccinate in the presence of prednisolone and hydrocortisone...

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Rohdewald P, Rehder J, Drehsen G, et al. Simultaneous determination of glucocorticoid alcohols, their succinates and hydrocortisone in plasma. J Pharm Biomed Anal. 1985;3(6):566-73doi: 10.1016/0731-7085(85)80074-1.
Rohdewald, P., Rehder, J., Drehsen, G., Hochhaus, G., Derendorf, H., & Möllmann, H. (1985). Simultaneous determination of glucocorticoid alcohols, their succinates and hydrocortisone in plasma. Journal of pharmaceutical and biomedical analysis, 3(6), 566-73. https://doi.org/10.1016/0731-7085(85)80074-1
Rohdewald, P, et al. "Simultaneous determination of glucocorticoid alcohols, their succinates and hydrocortisone in plasma." Journal of pharmaceutical and biomedical analysis vol. 3,6 (1985): 566-73. doi: https://doi.org/10.1016/0731-7085(85)80074-1
Rohdewald P, Rehder J, Drehsen G, Hochhaus G, Derendorf H, Möllmann H. Simultaneous determination of glucocorticoid alcohols, their succinates and hydrocortisone in plasma. J Pharm Biomed Anal. 1985;3(6):566-73. doi: 10.1016/0731-7085(85)80074-1. PMID: 16867648.
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P--P bond cleavage of tetraphenyltetraphosphane-1,4-diide facilitated by nickel(0).

Chemistry (Weinheim an der Bergstrasse, Germany)

Gómez-Ruiz S, Zahn S, Kirchner B, Böhlmann W, Hey-Hawkins E.
PMID: 18712742
Chemistry. 2008;14(29):8980-5. doi: 10.1002/chem.200801089.

One equivalent of [Na2(thf)5-(P4Ph4)] (1) reacts with one equivalent of [Ni(cod)2] (cod=1,5-cyclooctadiene) to give the unexpected ionic compound [Na(Et2O)3][Na3(Et2O)2Ni3(micro-P2Ph2)2-(P2Ph2)3] (2), whereas the reaction of [Ni(cod)2] with the less reactive [K2(pmdeta)2(P4Ph4)] (3) leads to the formation of [K(pmdeta)]2[Ni(P4Ph4)-(P2Ph2)] (4) (PMDETA=NMe(CH2CH2NMe2)2),...

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Gómez-Ruiz S, Zahn S, Kirchner B, et al. P--P bond cleavage of tetraphenyltetraphosphane-1,4-diide facilitated by nickel(0). Chemistry. 2008;14(29):8980-5doi: 10.1002/chem.200801089.
Gómez-Ruiz, S., Zahn, S., Kirchner, B., Böhlmann, W., & Hey-Hawkins, E. (2008). P--P bond cleavage of tetraphenyltetraphosphane-1,4-diide facilitated by nickel(0). Chemistry (Weinheim an der Bergstrasse, Germany), 14(29), 8980-5. https://doi.org/10.1002/chem.200801089
Gómez-Ruiz, Santiago, et al. "P--P bond cleavage of tetraphenyltetraphosphane-1,4-diide facilitated by nickel(0)." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 14,29 (2008): 8980-5. doi: https://doi.org/10.1002/chem.200801089
Gómez-Ruiz S, Zahn S, Kirchner B, Böhlmann W, Hey-Hawkins E. P--P bond cleavage of tetraphenyltetraphosphane-1,4-diide facilitated by nickel(0). Chemistry. 2008;14(29):8980-5. doi: 10.1002/chem.200801089. PMID: 18712742.
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Modulation of Neuropeptide-lnduced Membrane Currents by Protein Kinase C in Xenopus Oocytes Injected with GH Pituitary Cell Poly(A) RNA.

Journal of neuroendocrinology

Mahlmann S, Schwarz JR, Meyerhof W.
PMID: 19210484
J Neuroendocrinol. 1989 Feb;1(1):65-9. doi: 10.1111/j.1365-2826.1989.tb00078.x.

Abstract Protein kinase C was activated in Xenopus laevis oocytes by phorbol ester treatment and its effects on the inositol trisphosphate/Ca(2+) transmembrane signalling pathway analysed. Induction of the pathway was achieved by ligand stimulation of TRH receptors translated from...

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Mahlmann S, Schwarz JR, Meyerhof W. Modulation of Neuropeptide-lnduced Membrane Currents by Protein Kinase C in Xenopus Oocytes Injected with GH Pituitary Cell Poly(A) RNA. J Neuroendocrinol. 1989;1(1):65-9doi: 10.1111/j.1365-2826.1989.tb00078.x.
Mahlmann, S., Schwarz, J. R., & Meyerhof, W. (1989). Modulation of Neuropeptide-lnduced Membrane Currents by Protein Kinase C in Xenopus Oocytes Injected with GH Pituitary Cell Poly(A) RNA. Journal of neuroendocrinology, 1(1), 65-9. https://doi.org/10.1111/j.1365-2826.1989.tb00078.x
Mahlmann, S, et al. "Modulation of Neuropeptide-lnduced Membrane Currents by Protein Kinase C in Xenopus Oocytes Injected with GH Pituitary Cell Poly(A) RNA." Journal of neuroendocrinology vol. 1,1 (1989): 65-9. doi: https://doi.org/10.1111/j.1365-2826.1989.tb00078.x
Mahlmann S, Schwarz JR, Meyerhof W. Modulation of Neuropeptide-lnduced Membrane Currents by Protein Kinase C in Xenopus Oocytes Injected with GH Pituitary Cell Poly(A) RNA. J Neuroendocrinol. 1989 Feb;1(1):65-9. doi: 10.1111/j.1365-2826.1989.tb00078.x. PMID: 19210484.
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High-power vacuum-ultraviolet anti-Stokes Raman laser with atomic selenium.

Optics letters

Ludewigt K, Pfingsten W, Möhlmann C, Wellegehausen B.
PMID: 19738786
Opt Lett. 1987 Jan 01;12(1):39-41. doi: 10.1364/ol.12.000039.

High-power operation of a selenium anti-Stokes Raman laser has been realized by application of an ArF excimer laser as a primary pump source. Radiation at 169 and 146 nm was generated with conversion efficiencies of up to 2.3% and...

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Ludewigt K, Pfingsten W, Möhlmann C, et al. High-power vacuum-ultraviolet anti-Stokes Raman laser with atomic selenium. Opt Lett. 1987;12(1):39-41doi: 10.1364/ol.12.000039.
Ludewigt, K., Pfingsten, W., Möhlmann, C., & Wellegehausen, B. (1987). High-power vacuum-ultraviolet anti-Stokes Raman laser with atomic selenium. Optics letters, 12(1), 39-41. https://doi.org/10.1364/ol.12.000039
Ludewigt, K, et al. "High-power vacuum-ultraviolet anti-Stokes Raman laser with atomic selenium." Optics letters vol. 12,1 (1987): 39-41. doi: https://doi.org/10.1364/ol.12.000039
Ludewigt K, Pfingsten W, Möhlmann C, Wellegehausen B. High-power vacuum-ultraviolet anti-Stokes Raman laser with atomic selenium. Opt Lett. 1987 Jan 01;12(1):39-41. doi: 10.1364/ol.12.000039. PMID: 19738786.
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Optical and laser properties of (F(2)(+))(H) centers in sulfur-doped NaCl.

Optics letters

Möllmann K, Gellermann W.
PMID: 19844451
Opt Lett. 1994 Jun 01;19(11):804-6. doi: 10.1364/ol.19.000804.

We report the production and main optical and laser properties of (F(2)(+))(H) color centers in sulfur-doped NaCl crystals. Using a 1.06-microm Nd:YAG laser as the pump source, we realize continuous-wave and synchronously mode-locked laser operation. The laser is tunable...

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Möllmann K, Gellermann W. Optical and laser properties of (F(2)(+))(H) centers in sulfur-doped NaCl. Opt Lett. 1994;19(11):804-6doi: 10.1364/ol.19.000804.
Möllmann, K., & Gellermann, W. (1994). Optical and laser properties of (F(2)(+))(H) centers in sulfur-doped NaCl. Optics letters, 19(11), 804-6. https://doi.org/10.1364/ol.19.000804
Möllmann, K, and Gellermann, W. "Optical and laser properties of (F(2)(+))(H) centers in sulfur-doped NaCl." Optics letters vol. 19,11 (1994): 804-6. doi: https://doi.org/10.1364/ol.19.000804
Möllmann K, Gellermann W. Optical and laser properties of (F(2)(+))(H) centers in sulfur-doped NaCl. Opt Lett. 1994 Jun 01;19(11):804-6. doi: 10.1364/ol.19.000804. PMID: 19844451.
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Thyroid function tests in patients taking thyroid medication in Germany: Results from the population-based Study of Health in Pomerania (SHIP).

BMC research notes

Hannemann A, Friedrich N, Haring R, Krebs A, Völzke H, Alte D, Nauck M, Kohlmann T, Schober HC, Hoffmann W, Wallaschofski H.
PMID: 20712884
BMC Res Notes. 2010 Aug 16;3:227. doi: 10.1186/1756-0500-3-227.

BACKGROUND: Studies from iodine-sufficient areas have shown that a high proportion of patients taking medication for thyroid diseases have thyroid stimulating hormone (TSH) levels outside the reference range. Next to patient compliance, inadequate dosing adjustment resulting in under- and...

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Hannemann A, Friedrich N, Haring R, et al. Thyroid function tests in patients taking thyroid medication in Germany: Results from the population-based Study of Health in Pomerania (SHIP). BMC Res Notes. 2010;3:227doi: 10.1186/1756-0500-3-227.
Hannemann, A., Friedrich, N., Haring, R., Krebs, A., Völzke, H., Alte, D., Nauck, M., Kohlmann, T., Schober, H. C., Hoffmann, W., & Wallaschofski, H. (2010). Thyroid function tests in patients taking thyroid medication in Germany: Results from the population-based Study of Health in Pomerania (SHIP). BMC research notes, 3227. https://doi.org/10.1186/1756-0500-3-227
Hannemann, Anke, et al. "Thyroid function tests in patients taking thyroid medication in Germany: Results from the population-based Study of Health in Pomerania (SHIP)." BMC research notes vol. 3 (2010): 227. doi: https://doi.org/10.1186/1756-0500-3-227
Hannemann A, Friedrich N, Haring R, Krebs A, Völzke H, Alte D, Nauck M, Kohlmann T, Schober HC, Hoffmann W, Wallaschofski H. Thyroid function tests in patients taking thyroid medication in Germany: Results from the population-based Study of Health in Pomerania (SHIP). BMC Res Notes. 2010 Aug 16;3:227. doi: 10.1186/1756-0500-3-227. PMID: 20712884; PMCID: PMC2933586.
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Development of a Scoring System to Evaluate the Severity of Craniocervical Spinal Cord Compression in Patients with Mucopolysaccharidosis IVA (Morquio A Syndrome).

JIMD reports

Möllmann C, Lampe CG, Müller-Forell W, Scarpa M, Harmatz P, Schwarz M, Beck M, Lampe C.
PMID: 23580366
JIMD Rep. 2013;11:65-72. doi: 10.1007/8904_2013_223. Epub 2013 Apr 12.

BACKGROUND: As spinal cord compression at the craniocervical junction (CCJ) is a life-threatening manifestation in patients with mucopolysaccharidosis (MPS) IVA, surgical decompression should be performed before damage becomes irreversible. We evaluated the diagnostic value of several examinations for determining...

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Möllmann C, Lampe CG, Müller-Forell W, et al. Development of a Scoring System to Evaluate the Severity of Craniocervical Spinal Cord Compression in Patients with Mucopolysaccharidosis IVA (Morquio A Syndrome). JIMD Rep. 2013;11:65-72doi: 10.1007/8904_2013_223.
Möllmann, C., Lampe, C. G., Müller-Forell, W., Scarpa, M., Harmatz, P., Schwarz, M., Beck, M., & Lampe, C. (2013). Development of a Scoring System to Evaluate the Severity of Craniocervical Spinal Cord Compression in Patients with Mucopolysaccharidosis IVA (Morquio A Syndrome). JIMD reports, 1165-72. https://doi.org/10.1007/8904_2013_223
Möllmann, Christian, et al. "Development of a Scoring System to Evaluate the Severity of Craniocervical Spinal Cord Compression in Patients with Mucopolysaccharidosis IVA (Morquio A Syndrome)." JIMD reports vol. 11 (2013): 65-72. doi: https://doi.org/10.1007/8904_2013_223
Möllmann C, Lampe CG, Müller-Forell W, Scarpa M, Harmatz P, Schwarz M, Beck M, Lampe C. Development of a Scoring System to Evaluate the Severity of Craniocervical Spinal Cord Compression in Patients with Mucopolysaccharidosis IVA (Morquio A Syndrome). JIMD Rep. 2013;11:65-72. doi: 10.1007/8904_2013_223. Epub 2013 Apr 12. PMID: 23580366; PMCID: PMC3755552.
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About miRNAs, miRNA seeds, target genes and target pathways.

Oncotarget

Kehl T, Backes C, Kern F, Fehlmann T, Ludwig N, Meese E, Lenhof HP, Keller A.
PMID: 29291020
Oncotarget. 2017 Nov 09;8(63):107167-107175. doi: 10.18632/oncotarget.22363. eCollection 2017 Dec 05.

miRNAs are typically repressing gene expression by binding to the 3' UTR, leading to degradation of the mRNA. This process is dominated by the eight-base seed region of the miRNA. Further, miRNAs are known not only to target genes...

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Kehl T, Backes C, Kern F, et al. About miRNAs, miRNA seeds, target genes and target pathways. Oncotarget. 2017;8(63):107167-107175doi: 10.18632/oncotarget.22363.
Kehl, T., Backes, C., Kern, F., Fehlmann, T., Ludwig, N., Meese, E., Lenhof, H. P., & Keller, A. (2017). About miRNAs, miRNA seeds, target genes and target pathways. Oncotarget, 8(63), 107167-107175. https://doi.org/10.18632/oncotarget.22363
Kehl, Tim, et al. "About miRNAs, miRNA seeds, target genes and target pathways." Oncotarget vol. 8,63 (2017): 107167-107175. doi: https://doi.org/10.18632/oncotarget.22363
Kehl T, Backes C, Kern F, Fehlmann T, Ludwig N, Meese E, Lenhof HP, Keller A. About miRNAs, miRNA seeds, target genes and target pathways. Oncotarget. 2017 Nov 09;8(63):107167-107175. doi: 10.18632/oncotarget.22363. eCollection 2017 Dec 05. PMID: 29291020; PMCID: PMC5739805.
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Nrf2 Is a Central Regulator of Metabolic Reprogramming of Myeloid-Derived Suppressor Cells in Steady State and Sepsis.

Frontiers in immunology

Ohl K, Fragoulis A, Klemm P, Baumeister J, Klock W, Verjans E, Böll S, Möllmann J, Lehrke M, Costa I, Denecke B, Schippers A, Roth J, Wagner N, Wruck C, Tenbrock K.
PMID: 30034396
Front Immunol. 2018 Jul 06;9:1552. doi: 10.3389/fimmu.2018.01552. eCollection 2018.

Arising in inflammatory conditions, myeloid-derived suppressor cells (MDSCs) are constantly confronted with intracellular and extracellular reactive oxygen species molecules and oxidative stress. Generating mice with a constitutive activation of Nuclear factor (erythroid-derived 2)-like 2 (Nrf2) we show a pivotal...

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Ohl K, Fragoulis A, Klemm P, et al. Nrf2 Is a Central Regulator of Metabolic Reprogramming of Myeloid-Derived Suppressor Cells in Steady State and Sepsis. Front Immunol. 2018;9:1552doi: 10.3389/fimmu.2018.01552.
Ohl, K., Fragoulis, A., Klemm, P., Baumeister, J., Klock, W., Verjans, E., Böll, S., Möllmann, J., Lehrke, M., Costa, I., Denecke, B., Schippers, A., Roth, J., Wagner, N., Wruck, C., & Tenbrock, K. (2018). Nrf2 Is a Central Regulator of Metabolic Reprogramming of Myeloid-Derived Suppressor Cells in Steady State and Sepsis. Frontiers in immunology, 91552. https://doi.org/10.3389/fimmu.2018.01552
Ohl, Kim, et al. "Nrf2 Is a Central Regulator of Metabolic Reprogramming of Myeloid-Derived Suppressor Cells in Steady State and Sepsis." Frontiers in immunology vol. 9 (2018): 1552. doi: https://doi.org/10.3389/fimmu.2018.01552
Ohl K, Fragoulis A, Klemm P, Baumeister J, Klock W, Verjans E, Böll S, Möllmann J, Lehrke M, Costa I, Denecke B, Schippers A, Roth J, Wagner N, Wruck C, Tenbrock K. Nrf2 Is a Central Regulator of Metabolic Reprogramming of Myeloid-Derived Suppressor Cells in Steady State and Sepsis. Front Immunol. 2018 Jul 06;9:1552. doi: 10.3389/fimmu.2018.01552. eCollection 2018. PMID: 30034396; PMCID: PMC6043652.
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