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Intrinsic remote conditioning of the myocardium as a comprehensive cardiac response to ischemia and reperfusion.

Oncotarget

Pavo N, Lukovic D, Zlabinger K, Lorant D, Goliasch G, Winkler J, Pils D, Auer K, Ankersmit HJ, Giricz Z, Sárközy M, Jakab A, Garamvölgyi R, Emmert MY, Hoerstrup SP, Hausenloy DJ, Ferdinandy P, Maurer G, Gyöngyösi M.
PMID: 28978029
Oncotarget. 2017 Jun 12;8(40):67227-67240. doi: 10.18632/oncotarget.18438. eCollection 2017 Sep 15.

We have previously shown that distal anterior wall ischemia/reperfusion induces gene expression changes in the proximal anterior myocardial area, involving genes responsible for cardiac remodeling. Here we investigated the molecular signals of the ischemia non-affected remote lateral and posterior...

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Pavo N, Lukovic D, Zlabinger K, et al. Intrinsic remote conditioning of the myocardium as a comprehensive cardiac response to ischemia and reperfusion. Oncotarget. 2017;8(40):67227-67240doi: 10.18632/oncotarget.18438.
Pavo, N., Lukovic, D., Zlabinger, K., Lorant, D., Goliasch, G., Winkler, J., Pils, D., Auer, K., Ankersmit, H. J., Giricz, Z., Sárközy, M., Jakab, A., Garamvölgyi, R., Emmert, M. Y., Hoerstrup, S. P., Hausenloy, D. J., Ferdinandy, P., Maurer, G., & Gyöngyösi, M. (2017). Intrinsic remote conditioning of the myocardium as a comprehensive cardiac response to ischemia and reperfusion. Oncotarget, 8(40), 67227-67240. https://doi.org/10.18632/oncotarget.18438
Pavo, Noemi, et al. "Intrinsic remote conditioning of the myocardium as a comprehensive cardiac response to ischemia and reperfusion." Oncotarget vol. 8,40 (2017): 67227-67240. doi: https://doi.org/10.18632/oncotarget.18438
Pavo N, Lukovic D, Zlabinger K, Lorant D, Goliasch G, Winkler J, Pils D, Auer K, Ankersmit HJ, Giricz Z, Sárközy M, Jakab A, Garamvölgyi R, Emmert MY, Hoerstrup SP, Hausenloy DJ, Ferdinandy P, Maurer G, Gyöngyösi M. Intrinsic remote conditioning of the myocardium as a comprehensive cardiac response to ischemia and reperfusion. Oncotarget. 2017 Jun 12;8(40):67227-67240. doi: 10.18632/oncotarget.18438. eCollection 2017 Sep 15. PMID: 28978029; PMCID: PMC5620169.
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DC-Derived IL-10 Modulates Pro-inflammatory Cytokine Production and Promotes Induction of CD4.

Frontiers in immunology

Loevenich K, Ueffing K, Abel S, Hose M, Matuschewski K, Westendorf AM, Buer J, Hansen W.
PMID: 28293237
Front Immunol. 2017 Feb 28;8:152. doi: 10.3389/fimmu.2017.00152. eCollection 2017.

The cytokine IL-10 plays a crucial role during malaria infection by counteracting the pro-inflammatory immune response. We and others demonstrated that

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Loevenich K, Ueffing K, Abel S, et al. DC-Derived IL-10 Modulates Pro-inflammatory Cytokine Production and Promotes Induction of CD4. Front Immunol. 2017;8:152doi: 10.3389/fimmu.2017.00152.
Loevenich, K., Ueffing, K., Abel, S., Hose, M., Matuschewski, K., Westendorf, A. M., Buer, J., & Hansen, W. (2017). DC-Derived IL-10 Modulates Pro-inflammatory Cytokine Production and Promotes Induction of CD4. Frontiers in immunology, 8152. https://doi.org/10.3389/fimmu.2017.00152
Loevenich, Katharina, et al. "DC-Derived IL-10 Modulates Pro-inflammatory Cytokine Production and Promotes Induction of CD4." Frontiers in immunology vol. 8 (2017): 152. doi: https://doi.org/10.3389/fimmu.2017.00152
Loevenich K, Ueffing K, Abel S, Hose M, Matuschewski K, Westendorf AM, Buer J, Hansen W. DC-Derived IL-10 Modulates Pro-inflammatory Cytokine Production and Promotes Induction of CD4. Front Immunol. 2017 Feb 28;8:152. doi: 10.3389/fimmu.2017.00152. eCollection 2017. PMID: 28293237; PMCID: PMC5328999.
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Correction to: The pulvinar nucleus and antidepressant treatment: dynamic modeling of antidepressant response and remission with ultra-high field functional MRI.

Molecular psychiatry

Kraus C, Klöbl M, Tik M, Auer B, Vanicek T, Geissberger N, Pfabigan DM, Hahn A, Woletz M, Paul K, Komorowski A, Kasper S, Windischberger C, Lamm C, Lanzenberger R.
PMID: 29520037
Mol Psychiatry. 2019 May;24(5):772. doi: 10.1038/s41380-018-0032-6.

The author list was presented as last name, first name. The names should have been listed as:Christoph Kraus, Manfred Klöbl, Martin Tik, Bastian Auer, Thomas Vanicek, Nicole Geissberger, Daniela M. Pfabigan, Andreas Hahn, Michael Woletz, Katharina Paul, Arkadiusz Komorowski,...

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Kraus C, Klöbl M, Tik M, et al. Correction to: The pulvinar nucleus and antidepressant treatment: dynamic modeling of antidepressant response and remission with ultra-high field functional MRI. Mol Psychiatry. 2019;24(5):772doi: 10.1038/s41380-018-0032-6.
Kraus, C., Klöbl, M., Tik, M., Auer, B., Vanicek, T., Geissberger, N., Pfabigan, D. M., Hahn, A., Woletz, M., Paul, K., Komorowski, A., Kasper, S., Windischberger, C., Lamm, C., & Lanzenberger, R. (2019). Correction to: The pulvinar nucleus and antidepressant treatment: dynamic modeling of antidepressant response and remission with ultra-high field functional MRI. Molecular psychiatry, 24(5), 772. https://doi.org/10.1038/s41380-018-0032-6
Kraus, Christoph, et al. "Correction to: The pulvinar nucleus and antidepressant treatment: dynamic modeling of antidepressant response and remission with ultra-high field functional MRI." Molecular psychiatry vol. 24,5 (2019): 772. doi: https://doi.org/10.1038/s41380-018-0032-6
Kraus C, Klöbl M, Tik M, Auer B, Vanicek T, Geissberger N, Pfabigan DM, Hahn A, Woletz M, Paul K, Komorowski A, Kasper S, Windischberger C, Lamm C, Lanzenberger R. Correction to: The pulvinar nucleus and antidepressant treatment: dynamic modeling of antidepressant response and remission with ultra-high field functional MRI. Mol Psychiatry. 2019 May;24(5):772. doi: 10.1038/s41380-018-0032-6. PMID: 29520037; PMCID: PMC6755979.
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Noncovalent functionalization of solid-state nanopores via self-assembly of amphipols.

Nanoscale

Pérez-Mitta G, Burr L, Tuninetti JS, Trautmann C, Toimil-Molares ME, Azzaroni O.
PMID: 26676314
Nanoscale. 2016 Jan 21;8(3):1470-8. doi: 10.1039/c5nr08190d.

In recent years there has been increasing interest in the development of new methods for conferring functional features to nanopore-based fluidic devices. In this work, we describe for the first time the noncovalent integration of amphoteric-amphipathic polymers, also known...

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Pérez-Mitta G, Burr L, Tuninetti JS, et al. Noncovalent functionalization of solid-state nanopores via self-assembly of amphipols. Nanoscale. 2016;8(3):1470-8doi: 10.1039/c5nr08190d.
Pérez-Mitta, G., Burr, L., Tuninetti, J. S., Trautmann, C., Toimil-Molares, M. E., & Azzaroni, O. (2016). Noncovalent functionalization of solid-state nanopores via self-assembly of amphipols. Nanoscale, 8(3), 1470-8. https://doi.org/10.1039/c5nr08190d
Pérez-Mitta, Gonzalo, et al. "Noncovalent functionalization of solid-state nanopores via self-assembly of amphipols." Nanoscale vol. 8,3 (2016): 1470-8. doi: https://doi.org/10.1039/c5nr08190d
Pérez-Mitta G, Burr L, Tuninetti JS, Trautmann C, Toimil-Molares ME, Azzaroni O. Noncovalent functionalization of solid-state nanopores via self-assembly of amphipols. Nanoscale. 2016 Jan 21;8(3):1470-8. doi: 10.1039/c5nr08190d. PMID: 26676314.
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Design and Weighting Methods for a Nationally Representative Sample of HIV-infected Adults Receiving Medical Care in the United States-Medical Monitoring Project.

The open AIDS journal

Iachan R, Johnson CH, Harding RL, Kyle T, Saavedra P, Frazier EL, Beer L, Mattson CL, Skarbinski J.
PMID: 27651851
Open AIDS J. 2016 Aug 19;10:164-81. doi: 10.2174/1874613601610010164. eCollection 2016.

BACKGROUND: Health surveys of the general US population are inadequate for monitoring human immunodeficiency virus (HIV) infection because the relatively low prevalence of the disease (

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Iachan R, Johnson CH, Harding RL, et al. Design and Weighting Methods for a Nationally Representative Sample of HIV-infected Adults Receiving Medical Care in the United States-Medical Monitoring Project. Open AIDS J. 2016;10:164-81doi: 10.2174/1874613601610010164.
Iachan, R., Johnson, C. H., Harding, R. L., Kyle, T., Saavedra, P., Frazier, E. L., Beer, L., Mattson, C. L., & Skarbinski, J. (2016). Design and Weighting Methods for a Nationally Representative Sample of HIV-infected Adults Receiving Medical Care in the United States-Medical Monitoring Project. The open AIDS journal, 10164-81. https://doi.org/10.2174/1874613601610010164
Iachan, Ronaldo, et al. "Design and Weighting Methods for a Nationally Representative Sample of HIV-infected Adults Receiving Medical Care in the United States-Medical Monitoring Project." The open AIDS journal vol. 10 (2016): 164-81. doi: https://doi.org/10.2174/1874613601610010164
Iachan R, Johnson CH, Harding RL, Kyle T, Saavedra P, Frazier EL, Beer L, Mattson CL, Skarbinski J. Design and Weighting Methods for a Nationally Representative Sample of HIV-infected Adults Receiving Medical Care in the United States-Medical Monitoring Project. Open AIDS J. 2016 Aug 19;10:164-81. doi: 10.2174/1874613601610010164. eCollection 2016. PMID: 27651851; PMCID: PMC5013474.
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Benzo[2,1-c:3,4-c']bis(1,2,3-thiaselenazole) (BSe) and its charge trasfer chemistry. Crystal and electronic structure of [BSe]3[ClO4]2.

Inorganic chemistry

Beer L, Britten JF, Cordes AW, Clements OP, Oakley RT, Pink M, Reed RW.
PMID: 11511219
Inorg Chem. 2001 Aug 27;40(18):4705-9. doi: 10.1021/ic010357j.

The S-Se-N-based heterocycle benzo[2,1-c:3,4-c']bis(1,2,3-thiaselenazole) (BSe) can be prepared by the condensation of 1,4-diaminobenzene-2,3-dithiol with selenium tetrachloride. Crystals of this compound are not isomorphous with the related benzo[2,1-c:3,4-c']bis(1,2,3-dithiazole) (BT); a structure is adopted that allows for more extensive intermolecular Se-...

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Beer L, Britten JF, Cordes AW, et al. Benzo[2,1-c:3,4-c']bis(1,2,3-thiaselenazole) (BSe) and its charge trasfer chemistry. Crystal and electronic structure of [BSe]3[ClO4]2. Inorg Chem. 2001;40(18):4705-9doi: 10.1021/ic010357j.
Beer, L., Britten, J. F., Cordes, A. W., Clements, O. P., Oakley, R. T., Pink, M., & Reed, R. W. (2001). Benzo[2,1-c:3,4-c']bis(1,2,3-thiaselenazole) (BSe) and its charge trasfer chemistry. Crystal and electronic structure of [BSe]3[ClO4]2. Inorganic chemistry, 40(18), 4705-9. https://doi.org/10.1021/ic010357j
Beer, L, et al. "Benzo[2,1-c:3,4-c']bis(1,2,3-thiaselenazole) (BSe) and its charge trasfer chemistry. Crystal and electronic structure of [BSe]3[ClO4]2." Inorganic chemistry vol. 40,18 (2001): 4705-9. doi: https://doi.org/10.1021/ic010357j
Beer L, Britten JF, Cordes AW, Clements OP, Oakley RT, Pink M, Reed RW. Benzo[2,1-c:3,4-c']bis(1,2,3-thiaselenazole) (BSe) and its charge trasfer chemistry. Crystal and electronic structure of [BSe]3[ClO4]2. Inorg Chem. 2001 Aug 27;40(18):4705-9. doi: 10.1021/ic010357j. PMID: 11511219.
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Synthesis of a highly enantiomerically enriched silyllithium compound.

Chemical communications (Cambridge, England)

Strohmann C, Hörnig J, Auer D.
PMID: 12119713
Chem Commun (Camb). 2002 Apr 07;(7):766-7. doi: 10.1039/b111687h.

The highly enantiomerically enriched silyllithium compound lithiomethylphenyl(1-piperidinylmethyl)silane (4) reacts stereospecifically with chlorosilanes, but over a period of several hours slow racemization in solution at room temperature occurs, which can be suppressed by a transmetalation reaction with MgBr2(thf)4.

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Strohmann C, Hörnig J, Auer D. Synthesis of a highly enantiomerically enriched silyllithium compound. Chem Commun (Camb). 2002;(7):766-7doi: 10.1039/b111687h.
Strohmann, C., Hörnig, J., & Auer, D. (2002). Synthesis of a highly enantiomerically enriched silyllithium compound. Chemical communications (Cambridge, England), (7), 766-7. https://doi.org/10.1039/b111687h
Strohmann, Carsten, et al. "Synthesis of a highly enantiomerically enriched silyllithium compound." Chemical communications (Cambridge, England) vol. ,7 (2002): 766-7. doi: https://doi.org/10.1039/b111687h
Strohmann C, Hörnig J, Auer D. Synthesis of a highly enantiomerically enriched silyllithium compound. Chem Commun (Camb). 2002 Apr 07;(7):766-7. doi: 10.1039/b111687h. PMID: 12119713.
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[Pathophysiology and therapeutic aspects of left ventricular "remodeling" in the post-infarct phase].

Acta medica Austriaca

Auer J, Berent R, Eber B.
PMID: 11774772
Acta Med Austriaca. 2001;28(5):117-22. doi: 10.1046/j.1563-2571.2001.01030.x.

Left ventricular remodeling is the process by which ventricular size, shape, and function are regulated by mechanical, neurohormonal, and genetic factors. Remodeling may be physiological and adaptive during normal growth or pathological due to myocardial infarction, cardiomyopathy, hypertension, or...

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Auer J, Berent R, Eber B. Pathophysiologische und therapeutische Aspekte des linksventrikulären "Remodelings" in der Postinfarktphase. [Pathophysiology and therapeutic aspects of left ventricular "remodeling" in the post-infarct phase]. Acta Med Austriaca. 2001;28(5):117-22doi: 10.1046/j.1563-2571.2001.01030.x.
Auer, J., Berent, R., & Eber, B. (2001). Pathophysiologische und therapeutische Aspekte des linksventrikulären "Remodelings" in der Postinfarktphase. [Pathophysiology and therapeutic aspects of left ventricular "remodeling" in the post-infarct phase]. Acta medica Austriaca, 28(5), 117-22. https://doi.org/10.1046/j.1563-2571.2001.01030.x
Auer, J, et al. "Pathophysiologische und therapeutische Aspekte des linksventrikulären "Remodelings" in der Postinfarktphase." [Pathophysiology and therapeutic aspects of left ventricular "remodeling" in the post-infarct phase]. Acta medica Austriaca vol. 28,5 (2001): 117-22. doi: https://doi.org/10.1046/j.1563-2571.2001.01030.x
Auer J, Berent R, Eber B. Pathophysiologische und therapeutische Aspekte des linksventrikulären "Remodelings" in der Postinfarktphase. [Pathophysiology and therapeutic aspects of left ventricular "remodeling" in the post-infarct phase]. Acta Med Austriaca. 2001;28(5):117-22. doi: 10.1046/j.1563-2571.2001.01030.x. German. PMID: 11774772.
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Cancer of the vagina: Laminin-5gamma2 chain expression and prognosis.

International journal of gynecological cancer : official journal of the International Gynecological Cancer Society

Hellman K, Hellström AC, Silfverswärd C, Salo S, Aspenblad U, Nilsson B, Frankendal B, Tryggvasson K, Auer G.
PMID: 11240703
Int J Gynecol Cancer. 2000 Sep;10(5):391-396. doi: 10.1046/j.1525-1438.2000.010005391.x.

The purpose of this experiment was to investigate the expression and the prognostic impact of the gamma2 subchain of laminin-5 in vaginal malignancies. The outcome of the rare disease primary carcinoma of the vagina is poor and little is...

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Hellman K, Hellström AC, Silfverswärd C, et al. Cancer of the vagina: Laminin-5gamma2 chain expression and prognosis. Int J Gynecol Cancer. 2000;10(5):391-396doi: 10.1046/j.1525-1438.2000.010005391.x.
Hellman, K., Hellström, A. C., Silfverswärd, C., Salo, S., Aspenblad, U., Nilsson, B., Frankendal, B., Tryggvasson, K., & Auer, G. (2000). Cancer of the vagina: Laminin-5gamma2 chain expression and prognosis. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society, 10(5), 391-396. https://doi.org/10.1046/j.1525-1438.2000.010005391.x
Hellman, K., et al. "Cancer of the vagina: Laminin-5gamma2 chain expression and prognosis." International journal of gynecological cancer : official journal of the International Gynecological Cancer Society vol. 10,5 (2000): 391-396. doi: https://doi.org/10.1046/j.1525-1438.2000.010005391.x
Hellman K, Hellström AC, Silfverswärd C, Salo S, Aspenblad U, Nilsson B, Frankendal B, Tryggvasson K, Auer G. Cancer of the vagina: Laminin-5gamma2 chain expression and prognosis. Int J Gynecol Cancer. 2000 Sep;10(5):391-396. doi: 10.1046/j.1525-1438.2000.010005391.x. PMID: 11240703.
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A pi-stacked 1,2,3-dithiazolyl radical. Preparation and solid state characterization of (Cl2C3NS)(ClC2NS2).

Chemical communications (Cambridge, England)

Beer L, Cordes AW, Haddon RC, Itkis ME, Oakley RT, Reed RW, Robertson CM.
PMID: 12271651
Chem Commun (Camb). 2002 Sep 07;(17):1872-3. doi: 10.1039/b204855h.

Crystals of (Cl2C3NS)(ClC2NS2), an isothiazolyl-substituted 1,2,3-dithiazolyl radical, consist of evenly spaced, slipped pi-stacks; magnetic and conductivity measurements indicate the material is a Mott insulator with sigma RT = 2 x 10(-7) S cm-1.

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Beer L, Cordes AW, Haddon RC, et al. A pi-stacked 1,2,3-dithiazolyl radical. Preparation and solid state characterization of (Cl2C3NS)(ClC2NS2). Chem Commun (Camb). 2002;(17):1872-3doi: 10.1039/b204855h.
Beer, L., Cordes, A. W., Haddon, R. C., Itkis, M. E., Oakley, R. T., Reed, R. W., & Robertson, C. M. (2002). A pi-stacked 1,2,3-dithiazolyl radical. Preparation and solid state characterization of (Cl2C3NS)(ClC2NS2). Chemical communications (Cambridge, England), (17), 1872-3. https://doi.org/10.1039/b204855h
Beer, Leanne, et al. "A pi-stacked 1,2,3-dithiazolyl radical. Preparation and solid state characterization of (Cl2C3NS)(ClC2NS2)." Chemical communications (Cambridge, England) vol. ,17 (2002): 1872-3. doi: https://doi.org/10.1039/b204855h
Beer L, Cordes AW, Haddon RC, Itkis ME, Oakley RT, Reed RW, Robertson CM. A pi-stacked 1,2,3-dithiazolyl radical. Preparation and solid state characterization of (Cl2C3NS)(ClC2NS2). Chem Commun (Camb). 2002 Sep 07;(17):1872-3. doi: 10.1039/b204855h. PMID: 12271651.
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Reply.

Muscle & nerve

Siebner HR, Auer C.
PMID: 10883015
Muscle Nerve. 2000 Jul;23(7):1146. doi: 10.1002/1097-4598(200007)23:7<1146::aid-mus23>3.0.co;2-#.

No abstract available.

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Siebner HR, Auer C. Reply. Muscle Nerve. 2000;23(7):1146doi: 10.1002/1097-4598(200007)23:7<1146::aid-mus23>3.0.co;2-#.
Siebner, H. R., & Auer, C. (2000). Reply. Muscle & nerve, 23(7), 1146. https://doi.org/10.1002/1097-4598(200007)23:7<1146::aid-mus23>3.0.co;2-#
Siebner, and Auer. "Reply." Muscle & nerve vol. 23,7 (2000): 1146. doi: https://doi.org/10.1002/1097-4598(200007)23:7<1146::aid-mus23>3.0.co;2-#
Siebner HR, Auer C. Reply. Muscle Nerve. 2000 Jul;23(7):1146. doi: 10.1002/1097-4598(200007)23:7<1146::aid-mus23>3.0.co;2-#. PMID: 10883015.
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A highly enantiomerically enriched lithiosilane by selective cleavage of a silicon-phenyl bond with lithium.

Angewandte Chemie (International ed. in English)

Strohmann C, Däschlein C, Kellert M, Auer D.
PMID: 17516593
Angew Chem Int Ed Engl. 2007;46(25):4780-2. doi: 10.1002/anie.200604636.

No abstract available.

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Strohmann C, Däschlein C, Kellert M, et al. A highly enantiomerically enriched lithiosilane by selective cleavage of a silicon-phenyl bond with lithium. Angew Chem Int Ed Engl. 2007;46(25):4780-2doi: 10.1002/anie.200604636.
Strohmann, C., Däschlein, C., Kellert, M., & Auer, D. (2007). A highly enantiomerically enriched lithiosilane by selective cleavage of a silicon-phenyl bond with lithium. Angewandte Chemie (International ed. in English), 46(25), 4780-2. https://doi.org/10.1002/anie.200604636
Strohmann, Carsten, et al. "A highly enantiomerically enriched lithiosilane by selective cleavage of a silicon-phenyl bond with lithium." Angewandte Chemie (International ed. in English) vol. 46,25 (2007): 4780-2. doi: https://doi.org/10.1002/anie.200604636
Strohmann C, Däschlein C, Kellert M, Auer D. A highly enantiomerically enriched lithiosilane by selective cleavage of a silicon-phenyl bond with lithium. Angew Chem Int Ed Engl. 2007;46(25):4780-2. doi: 10.1002/anie.200604636. PMID: 17516593.
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