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14th St. Gallen International Breast Cancer Conference 2015: Evidence, Controversies, Consensus - Primary Therapy of Early Breast Cancer: Opinions Expressed by German Experts.

Breast care (Basel, Switzerland)

Jackisch C, Harbeck N, Huober J, von Minckwitz G, Gerber B, Kreipe HH, Liedtke C, Marschner N, Möbus V, Scheithauer H, Schneeweiss A, Thomssen C, Loibl S, Beckmann MW, Blohmer JU, Costa SD, Decker T, Diel I, Fasching PA, Fehm T, Janni W, Lück HJ, Maass N, Scharl A, Untch M.
PMID: 26557827
Breast Care (Basel). 2015 Jul;10(3):211-9. doi: 10.1159/000433590. Epub 2015 Jun 23.

The key topics of this year's 14th St. Gallen Consensus Conference on the diagnosis and therapy of primary breast cancer were again questions about breast surgery and axillary surgery, radio-oncology and systemic therapy options in consideration of tumor biology,...

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Jackisch C, Harbeck N, Huober J, et al. 14th St. Gallen International Breast Cancer Conference 2015: Evidence, Controversies, Consensus - Primary Therapy of Early Breast Cancer: Opinions Expressed by German Experts. Breast Care (Basel). 2015;10(3):211-9doi: 10.1159/000433590.
Jackisch, C., Harbeck, N., Huober, J., von Minckwitz, G., Gerber, B., Kreipe, H. H., Liedtke, C., Marschner, N., Möbus, V., Scheithauer, H., Schneeweiss, A., Thomssen, C., Loibl, S., Beckmann, M. W., Blohmer, J. U., Costa, S. D., Decker, T., Diel, I., Fasching, P. A., Fehm, T., Janni, W., Lück, H. J., Maass, N., Scharl, A., & Untch, M. (2015). 14th St. Gallen International Breast Cancer Conference 2015: Evidence, Controversies, Consensus - Primary Therapy of Early Breast Cancer: Opinions Expressed by German Experts. Breast care (Basel, Switzerland), 10(3), 211-9. https://doi.org/10.1159/000433590
Jackisch, Christian, et al. "14th St. Gallen International Breast Cancer Conference 2015: Evidence, Controversies, Consensus - Primary Therapy of Early Breast Cancer: Opinions Expressed by German Experts." Breast care (Basel, Switzerland) vol. 10,3 (2015): 211-9. doi: https://doi.org/10.1159/000433590
Jackisch C, Harbeck N, Huober J, von Minckwitz G, Gerber B, Kreipe HH, Liedtke C, Marschner N, Möbus V, Scheithauer H, Schneeweiss A, Thomssen C, Loibl S, Beckmann MW, Blohmer JU, Costa SD, Decker T, Diel I, Fasching PA, Fehm T, Janni W, Lück HJ, Maass N, Scharl A, Untch M. 14th St. Gallen International Breast Cancer Conference 2015: Evidence, Controversies, Consensus - Primary Therapy of Early Breast Cancer: Opinions Expressed by German Experts. Breast Care (Basel). 2015 Jul;10(3):211-9. doi: 10.1159/000433590. Epub 2015 Jun 23. PMID: 26557827; PMCID: PMC4569213.
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Synthesis, Crystal structure, and Hirshfeld Surface Analysis of a New Mixed Ligand Copper(II) Complex.

Acta chimica Slovenica

Shit S, Marschner C, Mitra S.
PMID: 26970797
Acta Chim Slov. 2016;63(1):129-37. doi: 10.17344/acsi.2015.2024.

A new mixed ligand copper(II) complex, [Cu(2,4-pydc)(pic)(H(2)O)]∙H(2)O (1) (where 2,4-pydc = pyridine-2,4-dicarboxylate, pic = 2-picolylamine) has been synthesized and characterized by elemental analysis, FT-IR and UV-Vis spectroscopic and thermogravimetric methods. Single crystal X-ray diffraction analysis reveals that copper(II) atom...

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Shit S, Marschner C, Mitra S. Synthesis, Crystal structure, and Hirshfeld Surface Analysis of a New Mixed Ligand Copper(II) Complex. Acta Chim Slov. 2016;63(1):129-37doi: 10.17344/acsi.2015.2024.
Shit, S., Marschner, C., & Mitra, S. (2016). Synthesis, Crystal structure, and Hirshfeld Surface Analysis of a New Mixed Ligand Copper(II) Complex. Acta chimica Slovenica, 63(1), 129-37. https://doi.org/10.17344/acsi.2015.2024
Shit, Shyamapada, et al. "Synthesis, Crystal structure, and Hirshfeld Surface Analysis of a New Mixed Ligand Copper(II) Complex." Acta chimica Slovenica vol. 63,1 (2016): 129-37. doi: https://doi.org/10.17344/acsi.2015.2024
Shit S, Marschner C, Mitra S. Synthesis, Crystal structure, and Hirshfeld Surface Analysis of a New Mixed Ligand Copper(II) Complex. Acta Chim Slov. 2016;63(1):129-37. doi: 10.17344/acsi.2015.2024. PMID: 26970797.
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Coordination Chemistry of Cyclic Disilylated Germylenes and Stannylenes with Group 11 Metals.

Organometallics

Hlina J, Arp H, Walewska M, Flörke U, Zangger K, Marschner C, Baumgartner J.
PMID: 25550678
Organometallics. 2014 Dec 22;33(24):7069-7077. doi: 10.1021/om500668r. Epub 2014 Nov 26.

Reactions of Et

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Hlina J, Arp H, Walewska M, et al. Coordination Chemistry of Cyclic Disilylated Germylenes and Stannylenes with Group 11 Metals. Organometallics. 2014;33(24):7069-7077doi: 10.1021/om500668r.
Hlina, J., Arp, H., Walewska, M., Flörke, U., Zangger, K., Marschner, C., & Baumgartner, J. (2014). Coordination Chemistry of Cyclic Disilylated Germylenes and Stannylenes with Group 11 Metals. Organometallics, 33(24), 7069-7077. https://doi.org/10.1021/om500668r
Hlina, Johann, et al. "Coordination Chemistry of Cyclic Disilylated Germylenes and Stannylenes with Group 11 Metals." Organometallics vol. 33,24 (2014): 7069-7077. doi: https://doi.org/10.1021/om500668r
Hlina J, Arp H, Walewska M, Flörke U, Zangger K, Marschner C, Baumgartner J. Coordination Chemistry of Cyclic Disilylated Germylenes and Stannylenes with Group 11 Metals. Organometallics. 2014 Dec 22;33(24):7069-7077. doi: 10.1021/om500668r. Epub 2014 Nov 26. PMID: 25550678; PMCID: PMC4276716.
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Wagner-Meerwein-Type Rearrangements of Germapolysilanes - A Stable Ion Study.

Organometallics

Albers L, Meshgi MA, Baumgartner J, Marschner C, Müller T.
PMID: 26294805
Organometallics. 2015 Aug 10;34(15):3756-3763. doi: 10.1021/acs.organomet.5b00431. Epub 2015 Jul 23.

The rearrangement of tris(trimethylsilyl)silyltrimethylgermane

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Albers L, Meshgi MA, Baumgartner J, et al. Wagner-Meerwein-Type Rearrangements of Germapolysilanes - A Stable Ion Study. Organometallics. 2015;34(15):3756-3763doi: 10.1021/acs.organomet.5b00431.
Albers, L., Meshgi, M. A., Baumgartner, J., Marschner, C., & Müller, T. (2015). Wagner-Meerwein-Type Rearrangements of Germapolysilanes - A Stable Ion Study. Organometallics, 34(15), 3756-3763. https://doi.org/10.1021/acs.organomet.5b00431
Albers, Lena, et al. "Wagner-Meerwein-Type Rearrangements of Germapolysilanes - A Stable Ion Study." Organometallics vol. 34,15 (2015): 3756-3763. doi: https://doi.org/10.1021/acs.organomet.5b00431
Albers L, Meshgi MA, Baumgartner J, Marschner C, Müller T. Wagner-Meerwein-Type Rearrangements of Germapolysilanes - A Stable Ion Study. Organometallics. 2015 Aug 10;34(15):3756-3763. doi: 10.1021/acs.organomet.5b00431. Epub 2015 Jul 23. PMID: 26294805; PMCID: PMC4534834.
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Oligosilanylated Antimony Compounds.

Organometallics

Zitz R, Gatterer K, Reinhold CR, Müller T, Baumgartner J, Marschner C.
PMID: 25937691
Organometallics. 2015 Apr 27;34(8):1419-1430. doi: 10.1021/om501075v. Epub 2015 Apr 10.

By reactions of magnesium oligosilanides with SbCl

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Zitz R, Gatterer K, Reinhold CR, et al. Oligosilanylated Antimony Compounds. Organometallics. 2015;34(8):1419-1430doi: 10.1021/om501075v.
Zitz, R., Gatterer, K., Reinhold, C. R., Müller, T., Baumgartner, J., & Marschner, C. (2015). Oligosilanylated Antimony Compounds. Organometallics, 34(8), 1419-1430. https://doi.org/10.1021/om501075v
Zitz, Rainer, et al. "Oligosilanylated Antimony Compounds." Organometallics vol. 34,8 (2015): 1419-1430. doi: https://doi.org/10.1021/om501075v
Zitz R, Gatterer K, Reinhold CR, Müller T, Baumgartner J, Marschner C. Oligosilanylated Antimony Compounds. Organometallics. 2015 Apr 27;34(8):1419-1430. doi: 10.1021/om501075v. Epub 2015 Apr 10. PMID: 25937691; PMCID: PMC4413694.
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First successful reaction of a silyl anion with hafnium tetrachloride.

Chemical communications (Cambridge, England)

Frank D, Baumgartner J, Marschner C.
PMID: 12109076
Chem Commun (Camb). 2002 Jun 07;(11):1190-1. doi: 10.1039/b201508k.

Hafnium tetrachloride reacts with the tris(trimethylsilyl)silyl potassium tmen adduct (1) to form a [tris(trimethylsilyl)silyl]trichlorohafnium tmen complex (2); reaction of 2 with 2,6-dimethylphenylisonitrile leads to insertion into the silicon hafnium bond (4).

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Frank D, Baumgartner J, Marschner C. First successful reaction of a silyl anion with hafnium tetrachloride. Chem Commun (Camb). 2002;(11):1190-1doi: 10.1039/b201508k.
Frank, D., Baumgartner, J., & Marschner, C. (2002). First successful reaction of a silyl anion with hafnium tetrachloride. Chemical communications (Cambridge, England), (11), 1190-1. https://doi.org/10.1039/b201508k
Frank, Dieter, et al. "First successful reaction of a silyl anion with hafnium tetrachloride." Chemical communications (Cambridge, England) vol. ,11 (2002): 1190-1. doi: https://doi.org/10.1039/b201508k
Frank D, Baumgartner J, Marschner C. First successful reaction of a silyl anion with hafnium tetrachloride. Chem Commun (Camb). 2002 Jun 07;(11):1190-1. doi: 10.1039/b201508k. PMID: 12109076.
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Involvement of superoxide radical in extracellular ferric reduction by iron-deficient bean roots.

Plant physiology

Cakmak I, van de Wetering DA, Marschner H, Bienfait HF.
PMID: 16665677
Plant Physiol. 1987 Sep;85(1):310-4. doi: 10.1104/pp.85.1.310.

The recent proposal of Tipton and Thowsen (Plant Physiol 79: 432-435) that iron-deficient plants reduce ferric chelates in cell walls by a system dependent on the leakage of malate from root cells was tested. Results are presented showing that...

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Cakmak I, van de Wetering DA, Marschner H, et al. Involvement of superoxide radical in extracellular ferric reduction by iron-deficient bean roots. Plant Physiol. 1987;85(1):310-4doi: 10.1104/pp.85.1.310.
Cakmak, I., van de Wetering, D. A., Marschner, H., & Bienfait, H. F. (1987). Involvement of superoxide radical in extracellular ferric reduction by iron-deficient bean roots. Plant physiology, 85(1), 310-4. https://doi.org/10.1104/pp.85.1.310
Cakmak, I, et al. "Involvement of superoxide radical in extracellular ferric reduction by iron-deficient bean roots." Plant physiology vol. 85,1 (1987): 310-4. doi: https://doi.org/10.1104/pp.85.1.310
Cakmak I, van de Wetering DA, Marschner H, Bienfait HF. Involvement of superoxide radical in extracellular ferric reduction by iron-deficient bean roots. Plant Physiol. 1987 Sep;85(1):310-4. doi: 10.1104/pp.85.1.310. PMID: 16665677; PMCID: PMC1054247.
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Iron Stress and Pyoverdin Production by a Fluorescent Pseudomonad in the Rhizosphere of White Lupine (Lupinus albus L.) and Barley (Hordeum vulgare L.).

Applied and environmental microbiology

Marschner P, Crowley DE.
PMID: 16535491
Appl Environ Microbiol. 1997 Jan;63(1):277-81. doi: 10.1128/aem.63.1.277-281.1997.

Induction of high-affinity iron transport during root colonization by Pseudomonas fluorescens Pf-5 (pvd-inaZ) was examined in lupine and barley growing in microcosms. P. fluorescens Pf-5 (pvd-inaZ) contains a plasmid carrying pvd-inaZ; thus, in this strain, ice nucleation activity is...

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Marschner P, Crowley DE. Iron Stress and Pyoverdin Production by a Fluorescent Pseudomonad in the Rhizosphere of White Lupine (Lupinus albus L.) and Barley (Hordeum vulgare L.). Appl Environ Microbiol. 1997;63(1):277-81doi: 10.1128/aem.63.1.277-281.1997.
Marschner, P., & Crowley, D. E. (1997). Iron Stress and Pyoverdin Production by a Fluorescent Pseudomonad in the Rhizosphere of White Lupine (Lupinus albus L.) and Barley (Hordeum vulgare L.). Applied and environmental microbiology, 63(1), 277-81. https://doi.org/10.1128/aem.63.1.277-281.1997
Marschner, P, and Crowley, D E. "Iron Stress and Pyoverdin Production by a Fluorescent Pseudomonad in the Rhizosphere of White Lupine (Lupinus albus L.) and Barley (Hordeum vulgare L.)." Applied and environmental microbiology vol. 63,1 (1997): 277-81. doi: https://doi.org/10.1128/aem.63.1.277-281.1997
Marschner P, Crowley DE. Iron Stress and Pyoverdin Production by a Fluorescent Pseudomonad in the Rhizosphere of White Lupine (Lupinus albus L.) and Barley (Hordeum vulgare L.). Appl Environ Microbiol. 1997 Jan;63(1):277-81. doi: 10.1128/aem.63.1.277-281.1997. PMID: 16535491; PMCID: PMC1389105.
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Open, cyclic, and bicyclic compounds of double silylated phosphorus and boron.

Dalton transactions (Cambridge, England : 2003)

Markov J, Fischer R, Wagner H, Noormofidi N, Baumgartner J, Marschner C.
PMID: 15249953
Dalton Trans. 2004 Jul 21;(14):2166-9. doi: 10.1039/B404073B. Epub 2004 Jun 03.

Salt elimination reactions of tris(trimethylsilyl)silyl potassium (1), and two 1,4-dipotassiooligosilanes (3, 5) with 2,2,6,6-tetramethylpiperidinodichloroborane and diethylaminodichlorophosphane have generated open (2), cyclic (4) and bicyclic (6) bora- and phosphaoligosilanes. A monosilylated phosphane and the two five-membered cyclosilanes have been subjected...

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Markov J, Fischer R, Wagner H, et al. Open, cyclic, and bicyclic compounds of double silylated phosphorus and boron. Dalton Trans. 2004;(14):2166-9doi: 10.1039/B404073B.
Markov, J., Fischer, R., Wagner, H., Noormofidi, N., Baumgartner, J., & Marschner, C. (2004). Open, cyclic, and bicyclic compounds of double silylated phosphorus and boron. Dalton transactions (Cambridge, England : 2003), (14), 2166-9. https://doi.org/10.1039/B404073B
Markov, Jelena, et al. "Open, cyclic, and bicyclic compounds of double silylated phosphorus and boron." Dalton transactions (Cambridge, England : 2003) vol. ,14 (2004): 2166-9. doi: https://doi.org/10.1039/B404073B
Markov J, Fischer R, Wagner H, Noormofidi N, Baumgartner J, Marschner C. Open, cyclic, and bicyclic compounds of double silylated phosphorus and boron. Dalton Trans. 2004 Jul 21;(14):2166-9. doi: 10.1039/B404073B. Epub 2004 Jun 03. PMID: 15249953.
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Oligosilylated group 4 titanocenes in the oxidation state +3.

Chemical communications (Cambridge, England)

Zirngast M, Flörke U, Baumgartner J, Marschner C.
PMID: 19753349
Chem Commun (Camb). 2009 Oct 07;(37):5538-40. doi: 10.1039/b910637e. Epub 2009 Aug 13.

Reactions of oligosilylanions with Cp2TiCl2 led to the formation of ate-complexes of silylated titanocenes, which form upon silylation of the intermediate K[Cp2TiCl2].18-crown-6.

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Zirngast M, Flörke U, Baumgartner J, et al. Oligosilylated group 4 titanocenes in the oxidation state +3. Chem Commun (Camb). 2009;(37):5538-40doi: 10.1039/b910637e.
Zirngast, M., Flörke, U., Baumgartner, J., & Marschner, C. (2009). Oligosilylated group 4 titanocenes in the oxidation state +3. Chemical communications (Cambridge, England), (37), 5538-40. https://doi.org/10.1039/b910637e
Zirngast, Michaela, et al. "Oligosilylated group 4 titanocenes in the oxidation state +3." Chemical communications (Cambridge, England) vol. ,37 (2009): 5538-40. doi: https://doi.org/10.1039/b910637e
Zirngast M, Flörke U, Baumgartner J, Marschner C. Oligosilylated group 4 titanocenes in the oxidation state +3. Chem Commun (Camb). 2009 Oct 07;(37):5538-40. doi: 10.1039/b910637e. Epub 2009 Aug 13. PMID: 19753349.
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Dispersion energy enforced dimerization of a cyclic disilylated plumbylene.

Journal of the American Chemical Society

Arp H, Baumgartner J, Marschner C, Zark P, Müller T.
PMID: 22455750
J Am Chem Soc. 2012 Apr 11;134(14):6409-15. doi: 10.1021/ja300654t. Epub 2012 Mar 28.

By reaction of 1,4-dipotassio-1,1,4,4-tetrakis(trimethylsilyl)tetramethyltetrasilane with PbBr(2) in the presence of triethylphosphine a base adduct of a cyclic disilylated plumbylene could be obtained. Phosphine abstraction with B(C(6)F(5))(3) led to formation of a base-free plumbylene dimer, which features an unexpected single...

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Arp H, Baumgartner J, Marschner C, et al. Dispersion energy enforced dimerization of a cyclic disilylated plumbylene. J Am Chem Soc. 2012;134(14):6409-15doi: 10.1021/ja300654t.
Arp, H., Baumgartner, J., Marschner, C., Zark, P., & Müller, T. (2012). Dispersion energy enforced dimerization of a cyclic disilylated plumbylene. Journal of the American Chemical Society, 134(14), 6409-15. https://doi.org/10.1021/ja300654t
Arp, Henning, et al. "Dispersion energy enforced dimerization of a cyclic disilylated plumbylene." Journal of the American Chemical Society vol. 134,14 (2012): 6409-15. doi: https://doi.org/10.1021/ja300654t
Arp H, Baumgartner J, Marschner C, Zark P, Müller T. Dispersion energy enforced dimerization of a cyclic disilylated plumbylene. J Am Chem Soc. 2012 Apr 11;134(14):6409-15. doi: 10.1021/ja300654t. Epub 2012 Mar 28. PMID: 22455750; PMCID: PMC3336735.
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Soil-Plant Transfer of Polychlorinated Dibenzo-p-dioxins and Dibenzofurans to Vegetables of the Cucumber Family (Cucurbitaceae).

Environmental science & technology

Huelster A, Mueller JF, Marschner H.
PMID: 22176237
Environ Sci Technol. 1994 Jun 01;28(6):1110-5. doi: 10.1021/es00055a021.

No abstract available.

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Huelster A, Mueller JF, Marschner H. Soil-Plant Transfer of Polychlorinated Dibenzo-p-dioxins and Dibenzofurans to Vegetables of the Cucumber Family (Cucurbitaceae). Environ Sci Technol. 1994;28(6):1110-5doi: 10.1021/es00055a021.
Huelster, A., Mueller, J. F., & Marschner, H. (1994). Soil-Plant Transfer of Polychlorinated Dibenzo-p-dioxins and Dibenzofurans to Vegetables of the Cucumber Family (Cucurbitaceae). Environmental science & technology, 28(6), 1110-5. https://doi.org/10.1021/es00055a021
Huelster, A, et al. "Soil-Plant Transfer of Polychlorinated Dibenzo-p-dioxins and Dibenzofurans to Vegetables of the Cucumber Family (Cucurbitaceae)." Environmental science & technology vol. 28,6 (1994): 1110-5. doi: https://doi.org/10.1021/es00055a021
Huelster A, Mueller JF, Marschner H. Soil-Plant Transfer of Polychlorinated Dibenzo-p-dioxins and Dibenzofurans to Vegetables of the Cucumber Family (Cucurbitaceae). Environ Sci Technol. 1994 Jun 01;28(6):1110-5. doi: 10.1021/es00055a021. PMID: 22176237.
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Showing 1 to 12 of 198 entries