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Poly(phenylene) and m-Terphenyl as Powerful Protecting Groups for the Preparation of Stable Organic Hydroxides.

Angewandte Chemie (International ed. in English)

Wright AG, Weissbach T, Holdcroft S.
PMID: 26948285
Angew Chem Int Ed Engl. 2016 Apr 04;55(15):4818-21. doi: 10.1002/anie.201511184. Epub 2016 Mar 07.

Four benzimidazolium hydroxide compounds, in which the C2-position is attached to a phenyl group possessing hydrogen, bromine, methyl groups, or phenyl groups at the ortho positions, are prepared and investigated for stability in a quantitative alkaline stability test. The...

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Wright AG, Weissbach T, Holdcroft S. Poly(phenylene) and m-Terphenyl as Powerful Protecting Groups for the Preparation of Stable Organic Hydroxides. Angew Chem Int Ed Engl. 2016;55(15):4818-21doi: 10.1002/anie.201511184.
Wright, A. G., Weissbach, T., & Holdcroft, S. (2016). Poly(phenylene) and m-Terphenyl as Powerful Protecting Groups for the Preparation of Stable Organic Hydroxides. Angewandte Chemie (International ed. in English), 55(15), 4818-21. https://doi.org/10.1002/anie.201511184
Wright, Andrew G, et al. "Poly(phenylene) and m-Terphenyl as Powerful Protecting Groups for the Preparation of Stable Organic Hydroxides." Angewandte Chemie (International ed. in English) vol. 55,15 (2016): 4818-21. doi: https://doi.org/10.1002/anie.201511184
Wright AG, Weissbach T, Holdcroft S. Poly(phenylene) and m-Terphenyl as Powerful Protecting Groups for the Preparation of Stable Organic Hydroxides. Angew Chem Int Ed Engl. 2016 Apr 04;55(15):4818-21. doi: 10.1002/anie.201511184. Epub 2016 Mar 07. PMID: 26948285.
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Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias.

Genes

Hebert E, Borngräber F, Schmidt A, Rakovic A, Brænne I, Weissbach A, Hampf J, Vollstedt EJ, Größer L, Schaake S, Müller M, Manzoor H, Jabusch HC, Alvarez-Fischer D, Kasten M, Kostic VS, Gasser T, Zeuner KE, Kim HJ, Jeon B, Bauer P, Altenmüller E, Klein C, Lohmann K.
PMID: 29057844
Genes (Basel). 2017 Oct 18;8(10). doi: 10.3390/genes8100276.

Mutations in RAB (member of the Ras superfamily) genes are increasingly recognized as cause of a variety of disorders including neurological conditions. While musician's dystonia (MD) and writer's dystonia (WD) are task-specific movement disorders, other dystonias persistently affect postures...

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Hebert E, Borngräber F, Schmidt A, et al. Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias. Genes (Basel). 2017;8(10)doi: 10.3390/genes8100276.
Hebert, E., Borngräber, F., Schmidt, A., Rakovic, A., Brænne, I., Weissbach, A., Hampf, J., Vollstedt, E. J., Größer, L., Schaake, S., Müller, M., Manzoor, H., Jabusch, H. C., Alvarez-Fischer, D., Kasten, M., Kostic, V. S., Gasser, T., Zeuner, K. E., Kim, H. J., Jeon, B., Bauer, P., Altenmüller, E., Klein, C., & Lohmann, K. (2017). Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias. Genes, 8(10), . https://doi.org/10.3390/genes8100276
Hebert, Eva, et al. "Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias." Genes vol. 8,10 (2017). doi: https://doi.org/10.3390/genes8100276
Hebert E, Borngräber F, Schmidt A, Rakovic A, Brænne I, Weissbach A, Hampf J, Vollstedt EJ, Größer L, Schaake S, Müller M, Manzoor H, Jabusch HC, Alvarez-Fischer D, Kasten M, Kostic VS, Gasser T, Zeuner KE, Kim HJ, Jeon B, Bauer P, Altenmüller E, Klein C, Lohmann K. Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias. Genes (Basel). 2017 Oct 18;8(10). doi: 10.3390/genes8100276. PMID: 29057844; PMCID: PMC5664126.
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Crystalline self-assembly into monolayers of folded oligomers at the air-water interface.

Chemistry (Weinheim an der Bergstrasse, Germany)

Lederer K, Godt A, Howes PB, Kjaer K, Als-Nielsen J, Lahav M, Wegner G, Leiserowitz L, Weissbuch I.
PMID: 10926223
Chemistry. 2000 Jun 16;6(12):2173-83. doi: 10.1002/1521-3765(20000616)6:12<2173::aid-chem2173>3.0.co;2-e.

Insertion of the 1,3-bis(ethynylene)benzene unit as a rigid spacer into a linear alkyl chain, thus separating the two resulting stems by 9 A. induces chain folding at the air-water interface. These folded molecules self-assemble into crystalline monolayers at this...

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Lederer K, Godt A, Howes PB, et al. Crystalline self-assembly into monolayers of folded oligomers at the air-water interface. Chemistry. 2000;6(12):2173-83doi: 10.1002/1521-3765(20000616)6:12<2173::aid-chem2173>3.0.co;2-e.
Lederer, K., Godt, A., Howes, P. B., Kjaer, K., Als-Nielsen, J., Lahav, M., Wegner, G., Leiserowitz, L., & Weissbuch, I. (2000). Crystalline self-assembly into monolayers of folded oligomers at the air-water interface. Chemistry (Weinheim an der Bergstrasse, Germany), 6(12), 2173-83. https://doi.org/10.1002/1521-3765(20000616)6:12<2173::aid-chem2173>3.0.co;2-e
Lederer, et al. "Crystalline self-assembly into monolayers of folded oligomers at the air-water interface." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 6,12 (2000): 2173-83. doi: https://doi.org/10.1002/1521-3765(20000616)6:12<2173::aid-chem2173>3.0.co;2-e
Lederer K, Godt A, Howes PB, Kjaer K, Als-Nielsen J, Lahav M, Wegner G, Leiserowitz L, Weissbuch I. Crystalline self-assembly into monolayers of folded oligomers at the air-water interface. Chemistry. 2000 Jun 16;6(12):2173-83. doi: 10.1002/1521-3765(20000616)6:12<2173::aid-chem2173>3.0.co;2-e. PMID: 10926223.
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Oriented crystalline monolayers and bilayers of 2 x 2 silver(I) grid architectures at the air-solution interface: their assembly and crystal structure elucidation.

Chemistry (Weinheim an der Bergstrasse, Germany)

Weissbuch I, Baxter PN, Kuzmenko I, Cohen H, Cohen S, Kjaer K, Howes PB, Als-Nielsen J, Lehn JM, Leiserowitz L, Lahav M.
PMID: 10807183
Chemistry. 2000 Feb 18;6(4):725-34. doi: 10.1002/(sici)1521-3765(20000218)6:4<725::aid-chem725>3.0.co;2-e.

Oriented crystalline monolayers, approximately 14 A thick, of a 2 x 2 Ag+ grid complex, self-assembled at the air-solution interface starting from an water-insoluble ligand 3,6-bis[2-(6-phenylpyridine)]pyridazine spread on silver-ion-containing solutions, were examined by grazing-incidence X-ray diffraction and specular X-ray...

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Weissbuch I, Baxter PN, Kuzmenko I, et al. Oriented crystalline monolayers and bilayers of 2 x 2 silver(I) grid architectures at the air-solution interface: their assembly and crystal structure elucidation. Chemistry. 2000;6(4):725-34doi: 10.1002/(sici)1521-3765(20000218)6:4<725::aid-chem725>3.0.co;2-e.
Weissbuch, I., Baxter, P. N., Kuzmenko, I., Cohen, H., Cohen, S., Kjaer, K., Howes, P. B., Als-Nielsen, J., Lehn, J. M., Leiserowitz, L., & Lahav, M. (2000). Oriented crystalline monolayers and bilayers of 2 x 2 silver(I) grid architectures at the air-solution interface: their assembly and crystal structure elucidation. Chemistry (Weinheim an der Bergstrasse, Germany), 6(4), 725-34. https://doi.org/10.1002/(sici)1521-3765(20000218)6:4<725::aid-chem725>3.0.co;2-e
Weissbuch, et al. "Oriented crystalline monolayers and bilayers of 2 x 2 silver(I) grid architectures at the air-solution interface: their assembly and crystal structure elucidation." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 6,4 (2000): 725-34. doi: https://doi.org/10.1002/(sici)1521-3765(20000218)6:4<725::aid-chem725>3.0.co;2-e
Weissbuch I, Baxter PN, Kuzmenko I, Cohen H, Cohen S, Kjaer K, Howes PB, Als-Nielsen J, Lehn JM, Leiserowitz L, Lahav M. Oriented crystalline monolayers and bilayers of 2 x 2 silver(I) grid architectures at the air-solution interface: their assembly and crystal structure elucidation. Chemistry. 2000 Feb 18;6(4):725-34. doi: 10.1002/(sici)1521-3765(20000218)6:4<725::aid-chem725>3.0.co;2-e. PMID: 10807183.
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UICC symposium on testicular cancer: Guidelines for standard care and future prospects.

International journal of cancer

Bokemeyer C, Bamberg M, Albers J, Schmoll H, Weissbach L.
PMID: 10602058
Int J Cancer. 1999 Dec 10;83(6):808. doi: 10.1002/(sici)1097-0215(19991210)83:6<808::aid-ijc19>3.0.co;2-c.

No abstract available.

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Bokemeyer C, Bamberg M, Albers J, et al. UICC symposium on testicular cancer: Guidelines for standard care and future prospects. Int J Cancer. 1999;83(6):808doi: 10.1002/(sici)1097-0215(19991210)83:6<808::aid-ijc19>3.0.co;2-c.
Bokemeyer, C., Bamberg, M., Albers, J., Schmoll, H., & Weissbach, L. (1999). UICC symposium on testicular cancer: Guidelines for standard care and future prospects. International journal of cancer, 83(6), 808. https://doi.org/10.1002/(sici)1097-0215(19991210)83:6<808::aid-ijc19>3.0.co;2-c
Bokemeyer, et al. "UICC symposium on testicular cancer: Guidelines for standard care and future prospects." International journal of cancer vol. 83,6 (1999): 808. doi: https://doi.org/10.1002/(sici)1097-0215(19991210)83:6<808::aid-ijc19>3.0.co;2-c
Bokemeyer C, Bamberg M, Albers J, Schmoll H, Weissbach L. UICC symposium on testicular cancer: Guidelines for standard care and future prospects. Int J Cancer. 1999 Dec 10;83(6):808. doi: 10.1002/(sici)1097-0215(19991210)83:6<808::aid-ijc19>3.0.co;2-c. PMID: 10602058.
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Clinical instructors' perceptions of behaviors that comprise entry-level clinical performance in physical therapist students: a qualitative study.

Physical therapy

Jette DU, Bertoni A, Coots R, Johnson H, McLaughlin C, Weisbach C.
PMID: 17601998
Phys Ther. 2007 Jul;87(7):833-43. doi: 10.2522/ptj.20070003.

BACKGROUND AND PURPOSE: The purpose of this study was to qualitatively explore clinical instructors' (CIs) perceptions of students' behaviors that comprise entry-level clinical performance, as well as how those perceptions were integrated into their decision making.SUBJECTS: The participants were...

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Jette DU, Bertoni A, Coots R, et al. Clinical instructors' perceptions of behaviors that comprise entry-level clinical performance in physical therapist students: a qualitative study. Phys Ther. 2007;87(7):833-43doi: 10.2522/ptj.20070003.
Jette, D. U., Bertoni, A., Coots, R., Johnson, H., McLaughlin, C., & Weisbach, C. (2007). Clinical instructors' perceptions of behaviors that comprise entry-level clinical performance in physical therapist students: a qualitative study. Physical therapy, 87(7), 833-43. https://doi.org/10.2522/ptj.20070003
Jette, Diane U, et al. "Clinical instructors' perceptions of behaviors that comprise entry-level clinical performance in physical therapist students: a qualitative study." Physical therapy vol. 87,7 (2007): 833-43. doi: https://doi.org/10.2522/ptj.20070003
Jette DU, Bertoni A, Coots R, Johnson H, McLaughlin C, Weisbach C. Clinical instructors' perceptions of behaviors that comprise entry-level clinical performance in physical therapist students: a qualitative study. Phys Ther. 2007 Jul;87(7):833-43. doi: 10.2522/ptj.20070003. PMID: 17601998.
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Serotonin, Norepinephrine, and Related Compounds in Bananas.

Science (New York, N.Y.)

Waalkes TP, Sjoerdsma A, Creveling CR, Weissbach H, Udenfriend S.
PMID: 17808884
Science. 1958 Mar 21;127(3299):648-50. doi: 10.1126/science.127.3299.648.

No abstract available.

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Waalkes TP, Sjoerdsma A, Creveling CR, et al. Serotonin, Norepinephrine, and Related Compounds in Bananas. Science. 1958;127(3299):648-50doi: 10.1126/science.127.3299.648.
Waalkes, T. P., Sjoerdsma, A., Creveling, C. R., Weissbach, H., & Udenfriend, S. (1958). Serotonin, Norepinephrine, and Related Compounds in Bananas. Science (New York, N.Y.), 127(3299), 648-50. https://doi.org/10.1126/science.127.3299.648
Waalkes, T P, et al. "Serotonin, Norepinephrine, and Related Compounds in Bananas." Science (New York, N.Y.) vol. 127,3299 (1958): 648-50. doi: https://doi.org/10.1126/science.127.3299.648
Waalkes TP, Sjoerdsma A, Creveling CR, Weissbach H, Udenfriend S. Serotonin, Norepinephrine, and Related Compounds in Bananas. Science. 1958 Mar 21;127(3299):648-50. doi: 10.1126/science.127.3299.648. PMID: 17808884.
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ISOLATION AND PROPERTIES OF B(12) COENZYMES CONTAINING BENZIMIDAZOLE OR DIMETHYLBENZIMIDAZOLE.

Proceedings of the National Academy of Sciences of the United States of America

Weissbach H, Toohey J, Barker HA.
PMID: 16590408
Proc Natl Acad Sci U S A. 1959 Apr;45(4):521-5. doi: 10.1073/pnas.45.4.521.

No abstract available.

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Weissbach H, Toohey J, Barker HA. ISOLATION AND PROPERTIES OF B(12) COENZYMES CONTAINING BENZIMIDAZOLE OR DIMETHYLBENZIMIDAZOLE. Proc Natl Acad Sci U S A. 1959;45(4):521-5doi: 10.1073/pnas.45.4.521.
Weissbach, H., Toohey, J., & Barker, H. A. (1959). ISOLATION AND PROPERTIES OF B(12) COENZYMES CONTAINING BENZIMIDAZOLE OR DIMETHYLBENZIMIDAZOLE. Proceedings of the National Academy of Sciences of the United States of America, 45(4), 521-5. https://doi.org/10.1073/pnas.45.4.521
Weissbach, H, et al. "ISOLATION AND PROPERTIES OF B(12) COENZYMES CONTAINING BENZIMIDAZOLE OR DIMETHYLBENZIMIDAZOLE." Proceedings of the National Academy of Sciences of the United States of America vol. 45,4 (1959): 521-5. doi: https://doi.org/10.1073/pnas.45.4.521
Weissbach H, Toohey J, Barker HA. ISOLATION AND PROPERTIES OF B(12) COENZYMES CONTAINING BENZIMIDAZOLE OR DIMETHYLBENZIMIDAZOLE. Proc Natl Acad Sci U S A. 1959 Apr;45(4):521-5. doi: 10.1073/pnas.45.4.521. PMID: 16590408; PMCID: PMC222591.
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Genetic recombination: genetic, physical, and biochemical aspects.

Science (New York, N.Y.)

Skalka A, Weissbach A, Bartl P.
PMID: 17789228
Science. 1974 Mar 22;183(4130):1218-9. doi: 10.1126/science.183.4130.1218.

No abstract available.

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Skalka A, Weissbach A, Bartl P. Genetic recombination: genetic, physical, and biochemical aspects. Science. 1974;183(4130):1218-9doi: 10.1126/science.183.4130.1218.
Skalka, A., Weissbach, A., & Bartl, P. (1974). Genetic recombination: genetic, physical, and biochemical aspects. Science (New York, N.Y.), 183(4130), 1218-9. https://doi.org/10.1126/science.183.4130.1218
Skalka, A, et al. "Genetic recombination: genetic, physical, and biochemical aspects." Science (New York, N.Y.) vol. 183,4130 (1974): 1218-9. doi: https://doi.org/10.1126/science.183.4130.1218
Skalka A, Weissbach A, Bartl P. Genetic recombination: genetic, physical, and biochemical aspects. Science. 1974 Mar 22;183(4130):1218-9. doi: 10.1126/science.183.4130.1218. PMID: 17789228.
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ELNES study of chemical solution deposited SrO(SrTiO(3))(n) Ruddlesden-Popper films: experiment and simulation.

Ultramicroscopy

Riedl T, Gemming T, Weissbach T, Seifert G, Gutmann E, Zschornak M, Meyer DC, Gemming S.
PMID: 19818559
Ultramicroscopy. 2009 Dec;110(1):26-32. doi: 10.1016/j.ultramic.2009.09.001. Epub 2009 Sep 17.

This article analyzes electron energy-loss near-edge fine structures of the SrO(SrTiO(3))(n=1) Ruddlesden-Popper system and of the parent compounds SrTiO(3) and SrO by comparison with first principles calculations. For that, the fine structures of chemical solution deposited Ruddlesden-Popper films have...

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Riedl T, Gemming T, Weissbach T, et al. ELNES study of chemical solution deposited SrO(SrTiO(3))(n) Ruddlesden-Popper films: experiment and simulation. Ultramicroscopy. 2009;110(1):26-32doi: 10.1016/j.ultramic.2009.09.001.
Riedl, T., Gemming, T., Weissbach, T., Seifert, G., Gutmann, E., Zschornak, M., Meyer, D. C., & Gemming, S. (2009). ELNES study of chemical solution deposited SrO(SrTiO(3))(n) Ruddlesden-Popper films: experiment and simulation. Ultramicroscopy, 110(1), 26-32. https://doi.org/10.1016/j.ultramic.2009.09.001
Riedl, T, et al. "ELNES study of chemical solution deposited SrO(SrTiO(3))(n) Ruddlesden-Popper films: experiment and simulation." Ultramicroscopy vol. 110,1 (2009): 26-32. doi: https://doi.org/10.1016/j.ultramic.2009.09.001
Riedl T, Gemming T, Weissbach T, Seifert G, Gutmann E, Zschornak M, Meyer DC, Gemming S. ELNES study of chemical solution deposited SrO(SrTiO(3))(n) Ruddlesden-Popper films: experiment and simulation. Ultramicroscopy. 2009 Dec;110(1):26-32. doi: 10.1016/j.ultramic.2009.09.001. Epub 2009 Sep 17. PMID: 19818559.
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Chloroplast DNA synthesis in light and dark grown cultured Nicotiana tabacum cells as determined by molecular hybridization.

Plant cell reports

Cannon G, Heinhorst S, Siedlecki J, Weissbach A.
PMID: 24253680
Plant Cell Rep. 1985 Apr;4(2):41-5. doi: 10.1007/BF00269202.

A simple method using molecular hybridization was devised to quantitatively measure chloroplast DNA synthesis in vivo. Total cellular DNA isolated from Nicotiana tabacum suspension cells, labeled with (3)H-thymidine, was hybridized to nitrocellulose membrane-bound cloned chloroplast DNA (ct DNA) fragments....

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Cannon G, Heinhorst S, Siedlecki J, et al. Chloroplast DNA synthesis in light and dark grown cultured Nicotiana tabacum cells as determined by molecular hybridization. Plant Cell Rep. 1985;4(2):41-5doi: 10.1007/BF00269202.
Cannon, G., Heinhorst, S., Siedlecki, J., & Weissbach, A. (1985). Chloroplast DNA synthesis in light and dark grown cultured Nicotiana tabacum cells as determined by molecular hybridization. Plant cell reports, 4(2), 41-5. https://doi.org/10.1007/BF00269202
Cannon, G, et al. "Chloroplast DNA synthesis in light and dark grown cultured Nicotiana tabacum cells as determined by molecular hybridization." Plant cell reports vol. 4,2 (1985): 41-5. doi: https://doi.org/10.1007/BF00269202
Cannon G, Heinhorst S, Siedlecki J, Weissbach A. Chloroplast DNA synthesis in light and dark grown cultured Nicotiana tabacum cells as determined by molecular hybridization. Plant Cell Rep. 1985 Apr;4(2):41-5. doi: 10.1007/BF00269202. PMID: 24253680.
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Sulfophenylated Terphenylene Copolymer Membranes and Ionomers.

ChemSusChem

Skalski TJG, Adamski M, Britton B, Schibli EM, Peckham TJ, Weissbach T, Moshisuki T, Lyonnard S, Frisken BJ, Holdcroft S.
PMID: 30251343
ChemSusChem. 2018 Dec 11;11(23):4033-4043. doi: 10.1002/cssc.201801965. Epub 2018 Nov 07.

The copolymerization of a prefunctionalized, tetrasulfonated oligophenylene monomer was investigated. The corresponding physical and electrochemical properties of the polymers were tuned by varying the ratio of hydrophobic to hydrophilic units within the polymers. Membranes prepared from these polymers possessed...

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Skalski TJG, Adamski M, Britton B, et al. Sulfophenylated Terphenylene Copolymer Membranes and Ionomers. ChemSusChem. 2018;11(23):4033-4043doi: 10.1002/cssc.201801965.
Skalski, T. J. G., Adamski, M., Britton, B., Schibli, E. M., Peckham, T. J., Weissbach, T., Moshisuki, T., Lyonnard, S., Frisken, B. J., & Holdcroft, S. (2018). Sulfophenylated Terphenylene Copolymer Membranes and Ionomers. ChemSusChem, 11(23), 4033-4043. https://doi.org/10.1002/cssc.201801965
Skalski, Thomas J G, et al. "Sulfophenylated Terphenylene Copolymer Membranes and Ionomers." ChemSusChem vol. 11,23 (2018): 4033-4043. doi: https://doi.org/10.1002/cssc.201801965
Skalski TJG, Adamski M, Britton B, Schibli EM, Peckham TJ, Weissbach T, Moshisuki T, Lyonnard S, Frisken BJ, Holdcroft S. Sulfophenylated Terphenylene Copolymer Membranes and Ionomers. ChemSusChem. 2018 Dec 11;11(23):4033-4043. doi: 10.1002/cssc.201801965. Epub 2018 Nov 07. PMID: 30251343.
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