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Localized lichen myxedematosus in childhood: what is the accurate diagnosis?.

International journal of dermatology

Fang X, Yang B, Zhou G, Zhang F.
PMID: 27667483
Int J Dermatol. 2017 Mar;56(3):333-336. doi: 10.1111/ijd.13429. Epub 2016 Sep 26.

No abstract available.

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Fang X, Yang B, Zhou G, et al. Localized lichen myxedematosus in childhood: what is the accurate diagnosis?. Int J Dermatol. 2016;56(3):333-336doi: 10.1111/ijd.13429.
Fang, X., Yang, B., Zhou, G., & Zhang, F. (2017). Localized lichen myxedematosus in childhood: what is the accurate diagnosis?. International journal of dermatology, 56(3), 333-336. https://doi.org/10.1111/ijd.13429
Fang, Xiangang, et al. "Localized lichen myxedematosus in childhood: what is the accurate diagnosis?." International journal of dermatology vol. 56,3 (2017): 333-336. doi: https://doi.org/10.1111/ijd.13429
Fang X, Yang B, Zhou G, Zhang F. Localized lichen myxedematosus in childhood: what is the accurate diagnosis?. Int J Dermatol. 2017 Mar;56(3):333-336. doi: 10.1111/ijd.13429. Epub 2016 Sep 26. PMID: 27667483.
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Abnormal topological organization in white matter structural networks in survivors of acute lymphoblastic leukaemia with chemotherapy treatment.

Oncotarget

Zou L, Su L, Qi R, Bao F, Fang X, Wang L, Zhai Z, Li D, Zheng S.
PMID: 28947994
Oncotarget. 2017 Jul 08;8(36):60568-60575. doi: 10.18632/oncotarget.19104. eCollection 2017 Sep 01.

Previous diffusion tensor imaging (DTI) studies have detected white matter (WM) integrity abnormalities in some specific fibre bundles in acute lymphoblastic leukaemia (ALL) patients with chemotherapy. However, little is known about the changes in the topological organization of the...

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Zou L, Su L, Qi R, et al. Abnormal topological organization in white matter structural networks in survivors of acute lymphoblastic leukaemia with chemotherapy treatment. Oncotarget. 2017;8(36):60568-60575doi: 10.18632/oncotarget.19104.
Zou, L., Su, L., Qi, R., Bao, F., Fang, X., Wang, L., Zhai, Z., Li, D., & Zheng, S. (2017). Abnormal topological organization in white matter structural networks in survivors of acute lymphoblastic leukaemia with chemotherapy treatment. Oncotarget, 8(36), 60568-60575. https://doi.org/10.18632/oncotarget.19104
Zou, Liwei, et al. "Abnormal topological organization in white matter structural networks in survivors of acute lymphoblastic leukaemia with chemotherapy treatment." Oncotarget vol. 8,36 (2017): 60568-60575. doi: https://doi.org/10.18632/oncotarget.19104
Zou L, Su L, Qi R, Bao F, Fang X, Wang L, Zhai Z, Li D, Zheng S. Abnormal topological organization in white matter structural networks in survivors of acute lymphoblastic leukaemia with chemotherapy treatment. Oncotarget. 2017 Jul 08;8(36):60568-60575. doi: 10.18632/oncotarget.19104. eCollection 2017 Sep 01. PMID: 28947994; PMCID: PMC5601162.
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Metal-Organic Framework for Emulsifying Carbon Dioxide and Water.

Angewandte Chemie (International ed. in English)

Liu C, Zhang J, Zheng L, Zhang J, Sang X, Kang X, Zhang B, Luo T, Tan X, Han B.
PMID: 27529754
Angew Chem Int Ed Engl. 2016 Sep 12;55(38):11372-6. doi: 10.1002/anie.201602150. Epub 2016 Aug 16.

Forming emulsions of carbon dioxide (CO2 ) and water can largely expand the utility of CO2 . Herein we propose for the first time the utilization of a metal-organic framework (MOF) for emulsifying CO2 and water. Owing to the...

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Liu C, Zhang J, Zheng L, et al. Metal-Organic Framework for Emulsifying Carbon Dioxide and Water. Angew Chem Int Ed Engl. 2016;55(38):11372-6doi: 10.1002/anie.201602150.
Liu, C., Zhang, J., Zheng, L., Zhang, J., Sang, X., Kang, X., Zhang, B., Luo, T., Tan, X., & Han, B. (2016). Metal-Organic Framework for Emulsifying Carbon Dioxide and Water. Angewandte Chemie (International ed. in English), 55(38), 11372-6. https://doi.org/10.1002/anie.201602150
Liu, Chengcheng, et al. "Metal-Organic Framework for Emulsifying Carbon Dioxide and Water." Angewandte Chemie (International ed. in English) vol. 55,38 (2016): 11372-6. doi: https://doi.org/10.1002/anie.201602150
Liu C, Zhang J, Zheng L, Zhang J, Sang X, Kang X, Zhang B, Luo T, Tan X, Han B. Metal-Organic Framework for Emulsifying Carbon Dioxide and Water. Angew Chem Int Ed Engl. 2016 Sep 12;55(38):11372-6. doi: 10.1002/anie.201602150. Epub 2016 Aug 16. PMID: 27529754.
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Credible evidence for the passivation effect of remnant PbI₂ in CH₃NHCH₃PbICH₃ films in improving the performance of perovskite solar cells.

Nanoscale

Wang S, Dong W, Fang X, Zhang Q, Zhou S, Deng Z, Tao R, Shao J, Xia R, Song C, Hu L, Zhu J.
PMID: 26939835
Nanoscale. 2016 Mar 28;8(12):6600-8. doi: 10.1039/c5nr08344c.

The role of remnant PbI2 in CH3NH3PbI3 films is still controversial, some investigations have revealed that the remnant PbI2 plays a passivation role, reduces the charge recombination in perovskite solar cells (PSCs), and improves the performance of PSCs, but...

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Wang S, Dong W, Fang X, et al. Credible evidence for the passivation effect of remnant PbI₂ in CH₃NHCH₃PbICH₃ films in improving the performance of perovskite solar cells. Nanoscale. 2016;8(12):6600-8doi: 10.1039/c5nr08344c.
Wang, S., Dong, W., Fang, X., Zhang, Q., Zhou, S., Deng, Z., Tao, R., Shao, J., Xia, R., Song, C., Hu, L., & Zhu, J. (2016). Credible evidence for the passivation effect of remnant PbI₂ in CH₃NHCH₃PbICH₃ films in improving the performance of perovskite solar cells. Nanoscale, 8(12), 6600-8. https://doi.org/10.1039/c5nr08344c
Wang, Shimao, et al. "Credible evidence for the passivation effect of remnant PbI₂ in CH₃NHCH₃PbICH₃ films in improving the performance of perovskite solar cells." Nanoscale vol. 8,12 (2016): 6600-8. doi: https://doi.org/10.1039/c5nr08344c
Wang S, Dong W, Fang X, Zhang Q, Zhou S, Deng Z, Tao R, Shao J, Xia R, Song C, Hu L, Zhu J. Credible evidence for the passivation effect of remnant PbI₂ in CH₃NHCH₃PbICH₃ films in improving the performance of perovskite solar cells. Nanoscale. 2016 Mar 28;8(12):6600-8. doi: 10.1039/c5nr08344c. PMID: 26939835.
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'Crystal Genes' in Metallic Liquids and Glasses.

Scientific reports

Sun Y, Zhang F, Ye Z, Zhang Y, Fang X, Ding Z, Wang CZ, Mendelev MI, Ott RT, Kramer MJ, Ho KM.
PMID: 27030071
Sci Rep. 2016 Mar 31;6:23734. doi: 10.1038/srep23734.

We analyze the underlying structural order that transcends liquid, glass and crystalline states in metallic systems. A genetic algorithm is applied to search for the most common energetically favorable packing motifs in crystalline structures. These motifs are in turn...

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Sun Y, Zhang F, Ye Z, et al. 'Crystal Genes' in Metallic Liquids and Glasses. Sci Rep. 2016;6:23734doi: 10.1038/srep23734.
Sun, Y., Zhang, F., Ye, Z., Zhang, Y., Fang, X., Ding, Z., Wang, C. Z., Mendelev, M. I., Ott, R. T., Kramer, M. J., & Ho, K. M. (2016). 'Crystal Genes' in Metallic Liquids and Glasses. Scientific reports, 623734. https://doi.org/10.1038/srep23734
Sun, Yang, et al. "'Crystal Genes' in Metallic Liquids and Glasses." Scientific reports vol. 6 (2016): 23734. doi: https://doi.org/10.1038/srep23734
Sun Y, Zhang F, Ye Z, Zhang Y, Fang X, Ding Z, Wang CZ, Mendelev MI, Ott RT, Kramer MJ, Ho KM. 'Crystal Genes' in Metallic Liquids and Glasses. Sci Rep. 2016 Mar 31;6:23734. doi: 10.1038/srep23734. PMID: 27030071; PMCID: PMC4814814.
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Crystal structure of bis-[tetra-kis-(tri-phenyl-phosphane-κP)silver(I)] (nitrilo-tri-acetato-κ(4) N,O,O',O'')(tri-phenyl-phosphane-κP)argentate(I) with an unknown amount of methanol as solvate.

Acta crystallographica. Section E, Crystallographic communications

Noll J, Korb M, Lang H.
PMID: 27006796
Acta Crystallogr E Crystallogr Commun. 2016 Feb 10;72:318-21. doi: 10.1107/S2056989016001262. eCollection 2016 Mar 01.

The structure of the title compound, [Ag(C18H15P)4]2[Ag(C6H6NO6)(C18H15P)], exhibits trigonal (P-3) symmetry, with a C 3 axis through all three complex ions, resulting in an asymmetric unit that contains one third of the atoms present in the formula unit. The...

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Noll J, Korb M, Lang H. Crystal structure of bis-[tetra-kis-(tri-phenyl-phosphane-κP)silver(I)] (nitrilo-tri-acetato-κ(4) N,O,O',O'')(tri-phenyl-phosphane-κP)argentate(I) with an unknown amount of methanol as solvate. Acta Crystallogr E Crystallogr Commun. 2016;72:318-21doi: 10.1107/S2056989016001262.
Noll, J., Korb, M., & Lang, H. (2016). Crystal structure of bis-[tetra-kis-(tri-phenyl-phosphane-κP)silver(I)] (nitrilo-tri-acetato-κ(4) N,O,O',O'')(tri-phenyl-phosphane-κP)argentate(I) with an unknown amount of methanol as solvate. Acta crystallographica. Section E, Crystallographic communications, 72318-21. https://doi.org/10.1107/S2056989016001262
Noll, Julian, et al. "Crystal structure of bis-[tetra-kis-(tri-phenyl-phosphane-κP)silver(I)] (nitrilo-tri-acetato-κ(4) N,O,O',O'')(tri-phenyl-phosphane-κP)argentate(I) with an unknown amount of methanol as solvate." Acta crystallographica. Section E, Crystallographic communications vol. 72 (2016): 318-21. doi: https://doi.org/10.1107/S2056989016001262
Noll J, Korb M, Lang H. Crystal structure of bis-[tetra-kis-(tri-phenyl-phosphane-κP)silver(I)] (nitrilo-tri-acetato-κ(4) N,O,O',O'')(tri-phenyl-phosphane-κP)argentate(I) with an unknown amount of methanol as solvate. Acta Crystallogr E Crystallogr Commun. 2016 Feb 10;72:318-21. doi: 10.1107/S2056989016001262. eCollection 2016 Mar 01. PMID: 27006796; PMCID: PMC4778820.
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Enantioselective Synthesis of 1,2-Dihydronaphthalenes via Oxidative N-Heterocyclic Carbene Catalysis.

Organic letters

Perveen S, Zhao Z, Zhang G, Liu J, Anwar M, Fang X.
PMID: 28485600
Org Lett. 2017 May 19;19(10):2470-2473. doi: 10.1021/acs.orglett.7b00555. Epub 2017 May 09.

1,2-Dihydronaphthalenes are important molecules in both medicinal and synthetic chemistry, but methods for the catalytic asymmetric construction of this class of molecules are limited. The diastereo- and enantioselective N-heterocyclic carbene-catalyzed cascade annulation reactions using benzodiketones and enals under oxidative...

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Perveen S, Zhao Z, Zhang G, et al. Enantioselective Synthesis of 1,2-Dihydronaphthalenes via Oxidative N-Heterocyclic Carbene Catalysis. Org Lett. 2017;19(10):2470-2473doi: 10.1021/acs.orglett.7b00555.
Perveen, S., Zhao, Z., Zhang, G., Liu, J., Anwar, M., & Fang, X. (2017). Enantioselective Synthesis of 1,2-Dihydronaphthalenes via Oxidative N-Heterocyclic Carbene Catalysis. Organic letters, 19(10), 2470-2473. https://doi.org/10.1021/acs.orglett.7b00555
Perveen, Saima, et al. "Enantioselective Synthesis of 1,2-Dihydronaphthalenes via Oxidative N-Heterocyclic Carbene Catalysis." Organic letters vol. 19,10 (2017): 2470-2473. doi: https://doi.org/10.1021/acs.orglett.7b00555
Perveen S, Zhao Z, Zhang G, Liu J, Anwar M, Fang X. Enantioselective Synthesis of 1,2-Dihydronaphthalenes via Oxidative N-Heterocyclic Carbene Catalysis. Org Lett. 2017 May 19;19(10):2470-2473. doi: 10.1021/acs.orglett.7b00555. Epub 2017 May 09. PMID: 28485600.
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Mucosal and Systemic Immune Responses to Influenza H7N9 Antigen HA1-2 Co-Delivered Intranasally with Flagellin or Polyethyleneimine in Mice and Chickens.

Frontiers in immunology

Song L, Xiong D, Song H, Wu L, Zhang M, Kang X, Pan Z, Jiao X.
PMID: 28424686
Front Immunol. 2017 Apr 05;8:326. doi: 10.3389/fimmu.2017.00326. eCollection 2017.

Consecutive cases of human infection with H7N9 influenza viruses since 2013 in China have prompted efforts to develop an effective treatment. Subunit vaccines introduced by intranasal administration can block an infection at its primary site; flagellin (fliC) and polyethyleneimine...

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Song L, Xiong D, Song H, et al. Mucosal and Systemic Immune Responses to Influenza H7N9 Antigen HA1-2 Co-Delivered Intranasally with Flagellin or Polyethyleneimine in Mice and Chickens. Front Immunol. 2017;8:326doi: 10.3389/fimmu.2017.00326.
Song, L., Xiong, D., Song, H., Wu, L., Zhang, M., Kang, X., Pan, Z., & Jiao, X. (2017). Mucosal and Systemic Immune Responses to Influenza H7N9 Antigen HA1-2 Co-Delivered Intranasally with Flagellin or Polyethyleneimine in Mice and Chickens. Frontiers in immunology, 8326. https://doi.org/10.3389/fimmu.2017.00326
Song, Li, et al. "Mucosal and Systemic Immune Responses to Influenza H7N9 Antigen HA1-2 Co-Delivered Intranasally with Flagellin or Polyethyleneimine in Mice and Chickens." Frontiers in immunology vol. 8 (2017): 326. doi: https://doi.org/10.3389/fimmu.2017.00326
Song L, Xiong D, Song H, Wu L, Zhang M, Kang X, Pan Z, Jiao X. Mucosal and Systemic Immune Responses to Influenza H7N9 Antigen HA1-2 Co-Delivered Intranasally with Flagellin or Polyethyleneimine in Mice and Chickens. Front Immunol. 2017 Apr 05;8:326. doi: 10.3389/fimmu.2017.00326. eCollection 2017. PMID: 28424686; PMCID: PMC5380672.
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Mono-, di- and tetrarhenium Fischer carbene complexes with thienothiophene substituents.

Dalton transactions (Cambridge, England : 2003)

Lamprecht Z, Radhakrishnan SG, Hildebrandt A, Lang H, Liles DC, Weststrate NA, Lotz S, Bezuidenhout DI.
PMID: 28975955
Dalton Trans. 2017 Oct 17;46(40):13983-13993. doi: 10.1039/c7dt02969a.

The oxidative cleaving of a rhenium-rhenium bond by bromine in binuclear Fischer carbene complexes proves to be an effective method to prepare mononuclear bromido-carbene complexes. The reaction of mono- and dilithiated thieno[2,3-b]thiophene (2,3-b-TTH

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Lamprecht Z, Radhakrishnan SG, Hildebrandt A, et al. Mono-, di- and tetrarhenium Fischer carbene complexes with thienothiophene substituents. Dalton Trans. 2017;46(40):13983-13993doi: 10.1039/c7dt02969a.
Lamprecht, Z., Radhakrishnan, S. G., Hildebrandt, A., Lang, H., Liles, D. C., Weststrate, N. A., Lotz, S., & Bezuidenhout, D. I. (2017). Mono-, di- and tetrarhenium Fischer carbene complexes with thienothiophene substituents. Dalton transactions (Cambridge, England : 2003), 46(40), 13983-13993. https://doi.org/10.1039/c7dt02969a
Lamprecht, Zandria, et al. "Mono-, di- and tetrarhenium Fischer carbene complexes with thienothiophene substituents." Dalton transactions (Cambridge, England : 2003) vol. 46,40 (2017): 13983-13993. doi: https://doi.org/10.1039/c7dt02969a
Lamprecht Z, Radhakrishnan SG, Hildebrandt A, Lang H, Liles DC, Weststrate NA, Lotz S, Bezuidenhout DI. Mono-, di- and tetrarhenium Fischer carbene complexes with thienothiophene substituents. Dalton Trans. 2017 Oct 17;46(40):13983-13993. doi: 10.1039/c7dt02969a. PMID: 28975955.
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Tricyanomethane and Its Ketenimine Tautomer: Generation from Different Precursors and Analysis in Solution, Argon Matrix, and as a Single Crystal.

Angewandte Chemie (International ed. in English)

Banert K, Chityala M, Hagedorn M, Beckers H, Stüker T, Riedel S, Rüffer T, Lang H.
PMID: 28510284
Angew Chem Int Ed Engl. 2017 Aug 01;56(32):9582-9586. doi: 10.1002/anie.201704561. Epub 2017 Jun 22.

Solutions of azidomethylidenemalononitrile were photolyzed at low temperatures to produce the corresponding 2H-azirine and tricyanomethane, which were analyzed by low-temperature NMR spectroscopy. The latter product was also observed after short thermolysis of the azide precursor in solution whereas irradiation...

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Banert K, Chityala M, Hagedorn M, et al. Tricyanomethane and Its Ketenimine Tautomer: Generation from Different Precursors and Analysis in Solution, Argon Matrix, and as a Single Crystal. Angew Chem Int Ed Engl. 2017;56(32):9582-9586doi: 10.1002/anie.201704561.
Banert, K., Chityala, M., Hagedorn, M., Beckers, H., Stüker, T., Riedel, S., Rüffer, T., & Lang, H. (2017). Tricyanomethane and Its Ketenimine Tautomer: Generation from Different Precursors and Analysis in Solution, Argon Matrix, and as a Single Crystal. Angewandte Chemie (International ed. in English), 56(32), 9582-9586. https://doi.org/10.1002/anie.201704561
Banert, Klaus, et al. "Tricyanomethane and Its Ketenimine Tautomer: Generation from Different Precursors and Analysis in Solution, Argon Matrix, and as a Single Crystal." Angewandte Chemie (International ed. in English) vol. 56,32 (2017): 9582-9586. doi: https://doi.org/10.1002/anie.201704561
Banert K, Chityala M, Hagedorn M, Beckers H, Stüker T, Riedel S, Rüffer T, Lang H. Tricyanomethane and Its Ketenimine Tautomer: Generation from Different Precursors and Analysis in Solution, Argon Matrix, and as a Single Crystal. Angew Chem Int Ed Engl. 2017 Aug 01;56(32):9582-9586. doi: 10.1002/anie.201704561. Epub 2017 Jun 22. PMID: 28510284.
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Structure and Reactivity of X-ray Amorphous Uranyl Peroxide, U2O7.

Inorganic chemistry

Odoh SO, Shamblin J, Colla CA, Hickam S, Lobeck HL, Lopez RA, Olds T, Szymanowski JE, Sigmon GE, Neuefeind J, Casey WH, Lang M, Gagliardi L, Burns PC.
PMID: 26974702
Inorg Chem. 2016 Apr 04;55(7):3541-6. doi: 10.1021/acs.inorgchem.6b00017. Epub 2016 Mar 14.

Recent accidents resulting in worker injury and radioactive contamination occurred due to pressurization of uranium yellowcake drums produced in the western U.S.A. The drums contained an X-ray amorphous reactive form of uranium oxide that may have contributed to the...

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Odoh SO, Shamblin J, Colla CA, et al. Structure and Reactivity of X-ray Amorphous Uranyl Peroxide, U2O7. Inorg Chem. 2016;55(7):3541-6doi: 10.1021/acs.inorgchem.6b00017.
Odoh, S. O., Shamblin, J., Colla, C. A., Hickam, S., Lobeck, H. L., Lopez, R. A., Olds, T., Szymanowski, J. E., Sigmon, G. E., Neuefeind, J., Casey, W. H., Lang, M., Gagliardi, L., & Burns, P. C. (2016). Structure and Reactivity of X-ray Amorphous Uranyl Peroxide, U2O7. Inorganic chemistry, 55(7), 3541-6. https://doi.org/10.1021/acs.inorgchem.6b00017
Odoh, Samuel O, et al. "Structure and Reactivity of X-ray Amorphous Uranyl Peroxide, U2O7." Inorganic chemistry vol. 55,7 (2016): 3541-6. doi: https://doi.org/10.1021/acs.inorgchem.6b00017
Odoh SO, Shamblin J, Colla CA, Hickam S, Lobeck HL, Lopez RA, Olds T, Szymanowski JE, Sigmon GE, Neuefeind J, Casey WH, Lang M, Gagliardi L, Burns PC. Structure and Reactivity of X-ray Amorphous Uranyl Peroxide, U2O7. Inorg Chem. 2016 Apr 04;55(7):3541-6. doi: 10.1021/acs.inorgchem.6b00017. Epub 2016 Mar 14. PMID: 26974702.
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Benzylic Functionalization of Anthrones via the Asymmetric Ring Opening of Oxabicycles Utilizing a Fourth-Generation Rhodium Catalytic System.

Chemistry (Weinheim an der Bergstrasse, Germany)

Loh CC, Fang X, Peters B, Lautens M.
PMID: 26310604
Chemistry. 2015 Sep 28;21(40):13883-7. doi: 10.1002/chem.201502718. Epub 2015 Aug 27.

While anthrones exist as privileged scaffolds in bioactive molecules, the enantioselective functionalization of anthrones is surprisingly scarce in the literature, with no asymmetric transition metal catalyzed example to date. Herein, we report the first asymmetric transition metal catalyzed benzylic...

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Loh CC, Fang X, Peters B, et al. Benzylic Functionalization of Anthrones via the Asymmetric Ring Opening of Oxabicycles Utilizing a Fourth-Generation Rhodium Catalytic System. Chemistry. 2015;21(40):13883-7doi: 10.1002/chem.201502718.
Loh, C. C., Fang, X., Peters, B., & Lautens, M. (2015). Benzylic Functionalization of Anthrones via the Asymmetric Ring Opening of Oxabicycles Utilizing a Fourth-Generation Rhodium Catalytic System. Chemistry (Weinheim an der Bergstrasse, Germany), 21(40), 13883-7. https://doi.org/10.1002/chem.201502718
Loh, Charles C J, et al. "Benzylic Functionalization of Anthrones via the Asymmetric Ring Opening of Oxabicycles Utilizing a Fourth-Generation Rhodium Catalytic System." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,40 (2015): 13883-7. doi: https://doi.org/10.1002/chem.201502718
Loh CC, Fang X, Peters B, Lautens M. Benzylic Functionalization of Anthrones via the Asymmetric Ring Opening of Oxabicycles Utilizing a Fourth-Generation Rhodium Catalytic System. Chemistry. 2015 Sep 28;21(40):13883-7. doi: 10.1002/chem.201502718. Epub 2015 Aug 27. PMID: 26310604.
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