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Automated integrative high-throughput phenotyping of plant shoots: a case study of the cold-tolerance of pea (Pisum sativum L.).

Plant methods

Humplík JF, Lazár D, Fürst T, Husičková A, Hýbl M, Spíchal L.
PMID: 25798184
Plant Methods. 2015 Mar 19;11:20. doi: 10.1186/s13007-015-0063-9. eCollection 2015.

BACKGROUND: Recently emerging approaches to high-throughput plant phenotyping have discovered their importance as tools in unravelling the complex questions of plant growth, development and response to the environment, both in basic and applied science. High-throughput methods have been also...

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Humplík JF, Lazár D, Fürst T, et al. Automated integrative high-throughput phenotyping of plant shoots: a case study of the cold-tolerance of pea (Pisum sativum L.). Plant Methods. 2015;11:20doi: 10.1186/s13007-015-0063-9.
Humplík, J. F., Lazár, D., Fürst, T., Husičková, A., Hýbl, M., & Spíchal, L. (2015). Automated integrative high-throughput phenotyping of plant shoots: a case study of the cold-tolerance of pea (Pisum sativum L.). Plant methods, 1120. https://doi.org/10.1186/s13007-015-0063-9
Humplík, Jan F, et al. "Automated integrative high-throughput phenotyping of plant shoots: a case study of the cold-tolerance of pea (Pisum sativum L.)." Plant methods vol. 11 (2015): 20. doi: https://doi.org/10.1186/s13007-015-0063-9
Humplík JF, Lazár D, Fürst T, Husičková A, Hýbl M, Spíchal L. Automated integrative high-throughput phenotyping of plant shoots: a case study of the cold-tolerance of pea (Pisum sativum L.). Plant Methods. 2015 Mar 19;11:20. doi: 10.1186/s13007-015-0063-9. eCollection 2015. PMID: 25798184; PMCID: PMC4369061.
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Bis(mesitoyl)phosphinic acid: photo-triggered release of metaphosphorous acid in solution.

Chemical communications (Cambridge, England)

Fast DE, Zalibera M, Lauer A, Eibel A, Schweigert C, Kelterer AM, Spichty M, Neshchadin D, Voll D, Ernst H, Liang Y, Dietliker K, Unterreiner AN, Barner-Kowollik C, Grützmacher H, Gescheidt G.
PMID: 27431207
Chem Commun (Camb). 2016 Aug 02;52(64):9917-20. doi: 10.1039/c6cc05219c.

Bis(mesitoyl)phosphinic acid and its sodium salt display a unique photo-induced reactivity: both derivatives stepwise release two mesitoyl radicals and, remarkably, metaphosphorous acid (previously postulated as transient species in the gas phase), providing a new phosphorus-based reagent.

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Fast DE, Zalibera M, Lauer A, et al. Bis(mesitoyl)phosphinic acid: photo-triggered release of metaphosphorous acid in solution. Chem Commun (Camb). 2016;52(64):9917-20doi: 10.1039/c6cc05219c.
Fast, D. E., Zalibera, M., Lauer, A., Eibel, A., Schweigert, C., Kelterer, A. M., Spichty, M., Neshchadin, D., Voll, D., Ernst, H., Liang, Y., Dietliker, K., Unterreiner, A. N., Barner-Kowollik, C., Grützmacher, H., & Gescheidt, G. (2016). Bis(mesitoyl)phosphinic acid: photo-triggered release of metaphosphorous acid in solution. Chemical communications (Cambridge, England), 52(64), 9917-20. https://doi.org/10.1039/c6cc05219c
Fast, David E, et al. "Bis(mesitoyl)phosphinic acid: photo-triggered release of metaphosphorous acid in solution." Chemical communications (Cambridge, England) vol. 52,64 (2016): 9917-20. doi: https://doi.org/10.1039/c6cc05219c
Fast DE, Zalibera M, Lauer A, Eibel A, Schweigert C, Kelterer AM, Spichty M, Neshchadin D, Voll D, Ernst H, Liang Y, Dietliker K, Unterreiner AN, Barner-Kowollik C, Grützmacher H, Gescheidt G. Bis(mesitoyl)phosphinic acid: photo-triggered release of metaphosphorous acid in solution. Chem Commun (Camb). 2016 Aug 02;52(64):9917-20. doi: 10.1039/c6cc05219c. PMID: 27431207.
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The Emerging Role of the Cytoskeleton in Chromosome Dynamics.

Frontiers in genetics

Spichal M, Fabre E.
PMID: 28580009
Front Genet. 2017 May 19;8:60. doi: 10.3389/fgene.2017.00060. eCollection 2017.

Chromosomes underlie a dynamic organization that fulfills functional roles in processes like transcription, DNA repair, nuclear envelope stability, and cell division. Chromosome dynamics depend on chromosome structure and cannot freely diffuse. Furthermore, chromosomes interact closely with their surrounding nuclear...

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Spichal M, Fabre E. The Emerging Role of the Cytoskeleton in Chromosome Dynamics. Front Genet. 2017;8:60doi: 10.3389/fgene.2017.00060.
Spichal, M., & Fabre, E. (2017). The Emerging Role of the Cytoskeleton in Chromosome Dynamics. Frontiers in genetics, 860. https://doi.org/10.3389/fgene.2017.00060
Spichal, Maya, and Fabre, Emmanuelle. "The Emerging Role of the Cytoskeleton in Chromosome Dynamics." Frontiers in genetics vol. 8 (2017): 60. doi: https://doi.org/10.3389/fgene.2017.00060
Spichal M, Fabre E. The Emerging Role of the Cytoskeleton in Chromosome Dynamics. Front Genet. 2017 May 19;8:60. doi: 10.3389/fgene.2017.00060. eCollection 2017. PMID: 28580009; PMCID: PMC5437106.
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Correlation of nanoscale behaviour of forces and macroscale surface wettability.

Nanoscale

Rana A, Patra A, Annamalai M, Srivastava A, Ghosh S, Stoerzinger K, Lee YL, Prakash S, Jueyuan RY, Goohpattader PS, Satyanarayana N, Gopinadhan K, Dykas MM, Poddar K, Saha S, Sarkar T, Kumar B, Bhatia CS, Giordano L, Shao-Horn Y, Venkatesan T.
PMID: 27510557
Nanoscale. 2016 Aug 25;8(34):15597-603. doi: 10.1039/c6nr02076c.

In this manuscript, we demonstrate a method based on atomic force microscopy which enables local probing of surface wettability. The maximum pull-off force, obtained from force spectroscopy shows a remarkable correlation with the macroscopically observed water contact angle, measured...

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Rana A, Patra A, Annamalai M, et al. Correlation of nanoscale behaviour of forces and macroscale surface wettability. Nanoscale. 2016;8(34):15597-603doi: 10.1039/c6nr02076c.
Rana, A., Patra, A., Annamalai, M., Srivastava, A., Ghosh, S., Stoerzinger, K., Lee, Y. L., Prakash, S., Jueyuan, R. Y., Goohpattader, P. S., Satyanarayana, N., Gopinadhan, K., Dykas, M. M., Poddar, K., Saha, S., Sarkar, T., Kumar, B., Bhatia, C. S., Giordano, L., Shao-Horn, Y., & Venkatesan, T. (2016). Correlation of nanoscale behaviour of forces and macroscale surface wettability. Nanoscale, 8(34), 15597-603. https://doi.org/10.1039/c6nr02076c
Rana, Abhimanyu, et al. "Correlation of nanoscale behaviour of forces and macroscale surface wettability." Nanoscale vol. 8,34 (2016): 15597-603. doi: https://doi.org/10.1039/c6nr02076c
Rana A, Patra A, Annamalai M, Srivastava A, Ghosh S, Stoerzinger K, Lee YL, Prakash S, Jueyuan RY, Goohpattader PS, Satyanarayana N, Gopinadhan K, Dykas MM, Poddar K, Saha S, Sarkar T, Kumar B, Bhatia CS, Giordano L, Shao-Horn Y, Venkatesan T. Correlation of nanoscale behaviour of forces and macroscale surface wettability. Nanoscale. 2016 Aug 25;8(34):15597-603. doi: 10.1039/c6nr02076c. PMID: 27510557.
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Carbanions Substituted by Transition Metals: Synthesis, Structure, and Configurational Restrictions of a Lithium Titanium Phosphonate.

Angewandte Chemie (International ed. in English)

Müller JF, Kulicke KJ, Neuburger M, Spichty M.
PMID: 11500899
Angew Chem Int Ed Engl. 2001 Aug 03;40(15):2890-2893. doi: 10.1002/1521-3773(20010803)40:15<2890::aid-anie2890>3.0.co;2-t.

No abstract available.

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Müller JF, Kulicke KJ, Neuburger M, et al. Carbanions Substituted by Transition Metals: Synthesis, Structure, and Configurational Restrictions of a Lithium Titanium Phosphonate. Angew Chem Int Ed Engl. 2001;40(15):2890-2893doi: 10.1002/1521-3773(20010803)40:15<2890::aid-anie2890>3.0.co;2-t.
Müller, J. F., Kulicke, K. J., Neuburger, M., & Spichty, M. (2001). Carbanions Substituted by Transition Metals: Synthesis, Structure, and Configurational Restrictions of a Lithium Titanium Phosphonate. Angewandte Chemie (International ed. in English), 40(15), 2890-2893. https://doi.org/10.1002/1521-3773(20010803)40:15<2890::aid-anie2890>3.0.co;2-t
Müller, Jürgen F. K., et al. "Carbanions Substituted by Transition Metals: Synthesis, Structure, and Configurational Restrictions of a Lithium Titanium Phosphonate." Angewandte Chemie (International ed. in English) vol. 40,15 (2001): 2890-2893. doi: https://doi.org/10.1002/1521-3773(20010803)40:15<2890::aid-anie2890>3.0.co;2-t
Müller JF, Kulicke KJ, Neuburger M, Spichty M. Carbanions Substituted by Transition Metals: Synthesis, Structure, and Configurational Restrictions of a Lithium Titanium Phosphonate. Angew Chem Int Ed Engl. 2001 Aug 03;40(15):2890-2893. doi: 10.1002/1521-3773(20010803)40:15<2890::aid-anie2890>3.0.co;2-t. PMID: 11500899.
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Hyalinized Uterine Mesenchymal Neoplasms with HMB-45-Positive Epithelioid Cells: Epithelioid Leiomyomas or Angiomyolipomas? Report of Four Cases.

International journal of surgical pathology

Michal M, Zamecnik M.
PMID: 11494009
Int J Surg Pathol. 2000 Oct;8(4):323-328. doi: 10.1177/106689690000800411.

We present 4 cases of uterine mesenchymal tumors that were located mostly in the myometrium in middle-aged women. Grossly the tumors vaguely resembled conventional leiomyomas. All tumors were extremely hyalinized. The tumor cells were remarkable because of their large...

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Michal M, Zamecnik M. Hyalinized Uterine Mesenchymal Neoplasms with HMB-45-Positive Epithelioid Cells: Epithelioid Leiomyomas or Angiomyolipomas? Report of Four Cases. Int J Surg Pathol. 2000;8(4):323-328doi: 10.1177/106689690000800411.
Michal, M., & Zamecnik, M. (2000). Hyalinized Uterine Mesenchymal Neoplasms with HMB-45-Positive Epithelioid Cells: Epithelioid Leiomyomas or Angiomyolipomas? Report of Four Cases. International journal of surgical pathology, 8(4), 323-328. https://doi.org/10.1177/106689690000800411
Michal, Michal, and Zamecnik, Michal. "Hyalinized Uterine Mesenchymal Neoplasms with HMB-45-Positive Epithelioid Cells: Epithelioid Leiomyomas or Angiomyolipomas? Report of Four Cases." International journal of surgical pathology vol. 8,4 (2000): 323-328. doi: https://doi.org/10.1177/106689690000800411
Michal M, Zamecnik M. Hyalinized Uterine Mesenchymal Neoplasms with HMB-45-Positive Epithelioid Cells: Epithelioid Leiomyomas or Angiomyolipomas? Report of Four Cases. Int J Surg Pathol. 2000 Oct;8(4):323-328. doi: 10.1177/106689690000800411. PMID: 11494009.
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Dimers of fluorinated methanes with carbonyl sulfide: the rotational spectrum and structure of difluoromethane-OCS.

The journal of physical chemistry. A

Serafin MM, Peebles SA.
PMID: 19007143
J Phys Chem A. 2008 Dec 11;112(49):12616-21. doi: 10.1021/jp8072393.

The pure rotational spectra of four isotopologues of the difluoromethane-carbonyl sulfide dimer have been measured in the 5-15 GHz region with use of pulsed-nozzle Fourier-transform microwave spectroscopy. The complex was determined to possess an ab plane of symmetry with...

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Serafin MM, Peebles SA. Dimers of fluorinated methanes with carbonyl sulfide: the rotational spectrum and structure of difluoromethane-OCS. J Phys Chem A. 2008;112(49):12616-21doi: 10.1021/jp8072393.
Serafin, M. M., & Peebles, S. A. (2008). Dimers of fluorinated methanes with carbonyl sulfide: the rotational spectrum and structure of difluoromethane-OCS. The journal of physical chemistry. A, 112(49), 12616-21. https://doi.org/10.1021/jp8072393
Serafin, Michal M, and Peebles, Sean A. "Dimers of fluorinated methanes with carbonyl sulfide: the rotational spectrum and structure of difluoromethane-OCS." The journal of physical chemistry. A vol. 112,49 (2008): 12616-21. doi: https://doi.org/10.1021/jp8072393
Serafin MM, Peebles SA. Dimers of fluorinated methanes with carbonyl sulfide: the rotational spectrum and structure of difluoromethane-OCS. J Phys Chem A. 2008 Dec 11;112(49):12616-21. doi: 10.1021/jp8072393. PMID: 19007143.
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Rotational spectrum of the dimethyl ether-acetylene complex: evidence for an effective C2v geometry.

The journal of physical chemistry. A

Newby JJ, Serafin MM, Peebles RA, Peebles SA.
PMID: 16839055
J Phys Chem A. 2005 Jun 23;109(24):5316-22. doi: 10.1021/jp0507593.

The rotational spectra for five isotopomers of the 1:1 weakly bound complex formed between dimethyl ether (DME) and acetylene (HCCH) have been measured by Fourier transform microwave spectroscopy. The experimental rotational constants, planar moments, and dipole moment components are...

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Newby JJ, Serafin MM, Peebles RA, et al. Rotational spectrum of the dimethyl ether-acetylene complex: evidence for an effective C2v geometry. J Phys Chem A. 2005;109(24):5316-22doi: 10.1021/jp0507593.
Newby, J. J., Serafin, M. M., Peebles, R. A., & Peebles, S. A. (2005). Rotational spectrum of the dimethyl ether-acetylene complex: evidence for an effective C2v geometry. The journal of physical chemistry. A, 109(24), 5316-22. https://doi.org/10.1021/jp0507593
Newby, Josh J, et al. "Rotational spectrum of the dimethyl ether-acetylene complex: evidence for an effective C2v geometry." The journal of physical chemistry. A vol. 109,24 (2005): 5316-22. doi: https://doi.org/10.1021/jp0507593
Newby JJ, Serafin MM, Peebles RA, Peebles SA. Rotational spectrum of the dimethyl ether-acetylene complex: evidence for an effective C2v geometry. J Phys Chem A. 2005 Jun 23;109(24):5316-22. doi: 10.1021/jp0507593. PMID: 16839055.
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Reversible synthesis and characterization of dynamic imino analogues of trimethine and pentamethine cyanine dyes.

Organic letters

Meguellati K, Spichty M, Ladame S.
PMID: 19193121
Org Lett. 2009 Mar 05;11(5):1123-6. doi: 10.1021/ol802913b.

A new family of unsymmetrical imine-based trimethine and pentamethine cyanine dye analogues is reported that can form under reversible and thermodynamically controlled conditions from non- or weakly emissive amine and aldehyde building blocks. These dynamic fluorophores show spectroscopic properties...

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Meguellati K, Spichty M, Ladame S. Reversible synthesis and characterization of dynamic imino analogues of trimethine and pentamethine cyanine dyes. Org Lett. 2009;11(5):1123-6doi: 10.1021/ol802913b.
Meguellati, K., Spichty, M., & Ladame, S. (2009). Reversible synthesis and characterization of dynamic imino analogues of trimethine and pentamethine cyanine dyes. Organic letters, 11(5), 1123-6. https://doi.org/10.1021/ol802913b
Meguellati, Kamel, et al. "Reversible synthesis and characterization of dynamic imino analogues of trimethine and pentamethine cyanine dyes." Organic letters vol. 11,5 (2009): 1123-6. doi: https://doi.org/10.1021/ol802913b
Meguellati K, Spichty M, Ladame S. Reversible synthesis and characterization of dynamic imino analogues of trimethine and pentamethine cyanine dyes. Org Lett. 2009 Mar 05;11(5):1123-6. doi: 10.1021/ol802913b. PMID: 19193121.
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Microwave spectrum, dipole moment, and internal dynamics of the methyl fluoride-carbonyl sulfide weakly bound complex.

The journal of physical chemistry. A

Serafin MM, Peebles SA.
PMID: 18217737
J Phys Chem A. 2008 Feb 21;112(7):1473-9. doi: 10.1021/jp710181z. Epub 2008 Jan 25.

Rotational spectra for the normal and four isotopically substituted species of the 1:1 complex between methyl fluoride (H3CF) and carbonyl sulfide (OCS) have been measured using Fourier-transform microwave spectroscopy in the 5-16 GHz frequency region. The observed spectra fit...

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Serafin MM, Peebles SA. Microwave spectrum, dipole moment, and internal dynamics of the methyl fluoride-carbonyl sulfide weakly bound complex. J Phys Chem A. 2008;112(7):1473-9doi: 10.1021/jp710181z.
Serafin, M. M., & Peebles, S. A. (2008). Microwave spectrum, dipole moment, and internal dynamics of the methyl fluoride-carbonyl sulfide weakly bound complex. The journal of physical chemistry. A, 112(7), 1473-9. https://doi.org/10.1021/jp710181z
Serafin, Michal M, and Peebles, Sean A. "Microwave spectrum, dipole moment, and internal dynamics of the methyl fluoride-carbonyl sulfide weakly bound complex." The journal of physical chemistry. A vol. 112,7 (2008): 1473-9. doi: https://doi.org/10.1021/jp710181z
Serafin MM, Peebles SA. Microwave spectrum, dipole moment, and internal dynamics of the methyl fluoride-carbonyl sulfide weakly bound complex. J Phys Chem A. 2008 Feb 21;112(7):1473-9. doi: 10.1021/jp710181z. Epub 2008 Jan 25. PMID: 18217737.
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Rotational spectra and conformational analysis of diethylsilane and diethyldifluorosilane.

The journal of physical chemistry. A

Peebles SA, Serafin MM, Peebles RA, Guirgis GA, Stidham HD.
PMID: 19243160
J Phys Chem A. 2009 Apr 02;113(13):3137-42. doi: 10.1021/jp811049n.

The rotational spectra belonging to the (28)Si isotopologue for three conformers of diethyldifluorosilane (Et(2)SiF(2)) and three conformers of diethylsilane (Et(2)SiH(2)) have been measured between 4 and 17 GHz by using pulsed-jet Fourier-transform microwave spectroscopy. Rotational spectra for the gauche-gauche,...

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Peebles SA, Serafin MM, Peebles RA, et al. Rotational spectra and conformational analysis of diethylsilane and diethyldifluorosilane. J Phys Chem A. 2009;113(13):3137-42doi: 10.1021/jp811049n.
Peebles, S. A., Serafin, M. M., Peebles, R. A., Guirgis, G. A., & Stidham, H. D. (2009). Rotational spectra and conformational analysis of diethylsilane and diethyldifluorosilane. The journal of physical chemistry. A, 113(13), 3137-42. https://doi.org/10.1021/jp811049n
Peebles, Sean A, et al. "Rotational spectra and conformational analysis of diethylsilane and diethyldifluorosilane." The journal of physical chemistry. A vol. 113,13 (2009): 3137-42. doi: https://doi.org/10.1021/jp811049n
Peebles SA, Serafin MM, Peebles RA, Guirgis GA, Stidham HD. Rotational spectra and conformational analysis of diethylsilane and diethyldifluorosilane. J Phys Chem A. 2009 Apr 02;113(13):3137-42. doi: 10.1021/jp811049n. PMID: 19243160.
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[Carney complex].

Ceskoslovenska patologie

Kacerovská D, Michal M, Síma R, Grossmann P, Kazakov DV.
PMID: 22145222
Cesk Patol. 2011 Oct;47(4):192-7.

Carney complex is a clinically and genetically heterogeneous disease, with at least two genetic loci including the PRKAR1A gene located on chromosome 17 and the CNC2 locus mapped to chromosome 2. Clinically this syndrome is characterized by multiple myxomas...

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Kacerovská D, Michal M, Síma R, et al. Carneyho komplex. [Carney complex]. Cesk Patol. 2011;47(4):192-7
Kacerovská, D., Michal, M., Síma, R., Grossmann, P., & Kazakov, D. V. (2011). Carneyho komplex. [Carney complex]. Ceskoslovenska patologie, 47(4), 192-7.
Kacerovská, D, et al. "Carneyho komplex." [Carney complex]. Ceskoslovenska patologie vol. 47,4 (2011): 192-7.
Kacerovská D, Michal M, Síma R, Grossmann P, Kazakov DV. Carneyho komplex. [Carney complex]. Cesk Patol. 2011 Oct;47(4):192-7. Czech. PMID: 22145222.
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Showing 1 to 12 of 229 entries