Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 97 entries
Sorted by: Best Match Show Resources per page
Interinstrumental method transfer of a capillary electrophoretic separation of angiotensin II and five derivatives: Evaluation and update of earlier developed guidelines.

Electrophoresis

De Cock B, Van Eeckhaut A, Stiens J, Mangelings D, Vander Heyden Y.
PMID: 26202748
Electrophoresis. 2015 Nov;36(21):2658-2664. doi: 10.1002/elps.201500273. Epub 2015 Sep 07.

The increased interest in the separation of peptides, proteins, immunoglobulins, and polynucleotides, led to an increased demand for appropriate analytical methodologies and instrumentation. CE, because of its unique separation mechanism and high efficiency, is frequently used in the analysis...

Cite
De Cock B, Van Eeckhaut A, Stiens J, et al. Interinstrumental method transfer of a capillary electrophoretic separation of angiotensin II and five derivatives: Evaluation and update of earlier developed guidelines. Electrophoresis. 2015;36(21):2658-2664doi: 10.1002/elps.201500273.
De Cock, B., Van Eeckhaut, A., Stiens, J., Mangelings, D., & Vander Heyden, Y. (2015). Interinstrumental method transfer of a capillary electrophoretic separation of angiotensin II and five derivatives: Evaluation and update of earlier developed guidelines. Electrophoresis, 36(21), 2658-2664. https://doi.org/10.1002/elps.201500273
De Cock, Bart, et al. "Interinstrumental method transfer of a capillary electrophoretic separation of angiotensin II and five derivatives: Evaluation and update of earlier developed guidelines." Electrophoresis vol. 36,21 (2015): 2658-2664. doi: https://doi.org/10.1002/elps.201500273
De Cock B, Van Eeckhaut A, Stiens J, Mangelings D, Vander Heyden Y. Interinstrumental method transfer of a capillary electrophoretic separation of angiotensin II and five derivatives: Evaluation and update of earlier developed guidelines. Electrophoresis. 2015 Nov;36(21):2658-2664. doi: 10.1002/elps.201500273. Epub 2015 Sep 07. PMID: 26202748.
Copy Download .nbib Format: NLM
Complex Thermodynamic Behavior of Single-Stranded Nucleic Acid Adsorption to Graphene Surfaces.

Langmuir : the ACS journal of surfaces and colloids

Ranganathan SV, Halvorsen K, Myers CA, Robertson NM, Yigit MV, Chen AA.
PMID: 27219463
Langmuir. 2016 Jun 21;32(24):6028-34. doi: 10.1021/acs.langmuir.6b00456. Epub 2016 Jun 06.

In just over a decade since its discovery, research on graphene has exploded due to a number of potential applications in electronics, materials, and medicine. In its water-soluble form of graphene oxide, the material has shown promise as a...

Cite
Ranganathan SV, Halvorsen K, Myers CA, et al. Complex Thermodynamic Behavior of Single-Stranded Nucleic Acid Adsorption to Graphene Surfaces. Langmuir. 2016;32(24):6028-34doi: 10.1021/acs.langmuir.6b00456.
Ranganathan, S. V., Halvorsen, K., Myers, C. A., Robertson, N. M., Yigit, M. V., & Chen, A. A. (2016). Complex Thermodynamic Behavior of Single-Stranded Nucleic Acid Adsorption to Graphene Surfaces. Langmuir : the ACS journal of surfaces and colloids, 32(24), 6028-34. https://doi.org/10.1021/acs.langmuir.6b00456
Ranganathan, Srivathsan V, et al. "Complex Thermodynamic Behavior of Single-Stranded Nucleic Acid Adsorption to Graphene Surfaces." Langmuir : the ACS journal of surfaces and colloids vol. 32,24 (2016): 6028-34. doi: https://doi.org/10.1021/acs.langmuir.6b00456
Ranganathan SV, Halvorsen K, Myers CA, Robertson NM, Yigit MV, Chen AA. Complex Thermodynamic Behavior of Single-Stranded Nucleic Acid Adsorption to Graphene Surfaces. Langmuir. 2016 Jun 21;32(24):6028-34. doi: 10.1021/acs.langmuir.6b00456. Epub 2016 Jun 06. PMID: 27219463.
Copy Download .nbib Format: NLM
A simple and general plant tissue extraction procedure for two-dimensional gel electrophoresis.

Plant cell reports

Mayer JE, Hahne G, Palme K, Schell J.
PMID: 24248456
Plant Cell Rep. 1987 Feb;6(1):77-81. doi: 10.1007/BF00269745.

A fast and simple extraction procedure of plant tissue for two-dimensional gel electrophoresis is presented. The procedure is especially useful for the extraction of plant cell suspension cultures, callus and other plant tissues having a high content of phenol...

Cite
Mayer JE, Hahne G, Palme K, et al. A simple and general plant tissue extraction procedure for two-dimensional gel electrophoresis. Plant Cell Rep. 1987;6(1):77-81doi: 10.1007/BF00269745.
Mayer, J. E., Hahne, G., Palme, K., & Schell, J. (1987). A simple and general plant tissue extraction procedure for two-dimensional gel electrophoresis. Plant cell reports, 6(1), 77-81. https://doi.org/10.1007/BF00269745
Mayer, J E, et al. "A simple and general plant tissue extraction procedure for two-dimensional gel electrophoresis." Plant cell reports vol. 6,1 (1987): 77-81. doi: https://doi.org/10.1007/BF00269745
Mayer JE, Hahne G, Palme K, Schell J. A simple and general plant tissue extraction procedure for two-dimensional gel electrophoresis. Plant Cell Rep. 1987 Feb;6(1):77-81. doi: 10.1007/BF00269745. PMID: 24248456.
Copy Download .nbib Format: NLM
ESR of Cu(2+) bound to polynucleotides and derivatives.

FEBS letters

Bemski G, Rieber M, Wust M.
PMID: 11945734
FEBS Lett. 1971 Apr;14(2):117-120. doi: 10.1016/0014-5793(71)80115-1.

Binding of Cu(2+) to polynucleotides has been found to occur at 1 Cu/5 polymer P and at similar molar ratios of copper to selected nucleic acid derivatives. Electron spin resonance (ESR) measurements show that the g-values and the hyperfine...

Cite
Bemski G, Rieber M, Wust M. ESR of Cu(2+) bound to polynucleotides and derivatives. FEBS Lett. 1971;14(2):117-120doi: 10.1016/0014-5793(71)80115-1.
Bemski, G., Rieber, M., & Wust, M. (1971). ESR of Cu(2+) bound to polynucleotides and derivatives. FEBS letters, 14(2), 117-120. https://doi.org/10.1016/0014-5793(71)80115-1
Bemski, G, et al. "ESR of Cu(2+) bound to polynucleotides and derivatives." FEBS letters vol. 14,2 (1971): 117-120. doi: https://doi.org/10.1016/0014-5793(71)80115-1
Bemski G, Rieber M, Wust M. ESR of Cu(2+) bound to polynucleotides and derivatives. FEBS Lett. 1971 Apr;14(2):117-120. doi: 10.1016/0014-5793(71)80115-1. PMID: 11945734.
Copy Download .nbib Format: NLM
Unique Catalysis and Regioselectivity Observed in the Poly(C)-Directed RNA Dimer Formation from 2-MeImpG: Kinetic Analysis as a Function of Monomer and Polymer Concentration.

The Journal of organic chemistry

Kanavarioti A, Baird EE, Hurley TB, Carruthers JA, Gangopadhyay S.
PMID: 11674755
J Org Chem. 1999 Oct 29;64(22):8323-8333. doi: 10.1021/jo991216q.

Polycytidylate, poly(C), serves as a scaffold or template to direct and catalyze the synthesis of long oligoguanylates from guanosine 5'-phosphate 2-methylimidazolide, 2-MeImpG. In the absence of poly(C), small amounts of three isomeric dimers, i.e., the 2'-5'-, the 3'-5'-, and...

Cite
Kanavarioti A, Baird EE, Hurley TB, et al. Unique Catalysis and Regioselectivity Observed in the Poly(C)-Directed RNA Dimer Formation from 2-MeImpG: Kinetic Analysis as a Function of Monomer and Polymer Concentration. J Org Chem. 1999;64(22):8323-8333doi: 10.1021/jo991216q.
Kanavarioti, A., Baird, E. E., Hurley, T. B., Carruthers, J. A., & Gangopadhyay, S. (1999). Unique Catalysis and Regioselectivity Observed in the Poly(C)-Directed RNA Dimer Formation from 2-MeImpG: Kinetic Analysis as a Function of Monomer and Polymer Concentration. The Journal of organic chemistry, 64(22), 8323-8333. https://doi.org/10.1021/jo991216q
Kanavarioti, Anastassia, et al. "Unique Catalysis and Regioselectivity Observed in the Poly(C)-Directed RNA Dimer Formation from 2-MeImpG: Kinetic Analysis as a Function of Monomer and Polymer Concentration." The Journal of organic chemistry vol. 64,22 (1999): 8323-8333. doi: https://doi.org/10.1021/jo991216q
Kanavarioti A, Baird EE, Hurley TB, Carruthers JA, Gangopadhyay S. Unique Catalysis and Regioselectivity Observed in the Poly(C)-Directed RNA Dimer Formation from 2-MeImpG: Kinetic Analysis as a Function of Monomer and Polymer Concentration. J Org Chem. 1999 Oct 29;64(22):8323-8333. doi: 10.1021/jo991216q. PMID: 11674755.
Copy Download .nbib Format: NLM
Optical properties of chemically synthetised polynucleotides containing D- or L-ribonucleosides.

FEBS letters

Fric I, Guschlbauer W, Holý A.
PMID: 11947686
FEBS Lett. 1970 Aug 31;9(5):261-264. doi: 10.1016/0014-5793(70)80371-4.

No abstract available.

Cite
Fric I, Guschlbauer W, Holý A. Optical properties of chemically synthetised polynucleotides containing D- or L-ribonucleosides. FEBS Lett. 1970;9(5):261-264doi: 10.1016/0014-5793(70)80371-4.
Fric, I., Guschlbauer, W., & Holý, A. (1970). Optical properties of chemically synthetised polynucleotides containing D- or L-ribonucleosides. FEBS letters, 9(5), 261-264. https://doi.org/10.1016/0014-5793(70)80371-4
Fric, I, et al. "Optical properties of chemically synthetised polynucleotides containing D- or L-ribonucleosides." FEBS letters vol. 9,5 (1970): 261-264. doi: https://doi.org/10.1016/0014-5793(70)80371-4
Fric I, Guschlbauer W, Holý A. Optical properties of chemically synthetised polynucleotides containing D- or L-ribonucleosides. FEBS Lett. 1970 Aug 31;9(5):261-264. doi: 10.1016/0014-5793(70)80371-4. PMID: 11947686.
Copy Download .nbib Format: NLM
A time-resolved fluorescence study of 4',6'-diamidine-2-phenylindole dihydrochloride binding to polynucleotides.

Biophysical chemistry

Cavatorta P, Masotti L, Szabo AG.
PMID: 17007778
Biophys Chem. 1985 Jun;22(1):11-6. doi: 10.1016/0301-4622(85)80021-1.

At phosphate/dye (P/D) ratios greater than 30 the quantum yield of 4',6'-diamidine-2-phenylindole dihydrochloride (DAPI)-DNA and DAPI-poly(d(A-T)) complexes was found to be 0.62 and 0.66, respectively. Contrary to earlier reports a fluorescence enhancement of DAPI-poly(d(G-C)) complexes was observed with a...

Cite
Cavatorta P, Masotti L, Szabo AG. A time-resolved fluorescence study of 4',6'-diamidine-2-phenylindole dihydrochloride binding to polynucleotides. Biophys Chem. 1985;22(1):11-6doi: 10.1016/0301-4622(85)80021-1.
Cavatorta, P., Masotti, L., & Szabo, A. G. (1985). A time-resolved fluorescence study of 4',6'-diamidine-2-phenylindole dihydrochloride binding to polynucleotides. Biophysical chemistry, 22(1), 11-6. https://doi.org/10.1016/0301-4622(85)80021-1
Cavatorta, P, et al. "A time-resolved fluorescence study of 4',6'-diamidine-2-phenylindole dihydrochloride binding to polynucleotides." Biophysical chemistry vol. 22,1 (1985): 11-6. doi: https://doi.org/10.1016/0301-4622(85)80021-1
Cavatorta P, Masotti L, Szabo AG. A time-resolved fluorescence study of 4',6'-diamidine-2-phenylindole dihydrochloride binding to polynucleotides. Biophys Chem. 1985 Jun;22(1):11-6. doi: 10.1016/0301-4622(85)80021-1. PMID: 17007778.
Copy Download .nbib Format: NLM
A HYBRID HELIX CONTAINING BOTH DEOXYRIBOSE AND RIBOSE POLYNUCLEOTIDES AND ITS RELATION TO THE TRANSFER OF INFORMATION BETWEEN THE NUCLEIC ACIDS.

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

Rich A.
PMID: 16590711
Proc Natl Acad Sci U S A. 1960 Aug;46(8):1044-53. doi: 10.1073/pnas.46.8.1044.

No abstract available.

Cite
Rich A. A HYBRID HELIX CONTAINING BOTH DEOXYRIBOSE AND RIBOSE POLYNUCLEOTIDES AND ITS RELATION TO THE TRANSFER OF INFORMATION BETWEEN THE NUCLEIC ACIDS. Proc Natl Acad Sci U S A. 1960;46(8):1044-53doi: 10.1073/pnas.46.8.1044.
Rich, A. (1960). A HYBRID HELIX CONTAINING BOTH DEOXYRIBOSE AND RIBOSE POLYNUCLEOTIDES AND ITS RELATION TO THE TRANSFER OF INFORMATION BETWEEN THE NUCLEIC ACIDS. Proceedings of the National Academy of Sciences of the United States of America, 46(8), 1044-53. https://doi.org/10.1073/pnas.46.8.1044
Rich, A. "A HYBRID HELIX CONTAINING BOTH DEOXYRIBOSE AND RIBOSE POLYNUCLEOTIDES AND ITS RELATION TO THE TRANSFER OF INFORMATION BETWEEN THE NUCLEIC ACIDS." Proceedings of the National Academy of Sciences of the United States of America vol. 46,8 (1960): 1044-53. doi: https://doi.org/10.1073/pnas.46.8.1044
Rich A. A HYBRID HELIX CONTAINING BOTH DEOXYRIBOSE AND RIBOSE POLYNUCLEOTIDES AND ITS RELATION TO THE TRANSFER OF INFORMATION BETWEEN THE NUCLEIC ACIDS. Proc Natl Acad Sci U S A. 1960 Aug;46(8):1044-53. doi: 10.1073/pnas.46.8.1044. PMID: 16590711; PMCID: PMC222998.
Copy Download .nbib Format: NLM
Nucleic Acid Polymerases: Possible Subunit Structure.

Science (New York, N.Y.)

Lee-Huang S, Cavalieri LF.
PMID: 17738156
Science. 1965 Jun 11;148(3676):1474-6. doi: 10.1126/science.148.3676.1474.

A hybrid polymerase which catalyzes the synthesis only of helical polynucleotides with one DNA-like strand and one RNA-like strand can be altered by certain treatments so that it will then synthesize DNA and RNA. There is evidence that the...

Cite
Lee-Huang S, Cavalieri LF. Nucleic Acid Polymerases: Possible Subunit Structure. Science. 1965;148(3676):1474-6doi: 10.1126/science.148.3676.1474.
Lee-Huang, S., & Cavalieri, L. F. (1965). Nucleic Acid Polymerases: Possible Subunit Structure. Science (New York, N.Y.), 148(3676), 1474-6. https://doi.org/10.1126/science.148.3676.1474
Lee-Huang, S, and Cavalieri, L F. "Nucleic Acid Polymerases: Possible Subunit Structure." Science (New York, N.Y.) vol. 148,3676 (1965): 1474-6. doi: https://doi.org/10.1126/science.148.3676.1474
Lee-Huang S, Cavalieri LF. Nucleic Acid Polymerases: Possible Subunit Structure. Science. 1965 Jun 11;148(3676):1474-6. doi: 10.1126/science.148.3676.1474. PMID: 17738156.
Copy Download .nbib Format: NLM
Studies on polynucleotides, lix. Further codon assignments from amino Acid incorporations directed by ribopolynucleotides containing repeating trinucleotide sequences.

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

Morgan AR, Wells RD, Khorana HG.
PMID: 16591436
Proc Natl Acad Sci U S A. 1966 Dec;56(6):1899-906. doi: 10.1073/pnas.56.6.1899.

No abstract available.

Cite
Morgan AR, Wells RD, Khorana HG. Studies on polynucleotides, lix. Further codon assignments from amino Acid incorporations directed by ribopolynucleotides containing repeating trinucleotide sequences. Proc Natl Acad Sci U S A. 1966;56(6):1899-906doi: 10.1073/pnas.56.6.1899.
Morgan, A. R., Wells, R. D., & Khorana, H. G. (1966). Studies on polynucleotides, lix. Further codon assignments from amino Acid incorporations directed by ribopolynucleotides containing repeating trinucleotide sequences. Proceedings of the National Academy of Sciences of the United States of America, 56(6), 1899-906. https://doi.org/10.1073/pnas.56.6.1899
Morgan, A R, et al. "Studies on polynucleotides, lix. Further codon assignments from amino Acid incorporations directed by ribopolynucleotides containing repeating trinucleotide sequences." Proceedings of the National Academy of Sciences of the United States of America vol. 56,6 (1966): 1899-906. doi: https://doi.org/10.1073/pnas.56.6.1899
Morgan AR, Wells RD, Khorana HG. Studies on polynucleotides, lix. Further codon assignments from amino Acid incorporations directed by ribopolynucleotides containing repeating trinucleotide sequences. Proc Natl Acad Sci U S A. 1966 Dec;56(6):1899-906. doi: 10.1073/pnas.56.6.1899. PMID: 16591436; PMCID: PMC220208.
Copy Download .nbib Format: NLM
Fast electron density methods in the life sciences--a routine application in the future?.

Organic & biomolecular chemistry

Luger P.
PMID: 18019525
Org Biomol Chem. 2007 Aug 21;5(16):2529-40. doi: 10.1039/b706235d.

The understanding of mutual recognition of biologically interacting systems on an atomic scale is of paramount importance in the life sciences. Electron density distributions that can be obtained from a high resolution X-ray diffraction experiment can provide--in addition to...

Cite
Luger P. Fast electron density methods in the life sciences--a routine application in the future?. Org Biomol Chem. 2007;5(16):2529-40doi: 10.1039/b706235d.
Luger, P. (2007). Fast electron density methods in the life sciences--a routine application in the future?. Organic & biomolecular chemistry, 5(16), 2529-40. https://doi.org/10.1039/b706235d
Luger, Peter. "Fast electron density methods in the life sciences--a routine application in the future?." Organic & biomolecular chemistry vol. 5,16 (2007): 2529-40. doi: https://doi.org/10.1039/b706235d
Luger P. Fast electron density methods in the life sciences--a routine application in the future?. Org Biomol Chem. 2007 Aug 21;5(16):2529-40. doi: 10.1039/b706235d. PMID: 18019525.
Copy Download .nbib Format: NLM
Conversions of the left-handed form and the protonated form of DNA back to the bound right-handed form by sanguinarine and ethidium: a comparative study.

Biophysical chemistry

Das S, Kumar GS, Maiti M.
PMID: 17027465
Biophys Chem. 1999 Feb 22;76(3):199-218. doi: 10.1016/s0301-4622(98)00238-5.

The interaction of sanguinarine and ethidium with right-handed (B-form), left-handed (Z-form) and left-handed protonated (designated as H(L)-form) structures of poly(dG-dC).poly(dG-dC) and poly(dG-me5dC).poly(dG-me5dC) was investigated by measuring the circular dichroism and UV absorption spectral analysis. Both sanguinarine and ethidium bind...

Cite
Das S, Kumar GS, Maiti M. Conversions of the left-handed form and the protonated form of DNA back to the bound right-handed form by sanguinarine and ethidium: a comparative study. Biophys Chem. 1999;76(3):199-218doi: 10.1016/s0301-4622(98)00238-5.
Das, S., Kumar, G. S., & Maiti, M. (1999). Conversions of the left-handed form and the protonated form of DNA back to the bound right-handed form by sanguinarine and ethidium: a comparative study. Biophysical chemistry, 76(3), 199-218. https://doi.org/10.1016/s0301-4622(98)00238-5
Das, S, et al. "Conversions of the left-handed form and the protonated form of DNA back to the bound right-handed form by sanguinarine and ethidium: a comparative study." Biophysical chemistry vol. 76,3 (1999): 199-218. doi: https://doi.org/10.1016/s0301-4622(98)00238-5
Das S, Kumar GS, Maiti M. Conversions of the left-handed form and the protonated form of DNA back to the bound right-handed form by sanguinarine and ethidium: a comparative study. Biophys Chem. 1999 Feb 22;76(3):199-218. doi: 10.1016/s0301-4622(98)00238-5. PMID: 17027465.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 97 entries