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Separation of 32P-labelled ribonucleic acid components. The use of polyethylenimine-cellulose (TLC) as a second dimension in separating oligoribonucleotides of '4.5 S' and 5 S from E. coli.

FEBS letters

Griffin BE.
PMID: 11945838
FEBS Lett. 1971 Jun 24;15(3):165-168. doi: 10.1016/0014-5793(71)80304-6.

No abstract available.

Cite
Griffin BE. Separation of 32P-labelled ribonucleic acid components. The use of polyethylenimine-cellulose (TLC) as a second dimension in separating oligoribonucleotides of '4.5 S' and 5 S from E. coli. FEBS Lett. 1971;15(3):165-168doi: 10.1016/0014-5793(71)80304-6.
Griffin, B. E. (1971). Separation of 32P-labelled ribonucleic acid components. The use of polyethylenimine-cellulose (TLC) as a second dimension in separating oligoribonucleotides of '4.5 S' and 5 S from E. coli. FEBS letters, 15(3), 165-168. https://doi.org/10.1016/0014-5793(71)80304-6
Griffin, B E.. "Separation of 32P-labelled ribonucleic acid components. The use of polyethylenimine-cellulose (TLC) as a second dimension in separating oligoribonucleotides of '4.5 S' and 5 S from E. coli." FEBS letters vol. 15,3 (1971): 165-168. doi: https://doi.org/10.1016/0014-5793(71)80304-6
Griffin BE. Separation of 32P-labelled ribonucleic acid components. The use of polyethylenimine-cellulose (TLC) as a second dimension in separating oligoribonucleotides of '4.5 S' and 5 S from E. coli. FEBS Lett. 1971 Jun 24;15(3):165-168. doi: 10.1016/0014-5793(71)80304-6. PMID: 11945838.
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Chloride channels and the reactions of cells to topography.

European cells & materials

Tobasnick G, Curtis AS.
PMID: 14562255
Eur Cell Mater. 2001 Dec 13;2:49-61. doi: 10.22203/ecm.v002a06.

The reactions of rat epitenon cells to substratum topography on the micrometric and nanometric scale such as groove-ridge structures include cell extension, elongation and orientation reactions. In this paper we report that stretch-sensitive chloride channels may be involved in...

Cite
Tobasnick G, Curtis AS. Chloride channels and the reactions of cells to topography. Eur Cell Mater. 2001;2:49-61doi: 10.22203/ecm.v002a06.
Tobasnick, G., & Curtis, A. S. (2001). Chloride channels and the reactions of cells to topography. European cells & materials, 249-61. https://doi.org/10.22203/ecm.v002a06
Tobasnick, G, and Curtis, A S. "Chloride channels and the reactions of cells to topography." European cells & materials vol. 2 (2001): 49-61. doi: https://doi.org/10.22203/ecm.v002a06
Tobasnick G, Curtis AS. Chloride channels and the reactions of cells to topography. Eur Cell Mater. 2001 Dec 13;2:49-61. doi: 10.22203/ecm.v002a06. PMID: 14562255.
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Photooxidation of nucleic acids on metal oxides: physico-chemical and astrobiological perspectives.

The journal of physical chemistry. C, Nanomaterials and interfaces

Shkrob IA, Marin TM, Adhikary A, Sevilla MD.
PMID: 21399705
J Phys Chem C Nanomater Interfaces. 2011 Feb 07;115(8):3393-3403. doi: 10.1021/jp110682c.

Photocatalytic oxidation of nucleic acid components on aqueous metal oxides (TiO(2), α-FeOOH, and α-Fe(2)O(3)) has been studied. The oxidation of purine nucleotides results in the formation of the purine radical cations and sugar-phosphate radicals, whereas the oxidation of pyrimidine...

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Shkrob IA, Marin TM, Adhikary A, et al. Photooxidation of nucleic acids on metal oxides: physico-chemical and astrobiological perspectives. J Phys Chem C Nanomater Interfaces. 2011;115(8):3393-3403doi: 10.1021/jp110682c.
Shkrob, I. A., Marin, T. M., Adhikary, A., & Sevilla, M. D. (2011). Photooxidation of nucleic acids on metal oxides: physico-chemical and astrobiological perspectives. The journal of physical chemistry. C, Nanomaterials and interfaces, 115(8), 3393-3403. https://doi.org/10.1021/jp110682c
Shkrob, Ilya A, et al. "Photooxidation of nucleic acids on metal oxides: physico-chemical and astrobiological perspectives." The journal of physical chemistry. C, Nanomaterials and interfaces vol. 115,8 (2011): 3393-3403. doi: https://doi.org/10.1021/jp110682c
Shkrob IA, Marin TM, Adhikary A, Sevilla MD. Photooxidation of nucleic acids on metal oxides: physico-chemical and astrobiological perspectives. J Phys Chem C Nanomater Interfaces. 2011 Feb 07;115(8):3393-3403. doi: 10.1021/jp110682c. PMID: 21399705; PMCID: PMC3049938.
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Pre-Clinical and Clinical Efficiency of Complexes of Oligoribonucleotides with D-Mannitol against Respiratory Viruses.

Pharmaceutics

Melnichuk N, Zarubaev V, Iosyk I, Andreychyn M, Semernikova L, Tkachuk Z.
PMID: 29783756
Pharmaceutics. 2018 May 19;10(2). doi: 10.3390/pharmaceutics10020059.

Oligoribonucleotides-D-mannitol (ORNs-D-M) complexes possess antiviral, anti-inflammatory, and immunomodulatory actions. The aim of the present study was to evaluated an antiviral effect of ORNs-D-M against parainfluenza virus type 3 (PIV3); influenza CA709, PR834; avian influenza virus H5N2 (AIV) in vitro...

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Melnichuk N, Zarubaev V, Iosyk I, et al. Pre-Clinical and Clinical Efficiency of Complexes of Oligoribonucleotides with D-Mannitol against Respiratory Viruses. Pharmaceutics. 2018;10(2)doi: 10.3390/pharmaceutics10020059.
Melnichuk, N., Zarubaev, V., Iosyk, I., Andreychyn, M., Semernikova, L., & Tkachuk, Z. (2018). Pre-Clinical and Clinical Efficiency of Complexes of Oligoribonucleotides with D-Mannitol against Respiratory Viruses. Pharmaceutics, 10(2), . https://doi.org/10.3390/pharmaceutics10020059
Melnichuk, Nataliia, et al. "Pre-Clinical and Clinical Efficiency of Complexes of Oligoribonucleotides with D-Mannitol against Respiratory Viruses." Pharmaceutics vol. 10,2 (2018). doi: https://doi.org/10.3390/pharmaceutics10020059
Melnichuk N, Zarubaev V, Iosyk I, Andreychyn M, Semernikova L, Tkachuk Z. Pre-Clinical and Clinical Efficiency of Complexes of Oligoribonucleotides with D-Mannitol against Respiratory Viruses. Pharmaceutics. 2018 May 19;10(2). doi: 10.3390/pharmaceutics10020059. PMID: 29783756; PMCID: PMC6027485.
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Efficient access to .

Monatshefte fur chemie

Falschlunger C, Micura R.
PMID: 31178603
Monatsh Chem. 2019;150(5):795-800. doi: 10.1007/s00706-019-02390-x. Epub 2019 Apr 29.

No abstract available.

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Falschlunger C, Micura R. Efficient access to . Monatsh Chem. 2019;150(5):795-800doi: 10.1007/s00706-019-02390-x.
Falschlunger, C., & Micura, R. (2019). Efficient access to . Monatshefte fur chemie, 150(5), 795-800. https://doi.org/10.1007/s00706-019-02390-x
Falschlunger, Christoph, and Micura, Ronald. "Efficient access to ." Monatshefte fur chemie vol. 150,5 (2019): 795-800. doi: https://doi.org/10.1007/s00706-019-02390-x
Falschlunger C, Micura R. Efficient access to . Monatsh Chem. 2019;150(5):795-800. doi: 10.1007/s00706-019-02390-x. Epub 2019 Apr 29. PMID: 31178603; PMCID: PMC6534076.
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The Cellular Processing Capacity Limits the Amounts of Chimeric U7 snRNA Available for Antisense Delivery.

Molecular therapy. Nucleic acids

Eckenfelder A, Tordo J, Babbs A, Davies KE, Goyenvalle A, Danos O.
PMID: 23344083
Mol Ther Nucleic Acids. 2012 Jun 26;1:e31. doi: 10.1038/mtna.2012.24.

Many genetic diseases are induced by mutations disturbing the maturation of pre-mRNAs, often affecting splicing. Antisense oligoribonucleotides (AONs) have been used to modulate splicing thereby circumventing the deleterious effects of mutations. Stable delivery of antisense sequences is achieved by...

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Eckenfelder A, Tordo J, Babbs A, et al. The Cellular Processing Capacity Limits the Amounts of Chimeric U7 snRNA Available for Antisense Delivery. Mol Ther Nucleic Acids. 2012;1:e31doi: 10.1038/mtna.2012.24.
Eckenfelder, A., Tordo, J., Babbs, A., Davies, K. E., Goyenvalle, A., & Danos, O. (2012). The Cellular Processing Capacity Limits the Amounts of Chimeric U7 snRNA Available for Antisense Delivery. Molecular therapy. Nucleic acids, 1e31. https://doi.org/10.1038/mtna.2012.24
Eckenfelder, Agathe, et al. "The Cellular Processing Capacity Limits the Amounts of Chimeric U7 snRNA Available for Antisense Delivery." Molecular therapy. Nucleic acids vol. 1 (2012): e31. doi: https://doi.org/10.1038/mtna.2012.24
Eckenfelder A, Tordo J, Babbs A, Davies KE, Goyenvalle A, Danos O. The Cellular Processing Capacity Limits the Amounts of Chimeric U7 snRNA Available for Antisense Delivery. Mol Ther Nucleic Acids. 2012 Jun 26;1:e31. doi: 10.1038/mtna.2012.24. PMID: 23344083; PMCID: PMC3390224.
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Draft Genome Sequence of Bacillus pumilus 7P, Isolated from the Soil of the Tatarstan Republic, Russia.

Genome announcements

Shagimardanova EI, Toymentseva AA, Balaban NP, Mardanova AM, Danilova YV, Gusev OA, Kostryukova E, Karpova I, Manolov A, Alexeev D, Sharipova MR.
PMID: 24926064
Genome Announc. 2014 Jun 12;2(3). doi: 10.1128/genomeA.00599-14.

Here, we present a draft genome sequence of Bacillus pumilus strain 7P. This strain was isolated from soil as an extracellular RNase-producing microorganism. The RNase of B. pumilus 7P is considered to be a potential antiviral and therapeutic antitumor...

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Shagimardanova EI, Toymentseva AA, Balaban NP, et al. Draft Genome Sequence of Bacillus pumilus 7P, Isolated from the Soil of the Tatarstan Republic, Russia. Genome Announc. 2014;2(3)doi: 10.1128/genomeA.00599-14.
Shagimardanova, E. I., Toymentseva, A. A., Balaban, N. P., Mardanova, A. M., Danilova, Y. V., Gusev, O. A., Kostryukova, E., Karpova, I., Manolov, A., Alexeev, D., & Sharipova, M. R. (2014). Draft Genome Sequence of Bacillus pumilus 7P, Isolated from the Soil of the Tatarstan Republic, Russia. Genome announcements, 2(3), . https://doi.org/10.1128/genomeA.00599-14
Shagimardanova, Elena I, et al. "Draft Genome Sequence of Bacillus pumilus 7P, Isolated from the Soil of the Tatarstan Republic, Russia." Genome announcements vol. 2,3 (2014). doi: https://doi.org/10.1128/genomeA.00599-14
Shagimardanova EI, Toymentseva AA, Balaban NP, Mardanova AM, Danilova YV, Gusev OA, Kostryukova E, Karpova I, Manolov A, Alexeev D, Sharipova MR. Draft Genome Sequence of Bacillus pumilus 7P, Isolated from the Soil of the Tatarstan Republic, Russia. Genome Announc. 2014 Jun 12;2(3). doi: 10.1128/genomeA.00599-14. PMID: 24926064; PMCID: PMC4056307.
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Oligoarginine peptides slow strand annealing and assist non-enzymatic RNA replication.

Nature chemistry

Jia TZ, Fahrenbach AC, Kamat NP, Adamala KP, Szostak JW.
PMID: 27657866
Nat Chem. 2016 Oct;8(10):915-21. doi: 10.1038/nchem.2551. Epub 2016 Jun 27.

The non-enzymatic replication of RNA is thought to have been a critical process required for the origin of life. One unsolved difficulty with non-enzymatic RNA replication is that template-directed copying of RNA results in a double-stranded product. After strand...

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Jia TZ, Fahrenbach AC, Kamat NP, et al. Oligoarginine peptides slow strand annealing and assist non-enzymatic RNA replication. Nat Chem. 2016;8(10):915-21doi: 10.1038/nchem.2551.
Jia, T. Z., Fahrenbach, A. C., Kamat, N. P., Adamala, K. P., & Szostak, J. W. (2016). Oligoarginine peptides slow strand annealing and assist non-enzymatic RNA replication. Nature chemistry, 8(10), 915-21. https://doi.org/10.1038/nchem.2551
Jia, Tony Z, et al. "Oligoarginine peptides slow strand annealing and assist non-enzymatic RNA replication." Nature chemistry vol. 8,10 (2016): 915-21. doi: https://doi.org/10.1038/nchem.2551
Jia TZ, Fahrenbach AC, Kamat NP, Adamala KP, Szostak JW. Oligoarginine peptides slow strand annealing and assist non-enzymatic RNA replication. Nat Chem. 2016 Oct;8(10):915-21. doi: 10.1038/nchem.2551. Epub 2016 Jun 27. PMID: 27657866; PMCID: PMC5061144.
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The model structure of the hammerhead ribozyme formed by RNAs of reciprocal chirality.

Bioscience reports

Wyszko E, Popenda M, Gudanis D, Sarzyńska J, Belter A, Perrigue P, Skowronek P, Rolle K, Barciszewski J.
PMID: 33351058
Biosci Rep. 2021 Jan 29;41(1). doi: 10.1042/BSR20203424.

RNA-based tools are frequently used to modulate gene expression in living cells. However, the stability and effectiveness of such RNA-based tools is limited by cellular nuclease activity. One way to increase RNA's resistance to nucleases is to replace its...

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Wyszko E, Popenda M, Gudanis D, et al. The model structure of the hammerhead ribozyme formed by RNAs of reciprocal chirality. Biosci Rep. 2021;41(1)doi: 10.1042/BSR20203424.
Wyszko, E., Popenda, M., Gudanis, D., Sarzyńska, J., Belter, A., Perrigue, P., Skowronek, P., Rolle, K., & Barciszewski, J. (2021). The model structure of the hammerhead ribozyme formed by RNAs of reciprocal chirality. Bioscience reports, 41(1), . https://doi.org/10.1042/BSR20203424
Wyszko, Eliza, et al. "The model structure of the hammerhead ribozyme formed by RNAs of reciprocal chirality." Bioscience reports vol. 41,1 (2021). doi: https://doi.org/10.1042/BSR20203424
Wyszko E, Popenda M, Gudanis D, Sarzyńska J, Belter A, Perrigue P, Skowronek P, Rolle K, Barciszewski J. The model structure of the hammerhead ribozyme formed by RNAs of reciprocal chirality. Biosci Rep. 2021 Jan 29;41(1). doi: 10.1042/BSR20203424. PMID: 33351058; PMCID: PMC7796190.
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Assessment of configurations and chemistries of bridged nucleic acids-containing oligomers as external guide sequences: a methodology for inhibition of expression of antibiotic resistance genes.

Biology methods & protocols

Jackson A, Jani S, Sala CD, Soler-Bistué AJ, Zorreguieta A, Tolmasky ME.
PMID: 27857983
Biol Methods Protoc. 2016 Mar;1(1). doi: 10.1093/biomethods/bpw001. Epub 2016 Mar 01.

EGSs (external guide sequences) are short antisense oligoribonucleotides that elicit RNase P-mediated cleavage of a target mRNA, which results in inhibition of gene expression. EGS technology is used to inhibit expression of a wide variety of genes, a strategy...

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Jackson A, Jani S, Sala CD, et al. Assessment of configurations and chemistries of bridged nucleic acids-containing oligomers as external guide sequences: a methodology for inhibition of expression of antibiotic resistance genes. Biol Methods Protoc. 2016;1(1)doi: 10.1093/biomethods/bpw001.
Jackson, A., Jani, S., Sala, C. D., Soler-Bistué, A. J., Zorreguieta, A., & Tolmasky, M. E. (2016). Assessment of configurations and chemistries of bridged nucleic acids-containing oligomers as external guide sequences: a methodology for inhibition of expression of antibiotic resistance genes. Biology methods & protocols, 1(1), . https://doi.org/10.1093/biomethods/bpw001
Jackson, Alexis, et al. "Assessment of configurations and chemistries of bridged nucleic acids-containing oligomers as external guide sequences: a methodology for inhibition of expression of antibiotic resistance genes." Biology methods & protocols vol. 1,1 (2016). doi: https://doi.org/10.1093/biomethods/bpw001
Jackson A, Jani S, Sala CD, Soler-Bistué AJ, Zorreguieta A, Tolmasky ME. Assessment of configurations and chemistries of bridged nucleic acids-containing oligomers as external guide sequences: a methodology for inhibition of expression of antibiotic resistance genes. Biol Methods Protoc. 2016 Mar;1(1). doi: 10.1093/biomethods/bpw001. Epub 2016 Mar 01. PMID: 27857983; PMCID: PMC5108630.
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Oligoribonucleotides as primer for terminal deoxynucleotidyl transferase.

FEBS letters

Feix G.
PMID: 11946141
FEBS Lett. 1971 Nov 01;18(2):280-282. doi: 10.1016/0014-5793(71)80465-9.

No abstract available.

Cite
Feix G. Oligoribonucleotides as primer for terminal deoxynucleotidyl transferase. FEBS Lett. 1971;18(2):280-282doi: 10.1016/0014-5793(71)80465-9.
Feix, G. (1971). Oligoribonucleotides as primer for terminal deoxynucleotidyl transferase. FEBS letters, 18(2), 280-282. https://doi.org/10.1016/0014-5793(71)80465-9
Feix, G. "Oligoribonucleotides as primer for terminal deoxynucleotidyl transferase." FEBS letters vol. 18,2 (1971): 280-282. doi: https://doi.org/10.1016/0014-5793(71)80465-9
Feix G. Oligoribonucleotides as primer for terminal deoxynucleotidyl transferase. FEBS Lett. 1971 Nov 01;18(2):280-282. doi: 10.1016/0014-5793(71)80465-9. PMID: 11946141.
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Evidence for RNA-Oligonucleotides in Plant Vacuoles Isolated from Cultured Tomato Cells.

Plant physiology

Abel S, Blume B, Glund K.
PMID: 16667812
Plant Physiol. 1990 Nov;94(3):1163-71. doi: 10.1104/pp.94.3.1163.

We have shown that highly purified vacuoles of suspension-cultured tomato (Lycopersicon esculentum) cells contain RNA-oligonucleotides, using two different approaches to label and detect RNA: (a) in vivo labeling of cellular RNA with [5-(3)H]uridine, followed by preparation of vacuoles from...

Cite
Abel S, Blume B, Glund K. Evidence for RNA-Oligonucleotides in Plant Vacuoles Isolated from Cultured Tomato Cells. Plant Physiol. 1990;94(3):1163-71doi: 10.1104/pp.94.3.1163.
Abel, S., Blume, B., & Glund, K. (1990). Evidence for RNA-Oligonucleotides in Plant Vacuoles Isolated from Cultured Tomato Cells. Plant physiology, 94(3), 1163-71. https://doi.org/10.1104/pp.94.3.1163
Abel, S, et al. "Evidence for RNA-Oligonucleotides in Plant Vacuoles Isolated from Cultured Tomato Cells." Plant physiology vol. 94,3 (1990): 1163-71. doi: https://doi.org/10.1104/pp.94.3.1163
Abel S, Blume B, Glund K. Evidence for RNA-Oligonucleotides in Plant Vacuoles Isolated from Cultured Tomato Cells. Plant Physiol. 1990 Nov;94(3):1163-71. doi: 10.1104/pp.94.3.1163. PMID: 16667812; PMCID: PMC1077357.
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Showing 1 to 12 of 30 entries