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Showing 13 to 24 of 241 entries
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Characterization of an HSP70 Cognate Gene Family in Arabidopsis.

Plant physiology

Wu CH, Caspar T, Browse J, Lindquist S, Somerville C.
PMID: 16666375
Plant Physiol. 1988 Nov;88(3):731-40. doi: 10.1104/pp.88.3.731.

Analysis of the polypeptide composition of extracts from heat-shocked leaves of Arabidopsis indicated the presence of at least 12 HSP70-related polypeptides, most of which were constitutively expressed. In vitro translation of mRNA from heat-shocked and control leaves indicated that...

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Wu CH, Caspar T, Browse J, et al. Characterization of an HSP70 Cognate Gene Family in Arabidopsis. Plant Physiol. 1988;88(3):731-40doi: 10.1104/pp.88.3.731.
Wu, C. H., Caspar, T., Browse, J., Lindquist, S., & Somerville, C. (1988). Characterization of an HSP70 Cognate Gene Family in Arabidopsis. Plant physiology, 88(3), 731-40. https://doi.org/10.1104/pp.88.3.731
Wu, C H, et al. "Characterization of an HSP70 Cognate Gene Family in Arabidopsis." Plant physiology vol. 88,3 (1988): 731-40. doi: https://doi.org/10.1104/pp.88.3.731
Wu CH, Caspar T, Browse J, Lindquist S, Somerville C. Characterization of an HSP70 Cognate Gene Family in Arabidopsis. Plant Physiol. 1988 Nov;88(3):731-40. doi: 10.1104/pp.88.3.731. PMID: 16666375; PMCID: PMC1055652.
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Comparing bacterial DNA microarray fingerprints.

Statistical applications in genetics and molecular biology

Willse A, Chandler DP, White A, Protic M, Daly DS, Wunschel S.
PMID: 16646836
Stat Appl Genet Mol Biol. 2005;4:Article19. doi: 10.2202/1544-6115.1162. Epub 2005 Aug 15.

Epidemiologic and forensic investigations often require assays to detect subtle genetic differences between closely related microorganisms. Typically, gel electrophoresis is used to compare randomly amplified DNA fragments between microbial samples, where the patterns of DNA fragment sizes are viewed...

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Willse A, Chandler DP, White A, et al. Comparing bacterial DNA microarray fingerprints. Stat Appl Genet Mol Biol. 2005;4:Article19doi: 10.2202/1544-6115.1162.
Willse, A., Chandler, D. P., White, A., Protic, M., Daly, D. S., & Wunschel, S. (2005). Comparing bacterial DNA microarray fingerprints. Statistical applications in genetics and molecular biology, 4Article19. https://doi.org/10.2202/1544-6115.1162
Willse, Alan, et al. "Comparing bacterial DNA microarray fingerprints." Statistical applications in genetics and molecular biology vol. 4 (2005): Article19. doi: https://doi.org/10.2202/1544-6115.1162
Willse A, Chandler DP, White A, Protic M, Daly DS, Wunschel S. Comparing bacterial DNA microarray fingerprints. Stat Appl Genet Mol Biol. 2005;4:Article19. doi: 10.2202/1544-6115.1162. Epub 2005 Aug 15. PMID: 16646836.
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Terminal restriction pattern analysis of 16S rRNA genes for the characterization of bacterial communities of activated sludge.

Journal of bioscience and bioengineering

Hiraishi A, Iwasaki M, Shinjo H.
PMID: 16232834
J Biosci Bioeng. 2000;90(2):148-56. doi: 10.1016/s1389-1723(00)80102-4.

A culture-independent molecular technique using terminal restriction fragment length polymorphism (T-RFLP) of 16S rRNA genes was applied to the characterization of bacterial communities of activated sludge taken from different municipal sewage treatment plants. 16S rDNA fragments from the bulk...

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Hiraishi A, Iwasaki M, Shinjo H. Terminal restriction pattern analysis of 16S rRNA genes for the characterization of bacterial communities of activated sludge. J Biosci Bioeng. 2000;90(2):148-56doi: 10.1016/s1389-1723(00)80102-4.
Hiraishi, A., Iwasaki, M., & Shinjo, H. (2000). Terminal restriction pattern analysis of 16S rRNA genes for the characterization of bacterial communities of activated sludge. Journal of bioscience and bioengineering, 90(2), 148-56. https://doi.org/10.1016/s1389-1723(00)80102-4
Hiraishi, A, et al. "Terminal restriction pattern analysis of 16S rRNA genes for the characterization of bacterial communities of activated sludge." Journal of bioscience and bioengineering vol. 90,2 (2000): 148-56. doi: https://doi.org/10.1016/s1389-1723(00)80102-4
Hiraishi A, Iwasaki M, Shinjo H. Terminal restriction pattern analysis of 16S rRNA genes for the characterization of bacterial communities of activated sludge. J Biosci Bioeng. 2000;90(2):148-56. doi: 10.1016/s1389-1723(00)80102-4. PMID: 16232834.
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Community analysis of the bacterial assemblages in the winter cover and pelagic layers of a high mountain lake by in situ hybridization.

Applied and environmental microbiology

Alfreider A, Pernthaler J, Amann R, Sattler B, Glockner F, Wille A, Psenner R.
PMID: 16535341
Appl Environ Microbiol. 1996 Jun;62(6):2138-44. doi: 10.1128/aem.62.6.2138-2144.1996.

The bacterial community structure in the winter cover and pelagic zone of a high mountain lake was analyzed by in situ hybridization with fluorescently labeled rRNA-targeted oligonucleotide probes. Cells fixed on membrane filters were hybridized with a probe specific...

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Alfreider A, Pernthaler J, Amann R, et al. Community analysis of the bacterial assemblages in the winter cover and pelagic layers of a high mountain lake by in situ hybridization. Appl Environ Microbiol. 1996;62(6):2138-44doi: 10.1128/aem.62.6.2138-2144.1996.
Alfreider, A., Pernthaler, J., Amann, R., Sattler, B., Glockner, F., Wille, A., & Psenner, R. (1996). Community analysis of the bacterial assemblages in the winter cover and pelagic layers of a high mountain lake by in situ hybridization. Applied and environmental microbiology, 62(6), 2138-44. https://doi.org/10.1128/aem.62.6.2138-2144.1996
Alfreider, A, et al. "Community analysis of the bacterial assemblages in the winter cover and pelagic layers of a high mountain lake by in situ hybridization." Applied and environmental microbiology vol. 62,6 (1996): 2138-44. doi: https://doi.org/10.1128/aem.62.6.2138-2144.1996
Alfreider A, Pernthaler J, Amann R, Sattler B, Glockner F, Wille A, Psenner R. Community analysis of the bacterial assemblages in the winter cover and pelagic layers of a high mountain lake by in situ hybridization. Appl Environ Microbiol. 1996 Jun;62(6):2138-44. doi: 10.1128/aem.62.6.2138-2144.1996. PMID: 16535341; PMCID: PMC1388879.
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Morphological and compositional shifts in an experimental bacterial community influenced by protists with contrasting feeding modes.

Applied and environmental microbiology

Simek K, Vrba J, Pernthaler J, Posch T, Hartman P, Nedoma J, Psenner R.
PMID: 16535515
Appl Environ Microbiol. 1997 Feb;63(2):587-95. doi: 10.1128/aem.63.2.587-595.1997.

In a two-stage continuous-flow system, we studied the impacts of different protozoan feeding modes on the morphology and taxonomic structure of mixed bacterial consortia, which were utilizing organic carbon released by a pure culture of a Rhodomonas sp. grown...

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Simek K, Vrba J, Pernthaler J, et al. Morphological and compositional shifts in an experimental bacterial community influenced by protists with contrasting feeding modes. Appl Environ Microbiol. 1997;63(2):587-95doi: 10.1128/aem.63.2.587-595.1997.
Simek, K., Vrba, J., Pernthaler, J., Posch, T., Hartman, P., Nedoma, J., & Psenner, R. (1997). Morphological and compositional shifts in an experimental bacterial community influenced by protists with contrasting feeding modes. Applied and environmental microbiology, 63(2), 587-95. https://doi.org/10.1128/aem.63.2.587-595.1997
Simek, K, et al. "Morphological and compositional shifts in an experimental bacterial community influenced by protists with contrasting feeding modes." Applied and environmental microbiology vol. 63,2 (1997): 587-95. doi: https://doi.org/10.1128/aem.63.2.587-595.1997
Simek K, Vrba J, Pernthaler J, Posch T, Hartman P, Nedoma J, Psenner R. Morphological and compositional shifts in an experimental bacterial community influenced by protists with contrasting feeding modes. Appl Environ Microbiol. 1997 Feb;63(2):587-95. doi: 10.1128/aem.63.2.587-595.1997. PMID: 16535515; PMCID: PMC1389521.
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A New Sensitive, Whole-Cell Hybridization Technique for Detection of Bacteria Involving a Biotinylated Oligonucleotide Probe Targeting rRNA and Tyramide Signal Amplification.

Applied and environmental microbiology

Lebaron P, Catala P, Fajon C, Joux F, Baudart J, Bernard L.
PMID: 16535676
Appl Environ Microbiol. 1997 Aug;63(8):3274-8. doi: 10.1128/aem.63.8.3274-3278.1997.

A tyramide signal amplification system with biotinylated oligonucleotide probes and streptavidin-horseradish peroxidase was used to increase the sensitivity of fluorescent in situ hybridization techniques. When applied to both gram-negative and -positive bacteria immobilized on glass slides, a 7- to...

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Lebaron P, Catala P, Fajon C, et al. A New Sensitive, Whole-Cell Hybridization Technique for Detection of Bacteria Involving a Biotinylated Oligonucleotide Probe Targeting rRNA and Tyramide Signal Amplification. Appl Environ Microbiol. 1997;63(8):3274-8doi: 10.1128/aem.63.8.3274-3278.1997.
Lebaron, P., Catala, P., Fajon, C., Joux, F., Baudart, J., & Bernard, L. (1997). A New Sensitive, Whole-Cell Hybridization Technique for Detection of Bacteria Involving a Biotinylated Oligonucleotide Probe Targeting rRNA and Tyramide Signal Amplification. Applied and environmental microbiology, 63(8), 3274-8. https://doi.org/10.1128/aem.63.8.3274-3278.1997
Lebaron, P, et al. "A New Sensitive, Whole-Cell Hybridization Technique for Detection of Bacteria Involving a Biotinylated Oligonucleotide Probe Targeting rRNA and Tyramide Signal Amplification." Applied and environmental microbiology vol. 63,8 (1997): 3274-8. doi: https://doi.org/10.1128/aem.63.8.3274-3278.1997
Lebaron P, Catala P, Fajon C, Joux F, Baudart J, Bernard L. A New Sensitive, Whole-Cell Hybridization Technique for Detection of Bacteria Involving a Biotinylated Oligonucleotide Probe Targeting rRNA and Tyramide Signal Amplification. Appl Environ Microbiol. 1997 Aug;63(8):3274-8. doi: 10.1128/aem.63.8.3274-3278.1997. PMID: 16535676; PMCID: PMC1389231.
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In situ classification and image cytometry of pelagic bacteria from a high mountain lake (gossenkollesee, austria).

Applied and environmental microbiology

Pernthaler J, Alfreider A, Posch T, Andreatta S, Psenner R.
PMID: 16535752
Appl Environ Microbiol. 1997 Dec;63(12):4778-83. doi: 10.1128/aem.63.12.4778-4783.1997.

We describe a procedure to measure the cell sizes of pelagic bacteria after determinative hybridization with rRNA-targeted fluorescently labeled oligonucleotide probes. Our approach is based on established image analysis techniques modified for objects simultaneously stained with two fluorescent dyes....

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Pernthaler J, Alfreider A, Posch T, et al. In situ classification and image cytometry of pelagic bacteria from a high mountain lake (gossenkollesee, austria). Appl Environ Microbiol. 1997;63(12):4778-83doi: 10.1128/aem.63.12.4778-4783.1997.
Pernthaler, J., Alfreider, A., Posch, T., Andreatta, S., & Psenner, R. (1997). In situ classification and image cytometry of pelagic bacteria from a high mountain lake (gossenkollesee, austria). Applied and environmental microbiology, 63(12), 4778-83. https://doi.org/10.1128/aem.63.12.4778-4783.1997
Pernthaler, J, et al. "In situ classification and image cytometry of pelagic bacteria from a high mountain lake (gossenkollesee, austria)." Applied and environmental microbiology vol. 63,12 (1997): 4778-83. doi: https://doi.org/10.1128/aem.63.12.4778-4783.1997
Pernthaler J, Alfreider A, Posch T, Andreatta S, Psenner R. In situ classification and image cytometry of pelagic bacteria from a high mountain lake (gossenkollesee, austria). Appl Environ Microbiol. 1997 Dec;63(12):4778-83. doi: 10.1128/aem.63.12.4778-4783.1997. PMID: 16535752; PMCID: PMC1389308.
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Group-Specific 16S rRNA-Targeted Oligonucleotide Probes To Identify Thermophilic Bacteria in Marine Hydrothermal Vents.

Applied and environmental microbiology

Harmsen H, Prieur D, Jeanthon C.
PMID: 16535717
Appl Environ Microbiol. 1997 Oct;63(10):4061-8. doi: 10.1128/aem.63.10.4061-4068.1997.

Four 16S rRNA-targeted oligonucleotide probes were designed for the detection of thermophilic members of the domain Bacteria known to thrive in marine hydrothermal systems. We developed and characterized probes encompassing most of the thermophilic members of the genus Bacillus,...

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Harmsen H, Prieur D, Jeanthon C. Group-Specific 16S rRNA-Targeted Oligonucleotide Probes To Identify Thermophilic Bacteria in Marine Hydrothermal Vents. Appl Environ Microbiol. 1997;63(10):4061-8doi: 10.1128/aem.63.10.4061-4068.1997.
Harmsen, H., Prieur, D., & Jeanthon, C. (1997). Group-Specific 16S rRNA-Targeted Oligonucleotide Probes To Identify Thermophilic Bacteria in Marine Hydrothermal Vents. Applied and environmental microbiology, 63(10), 4061-8. https://doi.org/10.1128/aem.63.10.4061-4068.1997
Harmsen, H, et al. "Group-Specific 16S rRNA-Targeted Oligonucleotide Probes To Identify Thermophilic Bacteria in Marine Hydrothermal Vents." Applied and environmental microbiology vol. 63,10 (1997): 4061-8. doi: https://doi.org/10.1128/aem.63.10.4061-4068.1997
Harmsen H, Prieur D, Jeanthon C. Group-Specific 16S rRNA-Targeted Oligonucleotide Probes To Identify Thermophilic Bacteria in Marine Hydrothermal Vents. Appl Environ Microbiol. 1997 Oct;63(10):4061-8. doi: 10.1128/aem.63.10.4061-4068.1997. PMID: 16535717; PMCID: PMC1389273.
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Characterization of the Cricket Hindgut Microbiota with Fluorescently Labeled rRNA-Targeted Oligonucleotide Probes.

Applied and environmental microbiology

Santo Domingo JW, Kaufman MG, Klug MJ, Tiedje JM.
PMID: 16349506
Appl Environ Microbiol. 1998 Feb;64(2):752-5. doi: 10.1128/AEM.64.2.752-755.1998.

Most cricket hindgut microorganisms (60 to 80%) were detected with a universal fluorescent rRNA-targeted probe and found to be eubacteria. Group-specific probes showed that the hindguts of five different cricket species harbor similar bacterial groups, although in different proportions,...

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Santo Domingo JW, Kaufman MG, Klug MJ, et al. Characterization of the Cricket Hindgut Microbiota with Fluorescently Labeled rRNA-Targeted Oligonucleotide Probes. Appl Environ Microbiol. 1998;64(2):752-5doi: 10.1128/AEM.64.2.752-755.1998.
Santo Domingo, J. W., Kaufman, M. G., Klug, M. J., & Tiedje, J. M. (1998). Characterization of the Cricket Hindgut Microbiota with Fluorescently Labeled rRNA-Targeted Oligonucleotide Probes. Applied and environmental microbiology, 64(2), 752-5. https://doi.org/10.1128/AEM.64.2.752-755.1998
Santo Domingo, J W, et al. "Characterization of the Cricket Hindgut Microbiota with Fluorescently Labeled rRNA-Targeted Oligonucleotide Probes." Applied and environmental microbiology vol. 64,2 (1998): 752-5. doi: https://doi.org/10.1128/AEM.64.2.752-755.1998
Santo Domingo JW, Kaufman MG, Klug MJ, Tiedje JM. Characterization of the Cricket Hindgut Microbiota with Fluorescently Labeled rRNA-Targeted Oligonucleotide Probes. Appl Environ Microbiol. 1998 Feb;64(2):752-5. doi: 10.1128/AEM.64.2.752-755.1998. PMID: 16349506; PMCID: PMC106112.
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Molecular Cloning and Characterization of c-erb-A mRNA Species in Mouse Neuroblastoma Cells.

Journal of neuroendocrinology

Moeller M, Rapoport B, Gavin LA.
PMID: 19210427
J Neuroendocrinol. 1989 Oct 01;1(5):351-6. doi: 10.1111/j.1365-2826.1989.tb00128.x.

UNLABELLED: Abstract The mouse neuroblastoma cell line is an excellent model in which to study thyroid hormone action and metabolism, particularly in neural tissue. We therefore undertook the molecular cloning and characterization in these cells of putative thyroid hormone...

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Moeller M, Rapoport B, Gavin LA. Molecular Cloning and Characterization of c-erb-A mRNA Species in Mouse Neuroblastoma Cells. J Neuroendocrinol. 1989;1(5):351-6doi: 10.1111/j.1365-2826.1989.tb00128.x.
Moeller, M., Rapoport, B., & Gavin, L. A. (1989). Molecular Cloning and Characterization of c-erb-A mRNA Species in Mouse Neuroblastoma Cells. Journal of neuroendocrinology, 1(5), 351-6. https://doi.org/10.1111/j.1365-2826.1989.tb00128.x
Moeller, M, et al. "Molecular Cloning and Characterization of c-erb-A mRNA Species in Mouse Neuroblastoma Cells." Journal of neuroendocrinology vol. 1,5 (1989): 351-6. doi: https://doi.org/10.1111/j.1365-2826.1989.tb00128.x
Moeller M, Rapoport B, Gavin LA. Molecular Cloning and Characterization of c-erb-A mRNA Species in Mouse Neuroblastoma Cells. J Neuroendocrinol. 1989 Oct 01;1(5):351-6. doi: 10.1111/j.1365-2826.1989.tb00128.x. PMID: 19210427.
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Design and characterization of two-dye and three-dye binary fluorescent probes for mRNA detection.

Tetrahedron

Martí AA, Li X, Jockusch S, Stevens N, Li Z, Raveendra B, Kalachikov S, Morozova I, Russo JJ, Akins DL, Ju J, Turro NJ.
PMID: 19907676
Tetrahedron. 2007 Apr 23;63(17):3591-3600. doi: 10.1016/j.tet.2006.08.109.

We report the design, synthesis and characterization of binary oligonucleotide probes for mRNA detection. The probes were designed to avoid common problems found in standard binary probes such as direct excitation of the acceptor fluorophore and overlap between the...

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Martí AA, Li X, Jockusch S, et al. Design and characterization of two-dye and three-dye binary fluorescent probes for mRNA detection. Tetrahedron. 2007;63(17):3591-3600doi: 10.1016/j.tet.2006.08.109.
Martí, A. A., Li, X., Jockusch, S., Stevens, N., Li, Z., Raveendra, B., Kalachikov, S., Morozova, I., Russo, J. J., Akins, D. L., Ju, J., & Turro, N. J. (2007). Design and characterization of two-dye and three-dye binary fluorescent probes for mRNA detection. Tetrahedron, 63(17), 3591-3600. https://doi.org/10.1016/j.tet.2006.08.109
Martí, Angel A, et al. "Design and characterization of two-dye and three-dye binary fluorescent probes for mRNA detection." Tetrahedron vol. 63,17 (2007): 3591-3600. doi: https://doi.org/10.1016/j.tet.2006.08.109
Martí AA, Li X, Jockusch S, Stevens N, Li Z, Raveendra B, Kalachikov S, Morozova I, Russo JJ, Akins DL, Ju J, Turro NJ. Design and characterization of two-dye and three-dye binary fluorescent probes for mRNA detection. Tetrahedron. 2007 Apr 23;63(17):3591-3600. doi: 10.1016/j.tet.2006.08.109. PMID: 19907676; PMCID: PMC2775546.
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Oligonucleotide probes for DNA fingerprinting in horses.

Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie

Wilke K, Weimann M, Jung M, Geldermann H.
PMID: 21395728
J Anim Breed Genet. 1993 Jan 12;110(1):301-4. doi: 10.1111/j.1439-0388.1993.tb00741.x.

SUMMARY: 10 different oligonucleotide probes were evaluated for DNA fingerprinting in horses. Five probes were able to detect polymorphic bands. The probes (GT)(8) , (GTG)(5) and (GGAT)(4) are most informative for individual identification and were used to analyze a...

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Wilke K, Weimann M, Jung M, et al. Oligonucleotide probes for DNA fingerprinting in horses. J Anim Breed Genet. 1993;110(1):301-4doi: 10.1111/j.1439-0388.1993.tb00741.x.
Wilke, K., Weimann, M., Jung, M., & Geldermann, H. (1993). Oligonucleotide probes for DNA fingerprinting in horses. Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie, 110(1), 301-4. https://doi.org/10.1111/j.1439-0388.1993.tb00741.x
Wilke, K, et al. "Oligonucleotide probes for DNA fingerprinting in horses." Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie vol. 110,1 (1993): 301-4. doi: https://doi.org/10.1111/j.1439-0388.1993.tb00741.x
Wilke K, Weimann M, Jung M, Geldermann H. Oligonucleotide probes for DNA fingerprinting in horses. J Anim Breed Genet. 1993 Jan 12;110(1):301-4. doi: 10.1111/j.1439-0388.1993.tb00741.x. PMID: 21395728.
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Showing 13 to 24 of 241 entries