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Subfamilies of histone H3 and H4 genes are located on most, possibly all of the chromosomes in maize.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik

Chaubet N, Philipps G, Gigot C, Guitton C, Bouvet N, Freyssinet G, Schneerman M, Weber DE.
PMID: 24201340
Theor Appl Genet. 1992 Aug;84(5):555-9. doi: 10.1007/BF00224151.

It has been previously shown that in the genome of maize the multiple copies of the histone H3 and H4 multigenic families are organized into eight to ten subfamilies each containing a variable number of copies. Each subfamily is...

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Chaubet N, Philipps G, Gigot C, et al. Subfamilies of histone H3 and H4 genes are located on most, possibly all of the chromosomes in maize. Theor Appl Genet. 1992;84(5):555-9doi: 10.1007/BF00224151.
Chaubet, N., Philipps, G., Gigot, C., Guitton, C., Bouvet, N., Freyssinet, G., Schneerman, M., & Weber, D. E. (1992). Subfamilies of histone H3 and H4 genes are located on most, possibly all of the chromosomes in maize. TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 84(5), 555-9. https://doi.org/10.1007/BF00224151
Chaubet, N, et al. "Subfamilies of histone H3 and H4 genes are located on most, possibly all of the chromosomes in maize." TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik vol. 84,5 (1992): 555-9. doi: https://doi.org/10.1007/BF00224151
Chaubet N, Philipps G, Gigot C, Guitton C, Bouvet N, Freyssinet G, Schneerman M, Weber DE. Subfamilies of histone H3 and H4 genes are located on most, possibly all of the chromosomes in maize. Theor Appl Genet. 1992 Aug;84(5):555-9. doi: 10.1007/BF00224151. PMID: 24201340.
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Callus and embryoid formation from protoplasts of Helianthus annuus.

Plant cell reports

Moyne AL, Thor V, Pelissier B, Bergounioux C, Freyssinet G, Gadal P.
PMID: 24240264
Plant Cell Rep. 1988 Oct;7(6):437-40. doi: 10.1007/BF00269532.

Sunflower hypocotyl protoplasts have been isolated and cultured. Optimum plating density for cell division and colony formation was in the range of 5 to 7×10(4) cells/mi in an agarose medium supplemented with BAP (1 mg/l) and NAA (1 mg/l)....

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Moyne AL, Thor V, Pelissier B, et al. Callus and embryoid formation from protoplasts of Helianthus annuus. Plant Cell Rep. 1988;7(6):437-40doi: 10.1007/BF00269532.
Moyne, A. L., Thor, V., Pelissier, B., Bergounioux, C., Freyssinet, G., & Gadal, P. (1988). Callus and embryoid formation from protoplasts of Helianthus annuus. Plant cell reports, 7(6), 437-40. https://doi.org/10.1007/BF00269532
Moyne, A L, et al. "Callus and embryoid formation from protoplasts of Helianthus annuus." Plant cell reports vol. 7,6 (1988): 437-40. doi: https://doi.org/10.1007/BF00269532
Moyne AL, Thor V, Pelissier B, Bergounioux C, Freyssinet G, Gadal P. Callus and embryoid formation from protoplasts of Helianthus annuus. Plant Cell Rep. 1988 Oct;7(6):437-40. doi: 10.1007/BF00269532. PMID: 24240264.
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The chloroplast and cytoplasmic ribosomes of euglena: I. Stability of chloroplast ribosomes prepared by an improved procedure.

Plant physiology

Schwartzbach SD, Freyssinet G, Schiff JA.
PMID: 16658740
Plant Physiol. 1974 Apr;53(4):533-42. doi: 10.1104/pp.53.4.533.

A new isolation procedure has resulted in an improved yield of stable 68S chloroplast ribosomes from Euglena gracilis var. bacillaris. Chloroplasts are isolated by suspending the cells in buffer I (sorbitol, 250 mm; sucrose, 250 mm; Ficoll, 2.5% [w/v];...

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Schwartzbach SD, Freyssinet G, Schiff JA. The chloroplast and cytoplasmic ribosomes of euglena: I. Stability of chloroplast ribosomes prepared by an improved procedure. Plant Physiol. 1974;53(4):533-42doi: 10.1104/pp.53.4.533.
Schwartzbach, S. D., Freyssinet, G., & Schiff, J. A. (1974). The chloroplast and cytoplasmic ribosomes of euglena: I. Stability of chloroplast ribosomes prepared by an improved procedure. Plant physiology, 53(4), 533-42. https://doi.org/10.1104/pp.53.4.533
Schwartzbach, S D, et al. "The chloroplast and cytoplasmic ribosomes of euglena: I. Stability of chloroplast ribosomes prepared by an improved procedure." Plant physiology vol. 53,4 (1974): 533-42. doi: https://doi.org/10.1104/pp.53.4.533
Schwartzbach SD, Freyssinet G, Schiff JA. The chloroplast and cytoplasmic ribosomes of euglena: I. Stability of chloroplast ribosomes prepared by an improved procedure. Plant Physiol. 1974 Apr;53(4):533-42. doi: 10.1104/pp.53.4.533. PMID: 16658740; PMCID: PMC541394.
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Influence of Culture Conditions on the Length of the Lag Period of Chlorophyll Synthesis in Preilluminated Dark-grown Euglena.

Plant physiology

Freyssinet G.
PMID: 16659579
Plant Physiol. 1976 May;57(5):831-5. doi: 10.1104/pp.57.5.831.

Two parameters of the potentiation process, the lengths of preillumination and of the subsequent dark phase have been determined for Euglena cells which had been grown in the dark under two different culture conditions. In both cases a maximum...

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Freyssinet G. Influence of Culture Conditions on the Length of the Lag Period of Chlorophyll Synthesis in Preilluminated Dark-grown Euglena. Plant Physiol. 1976;57(5):831-5doi: 10.1104/pp.57.5.831.
Freyssinet, G. (1976). Influence of Culture Conditions on the Length of the Lag Period of Chlorophyll Synthesis in Preilluminated Dark-grown Euglena. Plant physiology, 57(5), 831-5. https://doi.org/10.1104/pp.57.5.831
Freyssinet, G. "Influence of Culture Conditions on the Length of the Lag Period of Chlorophyll Synthesis in Preilluminated Dark-grown Euglena." Plant physiology vol. 57,5 (1976): 831-5. doi: https://doi.org/10.1104/pp.57.5.831
Freyssinet G. Influence of Culture Conditions on the Length of the Lag Period of Chlorophyll Synthesis in Preilluminated Dark-grown Euglena. Plant Physiol. 1976 May;57(5):831-5. doi: 10.1104/pp.57.5.831. PMID: 16659579; PMCID: PMC542127.
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Genotypic variation of quantitative trait loci controlling in vitro androgenesis in maize.

Genome

Murigneux A, Bentolila S, Hardy T, Baud S, Guitton C, Jullien H, Tahar SB, Freyssinet G, Beckert M.
PMID: 18470136
Genome. 1994 Dec;37(6):970-6. doi: 10.1139/g94-137.

A quantitative trait loci (QTL) analysis for androgenetic capability has been conducted on three different crosses in maize, including very high and nonresponding lines for androgenesis. The doubled haploid lines derived by anther culture from the crosses DH5 x...

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Murigneux A, Bentolila S, Hardy T, et al. Genotypic variation of quantitative trait loci controlling in vitro androgenesis in maize. Genome. 1994;37(6):970-6doi: 10.1139/g94-137.
Murigneux, A., Bentolila, S., Hardy, T., Baud, S., Guitton, C., Jullien, H., Tahar, S. B., Freyssinet, G., & Beckert, M. (1994). Genotypic variation of quantitative trait loci controlling in vitro androgenesis in maize. Genome, 37(6), 970-6. https://doi.org/10.1139/g94-137
Murigneux, A, et al. "Genotypic variation of quantitative trait loci controlling in vitro androgenesis in maize." Genome vol. 37,6 (1994): 970-6. doi: https://doi.org/10.1139/g94-137
Murigneux A, Bentolila S, Hardy T, Baud S, Guitton C, Jullien H, Tahar SB, Freyssinet G, Beckert M. Genotypic variation of quantitative trait loci controlling in vitro androgenesis in maize. Genome. 1994 Dec;37(6):970-6. doi: 10.1139/g94-137. PMID: 18470136.
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Does high mitochondrial efficiency carry an oxidative cost? The case of the African pygmy mouse (Mus mattheyi).

Comparative biochemistry and physiology. Part A, Molecular & integrative physiology

Boël M, Veyrunes F, Durieux AC, Freyssenet D, Voituron Y, Roussel D.
PMID: 34748935
Comp Biochem Physiol A Mol Integr Physiol. 2021 Nov 05;264:111111. doi: 10.1016/j.cbpa.2021.111111. Epub 2021 Nov 05.

Skeletal muscle mitochondria of the African pygmy mouse Mus mattheyi exhibit markedly reduced oxygen consumption and ATP synthesis rates but a higher mitochondrial efficiency than what would be expected from allometric trends. In the present study, we assessed whether...

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Boël M, Veyrunes F, Durieux AC, et al. Does high mitochondrial efficiency carry an oxidative cost? The case of the African pygmy mouse (Mus mattheyi). Comp Biochem Physiol A Mol Integr Physiol. 2021;264:111111doi: 10.1016/j.cbpa.2021.111111.
Boël, M., Veyrunes, F., Durieux, A. C., Freyssenet, D., Voituron, Y., & Roussel, D. (2021). Does high mitochondrial efficiency carry an oxidative cost? The case of the African pygmy mouse (Mus mattheyi). Comparative biochemistry and physiology. Part A, Molecular & integrative physiology, 264111111. https://doi.org/10.1016/j.cbpa.2021.111111
Boël, Mélanie, et al. "Does high mitochondrial efficiency carry an oxidative cost? The case of the African pygmy mouse (Mus mattheyi)." Comparative biochemistry and physiology. Part A, Molecular & integrative physiology vol. 264 (2021): 111111. doi: https://doi.org/10.1016/j.cbpa.2021.111111
Boël M, Veyrunes F, Durieux AC, Freyssenet D, Voituron Y, Roussel D. Does high mitochondrial efficiency carry an oxidative cost? The case of the African pygmy mouse (Mus mattheyi). Comp Biochem Physiol A Mol Integr Physiol. 2021 Nov 05;264:111111. doi: 10.1016/j.cbpa.2021.111111. Epub 2021 Nov 05. PMID: 34748935.
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Early Deconditioning of Human Skeletal Muscles and the Effects of a Thigh Cuff Countermeasure.

International journal of molecular sciences

Fovet T, Guilhot C, Stevens L, Montel V, Delobel P, Roumanille R, Semporé MY, Freyssenet D, Py G, Brioche T, Chopard A.
PMID: 34769492
Int J Mol Sci. 2021 Nov 08;22(21). doi: 10.3390/ijms222112064.

Muscle deconditioning is a major consequence of a wide range of conditions from spaceflight to a sedentary lifestyle, and occurs as a result of muscle inactivity, leading to a rapid decrease in muscle strength, mass, and oxidative capacity. The...

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Fovet T, Guilhot C, Stevens L, et al. Early Deconditioning of Human Skeletal Muscles and the Effects of a Thigh Cuff Countermeasure. Int J Mol Sci. 2021;22(21)doi: 10.3390/ijms222112064.
Fovet, T., Guilhot, C., Stevens, L., Montel, V., Delobel, P., Roumanille, R., Semporé, M. Y., Freyssenet, D., Py, G., Brioche, T., & Chopard, A. (2021). Early Deconditioning of Human Skeletal Muscles and the Effects of a Thigh Cuff Countermeasure. International journal of molecular sciences, 22(21), . https://doi.org/10.3390/ijms222112064
Fovet, Théo, et al. "Early Deconditioning of Human Skeletal Muscles and the Effects of a Thigh Cuff Countermeasure." International journal of molecular sciences vol. 22,21 (2021). doi: https://doi.org/10.3390/ijms222112064
Fovet T, Guilhot C, Stevens L, Montel V, Delobel P, Roumanille R, Semporé MY, Freyssenet D, Py G, Brioche T, Chopard A. Early Deconditioning of Human Skeletal Muscles and the Effects of a Thigh Cuff Countermeasure. Int J Mol Sci. 2021 Nov 08;22(21). doi: 10.3390/ijms222112064. PMID: 34769492; PMCID: PMC8584355.
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Tissue-Specific Expression of Germin-Like Oxalate Oxidase during Development and Fungal Infection of Barley Seedlings.

Plant physiology

Dumas B, Freyssinet G, Pallett KE.
PMID: 12228419
Plant Physiol. 1995 Apr;107(4):1091-1096. doi: 10.1104/pp.107.4.1091.

Oxalate oxidase activity was detected in situ during the development of barley seedlings. The presence of germin-like oxalate oxidase was confirmed by immunoblotting using an antibody directed against wheat germin produced in Escherichia coli, which is shown to cross-react...

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Dumas B, Freyssinet G, Pallett KE. Tissue-Specific Expression of Germin-Like Oxalate Oxidase during Development and Fungal Infection of Barley Seedlings. Plant Physiol. 1995;107(4):1091-1096doi: 10.1104/pp.107.4.1091.
Dumas, B., Freyssinet, G., & Pallett, K. E. (1995). Tissue-Specific Expression of Germin-Like Oxalate Oxidase during Development and Fungal Infection of Barley Seedlings. Plant physiology, 107(4), 1091-1096. https://doi.org/10.1104/pp.107.4.1091
Dumas, B., et al. "Tissue-Specific Expression of Germin-Like Oxalate Oxidase during Development and Fungal Infection of Barley Seedlings." Plant physiology vol. 107,4 (1995): 1091-1096. doi: https://doi.org/10.1104/pp.107.4.1091
Dumas B, Freyssinet G, Pallett KE. Tissue-Specific Expression of Germin-Like Oxalate Oxidase during Development and Fungal Infection of Barley Seedlings. Plant Physiol. 1995 Apr;107(4):1091-1096. doi: 10.1104/pp.107.4.1091. PMID: 12228419; PMCID: PMC157241.
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Expression of Chloroplast and Mitochondrial Genes during Microsporogenesis in Maize.

Plant physiology

Monéger F, Mandaron P, Niogret MF, Freyssinet G, Mache R.
PMID: 16668897
Plant Physiol. 1992 Jun;99(2):396-400. doi: 10.1104/pp.99.2.396.

Mitochondrial and plastid gene expression has been examined during maize (Zea mays) microsporogenesis. Accumulation of transcripts was found for three mitochondrial genes studied (cob, atp6, and atp9) at the mid-term of pollen development. In contrast, these mitochondrial transcripts were...

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Monéger F, Mandaron P, Niogret MF, et al. Expression of Chloroplast and Mitochondrial Genes during Microsporogenesis in Maize. Plant Physiol. 1992;99(2):396-400doi: 10.1104/pp.99.2.396.
Monéger, F., Mandaron, P., Niogret, M. F., Freyssinet, G., & Mache, R. (1992). Expression of Chloroplast and Mitochondrial Genes during Microsporogenesis in Maize. Plant physiology, 99(2), 396-400. https://doi.org/10.1104/pp.99.2.396
Monéger, F, et al. "Expression of Chloroplast and Mitochondrial Genes during Microsporogenesis in Maize." Plant physiology vol. 99,2 (1992): 396-400. doi: https://doi.org/10.1104/pp.99.2.396
Monéger F, Mandaron P, Niogret MF, Freyssinet G, Mache R. Expression of Chloroplast and Mitochondrial Genes during Microsporogenesis in Maize. Plant Physiol. 1992 Jun;99(2):396-400. doi: 10.1104/pp.99.2.396. PMID: 16668897; PMCID: PMC1080474.
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Relation between Paramylum Content and the Length of the Lag Period of Chlorophyll Synthesis during Greening of Dark-grown Euglena gracilis.

Plant physiology

Freyssinet G, Schwob C.
PMID: 16659578
Plant Physiol. 1976 May;57(5):824-30. doi: 10.1104/pp.57.5.824.

Euglena cells, strains Z and bacillaris, were grown in the dark under various nutritional deficiencies. After 3 days of nondivision, cells were transferred to the light, and the following parameters were measured: the paramylum content at the time of...

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Freyssinet G, Schwob C. Relation between Paramylum Content and the Length of the Lag Period of Chlorophyll Synthesis during Greening of Dark-grown Euglena gracilis. Plant Physiol. 1976;57(5):824-30doi: 10.1104/pp.57.5.824.
Freyssinet, G., & Schwob, C. (1976). Relation between Paramylum Content and the Length of the Lag Period of Chlorophyll Synthesis during Greening of Dark-grown Euglena gracilis. Plant physiology, 57(5), 824-30. https://doi.org/10.1104/pp.57.5.824
Freyssinet, G, and Schwob, C. "Relation between Paramylum Content and the Length of the Lag Period of Chlorophyll Synthesis during Greening of Dark-grown Euglena gracilis." Plant physiology vol. 57,5 (1976): 824-30. doi: https://doi.org/10.1104/pp.57.5.824
Freyssinet G, Schwob C. Relation between Paramylum Content and the Length of the Lag Period of Chlorophyll Synthesis during Greening of Dark-grown Euglena gracilis. Plant Physiol. 1976 May;57(5):824-30. doi: 10.1104/pp.57.5.824. PMID: 16659578; PMCID: PMC542126.
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Purification and Characterization of Extracellular Pectinolytic Enzymes Produced by Sclerotinia sclerotiorum.

Applied and environmental microbiology

Riou C, Freyssinet G, Fevre M.
PMID: 16348646
Appl Environ Microbiol. 1992 Feb;58(2):578-83. doi: 10.1128/aem.58.2.578-583.1992.

An exopolygalacturonase (exoPG) and an exopolymethylgalacturonase (exoPMG) produced by Sclerotinia sclerotiorum have been purified by ammonium sulfate precipitation, gel filtration, and ion exchange chromatography. The exoPG and the exoPMG were purified 66- and 50-fold, respectively, by using a series...

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Riou C, Freyssinet G, Fevre M. Purification and Characterization of Extracellular Pectinolytic Enzymes Produced by Sclerotinia sclerotiorum. Appl Environ Microbiol. 1992;58(2):578-83doi: 10.1128/aem.58.2.578-583.1992.
Riou, C., Freyssinet, G., & Fevre, M. (1992). Purification and Characterization of Extracellular Pectinolytic Enzymes Produced by Sclerotinia sclerotiorum. Applied and environmental microbiology, 58(2), 578-83. https://doi.org/10.1128/aem.58.2.578-583.1992
Riou, C, et al. "Purification and Characterization of Extracellular Pectinolytic Enzymes Produced by Sclerotinia sclerotiorum." Applied and environmental microbiology vol. 58,2 (1992): 578-83. doi: https://doi.org/10.1128/aem.58.2.578-583.1992
Riou C, Freyssinet G, Fevre M. Purification and Characterization of Extracellular Pectinolytic Enzymes Produced by Sclerotinia sclerotiorum. Appl Environ Microbiol. 1992 Feb;58(2):578-83. doi: 10.1128/aem.58.2.578-583.1992. PMID: 16348646; PMCID: PMC195287.
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Transformed calli obtained by direct gene transfer into sunflower protoplasts.

Plant cell reports

Moyne AL, Tagu D, Thor V, Bergounioux C, Freyssinet G, Gadal P.
PMID: 24232994
Plant Cell Rep. 1989 Feb;8(2):97-100. doi: 10.1007/BF00716848.

Helianthus annuus protoplasts were transformed with the plasmid pCaMVNEO (Frommet al. 1986) conferring kanamycin resistance to plant. Transformed calli were selected with a frequency of 4 calli for 10(6) treated protoplasts. DNA was extracted from kanamycin resistant calli. Analysis...

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Moyne AL, Tagu D, Thor V, et al. Transformed calli obtained by direct gene transfer into sunflower protoplasts. Plant Cell Rep. 1989;8(2):97-100doi: 10.1007/BF00716848.
Moyne, A. L., Tagu, D., Thor, V., Bergounioux, C., Freyssinet, G., & Gadal, P. (1989). Transformed calli obtained by direct gene transfer into sunflower protoplasts. Plant cell reports, 8(2), 97-100. https://doi.org/10.1007/BF00716848
Moyne, A L, et al. "Transformed calli obtained by direct gene transfer into sunflower protoplasts." Plant cell reports vol. 8,2 (1989): 97-100. doi: https://doi.org/10.1007/BF00716848
Moyne AL, Tagu D, Thor V, Bergounioux C, Freyssinet G, Gadal P. Transformed calli obtained by direct gene transfer into sunflower protoplasts. Plant Cell Rep. 1989 Feb;8(2):97-100. doi: 10.1007/BF00716848. PMID: 24232994.
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Showing 1 to 12 of 24 entries