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1

Molekularne odpowiedzi aparatu fotosyntetycznego roślin na długoterminowe zmiany natężenia światła

100%
Adamiec M., Jackowski G.
Postępy Biochemii
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2008
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tom 54
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nr 4
2

UV radiation in HCT 116 cells influences intracellular H2O2 and glutathione levels, antioxidant expression, and protein glutathionylation

100%
Adamiec M., Skonieczna M.
Acta Biochimica Polonica
|
2019
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tom 66
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nr 4
3

The fuel cell as the source of energy in the driving system of an electrical grass mower – studies of the functional model

100%
Adamiec M., Kuna-Broniowski M.
Electronic Journal of Polish Agricultural Universities. Series Agricultural Engineering
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2008
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tom 11
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nr 2
4

Erratum to: Arabidopsis thaliana intramembrane proteases

81%
Adamiec M., Ciesielska M., Zalas P., Lucinski R.
Acta Physiologiae Plantarum
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2017
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tom 39
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nr 09
5

The chloroplast genome: a review

81%
Dobrogojski J., Adamiec M., Lucinski R.
Acta Physiologiae Plantarum
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2020
|
tom 42
|
nr 06
6

Arabidopsis thaliana intramembrane proteases

81%
Adamiec M., Ciesielska M., Zalas P., Lucinski R.
Acta Physiologiae Plantarum
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2017
|
tom 39
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nr 07
7
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AtDeg2 - a chloroplast protein with dual protease/chaperone activity

81%
Jagodzik P., Adamiec M., Jackowski G.
Acta Societatis Botanicorum Poloniae
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2014
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tom 83
|
nr 3
Chloroplast protease AtDeg2 (an ATP-independent serine endopeptidase) is cytosolically synthesized as a precursor, which is imported into the chloroplast stroma and deprived of its transit peptide. Then the mature protein undergoes routing to its functional location at the stromal side of thylakoid membrane. In its linear structure AtDeg2 molecule contains the protease domain with catalytic triad (HDS) and two PDZ domains (PDZ1 and PDZ2). In vivo AtDeg2 most probably exists as a supposedly inactive haxamer, which may change its oligomeric stage to form active 12-mer, or 24-mer. AtDeg2 has recently been demonstrated to exhibit dual protease/chaperone function. This review is focused on the current awareness with regard to AtDeg2 structure and functional significance.
8
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Badania nad wykorzystaniem ogniw fotowoltaicznych w rolnictwie i przemysle rolno-spozywczym. Czesc II. Badania laboratoryjne

81%
Adamiec M., Kuna-Broniowski M., Kuna-Broniowska I.
Acta Scientiarum Polonorum. Technica Agraria
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2003
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tom 02
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nr 1
61-66
9
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Badania nad wykorzystaniem ogniw fotowoltaicznych w rolnictwie i przemysle rolno-spozywczym. Czesc I. Podstawy teoretyczne

81%
Adamiec M., Kuna-Broniowski M., Kuna-Broniowska I.
Acta Scientiarum Polonorum. Technica Agraria
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2002
|
tom 01
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nr 1
41-51
10

Redox state of plastoquionone pool regulates expression of Arabidopsis thaliana genes in response to elevated irradiance

80%
Adamiec M., Drath M., Jackowski G.
Acta Biochimica Polonica
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2008
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tom 55
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nr 1
DNA microarray technology was applied to gain insight into the role of the redox state of PQ pool as a retrograde factor mediating differential expression of Arabidopsis nuclear genes during the acclimation to changing irradiance. DNA microarray chips containing probes corresponding to 24000 Arabidopsis nuclear genes were screened with cRNA samples prepared from leaves of plants exposed for 5 h to low irradiance (control) vs. medium, high and excessive irradiances (MI, HI and EI, respectively). Six hundred and sixty three genes were differentially expressed as a result of an exposure to at least one elevated irradiance. Among 663 differentially expressed genes a total of 50 were reverted by DCMU - 24 ones modulated at medium irradiance, 32 ones modulated at high irradiance and a single one modulated at excessive irradiance. We postulate that their expression is regulated by redox state of plastoquinone (PQ) pool. Thus the PQ-mediated redox regulation of expression of Arabidopsis nuclear genes is probably limited to the irradiance window representing non-stressing conditions. We found that the promoter regions of the PQ-regulated genes contained conserved elements, suggesting transcriptional control by a shared set of trans-acting factors which participate in signal transduction from the redox state of the PQ pool.
11

Wpływ leczenia bisoprololem na wydzielanie insuliny, peptydu C (PPC), ghreliny i glukozo-zależnegoinsulinotropowego peptydu (GIP) u kobiet z nadciśnieniem pierwotnym

71%
Adamiec M., Sztefko K., Kawecka-Jaszcz K., Posnik-Urbanska A., Czarnecka D.
Diagnostyka Laboratoryjna
|
2007
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tom 43
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nr 3
12
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Dynamics of excitation energy transfer in PSII particles of Arabidopsis thaliana mutant clpC1

61%
Adamiec M., Lucinski R., Gibasiewicz K., Giera W., Sipinska W., Jackowski G.
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology
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2013
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tom 94
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nr 3
13
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Chloroplast protease/chaperone AtDeg2 influences cotyledons opening and reproductive development in Arabidopsis

51%
Adamiec M., Jagodzik P., Wyka T. P., Ludwikow A., Mitula F., Misztal L., Lucinski R., Jackowski G.
Acta Societatis Botanicorum Poloniae
|
2018
|
tom 87
|
nr 2
AtDeg2 is a chloroplast protein with dual protease/chaperone activity. Since data on how the individual activities of AtDeg2 affect growth and development of Arabidopsis thaliana plants is missing, two transgenic lines were prepared that express mutated AtDeg2 versions that have either only protease or chaperone activity and a comprehensive ontogenesis stage-based study was performed comprising wild type (WT) plants and insertional mutants that do not express AtDeg2, as well as the two transgenic lines. The repression of both AtDeg2 activities in deg2-3 mutants altered just a few phenotypic traits including the time when cotyledons were fully opened, the time when 10% flowers were open as well as the number of inflorescence branches and seed length in plants which have completed their generative development. It was demonstrated that complete opening of cotyledons as well as the number of inflorescence branches and seed length in plants which have completed their generative development required involvement of both AtDeg2 activities, whereas the time when 10% of flowers were open was controlled by AtDeg2 protease activity. These results show for the first time that the chaperone activity of AtDeg2 is needed for some elements of generative development of A. thaliana plants to proceed normally. So far, the chaperone activity of AtDeg2 was confirmed based on in vitro assays only.
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