Zobrazeno 1 - 10
of 208
pro vyhledávání: '"B. Pelissier"'
Publikováno v:
BMC Biotechnology, Vol 21, Iss 1, Pp 1-13 (2021)
Abstract Background Phakopsora pachyrhizi is a biotrophic fungal pathogen responsible for the Asian soybean rust disease causing important yield losses in tropical and subtropical soybean-producing countries. P. pachyrhizi triggers important transcri
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https://doaj.org/article/13a1c56ce81949febe8658bee45ef116
Akademický článek
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Akademický článek
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Autor:
H. Mehdi, F. Réveret, C. Robert-Goumet, L. Bideux, B. Gruzza, P.E. Hoggan, J. Leymarie, Y. Andre, E. Gil, B. Pelissier, T. Levert, D. Paget, G. Monier
Publikováno v:
Applied Surface Science
Applied Surface Science, 2022, 579, pp.152191. ⟨10.1016/j.apsusc.2021.152191⟩
Applied Surface Science, 2022, 579, pp.152191. ⟨10.1016/j.apsusc.2021.152191⟩
International audience; GaAs(001) substrates nitrided with N 2 plasma at various temperatures were investigated after being exposed to air for 40 days. They were studied by means of parallel angle-resolved X-ray photoelectron spectroscopy, scanning e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdecb811a447fb747a577c4c5c5a8da9
https://hal.science/hal-03515255
https://hal.science/hal-03515255
Additional file 7: Figure S6. Detection of GFP fluorescence in stable transgenic soybeans. Leaves of two T1 lines (129 and 133) transformed with the pGmCHIT1:GFP construction were observed using a dissection scope (Leica Z16 APO) under GFP filter and
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https://explore.openaire.eu/search/publication?articleId=doi_________::4f4e3d128e3bc25d23723a5854ce74cc
Additional file 9: Table S2. Primers used for PCR and qPCR. *from Hirschburger et al., 2015 [32], ** from Mazarei et al., 2007 [64], *** from Zhong et al., 2014 [70].
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https://explore.openaire.eu/search/publication?articleId=doi_________::97f9b5a4ba57f68d0034098e7520e30c
Additional file 6: Figure S5. The GmCHIT1 promoter and potential cis-regulatory elements identified. (a) List of the cis-regulatory elements related to pathogen infection identified in the GmCHIT1 promoter. (b) Map of the GmCHIT1 promoter. AUX: auxin
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https://explore.openaire.eu/search/publication?articleId=doi_________::07f1d216efe5d48a1c9f72fe60bb4dc1
Additional file 5: Figure S4. Multiple Sequence Alignment of GmCHIT (KRH29572.1) with plant homologous proteins (from BLASTP analysis). Similar residues are colored according to BLOSUM62 score: Max: 3.0 Low: 0.5.
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https://explore.openaire.eu/search/publication?articleId=doi_________::86a0d8aa3c7b8363f4ef1b910ca16796
Additional file 8: Figure S7. GmCHIT1 promoter expression following salicylic acid treatment. (a) GFP fluorescence in line 131 (pGmCHIT1:GFP) and WT detached leaves following SA (+) or mock (-) treatments. Graphics represent the fluorescence intensit
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https://explore.openaire.eu/search/publication?articleId=doi_________::397890d4c28d2fa444bbe29e8e057c58
Additional file 4: Figure S3. GmCHIT protein KRH29572.1 homologs, their functions and % of identity. From BLASTP analysis (NCBI).
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https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28f5f4ab663f233e61384b4ddf393af6