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Irene García

Researcher at Spanish National Research Council

Publications -  47
Citations -  2750

Irene García is an academic researcher from Spanish National Research Council. The author has contributed to research in topics: Mutant & Cysteine. The author has an hindex of 27, co-authored 45 publications receiving 2315 citations. Previous affiliations of Irene García include University of Seville & University of Paris.

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An O-Acetylserine(thiol)lyase Homolog with l-Cysteine Desulfhydrase Activity Regulates Cysteine Homeostasis in Arabidopsis

TL;DR: The results suggest that DES1 from Arabidopsis is an l-Cys desulfhydrase involved in maintaining Cys homeostasis, mainly at late developmental stages or under environmental perturbations.
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Cysteine and cysteine-related signaling pathways in arabidopsis thaliana

TL;DR: The research has been demonstrated that cytosolic sulfide and chloroplastic S-sulfocysteine act as signaling molecules regulating autophagy and protecting the photosystems, respectively.
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Cysteine-generated sulfide in the cytosol negatively regulates autophagy and modulates the transcriptional profile in arabidopsis

TL;DR: The results suggest that cysteine-generated sulfide in the cytosol negatively regulates autophagy and modulates the transcriptional profile of Arabidopsis, and sulfide is able to reverse ATG8 accumulation and lipidation, suggesting a general effect of sulfide on autophile regulation that is unrelated to sulfur or nitrogen limitation stress.
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Hair removal methods: A comparative study for dermoscopy images

TL;DR: “melanoma texture” is referred to as a rationale for supporting the need for the proposed hair detection and repair techniques, which incompletely represents why hair removal is an important operation for skin lesion analysis.
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Cloning and characterization of a chitinase (CHIT42) cDNA from the mycoparasitic fungus Trichoderma harzianum

TL;DR: A cDNA of Trichoderma harzianum (chit42), coding for an endochitinase of 42 kDa, has been cloned using synthetic oligonucleotides corresponding to aminoacid sequences of the purified chit inase, revealing post-translational processing of a putative signal peptide and a second peptide of 12 amino acids.