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Bonnie Bartel

Researcher at Rice University

Publications -  118
Citations -  31566

Bonnie Bartel is an academic researcher from Rice University. The author has contributed to research in topics: Arabidopsis & Peroxisome. The author has an hindex of 66, co-authored 112 publications receiving 28674 citations. Previous affiliations of Bonnie Bartel include Massachusetts Institute of Technology & Bethel University.

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Arabidopsis iba response5 suppressors separate responses to various hormones.

TL;DR: One ibr5 suppressor carried a mutation in PLEIOTROPIC DRUG RESISTANCE9 (PDR9/ABCG37/At3g53480), which encodes an ATP-binding cassette transporter previously implicated in cellular efflux of the synthetic auxin 2,4-dichlorophenoxyacetic acid.
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Genetic Dissection of Peroxisome-associated Matrix Protein Degradation in Arabidopsis thaliana

TL;DR: The isolation of pex6-2 as a pfl mutant supports the hypothesis that matrix proteins can exit the peroxisome for cytosolic degradation, and identifies persistent GFP-ICL fluorescence (pfl) mutants.
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Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

Daniel J. Klionsky, +2522 more
- 01 Jan 2016 - 
TL;DR: Author(s): Klionsky, DJ; Abdelmohsen, K; Abe, A; Abedin, MJ; Abeliovich, H; A Frozena, AA; Adachi, H, Adeli, K, Adhihetty, PJ; Adler, SG; Agam, G; Agarwal, R; Aghi, MK; Agnello, M; Agostinis, P; Aguilar, PV; Aguirre-Ghis
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A new path to auxin.

TL;DR: Two independent genetic screens have converged to support a previously conjectured auxin biosynthetic pathway that is responsible for providing auxin during plant development and in response to environmental cues.
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IAR4, a Gene Required for Auxin Conjugate Sensitivity in Arabidopsis, Encodes a Pyruvate Dehydrogenase E1α Homolog

TL;DR: The isolation and characterization of the Arabidopsis iar4 mutant, which has reduced sensitivity to several IAA-amino acid conjugates, is reported, and it is found that disruption of the previously described mitochondrial pyruvate dehydrogenase E1α-subunit does not alter I AA-Ala responsiveness or confer any obvious phenotypes.