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Items: 11

1.

Cytokinin treatment modifies litchi fruit pericarp anatomy leading to reduced susceptibility to post-harvest pericarp browning.

Fahima A, Levinkron S, Maytal Y, Hugger A, Lax I, Huang X, Eyal Y, Lichter A, Goren M, Stern RA, Harpaz-Saad S.

Plant Sci. 2019 Jun;283:41-50. doi: 10.1016/j.plantsci.2019.02.006. Epub 2019 Feb 13.

PMID:
31128712
2.

The role of COBRA-LIKE 2 function, as part of the complex network of interacting pathways regulating Arabidopsis seed mucilage polysaccharide matrix organization.

Ben-Tov D, Idan-Molakandov A, Hugger A, Ben-Shlush I, Günl M, Yang B, Usadel B, Harpaz-Saad S.

Plant J. 2018 May;94(3):497-512. doi: 10.1111/tpj.13871. Epub 2018 Mar 23.

3.

Permanently open stomata of aquatic angiosperms display modified cellulose crystallinity patterns.

Shtein I, Popper ZA, Harpaz-Saad S.

Plant Signal Behav. 2017 Jul 3;12(7):e1339858. doi: 10.1080/15592324.2017.1339858. Epub 2017 Jul 18.

4.

Stomatal cell wall composition: distinctive structural patterns associated with different phylogenetic groups.

Shtein I, Shelef Y, Marom Z, Zelinger E, Schwartz A, Popper ZA, Bar-On B, Harpaz-Saad S.

Ann Bot. 2017 Apr 1;119(6):1021-1033. doi: 10.1093/aob/mcw275.

5.

COBRA-LIKE2, a member of the glycosylphosphatidylinositol-anchored COBRA-LIKE family, plays a role in cellulose deposition in arabidopsis seed coat mucilage secretory cells.

Ben-Tov D, Abraham Y, Stav S, Thompson K, Loraine A, Elbaum R, de Souza A, Pauly M, Kieber JJ, Harpaz-Saad S.

Plant Physiol. 2015 Mar;167(3):711-24. doi: 10.1104/pp.114.240671. Epub 2015 Jan 12.

6.

The FEI2-SOS5 pathway and CELLULOSE SYNTHASE 5 are required for cellulose biosynthesis in the Arabidopsis seed coat and affect pectin mucilage structure.

Harpaz-Saad S, Western TL, Kieber JJ.

Plant Signal Behav. 2012 Feb;7(2):285-8. doi: 10.4161/psb.18819. Epub 2012 Feb 1.

7.

Cellulose synthesis via the FEI2 RLK/SOS5 pathway and cellulose synthase 5 is required for the structure of seed coat mucilage in Arabidopsis.

Harpaz-Saad S, McFarlane HE, Xu S, Divi UK, Forward B, Western TL, Kieber JJ.

Plant J. 2011 Dec;68(6):941-53. doi: 10.1111/j.1365-313X.2011.04760.x. Epub 2011 Oct 10.

8.

Dual N- and C-terminal processing of citrus chlorophyllase precursor within the plastid membranes leads to the mature enzyme.

Azoulay-Shemer T, Harpaz-Saad S, Cohen-Peer R, Mett A, Spicer V, Lovat N, Krokhin O, Brand A, Gidoni D, Standing KG, Goldschmidt EE, Eyal Y.

Plant Cell Physiol. 2011 Jan;52(1):70-83. doi: 10.1093/pcp/pcq174. Epub 2010 Nov 11.

PMID:
21071427
9.

The NAC-domain transcription factor GOBLET specifies leaflet boundaries in compound tomato leaves.

Berger Y, Harpaz-Saad S, Brand A, Melnik H, Sirding N, Alvarez JP, Zinder M, Samach A, Eshed Y, Ori N.

Development. 2009 Mar;136(5):823-32. doi: 10.1242/dev.031625. Epub 2009 Jan 28.

10.

Citrus chlorophyllase dynamics at ethylene-induced fruit color-break: a study of chlorophyllase expression, posttranslational processing kinetics, and in situ intracellular localization.

Azoulay Shemer T, Harpaz-Saad S, Belausov E, Lovat N, Krokhin O, Spicer V, Standing KG, Goldschmidt EE, Eyal Y.

Plant Physiol. 2008 Sep;148(1):108-18. doi: 10.1104/pp.108.124933. Epub 2008 Jul 16.

11.

Chlorophyllase is a rate-limiting enzyme in chlorophyll catabolism and is posttranslationally regulated.

Harpaz-Saad S, Azoulay T, Arazi T, Ben-Yaakov E, Mett A, Shiboleth YM, Hörtensteiner S, Gidoni D, Gal-On A, Goldschmidt EE, Eyal Y.

Plant Cell. 2007 Mar;19(3):1007-22. Epub 2007 Mar 16.

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