@article{GendreBaralDangetal.2019,
  author    = {Gendre, Delphine and Baral, Anirban and Dang, Xie and Esnay, Nicolas and Boutte, Yohann and Stanislas, Thomas and Vain, Thomas and Claverol, Stephane and Gustavsson, Anna and Lin, Deshu and Grebe, Markus and Bhalerao, Rishikesh P.},
  title     = {Rho-of-plant activated root hair formation requires Arabidopsis YIP4a/b gene function},
  series = {Development : Company of Biologists},
  volume    = {146},
  journal   = {Development : Company of Biologists},
  number    = {5},
  publisher = {The Company of Biologists},
  address   = {Cambridge},
  issn      = {0950-1991},
  doi       = {10.1242/dev.168559},
  pages     = {7},
  year      = {2019},
  abstract  = {Root hairs are protrusions from root epidermal cells with crucial roles in plant soil interactions. Although much is known about patterning, polarity and tip growth of root hairs, contributions of membrane trafficking to hair initiation remain poorly understood. Here, we demonstrate that the trans-Golgi network-localized YPT-INTERACTING PROTEIN 4a and YPT-INTERACTING PROTEIN 4b (YIP4a/b) contribute to activation and plasma membrane accumulation of Rho-of-plant (ROP) small GTPases during hair initiation, identifying YIP4a/b as central trafficking components in ROP-dependent root hair formation.},
  language  = {en}
}
@article{HilsonAllemeerschAltmannetal.2004,
  author    = {Hilson, Pierre and Allemeersch, Joke and Altmann, Thomas and Aubourg, Sebastien and Avon, Alexandra and Beynon, Jim and Bhalerao, Rishikesh P. and Bitton, Frederique and Caboche, Michel and Cannoot, Bernard and Chardakov, Vasil and Cognet-Holliger, Cecile and Colot, Vincent and Crowe, Mark and Darimont, Caroline and Durinck, Steffen and Eickhoff, Holger and deLongevialle, Andeol Falcon and Farmer, Edward E. and Grant, Murray and Kuiper, Martin T. R. and Lehrach, Hans and Leon, Celine and Leyva, Antonio and Lundeberg, Joakim and Lurin, Claire and Moreau, Yves},
  title     = {Versatile gene-specific sequence tags for arabidopsis functional genomics : transcript profiling and reserve genetics applications},
  year      = {2004},
  abstract  = {Microarray transcript profiling and RNA interference are two new technologies crucial for large-scale gene function studies in multicellular eukaryotes. Both rely on sequence-specific hybridization between complementary nucleic acid strands, inciting us to create a collection of gene-specific sequence tags (GSTs) representing at least 21,500 Arabidopsis genes and which are compatible with both approaches. The GSTs were carefully selected to ensure that each of them shared no significant similarity with any other region in the Arabidopsis genome. They were synthesized by PCR amplification from genomic DNA. Spotted microarrays fabricated from the GSTs show good dynamic range, specificity, and sensitivity in transcript profiling experiments. The GSTs have also been transferred to bacterial plasmid vectors via recombinational cloning protocols. These cloned GSTs constitute the ideal starting point for a variety of functional approaches, including reverse genetics. We have subcloned GSTs on a large scale into vectors designed for gene silencing in plant cells. We show that in planta expression of GST hairpin RNA results in the expected phenotypes in silenced Arabidopsis lines. These versatile GST resources provide novel and powerful tools for functional genomics},
  language  = {en}
}