Search Results - "Legouis, R"

X Chromosome-Linked Kallmann Syndrome: Stop Mutations Validate the Candidate Gene by Hardelin, Jean-Pierre, Levilliers, Jacqueline, del Castillo, Ignacio, Cohen-Salmon, Martine, Legouis, Renaud, Blanchard, Stephane, Compain, Sylvie, Bouloux, Pierre, Kirk, Jeremy, Moraine, Claude, Chaussain, Jean-Louis, Weissenbach, Jean, Petit, Christine

“…Kallmann syndrome represents the association of hypogonadotropic hypogonadism with anosmia. This syndrome is from a defect in the embryonic migratory pathway…”
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Postfertilization Autophagy of Sperm Organelles Prevents Paternal Mitochondrial DNA Transmission by Rawi, Sara Al, Louvet-Vallée, Sophie, Djeddi, Abderazak, Sachse, Martin, Culetto, Emmanuel, Hajjar, Connie, Boyd, Lynn, Legouis, Renaud, Galy, Vincent

“…In sexual reproduction of most animals, the spermatozoon provides DNA and centrioles, together with some cytoplasm and organelles, to the oocyte that is being…”
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Expression of the KAL Gene in Multiple Neuronal Sites During Chicken Development by Legouis, Renaud, Lievre, Christiane Ayer-Le, Leibovici, Michel, Lapointe, Francoise, Petit, Christine

“…The human KAL gene is responsible for the X chromosome-linked Kallmann syndrome. A partial cDNA sequence from the chicken KAL homologue was determined and used…”
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Developmental and cellular functions of the ESCRT machinery in pluricellular organisms by Michelet, Xavier, Djeddi, Abderazak, Legouis, Renaud

“…ESCRTs (endosomal sorting complexes required for transport) were first discovered in yeast and are known to be required in the biogenesis of the MVB…”
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CeVPS‐27 is an Endosomal Protein Required for the Molting and the Endocytic Trafficking of the Low‐Density Lipoprotein Receptor‐Related Protein 1 in Caenorhabditis elegans by Roudier, Nathalie, Lefebvre, Christophe, Legouis, Renaud

“…Class E vacuolar protein‐sorting (Vps) proteins were first described in yeast as being involved in receptor‐mediated endocytosis and multivesicular body…”
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Isolation and characterization of the gene responsible for the X chromosome-linked Kallmann syndrome by Legouis, R, Cohen-Salmon, M, Del Castillo, I, Petit, C

“…Kallmann de Morsier Syndrome is defined by the association of an hypogonadism with an anosmia. The hypogonadism is due to a deficiency of GnRH…”
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Assembly of C. elegans apical junctions involves positioning and compaction by LET-413 and protein aggregation by the MAGUK protein DLG-1 by McMahon, L, Legouis, R, Vonesch, J L, Labouesse, M

“…Specialised subapical junctions play a critical role in maintaining epithelial cell polarity and tissue integrity, and provide a platform for intracellular…”
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Characterization and chromosomal assignment of a human cDNA encoding a protein related to the murine 102-kDa cadherin-associated protein (alpha-catenin) by Claverie, J M, Hardelin, J P, Legouis, R, Levilliers, J, Bougueleret, L, Mattei, M G, Petit, C

“…We report the characterization of a human cDNA encompassing the complete coding region of a 945-residue putative protein (CAP-R) 80% identical to the recently…”
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A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3) by BOULOUX, P.-M. G, HARDELIN, J.-P, MUNROE, P, KIRK, J. M. W, LEGOUIS, R, LEVILLIERS, J, HAZAN, J, WEISSENBACH, J, PETIT, C

“…Images…”
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The Caenorhabditis elegans vab-10 Spectraplakin Isoforms Protect the Epidermis against Internal and External Forces by Bosher, Julia M., Hahn, Bum-Soo, Legouis, Renaud, Sookhareea, Satis, Weimer, Robby M., Gansmuller, Anne, Chisholm, Andrew D., Rose, Ann M., Bessereau, Jean-Louis, Labouesse, Michel

“…Morphogenesis of the Caenorhabditis elegans embryo is driven by actin microfilaments in the epidermis and by sarcomeres in body wall muscles. Both tissues are…”
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Basolateral targeting by leucine-rich repeat domains in epithelial cells by Legouis, Renaud, Jaulin-Bastard, Fanny, Schott, Sonia, Navarro, Christel, Borg, Jean-Paul, Labouesse, Michel

“…The asymmetric distribution of proteins to basolateral and apical membranes is an important feature of epithelial cell polarity. To investigate how basolateral…”
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LET-413 is a basolateral protein required for the assembly of adherens junctions in Caenorhabditis elegans by Labouesse, Michel, Legouis, Renaud, Gansmuller, Anne, Sookhareea, Satis, Bosher, Julia M, Baillie, David L

“…Epithelial cells are polarized, with apical and basal compartments demarcated by tight and adherens junctions. Proper establishment of these subapical…”
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PAR-3 is required for epithelial cell polarity in the distal spermatheca of C. elegans by Aono, Shinya, Legouis, Renaud, Hoose, Wendy A, Kemphues, Kenneth J

“…PAR-3 is localized asymmetrically in epithelial cells in a variety of animals from Caenorhabditis elegans to mammals. Although C. elegans PAR-3 is known to act…”
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Epithelial biology: lessons from Caenorhabditis elegans by Michaux, G, Legouis, R, Labouesse, M

“…Epithelial cells are essential and abundant in all multicellular animals where their dynamic cell shape changes orchestrate morphogenesis of the embryo and…”
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The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules by Legouis, R, Hardelin, J P, Levilliers, J, Claverie, J M, Compain, S, Wunderle, V, Millasseau, P, Le Paslier, D, Cohen, D, Caterina, D

“…Kallmann syndrome associates hypogonadotropic hypogonadism and anosmia and is probably due to a defect in the embryonic migration of olfactory and…”
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Collective nomenclature for LAP proteins by Bilder, David, Birnbaum, Daniel, Borg, Jean-Paul, Bryant, Peter, Huigbretse, Jon, Jansen, Erik, Kennedy, Mary B, Labouesse, Michel, Legouis, Renaud, Mechler, Bernard, Perrimon, Norbert, Petit, Marleen, Sinha, Pradip

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Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous system by Soussi-Yanicostas, N, Hardelin, J P, Arroyo-Jimenez, M M, Ardouin, O, Legouis, R, Levilliers, J, Traincard, F, Betton, J M, Cabanié, L, Petit, C

“…The KAL gene is responsible for the X-chromosome linked form of Kallmann's syndrome in humans. Upon transfection of CHO cells with a human KAL cDNA, the…”
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Xp22.3 deletions in isolated familial Kallmann's syndrome by Hardelin, J P, Levilliers, J, Young, J, Pholsena, M, Legouis, R, Kirk, J, Bouloux, P, Petit, C, Schaison, G

“…Several familial cases of Kallmann's syndrome (KS) have been reported, among which the X-chromosome-linked mode of inheritance is the most frequent. The gene…”
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Les mécanismes de transduction du signal olfactif: Les maladies génétiques sensorielles by LEGOUIS, R

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Characterization of the chicken and quail homologues of the human gene responsible for the X-linked Kallmann syndrome by Legouis, R, Cohen-Salmon, M, del Castillo, I, Levilliers, J, Capy, L, Mornow, J P, Petit, C

“…The human KAL gene, responsible for the X-linked Kallmann syndrome, was isolated previously. Southern blot analysis using human cDNA probes detected…”
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