Search Results - "Creveaux, I"

Fetal midgut volvulus as a sign for cystic fibrosis by Durand, M., Coste, K., Martin, A., Scheye, T., Creveaux, I., Vanlieferinghen, P., Laurichesse-Delmas, H., Dechelotte, P. J., Labbe, A., Jacquetin, B., Lemery, D., Gallot, D.

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SCO-spondin is evolutionarily conserved in the central nervous system of the chordate phylum by Gobron, S, Creveaux, I, Meiniel, R, Didier, R, Dastugue, B, Meiniel, A

“…Bovine subcommissural organ-spondin was shown to be a brain-secreted glycoprotein specifically expressed in the subcommissural organ, an ependymal…”
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Follicular bronchiolitis presenting in a cystic fibrosis patient 15 years after the initial diagnosis by Labbé, A, Creveaux, I

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De novo interstitial direct duplication of Xq21.1q25 associated with skewed X-inactivation pattern by Tachdjian, G., Aboura, A., Benkhalifa, M., Creveaux, I., Foix-Hélias, L., Gadisseux, J.F., Boespflug-Tanguy, O., Mohammed, M., Labrune, P.

“…Genotype‐phenotype correlation in women with an abnormal phenotype associated with a duplication of the long arm of the X chromosome remains unclear. We report…”
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Paracetamol and Pain Modulation by TRPV1, UGT2B15, SULT1A1 Genotypes: A Randomized Clinical Trial in Healthy Volunteers by Pickering, Gisèle, Creveaux, Isabelle, Macian, Nicolas, Pereira, Bruno

“…Abstract Background The influence of the genetic polymorphism of enzymes and receptors involved in paracetamol metabolism and mechanism of action has not been…”
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Screening for cystic fibrosis transmembrane conductance regulator gene mutations in men included in an intracytoplasmic sperm injection programme by Boucher, D., Creveaux, I., Grizard, G., Jimenez, C., Hermabessière, J., Dastugue, B.

“…The present study was undertaken to evaluate the frequency and nature of mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene in…”
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Specific transcripts analysed by in situ hybridization in the subcommissural organ of bovine embryos by Meiniel, R, Creveaux, I, Dastugue, B, Meiniel, A

“…The subcommissural organ (SCO) secretes specific glycoproteins into the cerebrospinal fluid that aggregate to constitute Reissner's fiber (RF), a thread-like…”
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Use of a heterologous monoclonal antibody for cloning and detection of glial fibrillary acidic protein in the bovine ventricular ependyma by Bouchard, P, Ravet, V, Meiniel, R, Creveaux, I, Meiniel, A, Vellet, A, Vigues, B

“…From protozoans to vertebrates, ciliated cells are characterized by well-developed cytoskeletal structures. An outstanding example is the epiplasm, a thick,…”
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Localization of the SCO-spondin gene to cattle chromosome 4 by Popescu, C P, Hayes, H, Meiniel, R, Creveaux, I, Meiniel, A

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Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome by Harbuz, Radu, Lespinasse, James, Boulet, Stéphanie, Francannet, Christine, Creveaux, Isabelle, Benkhelifa, Mariem, Jouk, Pierre-Simon, Lunardi, Joël, Ray, Pierre F.

“…Objective Molecular diagnosis and prenatal care of two pregnant women at risk of transmitting immunodysregulation, polyendocrinopathy, enteropathy X‐linked…”
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La photokératectomie thérapeutique dans le traitement de la dystrophie grillagée de type I by Chiambaretta, F., Rozier, B., Pilon, F., Gérard, M., Coulangeon, L.M., Creveaux, I., Rigal, D.

“…La dystrophie cornéenne grillagée de type I est due à des mutations du gène BIGH3 et se caractérise par la présence de dépôts stromaux linéaires superficiels…”
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Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France by Claustres, Mireille, Guittard, Caroline, Bozon, Dominique, Chevalier, Françoise, Verlingue, Claudine, Ferec, Claude, Girodon, Emanuelle, Cazeneuve, Cécile, Bienvenu, Thierry, Lalau, Guy, Dumur, Viviane, Feldmann, Delphine, Bieth, Eric, Blayau, Martine, Clavel, Christine, Creveaux, Isabelle, Malinge, Marie-Claire, Monnier, Nicole, Malzac, Perrine, Mittre, Hervé, Chomel, Jean-Claude, Bonnefont, Jean-Paul, Iron, Albert, Chery, Michèle, Georges, Marie Des

“…We have collated the results of cystic fibrosis (CF) mutation analysis conducted in 19 laboratories in France. We have analyzed 7,420 CF alleles, demonstrating…”
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Subcommissural organ/Reissner's fiber complex: Characterization of SCO-spondin, a glycoprotein with potent activity on neurite outgrowth by Gobron, Stéphane, Creveaux, Isabelle, Meiniel, Robert, Didier, Robert, Herbet, Alain, Bamdad, Mahchid, El Bitar, Fadia, Dastugue, Bernard, Meiniel, Annie

“…In the developing vertebrate nervous system, several proteins of the thrombospondin superfamily act on axonal pathfinding. By successive screening of a…”
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SCO-spondin: a new member of the thrombospondin family secreted by the subcommissural organ is a candidate in the modulation of neuronal aggregation by Gobron, S, Monnerie, H, Meiniel, R, Creveaux, I, Lehmann, W, Lamalle, D, Dastugue, B, Meiniel, A

“…A number of cues are known to influence neuronal development including growth factors, cell-adhesion molecules, components of the extracellular matrix and…”
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La maladie de Hashimoto est la deuxième plus fréquente maladie auto-immune dans les familles atteintes de polyarthrite rhumatoïde by Serova-Erard, A., Cattan, J., Dubost, J.J., Fournier, E., Bardin, T., Petit-Teixeira, E., Creveaux, I., Tauveron, I., Gerbaud, L., Cornélis, F.

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Mouse SCO-spondin, a gene of the thrombospondin type 1 repeat (TSR) superfamily expressed in the brain by Gonçalves-Mendes, Nicolas, Simon-Chazottes, Dominique, Creveaux, Isabelle, Meiniel, Annie, Guénet, Jean-Louis, Meiniel, Robert

“…SCO-spondin is specifically expressed in the subcommissural organ (SCO), a secretory ependymal differentiation lining the roof of the third ventricular cavity…”
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Élévation de la transcription d’IL-1β dans les abcès aseptiques by Bardy, A., Creveaux, I., Déchelotte, P., Kémény, J.-L., Rioux-Leclercq, N., Aumaitre, O., Andre, M.

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TREX1 est-il impliqué dans les manifestations neuropsychiatriques du lupus systémique ? Étude du génotype sur une cohorte française by Guettrot-Imbert, G., Costedoat-Chalumeau, N., Nachury, C., Blanc, P., Dion, A., Hullot, J.-S., Piette, J.-C., Amoura, Z., Aumaitre, O., Creveaux, I., Andre, M.

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SCO-spondin and RF-GlyI: Two designations for the same glycoprotein secreted by the subcommissural organ by Didier, Robert, Creveaux, Isabelle, Meiniel, Robert, Herbet, Alain, Dastugue, Bernard, Meiniel, Annie

“…SCO‐spondin and RF‐GlyI are two designations for cDNAs strongly expressed in the bovine subcommissural organ (SCO), characterized, respectively, in 1996 and…”
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Phototherapeutic keratectomy in the treatment of lattice corneal dystrophy type I by Chiambaretta, F, Rozier, B, Pilon, F, Gérard, M, Coulangeon, L M, Creveaux, I, Rigal, D

“…Lattice corneal dystrophy type I is an autosomal dominant corneal dystrophy caused by allelic mutations of the BIGH3 gene. Type I dystrophy is recognized…”
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