Kết quả tìm kiếm - Juliette Nectoux
- Đang hiển thị 1 - 10 kết quả của 10
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1
A quantitative gene expression study suggests a role for angiopoietins in focal nodular hyperplasia Bằng Valérie Paradis, Ivan Bièche, Delphine Dargère, Ingrid Laurendeau, Juliette Nectoux, Claude Degott, Jacques Belghiti, Michel Vidaud, Pierre Bédossa
Được phát hành 2003Artigo -
2
Droplet digital PCR combined with minisequencing, a new approach to analyze fetal DNA from maternal blood: application to the non-invasive prenatal diagnosis of achondroplasia Bằng Lucie Orhant, Olivia Anselem, Mélanie Fradin, Pierre Hadrien Becker, Caroline Beugnet, Nathalie Deburgrave, Gilles Tafuri, Franck Letourneur, François Goffinet, Laïla El Khattabi, France Leturcq, Thierry Bienvenu, Vassilis Tsatsaris, Juliette Nectoux
Được phát hành 2016Artigo -
3
Targeted next-generation sequencing for differential diagnosis of neurofibromatosis type 2, schwannomatosis, and meningiomatosis Bằng Camille Louvrier, Éric Pasmant, Audrey Briand‐Suleau, Joëlle Cohen, Patrick Nitschké, Juliette Nectoux, Lucie Orhant, Cécile Zordan, Cyril Goizet, Stéphane Goutagny, Dominique Lallemand, Michel Vidaud, Dominique Vidaud, Michel Kalamarides, Béatrice Parfait
Được phát hành 2018Artigo -
4
Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes Bằng Chloé Delépine, Hamid Méziane, Juliette Nectoux, Matthieu Opitz, Amos B. Smith, Carlo Ballatore, Yoann Saillour, Annelise Bennaceur‐Griscelli, Qiang Chang, Emily Cunningham Williams, Maxime Dahan, Aurélien Duboin, Pierre Billuart, Yann Hérault, Thierry Bienvenu
Được phát hành 2015Artigo -
5
Could Digital PCR Be an Alternative as a Non-Invasive Prenatal Test for Trisomy 21: A Proof of Concept Study Bằng Laïla El Khattabi, Christelle Rouillac-Le Sciellour, Dominique Le Tessier, Armelle Luscan, Audrey Coustier, Raphaël Porcher, Rakia Bhouri, Juliette Nectoux, Valérie Serazin, Thibaut Quibel, Laurent Mandelbrot, Vassilis Tsatsaris, François Vialard, Jean‐Michel Dupont
Được phát hành 2016Artigo -
6
Myopathologic trajectory in Duchenne muscular dystrophy (DMD) reveals lack of regeneration due to senescence in satellite cells Bằng Nastasia Cardone, Valentina Taglietti, Serena Baratto, Kaouthar Kefi, Baptiste Periou, Cyril Gitiaux, Christine Barnérias, Peggy Lafuste, France Leturcq Pharm, Juliette Nectoux Pharm, Chiara Panicucci, Isabelle Desguerre, Claudio Bruno, François‐Jérôme Authier, Chiara Fiorillo, Frédéric Relaix, Edoardo Malfatti
Được phát hành 2023Artigo -
7
Key clinical features to identify girls with CDKL5 mutations Bằng Nadia Bahi‐Buisson, Juliette Nectoux, Haydeé Rosas‐Vargas, Mathieu Milh, Nathalie Boddaert, Benoı̂t Girard, Claude Cancès, Dorothée Ville, Alexandra Afenjar, Marlène Rio, Delphine Héron, Marie Ange N'Guyen Morel, Alexis Arzimanoglou, Christophe Philippe, Philippe Jonveaux, Jamel Chelly, Thierry Bienvenu
Được phát hành 2008Artigo -
8
Novel FOXG1 mutations associated with the congenital variant of Rett syndrome Bằng Maria Antonietta Mencarelli, Ariele Spanhol-Rosseto, Rosangela Artuso, Dalila Rondinella, Roberta De Filippis, Nadia Bahi‐Buisson, Juliette Nectoux, R. Rubinsztajn, Thierry Bienvenu, A. Moncla, B. Chabrol, Laurent Villard, Zita Krūmiņa, Judith Armstrong, Ana Roche, M. Pineda, Eva Gak, Francesca Mari, Francesca Ariani, Alessandra Renieri
Được phát hành 2009Artigo -
9
A new titinopathy Bằng Rafael de Cid, Rabah Ben Yaou, Carinne Roudaut, Karine Charton, Sylvain Baulande, France Leturcq, Norma B. Romero, Edoardo Malfatti, Maud Beuvin, Anna Vihola, Audrey Criqui, Isabelle Nelson, Juliette Nectoux, Laurène Ben Aim, Christophe Caloustian, Robert Olaso, Bjarne Udd, Gisèle Bonne, B. Eymard, Isabelle Richard
Được phát hành 2015Artigo -
10
Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization Bằng Gina O’Grady, Heather Best, Tamar E. Sztal, Vanessa Schartner, Myriam Sanjuan-Vazquez, Sandra Donkervoort, Osório Lopes Abath Neto, R. Bryan Sutton, Biljana Ilkovski, Norma B. Romero, Tanya Stojkovic, Jahannaz Dastgir, Leigh B. Waddell, Anne Boland, Ying Hu, Caitlin Williams, Avnika A. Ruparelia, Thierry Maisonobe, Anthony Peduto, Stephen W. Reddel, Monkol Lek, Taru Tukiainen, Beryl B. Cummings, Himanshu Joshi, Juliette Nectoux, Susan Brammah, Jean‐François Deleuze, Viola Oorschot Ing, Georg Ramm, Didem Ardıçlı, Kristen L. Nowak, Beril Talim, Haluk Topaloğlu, Nigel G. Laing, Kathryn N. North, Daniel G. MacArthur, Sylvie Friant, Nigel F. Clarke, Robert J. Bryson‐Richardson, Carsten G. Bönnemann, Jocelyn Laporte, Sandra T. Cooper
Được phát hành 2016Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Medicine
Gene
Genetics
Internal medicine
Bioinformatics
Mutation
Neuroscience
Pathology
Biochemistry
Cell biology
Dystrophin
Muscular dystrophy
Myocyte
Pediatrics
Rett syndrome
Achondroplasia
Adenoma
Anatomy
Angiopoietin
Cell-free fetal DNA
Cirrhosis
Computational biology
Computer science
Differential diagnosis
Digital polymerase chain reaction
Duchenne muscular dystrophy
Encephalopathy
Endocrinology
Enzyme