Хайлтын үр дүнгүүд - Suonavy Khung
- 5-н 1 - 5 үр дүнгүүдийг харуулж байна
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Hippocampal Radial Glial Subtypes and Their Neurogenic Potential in Human Fetuses and Healthy and Alzheimer’s Disease Adults -н Sara Cipriani, Isidró Ferrer, Eleonora Aronica, Gábor G. Kovács, Catherine Verney, Jeannette Nardelli, Suonavy Khung, Anne‐Lise Delezoide, Ivan Milenković, Sowmyalakshmí Rasika, Philippe Manivet, Jean‐Louis Bénifla, Nicolas Deriot, Pierre Gressèns, Homa Adle‐Biassette
Хэвлэсэн 2018Artigo -
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Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation -н Valentina Grampa, Marion Delous, Mohamad Zaidan, Gweltas Odye, Sophie Thomas, Nadia Elkhartoufi, Emilie Filhol, Olivier Niel, Flora Silbermann, Corinne Lebreton, Sophie Collardeau‐Frachon, Isabelle Rouvet, Jean‐Luc Alessandri, Louise Devisme, Anne Dieux‐Coëslier, Marie‐Pierre Cordier, Yline Capri, Suonavy Khung‐Savatovsky, Sabine Sigaudy, Rémi Salomon, Corinne Antignac, Marie‐Claire Gubler, Alexandre Benmerah, Fabiola Terzi, Tania Attié‐Bitach, Marc Jeanpierre, Sophie Saunier
Хэвлэсэн 2016Artigo -
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<i>CC2D2A</i>mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation -н Soumaya Mougou-Zerelli, Sophie Thomas, Emmanuelle Szenker‐Ravi, Sophie Audollent, Nadia Elkhartoufi, Candice Babarit, Stéphane Romano, Rémi Salomon, Jeanne Amiel, Chantal Esculpavit, Marie Gonzalès, Estelle Escudier, Bruno Leheup, Philippe Loget, Sylvie Odent, J. Roume, Marion Gérard, Anne-Lise Delezoide, Suonavy Khung, Sophie Patrier, Marie-Pierre Cordier, Raymonde Bouvier, Jéléna Martinovic, Marie‐Claire Gubler, Nathalie Boddaert, Arnold Münnich, Férechté Encha‐Razavi, Enza Maria Valente, Ali Saâd, Sophie Saunier, Michel Vekemans, Tania Attié‐Bitach
Хэвлэсэн 2009Artigo -
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Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita -н Annie Laquerrière, Dana Jaber, Emanuela Abiusi, Jérôme Maluenda, Dan Mejlachowicz, Alexandre Vivanti, Klaus Dieterich, Radka Stoeva, Loïc Quevarec, Flora Nolent, Valérie Biancalana, Philippe Latour, Damien Sternberg, Yline Capri, Alain Verloès, Bettina Bessières, Laurence Lœuillet, Tania Attié‐Bitach, Jéléna Martinovic, Sophie Blesson, Florence Petit, Claire Bénéteau, Sandra Whalen, Florent Marguet, Jérôme Bouligand, Delphine Héron, Géraldine Viot, Jeanne Amiel, Daniel Amram, Céline Bellesme, Martine Bucourt, Laurence Faivre, Pierre‐Simon Jouk, Suonavy Khung, Sabine Sigaudy, Anne‐Lise Delezoide, Alice Goldenberg, Marie‐Line Jacquemont, Laëtitia Lambert, Valérie Layet, Stanislas Lyonnet, Arnold Münnich, Lionel Van Maldergem, Juliette Piard, Fabien Guimiot, P. Landrieu, Pascaline Létard, Fanny Pelluard, Laurence Perrin, Marie‐Hélène Saint‐Frison, Haluk Topaloğlu, Laetitia Trestard, Catherine Vincent‐Delorme, Helge Amthor, Christine Barnérias, Alexandra Benachi, Éric Bieth, Elise Boucher, Valérie Cormier‐Daire, Andrée Delahaye‐Duriez, Isabelle Desguerre, B. Eymard, Christine Francannet, Sarah Grotto, Didier Lacombe, Fanny Laffargue, Marine Legendre, Dominique Martin–Coignard, André Mégarbané, Sandra Mercier, Mathilde Nizon, Luc Rigonnot, Fabienne Prieur, Chloé Quēlin, Hanitra Ranjatoelina-Randrianaivo, Nicoletta Resta, Annick Toutain, Hélène Verhelst, Marie Vincent, Estelle Colin, Catherine Fallet‐Bianco, Michèle Granier, R Grigorescu, Julien Saada, Marie Gonzalès, Anne Guiochon‐Mantel, Jean‐Louis Bessereau, Marcel Tawk, Marta Gut, Cyril Gitiaux, Judith Melki
Хэвлэсэн 2021Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Biology
Gene
Genetics
Phenotype
Ciliopathies
Cilium
Exome sequencing
Medicine
Missense mutation
Agenesis
Alzheimer's disease
Anatomy
Aneuploidy
Arthrogryposis
Arthrogryposis multiplex congenita
Bioinformatics
Cancer research
Candidate gene
Cell biology
Cerebellar hypoplasia (non-human)
Cerebellum
Chromosome
Ciliogenesis
Ciliopathy
Craniofacial
DNA sequencing
Disease
Disease gene identification
Down syndrome
Exome