نتائج البحث - Nabil Mohsin
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Nanolayered composite with enhanced ultraviolet ray absorption properties from simultaneous intercalation of sunscreen molecules حسب Megat Nabil Mohsin, Sumaiyah, Hussein, Mohd Zobir, Sarijo, Siti Halimah, Fakurazi, Sharida, Arulselvan, Palanisamy, Taufiq-Yap, Yun Hin
منشور في 2018نص -
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Mutations in INF2 Are a Major Cause of Autosomal Dominant Focal Segmental Glomerulosclerosis حسب Olivia Boyer, Geneviève Benoît, Olivier Gribouval, Fabien Névo, Marie-Josèphe Tête, Jacques Dantal, Brigitte Gilbert‐Dussardier, Guy Touchard, Alexandre Karras, Claire Presne, Jean‐Pierre Grünfeld, Christophe Legendre, Dominique Joly, Philippe Rieu, Nabil Mohsin, Thierry Hannedouche, Valérie Moal, Marie‐Claire Gubler, Isabelle Broutin, Géraldine Mollet, Corinne Antignac
منشور في 2011Artigo -
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<i>NPHS2</i>Mutations in Steroid-Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum حسب Karim Bouchireb, Olivia Boyer, Olivier Gribouval, Fabien Névo, Evelyne Huynh-Cong, Vincent Morinière, Raphaëlle Campait, Elisabet Ars, Damien Brackman, Jacques Dantal, Philippe Eckart, Maddalena Gigante, Beata S. Lipska‐Ziętkiewicz, A. Liutkus, André Mégarbané, Nabil Mohsin, Fatih Özaltın, Moin A. Saleem, Franz Schaefer, Kenza Soulami, Roser Torrá, Nicolas Garcelon, Géraldine Mollet, Karin Dahan, Corinne Antignac
منشور في 2013Revisão -
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The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies حسب Friederike Petzold, Katy Billot, Xiaoyi Chen, C. Henry, Emilie Filhol, Yoann Martin, Marina Avramescu, Maxime Douillet, Vincent Morinière, Pauline Krug, Marc Jeanpierre, Kálmán Tory, Olivia Boyer, Anita Burgun, Aude Servais, Rémi Salomon, Alexandre Benmerah, Laurence Heidet, Nicolas Garcelon, Corinne Antignac, Mohamad Zaidan, Sophie Saunier, Tania Attié‐Bitach, Valerie Comier-Daire, Jean‐Michel Rozet, Yaacov Frishberg, Brigitte Llanas, M. Broyer, Nabil Mohsin, Marie‐Alice Macher, Nicole Philip, Véronique Baudouin, D. Brackman, Chantal Loirat, Marina Charbit, Maud Dehennault, C. Guyot, Pierre Bataille, Mariet Elting, Georges Deschênes, Andrea Gropman, Geneviève Guest, Marie‐France Gagnadoux, Philippe Nicoud, Pierre Cochat, Bruno Ranchin, A Bensman, Anne‐Marie Guerrot, Bertrand Knebelmann, İlmay Bilge, Bruno Daniele, Stéphane Burtey, Caroline Rousset Rouvière, Valérie Caudwell, Denis Morin, Hélène Dollfus, Anne Maisin, Christian Hamel, Éric Bieth, Sophie Gié, Judith Goodship, G. Roussey, Hermine La Selve, Hubert Nivet, Lucie Bessenay, Mathilde Caillez, Jean Bernard Palcoux, Stéphane L. Benoit, Philippe Dubot, Marc Fila, Fabienne Giuliano, Daouya Iftene, M. Kessler, Thérèsa Kwon, A. Lahoche, Audrey Laurent, Anne-Laure Leclerc, David V. Milford, Thomas J. Neuhaus, Sylvie Odent, Philippe Eckart, Dominique Chauveau, Patrick Niaudet, Horacio A. Repetto, Sophie Taque, Alexandra Bruel, Alexandra Noel-Botte, Emma Allain Launay, Lisa Allard, Dany Anlicheau, Anne-Laure Adra, Arnaud Garnier, Arvind Nagra, Remy Baatard, Justine Bacchetta, Banu Sadıkoğlu, Christine Barnérias, Anne Barthélémy, Lina Basel, Nader Bassilios
منشور في 2023Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Mutation
Phenotype
Focal segmental glomerulosclerosis
Glomerulonephritis
Kidney
Missense mutation
Podocyte
Proteinuria
Actin
Actin cytoskeleton
Bardet–Biedl syndrome
Cell
Cell biology
Ciliogenesis
Ciliopathies
Ciliopathy
Cilium
Compound heterozygosity
Cystic kidney disease
Cytoskeleton
Endocrinology
Exome sequencing
Exon
Formins
Genetic heterogeneity
Haploinsufficiency
Intraflagellar transport