Francoise Helmbacher
Affiliations: | IBDML, Luminy-Marseille, Marseille, Provence-Alpes-Côte d'Azur, France |
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"Francoise Helmbacher"Mean distance: 16.47 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentorPatrick Charnay | grad student | 1993-1999 | ENS Paris |
Ruediger Klein | post-doc | 1999-2004 | Max Planck Institute for Neurobiology, Munich |
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Publications
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Helmbacher F, Stricker S. (2020) Tissue cross talks governing limb muscle development and regeneration. Seminars in Cell & Developmental Biology. 104: 14-30 |
Jones MR, Lingampally A, Dilai S, et al. (2019) Characterization of and Reporter Lines in the Context of Fibroblast Growth Factor 10 Signaling During Mouse Embryonic Lung Development. Frontiers in Genetics. 10: 178 |
Petitpré C, Wu H, Sharma A, et al. (2018) Neuronal heterogeneity and stereotyped connectivity in the auditory afferent system. Nature Communications. 9: 3691 |
Helmbacher F. (2018) Tissue-specific activities of the Fat1 cadherin cooperate to control neuromuscular morphogenesis. Plos Biology. 16: e2004734 |
Lamballe F, Toscano S, Conti F, et al. (2016) Coordination of signalling networks and tumorigenic properties by ABL in glioblastoma cells. Oncotarget |
Fan Y, Richelme S, Avazeri E, et al. (2015) Tissue-Specific Gain of RTK Signalling Uncovers Selective Cell Vulnerability during Embryogenesis. Plos Genetics. 11: e1005533 |
Bagherie-Lachidan M, Reginensi A, Zaveri HP, et al. (2015) Stromal Fat4 acts non-autonomously with Dachsous1/2 to restrict the nephron progenitor pool. Development (Cambridge, England) |
Mariot V, Roche S, Hourdé C, et al. (2015) Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophy. Annals of Neurology |
Puppo F, Dionnet E, Gaillard MC, et al. (2015) Identification of variants in the 4q35 gene FAT1 in patients with a facioscapulohumeral dystrophy-like phenotype. Human Mutation. 36: 443-53 |
Mariot V, Roche S, Hourdé C, et al. (2015) Correlation between low FAT1 expression and early affected muscle in FSHD Neuromuscular Disorders. 25 |