Year |
Citation |
Score |
2020 |
Helmbacher F, Stricker S. Tissue cross talks governing limb muscle development and regeneration. Seminars in Cell & Developmental Biology. 104: 14-30. PMID 32517852 DOI: 10.1016/J.Semcdb.2020.05.005 |
0.336 |
|
2019 |
Jones MR, Lingampally A, Dilai S, Shrestha A, Stripp B, Helmbacher F, Chen C, Chao CM, Bellusci S. Characterization of and Reporter Lines in the Context of Fibroblast Growth Factor 10 Signaling During Mouse Embryonic Lung Development. Frontiers in Genetics. 10: 178. PMID 30923534 DOI: 10.3389/Fgene.2019.00178 |
0.36 |
|
2018 |
Petitpré C, Wu H, Sharma A, Tokarska A, Fontanet P, Wang Y, Helmbacher F, Yackle K, Silberberg G, Hadjab S, Lallemend F. Neuronal heterogeneity and stereotyped connectivity in the auditory afferent system. Nature Communications. 9: 3691. PMID 30209249 DOI: 10.1038/S41467-018-06033-3 |
0.377 |
|
2018 |
Helmbacher F. Tissue-specific activities of the Fat1 cadherin cooperate to control neuromuscular morphogenesis. Plos Biology. 16: e2004734. PMID 29768404 DOI: 10.1371/Journal.Pbio.2004734 |
0.473 |
|
2016 |
Lamballe F, Toscano S, Conti F, Arechederra M, Baeza N, Figarella-Branger D, Helmbacher F, Maina F. Coordination of signalling networks and tumorigenic properties by ABL in glioblastoma cells. Oncotarget. PMID 27732969 DOI: 10.18632/Oncotarget.12546 |
0.632 |
|
2015 |
Fan Y, Richelme S, Avazeri E, Audebert S, Helmbacher F, Dono R, Maina F. Tissue-Specific Gain of RTK Signalling Uncovers Selective Cell Vulnerability during Embryogenesis. Plos Genetics. 11: e1005533. PMID 26393505 DOI: 10.1371/Journal.Pgen.1005533 |
0.674 |
|
2015 |
Bagherie-Lachidan M, Reginensi A, Zaveri HP, Scott DA, Helmbacher F, McNeill H. Stromal Fat4 acts non-autonomously with Dachsous1/2 to restrict the nephron progenitor pool. Development (Cambridge, England). PMID 26116661 DOI: 10.1242/Dev.122648 |
0.362 |
|
2015 |
Mariot V, Roche S, Hourdé C, Portilho D, Sacconi S, Puppo F, Duguez S, Rameau P, Caruso N, Delezoide AL, Desnuelle C, Bessières B, Collardeau S, Feasson L, Maisonobe T, ... ... Helmbacher F, et al. Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophy. Annals of Neurology. PMID 26018399 DOI: 10.1002/Ana.24446 |
0.349 |
|
2015 |
Puppo F, Dionnet E, Gaillard MC, Gaildrat P, Castro C, Vovan C, Bertaux K, Bernard R, Attarian S, Goto K, Nishino I, Hayashi Y, Magdinier F, Krahn M, Helmbacher F, et al. Identification of variants in the 4q35 gene FAT1 in patients with a facioscapulohumeral dystrophy-like phenotype. Human Mutation. 36: 443-53. PMID 25615407 DOI: 10.1002/Humu.22760 |
0.303 |
|
2015 |
Mariot V, Roche S, Hourdé C, Portilho D, Sacconi S, Puppo F, Duguez S, Rameau P, Caruso N, Delezoide A, Desnuelle C, Bessières B, Collardeau S, Feasson L, Maisonobe T, ... ... Helmbacher F, et al. Correlation between low FAT1 expression and early affected muscle in FSHD Neuromuscular Disorders. 25. DOI: 10.1016/J.Nmd.2015.06.448 |
0.318 |
|
2014 |
Caruso N, Herberth B, Lamballe F, Arce-Gorvel V, Maina F, Helmbacher F. Plasticity versus specificity in RTK signalling modalities for distinct biological outcomes in motor neurons. Bmc Biology. 12: 56. PMID 25124859 DOI: 10.1186/S12915-014-0056-6 |
0.721 |
|
2014 |
Chai G, Zhou L, Manto M, Helmbacher F, Clotman F, Goffinet AM, Tissir F. Celsr3 is required in motor neurons to steer their axons in the hindlimb. Nature Neuroscience. 17: 1171-9. PMID 25108913 DOI: 10.1038/Nn.3784 |
0.456 |
|
2014 |
Puppo F, Sebbagh M, Helmbacher F, Levy N, Krahn M, Bartoli M. G.P.14 Neuromuscular Disorders. 24: 798. DOI: 10.1016/J.Nmd.2014.06.028 |
0.411 |
|
2014 |
Puppo F, Dionnet E, Gaildrat P, Castro C, Bernard R, Salort-Campana E, Shahram A, Nishino I, Krahn M, Helmbacher F, Levy N, Bartoli M. G.P.12 Neuromuscular Disorders. 24: 797-798. DOI: 10.1016/J.Nmd.2014.06.026 |
0.313 |
|
2013 |
Caruso N, Herberth B, Bartoli M, Puppo F, Dumonceaux J, Zimmermann A, Denadai S, Lebossé M, Roche S, Geng L, Magdinier F, Attarian S, Bernard R, Maina F, Levy N, ... Helmbacher F, et al. Deregulation of the protocadherin gene FAT1 alters muscle shapes: implications for the pathogenesis of facioscapulohumeral dystrophy. Plos Genetics. 9: e1003550. PMID 23785297 DOI: 10.1371/Journal.Pgen.1003550 |
0.606 |
|
2012 |
Charoy C, Nawabi H, Reynaud F, Derrington E, Bozon M, Wright K, Falk J, Helmbacher F, Kindbeiter K, Castellani V. gdnf activates midline repulsion by Semaphorin3B via NCAM during commissural axon guidance. Neuron. 75: 1051-66. PMID 22998873 DOI: 10.1016/J.Neuron.2012.08.021 |
0.435 |
|
2011 |
Lamballe F, Genestine M, Caruso N, Arce V, Richelme S, Helmbacher F, Maina F. Pool-specific regulation of motor neuron survival by neurotrophic support. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 11144-58. PMID 21813676 DOI: 10.1523/Jneurosci.2198-11.2011 |
0.701 |
|
2011 |
Genestine M, Caricati E, Fico A, Richelme S, Hassani H, Sunyach C, Lamballe F, Panzica GC, Pettmann B, Helmbacher F, Raoul C, Maina F, Dono R. Enhanced neuronal Met signalling levels in ALS mice delay disease onset. Cell Death & Disease. 2: e130. PMID 21412276 DOI: 10.1038/Cddis.2011.11 |
0.692 |
|
2010 |
Gascon E, Gaillard S, Malapert P, Liu Y, Rodat-Despoix L, Samokhvalov IM, Delmas P, Helmbacher F, Maina F, Moqrich A. Hepatocyte growth factor-Met signaling is required for Runx1 extinction and peptidergic differentiation in primary nociceptive neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 12414-23. PMID 20844136 DOI: 10.1523/Jneurosci.3135-10.2010 |
0.675 |
|
2006 |
Kramer ER, Knott L, Su F, Dessaud E, Krull CE, Helmbacher F, Klein R. Cooperation between GDNF/Ret and ephrinA/EphA4 signals for motor-axon pathway selection in the limb. Neuron. 50: 35-47. PMID 16600854 DOI: 10.1016/J.Neuron.2006.02.020 |
0.697 |
|
2003 |
Helmbacher F, Dessaud E, Arber S, deLapeyrière O, Henderson CE, Klein R, Maina F. Met signaling is required for recruitment of motor neurons to PEA3-positive motor pools. Neuron. 39: 767-77. PMID 12948444 DOI: 10.1016/S0896-6273(03)00493-8 |
0.719 |
|
2001 |
Maina F, Panté G, Helmbacher F, Andres R, Porthin A, Davies AM, Ponzetto C, Klein R. Coupling Met to specific pathways results in distinct developmental outcomes. Molecular Cell. 7: 1293-306. PMID 11430831 DOI: 10.1016/S1097-2765(01)00261-1 |
0.655 |
|
2001 |
Yokoyama N, Romero MI, Cowan CA, Galvan P, Helmbacher F, Charnay P, Parada LF, Henkemeyer M. Forward signaling mediated by ephrin-B3 prevents contralateral corticospinal axons from recrossing the spinal cord midline. Neuron. 29: 85-97. PMID 11182083 DOI: 10.1016/S0896-6273(01)00182-9 |
0.618 |
|
2001 |
Adams RH, Diella F, Hennig S, Helmbacher F, Deutsch U, Klein R. The cytoplasmic domain of the ligand ephrinB2 is required for vascular morphogenesis but not cranial neural crest migration. Cell. 104: 57-69. PMID 11163240 DOI: 10.1016/S0092-8674(01)00191-X |
0.377 |
|
2000 |
Helmbacher F, Schneider-Maunoury S, Topilko P, Tiret L, Charnay P. Targeting of the EphA4 tyrosine kinase receptor affects dorsal/ventral pathfinding of limb motor axons. Development (Cambridge, England). 127: 3313-24. PMID 10887087 |
0.574 |
|
1998 |
Helmbacher F, Pujades C, Desmarquet C, Frain M, Rijli FM, Chambon P, Charnay P. Hoxa1 and Krox-20 synergize to control the development of rhombomere 3. Development (Cambridge, England). 125: 4739-48. PMID 9806922 |
0.494 |
|
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