F. Helmbacher

发表

Neuronal heterogeneity and stereotyped connectivity in the auditory afferent system

G. Silberberg, Charles Petitpré, Haohao Wu, 2018, Nature Communications.

Characterization of Tg(Etv4-GFP) and Etv5RFP Reporter Lines in the Context of Fibroblast Growth Factor 10 Signaling During Mouse Embryonic Lung Development

B. Stripp, Matthew R. Jones, S. Bellusci, 2019, Front. Genet..

Cooperation between GDNF/Ret and ephrinA/EphA4 Signals for Motor-Axon Pathway Selection in the Limb

Rüdiger Klein, Catherine E. Krull, R. Klein, 2006, Neuron.

Stromal Fat4 acts non-autonomously with Dchs1/2 to restrict the nephron progenitor pool

B. Blencowe, Q. Pan, H. McNeill, 2015, Development.

Astrocyte-intrinsic and -extrinsic Fat1 activities regulate astrocyte development and angiogenesis in the retina.

F. Helmbacher, 2022, Development.

Fat1 regulates astrocyte maturation and angiogenesis in the retina

F. Helmbacher, 2020, bioRxiv.

Enhanced neuronal Met signalling levels in ALS mice delay disease onset

B. Pettmann, C. Sunyach, C. Raoul, 2011, Cell Death and Disease.

An intragenic FAT1 regulatory element deleted in muscular dystrophy patients drives muscle and mesenchyme expression during development

F. Helmbacher, Tarana Nigam, Angela K. Zimmermann, 2022, bioRxiv.

Coordination of signalling networks and tumorigenic properties by ABL in glioblastoma cells

D. Figarella-Branger, F. Helmbacher, F. Conti, 2016, Oncotarget.

Fat1 deletion promotes hybrid EMT state, tumour stemness and metastasis

C. Sotiriou, C. Decaestecker, I. Salmon, 2020, Nature.

Neuronal heterogeneity and stereotyped connectivity in the auditory afferent system

G. Silberberg, Charles Petitpré, Haohao Wu, 2018, Nature Communications.

Hepatocyte Growth Factor-Met Signaling Is Required for Runx1 Extinction and Peptidergic Differentiation in Primary Nociceptive Neurons

A. Moqrich, P. Delmas, I. Samokhvalov, 2010, The Journal of Neuroscience.

Tissue cross talks governing limb muscle development and regeneration.

F. Helmbacher, S. Stricker, 2020, Seminars in cell & developmental biology.

Identification of Variants in the 4q35 Gene FAT1 in Patients with a Facioscapulohumeral Dystrophy‐Like Phenotype

F. Puppo, Y. Hayashi, I. Nishino, 2015, Human mutation.

Deregulation of the Protocadherin Gene FAT1 Alters Muscle Shapes: Implications for the Pathogenesis of Facioscapulohumeral Dystrophy

F. Puppo, B. Herberth, F. Magdinier, 2013, PLoS genetics.

Tissue-Specific Gain of RTK Signalling Uncovers Selective Cell Vulnerability during Embryogenesis

S. Audebert, F. Helmbacher, F. Maina, 2015, PLoS genetics.

Coupling Met to specific pathways results in distinct developmental outcomes.

A. Davies, R. Klein, F. Helmbacher, 2001, Molecular cell.

Targeting of the EphA4 tyrosine kinase receptor affects dorsal/ventral pathfinding of limb motor axons.

S. Schneider-Maunoury, P. Topilko, P. Charnay, 2000, Development.

Forward Signaling Mediated by Ephrin-B3 Prevents Contralateral Corticospinal Axons from Recrossing the Spinal Cord Midline

Mario I. Romero, Chad A. Cowan, Patrick Charnay, 2001, Neuron.

Celsr3 is required in motor neurons to steer their axons in the hindlimb

M. Manto, A. Goffinet, Libing Zhou, 2014, Nature Neuroscience.

Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophy

F. Puppo, F. Magdinier, G. Butler-Browne, 2015, Annals of neurology.

Fat1 deletion promotes hybrid EMT state, tumour stemness and metastasis

C. Sotiriou, C. Decaestecker, I. Salmon, 2020, Nature.

gdnf Activates Midline Repulsion by Semaphorin3B via NCAM during Commissural Axon Guidance

V. Castellani, K. Wright, F. Helmbacher, 2012, Neuron.

Tissue-specific activities of the Fat1 cadherin cooperate to control neuromuscular morphogenesis

F. Helmbacher, 2017, bioRxiv.

Pool-Specific Regulation of Motor Neuron Survival by Neurotrophic Support

M. Genestine, F. Helmbacher, F. Maina, 2011, The Journal of Neuroscience.

G.O.15 Correlation between low FAT1 expression and early affected muscle in FSHD

F. Puppo, F. Magdinier, G. Butler-Browne, 2015, Neuromuscular Disorders.

G.P.12 Molecular defects in FAT1 are associated to facioscapulohumeral dystrophy (FSHD)

F. Puppo, I. Nishino, M. Bartoli, 2014, Neuromuscular Disorders.

Hoxa1 and Krox-20 synergize to control the development of rhombomere 3.

P. Chambon, M. Frain, F. Rijli, 1998, Development.

Met Signaling Is Required for Recruitment of Motor Neurons to PEA3-Positive Motor Pools

S. Arber, C. Henderson, R. Klein, 2003, Neuron.

The Cytoplasmic Domain of the Ligand EphrinB2 Is Required for Vascular Morphogenesis but Not Cranial Neural Crest Migration

F. Diella, R. Klein, R. Adams, 2001, Cell.

Endothelial FAT1 inhibits angiogenesis by controlling YAP/TAZ protein degradation via E3 ligase MIB2

M. Potente, S. Offermanns, N. Wettschureck, 2023, Nature Communications.

Requirement of FAT and DCHS protocadherins during hypothalamic-pituitary development

F. Faucz, C. Stratakis, N. Pankratz, 2020, JCI insight.

Plasticity versus specificity in RTK signalling modalities for distinct biological outcomes in motor neurons

B. Herberth, F. Helmbacher, F. Maina, 2014, BMC Biology.

Identification of variants in the 4 q 35 gene FAT 1 in patients with a Facioscapulohumeral dystrophy ( FSHD )-like phenotype

F. Puppo, Y. Hayashi, I. Nishino, 2015 .

Hepatocyte Growth Factor-Met Signaling Is Required for Runx1 Extinction and Peptidergic Differentiation in Primary Nociceptive Neurons

A. Moqrich, P. Delmas, I. Samokhvalov, 2010, The Journal of Neuroscience.