Defects in pathfinding by cranial neural crest cells in mice lacking the neuregulin receptor ErbB4

The Molecular Biology of Axon Guidance

Tessier‐Lavigne, M., & Goodman, C. S. (1996) · Science · doi:10.1126/science.274.5290.1123 · Cited by 3,311

Multiple essential functions of neuregulin in development

Meyer, D., & Birchmeier, C. (1995) · Nature · doi:10.1038/378386a0 · Cited by 1,273

Aberrant neural and cardiac development in mice lacking the ErbB4 neuregulin receptor

Gassmann, M., Casagranda, F., Orioli, D., Simon, H. H., Lai, C., Klein, R., & Lemke, G. (1995) · Nature · doi:10.1038/378390a0 · Cited by 1,151

Patterning the Vertebrate Neuraxis

Lumsden, A., & Krumlauf, R. K. (1996) · Science · doi:10.1126/science.274.5290.1109 · Cited by 1,142

Conversion of Xenopus Ectoderm into Neurons by NeuroD, a Basic Helix-Loop-Helix Protein

Lee, J. E., Hollenberg, S. M., Snider, L., Turner, D. L., Lipnick, N., & Weintraub, H. (1995) · Science · doi:10.1126/science.7754368 · Cited by 1,023

[22] Detection of messenger RNA by in Situ hybridization to tissue sections and whole mounts

Wilkinson, D. G., & Nieto, M. A. (1993) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(93)25025-w · Cited by 794

Sox10, a Novel Transcriptional Modulator in Glial Cells

Kuhlbrodt, K., Herbarth, B., Sock, E., Hermans-Borgmeyer, I., & Wegner, M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-01-00237.1998 · Cited by 781

neurogenin1 Is Essential for the Determination of Neuronal Precursors for Proximal Cranial Sensory Ganglia

Ma, Q., Chen, Z., Barrantes, I. D. B., de la Pompa, J. L., & Anderson, D. J. (1998) · Neuron · doi:10.1016/s0896-6273(00)80988-5 · Cited by 735

Ligand-specific activation of HER4/p180erbB4, a fourth member of the epidermal growth factor receptor family.

Plowman, G. D., Culouscou, J., Whitney, G. S., Green, J. M., Carlton, G. W., Foy, L., NEUBAUER, M., & SHOYAB, M. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.5.1746 · Cited by 714

Contributions of placodal and neural crest cells to avian cranial peripheral ganglia

D'amico‐Martel, A., & Noden, D. M. (1983) · American Journal of Anatomy · doi:10.1002/aja.1001660406 · Cited by 708

Altered immunoreactivity of ErbB4, a causative gene product for ALS19, in the spinal cord of patients with sporadic ALS

Takahashi, Y., Uchino, A., Shioya, A., Sano, T., Matsumoto, C., Numata‐Uematsu, Y., Nagano, S., Araki, T., Murayama, S., & Saito, Y. (2019) · Neuropathology · doi:10.1111/neup.12558 · Cited by 25

Embryology of the Head and Neck

Catala, M. (2005) · Springer eBooks · doi:10.1007/3-540-26398-5_28 · Cited by 23

Expression of EGFR-family proteins in the brain: role in development, health and disease

Novak, U., Walker, F., & Kaye, A. H. (2001) · Journal of Clinical Neuroscience · doi:10.1054/jocn.2000.0799 · Cited by 22

ErbB-4: a receptor tyrosine kinase

Zhou, W., & Carpenter, G. (2002) · Inflammation Research · doi:10.1007/bf02684009 · Cited by 22

Neural Crest and Cranial Ectodermal Placodes

Baker, C. V. H. (2006) · Kluwer Academic Publishers-Plenum Publishers eBooks · doi:10.1007/0-387-28117-7_4 · Cited by 20

Neuregulin signaling in neurons depends on ErbB4 interaction with PSD-95

Murphy, S. P., & Bielby‐Clarke, K. (2008) · Brain Research · doi:10.1016/j.brainres.2008.02.063 · Cited by 20

Neural Crest Cells

Trainor, P. A., Bronner-Fraser, M. E., & Krumlauf, R. K. (2004) · Elsevier eBooks · doi:10.1016/b978-012436643-5/50028-6 · Cited by 19

Xenopus Teashirt1 regulates posterior identity in brain and cranial neural crest

Koebernick, K., Kashef, J., Pieler, T., & Wedlich, D. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.06.041 · Cited by 19

Calpain-Dependent ErbB4 Cleavage Is Involved in Brain Ischemia-Induced Neuronal Death

Lu, Y., Gao, Y., Tao, R., Liao, M., Huang, J., Wu, G., Han, F., & Li, X.-M. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9275-2 · Cited by 18

The Role of NRG3 in Mammary Development

Howard, B. A. (2008) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-008-9082-8 · Cited by 18

Extensive expression of craniofacial related homeobox genes in canine mammary sarcomas

Wensman, H., Göransson, H., Leuchowius, K., Strömberg, S., Pontén, F., Isaksson, A., Rutteman, G. R., Heldin, N., Pejler, G., & Hellmén, E. (2008) · Breast Cancer Research and Treatment · doi:10.1007/s10549-008-0243-7 · Cited by 18

Expression of ErbB3, ErbB4, and neuregulin‐1 mRNA during tooth development

Fried, K., Risling, M., Tidcombe, H., Gassmann, M., & Lillesaar, C. (2002) · Developmental Dynamics · doi:10.1002/dvdy.10114 · Cited by 18

Cellular organization and boundary formation in craniofacial development

Kindberg, A. A., & Bush, J. O. (2018) · genesis · doi:10.1002/dvg.23271 · Cited by 19

Recent advances in understanding transforming growth factor β regulation of orofacial development

Greene, R. M., & Pisano, M. M. (2005) · Human & Experimental Toxicology · doi:10.1191/0960327105ht492oa · Cited by 17

The Postmigratory Alar Topography of Visceral Cranial Nerve Efferents Challenges the Classical Model of Hindbrain Columns

Puelles, L., Tvrdík, P., & Martı́nez-de-la-Torre, M. (2018) · The Anatomical Record · doi:10.1002/ar.23830 · Cited by 16

LATS1/2 control TGFB-directed epithelial-to-mesenchymal transition in the murine dorsal cranial neuroepithelium through YAP regulation

Martinez‐Traverso, I. M., Steimle, J. D., Zhao, X., Wang, J., & Martin, J. F. (2022) · Development · doi:10.1242/dev.200860 · Cited by 16

Regulation of functional nitric oxide synthase‐1 expression in cerebellar granule neurons by heregulin is post‐transcriptional, and involves mitogen‐activated protein kinase

Krainock, R., & Murphy, S. P. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00420.x · Cited by 15

Neuregulin‐1 is a chemoattractant and chemokinetic molecule for trunk neural crest cells

de Bellard, M. E., Ortega, B., Sao, S., Kim, L., Herman, J., & Zuhdi, N. (2018) · Developmental Dynamics · doi:10.1002/dvdy.24625 · Cited by 14

Mouse Embryo Culture for the Study of Neural Crest Cells

Muñoz, W. A., & Trainor, P. A. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9412-0_9 · Cited by 11

EGF Mediates Survival of Rat Cochlear Sensory Cells via an NF-κB Dependent Mechanism In Vitro

Zheng, Y., Rayner, M., Ling, F., Hu, X., Zheng, X., Bearth, E., & Lin, J. (2008) · The Open Neuroscience Journal · doi:10.2174/1874082000802010009 · Cited by 13

Neuregulins

Falls, D. L. (2003) · Elsevier eBooks · doi:10.1016/b978-012160281-9/50003-7 · Cited by 12

Exon level machine learning analyses elucidate novel candidate miRNA targets in an avian model of fetal alcohol spectrum disorder

Al‐Shaer, A. E., Flentke, G. R., Berres, M. E., Garic, A., & Smith, S. M. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006937 · Cited by 11

Heparin-binding epidermal growth factor–like growth factor promotes murine enteric nervous system development and enteric neural crest cell migration

Zhou, Y., James, I., & Besner, G. E. (2012) · Journal of Pediatric Surgery · doi:10.1016/j.jpedsurg.2012.05.008 · Cited by 11

Hypoxia-inducible Factor-1α Induces ErbB4 Signaling in the Differentiating Mammary Gland

Paatero, I., Seagroves, T. N., Vaparanta, K. M., Han, W., Jones, F. E., Johnson, R. S., & Elenius, K. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.533497 · Cited by 10

Analysis of Neural Crest Migration and Differentiation by Cross-species Transplantation

Griswold, S. L., & Lwigale, P. Y. (2012) · Journal of Visualized Experiments · doi:10.3791/3622 · Cited by 10

The Neural Crest and Craniofacial Malformations

ten Donkelaar, H. J., Vermeij‐Keers, C., & Mathijssen, I. M. J. (2014) · Springer eBooks · doi:10.1007/978-3-642-54687-7_5 · Cited by 10

Colec12 and Trail signaling confine cranial neural crest cell trajectories and promote collective cell migration

McLennan, R., Giniūnaitė, R., Hildebrand, K., Teddy, J. M., Kasemeier‐Kulesa, J. C., Castro, L. A. B., Baker, R. E., Maini, P. K., & Kulesa, P. M. (2023) · Developmental Dynamics · doi:10.1002/dvdy.569 · Cited by 9

The Emerging Roles of the Cephalic Neural Crest in Brain Development and Developmental Encephalopathies

Bruet, E., Amarante-Silva, D., Gorojankina, T., & Creuzet, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24129844 · Cited by 8

Identification and characterization of intermediate states in mammalian neural crest cell epithelial to mesenchymal transition and delamination

Zhao, R., Moore, E. L., Gogol, M., Unruh, J. R., Yu, Z., Scott, A. R., Wang, Y., Rajendran, N. K., & Trainor, P. A. (2024) · eLife · doi:10.7554/elife.92844 · Cited by 21

Genetic Identity of Neural Crest Cell Differentiation in Tissue and Organ Development

Kyriakoudi, S. A., Chatzi, D., Dermitzakis, I., Gargani, S., Μanthou, M. E., Meditskou, S., & Theotokis, P. (2024) · Frontiers in Bioscience-Landmark · doi:10.31083/j.fbl2907261 · Cited by 11

Dynamic Expression and Heterogeneous Intracellular Location of En-1 during Late Mouse Embryonic Development

Zhong, S., Chen, X.-S., Cai, Q., Luo, X. G., Chen, X., Liu, J., & Yao, Z. (2009) · Cells Tissues Organs · doi:10.1159/000260063 · Cited by 8

Involvement of CXCL10 in Neuronal Damage under the Condition of Spinal Cord Injury and the Potential Therapeutic Effect of Nrg1

Qiao, X.-Y., Wang, Y., Zhang, W., Li, Q., Liu, C., Dao, J.-J., Qiao, C.-M., Cui, C., Shen, Y., & Zhao, W. (2023) · Journal of Integrative Neuroscience · doi:10.31083/j.jin2204096 · Cited by 7

Paracrine regulation of neural crest EMT by placodal MMP28

Gouignard, N., Bibonne, A., Mata, J. F., Bajanca, F., Berki, B., Barriga, E. H., Saint‐Jeannet, J., & Théveneau, E. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3002261 · Cited by 8

Glial growth factor-2 promotes the survival, migration and bromodeoxyuridine incorporation of mammalian neural crest cells in caudal neural tube explant cultures

Bannerman, P. G. C., Puhalla, S., Sahai, A., Shieh, A., Berman, M., & Pleasure, D. (2000) · Developmental Brain Research · doi:10.1016/s0165-3806(00)00090-0 · Cited by 7

Neural Crest Cell and Placode Interactions in Cranial PNS Development

Fleenor, S. J., & Begbie, J. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-401730-6.00009-0 · Cited by 6

Dosage analysis of the 7q11.23 Williams region identifies BAZ1B as a major human gene patterning the modern human face and underlying self-domestication

Zanella, M., Vitriolo, A., Andirkó, A., Martins, P. T., Sturm, S., O’Rourke, T., Laugsch, M., Malerba, N., Skaros, A., Trattaro, S., et al. (2020) · Yearbook of pediatric endocrinology · doi:10.1530/ey.17.14.7 · Cited by 5

Dynamic expression of MMP28 during cranial morphogenesis

Gouignard, N., Théveneau, E., & Saint‐Jeannet, J. (2020) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2019.0559 · Cited by 5

Adult Rat Otic Placode-Derived Neurons and Sensory Epithelium Express All Four erbB Receptors: A Role in Regulating Vestibular Ganglion Neuron Viability

Matsunaga, T., Davis, J. G., & Greene, M. I. (2001) · DNA and Cell Biology · doi:10.1089/10445490152122424 · Cited by 5

Identification and characterization of intermediate states in mammalian neural crest cell epithelial to mesenchymal transition and delaminationPreprint

Zhao, R., Moore, E. L., Gogol, M., Unruh, J. R., Yu, Z., Scott, A. R., Wang, Y., Rajendran, N. K., & Trainor, P. A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.26.564204 · Cited by 5

Identification of in vivo roles of ErbB4-JMa and its direct nuclear signaling using a novel isoform-specific knock out mouse

Doherty, R. E., MacLeod, B. L., Nelson, M. M., Ibrahim, M. M. H., Borges, B. C., Jaradat, N. W., Finneran, M. C., Giger, R. J., & Corfas, G. (2022) · Scientific Reports · doi:10.1038/s41598-022-21598-2 · Cited by 6

Baicalin administration could rescue high glucose-induced craniofacial skeleton malformation by regulating neural crest development

Lü, J., Luo, Z., Sun, C., Wang, S.-M., Sun, D., Huang, R., Yang, X., Ding, Y., & Wang, G. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1295356 · Cited by 4

The Cardiac Neural Crest and Their Role in Development and Disease

Vincentz, J. W., & Firulli, A. B. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-401730-6.00012-0 · Cited by 4

Embryology of the Head and Neck

Catala, M. (2016) · Springer eBooks · doi:10.1007/978-3-662-46258-4_59-1 · Cited by 4

Identification and characterization of intermediate states in mammalian neural crest cell epithelial to mesenchymal transition and delaminationPreprint

Zhao, R., Moore, E. L., Gogol, M., Unruh, J. R., Yu, Z., Scott, A. R., Wang, Y., Rajendran, N. K., & Trainor, P. A. (2024) · eLife · doi:10.7554/elife.92844.2 · Cited by 4

Role of Cardiac Neural Crest Cells in Morphogenesis of the Heart and Great Vessels

Inman, K. E., Ezin, M., Bronner-Fraser, M. E., & Trainor, P. A. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-381332-9.00020-7 · Cited by 3

ErbB-4

Carpenter, G. F. (2003) · Elsevier eBooks · doi:10.1016/b978-012160281-9/50006-2 · Cited by 3

The Neural Crest and Craniofacial Malformations

ten Donkelaar, H. J., & Vermeij‐Keers, C. (2006) · Springer eBooks · doi:10.1007/3-540-34659-7_5 · Cited by 3

Hox gene control of neural crest cell, pharyngeal arch and craniofacial patterning">Hox gene control of neural crest cell, pharyngeal arch and craniofacial patterning

Iulianella, A., & Trainor, P. A. (2003) · Advances in developmental biology and biochemistry · doi:10.1016/s1569-1799(03)13006-7 · Cited by 2

Induced pluripotent stem cells-derived craniofacial mesenchymal progenitor cells

Srinivasan, A., Loberas, M., Toh, Y., & Hui, J. H. P. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85545-7.00010-7 · Cited by 2

Neuropilin 1 and 2 control cranial gangliogenesis and axon guidance through neural crest cells

Schwarz, Q., Vieira, J. M., Howard, B. A., Eickholt, B. J., & Ruhrberg, C. (2008) · Development · doi:10.1242/dev.033316 · Cited by 2

Changes in the Long Noncoding RNA Expression Profile in the Development of the Embryonic External Ear After BMP5 Gene Mutation

Liu, W., Jin, S., Lin, L., Yang, Q., & Jiang, H. (2023) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000009200 · Cited by 2

Identification and characterization of intermediate states in mammalian neural crest cell epithelial to mesenchymal transition and delaminationPreprint

Zhao, R., Moore, E. L., Gogol, M., Uhruh, J., Yu, Z., Scott, A. R., Wang, Y., Rajendran, N. K., & Trainor, P. A. (2024) · eLife · doi:10.7554/elife.92844.1 · Cited by 2

The Neural Crest and Craniofacial Malformations

Vermeij‐Keers, C., Mathijssen, I. M. J., Trainor, P. A., & ten Donkelaar, H. J. (2023) · Springer eBooks · doi:10.1007/978-3-031-26098-8_5 · Cited by 3

The Roles of Long-Term Hyperhomocysteinemia and Micronutrient Supplementation in the AppNL–G–F Model of Alzheimer’s Disease

Nieraad, H., de Bruin, N. M. W. J., Arne, O., Hofmann, M. C. J., Pannwitz, N., Resch, E., Luckhardt, S., Schneider, A., Trautmann, S., Schreiber, Y., et al. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.876826 · Cited by 1

Neuregulins

Seroogy, K. B., & ZHANG, L. (2006) · Elsevier eBooks · doi:10.1016/b978-012369442-3/50198-7 · Cited by 1

Mouse Models of Receptor Tyrosine Kinases

Holcmann, M., Amberg, N., Drobits, B., Glitzner, E., Komposch, K., Robson, J., Savarese, F., Srivatsa, S., Stulnig, G., & Sibilia, M. C. (2014) · Springer eBooks · doi:10.1007/978-1-4939-2053-2_11 · Cited by 1

Stem Cell Biology in the Craniofacial Apparatus

Parada, C., Akiyama, K., Chai, Y., & Shi, S. (2012) · Wiley eBooks · doi:10.1002/9781118704868.ch10 · Cited by 1

Neural Crest Cells

Trainor, P. A., Krumlauf, R. K., & Bronner-Fraser, M. E. (2004) · Elsevier eBooks · doi:10.1016/b978-012436643-5/50109-7 · Cited by 1

Retinoid signaling promotes frontonasal identity while repressing maxillary identity during craniofacial developmentPreprint

Xu, L., Wu, Y., Omi, M., Tsujimoto, T., Dang, Y., Wang, Q., Nie, X., Motooka, D., Ohara, H., Inubushi, T., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.09.730988 · Cited by 1

Differences in plasticity and expression of developmental genes in canine mammary Carcinomas and Sarcomas

Wensman, H. (2009) · Epsilon Open Archive (Sveriges lantbruksuniversitet biblioteket (Swedish University of Agricultural Sciences))

INVESTIGATION OF Hoxa2 GENE FUNCTION IN PALATE DEVELOPMENT USING A RETROVIRAL GENE DELIVERY SYSTEM

Wang, X. (2006) · University Library - University of Saskatchewan (University of Saskatchewan)

MED23: a Mediator subunit's role in global gene transcription, regulation of craniofacial development and WNT signaling.

Bhatt, S. (2013) · KU ScholarWorks (The University of Kansas)

Neuregulin Signaling and GABA A Receptor Expression in Cerebellar Granule Neurons

Xie, F. (2006) · Europe PMC (PubMed Central)

Universidade Federal de Santa Catarina Centro de Ciências Biológicas Programa de Pós-Graduação em Biologia Celular e do Desenvolvimento

Teixeira, B. L. (2011)

ErbB Membrane Tyrosine Kinase Receptors: Analyzing Migration in a Highly Complex Signaling System

Brossier, N. M., Byer, S. J., Peavler, L. T., & Carroll, S. L. (2012) · Neuromethods · doi:10.1007/978-1-61779-824-5_7

Sviluppo della faccia

Khonsari, R. H., & Catala, M. (2018) · EMC - Otorinolaringoiatria · doi:10.1016/s1639-870x(18)91438-8

Desarrollo de la cara

Khonsari, R. H., & Catala, M. (2018) · EMC - Otorrinolaringología · doi:10.1016/s1632-3475(18)91407-4

The biomechanics of collective neural crest cell chemotaxis

Shellard, A. (2018) · UCL Discovery (University College London)

CUBIERTAS PIROCLÁSTICAS CENOZOICAS EN LA PARTE SEPTENTRIONAL DEL VALLE MEDIO DEL MAGDALENA Y MESAS DE SANTANDER

Vergara, J. G., & Corchuelo, D. M. (2023) · Revista de la Academia Colombiana de Ciencias Exactas Físicas y Naturales · doi:10.18257/raccefyn.27(103).2003.2063

Reviewer #1 (Public Review): Identification and characterization of intermediate states in mammalian neural crest cell epithelial to mesenchymal transition and delamination

Zhao, R., Moore, E. L., Gogol, M. M., et al. (2024) · eLife · doi:10.7554/elife.92844.1.sa2

Reviewer #2 (Public Review): Identification and characterization of intermediate states in mammalian neural crest cell epithelial to mesenchymal transition and delamination

Zhao, R., Moore, E. L., Gogol, M. M., et al. (2024) · eLife · doi:10.7554/elife.92844.1.sa1

The craniofacial region

Iseki, S., & Morriss‐Kay, G. M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-23739-3.00019-5

Développement de la face

Khonsari, R. H., & Catala, M. (2026) · Encyclopédie médico-chirurgicale. Oto-rhino-laryngologie · doi:10.1016/s0246-0351(25)47403-0

Fibroblast growth factor receptor 1 in craniofacial and midbrain-hindbrain development

Trokovic, N. (2005) · Työväentutkimus Vuosikirja

Array-CNCC: precise aggregation and arrayed plating facilitate quantitative phenotyping of human cranial neural crest cells and craniofacial disease modellingPreprint

Ozga, E., Milto, K. M., Demurtas, M., Bates, L. E., Grimes, G. R., Azami, T., Su, J., Angelis, C. D., Trizzino, M., Nichols, J., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.18.696654

Study of Pax3 and Pax7 functions during the development of the mouse embryo

Zalc, A. (2014) · theses.fr (ABES) · doi:10.70675/1b3f0375zc09bz4e45z8c85z1e0f6985f9f2

Cell dynamics and genetic regulation in the zebrafish hindbrain morphogenesis

Kamaraj, M. (2022) · theses.fr (ABES) · doi:10.70675/459cae17zdb15z4613zae4cz9ff09675df75

The Role of SHH Signaling in Regulating Species-Specific Jaw Size

Vavrušová, Z. (2021) · theses.fr (ABES) · doi:10.70675/30249943zee54z48cfz9420zb883bf4c759f

Identification of apoptosis pathway in Treacher Collins Syndrome

Alsayegh, K. N. (2009) · VCU Scholars Compass (Virginia Commonwealth University) · doi:10.25772/9gqr-wq87

ErbB Ligands in Angiogenesis

Iivanainen, E. (2008) · UTUPub (University of Turku)

Neural and mammary gland defects in ErbB4 knockout mice genetically rescued from embryonic lethality

Tidcombe, H., Jackson-Fisher, A. J., Mathers, K., Stern, D. F., Gassmann, M., & Golding, J. P. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1436402100 · Cited by 260

Receptor tyrosine kinase ErbB4 modulates neuroblast migration and placement in the adult forebrain

Anton, E. S., Ghashghaei, H. T., Weber, J. L., McCann, C. M., Fischer, T. M., Cheung, I. D., Gassmann, M., Messing, A., Klein, R., Schwab, M. H., et al. (2004) · Nature Neuroscience · doi:10.1038/nn1345 · Cited by 256

Diverse roles of Notch signaling in cardiac cell differentiation, migration and ventricular morphogenesis

Bao, Z., Chau, M., Tuft, R. A., & Fogarty, K. E. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.03.403

erbB4

Mak, T. W., Penninger, J. M., Roder, J., Rossant, J., & Saunders, M. E. (1998) · Elsevier eBooks · doi:10.1016/b978-012466044-1/50168-x

Investigations into the role of ErbB4 in mouse development

Tidcombe, H. (2003) · OpenGrey (Institut de l'Information Scientifique et Technique)