The DOI matches its Crossref record; 50 of the 50 references it cites were found in a registry or an index.
G protein-coupled receptor 56 and collagen III, a receptor-ligand pair, regulates cortical development and lamination
Open accessAbstract
GPR56, an orphan G protein-coupled receptor (GPCR) from the family of adhesion GPCRs, plays an indispensable role in cortical development and lamination. Mutations in the GPR56 gene cause a malformed cerebral cortex in both humans and mice that resembles cobblestone lissencephaly, which is characterized by overmigration of neurons beyond the pial basement membrane. However, the molecular mechanisms through which GPR56 regulates cortical development remain elusive due to the unknown status of its ligand. Here we identify collagen, type III, alpha-1 (gene symbol Col3a1 ) as the ligand of GPR56 through an in vitro biotinylation/proteomics approach. Further studies demonstrated that Col3a1 null mutant mice exhibit overmigration of neurons beyond the pial basement membrane and a cobblestone-like cortical malformation similar to the phenotype seen in Gpr56 null mutant mice. Functional studies suggest that the interaction of collagen III with its receptor GPR56 inhibits neural migration in vitro. As for intracellular signaling, GPR56 couples to the Gα 12/13 family of G proteins and activates RhoA pathway upon ligand binding. Thus, collagen III regulates the proper lamination of the cerebral cortex by acting as the major ligand of GPR56 in the developing brain.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“GPR56 encodes an adhesion heterotrimeric guanine nucleotide–binding protein (G protein)–coupled receptor that is highly expressed in cortical progenitors (7, 16) and binds extracellular matrix proteins (17).”
From Evolutionarily Dynamic Alternative Splicing of GPR56 Regulates Regional Cerebral Cortical Patterning (2014) · cites this paper as [17]
In the citing paper
“GPR56 likely influences progenitor proliferation by stabilizing the basal process of radial neuroepithelial progenitors”
From Evolutionarily Dynamic Alternative Splicing of GPR56 Regulates Regional Cerebral Cortical Patterning (2014) · cites this paper as [17]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Regulation of the small GTP‐binding protein Rho by cell adhesion and the cytoskeleton
Ren, X. D., Kiosses, W. B., & Schwartz, M. A. (1999) · The EMBO Journal · doi:10.1093/emboj/18.3.578 · Cited by 1,575
Englund, C., Fink, A., Lau, C., Pham, D., Daza, R. A. M., Bulfone, A., Kowalczyk, T., & Hevner, R. F. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2899-04.2005 · Cited by 1,261
Development of the human cerebral cortex: Boulder Committee revisited
Bystron, I., Blakemore, C., & Rakic, P. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2252 · Cited by 977
C ELL M IGRATION IN THE F OREBRAIN
Marín, Ó., & Rubenstein, J. L. R. (2003) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.26.041002.131058 · Cited by 957
Perlecan Maintains the Integrity of Cartilage and Some Basement Membranes
Costell, M., Gustafsson, E., Aszódi, A., Mörgelin, M., Bloch, W., Hunziker, E. B., Addicks, K., Timpl, R., & Fässler, R. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.147.5.1109 · Cited by 672
Mechanisms of Cortical Development: A View From Mutations in Mice
Caviness, V. S., & RAKIC, P. T. (1978) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.01.030178.001501 · Cited by 653
Trekking across the Brain: The Journey of Neuronal Migration
Ayala, R., Shu, T., & Tsai, L.-H. (2007) · Cell · doi:10.1016/j.cell.2006.12.021 · Cited by 620
Liu, X., Wu, H., Byrne, M., Krane, S., & Jaenisch, R. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.5.1852 · Cited by 614
Graus-Porta, D., Blaess, S., Senften, M., Littlewood-Evans, A., Damsky, C. H., Huang, Z., Orban, P. C., Klein, R., Schittny, J. C., & Müller, U. (2001) · Neuron · doi:10.1016/s0896-6273(01)00374-9 · Cited by 569
Nieto, M., Monuki, E. S., Tang, H., Imitola, J., Haubst, N., Khoury, S. J., Cunningham, J., Götz, M., & Walsh, C. A. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20322 · Cited by 569
Cited by
Sorted by citations
Items 101–200 of 291
Jørgensen, A., Fagerheim, T., Rand‐Hendriksen, S., Lunde, P. I., Vorren, T., Pepin, M. G., Leistritz, D. F., & Byers, P. H. (2014) · European Journal of Human Genetics · doi:10.1038/ejhg.2014.181 · Cited by 46
Developmental disorders of the midbrain and hindbrain
Barkovich, A. J. (2012) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2012.00007 · Cited by 48
G Protein-Coupled Receptors in Myelinating Glia
Mogha, A., D’Rozario, M., & Monk, K. R. (2016) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2016.09.002 · Cited by 43
Stienen, S., Ferreira, J. P., Kobayashi, M., Preud’homme, G., Dobre, D., Machu, J., Duarte, K., Bresso, E., Devignes, M., López‐Andrés, N., et al. (2020) · Biomarkers · doi:10.1080/1354750x.2020.1727015 · Cited by 46
Emerging roles of adhesion G protein-coupled receptors
Rosa, M., Noel, T., Harris, M., & Ladds, G. (2021) · Biochemical Society Transactions · doi:10.1042/bst20201144 · Cited by 49
Dissecting signaling and functions of adhesion G protein–coupled receptors
Araç, D., Aust, G., Calebiro, D., Engel, F. B., Formstone, C. J., Goffinet, A. M., Hamann, J., Kittel, R. J., Liebscher, I., Lin, H., et al. (2012) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2012.06820.x · Cited by 45
Self-citationToriyama, M., Mizuno, N., Fukami, T., Iguchi, T., Toriyama, M., Tago, K., & Itoh, H. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.316307 · Cited by 44
GPR56 contributes to the development of acute myeloid leukemia in mice
Daria, D., Kirsten, N., Muranyi, A., Mulaw, M. A., Ihme, S., Kechter, A., Hollnagel, M., Bullinger, L., Döhner, K., Döhner, H., et al. (2016) · Leukemia · doi:10.1038/leu.2016.76 · Cited by 43
Takeuchi, M., Yamaguchi, S., Yonemura, S., Kakiguchi, K., Sato, Y., Higashiyama, T., Shimizu, T., & Hibi, M. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005587 · Cited by 44
Elrick, M. M., Samson, W. K., Corbett, J. A., Salvatori, A., Stein, L. M., Kolar, G. R., Naatz, A., & Yosten, G. L. C. (2015) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00369.2014 · Cited by 41
Loss of Col3a1, the Gene for Ehlers-Danlos Syndrome Type IV, Results in Neocortical Dyslamination
Jeong, S., Li, S., Luo, R., Strokes, N., & Piao, X. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029767 · Cited by 40
Self-citationClassification, Nomenclature, and Structural Aspects of Adhesion GPCRs
Krishnan, A., Nijmeijer, S., de Graaf, C., & Schiöth, H. B. (2016) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-41523-9_2 · Cited by 40
Bondarev, A. D., Attwood, M. M., Jonsson, J., Chubarev, V. N., Tarasov, V. V., & Schiöth, H. B. (2020) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2020.1791075 · Cited by 40
Parkin, J. D., San Antonio, J. D., Persikov, A. V., Dagher, H., Dalgleish, R., Jensen, S. T., Jeunemaitre, X., & Savige, J. (2017) · PLOS ONE · doi:10.1371/journal.pone.0175582 · Cited by 39
Irfan, M., Evonuk, K. S., & DeSilva, T. M. (2022) · The FEBS Journal · doi:10.1111/febs.16190 · Cited by 39
Jeong, S., Luo, R., Li, S., Strokes, N., & Piao, X. (2012) · Journal of Comparative Neurology · doi:10.1002/cne.23076 · Cited by 36
Self-citationMallat, Z., Tedgui, A., & Henrion, D. (2016) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.116.307909 · Cited by 39
Agonistic Antibodies Reveal the Function of GPR56 in Human Glioma U87-MG Cells
Ohta, S., Sakaguchi, S., Kobayashi, Y., Mizuno, N., Tago, K., & Itoh, H. (2015) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b14-00752 · Cited by 37
Chaudhry, P. M., & Piao, X. (2016) · Developmental Dynamics · doi:10.1002/dvdy.24473 · Cited by 37
Self-citationFricke, F., Lee, J., Michalak, M., Warnken, U. H., Haußer, I., Suarez‐Carmona, M., Halama, N., Schnölzer, M., Kopitz, J., & Gebert, J. F. (2017) · Cell Communication and Signaling · doi:10.1186/s12964-017-0169-y · Cited by 37
Daga, S., Rosenberger, A., Quehenberger, F., Krisper, N., Prietl, B., Reinisch, A., Zebisch, A., Sill, H., & Wölfler, A. (2019) · Cancer Medicine · doi:10.1002/cam4.2053 · Cited by 40
Schwann cell development: From neural crest to myelin sheath
Muppirala, A. N., Limbach, L. E., Bradford, E. F., & Petersen, S. C. (2020) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.398 · Cited by 36
Spatiotemporal Regulation of Rho GTPases in Neuronal Migration
Xu, Z., Chen, Y., & Chen, Y. (2019) · Cells · doi:10.3390/cells8060568 · Cited by 39
Quattrocchi, C. C., Zanni, G., Napolitano, A., Longo, D., Cordelli, D. M., Barresi, S., Randisi, F., Valente, E. M., Verdolotti, T., Genovese, E., et al. (2012) · Neurogenetics · doi:10.1007/s10048-012-0352-7 · Cited by 34
The genetic basis of hydrocephalus: genes, pathways, mechanisms, and global impact
Hale, A. T., Boudreau, H. S., Devulapalli, R. K., Duy, P. Q., Atchley, T. J., Dewan, M. C., Goolam, M., Fieggen, G. A. G., Spader, H. L., Smith, A. A., et al. (2024) · Fluids and Barriers of the CNS · doi:10.1186/s12987-024-00513-z · Cited by 33
Role of ADGRG1/GPR56 in Tumor Progression
Ng, K., Chen, T., Stacey, M. A., & Lin, H. (2021) · Cells · doi:10.3390/cells10123352 · Cited by 33
Fève, M., Saliou, J., Zeniou, M., Lennon, S., Carapito, C., Dong, J., DORSSELAER, A. V., Junier, M., Chneiweiss, H., Cianférani, S., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0091519 · Cited by 35
Atanes, P., Ruz‐Maldonado, I., Hawkes, R. G., Liu, B., Zhao, M., Huang, G. C., Al-Amily, I. M., Salehi, A. A., Amisten, S., & Persaud, S. J. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2778-z · Cited by 33
Nielsen, M. J., & Karsdal, M. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-809847-9.00003-9 · Cited by 33
GPR56: An adhesion GPCR involved in brain development, neurological disorders and cancer
Ganesh, R. A., Venkataraman, K., & Sirdeshmukh, R. (2020) · Brain Research · doi:10.1016/j.brainres.2020.147055 · Cited by 31
GPR56 in Cancer Progression: Current Status and Future Perspective
Yang, L., & Xu, L. (2012) · Future Oncology · doi:10.2217/fon.12.27 · Cited by 31
Adhesion GPCRs in Kidney Development and Disease
Cazorla‐Vázquez, S., & Engel, F. B. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00009 · Cited by 34
Vézain, M., Lecuyer, M., Rubio, M., Dupé, V., Ratié, L., David, V., Pasquier, L., Odent, S., Coutant, S., Tournier, I., et al. (2018) · Acta Neuropathologica Communications · doi:10.1186/s40478-018-0610-5 · Cited by 30
Chatterjee, T., Zhang, S., Posey, T. A., Jacob, J., Wu, L., Yu, W., Francisco, L. E., Liu, Q. J., & Carmon, K. S. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100261 · Cited by 28
Landscape of GPCR expression along the mouse nephron
Poll, B. G., Chen, L., Chou, C., Raghuram, V., & Knepper, M. A. (2021) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00077.2021 · Cited by 30
New functions and signaling mechanisms for the class of adhesion G protein–coupled receptors
Liebscher, I., Ackley, B. D., Araç, D., Ariestanti, D. M., Aust, G., Bae, B.-I., Bista, B. R., Bridges, J. P., Duman, J. G., Engel, F. B., et al. (2014) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12580 · Cited by 30
Self-citationThe Activation and Signaling Mechanisms of GPR56/ADGRG1 in Melanoma Cell
Huang, K., & Lin, H. (2018) · Frontiers in Oncology · doi:10.3389/fonc.2018.00304 · Cited by 29
Expression of orphan GPR56 correlates with tumor progression in human epithelial ovarian cancer
Liu, Z., Huang, Z., Yang, W., LI, Z., Xing, S., LI, H., HU, B., & LI, P. (2016) · Neoplasma · doi:10.4149/neo_2017_104 · Cited by 29
Rao, T. N., Marks-Bluth, J., Sullivan, J., Gupta, M. K., Chandrakanthan, V., Fitch, S. R., Ottersbach, K., Jang, Y. C., Piao, X., Kulkarni, R., et al. (2015) · Stem Cell Research · doi:10.1016/j.scr.2015.02.001 · Cited by 28
Self-citationAffinity proteomics identifies novel functional modules related to adhesion GPCRs
Knapp, B., Roedig, J., Boldt, K., Krzysko, J., Horn, N., Ueffing, M., & Uwe Wolfrum, B. (2019) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14220 · Cited by 28
Tethered agonists: a new mechanism underlying adhesion G protein-coupled receptor activation
Schöneberg, T., Liebscher, I., Luo, R., Monk, K. R., & Piao, X. (2015) · Journal of Receptors and Signal Transduction · doi:10.3109/10799893.2015.1072978 · Cited by 27
Self-citationPathophysiological impact of the adhesion G protein-coupled receptor family
Einspahr, J. M., & Tilley, D. G. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00445.2021 · Cited by 27
Rønnekleiv, O. K., Fang, Y., Zhang, C., Nestor, C. C., Mao, P., & Kelly, M. J. (2014) · Molecular Endocrinology · doi:10.1210/me.2014-1103 · Cited by 29
Kang, S. (2020) · Human Genetics · doi:10.1007/s00439-020-02124-8 · Cited by 27
Versatile Signaling Activity of Adhesion GPCRs
Kishore, A., & Hall, R. A. (2016) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-41523-9_7 · Cited by 26
Adhesion GPCR-Related Protein Networks
Knapp, B., & Uwe Wolfrum, B. (2016) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-41523-9_8 · Cited by 26
Adhesion GPCRs as a paradigm for understanding polycystin-1 G protein regulation
Maser, R. L., & Calvet, J. P. (2020) · Cellular Signalling · doi:10.1016/j.cellsig.2020.109637 · Cited by 26
Cauley, E. S., Hamed, A. A., Mohamed, I. N., Elseed, M. A., Martinez, S., Yahia, A., Abozar, F., Abubakr, R., Koko, M., Elsayed, L. E. O., et al. (2019) · Neurogenetics · doi:10.1007/s10048-019-00577-2 · Cited by 25
Self-citationAdhesion G-protein coupled receptors: Implications for metabolic function
Olaniru, O. E., & Persaud, S. J. (2019) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2019.02.012 · Cited by 23
Crucial contribution of GPR56/ADGRG1, expressed by breast cancer cells, to bone metastasis formation
Sasaki, S., Zhang, D., Iwabuchi, S., Tanabe, Y., Hashimoto, S., 山内, 明., Hayashi, K., Tsuchiya, H., Hayakawa, Y., Baba, T., et al. (2021) · Cancer Science · doi:10.1111/cas.15150 · Cited by 23
Unexpected redundancy of Gpr56 and Gpr97 during hematopoietic cell development and differentiation
Maglitto, A., Mariani, S. A., de Pater, E., Rodríguez‐Seoane, C., Vink, C. S., Piao, X., Lukke, M.-L., & Dzierzak, E. A. (2021) · Blood Advances · doi:10.1182/bloodadvances.2020003693 · Cited by 22
Self-citationSingh, J. P., Dagar, M., Dagar, G., Kumar, S., Rawal, S. K., Sharma, R. D., Tyagi, R. K., & Bagchi, G. (2020) · PLoS ONE · doi:10.1371/journal.pone.0226056 · Cited by 22
GPR56 Promotes Diabetic Kidney Disease Through eNOS Regulation in Glomerular Endothelial Cells
Wu, J., Wang, Z., Cai, M., Wang, X., Lo, B., Li, Q., He, C., Lee, K., & Fu, J. (2023) · Diabetes · doi:10.2337/db23-0124 · Cited by 22
Adhesion G-protein-coupled receptor, GPR56, is required for Müllerian duct development in the chick
Roly, Z. Y., Major, A. T., Fulcher, A. J., Estermann, M. A., Hirst, C. E., & Smith, C. A. (2019) · Journal of Endocrinology · doi:10.1530/joe-19-0419 · Cited by 22
Loohuis, N. F. M. O., Martens, G. J. M., van Bokhoven, H., Kaplan, B. B., Homberg, J. R., & Aschrafi, A. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2017.04.009 · Cited by 21
Adgrf5 contributes to patterning of the endothelial deep layer in retina
Niaudet, C., Petkova, M., Jung, B., Lu, S. Y., Laviña, B., Offermanns, S., Brakebusch, C., & Betsholtz, C. (2019) · Angiogenesis · doi:10.1007/s10456-019-09674-0 · Cited by 21
Adhesion G protein-coupled receptor gluing action guides tissue development and disease
Sreepada, A., Tiwari, M., & Pal, K. (2022) · Journal of Molecular Medicine · doi:10.1007/s00109-022-02240-0 · Cited by 24
Nijmeijer, S., Vischer, H. F., & Leurs, R. (2016) · Biochemical Pharmacology · doi:10.1016/j.bcp.2016.04.013 · Cited by 20
Al-Hasan, M., Martin, P. E., Shu, X., Patterson, S., & Bartholomew, C. (2021) · Biomolecules · doi:10.3390/biom11020156 · Cited by 21
Functions of G protein‐coupled receptor 56 in health and disease
Su, T., Guan, Q., Cheng, H., Zhu, Z., Jiang, C., Guo, P., Tai, Y., Sun, H., Wang, M., Wei, W., et al. (2022) · Acta Physiologica · doi:10.1111/apha.13866 · Cited by 20
Targeting adhesion G protein-coupled receptors. Current status and future perspectives
Ließmann, F., von Bredow, L., Meiler, J., & Liebscher, I. (2024) · Structure · doi:10.1016/j.str.2024.10.022 · Cited by 19
Role of Adhesion G Protein-Coupled Receptors in Immune Dysfunction and Disorder
Tseng, W.-Y., Stacey, M. A., & Lin, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065499 · Cited by 19
Adhesion G‐protein coupled receptor 56 is required for 3T3‐L1 adipogenesis
Hasan, M. A., Roy, P., Dolan, S., Martin, P. E., Patterson, S., & Bartholomew, C. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.29079 · Cited by 18
The adhesion G protein‐coupled receptor GPR56/ADGRG1 in cytotoxic lymphocytes
Hsiao, C., Vos, E., van Gisbergen, K. P. J. M., & Hamann, J. (2023) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.13841 · Cited by 17
Zhu, B., Wangzhou, A., Yu, D., Li, T., Schmidt, R., Florencio, S. L. D., Chao, L., Thurber, A. L., Zhou, M., Msheik, Z., et al. (2024) · Neuron · doi:10.1016/j.neuron.2025.06.020 · Cited by 17
Self-citationAdhesion G-Protein-Coupled Receptors: Elusive Hybrids Come of Age
Simundza, J., & Cowin, P. (2013) · Cell Communication & Adhesion · doi:10.3109/15419061.2013.855727 · Cited by 16
Olaniru, O. E., Cheng, J., Ast, J., Arvaniti, A., Atanes, P., Huang, G. C., King, A., Jones, P. M., Broichhagen, J., Hodson, D. J., et al. (2021) · Molecular Metabolism · doi:10.1016/j.molmet.2021.101285 · Cited by 16
Depletion of C3orf1/TIMMDC1 Inhibits Migration and Proliferation in 95D Lung Carcinoma Cells
Wu, H., Wang, W., & Xu, H. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms151120555 · Cited by 16
Tonni, G., Pattacini, P., Bonasoni, M. P., & Júnior, E. A. (2016) · Revista Brasileira Ginecologia e Obstetrícia · doi:10.1055/s-0036-1582126 · Cited by 16
Sawal, H. A., Harripaul, R., Mikhailov, A., Vleuten, K., Naeem, F., Nasr, T., Hassan, M. J., Vincent, J. B., Ayub, M., & Rafiq, M. (2017) · Journal of Pediatric Genetics · doi:10.1055/s-0037-1612591 · Cited by 16
Genomic landscape of diffuse glioma revealed by whole genome sequencing
Kinnersley, B., Jung, J., Cornish, A. J., Chubb, D., Laxton, R. C., Frangou, A., Gruber, A. J., Sud, A., Caravagna, G., Sottoriva, A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-59156-9 · Cited by 18
Ganesh, R. A., Sonpatki, P., Naik, D., John, A. E., Sathe, G. J., Lakshmikantha, A., Chandrachari, K. P., Bauer, L., Knäuper, V., Aeschlimann, D. P., et al. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.841890 · Cited by 14
Collagen VI Is a Gi-Biased Ligand of the Adhesion GPCR GPR126/ADGRG6
Wilde, C., Chaudhry, P. M., Luo, R., Simon, K., Piao, X., & Liebscher, I. (2023) · Cells · doi:10.3390/cells12111551 · Cited by 14
Self-citationYosten, G. L. C., Elrick, M. M., Salvatori, A., Stein, L. M., Kolar, G. R., Ren, J. T., Corbett, J. A., & Samson, W. K. (2015) · Peptides · doi:10.1016/j.peptides.2015.05.011 · Cited by 14
Murayama, A. Y., Kuwako, K.-I., Okahara, J., Bae, B.-I., Okuno, M., Mashiko, H., Shimogori, T., Walsh, C. A., Sasaki, E., & Okano, H. (2020) · Scientific Reports · doi:10.1038/s41598-020-78608-4 · Cited by 14
Non-muscle myosins control radial glial basal endfeet to mediate interneuron organization
D’Arcy, B. R., Lennox, A. L., Musso, C. M., Bracher, A., Escobar-Tomlienovich, C. F., Perez-Sanchez, S., & Silver, D. L. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3001926 · Cited by 14
Sigoillot, S. M., Monk, K. R., Piao, X., Selimi, F., & Harty, B. L. (2016) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-41523-9_12 · Cited by 15
Self-citationNakane, T., Angata, K., Sato, T., Kaji, H., & Narimatsu, H. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.006892 · Cited by 14
Röthe, J., Kraft, R., Ricken, A. M., Kaczmarek, I., Matz‐Soja, M., Winter, K., Dietzsch, A. N., Buchold, J., Ludwig, M., Liebscher, I., et al. (2024) · Communications Biology · doi:10.1038/s42003-024-05783-9 · Cited by 12
The relevance of adhesion G protein-coupled receptors in metabolic functions
Kaczmarek, I., Suchý, T., Prömel, S., Schöneberg, T., Liebscher, I., & Thor, D. (2021) · Biological Chemistry · doi:10.1515/hsz-2021-0146 · Cited by 14
Structural clarity is brought to adhesion G protein‐coupled receptor tethered agonism
Gupta, C., Bernadyn, T. F., & Tall, G. G. (2022) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.13831 · Cited by 13
Castello, M. A., & Gleeson, J. G. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.10.005 · Cited by 10
G protein-coupled receptor 56 regulates matrix production and motility of lung fibroblasts
Yang, J., Wang, Z., Leng, D., Dai, H., Wang, J., Liang, J., Jiang, D., & Wang, C. (2014) · Experimental Biology and Medicine · doi:10.1177/1535370214529395 · Cited by 13
Identification of Key Structural Motifs Involved in 7 Transmembrane Signaling of Adhesion GPCRs
Arimont, M., van der Woude, M., Leurs, R., Vischer, H. F., de Graaf, C., & Nijmeijer, S. (2019) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.8b00051 · Cited by 12
Adhesion GPCR GPR56 Expression Profiling in Human Tissues
Kaiser, F., Morawski, M., Krohn, K., Rayes, N., Hsiao, C., Quaas, M., & Aust, G. (2021) · Cells · doi:10.3390/cells10123557 · Cited by 12
Adhesion GPCRs Govern Polarity of Epithelia and Cell Migration
Strutt, D. I., Schnabel, R., Fiedler, F., & Prömel, S. (2016) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-41523-9_11 · Cited by 12
Adhesion G protein-coupled receptors
Langenhan, T., Anderson, G. R., Araç, D., Aust, G., Avila-Zozaya, M., Bagger, S. M., Barth, P., Berndt, S., Blacklow, S. C., Blanco-Redondo, B., et al. (2026) · Pharmacological Reviews · doi:10.1016/j.pharmr.2026.100116 · Cited by 15
Self-citationVizurraga, A., Robertson, M. J., Yu, M., Skiniotis, G., & Tall, G. G. (2023) · Molecular Pharmacology · doi:10.1124/molpharm.123.000688 · Cited by 11
Control of Skeletal Muscle Cell Growth and Size Through Adhesion GPCRs
White, J. P. (2016) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-41523-9_13 · Cited by 11
Speidell, A. P., Walton, S., Campbell, L. A., Tomassoni‐Ardori, F., Tessarollo, L., Corbo, C., Taraballi, F., & Mocchetti, I. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15818 · Cited by 10
Yang, T.-Y., Chiang, N., Tseng, W.-Y., Pan, H.-L., Peng, Y.-M., Shen, J., Wu, K.-A., Kuo, M., Chang, G.-W., & Lin, H. (2014) · Protein Expression and Purification · doi:10.1016/j.pep.2014.11.013 · Cited by 11
GPR56: A potential therapeutic target for neurological and psychiatric disorders
Qi, W., & Guan, W. (2024) · Biochemical Pharmacology · doi:10.1016/j.bcp.2024.116395 · Cited by 12
G protein selectivity profile of GPR56/ADGRG1 and its effect on downstream effectors
Jallouli, R., Moreno-Salinas, A. L., Laniel, A., Holleran, B. J., Avet, C., Jacob, J., Hoang, T., Lavoie, C. L., Carmon, K. S., Bouvier, M., et al. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05416-8 · Cited by 10
GPR56 S4 variant is required for microglia‐mediated synaptic pruning
Li, T., Luo, R., Schmidt, R., D'Alessandro, N., Kishore, P., Zhu, B., Yu, D., & Piao, X. (2022) · Glia · doi:10.1002/glia.24293 · Cited by 12
Self-citationCollagen I is a critical organizer of scarring and CNS regeneration failurePreprint
Bi, Y., Duan, W., & Silver, J. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.07.592424 · Cited by 11
Huang, K., Ng, K., Kuan-Yu, I., Chang, Y. C., Chen, H., Chiu, Y., Hung, C., Yu, W.-C., Chen, T., Stacey, M. A., et al. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02267-z · Cited by 9
Yang, F., Wang, W., Qiu, F., Qing, R., Gao, Q., Yan, X., Wu, D., Hui, H., Dang, R., Jiang, G., et al. (2026) · Nature Metabolism · doi:10.1038/s42255-025-01436-1 · Cited by 9
Deletion ofGpr128results in weight loss and increased intestinal contraction frequency
Ni, Y.-Y. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i2.498 · Cited by 9
Lee, J. Y. (2019) · Journal of Korean Neurosurgical Society · doi:10.3340/jkns.2019.0098 · Cited by 9
GPR56, a novel platelet collagen receptor that loves stress
Hers, I., & Mundell, S. J. (2021) · Journal of Thrombosis and Haemostasis · doi:10.1111/jth.15335 · Cited by 9
Metadata
- Authors
- Luo, R., Jeong, S.-J., Jin, Z., Strokes, N., Li, S., & Piao, X.
- Affiliations
- Boston Children's Hospital (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2011-07-18
- Volume
- 108
- Issue
- 31
- Pages
- 12925-12930
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3150909
- OpenAlex
- W2083047610
- Cited by
- 290
- References
- 50
- Citations by year
- 2026: 14 · 2025: 21 · 2024: 15 · 2023: 20 · 2022: 17 · 2021: 23 · 2020: 22 · 2019: 26 · 2018: 15 · 2017: 14 · 2016: 26 · 2015: 22 · 2014: 19 · 2013: 18 · 2012: 16
- FWCI
- 5.66
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01NS057536)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Fetal and Pediatric Neurological Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- GPR56, type III collagen, COL3A1, G protein-coupled receptor ligands, cortical lamination, cortical development, neuronal migration, cobblestone lissencephaly, adhesion GPCRs, RhoA signaling, cerebral cortex malformation
- MeSH terms
- Animals, Basement Membrane, Brain, Cell Movement, Cells, Cultured, Cerebral Cortex, Humans, Immunohistochemistry, Neurons, Protein Binding, Recombinant Proteins, Immunoblotting, Microscopy, Immunoelectron, Mice, Knockout, rhoA GTP-Binding Protein, Collagen Type III, NIH 3T3 Cells, Receptors, G-Protein-Coupled, GTP-Binding Protein alpha Subunits, G12-G13, Immunoprecipitation, Mice, Cobblestone Lissencephaly
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review