GPR56 Regulates Pial Basement Membrane Integrity and Cortical Lamination

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

Kobayashi, K., Nakahori, Y., Miyake, M., Matsumura, K., Kondo-Iida, E., Nomura, Y., Segawa, M., Yoshioka, M., Saito, K., Ōsawa, M., et al. (1998) · Nature · doi:10.1038/28653 · Cited by 811

Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophies

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Neuronal or Glial Progeny

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Reelin and brain development

Tissir, F., & Goffinet, A. M. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1113 · Cited by 767

Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1

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Perlecan Maintains the Integrity of Cartilage and Some Basement Membranes

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The tetraspanin web modulates immune-signalling complexes

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β1-Class Integrins Regulate the Development of Laminae and Folia in the Cerebral and Cerebellar Cortex

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

Expression of Cux‐1 and Cux‐2 in the subventricular zone and upper layers II–IV of the cerebral cortex

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The matrix reorganized: extracellular matrix remodeling and integrin signaling

Larsen, M., Artym, V. V., Green, J. A., & Yamada, K. M. (2006) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2006.08.009 · Cited by 541

Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesis

Pisano, T., Barkovich, A. J., Leventer, R. J., Squier, W., Scheffer, I. E., Parrini, E., Blasér, S., Marini, C., Robertson, S. P., Tortorella, G., et al. (2012) · Neurology · doi:10.1212/wnl.0b013e31826aac88 · Cited by 39

Characterization of G protein‐coupled receptor 56 protein expression in the mouse developing neocortex

Jeong, S., Luo, R., Li, S., Strokes, N., & Piao, X. (2012) · Journal of Comparative Neurology · doi:10.1002/cne.23076 · Cited by 36

Research models of neurodevelopmental disorders: The right model in the right place

Damianidou, E., Mouratidou, L., & Kyrousi, C. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.1031075 · Cited by 41

GPR56 Plays varying roles in endogenous cancer progression

Xu, L., Begum, S., Barry, M., Crowley, D. G., Yang, L., Bronson, R. T., & Hynes, R. O. (2010) · Clinical & Experimental Metastasis · doi:10.1007/s10585-010-9322-3 · Cited by 37

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

Adhesion G‐protein coupled receptors and extracellular matrix proteins: Roles in myelination and glial cell development

Chaudhry, P. M., & Piao, X. (2016) · Developmental Dynamics · doi:10.1002/dvdy.24473 · Cited by 37

A Novel GPR56 Mutation Causes Bilateral Frontoparietal Polymicrogyria

Luo, R., Yang, H. M., Jin, Z., Halley, D. J. J., Chang, B. S., MacPherson, L. K. R., Brueton, L. A., & Piao, X. (2011) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2011.02.004 · Cited by 36

The Novel Immune Checkpoint GPR56 Is Expressed on Tumor-Infiltrating Lymphocytes and Selectively Upregulated upon TCR Signaling

Bilemjian, V., Vlaming, M. R., Freile, J. Á., Huls, G. A., de Bruyn, M., & Bremer, E. (2022) · Cancers · doi:10.3390/cancers14133164 · Cited by 35

Spatiotemporal Regulation of Rho GTPases in Neuronal Migration

Xu, Z., Chen, Y., & Chen, Y. (2019) · Cells · doi:10.3390/cells8060568 · Cited by 39

Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotype

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

Subcellular mRNA localization and local translation of Arhgap11a in radial glial progenitors regulates cortical development

Pilaz, L., Liu, J., Joshi, K., Tsunekawa, Y., Musso, C. M., D’Arcy, B. R., Suzuki, I., Alsina, F. C., Pratiksha, K. C., Sethi, S., et al. (2023) · Neuron · doi:10.1016/j.neuron.2023.02.023 · Cited by 39

Moving messages in the developing brain—emerging roles for mRNA transport and local translation in neural stem cells

Pilaz, L., & Silver, D. L. (2017) · FEBS Letters · doi:10.1002/1873-3468.12626 · Cited by 31

Abnormal development of the human cerebral cortex

Squier, W., & Jansen, A. (2010) · Journal of Anatomy · doi:10.1111/j.1469-7580.2010.01288.x · Cited by 31

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

Anti-GPR56 monoclonal antibody potentiates GPR56-mediated Src-Fak signaling to modulate cell adhesion

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

Primary cellular meningeal defects cause neocortical dysplasia and dyslamination

Hecht, J. H., Siegenthaler, J. A., Patterson, K. P., & Pleasure, S. J. (2010) · Annals of Neurology · doi:10.1002/ana.22103 · Cited by 30

GPR56 is highly expressed in neural stem cells but downregulated during differentiation

Bai, Y., Du, L., Li, S., Zhang, Y., & Zhang, L. (2009) · Neuroreport · doi:10.1097/wnr.0b013e32832c92d7 · Cited by 30

The 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

High-level Gpr56 expression is dispensable for the maintenance and function of hematopoietic stem and progenitor cells in mice

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

The Adhesion G-Protein-Coupled Receptor, GPR56/ADGRG1, Inhibits Cell–Extracellular Matrix Signaling to Prevent Metastatic Melanoma Growth

Millar, M. W., Corson, N., & Xu, L. (2018) · Frontiers in Oncology · doi:10.3389/fonc.2018.00008 · 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

Cerebellar Cysts in Children: a Pattern Recognition Approach

Boltshauser, E., Scheer, I., Huisman, T. A. G. M., & Poretti, A. (2014) · The Cerebellum · doi:10.1007/s12311-014-0633-9 · Cited by 27

Cell type‐specific evaluation of ADGRG1 / GPR56 function in developmental central nervous system myelination

Chiou, B., Gao, C., Giera, S., Folts, C. J., Kishore, P., Yu, D., Oak, H. C., Jiang, R., & Piao, X. (2020) · Glia · doi:10.1002/glia.23906 · Cited by 26

Small Rho-GTPases and cortical malformations

Cappello, S. (2013) · Small GTPases · doi:10.4161/sgtp.23093 · Cited by 28

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

Cell‐autonomous and cell‐to‐cell signalling events in normal and altered neuronal migration

Manent, J., Beguin, S., Ganay, T., & Represa, A. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07867.x · Cited by 26

Local gene regulation in radial glia: Lessons from across the nervous system

D’Arcy, B. R., & Silver, D. L. (2020) · Traffic · doi:10.1111/tra.12769 · Cited by 22

Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556

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

Adhesion 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

Ariadne’s Thread in the Developing Cerebral Cortex: Mechanisms Enabling the Guiding Role of the Radial Glia Basal Process during Neuron Migration

Meyerink, B. L., Tiwari, N. K., & Pilaz, L. (2020) · Cells · doi:10.3390/cells10010003 · Cited by 23

Chapter 1 GPR56 and Its Related Diseases

Jin, Z., Luo, R., & Piao, X. (2009) · Progress in molecular biology and translational science · doi:10.1016/s1877-1173(09)89001-7 · 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

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

Assessment of fetal midbrain and hindbrain in mid‐sagittal cranial plane by three‐dimensional multiplanar sonography. Part 2: application of nomograms to fetuses with posterior fossa malformations

Leibovitz, Z., Shkolnik, C., Haratz, K. K., Malinger, G., Shapiro, I., & Lerman‐Sagie, T. (2014) · Ultrasound in Obstetrics and Gynecology · doi:10.1002/uog.13312 · Cited by 21

Seizure susceptibility in polymicrogyria: Clinical and experimental approaches

Takano, T. (2011) · Epilepsy Research · doi:10.1016/j.eplepsyres.2011.06.010 · 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

Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A)

Jayakody, H., Zarei, S., Nguyen, H., Dalton, J. C., Chen, K. S., Hudgins, L., Day, J., Withrow, K., Pandya, A., Teasley, J., et al. (2020) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlaa062 · 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

Adhesion G protein-coupled receptors in glioblastoma

Stephan, G., Ravn-Boess, N., & Placantonakis, D. G. (2021) · Neuro-Oncology Advances · doi:10.1093/noajnl/vdab046 · Cited by 19

Experimental models of human cortical malformations: from mammals to 'acortical' zebrafish

Costa, F. V., Zabegalov, K. N., Kolesnikova, T. O., de Abreu, M. S., Kotova, M. M., Petersen, E. V., & Kalueff, A. V. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105429 · Cited by 18

Subarachnoid cerebrospinal fluid is essential for normal development of the cerebral cortex

Miyan, J. A., Cains, S., Larcombe, S. J., Naz, N., Jimenez, A. R., Bueno, D., & Gato, A. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.11.011 · Cited by 17

Malformations of Cortical Development

Dobyns, W. B., Guerrini, R., & Leventer, R. J. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4377-0435-8.00026-3 · Cited by 17

Bilateral frontoparietal polymicrogyria (BFPP) syndrome secondary to a 16q12.1‐q21 chromosome deletion involving GPR56 gene

Borgatti, R., Marelli, S., Bernardini, L., Novelli, A., Cavallini, A. R., Tonelli, A., Bassi, M. T., & Dallapiccola, B. (2009) · Clinical Genetics · doi:10.1111/j.1399-0004.2009.01262.x · Cited by 15

Adhesion GPCR Function in Pulmonary Development and Disease

Ludwig, M., Seuwen, K., & Bridges, J. P. (2016) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-41523-9_14 · Cited by 15

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

The polymicrogyria-associated GPR56 promoter preferentially drives gene expression in developing GABAergic neurons in common marmosets

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

D egree of C ajal– R etzius Cell Mislocalization Correlates with the Severity of Structural Brain Defects in Mouse Models of Dystroglycanopathy

Booler, H. S., Williams, J. L. D., Hopkinson, M., & Brown, S. (2015) · Brain Pathology · doi:10.1111/bpa.12306 · Cited by 13

The β‐tubulin gene TUBB2B is involved in a large spectrum of neuronal migration disorders

Uribe, V. (2009) · Clinical Genetics · doi:10.1111/j.1399-0004.2009.01301.x · Cited by 13

Defects in neural guidepost structures and failure to remove leptomeningeal cells from the septal midline behind the interhemispheric fusion defects in Netrin1 deficient mice

Hakanen, J., & Salminen, M. (2015) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2015.08.005 · Cited by 14

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

Cellular and Axonal Constituents of Neocortical Molecular Layer Heterotopia

Ramos, R. L., Siu, N. Y., Brunken, W. J., Yee, K. T., Gabel, L. A., Dine, S. E. V., & Hoplight, B. J. (2014) · Developmental Neuroscience · doi:10.1159/000365100 · Cited by 12

Please eat (only part) of me: synaptic phosphatidylserine cues microglia to feast

Peet, G. C., Bennett, F. C., & Bennett, M. L. (2020) · The EMBO Journal · doi:10.15252/embj.2020105924 · 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

Subcellular mRNA localization and local translation of Arhgap11a in radial glial cells regulates cortical developmentPreprint

Pilaz, L., Joshi, K., Liu, J., Tsunekawa, Y., Alsina, F. C., Sethi, S., Suzuki, I., Vanderhaeghen, P., Polleux, F., & Silver, D. L. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.30.229724 · 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

Heart Development, Angiogenesis, and Blood-Brain Barrier Function Is Modulated by Adhesion GPCRs

Musa, G., Engel, F. B., & Niaudet, C. (2016) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-41523-9_16 · Cited by 12

Expression and immunoaffinity purification of recombinant soluble human GPR56 protein for the analysis of GPR56 receptor shedding by ELISA

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

GNG5 Controls the Number of Apical and Basal Progenitors and Alters Neuronal Migration During Cortical Development

Ayo-Martin, A. C., Kyrousi, C., Giaimo, R. D., & Cappello, S. (2020) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.578137 · Cited by 11

Adhesion-GPCRs in the CNS

Strokes, N., & Piao, X. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-7913-1_7 · Cited by 11

GPR56 Interacts with Extracellular Matrix and Regulates Cancer Progression

Xu, L. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-7913-1_8 · 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

Unravelling the genetic architecture of autosomal recessive epilepsy in the genomic era

Calhoun, J. D., & Carvill, G. L. (2018) · Journal of Neurogenetics · doi:10.1080/01677063.2018.1513509 · 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

The Development of Developmental Neuroscience

Mason, C. A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4648-09.2009 · Cited by 10

Radial glia progenitor polarity in health and disease

Viola, V., Chinnappa, K., & Francis, F. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1478283 · Cited by 10

Downstream signalling of the disease‐associated mutations on GPR56/ADGRG1

Cevheroğlu, O., Demir, N., Kesici, M. S., Özçubukçu, S., & Son, Ç. D. (2023) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.13873 · Cited by 9

Indomethacin induced gene regulation in the rat hippocampus

Sathyanesan, M., Girgenti, M. J., Warner‐Schmidt, J. L., & Newton, S. S. (2015) · Molecular Brain · doi:10.1186/s13041-015-0150-x · Cited by 9

Malformations of Cortical Development

Dobyns, W. B., Leventer, R. J., & Guerrini, R. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-37101-8.00029-1 · Cited by 10

Prolidase enzyme is required for extracellular matrix integrity and impacts on postnatal cerebellar cortex development

Insolia, V., Priori, E. C., Gasperini, C., Coppa, F., Cocchia, M., Iervasi, E., Ferrari, B., Besio, R., Maruelli, S., Bernocchi, G., et al. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24735 · Cited by 9

Loss of BAF (mSWI/SNF) chromatin-remodeling ATPase Brg1 causes multiple malformations of cortical development in mice

Jin, Y., Gao, X., Lu, M., Chen, G., Yang, X., Ren, N., Song, Y., Hou, C., Li, J., Liu, Q., et al. (2022) · Human Molecular Genetics · doi:10.1093/hmg/ddac127 · Cited by 7

Deletion of RIC8A in neural precursor cells leads to altered neurogenesis and neonatal lethality of mouse

Kask, K., Ruisu, K., Tikker, L., Karis, K., Saare, M., Meier, R., Karis, A., Tõnissoo, T., & Pooga, M. (2015) · Developmental Neurobiology · doi:10.1002/dneu.22264 · Cited by 8

An adhesion signaling axis involving Dystroglycan, β1-Integrin, and Cas adaptor proteins regulates the establishment of the cortical glial scaffold

Wong, W., Estep, J. A., Treptow, A. M., Rajabli, N., Jahncke, J. N., Ubina, T., Wright, K. M., & Riccomagno, M. M. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3002212 · Cited by 8

Symptomatic epilepsy

Shorvon, S. D., Andermann, F., & Guerrini, R. (2011) · Cambridge University Press eBooks · doi:10.1017/cbo9780511921001.016 · Cited by 7

Human Developmental Genetics

Tan, W., Gilmore, E. C., & Baris, H. N. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-383834-6.00018-5 · Cited by 9

GPR56, an Adhesion GPCR with Multiple Roles in Human Diseases, Current Status and Future Perspective

Fan, Y., Yan, X., & Guan, W. (2024) · Current Drug Targets · doi:10.2174/0113894501298344240507080149 · Cited by 6

Adhesion-GPCRs in the Male Reproductive Tract

Davies, B., & Kirchhoff, C. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-7913-1_16 · Cited by 6

Hindbrain Tangential Migration

Sotelo, C., & Chédotal, A. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00032-6 · Cited by 8

Sijunzi decoction may decrease apoptosis via stabilization of the extracellular matrix following cerebral ischaemia‑reperfusion in rats

Yang, P., Tian, Y., Deng, W., Cai, X., Liu, W., Li, L., & Huang, H. (2019) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2019.7878 · Cited by 6

The Genetics of Brain Malformations

Manzini, M. C., & Walsh, C. A. (2015) · Wiley eBooks · doi:10.1002/9781118524947.ch7 · Cited by 6

Loss of cardiomyocyte-specific adhesion G-protein-coupled receptor G1 (ADGRG1/GPR56) promotes pressure overload-induced heart failure

Einspahr, J. M., Xu, H., Roy, R., Dietz, N., Melchior, J., Raja, J., Carter, R. L., Piao, X., & Tilley, D. G. (2024) · Bioscience Reports · doi:10.1042/bsr20240826 · Cited by 5

Divergence and inheritance of neocortical heterotopia in inbred and genetically-engineered mice

Toia, A. R., Cuoco, J. A., Esposito, A. W., Ahsan, J., Joshi, A., Herron, B. J., Torres, G., Bolivar, V. J., & Ramos, R. L. (2016) · Neuroscience Letters · doi:10.1016/j.neulet.2016.12.038 · Cited by 5

Neuronal Migration Disorders

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