The transforming growth factor-β superfamily of receptors

TGFβ Signaling in Growth Control, Cancer, and Heritable Disorders

Massagué, J., Blain, S. W., & Lo, R. S. (2000) · Cell · doi:10.1016/s0092-8674(00)00121-5 · Cited by 2,391

Mechanism of activation of the TGF-β receptor

Wrana, J. L., Attisano, L., Wieser, R., Ventura, F., & Massagué, J. (1994) · Nature · doi:10.1038/370341a0 · Cited by 2,340

Transcriptional control by the TGF‐β/Smad signaling system

Massagué, J., & Wotton, D. (2000) · The EMBO Journal · doi:10.1093/emboj/19.8.1745 · Cited by 1,990

Identification of Smad7, a TGFβ-inducible antagonist of TGF-β signalling

Nakao, A., Afrakhte, M., Morn, A., Nakayama, T., Christian, J. L., Heuchel, R. L., Itoh, S., Kawabata, M., Heldin, N., Heldin, C., et al. (1997) · Nature · doi:10.1038/39369 · Cited by 1,796

SB-431542 Is a Potent and Specific Inhibitor of Transforming Growth Factor-β Superfamily Type I Activin Receptor-Like Kinase (ALK) Receptors ALK4, ALK5, and ALK7

Inman, G. J., Nicolás, F. J., Callahan, J. F., Harling, J. D., Gaster, L. M., Reith, A. D., Laping, N. J., & Hill, C. S. (2002) · Molecular Pharmacology · doi:10.1124/mol.62.1.65 · Cited by 1,636

Regulation of myostatin activity and muscle growth

Lee, S.-J., & McPherron, A. C. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.151270098 · Cited by 1,616

TGFβ signals through a heteromeric protein kinase receptor complex

Wrana, J. L., Attisano, L., Cárcamo, J. M., Zentella‐Dehesa, A., Doody, J. F., Laiho, M., Wang, X.-F., & Massagué, J. (1992) · Cell · doi:10.1016/0092-8674(92)90395-s · Cited by 1,528

Regulation of actin dynamics through phosphorylation of cofilin by LIM-kinase

Arber, S., Barbayannis, F. A., Hanser, H., Schneider, C., Stanyon, C. A., Bernard, O., & Caroni, P. (1998) · Nature · doi:10.1038/31729 · Cited by 1,426

Active and Inactive Protein Kinases: Structural Basis for Regulation

Johnson, L. N., Noble, M. E. M., & Owen, D. J. (1996) · Cell · doi:10.1016/s0092-8674(00)81092-2 · Cited by 1,396

Cartilage intermediate layer protein affects the progression of intervertebral disc degeneration by regulating the extracellular microenvironment (Review)

Liu, L., He, J., Liu, C., Yang, M., Fu, J., Yi, J., Ai, X., Liu, M., Zhuang, Y., Zhang, Y., et al. (2020) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2020.4832 · Cited by 29

Cloning and primary immunological study of TGF-β1 and its receptors TβR I /TβR II in tilapia(Oreochromis niloticus)

Zhan, X.-L., Ma, T., Wu, J., Yi, L., Wang, J., Gao, X.-K., & Li, W. (2015) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2015.03.008 · Cited by 29

Activin A is an anticatabolic autocrine cytokine in articular cartilage whose production is controlled by fibroblast growth factor 2 and NF‐κB

Alexander, S., Watt, F. E., Sawaji, Y., Hermansson, M., & Saklatvala, J. (2007) · Arthritis & Rheumatism · doi:10.1002/art.22953 · Cited by 29

Sulfur Dioxide Protects Against Collagen Accumulation in Pulmonary Artery in Association With Downregulation of the Transforming Growth Factor β1/Smad Pathway in Pulmonary Hypertensive Rats

Yu, W., Liu, D., Liang, C., Ochs, T., Chen, S., Chen, S. Y., Du, S., Tang, C., Huang, Y., Du, J., et al. (2016) · Journal of the American Heart Association · doi:10.1161/jaha.116.003910 · Cited by 29

Tgf-&Bgr; Regulation of Suture Morphogenesis and Growth

Rawlins, J. T., & Opperman, L. A. (2008) · KARGER eBooks · doi:10.1159/000115038 · Cited by 29

Application of Cytokines of the Bone Morphogenetic Protein (BMP) Family in Spinal Fusion - Effects on the Bone, Intervertebral Disc and Mesenchymal Stromal Cells

May, R. D., Frauchiger, D. A., Albers, C. E., Tekari, A., Benneker, L. M., Klenke, F. M., Hofstetter, W., & Gantenbein, B. (2019) · Current Stem Cell Research & Therapy · doi:10.2174/1574888x14666190628103528 · Cited by 28

The Transforming Growth Factor β Superfamily As Possible Biomarkers of Preeclampsia: A Comprehensive Review

Adu‐Gyamfi, E. A., Lamptey, J., Duan, F.-M., Wang, Y., & Ding, Y. (2019) · Biomarkers in Medicine · doi:10.2217/bmm-2019-0208 · Cited by 28

Murine FSH Production Depends on the Activin Type II Receptors ACVR2A and ACVR2B

Schang, G., Ongaro, L., Schultz, H., Wang, Y., Zhou, X., Brûlé, E., Boehm, U., Lee, S., & Bernard, D. J. (2020) · Endocrinology · doi:10.1210/endocr/bqaa056 · Cited by 27

Skeletal muscle-derived progenitors capable of differentiating into cardiomyocytes proliferate through myostatin-independent TGF-β family signaling

Nomura, T., Ueyama, T., Ashihara, E., Tateishi, K., Asada, S., Nakajima, N., Isodono, K., Takahashi, T., Matsubara, H., & Oh, H. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.11.087 · Cited by 27

Knockdown of BAMBI inhibits β-catenin and transforming growth factor β to suppress metastasis of gastric cancer cells

Liu, K., Song, X., Ma, H., LIU, L., WEN, X., Yu, J., WANG, L., & Hu, S. (2014) · Molecular Medicine Reports · doi:10.3892/mmr.2014.2305 · Cited by 27

Growth differentiation factor 5 is a key physiological regulator of dendrite growth during development

Osório, C., Chacón, P. J., Kisiswa, L., White, M. A., Wyatt, S. L., Rodrı́guez-Tébar, A., & Davies, A. M. (2013) · Development · doi:10.1242/dev.101378 · Cited by 26

Adenoviral delivery of dominant‐negative transforming growth factor β type II receptor up‐regulates transcriptional repressor SKI‐like oncogene, decreases matrix metalloproteinase 2 in hepatic stellate cell and prevents liver fibrosis in rats

Márquez-Aguirre, A. L., Sandoval-Rodriguez, A. S., González-Cuevas, J., Bueno‐Topete, M. R., Navarro‐Partida, J., Arellano-Olivera, I., Lucano‐Landeros, S., & Armendáriz‐Borunda, J. (2009) · The Journal of Gene Medicine · doi:10.1002/jgm.1303 · Cited by 26

Expression of bone morphogenetic proteins (BMPs), their receptors, and activins in normal and scarred conjunctiva: Role of BMP-6 and activin-A in conjunctival scarring?

Andreev, K., Zenkel, M., Kruse, F. E., Jünemann, A. G. M., & Schlötzer-Schrehardt, U. M. (2006) · Experimental Eye Research · doi:10.1016/j.exer.2006.06.003 · Cited by 26

Bone morphogenetic protein-6 enhances gonadotrophin-dependent progesterone and inhibin secretion and expression of mRNA transcripts encoding gonadotrophin receptors and inhibin/activin subunits in chicken granulosa cells

Al-Musawi, S. L., Gladwell, R. T., & Knight, P. G. (2007) · Reproduction · doi:10.1530/rep-07-0070 · Cited by 26

Endoplasmic Reticulum Associated Protein Degradation (ERAD) in the Pathology of Diseases Related to TGFβ Signaling Pathway: Future Therapeutic Perspectives

Gariballa, N., & Ali, B. R. (2020) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.575608 · Cited by 25

Ferroportin and Erythroid Cells: An Update

Cianetti, L., Gabbianelli, M., & Sposi, N. M. (2010) · Advances in Hematology · doi:10.1155/2010/404173 · Cited by 28

Transforming Growth Factor-β, Smads, and Cancer

Grady, W. M. (2005) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-05-0414 · Cited by 25

A Soluble Activin Receptor Type IIB Does Not Improve Blood Glucose in Streptozotocin-Treated Mice

Wang, Q., Guo, T., Portas, J., & McPherron, A. C. (2015) · International Journal of Biological Sciences · doi:10.7150/ijbs.10430 · Cited by 24

ERBB Receptor Activation Is Required for Profibrotic Responses to Transforming Growth Factor β

Andrianifahanana, M., Wilkes, M. C., Repellin, C. E., Edens, M., Kottom, T. J., Rahimi, R. A., & Leof, E. B. (2010) · Cancer Research · doi:10.1158/0008-5472.can-10-0232 · Cited by 25

Cytokine sensitivity screening highlights BMP4 pathway signaling as a therapeutic opportunity in ER + breast cancer

Shee, K., Jiang, A., Varn, F. S., Liu, S., Traphagen, N. A., Owens, P., Ma, C. X., Hoog, J., Cheng, C., Golub, T. R., et al. (2018) · The FASEB Journal · doi:10.1096/fj.201801241r · Cited by 25

Effect of grafting BMP2-derived peptide to nanoparticles on osteogenic and vasculogenic expression of stromal cells

Mercado‐Pagán, Á. E., Yang, X., He, X., & Jabbari, E. (2012) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.1487 · Cited by 24

Soluble activin receptor type IIB treatment does not cause fat loss in mice with diet‐induced obesity

McPherron, A. C., Guo, T., Wang, Q., & Portas, J. (2011) · Diabetes Obesity and Metabolism · doi:10.1111/j.1463-1326.2011.01520.x · Cited by 24

TGF ‐β cascade regulation by PPP 1 and its interactors –impact on prostate cancer development and therapy

Korrodi‐Gregório, L., Silva, J. V., Santos‐Sousa, L., Freitas, M. J., Felgueiras, J., & Fardilha, M. (2014) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12266 · Cited by 23

Differential Binding Activity of TGF-β Family Proteins to Select TGF-β Receptors

Khalil, A. M., Dotimas, H., Kahn, J., Lamerdin, J. E., Hayes, D. B., Gupta, P., & Franti, M. (2016) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.116.232322 · Cited by 27

Pretreatment with a soluble activin type IIB receptor/Fc fusion protein improves hypoxia-induced muscle dysfunction

Pistilli, E. E., Bogdanovich, S., Mosqueira, M., Lachey, J. L., Seehra, J. S., & Khurana, T. S. (2009) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00138.2009 · Cited by 25

Langerhans cells are strongly reduced in the skin of transgenic mice overexpressing follistatin in the epidermis

Stoitzner, P., Stössel, H., Wankell, M., Hofer, S., Heufler, C., Werner, S., & Romani, N. (2005) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2005.04.003 · Cited by 24

MicroRNAs in osteoblast differentiation and fracture healing: From pathogenesis to therapeutic implication

Yao, J., Xin, R., Zhao, C., & Yu, C.-F. (2024) · Injury · doi:10.1016/j.injury.2024.111410 · Cited by 23

Cellular targets of estrogen signaling in regeneration of inner ear sensory epithelia

McCullar, J. S., & Oesterle, E. C. (2009) · Hearing Research · doi:10.1016/j.heares.2009.01.012 · Cited by 25

Smad3‐dependent signaling underlies the TGF‐β1‐mediated enhancement in astrocytic iNOS expression

Hamby, M. E., Hewett, J. A., & Hewett, S. J. (2010) · Glia · doi:10.1002/glia.21005 · Cited by 23

The imbalance of masticatory muscle activity affects the asymmetric growth of condylar cartilage and subchondral bone in rats

Miyazaki, M., Yonemitsu, I., Takei, M., Kure-Hattori, I., & Ono, T. (2015) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2015.11.020 · Cited by 23

Genetic changes in nonepithelial ovarian cancer

Nieuwenhuysen, E. V., Lambrechts, S., Lambrechts, D., Leunen, K., Amant, F. C., & Vergote, I. B. (2013) · Expert Review of Anticancer Therapy · doi:10.1586/14737140.2013.811174 · Cited by 23

Bipolar properties of red seabream (Pagrus major) transforming growth factor-β in induction of the leucocytes migration

Cai, Z., Gao, C., Li, L., & Xing, K. (2010) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2010.01.011 · Cited by 22

ActRIIB blockade increases force‐generating capacity and preserves energy supply in exercising mdx mouse muscle in vivo

Béchir, N., Pecchi, É., Vilmen, C., Fur, Y. L., Amthor, H., Bernard, M., Bendahan, D., & Giannesini, B. (2016) · The FASEB Journal · doi:10.1096/fj.201600271rr · Cited by 22

Role of transforming growth factor β in cancer microenvironment

de la Cruz‐Merino, L., Henao‐Carrasco, F., García-Manrique, T., Fernández‐Salguero, P. M., & de Villena, M. C. M. (2009) · Clinical & Translational Oncology · doi:10.1007/s12094-009-0433-8 · Cited by 22

Smad3 deficiency increases cortical and hippocampal neuronal loss following traumatic brain injury

Villapol, S., Wang, Y., Adams, M., & Symes, A. J. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.10.008 · Cited by 21

The relationship of the active and latent forms of TGF-β1 with marrow fibrosis in essential thrombocythemia and primary myelofibrosis

Ponce, C. C., Chauffaille, M. D. L. L. F., Ihara, S. S. M., & Silva, M. R. R. (2011) · Medical Oncology · doi:10.1007/s12032-011-0144-1 · Cited by 22

Extra-ovarian expression and activity of growth differentiation factor 9

Wang, Y., Nicholls, P. K., Stanton, P. G., Harrison, C. A., Sarraj, M. A., Gilchrist, R. B., Findlay, J. K., & Farnworth, P. G. (2009) · Journal of Endocrinology · doi:10.1677/joe-08-0563 · Cited by 22

Adaptive and Innate Transforming Growth Factor β Signaling Impact Herpes Simplex Virus 1 Latency and Reactivation

Allen, S. J., Mott, K. R., Wechsler, S. L., Flavell, R. A., Town, T., & Ghiasi, H. (2011) · Journal of Virology · doi:10.1128/jvi.00678-11 · Cited by 22

Molecular Regulation of Cushion Morphogenesis

Camenisch, T. D., Runyan, R. B., & Markwald, R. R. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-381332-9.00018-9 · Cited by 23

Smad2/3 Activation Regulates Smad1/5/8 Signaling via a Negative Feedback Loop to Inhibit 3T3-L1 Adipogenesis

Aykul, S., Maust, J., Thamilselvan, V., Floer, M., & Martı́nez-Hackert, E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22168472 · Cited by 24

Hopes and opportunities of stem cells from human exfoliated deciduous teeth (SHED) in cartilage tissue regeneration

Mahdavi-Jouibari, F., Parseh, B., Kazeminejad, E., & Khosravi, A. (2023) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2023.1021024 · Cited by 22

Induced pluripotent stem cell-derived hepatocytes as an alternative to human adult hepatocytes.

Hernandez, I., Baio, J. M., Tsay, E., Martinez, A. F., Fuentes, T. I., Bailey, L. L., Hasaniya, N. W. M. A., & Kearns‐Jonker, M. (2012) · PubMed Central · Cited by 22

Derivation and applications of human hepatocyte-like cells

Li, S., Huang, S., Zhao, Y., Ding, Y.-J., Ma, D., & Ding, Q. (2019) · World Journal of Stem Cells · doi:10.4252/wjsc.v11.i8.535 · Cited by 19

Two Modulators of Skeletal Development: BMPs and Proteoglycans

Koosha, E., & Eames, B. F. (2022) · Journal of Developmental Biology · doi:10.3390/jdb10020015 · Cited by 21

Form-deprivation myopia induces decreased expression of bone morphogenetic protein-2, 5 in guinea pig sclera.

Wang, Q., Xue, M., Zhao, G., Liu, M.-G., Ma, Y.-N., & Ma, Y. (2015) · Europe PMC (PubMed Central) · doi:10.3980/j.issn.2222-3959.2015.01.07 · Cited by 20

Reducing betaglycan expression by RNA interference (RNAi) attenuates inhibin bioactivity in LβT2 gonadotropes

Escalona, R. M., Stenvers, K. L., Farnworth, P. G., Findlay, J. K., & Ooi, G. T. (2009) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2009.03.021 · Cited by 20

Paracrine effect of TGF-β1 on downregulation of gap junctional intercellular communication between human dermal fibroblasts

Stuhlmann, D., Steinbrenner, H., Wendlandt, B., Mitić, D. M., Sies, H., & Brenneisen, P. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.05.004 · Cited by 20

Synthetic peptides cytomodulin-1 (CM-1) and cytomodulin-2 (CM-2) promote collagen synthesis and wound healing in vitro

Lam, H., Li, S., Lou, N., Chu, J. S. F., & BHATNAGAR, R. S. (2005) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/iembs.2004.1404389 · Cited by 20

Transforming Growth Factor‐β (TGF‐β) and Programmed Cell Death in the Vertebrate Retina

Dünker, N. (2005) · International review of cytology · doi:10.1016/s0074-7696(05)45002-0 · Cited by 20

Monocrotaline pyrrole induces Smad nuclear accumulation and altered signaling expression in human pulmonary arterial endothelial cells

Ramos, M. I., Lamé, M. W., Segall, H. J., & Wilson, D. W. (2007) · Vascular Pharmacology · doi:10.1016/j.vph.2007.01.005 · Cited by 20

Functional polymorphisms in asporin and CILP together with joint loading predispose to hand osteoarthritis

Taipale, M., Solovieva, S. A., Leino‐Arjas, P., & Männikkö, M. (2017) · BMC Genetics · doi:10.1186/s12863-017-0585-4 · Cited by 19

Cell autonomous requirement of endocardial Smad4 during atrioventricular cushion development in mouse embryos

Song, L., Zhao, M., Wu, B., Zhou, B., Wang, Q., & Jiao, K. (2010) · Developmental Dynamics · doi:10.1002/dvdy.22493 · Cited by 19

Impact of Genetic and Pharmacologic Inhibition of Myostatin in a Murine Model of Osteogenesis Imperfecta

Omosule, C. L., Gremminger, V. L., AGUILLARD, A., Jeong, Y., Harrelson, E. N., Miloscio, L., Mastaitis, J. W., Rafique, A., Kleiner, S., Pfeiffer, F. M., et al. (2020) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.4223 · Cited by 21

TGF-β Superfamily Receptors—Targets for Antiangiogenic Therapy?

Otten, J., Bokemeyer, C., & Fiedler, W. (2010) · Journal of Oncology · doi:10.1155/2010/317068 · Cited by 19

Towards New Therapies for Parkinson's Disease

Finkelstein, D. I. (2011) · InTech eBooks · doi:10.5772/954 · Cited by 19

Halofuginone Attenuates Osteoarthritis by Rescuing Bone Remodeling in Subchondral Bone Through Oral Gavage

Mu, W., Xu, B., Ma, H., Li, J., Ji, B., Zhang, Z., Amat, A., & Cao, L. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00269 · Cited by 19

A narrative review of the relationship between TGF-β signaling and gynecological malignant tumor

Luo, F., Huang, Y., Li, Y., Zhao, X., Xie, Y., Zhang, Q., Mei, J., & Liu, X. (2021) · Annals of Translational Medicine · doi:10.21037/atm-21-4879 · Cited by 18

Recombinant protein drugs-based intra articular drug delivery systems for osteoarthritis therapy

Huang, H., Lin, Y., Jiang, Y., Yao, Q., Chen, R., Zhao, Y., & Kou, L. (2022) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2022.12.012 · Cited by 18

From bench to bedside: The promise of sotatercept in hematologic disorders

Lan, Z., Lv, Z., Zuo, W., & Xiao, Y. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115239 · Cited by 18

A TALEN ‐based specific transcript knock‐down of PIWIL 2 suppresses cell growth in HepG2 tumor cell

Chen, Y., Hu, W., Lu, Y., Jiang, S., Li, C., Chen, J., Tao, D., Liu, Y., Yang, Y., & Ma, Y. (2014) · Cell Proliferation · doi:10.1111/cpr.12120 · Cited by 18

Organically vs conventionally-grown dark and white chia seeds (Salvia hispanica L.): fatty acid composition, antioxidant activity and techno-functional properties

Alvites-Misajel, K., García-Gutiérrez, M., Miranda-Rodríguez, C., & Ramos-Escudero, F. (2019) · Grasas y Aceites · doi:10.3989/gya.0462181 · Cited by 17

Molecular pathways in experimental glaucoma models

Bugara, K., Pacwa, A., & Smędowski, A. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1363170 · Cited by 17

Positive selection drives the evolution of endocrine regulatory bone morphogenetic protein system in mammals

Ahmad, H. I., Ahmad, M. J., Adeel, M. M., Asif, A. R., & Du, X. (2018) · Oncotarget · doi:10.18632/oncotarget.24240 · Cited by 17

A Process for the Design and Development of Novel Bone Morphogenetic Protein-7 (BMP-7) Mimetics With an Example: THR-184

Carlson, W. D., Keck, P. C., Bosukonda, D., & Carlson, F. R. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.864509 · Cited by 17

The conditioned medium from a stable human GDF3-expressing CHO cell line, induces the differentiation of PC12 cells

Li, Q., Liu, X.-H., Wu, Y., An, J., Hexige, S., Ling, Y., Zhang, M., Yang, X., & Yu, L. (2011) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-011-1005-0 · Cited by 17

Analysis of the mRNA expression of the TGF‐Beta family in testicular cells and localization of the splice variant TGF‐β2B in testis

Konrad, L., Lüers, G. H., Völck‐Badouin, E., Keilani, M. M., Laible, L., Aumüller, G., & Hofmann, R. W. (2006) · Molecular Reproduction and Development · doi:10.1002/mrd.20399 · Cited by 17

Molecular signaling in pathogenesis of craniosynostosis: the role of fibroblast growth factor and transforming growth factor–β

Chim, H., Manjila, S. V., Cohen, A. R., & Gosain, A. K. (2011) · Neurosurgical FOCUS · doi:10.3171/2011.5.focus1197 · Cited by 18

New Anti-Nodal Monoclonal Antibodies Targeting the Nodal Pre-Helix Loop Involved in Cripto-1 Binding

Focà, A., Sanguigno, L., Focà, G., Strizzi, L., Iannitti, R., Palumbo, R., Hendrix, M. J. C., Leonardi, A., Ruvo, M., & Sandomenico, A. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms160921342 · Cited by 17

Diagnostic and Therapeutic Roles of the “Omics” in Hypoxic–Ischemic Encephalopathy in Neonates

Rasineni, G. K., Panigrahy, N., Rath, S. N., Chinnaboina, M., Konanki, R., Chirla, D., & Madduri, S. (2022) · Bioengineering · doi:10.3390/bioengineering9100498 · Cited by 18

Activin Potentiates Proliferation in Mature Avian Auditory Sensory Epithelium

McCullar, J. S., Ty, S., Campbell, S., & Oesterle, E. C. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5154-09.2010 · Cited by 16

Generation of a conditional mutant allele for Tab1 in mouse

Inagaki, M., Komatsu, Y., Scott, G. J., Yamada, G., Ray, M. K., Ninomiya‐Tsuji, J., & Mishina, Y. M. (2008) · genesis · doi:10.1002/dvg.20418 · Cited by 16

Development of an in vitro potency assay for therapeutic TGFβ antagonists: The A549 cell bioassay

Rapoza, M. L., Fu, D., & Sendak, R. A. (2006) · Journal of Immunological Methods · doi:10.1016/j.jim.2006.07.009 · Cited by 16

Extracellular matrix viscoelasticity regulates TGFβ1‐induced epithelial‐mesenchymal transition and apoptosis via integrin linked kinase

Sacco, J. L., Vaneman, Z. T., & Gomez, E. W. (2023) · Journal of Cellular Physiology · doi:10.1002/jcp.31165 · Cited by 14

From in vivo to in vitro: exploring the key molecular and cellular aspects of human female gametogenesis

Coxir, S. A., Costa, G. M. J., dos Santos, C. F., Alvarenga, R. D. L. L. S., & Lacerda, S. M. D. S. N. (2023) · Human Cell · doi:10.1007/s13577-023-00921-7 · Cited by 15

Bypassing Heterogeneity: The Road to Embryonic Stem Cell-Derived Cardiomyocyte Specification

Singh, A. M., & Terada, N. (2007) · Trends in Cardiovascular Medicine · doi:10.1016/j.tcm.2007.02.003 · Cited by 15

Genetics of Congenital Heart Defects: A Candidate Gene Approach

Lagendijk, A. K., Smith, K., & Bakkers, J. (2010) · Trends in Cardiovascular Medicine · doi:10.1016/j.tcm.2010.10.003 · Cited by 15

Pdgfrb is a direct regulatory target of TGFβ signaling in atrioventricular cushion mesenchymal cells

Peng, Y., Yan, S., Chen, D., Cui, X., & Jiao, K. (2017) · PLoS ONE · doi:10.1371/journal.pone.0175791 · Cited by 15

Inhibition of activin-like kinase 4/5 attenuates cancer cachexia associated muscle wasting

Levolger, S., Wiemer, E. A. C., van Vugt, J. L. A., Huisman, S. A., van Vledder, M. G., den Engel, S. V. D.-V., Ambagtsheer, G., IJzermans, J. N. M., & de Bruin, R. W. F. (2019) · Scientific Reports · doi:10.1038/s41598-019-46178-9 · Cited by 15

Transforming growth factor beta mediates apoptosis in the ganglion cell layer during all programmed cell death periods of the developing murine retina

Beier, M., Franke, A. G., Paunel‐Görgülü, A., Scheerer, N., & Dünker, N. (2006) · Neuroscience Research · doi:10.1016/j.neures.2006.07.002 · Cited by 15

Generation of hepatocyte-like cells from human induced pluripotent stem (iPS) cells by co-culturing embryoid body cells with liver non-parenchymal cell line TWNT-1.

Javed, M. S., Yaqoob, N., Iwamuro, M., Kobayashi, N., & Fujiwara, T. (2014) · PubMed · Cited by 14

Let-7b promotes alpaca hair growth via transcriptional repression of TGFβR I

Yan, S., Yu, Z., Liu, N., Wang, H., Jian-Shan, X., Gao, S., Cheng, J., Yu, X., Ting, W., Dong, C., et al. (2015) · Gene · doi:10.1016/j.gene.2015.11.022 · Cited by 14

The Role of Bone Morphogenetic Protein Receptor Type 2 (BMPR2) and the Prospects of Utilizing Induced Pluripotent Stem Cells (iPSCs) in Pulmonary Arterial Hypertension Disease Modeling

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Activin A in Nonalcoholic Fatty Liver Disease

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Theoretical and Clinical Considerations for Autologous Blood Preparations: Platelet‐Rich Plasma, Fibrin Sealants, and Plasma‐Rich Growth Factors

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Cell-based assays for kinase drug discovery

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BMP-7/TGF-β1 signalling in myoblasts: Components involved in signalling and BMP-7-dependent blockage of TGF-β-mediated CTGF expression

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Recent progress in pancreatic islet cell therapy

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Metastasis of Colorectal Cancer

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Regulation of Skeletogenic Pathways by m6A RNA Modification: A Comprehensive Review

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Population Based Model of Human Embryonic Stem Cell (hESC) Differentiation during Endoderm Induction

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Expression of TGFBR1, TGFBR2, TGFBR3, ACVR1B and ACVR2B is altered in ovaries of cows with cystic ovarian disease

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Optimizing Generation of Stem Cell-Derived Islet Cells

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Role of TGF-β Signaling in Neurogenic Regions After Brain Injury

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Obesity attenuates the effect of sleep apnea on active TGF-ß1 levels and tumor aggressiveness in patients with melanoma

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The modulation of apoptosis by cyclic AMP involves Akt and epidermal growth factor receptor

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Loss of inhibition over master pathways of bone mass regulation results in osteosclerotic bone metastases in prostate cancer

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New insights into the regulation of TGF‐β/Smad and MPK signaling pathway gene expressions by nasal allergen and methacholine challenge test in asthma

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TGF-β signaling in the ovary: Emerging roles in development and disease

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Bone morphogenic protein-2 regulates the myogenic differentiation of PMVECs in CBDL rat serum-induced pulmonary microvascular remodeling

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Transforming Growth Factor-β Receptors and Signal Transduction

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Receptor–Ligand Recognition in the TGFβ Family as Suggested by the Crystal Structures of BMP-2–BR-IAec and TGFβ3–TR-IIec

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