Signal transduction of bone morphogenetic protein receptors

TGF-β SIGNAL TRANSDUCTION

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Bone: Formation by Autoinduction

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

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Direct binding of Smad3 and Smad4 to critical TGFβ‐inducible elements in the promoter of human plasminogen activator inhibitor‐type 1 gene

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Identification of a Member of the MAPKKK Family as a Potential Mediator of TGF-β Signal Transduction

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The MAD-Related Protein Smad7 Associates with the TGFβ Receptor and Functions as an Antagonist of TGFβ Signaling

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TGF‐β receptor‐mediated signalling through Smad2, Smad3 and Smad4

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Smad6 inhibits signalling by the TGF-β superfamily

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Cardiac pathologies in relation to Smad-dependent pathways

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Enamel matrix proteins exhibit growth factor activity: A review of evidence at the cellular and molecular levels

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MODELLING VASCULAR MORPHOGENESIS: CURRENT VIEWS ON BLOOD VESSELS DEVELOPMENT

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Constitutive activation of BMP signalling abrogates experimental metastasis of OVCA429 cells via reduced cell adhesion

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The detrimental effects of glucocorticoids exposure during pregnancy on offspring’s cardiac functions mediated by hypermethylation of bone morphogenetic protein-4

Peng, J., Zhou, Y., Zhang, Z., Wang, Z., Gao, L.-T., Zhang, X., Zhou, F., Li, G., Chen, H., Yang, H., et al. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-0841-1 · Cited by 24

HGF/SF up-regulates the expression of bone morphogenetic protein 7 in prostate cancer cells

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BMP Signaling in Osteogenesis, Bone Remodeling and Repair

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Differential regulation of translation and endocytosis of alternatively spliced forms of the type II bone morphogenetic protein (BMP) receptor

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Failure of Tooth Formation Mediated by miR-135a Overexpression via BMP Signaling

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miR-98 is involved in missed abortion by targeting GDF6 and FAPP2

Zhu, Q., Dong, Y., Zhang, L., Ma, X., & Xia, H. (2020) · Reproduction · doi:10.1530/rep-19-0282 · Cited by 21

Activation of the BMP Canonical Signaling Pathway in Human Optic Nerve Head Tissue and Isolated Optic Nerve Head Astrocytes and Lamina Cribrosa Cells

Zode, G. S., Clark, A. F., & Wordinger, R. J. (2007) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.07-0127 · Cited by 21

Spinally upregulated noggin suppresses axonal and dendritic plasticity following dorsal rhizotomy

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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

Sword Bean (Canavalia gladiata) Pods Induce Differentiation in MC3T3-E1 Osteoblast Cells by Activating the BMP2/SMAD/RUNX2 Pathway

Hwang, Y. J., Hwang, H.-J., Go, H., Park, N., & Hwang, K. (2023) · Nutrients · doi:10.3390/nu15204372 · Cited by 20

Altered plasma membrane dynamics of bone morphogenetic protein receptor type Ia in a low bone mass mouse model

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Trapping of BMP receptors in distinct membrane domains inhibits their function in pulmonary arterial hypertension

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Bone morphogenetic protein receptor type Ia localization causes increased BMP2 signaling in mice exhibiting increased peak bone mass phenotype

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Compartmentalization of bone morphogenetic proteins and their antagonists in lymphoid progenitors and supporting microenvironments and functional implications

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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

The SIRT1 activator SRT2104 promotes BMP9-induced osteogenic and angiogenic differentiation in mesenchymal stem cells

Lu, Y., Ma, Z., Deng, R., Jiang, H., Chu, L., & Deng, Z.-L. (2022) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2022.111724 · Cited by 19

Sambucus Williamsii Hance Promotes MC3T3‐E1 Cells Proliferation and Differentiation via BMP‐2/Smad/p38/JNK/Runx2 Signaling Pathway

Yang, B., Lin, X., Yang, C., Tan, J., Li, W., & Kuang, H. (2015) · Phytotherapy Research · doi:10.1002/ptr.5482 · Cited by 19

Osteoblastogenic activity of ark shell protein hydrolysates with low molecular weight in mouse mesenchymal stem cells

Hyung, J.-H., Ahn, C., & Je, J. (2016) · RSC Advances · doi:10.1039/c6ra00898d · Cited by 19

CpG-Oligodeoxynucleotide Inhibits Smad-Dependent Bone Morphogenetic Protein Signaling: Effects on Myeloma Cell Apoptosis and In Vitro Osteoblastogenesis

Nørgaard, N. N., Holien, T., Jönsson, S., Hella, H., Espevik, T., Sundan, A., & Standal, T. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903605 · Cited by 19

Repulsive guidance molecule B inhibits metastasis and is associated with decreased mortality in non-small cell lung cancer

Li, J., Ye, L., Shi, X., Chen, J., Feng, F., Chen, Y., Xiao, Y., Shen, J., Li, P., Jiang, W. G., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.7463 · Cited by 19

Cellular response to bioactive ceramics

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The Pathogenic Effects of Fusobacterium nucleatum on the Proliferation, Osteogenic Differentiation, and Transcriptome of Osteoblasts

Gao, H., Sun, T., Yang, F., Yuan, J., Yang, M., Kang, W., Tang, D., Zhang, J., & Feng, Q. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00807 · Cited by 18

Oligodendrocytes Development and Wnt Signaling Pathway

Soomro, S. H., Jie, J., & Fu, H. Q. (2018) · International Journal of Human Anatomy · doi:10.14302/issn.2577-2279.ijha-18-2407 · Cited by 19

Recombinant Bone Morphogenetic Protein-2 (rhBMP-2) in High-Risk Foot and Ankle Surgery

Bibbo, C., & Haskell, M. D. (2007) · Techniques in Foot & Ankle Surgery · doi:10.1097/btf.0b013e33180620e9c · Cited by 18

Intracrine Signaling Mechanisms of Activin A and TGF-β

Gressner, O. A. (2011) · Vitamins and hormones · doi:10.1016/b978-0-12-385961-7.00004-4 · Cited by 17

BMPR2-pSMAD1/5 signaling pathway regulates RUNX2 expression and impacts the progression of dedifferentiated chondrosarcoma.

Yang, K., Tang, X., Guo, W., Xu, X., Ren, T., Ren, C.-M., Wang, S., Bao, X., Zhang, F., & Sun, K. (2016) · PubMed Central · 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

Mechanism of CK2.3, a Novel Mimetic Peptide of Bone Morphogenetic Protein Receptor Type IA, Mediated Osteogenesis

Vrathasha, V., Weidner, H., & Nohe, A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20102500 · Cited by 18

The Effects of Transforming Growth Factor-β2 on the Expression of Follistatin and Activin A in Normal and Glaucomatous Human Trabecular Meshwork Cells and Tissues

Fitzgerald, A. M., Benz, C. L., Clark, A. F., & Wordinger, R. J. (2012) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.12-10292 · Cited by 17

Bone Morphogenic Protein: An Elixir for Bone Grafting—A Review

Shah, P., Keppler, L., & Rutkowski, J. L. (2011) · Journal of Oral Implantology · doi:10.1563/aaid-joi-d-10-00196 · Cited by 17

The expression and potential function of bone morphogenetic proteins 2 and 4 in bovine trophectoderm

Pennington, K. A., & Ealy, A. D. (2012) · Reproductive Biology and Endocrinology · doi:10.1186/1477-7827-10-12 · Cited by 17

Regeneration of hair and other skin appendages: A microenvironment‐centric view

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Detection of mRNA Expression and Copy Number Variations Within the Goat FecB Gene Associated With Litter Size

Bi, Y., Feng, W., Kang, Y., Wang, K., Yang, Y., Qu, L., Chen, H., Lan, X., & Pan, C. (2021) · Frontiers in Veterinary Science · doi:10.3389/fvets.2021.758705 · Cited by 16

Bone formation by heterodimers through non-viral gene delivery of BMP-2/6 and BMP-2/7

Loozen, L. D., Vandersteen, A., Kragten, A. H. M., Öner, F. C., Dhert, W. J. A., Kruyt, M. C., & Alblas, J. (2018) · European Cells and Materials · doi:10.22203/ecm.v035a14 · Cited by 16

A BMP4-p38 MAPK signaling axis controls ISL1 protein stability and activity during cardiogenesis

Jing, Y., Ren, Y., Witzel, H. R., & Dobreva, G. D. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.06.017 · Cited by 16

Targeting bone morphogenetic protein signaling on renal and vascular diseases

Maciel, T. T., Kempf, H., & Campos, A. H. (2009) · Current Opinion in Nephrology & Hypertension · doi:10.1097/mnh.0b013e328332fc13 · Cited by 16

Visualizing Smad1/4 signaling response to bone morphogenetic Protein-4 activation by FRET biosensors

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Differential molecular regulation of processing and membrane expression of Type-I BMP receptors: implications for signaling

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Dynamic expression and regulatory mechanism of TGF-β signaling in chicken embryonic stem cells differentiating into spermatogonial stem cells

Zuo, Q., Jin, K., Zhang, Y., Song, J., & Li, B. (2017) · Bioscience Reports · doi:10.1042/bsr20170179 · Cited by 16

The Combination of icariin and constrained dynamic loading stimulation attenuates bone loss in ovariectomy‐induced osteoporotic mice

Wang, Q., Wang, G., Lu, Y., Cui, Y., Li, H., Li, R., Zhang, X., Zhang, C., & Liu, T. (2017) · Journal of Orthopaedic Research® · doi:10.1002/jor.23777 · Cited by 16

Modulation of granulosa cell function via CRISPR-Cas fuelled editing of BMPR-IB gene in goats (Capra hircus)

Kumar, S., Punetha, M., Jose, B., Bharati, J., Khanna, S., Sonwane, A., Green, J. A., Whitworth, K. M., & Sarkar, M. (2020) · Scientific Reports · doi:10.1038/s41598-020-77596-9 · Cited by 16

The Molecular Genetics and Cellular Mechanisms Underlying Pulmonary Arterial Hypertension

Machado, R. D. (2012) · Scientifica · doi:10.6064/2012/106576 · Cited by 15

Expression and functional role of Bone Morphogenetic Proteins (BMPs) in cyclical corpus luteum in buffalo ( Bubalus bubalis )

Rajesh, G., Paul, A., Mishra, S., Bharati, J., Thakur, N., Mondal, T., Soren, S., Harikumar, S. K., Narayanan, K., Chouhan, V. S., et al. (2016) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2016.10.016 · Cited by 15

Bone morphogenetic protein-7 and interferon-alpha synergistically suppress hepatitis C virus replicon

Sakamoto, N., Yoshimura, M., Kimura, T., Toyama, K., Sekine‐Osajima, Y., Watanabe, M., & Muramatsu, M. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.03.167 · Cited by 15

Physiologie du tissu osseux

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BMP signaling balances murine myeloid potential through SMAD-independent p38MAPK and NOTCH pathways

Cook, B. D., & Evans, T. (2014) · Blood · doi:10.1182/blood-2014-02-556993 · Cited by 15

Efficient retina formation requires suppression of both Activin and BMP signaling pathways in pluripotent cells

Wong, K. A., Trembley, M. A., Wahab, S. A., & Viczian, A. S. (2015) · Biology Open · doi:10.1242/bio.20149977 · Cited by 15

Role of Recombinant Human Bone Morphogenetic Protein-2 on Hindfoot Arthrodesis

Hreha, J., Krell, E. S., & Bibbo, C. (2016) · Foot and Ankle Clinics · doi:10.1016/j.fcl.2016.07.001 · Cited by 15

BMP modulators regulate the function of BMP during body patterning and disease progression

Yanagita, M. (2009) · BioFactors · doi:10.1002/biof.15 · Cited by 14

The pro-form of BMP-2 exhibits a delayed and reduced activity when compared to mature BMP-2

von Einem, S., Erler, S., Bigl, K., Frerich, B., & Schwarz, E. (2011) · Growth Factors · doi:10.3109/08977194.2011.561798 · Cited by 14

Role of bone morphogenetic proteins in adrenal physiology and disease

Johnsen, I. K., & Beuschlein, F. (2010) · Journal of Molecular Endocrinology · doi:10.1677/jme-10-0001 · Cited by 14

Gene Expression Profiling of Cells Involved in Periodontal Regeneration

Ivanovski, S., Lichanska, A. M., D’Aniello, E., Xiao, Y., & Waters, M. J. (2007) · Tissue Engineering · doi:10.1089/ten.2006.0082 · Cited by 14

Shedding of a soluble form of BMP receptor-IB controls bone cell responses to BMP

Singhatanadgit, W., Salih, V. M., & Olsen, I. (2006) · Bone · doi:10.1016/j.bone.2006.04.030 · Cited by 14

Brorin is required for neurogenesis, gliogenesis, and commissural axon guidance in the zebrafish forebrain

Miyake, A., Mekata, Y., Fujibayashi, H., Nakanishi, K., Konishi, M., & Itoh, N. (2017) · PLoS ONE · doi:10.1371/journal.pone.0176036 · Cited by 13

(+)-Cholesten-3-one induces differentiation of neural stem cells into dopaminergic neurons through BMP signaling

Chen, D., Meng, L.-J., Du, S.-H., Zhang, H., Li, H., Zhou, J.-H., Li, Y., Zeng, H., & Hua, Z. (2010) · Neuroscience Research · doi:10.1016/j.neures.2010.07.2043 · Cited by 13

Dysregulated Inflammatory Signaling upon Charcot-Marie-Tooth Type 1C Mutation of SIMPLE Protein

Li, W., Zhu, H., Zhao, X., Brancho, D., Liang, Y., Zou, Y., Bennett, C. L., & Chow, C.-W. (2015) · Molecular and Cellular Biology · doi:10.1128/mcb.00300-15 · Cited by 13

mRNA Expression of Bone Morphogenetic Proteins and Their Receptors in Human Renal Cell Carcinoma

Markić, D., Ćelić, T., Gršković, A., Španjol, J., Fučkar, Ž., Grahovac, B., Đorđević, G., & Bobinac, D. (2011) · Urologia Internationalis · doi:10.1159/000330797 · Cited by 13

Human Embryonic Stem Cell Technology: Large Scale Cell Amplification and Differentiation

Oh, S. K. W., & Choo, A. B. H. (2006) · Cytotechnology · doi:10.1007/s10616-005-3862-4 · Cited by 13

BMP signaling dynamics in embryonic orofacial tissue

Mukhopadhyay, P., Webb, C. L., Warner, D. R., Greene, R. M., & Pisano, M. (2008) · Journal of Cellular Physiology · doi:10.1002/jcp.21455 · Cited by 13

Identification of a functional variant for colorectal cancer risk mapping to chromosome 5q31.1

Ke, J., Lou, J., Chen, X., Li, J., Liu, C., Gong, Y., Yang, Y., Zhu, Y., Zhang, Y., Tian, J., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.9298 · Cited by 12

Expression of Human Hemojuvelin (HJV) Is Tightly Regulated by Two Upstream Open Reading Frames in HJV mRNA That Respond to Iron Overload in Hepatic Cells

Onofre, C., Tomé, F., Barbosa, C., Silva, A. L., & Romão, L. (2015) · Molecular and Cellular Biology · doi:10.1128/mcb.01462-14 · Cited by 12

Probing Embryonic Development Enables the Discovery of Unique Small-Molecule Bone Morphogenetic Protein Potentiators

Wesseler, F., Riege, D., Puthanveedu, M., Halver, J., Müller, E., Bertrand, J., Antonchick, A. P., Sievers, S., Waldmann, H., & Schade, D. (2022) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.1c01800 · Cited by 12

Phenotypic Discovery of Triazolo[1,5-c]quinazolines as a First-In-Class Bone Morphogenetic Protein Amplifier Chemotype

Wesseler, F., Lohmann, S., Riege, D., Halver, J., Roth, A., Pichlo, C., Weber, S., Takamiya, M., Müller, E., Ketzel, J., et al. (2022) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.2c01199 · Cited by 12

Bone Morphogenetic Protein-2 Conjugated to Quantum Dot®s is Biologically Functional

Halloran, D. R., Vrathasha, V., Durbano, H. W., & Nohe, A. (2020) · Nanomaterials · doi:10.3390/nano10061208 · Cited by 12

NRAGE: A potential rheostat during branching morphogenesis

Nikopoulos, G. N., Martins, J. F., Adams, T. L., Karaczyn, A. A., Adams, D. C., Vary, C., Oxburgh, L. H., & Verdi, J. M. (2009) · Mechanisms of Development · doi:10.1016/j.mod.2009.02.005 · Cited by 12

Molecular cloning, expression and characterization of the zebrafish bram1 gene, a BMP receptor-associated molecule

Wu, K.-M., Huang, C., Hwang, S. L., & Chang, Y. (2006) · Journal of Biomedical Science · doi:10.1007/s11373-005-9066-2 · Cited by 12

HIV and Bone Disease: A Perspective of the Role of microRNAs in Bone Biology upon HIV Infection

Carpio‐Cano, F. E. D., Cadena, R. A. D., & Sawaya, B. E. (2013) · Journal of Osteoporosis · doi:10.1155/2013/571418 · Cited by 11

Alcohol Exposure Causes Overexpression of Heart Development‐Related Genes by Affecting the Histone H3 Acetylation via BMP Signaling Pathway in Cardiomyoblast Cells

Shi, J. P., Zhao, W., Pan, B., Zheng, M., Si, L., Zhu, J., Liu, L., & Tian, J. (2016) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.13273 · Cited by 11

Tectorigenin Promotes Osteoblast Differentiation and in vivo Bone Healing, but Suppresses Osteoclast Differentiation and in vivo Bone Resorption.

Lee, S.-Y., Kim, G.-T., Yun, H., Kim, Y.-C., Kwon, I.-K., & Kim, E. (2018) · Europe PMC (PubMed Central) · doi:10.14348/molcells.2018.0056 · Cited by 11

Immunoexpression of bone morphogenetic protein-2 (BMP-2), BMP receptor type IA, and BMP receptor type II in metastatic and non-metastatic lower lip squamous cell carcinoma

de Carvalho, C. H. P., Nonaka, C. F. W., de Araújo, C. R. F., de Souza, L. B., & Pinto, L. P. (2010) · Journal of Oral Pathology and Medicine · doi:10.1111/j.1600-0714.2010.00974.x · Cited by 11

Binding of integrin α1 to bone morphogenetic protein receptor IA suggests a novel role of integrin α1β1 in bone morphogenetic protein 2 signalling

Zu, Y., Liang, X., Du, J., Zhou, S., & Yang, C. (2015) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2015.09.027 · Cited by 11

Bone morphogenetic protein signaling in vertebrate motor neurons and neuromuscular communication

Osses, N., & Henríquez, J. P. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00453 · Cited by 11

Transcriptome of pancreas-specificBmpr1a-deleted islets links to TPH1–5-HT axis

Jiang, F., Mishina, Y. M., Baten, A., Morahan, G., & Harrison, L. C. (2015) · Biology Open · doi:10.1242/bio.011858 · Cited by 11

9-Demethoxy-medicarpin promotes peak bone mass achievement and has bone conserving effect in ovariectomized mice: Positively regulates osteoblast functions and suppresses osteoclastogenesis

Goel, A., Raghuvanshi, A., Kumar, A., Gautam, A. K., Srivastava, K., Kureel, J., & Singh, D. R. (2015) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2015.04.023 · Cited by 11

Regulation of crucial lnc RNA s in differentiation of chicken embryonic stem cells to spermatogonia stem cells

Li, D., Ji, Y., Wang, F., Wang, Y., Wang, M., Zhang, C., Zhang, W., Lu, Z., Sun, C., Ahmed, M. F. E. M., et al. (2016) · Animal Genetics · doi:10.1111/age.12510 · Cited by 10

Endothelin-1 alters BMP signaling to promote proliferation of pulmonary artery smooth muscle cells

Maruyama, H., Sakai, S., & Ieda, M. (2022) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2022-0104 · Cited by 10

Bone morphogenetic proteins mediate crosstalk between cancer cells and the tumour microenvironment at primary tumours and metastases (Review)

Sun, Z., Cai, S., Zabkiewicz, C., Liu, C., & Ye, L. (2020) · International Journal of Oncology · doi:10.3892/ijo.2020.5030 · Cited by 10

Homocysteine upregulates hepcidin expression through BMP6/SMAD signaling pathway in hepatocytes

Luo, X., Luo, Z., Zhang, Z., Yang, H., Lai, B., Yao, Q., Xiao, L., & Wang, N. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.02.001 · Cited by 10

Effects of constrained dynamic loading, CKIP‑1 gene knockout and combination stimulations on bone loss caused by mechanical unloading

Han, B., Wei, S., Zhang, X., Li, H., Li, Y., Li, R., Li, K., & Zhang, X. (2018) · Molecular Medicine Reports · doi:10.3892/mmr.2018.9222 · Cited by 10

Neurogenesin-1 differentially inhibits the osteoblastic differentiation by bone morphogenetic proteins in C2C12 cells

Chandra, A., Itakura, T., Yang, Z. G., Tamakoshi, T., Xue, X., Wang, B., Ueki, T., Sato, K., Uezato, T., & Miura, N. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.03.195 · Cited by 10

Comparison of osteogenic potentials of human rat BMP4 and BMP6 gene therapy using [E1-] and [E1-,E2b-] adenoviral vectors

Li, H., Li, J. Z., Pittman, D. D., Amalfitano, A., Hankins, G. R., & Helm, G. A. (2006) · International Journal of Medical Sciences · doi:10.7150/ijms.3.97 · Cited by 10

Human pluripotent embryonal carcinoma NTERA2 cl.D1 cells maintain their typical morphology in an angiomyogenic medium

Simões, P. D., & Ramos, T. L. (2007) · Journal of Negative Results in BioMedicine · doi:10.1186/1477-5751-6-5 · Cited by 9

Genetic aspects of ameloblastoma: a brief review

Stolf, D., Karim, A. C., & Banerjee, A. G. (2007) · Biotechnology and Molecular Biology Reviews · doi:10.5897/bmbr2007.0012 · Cited by 9

Sulfation is required for bone morphogenetic protein 2-dependent Id1 induction

Osses, N., Gutiérrez, J., López‐Rovira, T., Ventura, F., & Brandan, E. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.04.029 · Cited by 9

Overexpression of constitutively active BMP-receptor-IB in mouse skin causes an ichthyosis-vulgaris-like disease

Yu, X., Espinoza‐Lewis, R. A., Sun, C., Lin, L., He, F., Xiong, W., Yang, J., Wang, A., & Chen, Y. (2010) · Cell and Tissue Research · doi:10.1007/s00441-010-1077-2 · Cited by 9

GDF‐9 promotes the growth of prostate cancer cells by protecting them from apoptosis

Bokobza, S., Ye, L., Kynaston, H., & Jiang, W. G. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22235 · Cited by 9

Osteoblastic differentiation and cell calcification of adamantinomatous craniopharyngioma induced by bone morphogenetic protein-2

Yan, X., Kang, D., Pan, J., Jiang, C., Lin, Y., & Qi, S. (2016) · Cancer Biomarkers · doi:10.3233/cbm-161576 · Cited by 9

A bone morphogenetic protein regulates the shell formation of Crassostrea gigas under ocean acidification

Gao, Y., Liu, Z., Zhu, T., Xin, X., Jin, Y., Wang, L., Liu, C., & Song, L. (2023) · Gene · doi:10.1016/j.gene.2023.147687 · Cited by 8

Ecotoxicological risk assessment of the novel psychoactive substance Esketamine: Emphasis on fish skeletal, behavioral, and vascular development

Zhang, Q., Wu, T., Luo, C., Xie, H., Wang, D., Peng, J., Wu, K., & Huang, W. (2024) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2024.135823 · Cited by 8

Loss of expression of growth differentiation factor-9 (GDF9) in human kidney cancer and regulation of growth and migration of kidney cancer cells by GDF9.

Du, P., Ye, L., Li, H., Ruge, F., Yang, Y., & Jiang, W. G. (2012) · PubMed · Cited by 8

Structural basis of BMP‐2 and BMP‐7 interactions with antagonists Gremlin‐1 and Noggin in Glioblastoma tumors

Choudhuri, K. S. R., & Mishra, S. (2020) · Journal of Computational Chemistry · doi:10.1002/jcc.26407 · Cited by 8

Generating Mature β-Cells From Embryonic Stem Cells

Tsaniras, S. C. (2011) · Vitamins and hormones · doi:10.1016/b978-0-12-386015-6.00025-1 · Cited by 8

Local immunomodulation with CD4 and CD8 antibodies, but not cyclosporine A, improves osteogenesis induced by ADhBMP9 gene therapy

Li, J. Z., Li, H., Hankins, G. R., Dunford, B., & Helm, G. A. (2005) · Gene Therapy · doi:10.1038/sj.gt.3302502 · Cited by 8

Sevuparin strongly reduces hepcidin expression in cells, mice, and healthy human volunteers

Asperti, M., Denardo, A., Gryzik, M., Persson, K. E. M., Westerberg, G., Öhd, J., & Poli, M. (2024) · HemaSphere · doi:10.1002/hem3.70035 · Cited by 7

Growth differentiation factor-9 expression is inversely correlated with an aggressive behaviour in human bladder cancer cells

Jiang, W. (2011) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2011.858 · Cited by 7

The effect of adenovirus-mediated siRNA targeting BMPR-II on UHMWPE-induced osteoclast formation

Wang, Y., Wu, N., Mu, Y.-Q., Zhang, R., Hu, M., Li, R., Chen, L., He, B., & Deng, Z. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2012.09.059 · Cited by 7

Cross‐talk between the bone morphogenetic protein pathway and other major signaling pathways results in tightly regulated cell‐specific outcomes

Herpin, A., & Cunningham, C. (2007) · FEBS Journal · doi:10.1111/j.1742-4658.2007.05840.x · Cited by 104

Controlling of bone morphogenetic protein signaling

Zeng, S., Chen, J., & Shen, H. (2010) · Cellular Signalling · doi:10.1016/j.cellsig.2009.12.007 · Cited by 35

Bone morphogenetic proteins and signal transduction pathways

Lu, D. (2013) · International journal of pediatrics · doi:10.3760/cma.j.issn.1673-4408.2013.06.005

Signaling cross-talk by bone morphogenetic proteins

Ghosh‐Choudhury, N., & Ghosh-Choudhury, G. (2008) · Birkhäuser Basel eBooks · doi:10.1007/978-3-7643-8552-1_9

Bone morphogenetic protein receptor signal transduction in human disease

Gomez‐Puerto, M. C., Iyengar, P. V., de Vinuesa, A. G., ten Dijke, P., & Sánchez‐Duffhues, G. (2018) · The Journal of Pathology · doi:10.1002/path.5170 · Cited by 239