Cited by 1,534Cellular Mechanics and InteractionsCell Adhesion Molecules ResearchBone and Dental Protein Studies

The DOI matches its Crossref record; 179 of the 182 references it cites were found in a registry or an index.

Extracellular matrix assembly: a multiscale deconstruction

Open access

Mouw, Janna K., Ou, Guanqing, Weaver, Valerie M.·2014·Nature Reviews Molecular Cell Biology

Open this paper in CoChat — free account

Abstract

The biochemical and biophysical properties of the extracellular matrix (ECM) dictate tissue-specific cell behaviour. The molecules that are associated with the ECM of each tissue, including collagens, proteoglycans, laminins and fibronectin, and the manner in which they are assembled determine the structure and the organization of the resultant ECM. The product is a specific ECM signature that is comprised of unique compositional and topographical features that both reflect and facilitate the functional requirements of the tissue.

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

Crossref · 10.1038/nrm3902

Cites

179 of 179 references verified0 citation errors · 0 not checkable

Statistics

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Epigenetic Regulations of GABAergic Neurotransmission: Relevance for Neurological Disorders and Epigenetic Therapy
Shrestha, S., & Offer, S. M. (2016) · Medical Epigenetics · doi:10.1159/000444713 · Cited by 8,951
Molecular Mechanisms of Stress-Responsive Changes in Collagen and Elastin Networks in Skin
Aziz, J., Shezali, H., Radzi, Z., Yahya, N. A., Abu Kassim, N. H., Czernuszka, J., & Rahman, M. T. (2016) · Skin Pharmacology and Physiology · doi:10.1159/000447017 · Cited by 7,323
Remodelling the extracellular matrix in development and disease
Bonnans, C., Chou, J., & Werb, Z. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3904 · Cited by 4,367
Essentials of glycobiology
Wiederschain, G. Y. (2009) · Biochemistry (Moscow) · doi:10.1134/s0006297909090156 · Cited by 4,089
Collagen Structure and Stability
Shoulders, M. D., & Raines, R. T. (2009) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.77.032207.120833 · Cited by 3,923
Matrix metalloproteinases and the regulation of tissue remodelling
Page-McCaw, A., Ewald, A. J., & Werb, Z. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2125 · Cited by 2,630
Essentials of Glycobiology
Varki, A. P., Cummings, R. D., Esko, J. D., Freeze, H. H., Stanley, P., Bertozzi, C. R., Hart, G. W., & Etzler, M. E. (1999) · Cited by 2,384
Matrix metalloproteinases and other matrix proteinases in relation to cariology: the era of dentin degradomics
Tjäderhane, L., Buzalaf, M. A. R., Carrilho, M., & Chaussain, C. (2015) · Caries Research · doi:10.1159/000363582 · Cited by 2,306
The Collagen Family
Ricard-Blum, S. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a004978 · Cited by 2,305
Extracellular Matrix Degradation and Remodeling in Development and Disease
Lu, P., Takai, K., Weaver, V. M., & Werb, Z. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005058 · Cited by 2,265
Self-citation

Flagged first, then by citations

Show all 182 references

3 of the 182 references couldn’t be matched to a known paper.

Research works printed but not linked: 1

Hulmes, D. J. S. in Collagen Struct. Mech. (ed. Fratzl, P.) 15–47 (Springer, 2008). This is a comprehensive review of intracellular and extracellular collagen biosynthesis and collagen fibril assembly.

Sorted by citations

Items 401–500 of 1,000

EPB41L5 controls podocyte extracellular matrix assembly by adhesome-dependent force transmission
Maier, J. I., Rogg, M., Helmstädter, M., Sammarco, A., Schilling, O., Sabass, B., Miner, J. H., Dengjel, J., Walz, G., Werner, M., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108883 · Cited by 40
Genomic Hippo Pathway Alterations and Persistent YAP/TAZ Activation: New Hallmarks in Head and Neck Cancer
Faraji, F., Ramirez, S. I., Quiroz, P. Y. A., Mendez-Molina, A. N., & Gutkind, J. S. (2022) · Cells · doi:10.3390/cells11081370 · Cited by 41
New Insights into ADAMTS Metalloproteases in the Central Nervous System
Mohamedi, Y., Fontanil, T., Cobo, T., Cal, S., & Obaya, Á. J. (2020) · Biomolecules · doi:10.3390/biom10030403 · Cited by 43
Temperature-dependent properties of fat in adipose tissue from pork, beef and lamb. Part 2: rheology and texture
Wijarnprecha, K., Fuhrmann, P. L., Gregson, C. M., Sillick, M., Sonwai, S., & Rousseau, D. (2022) · Food & Function · doi:10.1039/d2fo00582d · Cited by 39
Biochemical and biomechanical properties of the pacemaking sinoatrial node extracellular matrix are distinct from contractile left ventricular matrix
Gluck, J. M., Herren, A. W., Yechikov, S., Kao, H. K. J., Khan, A., Phinney, B. S., Chiamvimonvat, N., Chan, J. W., & Lieu, D. K. (2017) · PLoS ONE · doi:10.1371/journal.pone.0185125 · Cited by 39
DDR1 and MT1-MMP Expression Levels Are Determinant for Triggering BIK-Mediated Apoptosis by 3D Type I Collagen Matrix in Invasive Basal-Like Breast Carcinoma Cells
Saby, C., Collin, G., Sinane, M., Buache, É., Gulick, L. V., Saltel, F., Maquoi, E., & Morjani, H. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00462 · Cited by 39
Matrix decoded – A pancreatic extracellular matrix with organ specific cues guiding human iPSC differentiation
Berger, C., Bjørlykke, Y., Hahn, L., Mühlemann, M., Kreß, S., Walles, H., Luxenhofer, R., Ræder, H., Metzger, M., & Zdzieblo, D. (2020) · Biomaterials · doi:10.1016/j.biomaterials.2020.119766 · Cited by 42
Biomaterial Stiffness Guides Cross-talk between Chondrocytes: Implications for a Novel Cellular Response in Cartilage Tissue Engineering
Cai, L., Liu, W., Cui, Y., Liu, Y., Du, W., Zheng, L., Pi, C., Zhang, D., Xie, J., & Zhou, X. (2020) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.0c00367 · Cited by 39
Supramolecular assembly of protein building blocks: from folding to function
Kim, N. H., Choi, H., Shahzad, Z. M., Ki, H., Lee, J., Chae, H., & Kim, Y. H. (2022) · Nano Convergence · doi:10.1186/s40580-021-00294-3 · Cited by 42
Characterizing viscoelastic properties of breast cancer tissue in a mouse model using indentation
Qiu, S., Zhao, X., Chen, J., Zeng, J., Chen, S., Chen, L., Meng, Y., Liu, B., Shan, H., Gao, M., et al. (2018) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2018.01.007 · Cited by 39
Crisscross multilayering of cell sheets
Sarkar, T., Yashunsky, V., Brézin, L., Blanch-Mercader, C., Aryaksama, T., Lacroix, M., Risler, T., Joanny, J., & Silberzan, P. (2023) · PNAS Nexus · doi:10.1093/pnasnexus/pgad034 · Cited by 38
Recent Development of Fibrous Hydrogels: Properties, Applications and Perspectives
Luo, W., Ren, L., Hu, B., Zhang, H., Yang, Z., Jin, L., & Zhang, D. (2024) · Advanced Science · doi:10.1002/advs.202408657 · Cited by 38
Decellularized extracellular matrix for organoid and engineered organ culture
Guo, X., Liu, B., Zhang, Y., Cheong, S., Xu, T., Lu, F., & He, Y. (2024) · Journal of Tissue Engineering · doi:10.1177/20417314241300386 · Cited by 44
Macrophage infiltration regulates the adipose ECM reconstruction and the fibrosis process after fat grafting
Cai, J., Li, B., Liu, K., Li, G., & Lu, F. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.06.078 · Cited by 38
Engineered coatings for titanium implants to present ultra-low doses of BMP-7
Al-Jarsha, M. Y., Moulisová, V., Leal‐Egaña, A., Connell, A., Naudi, K. B., Ayoub, A. F., Dalby, M. J., & Salmerón‐Sánchez, M. (2018) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.7b01037 · Cited by 38
Regulating Mechanotransduction in Three Dimensions using Sub‐Cellular Scale, Crosslinkable Fibers of Controlled Diameter, Stiffness, and Alignment
Wang, M., Cui, C., Ibrahim, M. M., Han, B., Li, Q., Pacifici, M., Lawrence, J. T. R., Han, L., & Han, L. (2019) · Advanced Functional Materials · doi:10.1002/adfm.201808967 · Cited by 38
Substrate Compliance Directs the Osteogenic Lineages of Stem Cells from the Human Apical Papilla via the Processes of Mechanosensing and Mechanotransduction
Zhou, C., Zhang, D., Zou, J., Li, X., Zou, S., & Xie, J. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b07147 · Cited by 38
Coupling Polar Adhesion with Traction, Spring, and Torque Forces Allows High-Speed Helical Migration of the Protozoan Parasite Toxoplasma
Pavlou, G., Touquet, B., Vigetti, L., Renesto, P., Bougdour, A., Débarre, D., Balland, M., & Tardieux, I. (2020) · ACS Nano · doi:10.1021/acsnano.0c01893 · Cited by 38
In Vivo and Ex Vivo Pediatric Brain Tumor Models: An Overview
Li, Z., & Langhans, S. A. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.620831 · Cited by 39
Fibrous stroma: Driver and passenger in cancer development
Sharma, V., Letson, J., & Furuta, S. (2022) · Science Signaling · doi:10.1126/scisignal.abg3449 · Cited by 38
Receptor‐Level Proximity and Fastening of Ligands Modulates Stem Cell Differentiation
Bae, G., Kim, M., Thangam, R., Koo, T. M., Jang, W. Y., Yoon, J., Han, S., Yang, L., Kim, S. Y., Kang, N., et al. (2022) · Advanced Functional Materials · doi:10.1002/adfm.202200828 · Cited by 38
Periostin promotes secretion of fibronectin from the endoplasmic reticulum
Kii, I., Nishiyama, T., & Kudō, A. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.01.139 · Cited by 38
Mimicking the extracellular world: from natural to fully synthetic matrices utilizing supramolecular biomaterials
Rijns, L., Rutten, M. G. T. A., Vrehen, A. F., Aldana, A. A., Baker, M. B., & Dankers, P. Y. W. (2024) · Nanoscale · doi:10.1039/d4nr02088j · Cited by 37
Bioengineering Beige Adipose Tissue Therapeutics
Tharp, K. M., & Stahl, A. (2015) · Frontiers in Endocrinology · doi:10.3389/fendo.2015.00164 · Cited by 40
Three‐Dimensional Osteosarcoma Models for Advancing Drug Discovery and Development
Monteiro, C. F., Custódio, C. A., & Mano, J. F. (2018) · Advanced Therapeutics · doi:10.1002/adtp.201800108 · Cited by 37
Biofabrication and Characterization of Collagens with Different Hierarchical Architectures
Liu, X., Zheng, M., Wang, X., Luo, X., Hou, M., & Yue, O. (2019) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.9b01252 · Cited by 37
Binding Strength of Gram-Positive Bacterial Adhesins
Dufrêne, Y. F., & Viljoen, A. J. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01457 · Cited by 37
Zein supports scaffolding capacity toward mammalian cells and bactericidal and antiadhesive properties on poly(ε-caprolactone)/zein electrospun fibers
Plath, A. M. S., Facchi, S. P., Souza, P. R., Sabino, R. M., Corradini, E., Muniz, E. C., Popat, K. C., Cardozo‐Filho, L., Kipper, M. J., & Martins, A. F. (2021) · Materials Today Chemistry · doi:10.1016/j.mtchem.2021.100465 · Cited by 37
Integrin β1 orchestrates the abnormal cell-matrix attachment and invasive behaviour of E-cadherin dysfunctional cells
Figueiredo, J., Ferreira, R. M., Xu, H., Gonçalves, M., Barros-Carvalho, A., Cravo, J., Maia, A. F., Carneiro, P., Figueiredo, C., Smith, M. L., et al. (2021) · Gastric Cancer · doi:10.1007/s10120-021-01239-9 · Cited by 37
Transcriptomic Profile of New Gene Markers Encoding Proteins Responsible for Structure of Porcine Ovarian Granulosa Cells
Kulus, J., Kulus, M., Kranc, W., Jopek, K., Zdun, M., Józkowiak, M., Jaśkowski, J. M., Piotrowska‐Kempisty, H., Bukowska, D., Antosik, P., et al. (2021) · Biology · doi:10.3390/biology10111214 · Cited by 37
Silk Fibroin Nacre
Zhao, C., Liu, Y., Lv, Z., Cao, L., Ren, J., Shao, Z., & Ling, S. (2022) · Advanced Fiber Materials · doi:10.1007/s42765-022-00171-6 · Cited by 37
How do the Local Physical, Biochemical, and Mechanical Properties of an Injectable Synthetic Anisotropic Hydrogel Affect Oriented Nerve Growth?
Babu, S., Chen, I., Vedaraman, S., Gerardo‐Nava, J., Licht, C. J., Kittel, Y., Haraszti, T., Russo, J. D., & Laporte, L. D. (2022) · Advanced Functional Materials · doi:10.1002/adfm.202202468 · Cited by 37
A novel 3D in vitro metastasis model elucidates differential invasive strategies during and after breaching basement membrane
Guzman, A., Alemany, V. S., Nguyen, Y. T.-K., Zhang, C. R., & Kaufman, L. J. (2016) · Biomaterials · doi:10.1016/j.biomaterials.2016.11.014 · Cited by 38
TLR expression profile of human alveolar bone proper-derived stem/progenitor cells and osteoblasts
El‐Sayed, K. M. F., Boeckler, J., & Dörfer, C. E. (2017) · Journal of Cranio-Maxillofacial Surgery · doi:10.1016/j.jcms.2017.09.007 · Cited by 37
The impact of α-synuclein aggregates on blood-brain barrier integrity in the presence of neurovascular unit cells
Hourfar, H., Aliakbari, F., Aqdam, S. R., Nayeri, Z., Bardania, H., Otzen, D. E., & Morshedi, D. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.12.134 · Cited by 36
The Macrophage’s Role on Bone Remodeling and Osteogenesis: a Systematic Review
Orvalho, J. M., Fernandes, J. C. H., CASTILHO, R. M., & Fernandes, G. V. O. (2023) · Clinical Reviews in Bone and Mineral Metabolism · doi:10.1007/s12018-023-09286-9 · Cited by 37
Bioactive Nanostructured Scaffold-Based Approach for Tendon and Ligament Tissue Engineering
Govindaraju, D. T., Chen, C., Shalumon, K. T., Kao, H.-H., & Chen, J. (2023) · Nanomaterials · doi:10.3390/nano13121847 · Cited by 36
Elastic properties of hydrogels and decellularized tissue sections used in mechanobiology studies probed by atomic force microscopy
Garcia-Gimenez, A., Uriarte, J. J., Vieyra, J., Navajas, D., & Alcaraz, J. (2016) · Microscopy Research and Technique · doi:10.1002/jemt.22740 · Cited by 36
Dysregulated fibronectin trafficking by Hsp90 inhibition restricts prostate cancer cell invasion
Armstrong, H., Gillis, J. L., Johnson, I. R. D., Nassar, Z. D., Moldovan, M. V., Levrier, C., Sadowski, M. C., Chin, M. Y., Guns, E. S. T., Tarulli, G. A., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-19871-4 · Cited by 36
Collagen XII Is a Regulator of Corneal Stroma Structure and Function
Sun, M., Zafrullah, N., Devaux, F., Hemmavanh, C., Adams, S. M., Ziebarth, N., Koch, M., Birk, D. E., & Espana, E. M. (2020) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.61.5.61 · Cited by 36
Biomimetic Nanostructures Fabricated by Nanoimprint Lithography for Improved Cell‐Coupling
Nowduri, B., Schulte, S., Decker, D., Schäfer, K., & Saumer, M. (2020) · Advanced Functional Materials · doi:10.1002/adfm.202004227 · Cited by 36
Advances in 3D bioprinting for the biofabrication of tumor models
Sánchez-Salazar, M. G., Álvarez, M. M., & Santiago, G. T. (2020) · Bioprinting · doi:10.1016/j.bprint.2020.e00120 · Cited by 37
Sweet impersonators: Molecular mimicry of host glycans by bacteria
de Jong, H., Wösten, M. M. S. M., & Wennekes, T. (2021) · Glycobiology · doi:10.1093/glycob/cwab104 · Cited by 36
Exposure to trace levels of metals and fluoroquinolones increases inflammation and tumorigenesis risk of zebrafish embryos
Jia, D., Zhang, R., Shao, J., Zhang, W., Cai, L., & Sun, W. (2022) · Environmental Science and Ecotechnology · doi:10.1016/j.ese.2022.100162 · Cited by 36
From Small to Large-Scale: A Review of Recombinant Spider Silk and Collagen Bioproduction
Gomes, V., & Salgueiro, S. P. (2022) · Discover Materials · doi:10.1007/s43939-022-00024-4 · Cited by 35
Ligand Coupling and Decoupling Modulates Stem Cell Fate
Thangam, R., Kim, S. Y., Kang, N., Hong, H., Lee, H., Lee, S., Jeong, D., Tag, K., Kim, K., Zhu, Y., et al. (2023) · Advanced Functional Materials · doi:10.1002/adfm.202206673 · Cited by 35
Hierarchical Design of Tissue‐Mimetic Fibrillar Hydrogel Scaffolds
Pardo, A., Gómez‐Florit, M., Davidson, M. D., Öztürk-Öncel, M. Ö., Domingues, R. M. A., Burdick, J. A., & Gomes, M. E. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202303167 · Cited by 36
Promoting Diabetic Wound Healing through a Hydrogel‐Based Cascade Regulation Strategy of Fibroblast‐Macrophage
Jin, N., Wang, Z., Tang, X., Jin, N., & Wang, X. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202400526 · Cited by 35
Identification of ageing-associated naturally occurring peptides in human urine
Nkuipou‐Kenfack, E., Bhat, A. V., Klein, J., Jankowski, V., Mullen, W., Vlahou, A., Dakna, M., Koeck, T., Schanstra, J. P., Zürbig, P., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.5896 · Cited by 35
Signaling at the Crossroads: Matrix-Derived Proteoglycan and Reactive Oxygen Species Signaling
Nastase, M.-V., Janicova, A., Wygrecka, M., & Schaefer, L. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7165 · Cited by 36
Cell cycle–dependent force transmission in cancer cells
Panagiotakopoulou, M., Lendenmann, T., Pramotton, F. M., Giampietro, C., Stefopoulos, G., Dimos Poulikakos, A., & Ferrari, A. (2018) · Molecular Biology of the Cell · doi:10.1091/mbc.e17-12-0726 · Cited by 38
Dynamic Mechanical Control of Alginate-Fibronectin Hydrogels with Dual Crosslinking: Covalent and Ionic
Trujillo, S., Seow, M., Lueckgen, A., Salmeron-Sanchez, M., & Cipitria, A. (2021) · Polymers · doi:10.3390/polym13030433 · Cited by 35
Drug screening by uniform patient derived colorectal cancer hydro-organoids
Jung, Y. H., Choi, D., Park, K., Lee, S.-B., Kim, J., Kim, H., Jeong, H., Yang, J. H., Kim, J., Chung, S. H., et al. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.121004 · Cited by 35
Enantioselective Interaction between Cells and Chiral Hydroxyapatite Films
Zhou, C. H., Zhang, S., Ai, J., Li, P., Zhao, Y., Li, B., Han, L., Duan, Y., & Che, S. (2021) · Chemistry of Materials · doi:10.1021/acs.chemmater.1c02417 · Cited by 35
Nanoparticulates reduce tumor cell migration through affinity interactions with extracellular migrasomes and retraction fibers
Cheng, Y., Ren, J., Fan, S., Wu, P., Cong, W., Lin, Y., Lan, S., Song, S., Shao, B., Dai, W., et al. (2022) · Nanoscale Horizons · doi:10.1039/d2nh00067a · Cited by 35
Characterisation of 3D Bioprinted Human Breast Cancer Model for In Vitro Drug and Metabolic Targeting
Dankó, T., Petővári, G., Raffay, R. E., Sztankovics, D., Moldvai, D., Vetlényi, E., Krencz, I., Rókusz, A., Sipos, K., Visnovitz, T., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23137444 · Cited by 35
Exposing Differences in Monomer Exchange Rates of Multicomponent Supramolecular Polymers in Water
Baker, M. B., Gosens, R. P. J., Albertazzi, L., Matsumoto, N. M., Palmans, A. R. A., & Meijer, E. W. (2015) · ChemBioChem · doi:10.1002/cbic.201500606 · Cited by 35
Immune‐mediated ECM depletion improves tumour perfusion and payload delivery
Yeow, Y. L., Kotamraju, V. R., Wang, X., Chopra, M., Azme, N., Wu, J., Schoep, T. D., Delaney, D. S., Feindel, K. W., Li, J., et al. (2019) · EMBO Molecular Medicine · doi:10.15252/emmm.201910923 · Cited by 35
Decellularized mice colons as models to study the contribution of the extracellular matrix to cell behavior and colon cancer progression
Alabi, B. R., LaRanger, R., & Shay, J. W. (2019) · Acta Biomaterialia · doi:10.1016/j.actbio.2019.09.033 · Cited by 34
The versatile roles of ADAM8 in cancer cell migration, mechanics, and extracellular matrix remodeling
Mierke, C. T. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1130823 · Cited by 34
Macrostructure and Microenvironment Biomimetic Hydrogel: Design, Properties, and Tissue Engineering Application
Hu, S., Zeng, C., Jiang, Y., Kong, W., & Zhu, M. (2024) · Chemistry of Materials · doi:10.1021/acs.chemmater.3c02098 · Cited by 37
Tunable Macroscopic Alignment of Self-Assembling Peptide Nanofibers
Farsheed, A. C., Delgado, C. Z., Yu, L. T., Saeidifard, S., Swain, J. W. R., Makhoul, J. T., Thomas, A. J., Cole, C. C., Huitron, E. I. G., Grande-Allen, K. J., et al. (2024) · ACS Nano · doi:10.1021/acsnano.4c02030 · Cited by 34
PD-L2 of tumor-derived exosomes mediates the immune escape of cancer cells via the impaired T cell function
Liu, T., Cheng, S., Peng, B., Zang, H., Zhu, X., Wang, X., Zhao, X., Gu, Y., Pan, Y., Hu, H., et al. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-07191-7 · Cited by 35
The prognostic value and pathobiological significance of Glasgow microenvironment score in gastric cancer
Zhou, Z.-H., Ji, C., Zhu, J., Xiao, H., Zhao, H., Cui, Y., & Bian, X. (2017) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-017-2346-1 · Cited by 34
Inducible knockdown of procollagen I protects mice from liver fibrosis and leads to dysregulated matrix genes and attenuated inflammation
Molokanova, O., Schönig, K., Weng, S., Wang, X., Bros, M., Diken, M., Ohngemach, S., Karsdal, M. A., Strand, D. J., Nikolaev, A., et al. (2017) · Matrix Biology · doi:10.1016/j.matbio.2017.11.002 · Cited by 34
Molecular basis for governing the morphology of type-I collagen fibrils by Osteomodulin
Tashima, T., Nagatoishi, S., Caaveiro, J. M. M., Nakakido, M., Sagara, H., Kusano‐Arai, O., Iwanari, H., Mimuro, H., Hamakubo, T., Ohnuma, S., et al. (2018) · Communications Biology · doi:10.1038/s42003-018-0038-2 · Cited by 34
Cellular Processes by Which Osteoblasts and Osteocytes Control Bone Mineral Deposition and Maturation Revealed by Stage-Specific EphrinB2 Knockdown
Blank, M., & Sims, N. A. (2019) · Current Osteoporosis Reports · doi:10.1007/s11914-019-00524-y · Cited by 35
Peroxidasin is essential for endothelial cell survival and growth signaling by sulfilimine crosslink‐dependent matrix assembly
Lee, S. W., Kim, H. K., Naidansuren, P., Ham, K. A., Choi, H. S., Ahn, H., Kim, M., Kang, D. H., Kang, S. W., & Joe, Y. A. (2020) · The FASEB Journal · doi:10.1096/fj.201902899r · Cited by 34
Modulating barriers of tumor microenvironment through nanocarrier systems for improved cancer immunotherapy: a review of current status and future perspective
Lan, H., We, Z., Jin, K., Liu, Y., & Wang, Z. (2020) · Drug Delivery · doi:10.1080/10717544.2020.1809559 · Cited by 35
Using 3D in vitro cell culture models in anti-cancer drug discovery
Langhans, S. A. (2021) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2021.1912731 · Cited by 35
From structure to application: Progress and opportunities in peptide materials development
Lopez‐Silva, T. L., & Schneider, J. P. (2021) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2021.06.006 · Cited by 34
3D printed tissue models: From hydrogels to biomedical applications
Cadamuro, F., Nicotra, F., & Russo, L. (2023) · Journal of Controlled Release · doi:10.1016/j.jconrel.2023.01.048 · Cited by 35
CD98 heavy chain as a prognostic biomarker and target for cancer treatment
Pu, X., & Dubrovska, A. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1251100 · Cited by 35
Skin-Inspired Patterned Hydrogel with Strain-Stiffening Capability for Strain Sensors
Cui, J., Xu, R., Dong, W., Kaneko, T., Chen, M., & Shi, D. (2023) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.3c12127 · Cited by 33
Monoterpenoids: An upcoming class of therapeutic agents for modulating cancer metastasis
Mathur, A., Meena, A., & Luqman, S. (2023) · Phytotherapy Research · doi:10.1002/ptr.8081 · Cited by 33
Glioblastoma shift from bulk to infiltrative growth is guided by plexin-B2-mediated microglia alignment in invasive niches
Kang, S., Ughetta, M. E., Zhang, J. Y., Marallano, V. J., Sattiraju, A., Hannah, T., Wahane, S., Ramakrishnan, A., Estill, M. S., Tsankova, N. M., et al. (2025) · Nature Cancer · doi:10.1038/s43018-025-00985-4 · Cited by 34
Impact of breast cancer cells´ secretome on the brain metastatic niche remodeling
Carvalho, R., Paredes, J., & Ribeiro, A. S. (2019) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2019.10.011 · Cited by 35
Bidirectional Mechanical Response Between Cells and Their Microenvironment
Mierke, C. T. (2021) · Frontiers in Physics · doi:10.3389/fphy.2021.749830 · Cited by 36
Oxidation of human plasma fibronectin by inflammatory oxidants perturbs endothelial cell function
Vanichkitrungruang, S., Chuang, C. Y., Hawkins, C. L., Hammer, A., Höefler, G., Malle, E., & Davies, M. J. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.04.003 · Cited by 33
Design strategies for composite matrix and multifunctional polymeric scaffolds with enhanced bioactivity for bone tissue engineering
Shikha, K., Katiyar, S., Darshna, Anand, A., Singh, D., Singh, B. N., Mallick, S. P., Mishra, A., & Srivastava, P. (2022) · Frontiers in Chemistry · doi:10.3389/fchem.2022.1051678 · Cited by 32
Cartilage and bone injectable hydrogels: A review of injectability methods and treatment strategies for repair in tissue engineering
Shaygani, H., Mofrad, Y. M., Demneh, S. M. H. R., Hafezi, S., Almasi-Jaf, A., & Shamloo, A. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.136689 · Cited by 34
Three-dimensional organotypic matrices from alternative collagen sources as pre-clinical models for cell biology
Conway, J. R. W., Vennin, C., Cazet, A., Herrmann, D., Murphy, K. J., Warren, S. C., Wullkopf, L., Boulghourjian, A., Zaratzian, A., Silva, A. M. D., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-17177-5 · Cited by 32
Epidermal aspects of type VII collagen: Implications for dystrophic epidermolysis bullosa and epidermolysis bullosa acquisita
Watanabe, M., Natsuga, K., Shinkuma, S., & Shimizu, H. (2018) · The Journal of Dermatology · doi:10.1111/1346-8138.14222 · Cited by 32
MicroRNA-101a suppresses fibrotic programming in isolated cardiac fibroblasts and in vivo fibrosis following trans-aortic constriction
Zhou, Y., Shiok, T. C., Richards, M., & Wang, P. (2018) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2018.07.251 · Cited by 32
Dose-Dependent Antifibrotic Effect of Chrysin on Regression of Liver Fibrosis: The Role in Extracellular Matrix Remodeling
Baltă, C., Ciceu, A., Herman, H., Roșu, M., Boldura, O. M., & Hermenean, A. O. (2018) · Dose-Response · doi:10.1177/1559325818789835 · Cited by 32
Design of Bio-Conjugated Hydrogels for Regenerative Medicine Applications: From Polymer Scaffold to Biomolecule Choice
Chimisso, V., Aleman‐Garcia, M. A., Avsar, S. Y., Dinu, I. A., & Palivan, C. G. (2020) · Molecules · doi:10.3390/molecules25184090 · Cited by 32
Trypanosoma cruzi Induces the PARP1/AP-1 Pathway for Upregulation of Metalloproteinases and Transforming Growth Factor β in Macrophages: Role in Cardiac Fibroblast Differentiation and Fibrosis in Chagas Disease
Choudhuri, S., & Garg, N. J. (2020) · mBio · doi:10.1128/mbio.01853-20 · Cited by 32
Dual Functionalized Injectable Hybrid Extracellular Matrix Hydrogel for Burn Wounds
Bankoti, K., Rameshbabu, A. P., Datta, S., Goswami, P., Roy, M., Das, D., Ghosh, S. K., Das, A. K., Mitra, A., Pal, S., et al. (2020) · Biomacromolecules · doi:10.1021/acs.biomac.0c01400 · Cited by 32
Glioblastoma Vasculature: From its Critical Role in Tumor Survival to Relevant in Vitro Modelling
Pacheco, C., Martins, C., Monteiro, J., Baltazar, F., Costa, B. M., & Sarmento, B. F. C. C. (2022) · Frontiers in Drug Delivery · doi:10.3389/fddev.2022.823412 · Cited by 33
The Study of the Extracellular Matrix in Chronic Inflammation: A Way to Prevent Cancer Initiation?
Marangio, A., Biccari, A., D’Angelo, E., Sensi, F., Spolverato, G., Pucciarelli, S., & Agostini, M. (2022) · Cancers · doi:10.3390/cancers14235903 · Cited by 34
Molecular effects of a variable environment on Sydney rock oysters, Saccostrea glomerata: Thermal and low salinity stress, and their synergistic effect
Ertl, N. G., O’Connor, W. A., & Elizur, A. (2018) · Marine Genomics · doi:10.1016/j.margen.2018.10.003 · Cited by 35
Nanomechanical Analysis of Extracellular Matrix and Cells in Multicellular Spheroids
Vyas, V., Solomon, M. A., D’Souza, G. G. M., & Huey, B. D. (2019) · Cellular and Molecular Bioengineering · doi:10.1007/s12195-019-00577-0 · Cited by 36
Mutual adhesion of Lactobacillus spp. to intestinal cells: A review of perspectives on surface layer proteins and cell surface receptors
Zheng, Y., Zhao, J., Nie, X., Chitrakar, B., Gao, J., & Sang, Y. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.137031 · Cited by 31
Natural polymers for bone repair
Ramírez‐Rodríguez, G. B., Patrício, T., & López, J. D. (2019) · Elsevier eBooks · doi:10.1016/b978-0-08-102451-5.00008-1 · Cited by 31
Functionalized DNA Hydrogels Produced by Polymerase‐Catalyzed Incorporation of Non‐Natural Nucleotides as a Surface Coating for Cell Culture Applications
Finke, A., Schneider, A., Spreng, A., Leist, M., Niemeyer, C. M., & Marx, A. (2019) · Advanced Healthcare Materials · doi:10.1002/adhm.201900080 · Cited by 32
Poroelasticity of (bio)polymer networks during compression: theory and experiment
Punter, M. T. J. J. M., Vos, B. E., Mulder, B. M., & Koenderink, G. H. (2019) · Soft Matter · doi:10.1039/c9sm01973a · Cited by 31
Identification of Ppar γ -modulated miRNA hubs that target the fibrotic tumor microenvironment
Winkler, I., Bitter, C., Winkler, S., Weichenhan, D., Thavamani, A., Hengstler, J. G., Borkham‐Kamphorst, E., Kohlbacher, O., Plass, C., Geffers, R., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1909145117 · Cited by 33
Mechano-chemical enforcement of tendon apical ECM into nano-filaments during Drosophila flight muscle development
Chu, W.-C., & Hayashi, S. (2021) · Current Biology · doi:10.1016/j.cub.2021.01.010 · Cited by 31
The role of cell–matrix interactions in connective tissue mechanics
Muntz, I., Fenu, M., van Osch, G. J. V. M., & Koenderink, G. H. (2021) · Physical Biology · doi:10.1088/1478-3975/ac42b8 · Cited by 33
Association of breast cancer risk, density, and stiffness: global tissue stiffness on breast MR elastography (MRE)
Patel, B., Pepin, K. M., Brandt, K. R., Mazza, G. L., Pockaj, B. A., Chen, J., Zhou, Y., Northfelt, D., Anderson, K. S., Kling, J. M., et al. (2022) · Breast Cancer Research and Treatment · doi:10.1007/s10549-022-06607-2 · Cited by 31

Authors: Mouw, J. K., Ou, G., & Weaver, V. M.
Affiliations: University of California, San Francisco (US)
Corresponding author: Weaver, Valerie M.
ORCID: Mouw, Janna K.
Ou, Guanqing
Weaver, Valerie M.
Venue: Nature Reviews Molecular Cell Biology
Publisher: Springer Science and Business Media LLC
Published: 2014-11-05
Volume: 15
Issue: 12
Pages: 771-785
ISSN: 1471-0072 (ISSN-L)
1471-0080
DOI: 10.1038/nrm3902
PMC: PMC4682873
OpenAlex: W2023026872
Cited by: 1,534
References: 182
Citations by year: 2026: 118 · 2025: 130 · 2024: 172 · 2023: 162 · 2022: 138 · 2021: 179 · 2020: 164 · 2019: 134 · 2018: 109 · 2017: 111 · 2016: 76 · 2015: 35 · 2014: 2
FWCI: 7.48
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: www.springer.com/tdm (tdm)
Locations: Nature Reviews Molecular Cell Biology (publishedVersion)
PubMed (publishedVersion)
Europe PMC (PubMed Central) (acceptedVersion)
PubMed Central (acceptedVersion)
eScholarship (California Digital Library) (submittedVersion)
Funders: U.S. Department of Defense
National Cancer Institute (U01CA151925, R01CA085492, R01CA138818, U54CA143836)
National Institute of Environmental Health Sciences (U01ES019458)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Bone and Dental Protein Studies
Keywords: extracellular matrix assembly, collagen, proteoglycans, laminin, fibronectin, ECM composition, cell behavior
MeSH terms: Animals, Basement Membrane, Extracellular Matrix, Humans, Neurons, Proteoglycans, Extracellular Matrix Proteins

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

Extracellular matrix assembly: a multiscale deconstruction

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks