Relationships between degradability of silk scaffolds and osteogenesis
Open accessAbstract
Bone repairs represent a major focus in orthopedic medicine with biomaterials as a critical aspect of the regenerative process. However, only a limited set of biomaterials are utilized today and few studies relate biomaterial scaffold design to degradation rate and new bone formation. Matching biomaterial remodeling rate towards new bone formation is important in terms of the overall rate and quality of bone regeneration outcomes. We report on the osteogenesis and metabolism of human bone marrow derived mesenchymal stem cells (hMSCs) in 3D silk scaffolds. The scaffolds were prepared with two different degradation rates in order to study relationships between matrix degradation, cell metabolism and bone tissue formation in vitro. SEM, histology, chemical assays, real-time PCR and metabolic analyses were assessed to investigate these relationships. More extensively mineralized ECM formed in the scaffolds designed to degrade more rapidly, based on SEM, von Kossa and type I collagen staining and calcium content. Measures of osteogenic ECM were significantly higher in the more rapidly degrading scaffolds than in the more slowly degrading scaffolds over 56 days of study in vitro. Metabolic analysis, including glucose and lactate levels, confirmed the degradation rate differences with the two types of scaffolds, with the more rapidly degrading scaffolds supporting higher levels of glucose consumption and lactate synthesis by the hMSCs upon osteogenesis, in comparison to the more slowly degrading scaffolds. The results demonstrate that scaffold degradation rates directly impact the metabolism of hMSCs, and in turn the rate of osteogenesis. An understanding of the interplay between cellular metabolism and scaffold degradability should aid in the more rational design of scaffolds for bone regeneration needs both in vitro and in vivo.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
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?
Silk fibroin hydrolysates can enhance alkaline phosphatase activity in osteoblasts and their ability to undergo osteogenic differentiation.
“Moreover, the study also found that silk fibroin hydrolysates can enhance the activity of alkaline phosphatase (ALP) in osteoblasts and their ability to undergo osteogenic differentiation [33].”
From Recent Advances in Silk Fibroin-Based Composites for Bone Repair Applications: A Review (2025) · cites this paper as [33]
The Discussion reports that faster-degrading silk scaffolds promoted osteogenic differentiation, and the Gene expression results report higher ALP transcripts in those scaffolds. The study examined cells grown on scaffolds, not treatment with silk fibroin hydrolysates. Its Biochemical analysis does not report enhanced ALP activity; activity decreased from day 16 to day 56 in both scaffold groups. (LLM, conf=0.88)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Hydrogels for tissue engineering: scaffold design variables and applications
Drury, J. L., & Mooney, D. J. (2003) · Biomaterials · doi:10.1016/s0142-9612(03)00340-5 · Cited by 5,136 · see citing works
Biodegradable and bioactive porous polymer/inorganic composite scaffolds for bone tissue engineering
Rezwan, K., Chen, Q. Z., Blaker, J. J., & Boccaccini, A. R. (2006) · Biomaterials · doi:10.1016/j.biomaterials.2006.01.039 · Cited by 3,840 · see citing works
Altman, G. H., Diaz, F., Jakuba, C., Calabro, T., Horan, R. L., Chen, J., Lu, H., Richmond, J., & Kaplan, D. L. (2003) · Biomaterials · doi:10.1016/s0142-9612(02)00353-8 · Cited by 3,458 · see citing works
Self-citationTranscriptional regulation of genes encoding glycolytic enzymes by hypoxia-inducible factor 1.
Semenza, G., Roth, P. H., Fang, H. M., & Wang, G. L. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)31580-6 · Cited by 1,892 · see citing works
Determination of blood glucose using an oxidase-peroxidase system with a non-carcinogenic chromogen
Trinder, P. (1969) · Journal of Clinical Pathology · doi:10.1136/jcp.22.2.158 · Cited by 1,656 · see citing works
Navarro, M., Michiardi, A., Castaño, Ó., & Planell, J. A. (2008) · Journal of The Royal Society Interface · doi:10.1098/rsif.2008.0151 · Cited by 1,521 · see citing works
Three-dimensional aqueous-derived biomaterial scaffolds from silk fibroin
Kim, U., Park, J. H., Kim, H. J., Wada, M., & Kaplan, D. L. (2004) · Biomaterials · doi:10.1016/j.biomaterials.2004.07.044 · Cited by 979 · see citing works
Self-citationHypoxia-inducible factor 1: oxygen homeostasis and disease pathophysiology
Semenza, G. L. (2001) · Trends in Molecular Medicine · doi:10.1016/s1471-4914(01)02090-1 · Cited by 930 · see citing works
Porous 3-D Scaffolds from Regenerated Silk Fibroin
Nazarov, R., Jin, H., & Kaplan, D. L. (2004) · Biomacromolecules · doi:10.1021/bm034327e · Cited by 888 · see citing works
Self-citationBryant, S. J., & Anseth, K. S. (2002) · Journal of Biomedical Materials Research · doi:10.1002/jbm.1217 · Cited by 845 · see citing works
Benoit, D. S. W., Schwartz, M. P., Durney, A. R., & Anseth, K. S. (2008) · Nature Materials · doi:10.1038/nmat2269 · Cited by 825 · see citing works
In vivo degradation of three-dimensional silk fibroin scaffolds
Wang, Y., Rudym, D., Walsh, A., Abrahamsen, L., Kim, H.-J., Kim, H. S., Kirker‐Head, C. A., & Kaplan, D. L. (2008) · Biomaterials · doi:10.1016/j.biomaterials.2008.05.002 · Cited by 788 · see citing works
Self-citationEvolution of bone transplantation: molecular, cellular and tissue strategies to engineer human bone
Yaszemski, M. J., Payne, R. G., Hayes, W. C., Langer, R., & Mikos, A. G. (1996) · Biomaterials · doi:10.1016/0142-9612(96)85762-0 · Cited by 729 · see citing works
Osteopontin: a versatile regulator of inflammation and biomineralization
Giachelli, C. M., & Steitz, S. A. (2000) · Matrix Biology · doi:10.1016/s0945-053x(00)00108-6 · Cited by 586 · see citing works
Activation of the hypoxia-inducible factor-1α pathway accelerates bone regeneration
Wan, C., Gilbert, S. R., Wang, Y., Cao, X., Shen, X., Ramaswamy, G., Jacobsen, K. A., Al-Aql, Z. S., Eberhardt, A. W., Gerstenfeld, L. C., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708474105 · Cited by 517 · see citing works
Ganss, B., Kim, R. H., & Sodek, J. (1999) · Critical Reviews in Oral Biology & Medicine · doi:10.1177/10454411990100010401 · Cited by 490 · see citing works
Enzymatic degradation behavior of porous silk fibroin sheets
Li, M., Ogiso, M., & Minoura, N. (2002) · Biomaterials · doi:10.1016/s0142-9612(02)00326-5 · Cited by 457 · see citing works
Regulating Bone Formation via Controlled Scaffold Degradation
Alsberg, E., Kong, H., Hirano, Y., Smith, M. K., Albeiruti, A., & Mooney, D. J. (2003) · Journal of Dental Research · doi:10.1177/154405910308201111 · Cited by 327 · see citing works
Influence of macroporous protein scaffolds on bone tissue engineering from bone marrow stem cells
Kim, H. J., Kim, U., Vunjak‐Novakovic, G., Min, B., & Kaplan, D. L. (2004) · Biomaterials · doi:10.1016/j.biomaterials.2004.11.013 · Cited by 301 · see citing works
Self-citationBone tissue engineering with premineralized silk scaffolds
Kim, H. J., Kim, U., Kim, H. S., Li, C., Wada, M., Leisk, G. G., & Kaplan, D. L. (2008) · Bone · doi:10.1016/j.bone.2008.02.007 · Cited by 294 · see citing works
Self-citationBiodegradable polymers as biomaterials
Pişkın, E. (1995) · Journal of Biomaterials Science Polymer Edition · doi:10.1163/156856295x00175 · Cited by 288 · see citing works
Lian, J. B., & Stein, G. S. (1995) · Europe PMC (PubMed Central) · Cited by 283 · see citing works
Matricellular proteins: Extracellular modulators of bone development, remodeling, and regeneration
Alford, A. I., & Hankenson, K. D. (2006) · Bone · doi:10.1016/j.bone.2005.11.017 · Cited by 265 · see citing works
Evidence for a negative Pasteur effect in articular cartilage
Lee, R. B., & Urban, J. P. G. (1997) · Biochemical Journal · doi:10.1042/bj3210095 · Cited by 236 · see citing works
Bioactive scaffolds for bone and ligament tissue
Guarino, V., Causa, F., & Ambrosio, L. (2007) · Expert Review of Medical Devices · doi:10.1586/17434440.4.3.405 · Cited by 226 · see citing works
Tissue engineering for bone defect healing: an update on a multi-component approach.
Drosse, I., Volkmer, E., Capanna, R., Biase, P. D., Mutschler, W., & Schieker, M. (2008) · Injury · doi:10.1016/s0020-1383(08)70011-1 · Cited by 221 · see citing works
Stem cells for regenerative medicine: advances in the engineering of tissues and organs
Ringe, J., Kaps, C., Burmester, G.-R. X. F. D., & Sittinger, M. (2002) · Die Naturwissenschaften · doi:10.1007/s00114-002-0344-9 · Cited by 220 · see citing works
On scaffold designing for bone regeneration: A computational multiscale approach
Sanz‐Herrera, J. A., García‐Aznar, J. M., & Doblaré, M. (2008) · Acta Biomaterialia · doi:10.1016/j.actbio.2008.06.021 · Cited by 214 · see citing works
Applications of amino acid derivatization with 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate
Cohen, S. A., & Antonis, K. M. D. (1994) · Journal of Chromatography A · doi:10.1016/0021-9673(93)e0821-b · Cited by 208 · see citing works
Processing methods to control silk fibroin film biomaterial features
Lawrence, B. D., Omenetto, F. G., Chui, K., & Kaplan, D. L. (2008) · Journal of Materials Science · doi:10.1007/s10853-008-2961-y · Cited by 205 · see citing works
Self-citationMesenchymal stem cells cultured on a collagen scaffold: In vitro osteogenic differentiation
Donzelli, E., Salvadè, A., Mimo, P., et al. (2006) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2006.07.007 · Cited by 191 · see citing works
The Metabolism of Proline as Microenvironmental Stress Substrate
Phang, J. M., Pandhare, J., & Liu, Y. (2008) · Journal of Nutrition · doi:10.1093/jn/138.10.2008s · Cited by 175 · see citing works
Wu, C., Ramaswamy, Y., Boughton, P. C., et al. (2007) · Acta Biomaterialia · doi:10.1016/j.actbio.2007.08.010 · Cited by 164 · see citing works
Buckbinder, L., Crawford, D. T., Qi, H., Ke, H. Z., OLSON, L. M., Long, K. R., Bonnette, P. C., Baumann, A. P., Hambor, J., GRASSER, W. A., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701421104 · Cited by 163 · see citing works
Pham, Q. P., Kasper, F. K., Baggett, L. S., Raphael, R. M., Jansen, J. A., & Mikos, A. G. (2008) · Biomaterials · doi:10.1016/j.biomaterials.2008.02.025 · Cited by 150 · see citing works
Tissue‐engineered Cartilage Using Fibrin/Hyaluronan Composite Gel and Its In Vivo Implantation
Park, S., Park, S. R., Chung, S. I., et al. (2005) · Artificial Organs · doi:10.1111/j.1525-1594.2005.00137.x · Cited by 147 · see citing works
Self-citationStucki, U., Schmid, J., Hämmerle, C., et al. (2001) · Clinical Oral Implants Research · doi:10.1034/j.1600-0501.2001.012002121.x · Cited by 145 · see citing works
Bone Regeneration on Macroporous Aqueous‐Derived Silk 3‐D Scaffolds
Kim, H. J., Kim, U., Leisk, G. G., Bayan, C., Georgakoudi, I., & Kaplan, D. L. (2007) · Macromolecular Bioscience · doi:10.1002/mabi.200700030 · Cited by 145 · see citing works
Self-citationKasugai, S., Nagata, T., & Sodek, J. (1992) · Journal of Cellular Physiology · doi:10.1002/jcp.1041520305 · Cited by 144 · see citing works
Effect of Scaffold Design on Bone Morphology In Vitro
Uebersax, L., Hagenmüller, H., Hofmann, S., Gruenblatt, E., Müller, R., Vunjak‐Novakovic, G., Kaplan, D. L., Merkle, H. P., & Meinel, L. (2006) · Tissue Engineering · doi:10.1089/ten.2006.12.3417 · Cited by 143 · see citing works
Self-citationMaterials in particulate form for tissue engineering. 2. Applications in bone
Silva, G. A., Coutinho, O. P., Ducheyne, P., & Reis, R. L. (2007) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.1 · Cited by 131 · see citing works
Lian, J. B., & Stein, G. S. (1993) · PubMed · Cited by 122 · see citing works
Oxygen tension is an important mediator of the transformation of osteoblasts to osteocytes
Hirao, M., Hashimoto, J., Yamasaki, N., Ando, W., Tsuboi, H., Myoui, A., & Yoshikawa, H. (2007) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-007-0765-9 · Cited by 122 · see citing works
Ge, Z., Tian, X., Heng, B. C., et al. (2009) · Biomedical Materials · doi:10.1088/1748-6041/4/2/021001 · Cited by 118 · see citing works
Comparative Aspects of Tissue Glutamine and Proline Metabolism
Bertolo, R. F. P., & Burrin, D. G. (2008) · Journal of Nutrition · doi:10.1093/jn/138.10.2032s · Cited by 94 · see citing works
An enzymatic fluorometric method for the determination of lactic acid in serum.
Loomis, M. E. (1961) · PubMed · Cited by 88 · see citing works
Byrne, E. M., Farrell, E., McMahon, L. A., Haugh, M. G., O’Brien, F. J., Campbell, V. A., Prendergast, P. J., & O'Connell, B. C. (2008) · Journal of Materials Science Materials in Medicine · doi:10.1007/s10856-008-3506-2 · Cited by 86 · see citing works
Heywood, H. K., Bader, D. L., & Lee, D. A. (2005) · Journal of Cellular Physiology · doi:10.1002/jcp.20491 · Cited by 82 · see citing works
Holtorf, H. L., Jansen, J. A., & Mikos, A. G. (2005) · Biomaterials · doi:10.1016/j.biomaterials.2005.04.006 · Cited by 82 · see citing works
Controlled Release Scaffolds for Bone Tissue Engineering
Cartmell, S. (2009) · Journal of Pharmaceutical Sciences · doi:10.1002/jps.21431 · Cited by 66 · see citing works
Profiling of dynamic changes in hypermetabolic livers
Lee, K., Francois Berthiaume, B., Stephanopoulos, G. N., & Yarmush, M. L. (2003) · Biotechnology and Bioengineering · doi:10.1002/bit.10682 · Cited by 64 · see citing works
Self-citationKnabe, C., Berger, G., Gildenhaar, R., et al. (2004) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.20131 · Cited by 64 · see citing works
Koukourakis, M. I., Pitiakoudis, M., Giatromanolaki, A. N., Tsarouha, A., Polychronidis, A., Sivridis, E., & Simopoulos, C. (2006) · Cancer Science · doi:10.1111/j.1349-7006.2006.00298.x · Cited by 61 · see citing works
Follmar, K. E., DeCroos, F. C., Prichard, H. L., Wang, H. T., Erdmann, D., & Olbrich, K. C. (2006) · Tissue Engineering · doi:10.1089/ten.2006.12.3525 · Cited by 58 · see citing works
The role of glutamate in the regulation of bone mass and architecture.
Skerry, T. M. (2008) · PubMed · Cited by 55 · see citing works
A mathematical approach to bone tissue engineering
Sanz‐Herrera, J. A., García‐Aznar, J. M., & Doblaré, M. (2009) · Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences · doi:10.1098/rsta.2009.0055 · Cited by 54 · see citing works
Glutamate signalling and its potential application to tissue engineering of bone
Mason, D. J. (2004) · European Cells and Materials · doi:10.22203/ecm.v007a02 · Cited by 49 · see citing works
Knabe, C., Berger, G., Gildenhaar, R., et al. (2003) · Biomaterials · doi:10.1016/s0142-9612(03)00525-8 · Cited by 48 · see citing works
Metabolic and Functional Characterization of Human Adipose-Derived Stem Cells in Tissue Engineering
Mischen, B. T., Follmar, K. E., Moyer, K. E., Buehrer, B. M., Olbrich, K. C., Levin, L. S., Klitzman, B. M., & Erdmann, D. (2008) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0b013e318180ec9f · Cited by 47 · see citing works
Collagen and Disorders of Bone
Smith, R. F. (1980) · Clinical Science · doi:10.1042/cs0590215 · Cited by 46 · see citing works
Introduction: Glutamate transport, metabolism, and physiological responses
Hediger, M. A., & Welbourne, T. C. (1999) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.1999.277.4.f477 · Cited by 45 · see citing works
Analysis of Collagen Synthesis
Diegelmann, R. F. (2003) · Humana Press eBooks · doi:10.1385/1-59259-332-1:349 · Cited by 42 · see citing works
Leong, D. T., Nah, W., Gupta, A., Hutmacher, D. W., & Woodruff, M. A. (2008) · Current Drug Discovery Technologies · doi:10.2174/157016308786733537 · Cited by 35 · see citing works
Boehm, J. R., Kutz, S. M., Sage, E. H., Staiano‐Coico, L., & Higgins, P. J. (1999) · Journal of Cellular Physiology · doi:10.1002/(sici)1097-4652(199910)181:1 · Cited by 32 · see citing works
Reduced Collagen Degradation in Polytraumas with Traumatic Brain Injury Causes Enhanced Osteogenesis
Andermahr, J., Elsner, A., Brings, A. E., et al. (2006) · Journal of Neurotrauma · doi:10.1089/neu.2006.23.708 · Cited by 31 · see citing works
Hwang, D., & Ismail‐Beigi, F. (2002) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2002.2758 · Cited by 30 · see citing works
Quantitative Screening of Engineered Implants in a Long Bone Defect Model in Rabbits
Bakker, A. D., Schrooten, J., Cleynenbreugel, T. V., et al. (2008) · Tissue Engineering Part C Methods · doi:10.1089/ten.tec.2008.0022 · Cited by 29 · see citing works
Bone Matrix Proteins: More Than Markers
Young, M. F. (2003) · Calcified Tissue International · doi:10.1007/s00223-002-1017-6 · Cited by 28 · see citing works
An inverse method for predicting tissue-level mechanics from cellular mechanical input
Kim, W., Tretheway, D. C., & Kohles, S. S. (2009) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2008.11.014 · Cited by 22 · see citing works
Extracellular matrix remodeling—Methods to quantify cell–matrix interactions
Abraham, L. C., Dice, J. F., Finn, P. F., Mesires, N. T., Lee, K., & Kaplan, D. L. (2006) · Biomaterials · doi:10.1016/j.biomaterials.2006.07.001 · Cited by 21 · see citing works
Self-citationLysyl hydroxylation in collagens from hyperplastic callus and embryonic bones
Lehmann, H., Bodo, M., Frohn, C., et al. (1992) · Biochemical Journal · doi:10.1042/bj2820313 · Cited by 19 · see citing works
Impact of collagen structure on matrix trafficking by human fibroblasts
Abraham, L. C., Vorrasi, J., & Kaplan, D. L. (2004) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.30057 · Cited by 19 · see citing works
Self-citationAdhesion molecule expression by osteogenic cells cultured on various biodegradable scaffolds
Shur, I., Zilberman, M., Benayahu, D., et al. (2005) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.30507 · Cited by 15 · see citing works
Dynamics of the cell and its extracellular matrix-a simple mathematical approach
Saha, A. K., & Mazumdar, J. (2003) · IEEE Transactions on NanoBioscience · doi:10.1109/tnb.2003.813921 · Cited by 9 · see citing works
Myllylä, R., Tryggvason, K., Kivirikko, K. I., et al. (1981) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/0304-4165(81)90381-0 · Cited by 8 · see citing works
Pollok, J., & Vacanti, J. P. (1996) · PubMed · Cited by 6 · see citing works
[The state and perspective in bone regeneration].
Imai, Y., & Takaoka, K. (2008) · PubMed · Cited by 5 · see citing works
Osteogenic Influence of Lysine in Porous Hydroxyapatite Scaffold
Tsuji, N., Yoshikawa, M., Shimomura, Y., et al. (2007) · Key engineering materials · doi:10.4028/www.scientific.net/kem.361-363.1189 · Cited by 3 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Silk fibroin biomaterials for tissue regenerations
Kundu, B., Rajkhowa, R., Kundu, S. C., & Wang, X. (2013) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2012.09.043 · Cited by 1,391 · see citing works
High-strength silk protein scaffolds for bone repair
Mandal, B. B., Grinberg, A., Seok Gil, E., Panilaitis, B., & Kaplan, D. L. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1119474109 · Cited by 401 · see citing works
Self-citationScaffold degradation in bone tissue engineering: An overview
Tajvar, S., Hadjizadeh, A., & Samandari, S. S. (2023) · International Biodeterioration & Biodegradation · doi:10.1016/j.ibiod.2023.105599 · Cited by 291 · see citing works
Shahriarpanah, S., Nourmohammadi, J., & Amoabediny, G. (2016) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2016.09.045 · Cited by 72 · see citing works
Jung, S.-R., Song, N.-J., Yang, D. K., Cho, Y.-J., Kim, B.-J., Hong, J.-W., Yun, U. J., Jo, D.-G., Lee, Y. M., Choi, S. Y., et al. (2013) · Nutrition Research · doi:10.1016/j.nutres.2012.11.006 · Cited by 64 · see citing works
Recent Advances in Silk Fibroin-Based Composites for Bone Repair Applications: A Review
Zhu, S., Zhang, Q., Xu, X., Liu, Z., Cheng, G., Long, D., Cheng, L., & Dai, F. (2025) · Polymers · doi:10.3390/polym17060772 · Cited by 36 · see citing works
“Moreover, the study also found that silk fibroin hydrolysates can enhance the activity of alkaline phosphatase (ALP) in osteoblasts and their ability to undergo osteogenic differentiation [33].”
- Authors
- Park, S.-H., Gil, E. S., Shi, H., Kim, H. J., Lee, K., & Kaplan, D. L.
- Affiliations
- Tufts University (US)
- Corresponding author
- Kaplan, David L.
- Venue
- Biomaterials
- Publisher
- Elsevier BV
- Published
- 2010-08
- Volume
- 31
- Issue
- 24
- Pages
- 6162-6172
- ISSN
- 0142-9612 (ISSN-L)
- PMC
- PMC2891356
- OpenAlex
- W1977959012
- Cited by
- 196
- References
- 78
- Citations by year
- 2026: 14 · 2025: 20 · 2024: 9 · 2023: 14 · 2022: 14 · 2021: 16 · 2020: 12 · 2019: 13 · 2018: 10 · 2017: 6 · 2016: 10 · 2015: 10 · 2014: 11 · 2013: 8 · 2012: 11
- FWCI
- 7.00
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Biomaterials (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Ministry of Education and Human Resources Development (KRF-2007-357-D00296)
- National Institutes of Health (EB002520, EB003210P41)
- National Research Foundation of Korea
- Topics
- Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
- Physical Sciences › Materials Science › Biomaterials › Silk-based biomaterials and applications
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Keywords
- silk scaffolds, scaffold degradation rate, bone formation, bone marrow mesenchymal stem cells, bone regeneration, cellular metabolism, glucose utilization, lactic acid production, extracellular matrix mineralization, type I collagen
- MeSH terms
- Adult, Amino Acids, Cell Differentiation, Cells, Cultured, Culture Media, Gene Expression Regulation, Humans, Immunohistochemistry, Male, Models, Biological, Osteogenesis, RNA, Messenger, Biomarkers, Silk, Tissue Scaffolds, Mesenchymal Stem Cells
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