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5. Basic Bone Biology

Author

Allen, Matthew R., Metzger, Corinne E., Ahn, Jaimo, Hankenson, Kurt D., Guastaldi, Fernando P.S., editor, and Mahadik, Bhushan, editor

Published
2022
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8. Osteoporosis GWAS-implicated DNM3 locus contextually regulates osteoblastic and chondrogenic fate of mesenchymal stem/progenitor cells through oscillating miR-199a-5p levels

Author

Kaur, Gurcharan, primary, Pippin, James A, additional, Chang, Solomon, additional, Redmond, Justin, additional, Chesi, Alessandra, additional, Wells, Andrew D, additional, Maerz, Tristan, additional, Grant, Struan F A, additional, Coleman, Rhima M, additional, Hankenson, Kurt D, additional, and Wagley, Yadav, additional

Published
2024
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9. Cellular biology of fracture healing

Author

Bahney, Chelsea S, Zondervan, Robert L, Allison, Patrick, Theologis, Alekos, Ashley, Jason W, Ahn, Jaimo, Miclau, Theodore, Marcucio, Ralph S, and Hankenson, Kurt D

Subjects
Genetics, Regenerative Medicine, Stem Cell Research - Nonembryonic - Non-Human, Stem Cell Research, Physical Injury - Accidents and Adverse Effects, Osteoporosis, 5.2 Cellular and gene therapies, Underpinning research, Development of treatments and therapeutic interventions, 2.1 Biological and endogenous factors, 1.1 Normal biological development and functioning, Aetiology, Musculoskeletal, Animals, Bony Callus, Chondrocytes, Endothelial Progenitor Cells, Fracture Healing, Humans, Mesenchymal Stem Cells, Neovascularization, Physiologic, Osteoblasts, Osteoclasts, Osteogenesis, Signal Transduction, bone repair, fracture healing, bone regeneration, Biomedical Engineering, Clinical Sciences, Human Movement and Sports Sciences, Orthopedics
Abstract

The biology of bone healing is a rapidly developing science. Advances in transgenic and gene-targeted mice have enabled tissue and cell-specific investigations of skeletal regeneration. As an example, only recently has it been recognized that chondrocytes convert to osteoblasts during healing bone, and only several years prior, seminal publications reported definitively that the primary tissues contributing bone forming cells during regeneration were the periosteum and endosteum. While genetically modified animals offer incredible insights into the temporal and spatial importance of various gene products, the complexity and rapidity of healing-coupled with the heterogeneity of animal models-renders studies of regenerative biology challenging. Herein, cells that play a key role in bone healing will be reviewed and extracellular mediators regulating their behavior discussed. We will focus on recent studies that explore novel roles of inflammation in bone healing, and the origins and fates of various cells in the fracture environment. © 2018 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res.

Published
2019

13. Stimulating Fracture Healing in Ischemic Environments: Does Oxygen Direct Stem Cell Fate during Fracture Healing?

Author

Miclau, Katherine R, Brazina, Sloane A, Bahney, Chelsea S, Hankenson, Kurt D, Hunt, Thomas K, Marcucio, Ralph S, and Miclau, Theodore

Subjects
Medical Biotechnology, Biomedical and Clinical Sciences, Physical Injury - Accidents and Adverse Effects, Stem Cell Research - Nonembryonic - Non-Human, Stem Cell Research, Regenerative Medicine, 1.1 Normal biological development and functioning, Underpinning research, Development of treatments and therapeutic interventions, 5.2 Cellular and gene therapies, Musculoskeletal, fractures, bone, repair, ischemia, oxygen, stem cell, differentiation, stimulation, Biological sciences, Biomedical and clinical sciences
Abstract

Bone fractures represent an enormous societal and economic burden as one of the most prevalent causes of disability worldwide. Each year, nearly 15 million people are affected by fractures in the United States alone. Data indicate that the blood supply is critical for fracture healing; as data indicate that concomitant bone and vascular injury are major risk factors for non-union. However, the various role(s) that the vasculature plays remains speculative. Fracture stabilization dictates stem cell fate choices during repair. In stabilized fractures stem cells differentiate directly into osteoblasts and heal the injury by intramembranous ossification. In contrast, in non-stable fractures stem cells differentiate into chondrocytes and the bone heals through endochondral ossification, where a cartilage template transforms into bone as the chondrocytes transform into osteoblasts. One suggested role of the vasculature has been to participate in the stem cell fate decisions due to delivery of oxygen. In stable fractures, the blood vessels are thought to remain intact and promote osteogenesis, while in non-stable fractures, continual disruption of the vasculature creates hypoxia that favors formation of cartilage, which is avascular. However, recent data suggests that non-stable fractures are more vascularized than stable fractures, that oxygen does not appear associated with differentiation of stem cells into chondrocytes and osteoblasts, that cartilage is not hypoxic, and that oxygen, not sustained hypoxia, is required for angiogenesis. These unexpected results, which contrast other published studies, are indicative of the need to better understand the complex, spatio-temporal regulation of vascularization and oxygenation in fracture healing. This work has also revealed that oxygen, along with the promotion of angiogenesis, may be novel adjuvants that can stimulate healing in select patient populations.

Published
2017

14. An Intact Periosteum is Required for Recombinant Human Jagged1 Guided Bone Regeneration in Calvaria Critical-size Defect Healing

Author

Senos, Rafael, Chen, Matheus Ton Yan, Panse, Isabella, Stella, Jose Joaquin, and Hankenson, Kurt D.

Abstract

The need to promote calvaria bone healing as a consequence of injury or craniotomy is a major clinical issue. Previous reports tested recombinant human Jagged1 (rhJagged1) treatment for critical-size calvaria defects in the absence of periosteum, and this resulted in significant new bone formation. As the periosteum contributes to healing by serving as a source of progenitor cells, the present study aimed to examine whether significantly more bone is formed when the periosteum is intact for using rhJagged1 to treat critical-size parietal bone defects in mice. Fifteen healthy adult mice, 34 to 65 weeks of age, 26.9 to 48.2 g, were divided into different groups that compared the critical-size defects treated with either phosphate-buffered saline or rhJagged1 protein in either the presence or absence of periosteum. The results indicated that more bone was formed in the presence of periosteum when rhJagged1 is delivered [35% bone volume per tissue volume (BV/TV); P= 0.02] relative to nonperiosteum. Recombinant human Jagged1 protein delivered in the absence of periosteum had the next most new bone formed (25% BV/TV). Defects with phosphate-buffered saline delivered in the absence or presence of periosteum had the least new bone formed (15% and 18% BV/TV, respectively; P= 0.48). The results also show that rhJagged1 does not form ectopic or hypertrophic bone. The usage of rhJagged1 to treat critical-size defects in calvaria is promising clinically, but to maximize clinical efficacy it will require that the periosteum be intact on the noninjured portions of calvaria.

Published
2024
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16. Regulating the proinflammatory response to implanted composite biomaterials comprising polylactide and hydroxyapatite by targeting immunometabolism

Author

Maduka, Chima V, primary, Makela, Ashley V, additional, Ural, Evran, additional, Stivers, Katlin B, additional, Kuhnert, Maxwell M, additional, Tundo, Anthony, additional, Alhaj, Mohammed, additional, Hoque Apu, Ehsanul, additional, Ashammakhi, Nureddin, additional, Hankenson, Kurt D, additional, Narayan, Ramani, additional, Elisseeff, Jennifer H, additional, and Contag, Christopher H, additional

Published
2023
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17. Genome-wide association study implicates novel loci and reveals candidate effector genes for longitudinal pediatric bone accrual

Author

Cousminer, Diana L., Wagley, Yadav, Pippin, James A., Elhakeem, Ahmed, Way, Gregory P., Pahl, Matthew C., McCormack, Shana E., Chesi, Alessandra, Mitchell, Jonathan A., Kindler, Joseph M., Baird, Denis, Hartley, April, Howe, Laura, Kalkwarf, Heidi J., Lappe, Joan M., Lu, Sumei, Leonard, Michelle E., Johnson, Matthew E., Hakonarson, Hakon, Gilsanz, Vicente, Shepherd, John A., Oberfield, Sharon E., Greene, Casey S., Kelly, Andrea, Lawlor, Deborah A., Voight, Benjamin F., Wells, Andrew D., Zemel, Babette S., Hankenson, Kurt D., and Grant, Struan F. A.

Published
2021
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18. Polylactide Degradation Activates Immune Cells by Metabolic Reprogramming

Author

Maduka, Chima V., primary, Alhaj, Mohammed, additional, Ural, Evran, additional, Habeeb, Oluwatosin M., additional, Kuhnert, Maxwell M., additional, Smith, Kylie, additional, Makela, Ashley V., additional, Pope, Hunter, additional, Chen, Shoue, additional, Hix, Jeremy M., additional, Mallett, Christiane L., additional, Chung, Seock‐Jin, additional, Hakun, Maxwell, additional, Tundo, Anthony, additional, Zinn, Kurt R., additional, Hankenson, Kurt D., additional, Goodman, Stuart B., additional, Narayan, Ramani, additional, and Contag, Christopher H., additional

Published
2023
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19. 3D genomic features across >50 diverse cell types reveal insights into the genomic architecture of childhood obesity

Author

Trang, Khanh B, primary, Pahl, Matthew C, additional, Pippin, James A, additional, Su, Chun, additional, Littleton, Sheridan H, additional, Sharma, Prabhat, additional, Kulkarni, Nikhil N, additional, Ghanem, Louis R, additional, Terry, Natalie A, additional, O'Brien, Joan M, additional, Wagley, Yadav, additional, Hankenson, Kurt D, additional, Jermusyk, Ashley, additional, Hoskins, Jason W, additional, Amundadottir, Laufey T, additional, Xu, Mai, additional, Brown, Kevin M, additional, Anderson, Stewart A, additional, Yang, Wenli, additional, Titchenell, Paul M, additional, Seale, Patrick, additional, Cook, Laura, additional, Levings, Megan K, additional, Zemel, Babette S, additional, Chesi, Alessandra, additional, Wells, Andrew D, additional, and Grant, Struan FA, additional

Published
2023
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20. Immunometabolic cues recompose and reprogram the microenvironment around biomaterials

Author

Maduka, Chima V, primary, Schmitter-Sanchez, Axel D, additional, Makela, Ashley V, additional, Ural, Evran, additional, Stivers, Katlin B, additional, Pope, Hunter, additional, Kuhnert, Maxwell M, additional, Habeeb, Oluwatosin M, additional, Tundo, Anthony, additional, Alhaj, Mohammed, additional, Kiselev, Artem, additional, Chen, Shoue, additional, Olive, Andrew J, additional, Hankenson, Kurt D D, additional, Narayan, Ramani, additional, Park, Sangbum, additional, Elisseeff, Jennifer H, additional, and Contag, Christopher H, additional

Published
2023
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21. List of Contributors

Author

Abraham, David, primary, Almeida, Maria, additional, Ambrogini, Elena, additional, Arnold, Andrew, additional, Bakos, Bence, additional, Bergwitz, Clemens, additional, Bikle, Daniel D., additional, Bilezikian, John P., additional, Binkley, Neil, additional, Bisello, Alessandro, additional, Bonewald, L.F., additional, Bou-Gharios, George, additional, Bouillon, Roger, additional, Bouxsein, Mary L., additional, Boyce, Brendan F., additional, Boyd, Steven, additional, Brandi, Maria Luisa, additional, Burr, David B., additional, Calvi, Laura M., additional, Canalis, Ernesto, additional, Cao, Xu, additional, Carmeliet, Geert, additional, Carpenter, Thomas O., additional, Chang, Wenhan, additional, Chim, Shek Man, additional, Choudhary, Shilpa, additional, Christakos, Sylvia, additional, Chun, Yong-Hee Patricia, additional, Cipriani, Cristiana, additional, Civitelli, Roberto, additional, Clemens, Thomas L., additional, Collins, Michael T., additional, Conte, Caterina, additional, Cooper, Mark S., additional, Cornish, Jillian, additional, Cremers, Serge, additional, Dawson-Hughes, Bess, additional, de Crombrugghe, Benoit, additional, DeLuca, Hector F., additional, Dempster, David W., additional, Drake, Matthew T., additional, Ducy, Patricia, additional, Ebetino, Frank H., additional, Engelke, Klaus, additional, Erben, Reinhold G., additional, Eyre, David R., additional, Farber, Charles R., additional, Feigenson, Marina, additional, Ferron, Mathieu, additional, Florenzano, Pablo, additional, Fontana, Francesca, additional, Foster, Brian L., additional, Friedman, Peter A., additional, Fukumoto, Seiji, additional, Gamer, Laura W., additional, Gardella, Thomas J., additional, Garnero, Patrick, additional, Genant, Harry K., additional, Giusti, Francesca, additional, Göbel, Andy, additional, Goltzman, David, additional, Gorski, Jeffrey P., additional, Griffith, James, additional, G Russell, R. Graham, additional, Hankenson, Kurt D., additional, Hannan, Fadil M., additional, Harris, Stephen E., additional, Hartley, Iris R., additional, Hartmann, Christine, additional, Heaney, Robert P., additional, Hendy, Geoffrey N., additional, Hilton, Matthew J., additional, Hofbauer, Lorenz C., additional, Holdsworth, Gill, additional, Hsu, Yi-Hsiang, additional, Hudson, David M., additional, Hurley, Marja, additional, Insogna, Karl L., additional, Jilka, Robert L., additional, Johnson, Mark L., additional, Johnson, Rachelle W., additional, Jones, Glenville, additional, Judex, Stefan, additional, Jüppner, Harald, additional, Kalajzic, Ivo, additional, Karsenty, Gérard, additional, Ke, Hua Zhu, additional, Khosla, Sundeep, additional, Kiel, Douglas P., additional, Klein-Nulend, J., additional, Ko, Frank C., additional, Kobayashi, Yasuhiro, additional, Konrad, Martin, additional, Kostenuik, Paul J., additional, Kovacs, Christopher S., additional, Kremer, Richard, additional, Krishnan, Venkatesh, additional, Kronenberg, Henry M., additional, Lakatos, Peter A., additional, Liberman, Uri A., additional, Lorenzo, Joseph A., additional, Lynch, Conor C., additional, Lyons, Karen M., additional, Ma, Y. Linda, additional, Maes, Christa, additional, Mannstadt, Michael, additional, Manolagas, Stavros, additional, Marcus, Robert, additional, Maridas, David E., additional, Marie, Pierre J., additional, Marini, Francesca, additional, Markovac, Jasna, additional, Martin, T. John, additional, Matthews, Brya G., additional, Maurizi, Antonio, additional, Mirfakhraee, Sasan, additional, Moe, Sharon M., additional, Monroe, David G., additional, Moreira, Carolina A., additional, Müller, Ralph, additional, Musson, David S., additional, Nakatani, Teruyo, additional, Naot, Dorit, additional, Napoli, Nicola, additional, Naveh-Many, Tally, additional, Nemeth, Edward F., additional, Nickolas, Thomas L., additional, Ominsky, Michael S., additional, Ono, Noriaki, additional, Ornitz, David M., additional, Partridge, Nicola C., additional, Patel, Vihitaben S., additional, Pike, J. Wesley, additional, Pilbeam, Carol, additional, Plum, Lori, additional, Potts, John T., additional, Puzas, J. Edward, additional, Rachner, Tilman D., additional, Rakian, Audrey, additional, Rakian, Rubie, additional, Renthal, Nora E., additional, Rhoades (Sterling), Julie A., additional, Riminucci, Mara, additional, Roberts, Scott J., additional, Robey, Pamela Gehron, additional, Rogers, Michael J., additional, Roodman, G. David, additional, Rosen, Clifford J., additional, Rosen, Vicki, additional, Rowe, David W., additional, Rubin, Janet, additional, Rubin, Clinton T., additional, Schlingmann, Karl P., additional, Seeman, Ego, additional, Seibel, Markus J., additional, Sempos, Chris, additional, Shoback, Dolores M., additional, Silve, Caroline, additional, Silver, Justin, additional, Sims, Natalie A., additional, Singer, Frederick R., additional, Stains, Joseph P., additional, Stegen, Steve, additional, Stern, Paula H., additional, Tabacco, Gaia, additional, Takacs, Istvan, additional, Takahashi, Naoyuki, additional, Tay, Donovan, additional, Teti, Anna, additional, Thakker, Rajesh V., additional, Tomlinson, Ryan E., additional, Tonelli, Francesco, additional, Towler, Dwight A., additional, Tsourdi, Elena, additional, Tu, Chia-Ling, additional, Udagawa, Nobuyuki, additional, Weaver, Connie M., additional, Wein, Marc N., additional, Weinstein, Lee S., additional, Weis, MaryAnn, additional, Whyte, Michael P., additional, Williams, Bart O., additional, Xu, Xin, additional, Yakar, Shoshana, additional, Yang, Yingzi, additional, Zanotti, Stefano, additional, and Zhou, Hong, additional

Published
2020
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26. Tailored Coatings for Enhanced Performance of Zinc–Magnesium Alloys in Absorbable Implants

Author

Hernández-Escobar, David, Pajares-Chamorro, Natalia, Chatzistavrou, Xanthippi, Hankenson, Kurt D., Hammer, Neal D., and Boehlert, Carl J.

Abstract

Absorbable metals exhibit potential for next-generation temporary medical implants, dissolving safely in the body during tissue healing and regeneration. Their commercial incorporation could substantially diminish the need for additional surgeries and complications that are tied to permanent devices. Despite extensive research on magnesium (Mg) and iron (Fe), achieving the optimal combination of mechanical properties, biocompatibility, and controlled degradation rate for absorbable implants remains a challenge. Zinc (Zn) and Zn-based alloys emerged as an attractive alternative for absorbable implants, due to favorable combination of in vivobiocompatibility and degradation behavior. Moreover, the development of suitable coatings can enhance their biological characteristics and tailor their degradation process. In this work, four different biodegradable coatings (based on zinc phosphate (ZnP), collagen (Col), and Ag-doped bioactive glass nanoparticles (AgBGNs)) were synthesized by chemical conversion, spin-coating, or a combination of both on Zn-3Mg substrates. This study assessed the impact of the coatings on in vitrodegradation behavior, cytocompatibility, and antibacterial activity. The ZnP-coated samples demonstrated controlled weight loss and a decreased corrosion rate over time, maintaining a physiological pH. Extracts from the uncoated, ZnP-coated, and Col-AgBGN-coated samples showed higher cell viability with increasing concentration. Bacterial viability was significantly impaired in all coated samples, particularly in the Col-AgBGN coating. This study showcases the potential of a strategic material-coating combination to effectively tackle multiple challenges encountered in current medical implant technologies by modifying the properties of absorbable metals to tailor patient treatments.

Published
2024
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28. Comparison of true blood loss between short and long cephalomedullary nail fixation of geriatric hip fractures, a retrospective cohort study.

Author

Schaffer, Nathaniel E., Singh, Manak, McHugh, Michael A., Perdue, Aaron M., Ahn, Jaimo, MOTR Collaborative, Alford, Andrea I., Davenport, Ryan, Eichman, Jack, Farrar, Nicholas, Fuster, Francisco, Guthrie, S. Trent, Hakeos, William M., Hankenson, Kurt D., Hoegler, Joseph J., Muscatelli, Stefano R., Offerman, Alexandra, Piche, Joshua, Walley, Kempland C., and Weick, Jack

Subjects
ORTHOPEDIC implants, CONFIDENCE intervals, BLOOD transfusion, HIP fractures, RETROSPECTIVE studies, ACQUISITION of data, REGRESSION analysis, COMPARATIVE studies, FRACTURE fixation, MEDICAL records, DESCRIPTIVE statistics, RESEARCH funding, BLOOD loss estimation, ELDER care, LONGITUDINAL method, OLD age
Abstract

Purpose: Existing literature is discrepant on the differences in blood loss and need for transfusion between short and long cephalomedullary nails used for extracapsular geriatric hip fractures. However, prior studies used the inaccurate estimated rather than the more accurate 'calculated' blood loss based on hematocrit dilution (Gibon in IO 37:735–739, 2013, Mercuriali in CMRO 13:465–478, 1996). This study sought to clarify whether use of short nails is associated with clinically meaningful reductions in calculated blood loss and resultant need for transfusion. Methods: A retrospective cohort study using bivariate and propensity score-weighted linear regression analyses was conducted examining 1442 geriatric (ages 60–105) patients undergoing cephalomedullary fixation of extracapsular hip fractures over 10 years at two trauma centers. Implant dimensions, pre and postoperative laboratory values, preoperative medications, and comorbidities were recorded. Two groups were compared based on nail length (greater or less than 235 mm). Results: Short nails were associated with a 26% reduction in calculated blood loss (95% confidence interval: 17–35%; p < 10–14) and a 24-min (36%) reduction in mean operative time (95% confidence interval: 21–26 min; p < 10–71). The absolute reduction in transfusion risk was 21% (95% confidence interval: 16–26%; p < 10–13) yielding a number needed to treat of 4.8 (95% confidence interval: 3.9–6.4) with short nails to prevent one transfusion. No difference in reoperation, periprosthetic fracture, or mortality was noted between groups. Conclusion: Use of short compared to long cephalomedullary nails for geriatric extracapsular hip fractures confers reduced blood loss, need for transfusion, and operative time without a difference in complications. [ABSTRACT FROM AUTHOR]

Published
2023
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33. Constitutive bone marrow adipocytes suppress local bone formation

Author

Li, Ziru, primary, Bagchi, Devika P., additional, Zhu, Junxiong, additional, Bowers, Emily, additional, Yu, Hui, additional, Hardij, Julie, additional, Mori, Hiroyuki, additional, Granger, Katrina, additional, Skjaerlund, Jon, additional, Mandair, Gurjit, additional, Abrishami, Simin, additional, Singer, Kanakadurga, additional, Hankenson, Kurt D., additional, Rosen, Clifford J., additional, and MacDougald, Ormond A., additional

Published
2022
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36. Synovial fibroblasts assume distinct functional identities and secrete R-spondin 2 in osteoarthritis

Author

Knights, Alexander J, primary, Farrell, Easton C, additional, Ellis, Olivia M, additional, Lammlin, Lindsey, additional, Junginger, Lucas M, additional, Rzeczycki, Phillip M, additional, Bergman, Rachel F, additional, Pervez, Rida, additional, Cruz, Monique, additional, Knight, Eleanor, additional, Farmer, Dennis, additional, Samani, Alexa A, additional, Wu, Chia-Lung, additional, Hankenson, Kurt D, additional, and Maerz, Tristan, additional

Published
2022
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37. Polylactide Degradation Activates Immune Cells by Metabolic Reprogramming

Author

Maduka, Chima V., primary, Alhaj, Mohammed, additional, Ural, Evran, additional, Habeeb, Michael O., additional, Kuhnert, Maxwell M., additional, Smith, Kylie, additional, Makela, Ashley V., additional, Pope, Hunter, additional, Chen, Shoue, additional, Hix, Jeremy M., additional, Mallett, Christiane L., additional, Chung, Seock-Jin, additional, Hakun, Maxwell, additional, Tundo, Anthony, additional, Zinn, Kurt R., additional, Hankenson, Kurt D., additional, Goodman, Stuart B., additional, Narayan, Ramani, additional, and Contag, Christopher H., additional

Published
2022
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43. Lipolysis of bone marrow adipocytes is required to fuel bone and the marrow niche during energy deficits

Author

Li, Ziru, primary, Bowers, Emily, additional, Zhu, Junxiong, additional, Yu, Hui, additional, Hardij, Julie, additional, Bagchi, Devika P, additional, Mori, Hiroyuki, additional, Lewis, Kenneth T, additional, Granger, Katrina, additional, Schill, Rebecca L, additional, Romanelli, Steven M, additional, Abrishami, Simin, additional, Hankenson, Kurt D, additional, Singer, Kanakadurga, additional, Rosen, Clifford J, additional, and MacDougald, Ormond A, additional

Published
2022
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44. Author response: Lipolysis of bone marrow adipocytes is required to fuel bone and the marrow niche during energy deficits

Author

Li, Ziru, primary, Bowers, Emily, additional, Zhu, Junxiong, additional, Yu, Hui, additional, Hardij, Julie, additional, Bagchi, Devika P, additional, Mori, Hiroyuki, additional, Lewis, Kenneth T, additional, Granger, Katrina, additional, Schill, Rebecca L, additional, Romanelli, Steven M, additional, Abrishami, Simin, additional, Hankenson, Kurt D, additional, Singer, Kanakadurga, additional, Rosen, Clifford J, additional, and MacDougald, Ormond A, additional

Published
2022
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45. Synovial fibroblasts assume distinct functional identities and secrete R-spondin 2 to drive osteoarthritis

Author

Knights, Alexander J., primary, Farrell, Easton C., additional, Ellis, Olivia M., additional, Lammlin, Lindsey, additional, Junginger, Lucas M., additional, Rzeczycki, Phillip M., additional, Bergman, Rachel F., additional, Pervez, Rida, additional, Cruz, Monique, additional, Samani, Alexa A., additional, Wu, Chia-Lung, additional, Hankenson, Kurt D., additional, and Maerz, Tristan, additional

Published
2022
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47. Notch signaling enhances bone regeneration in the zebrafish mandible

Author

Kraus, Jessica M., primary, Giovannone, Dion, additional, Rydzik, Renata, additional, Balsbaugh, Jeremy L., additional, Moss, Isaac L., additional, Schwedler, Jennifer L., additional, Bertrand, Julien Y., additional, Traver, David, additional, Hankenson, Kurt D., additional, Crump, J. Gage, additional, and Youngstrom, Daniel W., additional

Published
2022
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