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Cited by in CrossRef
For: Bottino R, Trucco M. Use of genetically-engineered pig donors in islet transplantation. World J Transplant 2015; 5(4): 243-250 [PMID: 26722651 DOI: 10.5500/wjt.v5.i4.243]
URL: https://www.wjgnet.com/2220-3230/full/v5/i4/243.htm
Number Citing Articles
1
Rajeswar Chinnuswami, Abid Hussain, Gopalakrishnan Loganathan, Siddharth Narayanan, Gene D. Porter, Appakalai N. Balamurugan. Xenotransplantation - Comprehensive Study2020;  doi: 10.5772/intechopen.90437
2
Tian-Yu Lu, Xue-Ling Xu, Xu-Guang Du, Jin-Hua Wei, Jia-Nan Yu, Shou-Long Deng, Chuan Qin. Advances in Innate Immunity to Overcome Immune Rejection during XenotransplantationCells 2022; 11(23): 3865 doi: 10.3390/cells11233865
3
Yumin Li, Cong He, Rui Liu, Zhongdang Xiao, Bo Sun. Stem cells therapy for diabetes: from past to futureCytotherapy 2023; 25(11): 1125 doi: 10.1016/j.jcyt.2023.04.012
4
Hee Jung Kang, Haneulnari Lee, Eun Mi Park, Jong‐Min Kim, Byoung‐Hoon Min, Chung‐Gyu Park. D‐dimer level, in association with humoral responses, negatively correlates with survival of porcine islet grafts in non‐human primates with immunosuppressionXenotransplantation 2017; 24(3) doi: 10.1111/xen.12299
5
Wayne Hawthorne. Xenotransplantation - New Insights2017;  doi: 10.5772/intechopen.69379
6
Jessie M. Barra, Veronika Kozlovskaya, Jessica D. Kepple, Karen L. Seeberger, Purushothaman Kuppan, Chad S. Hunter, Gregory S. Korbutt, Eugenia Kharlampieva, Hubert M. Tse. Xenotransplantation of tannic acid‐encapsulated neonatal porcine islets decreases proinflammatory innate immune responsesXenotransplantation 2021; 28(6) doi: 10.1111/xen.12706
7
Anissa Gamble, Antonio Bruni, A.M. James Shapiro. Encyclopedia of Endocrine Diseases2019; : 259 doi: 10.1016/B978-0-12-801238-3.66107-X
8
Jessica D. Kepple, Jessie M. Barra, Martin E. Young, Chad S. Hunter, Hubert M. Tse. Islet transplantation into brown adipose tissue can delay immune rejectionJCI Insight 2022; 7(4) doi: 10.1172/jci.insight.152800
9
Hien Lau, Nicole Corrales, Samuel Rodriguez, Colleen Luong, Mohammadreza Mohammadi, Veria Khosrawipour, Shiri Li, Michael Alexander, Paul de Vos, Jonathan R. T. Lakey, Zoltán Rakonczay. Dose-dependent effects of necrostatin-1 supplementation to tissue culture media of young porcine isletsPLOS ONE 2020; 15(12): e0243506 doi: 10.1371/journal.pone.0243506
10
Nikolai Klymiuk, Barbara Ludwig, Jochen Seissler, Bruno Reichart, Eckhard Wolf. Current Concepts of Using Pigs as a Source for Beta-Cell Replacement Therapy of Type 1 DiabetesCurrent Molecular Biology Reports 2016; 2(2): 73 doi: 10.1007/s40610-016-0039-1
11
Jennifer Croden, Wenlong Huang, Gina R. Rayat. Xenotransplantation - New Insights2017;  doi: 10.5772/intechopen.68999
12
Karen L Seeberger, Bassem F Salama, Sandra Kelly, Mandy Rosko, Chelsea Castro, Jessica DesAulniers, Gregory S Korbutt. Heterogenous expression of endocrine and progenitor cells within the neonatal porcine pancreatic lobes–Implications for neonatal porcine islet xenotransplantationXenotransplantation 2023; 30(2) doi: 10.1111/xen.12793
13
Marco Farina, Jenolyn F. Alexander, Usha Thekkedath, Mauro Ferrari, Alessandro Grattoni. Cell encapsulation: Overcoming barriers in cell transplantation in diabetes and beyondAdvanced Drug Delivery Reviews 2019; 139: 92 doi: 10.1016/j.addr.2018.04.018
14
Hee Jung Kang, Haneulnari Lee, Eun Mi Park, Jong‐Min Kim, Jun‐Seop Shin, Chung‐Gyu Park. The value of glycated albumin for the prediction of graft outcome in the non‐human primate porcine islet transplantation modelXenotransplantation 2018; 25(2) doi: 10.1111/xen.12384
15
W.F. Kendall, E.C. Opara. Transplantation, Bioengineering, and Regeneration of the Endocrine Pancreas2020; : 761 doi: 10.1016/B978-0-12-814833-4.00061-7
16
Paul de Vos. Cell TherapyMolecular and Translational Medicine 2017; : 121 doi: 10.1007/978-3-319-57153-9_7
17
Maheswaran Dhanasekaran, Johnathan J. George, Gopalakrishnan Loganathan, Siddharth Narayanan, Michael G. Hughes, Stuart K. Williams, Appakalai N. Balamurugan. Pig islet xenotransplantationCurrent Opinion in Organ Transplantation 2017; 22(5): 452 doi: 10.1097/MOT.0000000000000455
18
Jeske Noordergraaf, Adrienne Schucker, Mike Martin, Henk‐jan Schuurman, Brianne Ordway, Kevin Cooley, Marie Sheffler, Kara Theis, Chasa Armstrong, Laura Klein, Doug Hansen, Megan Olson, Lisa Schlechter, Tom Spizzo. Pathogen elimination and prevention within a regulated, Designated Pathogen Free, closed pig herd for long‐term breeding and production of xenotransplantation materialsXenotransplantation 2018; 25(4) doi: 10.1111/xen.12428
19
Cheorl-Ho Kim. Glycoimmunology in Xenotransplantation2024; : 61 doi: 10.1007/978-981-99-7691-1_8
20
Alexandra M. Smink, Shiri Li, Don T. Hertsig, Bart J. de Haan, Leendert Schwab, Aart A. van Apeldoorn, Eelco de Koning, Marijke M. Faas, Jonathan R.T. Lakey, Paul de Vos. The Efficacy of a Prevascularized, Retrievable Poly(D,L,-lactide-co-ε-caprolactone) Subcutaneous Scaffold as Transplantation Site for Pancreatic IsletsTransplantation 2017; 101(4): e112 doi: 10.1097/TP.0000000000001663
21
Cheorl-Ho Kim. Glycoimmunology in Xenotransplantation2024; : 307 doi: 10.1007/978-981-99-7691-1_20
22
Juliet A. Emamaullee, Andrew Pepper, A.M. James Shapiro. Principles of Regenerative Medicine2019; : 987 doi: 10.1016/B978-0-12-809880-6.00056-4
23
Rana El Nahas, Mohammad Ameen Al-Aghbar, Laura Herrero, Nicholas van Panhuys, Meritxell Espino-Guarch. Applications of Genome-Editing Technologies for Type 1 DiabetesInternational Journal of Molecular Sciences 2023; 25(1): 344 doi: 10.3390/ijms25010344