English
Русский
English
References of the article: “In vitro models of thrombosis and hemostasis”
  1. Arterial thrombosis—insidious, unpredictable and deadly

    S. Jackson

    Nature Medicine. 2011, 17, 1423-1436

    https://doi.org/10.1038/nm.2515

    Article|Google Scholar

  2. Murine Models of Vascular Thrombosis

    R. Westrick, M. Winn, D. Eitzman

    Arteriosclerosis, Thrombosis, and Vascular Biology. 2007, 27, 2079-2093

    https://doi.org/10.1161/ATVBAHA.107.142810

    Article|Google Scholar

  3. High-throughput measurement of human platelet aggregation under flow: application in hemostasis and beyond

    S. Brouns, J. van Geffen, J. Heemskerk

    Platelets. 2018, 29, 662-669

    https://doi.org/10.1080/09537104.2018.1447660

    Article|Google Scholar

  4. The use of microfluidics in hemostasis

    K. Neeves, A. Onasoga, A. Wufsus

    Current Opinion in Hematology. 2013, 20, 417-423

    https://doi.org/10.1097/moh.0b013e3283642186

    Article|Google Scholar

  5. Subcommittee on Biorheology. In vitro flow‐based assay: From simple toward more sophisticated models for mimicking hemostasis and thrombosis.

    5. Mangin PH, Neeves KB, Lam WA, Cosemans JM, Korin N, Kerrigan SW, Panteleev MA

    Journal of Thrombosis and Haemostasis. 2021, 19, 582-7

    https://doi.org/10.1111/jth.15143

    Article|Google Scholar

  6. In Silico Hemostasis Modeling and Prediction

    D. Nechipurenko, A. Shibeko, A. Sveshnikova, M. Panteleev

    Hämostaseologie. 2020, 40, 524-535

    https://doi.org/10.1055/a-1213-2117

    Article|Google Scholar

  7. Microfluidic focal thrombosis model for measuring murine platelet deposition and stability: PAR4 signaling enhances shear-resistance of platelet aggregates

    K. NEEVES, S. MALONEY, K. FONG, A. SCHMAIER, M. KAHN, L. BRASS, S. DIAMOND

    Journal of Thrombosis and Haemostasis. 2008, 6, 2193-2201

    https://doi.org/10.1111/j.1538-7836.2008.03188.x

    Article|Google Scholar

  8. Side view thrombosis microfluidic device with controllable wall shear rate and transthrombus pressure gradient

    R. Muthard, S. Diamond

    Lab on a Chip. 2013, 13, 1883

    https://doi.org/10.1039/C3LC41332B

    Article|Google Scholar

  9. Tissue‐engineered 3D microvessel and capillary network models for the study of vascular phenomena

    M. Bogorad, J. DeStefano, A. Wong, P. Searson

    Microcirculation. 2017, 24,

    https://doi.org/10.1111/micc.12360

    Article|Google Scholar

  10. Microengineered human blood–brain barrier platform for understanding nanoparticle transport mechanisms

    S. Ahn, Y. Sei, H. Park, J. Kim, Y. Ryu, J. Choi, H. Sung, T. MacDonald, A. Levey, Y. Kim

    Nature Communications. 2020, 11,

    https://doi.org/10.1038/s41467-019-13896-7

    Article|Google Scholar

  11. Engineering of Hydrogel Materials with Perfusable Microchannels for Building Vascularized Tissues

    R. Xie, W. Zheng, L. Guan, Y. Ai, Q. Liang

    Small. 2020, 16, 1902838

    https://doi.org/10.1002/smll.201902838

    Article|Google Scholar

  12. Bioprinted thrombosis-on-a-chip

    Y. Zhang, F. Davoudi, P. Walch, A. Manbachi, X. Luo, V. Dell'Erba, A. Miri, H. Albadawi, A. Arneri, X. Li, X. Wang, M. Dokmeci, A. Khademhosseini, R. Oklu

    Lab on a Chip. , 16, 4097-4105

    https://doi.org/10.1039/C6LC00380J

    Article|Google Scholar

  13. Pharmacological Blockade of Glycoprotein VI Promotes Thrombus Disaggregation in the Absence of Thrombin

    M. Ahmed, V. Kaneva, S. Loyau, D. Nechipurenko, N. Receveur, M. Le Bris, E. Janus-Bell, M. Didelot, A. Rauch, S. Susen, N. Chakfé, F. Lanza, E. Gardiner, R. Andrews, M. Panteleev, C. Gachet, M. Jandrot-Perrus, P. Mangin

    Arteriosclerosis, Thrombosis, and Vascular Biology. 2020, 40, 2127-2142

    https://doi.org/10.1161/ATVBAHA.120.314301

    Article|Google Scholar

  14. Clot Contraction Drives the Translocation of Procoagulant Platelets to Thrombus Surface

    D. Nechipurenko, N. Receveur, A. Yakimenko, T. Shepelyuk, A. Yakusheva, R. Kerimov, S. Obydennyy, A. Eckly, C. Léon, C. Gachet, E. Grishchuk, F. Ataullakhanov, P. Mangin, M. Panteleev

    Arteriosclerosis, Thrombosis, and Vascular Biology. 2019, 39, 37-47

    https://doi.org/10.1161/ATVBAHA.118.311390

    Article|Google Scholar

  15. Core and shell platelets of a thrombus: A new microfluidic assay to study mechanics and biochemistry

    M. DeCortin, L. Brass, S. Diamond

    Research and Practice in Thrombosis and Haemostasis. 2020, 4, 1158-1166

    https://doi.org/10.1002/rth2.12405

    Article|Google Scholar

  16. Coagulation factors bound to procoagulant platelets concentrate in cap structures to promote clotting

    N. Podoplelova, A. Sveshnikova, Y. Kotova, A. Eckly, N. Receveur, D. Nechipurenko, S. Obydennyi, I. Kireev, C. Gachet, F. Ataullakhanov, P. Mangin, M. Panteleev

    Blood. 2016, 128, 1745-1755

    https://doi.org/10.1182/blood-2016-02-696898

    Article|Google Scholar

  17. Platelet Control of Fibrin Distribution and Microelasticity in Thrombus Formation Under Flow

    F. Swieringa, C. Baaten, R. Verdoold, T. Mastenbroek, N. Rijnveld, K. van der Laan, E. Breel, P. Collins, M. Lancé, Y. Henskens, J. Cosemans, J. Heemskerk, P. van der Meijden

    Arteriosclerosis, Thrombosis, and Vascular Biology. 2016, 36, 692-699

    https://doi.org/10.1161/ATVBAHA.115.306537

    Article|Google Scholar

  18. Contribution of platelet glycoprotein VI to the thrombogenic effect of collagens in fibrous atherosclerotic lesions

    J. Cosemans, M. Kuijpers, C. Lecut, S. Loubele, S. Heeneman, M. Jandrot-Perrus, J. Heemskerk

    Atherosclerosis. 2005, 181, 19-27

    https://doi.org/10.1016/j.atherosclerosis.2004.12.037

    Article|Google Scholar

  19. Identification of platelet function defects by multi-parameter assessment of thrombus formation

    S. de Witt, F. Swieringa, R. Cavill, M. Lamers, R. van Kruchten, T. Mastenbroek, C. Baaten, S. Coort, N. Pugh, A. Schulz, I. Scharrer, K. Jurk, B. Zieger, K. Clemetson, R. Farndale, J. Heemskerk, J. Cosemans

    Nature Communications. 2014, 5,

    https://doi.org/10.1038/ncomms5257

    Article|Google Scholar

  20. Atherosclerotic geometries exacerbate pathological thrombus formation poststenosis in a von Willebrand factor-dependent manner

    E. Westein, A. van der Meer, M. Kuijpers, J. Frimat, A. van den Berg, J. Heemskerk

    Proceedings of the National Academy of Sciences. 2013, 110, 1357-1362

    https://doi.org/10.1073/pnas.1209905110

    Article|Google Scholar

  21. A shear gradient–dependent platelet aggregation mechanism drives thrombus formation

    W. Nesbitt, E. Westein, F. Tovar-Lopez, E. Tolouei, A. Mitchell, J. Fu, J. Carberry, A. Fouras, S. Jackson

    Nature Medicine. 2009, 15, 665-673

    https://doi.org/10.1038/nm.1955

    Article|Google Scholar

  22. Shear rate gradients promote a bi-phasic thrombus formation on weak adhesive proteins, such as fibrinogen in a von Willebrand factor-dependent manner.

    Receveur, Nicolas, Dmitry Nechipurenko, Yannick Knapp, Aleksandra Yakusheva, Eric Maurer, Cécile V. Denis, François Lanza, Mikhail Panteleev, Christian Gachet, and Pierre H. Mangin.

    Haematologica. 2020, 105,

    https://doi.org/10.3324/haematol.2019.235754

    Article|Google Scholar

  23. Thrombin Flux and Wall Shear Rate Regulate Fibrin Fiber Deposition State during Polymerization under Flow

    K. Neeves, D. Illing, S. Diamond

    Biophysical Journal. 2010, 98, 1344-1352

    https://doi.org/10.1016/j.bpj.2009.12.4275

    Article|Google Scholar

  24. Thrombin generation and fibrin formation under flow on biomimetic tissue factor-rich surfaces

    A. Onasoga-Jarvis, T. Puls, S. O'Brien, L. Kuang, H. Liang, K. Neeves

    Journal of Thrombosis and Haemostasis. 2014, 12, 373-382

    https://doi.org/10.1111/jth.12491

    Article|Google Scholar

  25. Impact of Tissue Factor Localization on Blood Clot Structure and Resistance under Venous Shear

    V. Govindarajan, S. Zhu, R. Li, Y. Lu, S. Diamond, J. Reifman, A. Mitrophanov

    Biophysical Journal. 2018, 114, 978-991

    https://doi.org/10.1016/j.bpj.2017.12.034

    Article|Google Scholar

  26. Dynamics of Blood Flow and Thrombus Formation in a Multi-Bypass Microfluidic Ladder Network

    J. Zilberman-Rudenko, J. Sylman, H. Lakshmanan, O. McCarty, J. Maddala

    Cellular and Molecular Bioengineering. 2017, 10, 16-29

    https://doi.org/10.1007/s12195-016-0470-7

    Article|Google Scholar

  27. High Shear Thrombus Formation under Pulsatile and Steady Flow

    L. Casa, D. Ku

    Cardiovascular Engineering and Technology. 2014, 5, 154-163

    https://doi.org/10.1007/s13239-014-0180-z

    Article|Google Scholar

  28. The influence of the pulsatility of the blood flow on the extent of platelet adhesion.

    Zhao XM, Wu YP, Cai HX, Wei R, Lisman T, Han JJ, Xia ZL, de Groot PG

    Thrombosis research. 2008, 121, 821-5

    https://doi.org/10.1016/j.thromres.2007.07.013

    Article|Google Scholar

  29. A novel mouse-driven ex vivo flow chamber for the study of leukocyte and platelet function

    A. Hafezi-Moghadam, K. Thomas, C. Cornelssen

    American Journal of Physiology-Cell Physiology. 2004, 286, C876-C892

    https://doi.org/10.1152/ajpcell.00500.2003

    Article|Google Scholar

  30. Platelets Drive Thrombus Propagation in a Hematocrit and Glycoprotein VI–Dependent Manner in an In Vitro Venous Thrombosis Model

    M. Lehmann, R. Schoeman, P. Krohl, A. Wallbank, J. Samaniuk, M. Jandrot-Perrus, K. Neeves

    Arteriosclerosis, Thrombosis, and Vascular Biology. 2018, 38, 1052-1062

    https://doi.org/10.1161/ATVBAHA.118.310731

    Article|Google Scholar

  31. Point-of-Care Diagnostic Assays and Novel Preclinical Technologies for Hemostasis and Thrombosis

    C. Caruso, W. Lam

    Seminars in Thrombosis and Hemostasis. 2021, 47, 120-128

    https://doi.org/10.1055/s-0041-1723798

    Article|Google Scholar

  32. A Microfluidic Model of Hemostasis Sensitive to Platelet Function and Coagulation

    R. Schoeman, K. Rana, N. Danes, M. Lehmann, J. Di Paola, A. Fogelson, K. Leiderman, K. Neeves

    Cellular and Molecular Bioengineering. 2017, 10, 3-15

    https://doi.org/10.1007/s12195-016-0469-0

    Article|Google Scholar

  33. A microengineered vascularized bleeding model that integrates the principal components of hemostasis

    Y. Sakurai, E. Hardy, B. Ahn, R. Tran, M. Fay, J. Ciciliano, R. Mannino, D. Myers, Y. Qiu, M. Carden, W. Baldwin, S. Meeks, G. Gilbert, S. Jobe, W. Lam

    Nature Communications. 2018, 9,

    https://doi.org/10.1038/s41467-018-02990-x

    Article|Google Scholar

  34. A Human Vascular Injury‐on‐a‐Chip Model of Hemostasis

    I. Poventud‐Fuentes, K. Kwon, J. Seo, M. Tomaiuolo, T. Stalker, L. Brass, D. Huh

    Small. 2021, 17, 2004889

    https://doi.org/10.1002/smll.202004889

    Article|Google Scholar