Clinical trial NCT02824471 - References

Sickle Cell Disease — Sickle Cell Disease Biofluid Chip Technology (SCD BioChip)

Citation(s)

•   Almeida CB, Scheiermann C, Jang JE, Prophete C, Costa FF, Conran N, Frenette PS
  Hydroxyurea and a cGMP-amplifying agent have immediate benefits on acute vaso-occlusive events in sickle cell disease mice. Blood. 2012 Oct 4;120(14):2879-88. doi: 10.1182/blood-2012-02-409524. Epub 2012 Jul 25.
•   Anjum F, Lazar J, Zein J, Jamaleddine G, Demetis S, Wadgaonkar R
  Characterization of altered patterns of endothelial progenitor cells in sickle cell disease related pulmonary arterial hypertension. Pulm Circ. 2012 Jan-Mar;2(1):54-60. doi: 10.4103/2045-8932.94834.
•   Ayyappan, S
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  Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans. Blood. 2012 Aug 30;120(9):1961-2. doi: 10.1182/blood-2012-06-432849. No abstract available.
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•   Barabino GA, McIntire LV, Eskin SG, Sears DA, Udden M
  Rheological studies of erythrocyte-endothelial cell interactions in sickle cell disease. Prog Clin Biol Res. 1987;240:113-27.
•   Barabino GA, Wise RJ, Woodbury VA, Zhang B, Bridges KA, Hebbel RP, Lawler J, Ewenstein BM
  Inhibition of sickle erythrocyte adhesion to immobilized thrombospondin by von Willebrand factor under dynamic flow conditions. Blood. 1997 Apr 1;89(7):2560-7.
•   Bartolucci P, Chaar V, Picot J, Bachir D, Habibi A, Fauroux C, Galacteros F, Colin Y, Le Van Kim C, El Nemer W
  Decreased sickle red blood cell adhesion to laminin by hydroxyurea is associated with inhibition of Lu/BCAM protein phosphorylation. Blood. 2010 Sep 23;116(12):2152-9. doi: 10.1182/blood-2009-12-257444. Epub 2010 Jun 21.
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  Thrombospondin from activated platelets promotes sickle erythrocyte adherence to human microvascular endothelium under physiologic flow: a potential role for platelet activation in sickle cell vaso-occlusion. Blood. 1993 Apr 15;81(8):2137-43.
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  A method to identify California's sickle-cell disease population and its linkage to the California Cancer Registry. J Registry Manag. 2012 Summer;39(2):53-61.
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  Participation of Mac-1, LFA-1 and VLA-4 integrins in the in vitro adhesion of sickle cell disease neutrophils to endothelial layers, and reversal of adhesion by simvastatin. Haematologica. 2011 Apr;96(4):526-33. doi: 10.3324/haematol.2010.032912. Epub 2010 Dec 20.
•   Chaar V, Picot J, Renaud O, Bartolucci P, Nzouakou R, Bachir D, Galacteros F, Colin Y, Le Van Kim C, El Nemer W
  Aggregation of mononuclear and red blood cells through an alpha4beta1-Lu/basal cell adhesion molecule interaction in sickle cell disease. Haematologica. 2010 Nov;95(11):1841-8. doi: 10.3324/haematol.2010.026294. Epub 2010 Jun 18.
•   Chang J, Patton JT, Sarkar A, Ernst B, Magnani JL, Frenette PS
  GMI-1070, a novel pan-selectin antagonist, reverses acute vascular occlusions in sickle cell mice. Blood. 2010 Sep 9;116(10):1779-86. doi: 10.1182/blood-2009-12-260513. Epub 2010 May 27.
•   Charache S, Terrin ML, Moore RD, Dover GJ, Barton FB, Eckert SV, McMahon RP, Bonds DR
  Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia. N Engl J Med. 1995 May 18;332(20):1317-22. doi: 10.1056/NEJM199505183322001.
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•   Connes P, Coates TD
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  Short survival of phosphatidylserine-exposing red blood cells in murine sickle cell anemia. Blood. 2001 Sep 1;98(5):1577-84. doi: 10.1182/blood.v98.5.1577.
•   de Jong K, Larkin SK, Styles LA, Bookchin RM, Kuypers FA
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  Adherent leukocytes capture sickle erythrocytes in an in vitro flow model of vaso-occlusion. Am J Hematol. 2007 Apr;82(4):266-75. doi: 10.1002/ajh.20819.
•   Frenette PS, Atweh GF
  Sickle cell disease: old discoveries, new concepts, and future promise. J Clin Invest. 2007 Apr;117(4):850-8. doi: 10.1172/JCI30920.
•   Frenette PS
  Sickle cell vaso-occlusion: multistep and multicellular paradigm. Curr Opin Hematol. 2002 Mar;9(2):101-6. doi: 10.1097/00062752-200203000-00003.
•   Frenette PS
  Sickle cell vasoocclusion: heterotypic, multicellular aggregations driven by leukocyte adhesion. Microcirculation. 2004 Mar;11(2):167-77.
•   Gauthier E, Rahuel C, Wautier MP, El Nemer W, Gane P, Wautier JL, Cartron JP, Colin Y, Le Van Kim C
  Protein kinase A-dependent phosphorylation of Lutheran/basal cell adhesion molecule glycoprotein regulates cell adhesion to laminin alpha5. J Biol Chem. 2005 Aug 26;280(34):30055-62. doi: 10.1074/jbc.M503293200. Epub 2005 Jun 23.
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  Controlled viable release of selectively captured label-free cells in microchannels. Lab Chip. 2011 Dec 7;11(23):3979-89. doi: 10.1039/c1lc20487d. Epub 2011 Oct 14.
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  Smart interface materials integrated with microfluidics for on-demand local capture and release of cells. Adv Healthc Mater. 2012 Sep;1(5):661-8. doi: 10.1002/adhm.201200009. Epub 2012 Jul 9.
•   Gurkan UA, Tasoglu S, Kavaz D, Demirel MC, Demirci U
  Emerging technologies for assembly of microscale hydrogels. Adv Healthc Mater. 2012 Mar;1(2):149-158. doi: 10.1002/adhm.201200011.
•   Hebbel RP, Boogaerts MA, Eaton JW, Steinberg MH
  Erythrocyte adherence to endothelium in sickle-cell anemia. A possible determinant of disease severity. N Engl J Med. 1980 May 1;302(18):992-5. doi: 10.1056/NEJM198005013021803.
•   Hebbel RP, Boogaerts MA, Koresawa S, Jacob HS, Eaton JW, Steinberg MH
  Erytrocyte adherence to endothelium as a determinant of vasocclusive severity in sickle cell disease. Trans Assoc Am Physicians. 1980;93:94-9. No abstract available.
•   Hebbel RP, Eaton JW, Steinberg MH, White JG
  Erythrocyte/endothelial interactions and the vasocclusive severity of sickle cell disease. Prog Clin Biol Res. 1981;55:145-62.
•   Hebbel RP, Yamada O, Moldow CF, Jacob HS, White JG, Eaton JW
  Abnormal adherence of sickle erythrocytes to cultured vascular endothelium: possible mechanism for microvascular occlusion in sickle cell disease. J Clin Invest. 1980 Jan;65(1):154-60. doi: 10.1172/JCI109646.
•   Herrick JB
  Peculiar elongated and sickle-shaped red blood corpuscles in a case of severe anemia. 1910. Yale J Biol Med. 2001 May-Jun;74(3):179-84. No abstract available.
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  Intravenous immunoglobulins modulate neutrophil activation and vascular injury through FcgammaRIII and SHP-1. Circ Res. 2012 Apr 13;110(8):1057-66. doi: 10.1161/CIRCRESAHA.112.266411. Epub 2012 Mar 13.
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  Vasculopathy in sickle cell disease: Biology, pathophysiology, genetics, translational medicine, and new research directions. Am J Hematol. 2009 Sep;84(9):618-25. doi: 10.1002/ajh.21475.
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  DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease. Proc Natl Acad Sci U S A. 2008 Aug 19;105(33):11869-74. doi: 10.1073/pnas.0804799105. Epub 2008 Jul 30.
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•   Luck L, Zeng L, Hiti AL, Weinberg KI, Malik P
  Human CD34(+) and CD34(+)CD38(-) hematopoietic progenitors in sickle cell disease differ phenotypically and functionally from normal and suggest distinct subpopulations that generate F cells. Exp Hematol. 2004 May;32(5):483-93. doi: 10.1016/j.exphem.2004.02.003.
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  Hospitalization for pain in patients with sickle cell disease treated with sildenafil for elevated TRV and low exercise capacity. Blood. 2011 Jul 28;118(4):855-64. doi: 10.1182/blood-2010-09-306167. Epub 2011 Apr 28.
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Sickle Cell Disease (SCD) Biochip': Towards a Simple and Reliable Way to Monitor Sickle Cell Disease

Details for clinical trial NCT02824471