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Hemoglobin S gelation and sickle cell disease
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“The rate and extent of polymerization is modified by the erythrocyte HbF concentration. 2”
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Cites
ON THE NATURE OF ALLOSTERIC TRANSITIONS: A PLAUSIBLE MODEL.
Monod, J., Wyman, J., & Changeux, J. (1965) · Journal of Molecular Biology · doi:10.1016/s0022-2836(65)80285-6 · Cited by 7,681
Krogh, A. (1919) · The Journal of Physiology · doi:10.1113/jphysiol.1919.sp001839 · Cited by 1,433
Hydroxyurea enhances fetal hemoglobin production in sickle cell anemia.
Platt, O., Orkin, S. H., Dover, G., Beardsley, G. P., Miller, B. A., & Nathan, D. G. (1984) · Journal of Clinical Investigation · doi:10.1172/jci111464 · Cited by 532
Hofrichter, J., Ross, P. D., & Eaton, W. A. (1974) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.71.12.4864 · Cited by 520
Self-citationErythrocyte Adherence to Endothelium in Sickle-Cell Anemia
Hebbel, R. P., Boogaerts, M., Eaton, J. W., & Steinberg, M. H. (1980) · New England Journal of Medicine · doi:10.1056/nejm198005013021803 · Cited by 518
Kinetics of sickle hemoglobin polymerization
Ferrone, F. A., Hofrichter, J., & Eaton, W. A. (1985) · Journal of Molecular Biology · doi:10.1016/0022-2836(85)90175-5 · Cited by 505
Self-citationAbnormal Adherence of Sickle Erythrocytes to Cultured Vascular Endothelium
Hebbel, R. P., Yamada, O., Moldow, C. F., Jacob, H. S., White, J. G., & Eaton, J. W. (1980) · Journal of Clinical Investigation · doi:10.1172/jci109646 · Cited by 421
Abnormal rheology of oxygenated blood in sickle cell anemia
Chien, S., Usami, S., & Bertles, J. F. (1970) · Journal of Clinical Investigation · doi:10.1172/jci106273 · Cited by 358
Is there a threshold level of fetal hemoglobin that ameliorates morbidity in sickle cell anemia?
Powars, D., Weiss, J., Chan, L., & Schroeder, W. (1984) · Blood · doi:10.1182/blood.v63.4.921.921 · Cited by 314
Hemoglobin as a receptor of drugs and peptides: x-ray studies of the stereochemistry of binding
Perutz, M. F., Fermi, G., Abraham, D. J., Poyart, C., & Bursaux, E. (1986) · Journal of the American Chemical Society · doi:10.1021/ja00265a036 · Cited by 299
Cited by
Sorted by citations
Items 101–200 of 423
Effect of cell age and phenylhydrazine on the cation transport properties of rabbit erythrocytes
Brugnara, C., & Franceschi, L. D. (1993) · Journal of Cellular Physiology · doi:10.1002/jcp.1041540209 · Cited by 56
Transgenic mice expressing human sickle hemoglobin are partially resistant to rodent malaria
Shear, H. L., Roth, E. J., Fabry, M. E., Costantini, F. D., Pachnis, A., Hood, A. T., & Nagel, R. L. (1993) · Blood · doi:10.1182/blood.v81.1.222.222 · Cited by 56
Rate of deoxygenation and rheologic behavior of blood in sickle cell anemia
Kaul, D., & Xue, H. (1991) · Blood · doi:10.1182/blood.v77.6.1353.1353 · Cited by 56
Fabry, M. E., Romero, J. R., Buchanan, I., Suzuka, S. M., Stamatoyannopoulos, G., Nagel, R. L., & CANESSA, M. L. (1991) · Blood · doi:10.1182/blood.v78.1.217.bloodjournal781217 · Cited by 56
Moeckel, G. W., Shadman, R., Fogel, J. M., & Sadrzadeh, S. M. H. (2002) · Life Sciences · doi:10.1016/s0024-3205(02)02035-0 · Cited by 55
Asma, S., Kozanoğlu, İ., Tarım, E., Sarıtürk, Ç., Gereklioğlu, Ç., Akdeniz, A., Kasar, M., Turgut, N. H., Yeral, M., Kandemir, F., et al. (2014) · Transfusion · doi:10.1111/trf.12780 · Cited by 54
Autoxidation, dehydration, and adhesivity may be related abnormalities of sickle erythrocytes
Hebbel, R. P., Ney, P. A., & Foker, W. (1989) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1989.256.3.c579 · Cited by 54
Eaton, W. A. (2019) · American Journal of Hematology · doi:10.1002/ajh.25687 · Cited by 57
Self-citationHematopoietic Stem Cell Gene-Addition/Editing Therapy in Sickle Cell Disease
Germino-Watnick, P., Hinds, M., Le, A., Chu, R., Liu, X., & Uchida, N. (2022) · Cells · doi:10.3390/cells11111843 · Cited by 63
Kaul, D. K., Fabry, M. E., & Nagel, R. L. (1989) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1989.tb24179.x · Cited by 53
Free energy of sickling: A simulation analysis.
Kuczera, K., Gao, J., Tidor, B., & Karplus, M. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.21.8481 · Cited by 53
Franceschi, L. D., Brugnara, C., Rouyer‐Fessard, P., Jouault, H., & Beuzard, Y. (1999) · Blood · doi:10.1182/blood.v94.12.4307 · Cited by 52
Deoxygenation-induced cation fluxes in sickle cells: II. Inhibition by stilbene disulfonates
Joiner, C. (1990) · Blood · doi:10.1182/blood.v76.1.212.212 · Cited by 51
Grubina, R., Basu, S., Tiso, M., Kim‐Shapiro, D. B., & Gladwin, M. T. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m705222200 · Cited by 50
Vitoux, D., Olivieri, O., Garay, R. P., Cragoe, E. J., Galactéros, F., & Beuzard, Y. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.11.4273 · Cited by 50
Browning, J., Staines, H. M., Robinson, H., Powell, T., Ellory, J. C., & Gibson, J. S. (2006) · Blood · doi:10.1182/blood-2006-03-001404 · Cited by 49
Wajer, S. D., Taomoto, M., McLeod, D. S., McCally, R. L., Nishiwaki, H., Fabry, M. E., Nagel, R. L., & Lutty, G. A. (2000) · Microvascular Research · doi:10.1006/mvre.2000.2270 · Cited by 49
Nucleus factory on cavitation bubble for amyloid β fibril
Nakajima, K., Ogi, H., Adachi, K., Noi, K., Hirao, M., Yagi, H., & Goto, Y. (2016) · Scientific Reports · doi:10.1038/srep22015 · Cited by 49
Kiessling, K., Roberts, N. B., Gibson, J. S., & Ellory, J. C. (2000) · The Hematology Journal · doi:10.1038/sj.thj.6200033 · Cited by 47
2015 Clinical trials update in sickle cell anemia
Archer, N. M., Galactéros, F., & Brugnara, C. (2015) · American Journal of Hematology · doi:10.1002/ajh.24116 · Cited by 49
Established and experimental treatments for sickle cell disease.
Franceschi, L. D., & Corrocher, R. (2004) · PubMed · Cited by 47
Kinetic assay shows that increasing red cell volume could be a treatment for sickle cell disease
Li, Q., Henry, E. R., Hofrichter, J., Smith, J. F., Cellmer, T., Dunkelberger, E. B., Metaferia, B. B., Jones-Straehle, S., Boutom, S., Christoph, G. W., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1619054114 · Cited by 47
Self-citationSickle Cell Protection from Malaria
Eridani, S. (2011) · Hematology Reports · doi:10.4081/hr.2011.e24 · Cited by 47
The panoply of animal models for sickle cell anaemia
Nagel, R. L., & Fabry, M. E. (2001) · British Journal of Haematology · doi:10.1046/j.1365-2141.2001.02286.x · Cited by 47
Unusual causes of abdominal pain: sickle cell anemia
Ahmed, S., Shahid, R. K., & Russo, L. A. (2005) · Best Practice & Research Clinical Gastroenterology · doi:10.1016/j.bpg.2004.11.007 · Cited by 46
Dong, C., Chadwick, R. S., & Schechter, A. N. (1992) · Biophysical Journal · doi:10.1016/s0006-3495(92)81655-7 · Cited by 45
Fluorescence measurements of the labile iron pool of sickle erythrocytes
Darbari, D. S., Loyevsky, M., Gordeuk, V. R., Kark, J. A., Castro, O. L., RANA, S. R., Apprey, V., & Kurantsin‐Mills, J. (2003) · Blood · doi:10.1182/blood-2002-03-0914 · Cited by 43
Improvement of sickle cell anemia by iron‐limited erythropoiesis
Castro, O. L., Poillon, W. N., Finke, H., & Massac, E. (1994) · American Journal of Hematology · doi:10.1002/ajh.2830470203 · Cited by 43
Oxidative stress and phosphatidylserine exposure in red cells from patients with sickle cell anaemia
Hannemann, A., Rees, D. C., Brewin, J. N., Noe, A., Low, B., & Gibson, J. S. (2018) · British Journal of Haematology · doi:10.1111/bjh.15441 · Cited by 43
Pharmacotherapy in sickle cell disease – state of the art and future prospects
Hankins, J. S., & Aygün, B. (2009) · British Journal of Haematology · doi:10.1111/j.1365-2141.2009.07602.x · Cited by 43
The Properties of Red Blood Cells from Patients Heterozygous for HbS and HbC (HbSC Genotype)
Hannemann, A., Weiss, E., Rees, D. C., Dalibalta, S., Ellory, J. C., & Gibson, J. S. (2010) · Anemia · doi:10.1155/2011/248527 · Cited by 42
Balushi, H. W. M. A., Hannemann, A., Rees, D. C., Brewin, J. N., & Gibson, J. S. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00976 · Cited by 40
Linus Pauling and sickle cell disease
Eaton, W. A. (2002) · Biophysical Chemistry · doi:10.1016/s0301-4622(02)00269-7 · Cited by 42
Self-citationRheologic impairment of sickle RBCs induced by repetitive cycles of deoxygenation-reoxygenation
Nash, G. B., Johnson, C., & Meiselman, H. J. (1988) · Blood · doi:10.1182/blood.v72.2.539.539 · Cited by 42
Veluswamy, S., Shah, P., Denton, C. C., Chalacheva, P., Khoo, M. C. K., & Coates, T. D. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8101690 · Cited by 41
Kennan, R. P., Suzuka, S. M., Nagel, R. L., & Fabry, M. E. (2004) · Magnetic Resonance in Medicine · doi:10.1002/mrm.20014 · Cited by 41
Zehtabchi, S., Sinert, R. H., Rinnert, S., Chang, B., Heinis, C., Altura, R. A., Altura, B. T., & Altura, B. M. (2004) · American Journal of Hematology · doi:10.1002/ajh.20187 · Cited by 40
Intracellular Hemoglobin S Polymerization and the Clinical Severity of Sickle Cell Anemia
Poillon, W. N., Kim, B. C., & Castro, O. L. (1998) · Blood · doi:10.1182/blood.v91.5.1777 · Cited by 40
Sociodemographic aspects and quality of life of patients with sickle cell anemia
dos Santos, J. P., & Neto, M. G. (2013) · Revista Brasileira de Hematologia e Hemoterapia · doi:10.5581/1516-8484.20130093 · Cited by 39
Pathophysiology of Abnormal Cell Volume in Human Red Cells
Ellory, J. C., Gibson, J. S., & Stewart, G. W. (1998) · KARGER eBooks · doi:10.1159/000059915 · Cited by 39
Sickle cell rheology is determined by polymer fraction–not cell morphology
Hiruma, H., Noguchi, C. T., Uyesaka, N., Hasegawa, S., Blanchette‐Mackie, E. J., Schechter, A. N., & Rodgers, G. P. (1995) · American Journal of Hematology · doi:10.1002/ajh.2830480105 · Cited by 38
CRISPR/Cas9-based gene-editing technology for sickle cell disease
Ma, L., Yang, S., Peng, Q., Zhang, J., & Zhang, J. (2023) · Gene · doi:10.1016/j.gene.2023.147480 · Cited by 45
Gene Therapy for Sickle Cell Disease : A Lentiviral Vector Comparison Study
Urbinati, F., Fernandez, B. C., Masiuk, K. E., Poletti, V., Hollis, R. P., Koziol, C., Kaufman, M. L., Brown, D., Mavilio, F., & Kohn, D. B. (2018) · Human Gene Therapy · doi:10.1089/hum.2018.061 · Cited by 40
Hannemann, A., Rees, D. C., Tewari, S., & Gibson, J. S. (2015) · EBioMedicine · doi:10.1016/j.ebiom.2015.09.026 · Cited by 37
Hydroxyurea and erythropoietin therapy in sickle cell anemia.
Goldberg, M. A., Brugnara, C., Dover, G., Schapira, L., Lacroix, L., & Bunn, H. F. (1992) · PubMed · Cited by 37
Deoxygenation of sickle red blood cells stimulates KCl cotransport without affecting Na+/H+exchange
Joiner, C. H., Jiang, M., Fathallah, H., Giraud, F., & Franco, R. (1998) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1998.274.6.c1466 · Cited by 37
A Prospective Longitudinal Brain Morphometry Study of Children with Sickle Cell Disease
Chen, R., Arkuszewski, M., Krejza, J., Zimmerman, R. A., Herskovits, E. H., & Melhem, E. R. (2014) · American Journal of Neuroradiology · doi:10.3174/ajnr.a4101 · Cited by 35
Carden, M. A., Fasano, R. M., & Meier, E. R. (2019) · Blood Reviews · doi:10.1016/j.blre.2019.100637 · Cited by 38
Regioselective Covalent Modification of Hemoglobin in Search of Antisickling Agents
Park, S., Hayes, B. L., Marankan, F., Mulhearn, D. C., Wanna, L., Mesecar, A. D., Santarsiero, B. D., Johnson, M. E., & Venton, D. L. (2003) · Journal of Medicinal Chemistry · doi:10.1021/jm020361k · Cited by 35
Heme Redox Properties of S-Nitrosated Hemoglobin A0 and Hemoglobin S
Bonaventura, C., Taboy, C. H., Low, P. S., Stevens, R. D., Lafon, C., & Crumbliss, A. L. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m107658200 · Cited by 34
Emerging pharmacotherapeutic approaches for the management of sickle cell disease
Torres, L. S., & Conran, N. (2018) · Expert Opinion on Pharmacotherapy · doi:10.1080/14656566.2018.1548610 · Cited by 35
Li, W., Xu, X., Liu, P., Strouse, J. J., Casella, J. F., Lu, H., van Zijl, P. C. M., & Qin, Q. (2019) · Magnetic Resonance in Medicine · doi:10.1002/mrm.27972 · Cited by 34
The conductance of red blood cells from sickle cell patients: ion selectivity and inhibitors
Ma, Y., Rees, D. C., Gibson, J. S., & Ellory, J. C. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.229609 · Cited by 34
Fabry, M. E., Rajanayagam, V., Fine, E. J., Holland, S. K., Gore, J. C., Nagel, R. L., & Kaul, D. K. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.10.3808 · Cited by 34
Review of Sickle Cell Disease and Spinal Pathology
Rudy, H. L., Yang, D. C.-S., Nam, A. D., & Cho, W. (2018) · Global Spine Journal · doi:10.1177/2192568218799074 · Cited by 34
Zhou, Z., Behymer, M., & Guchhait, P. (2010) · Anemia · doi:10.1155/2011/918916 · Cited by 36
Biondani, A., Turrini, F., Carta, F., Mattè, A., Filippini, A., Siciliano, A., Beuzard, Y., & Franceschi, L. D. (2008) · PROTEOMICS - CLINICAL APPLICATIONS · doi:10.1002/prca.200780058 · Cited by 33
Smolinski, P. A., Offermann, M. K., Eckman, J., & Wick, T. M. (1995) · Blood · doi:10.1182/blood.v85.10.2945.bloodjournal85102945 · Cited by 33
Anesthesia and Hemoglobinopathies
Firth, P. G. (2009) · Anesthesiology Clinics · doi:10.1016/j.anclin.2009.05.001 · Cited by 33
Pleiotropic and epistatic effects in sickle cell anemia
Nagel, R. L. (2001) · Current Opinion in Hematology · doi:10.1097/00062752-200103000-00008 · Cited by 32
Gene Replacement Therapy for Sickle Cell Disease and Other Blood Disorders
Townes, T. M. (2008) · Hematology · doi:10.1182/asheducation-2008.1.193 · Cited by 30
Immuotactoid Glomerulopathy (Fibrillary Glomerulonephritis)
Korbet, S. M., Schwartz, M. M., & Lewis, E. J. (2006) · Clinical Journal of the American Society of Nephrology · doi:10.2215/cjn.01140406 · Cited by 31
Pathophysiology and treatment of sickle cell disease.
Raphael, R. I. (2005) · PubMed · Cited by 30
Sickle cell disease and dental treatment.
Piccin, A., Fleming, P., Eakins, E., McGovern, E., Smith, O. P., & McMahon, C. (2008) · PubMed · Cited by 28
White, J. U., Krishnamoorthy, S., Gupta, D., Lancelot, M. M., Moore, N., Sarnaik, S. A., Hobbs, W. E., Light, D. R., & Hines, P. C. (2016) · British Journal of Haematology · doi:10.1111/bjh.14158 · Cited by 29
Carden, M. A., Fay, M. E., Sakurai, Y., McFarland, B., Blanche, S., DiPrete, C., Joiner, C. H., Sulchek, T., & Lam, W. A. (2017) · Microcirculation · doi:10.1111/micc.12353 · Cited by 29
Caprio, G. D., Schonbrun, E. F., Gonçalves, B. P., Valdez, J. M., Wood, D. K., & Higgins, J. M. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1914056116 · Cited by 30
Carden, M. A., Brousseau, D. C., Ahmad, F. A., Bennett, J. E., Bhatt, S. R., Bogie, A. L., Brown, K., Casper, T. C., Chapman, L. L., Chumpitazi, C. E., et al. (2019) · American Journal of Hematology · doi:10.1002/ajh.25471 · Cited by 30
Mandal, A. K., Mitra, A., & Das, R. (2020) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-030-41769-7_12 · Cited by 30
Sickle cell vaso-occlusion: The dialectic between red cells and white cells
Conran, N., & Embury, S. H. (2021) · Experimental Biology and Medicine · doi:10.1177/15353702211005392 · Cited by 31
Metaferia, B. B., Cellmer, T., Dunkelberger, E. B., Li, Q., Henry, E. R., Hofrichter, J., Staton, D., Hsieh, M. M., Conrey, A. K., Tisdale, J. F., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2210779119 · Cited by 30
Self-citationUniversality of supersaturation in protein-fiber formation
Cellmer, T., Ferrone, F. A., & Eaton, W. A. (2016) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.3197 · Cited by 28
Self-citationHaematological Diseases in the Tropics
Thachil, J. V., Owusu‐Ofori, S., & Bates, I. (2013) · Elsevier eBooks · doi:10.1016/b978-0-7020-5101-2.00066-2 · Cited by 29
RENAL FAILURE IN SICKLE CELL ANEMIA
Wong, W.-Y., Elliott-Mills, D. D., & Powars, D. R. (1996) · Hematology/Oncology Clinics of North America · doi:10.1016/s0889-8588(05)70403-2 · Cited by 28
Deoxygenation-Induced Non-Electrolyte Pathway in Red Cells from Sickle Cell Patients
Browning, J., Robinson, H., Ellory, C., & Gibson, J. S. (2007) · Cellular Physiology and Biochemistry · doi:10.1159/000099204 · Cited by 28
Sulfhydryl oxidation and activation of red cell K(+)-Cl- cotransport in the transgenic SAD mouse
Franceschi, L. D., Beuzard, Y., & Brugnara, C. (1995) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1995.269.4.c899 · Cited by 28
Probing the Twisted Structure of Sickle Hemoglobin Fibers via Particle Simulations
Lu, L., Li, X., Vekilov, P. G., & Karniadakis, G. E. (2016) · Biophysical Journal · doi:10.1016/j.bpj.2016.04.002 · Cited by 27
Overview of Sickle Cell Anemia Pathophysiology
Steinberg, M. H. (2016) · Springer eBooks · doi:10.1007/978-3-319-06713-1_3 · Cited by 26
Yoda1 and phosphatidylserine exposure in red cells from patients with sickle cell anaemia
Wadud, R., Hannemann, A., Rees, D. C., Brewin, J. N., & Gibson, J. S. (2020) · Scientific Reports · doi:10.1038/s41598-020-76979-2 · Cited by 28
Hannemann, A., Cytlak, U., Rees, D. C., Tewari, S., & Gibson, J. S. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.277681 · Cited by 27
Carbamazepine-induced thrombocytopenia defined by a challenge test
Ishikita, T., Ishiguro, A., Fujisawa, K., Tsukimoto, I., & Shimbo, T. (1999) · American Journal of Hematology · doi:10.1002/(sici)1096-8652(199909)62:1 · Cited by 17
Gibson, J. S., Khan, A. M., Speake, P. F., & Ellory, J. C. (2001) · The FASEB Journal · doi:10.1096/fj.00-0177com · Cited by 27
Cytlak, U., Hannemann, A., Rees, D. C., & Gibson, J. S. (2013) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-013-1308-y · Cited by 26
Rheological and Adherence Properties of Sickle Cellsa
Mohandas, N., & Evans, E. A. (1989) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1989.tb24180.x · Cited by 26
Basu, A., Saha, S., Karmakar, S., Chakravarty, S., Banerjee, D., Dash, B. P., & Chakrabarti, A. (2013) · PROTEOMICS · doi:10.1002/pmic.201300177 · Cited by 25
Abdulmalik, O. Y., Pagare, P. P., Huang, B., Xu, G. G., Ghatge, M. S., Xu, X., Chen, Q., Anabaraonye, N., Musayev, F. N., Omar, A. M., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-77171-2 · Cited by 25
Supersaturation, a Critical Factor Underlying Proteostasis of Amyloid Fibril Formation
Goto, Y., Nakajima, K., Yamamoto, S., & Yamaguchi, K. (2024) · Journal of Molecular Biology · doi:10.1016/j.jmb.2024.168475 · Cited by 26
Lu, X., Chaudhury, A., Higgins, J. M., & Wood, D. K. (2018) · American Journal of Hematology · doi:10.1002/ajh.25227 · Cited by 24
Enhanced polymerization of recombinant human deoxyhemoglobin beta 6 Glu----Ile.
Baudin‐Creuza, V., Pagnier, J., Marden, M. C., Brohard-Bohn, B., Lacaze, N., KISTER, J., Schaad, O., Edelstein, S. J., & Poyart, C. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.5.1845 · Cited by 24
Abnormal permeability pathways in human red blood cells
Ellory, J. C., Robinson, H., Browning, J., Stewart, G. W., Gehl, K. A., & Gibson, J. S. (2007) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2007.02.011 · Cited by 24
Sickle Cell Trait, Heroic Exercise, and Fatal Collapse
Eichner, E. R. (1993) · The Physician and Sportsmedicine · doi:10.1080/00913847.1993.11710400 · Cited by 24
Stivala, S., Gobbato, S., Bonetti, N. R., Camici, G. G., Lüscher, T. F., & Beer, J. H. (2021) · Journal of Thrombosis and Haemostasis · doi:10.1111/jth.15581 · Cited by 23
What's New in the Pathophysiology of Sickle Cell Disease?
Adekile, A. D. (2013) · Medical Principles and Practice · doi:10.1159/000350283 · Cited by 23
Lu, X., Galarneau, M., Higgins, J. M., & Wood, D. K. (2017) · Microcirculation · doi:10.1111/micc.12357 · Cited by 23
Effect of 1-chloro-2,4-dinitrobenzene on K+ transport in normal and sickle human red blood cells
Muzyamba, M. C., & Gibson, J. S. (2003) · The Journal of Physiology · doi:10.1111/j.1469-7793.2003.00903.x · Cited by 23
Therapeutic Strategies for Prevention of Sickle Cell Dehydration
Brugnara, C. (2001) · Blood Cells Molecules and Diseases · doi:10.1006/bcmd.2000.0366 · Cited by 23
A New Therapeutic Approach for Sickle Cell Disease
Brugnara, C., Franceschi, L. D., Armsby, C. C., Saadane, N., Trudel, M., Beuzard, Y., Rittenhouse, A. R., Rifai, N., Platt, O. S., & Alper, S. L. (1995) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1995.tb32411.x · Cited by 23
Immunotactoid Glomerulopathy: The Case for Occam's Razor
Schwartz, M. M. (1993) · American Journal of Kidney Diseases · doi:10.1016/s0272-6386(12)70150-6 · Cited by 23
Dalibalta, S., Ellory, J. C., Browning, J., Wilkins, R. J., Rees, D. C., & Gibson, J. S. (2010) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2010.02.010 · Cited by 22
AN OVERVIEW ON SICKLE CELL DISEASE PROFILE
Kaur, M., Dangi, C. B. S., & Singh, M. (2013) · Cited by 22
Metadata
- Authors
- Eaton, W., & Hofrichter, J.
- Affiliations
- National Institutes of Health (US)
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 1987-11-01
- Volume
- 70
- Issue
- 5
- Pages
- 1245-1266
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W1919238100
- Cited by
- 425
- References
- 143
- Citations by year
- 2026: 10 · 2025: 2 · 2024: 9 · 2023: 13 · 2022: 12 · 2021: 16 · 2020: 11 · 2019: 23 · 2018: 18 · 2017: 16 · 2016: 15 · 2015: 8 · 2014: 8 · 2013: 18 · 2012: 14
- FWCI
- 12.91
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Blood (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Genetics (clinical) › Hemoglobinopathies and Related Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Hemoglobin structure and function
- Health Sciences › Medicine › Hematology › Blood properties and coagulation
- Keywords
- hemoglobin S, sickle cell disease, hemoglobin polymerization, vaso-occlusive crisis
- MeSH terms
- Anemia, Sickle Cell, Gels, Hemoglobin, Sickle, Humans, Oxyhemoglobins, Protein Conformation
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