Molecular and cellular pathogenesis of hemoglobin SC disease.
about
Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell traitIntracellular polymerization. Disease severity and therapeutic predictions.Kinetic assay shows that increasing red cell volume could be a treatment for sickle cell disease.Human bulbar conjunctival hemodynamics in hemoglobin SS and SC disease.Reconstructing sickle cell disease: a data-based analysis of the "hyperhemolysis paradigm" for pulmonary hypertension from the perspective of evidence-based medicine.Intracellular polymerization of sickle hemoglobin. Effects of cell heterogeneity.Dyspnea with hemoglobin SC disease.Polymerization in erythrocytes containing S and non-S hemoglobinsThe Properties of Red Blood Cells from Patients Heterozygous for HbS and HbC (HbSC Genotype)The rules of variation: amino acid exchange according to the rotating circular genetic code.Elevated hypercoagulability markers in hemoglobin SC disease.Effect of red blood cell variants on childhood malaria in Mali: a prospective cohort study.Hemoglobin sickle cell disease complications: a clinical study of 179 casesSparing effect of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S at physiologic ligand saturations.Practicing biochemistry without a licenseA non-electrolyte haemolysis assay for diagnosis and prognosis of sickle cell disease.Detrimental effects of adenosine signaling in sickle cell disease.Role of oxidative stress in the pathogenesis of sickle cell disease.Classification of the disorders of hemoglobinRole of Exercise-Induced Oxidative Stress in Sickle Cell Trait and Disease.Current perspectives on the kinetics of hemoglobin S gelation.Universality of supersaturation in protein-fiber formation.Medullary Microvascular Thrombosis and Injury in Sickle Hemoglobin C Disease.A model for the sickle hemoglobin fiber using both mutation sitesOutcome in hemoglobin SC disease: a four-decade observational study of clinical, hematologic, and genetic factors.Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.Increased oxidative stress alters nucleosides metabolite levels in sickle cell anemia.Sickle cell maculopathy: Identification of systemic risk factors, and microstructural analysis of individual retinal layers of the macula.
P2860
Q24629836-1958295F-3869-4167-A51A-517C142B06C5Q30807725-B8634B7C-6AEC-4585-9547-88F97BC18C0EQ30837666-CF916813-3882-4B13-8715-8DDCBB2407D0Q33692837-6E056D2D-7A5C-449D-9403-4156A0E0E16DQ33803027-2CD02CD7-0C37-48DA-933F-D7A4AB9B1627Q33822227-1217E110-001C-4274-830F-A3598F85B382Q34116422-B5CF9703-0BB3-4C67-BB60-3EAC503101E5Q34535078-C576502A-C14C-4DDC-8777-531C25E50E50Q34734929-40364798-695F-4E71-B7FA-2F824B4B5BEEQ35088718-3D4DD36F-825A-4EBD-A37A-4EEE25DA0622Q35236050-A78BD806-C987-426F-9D1F-05BAD78D92E8Q35564214-91331527-0CD5-41F4-BACE-E87EFA06A915Q36132987-EE447D46-368A-4D5E-835E-B89229979A3BQ36333394-5AC88919-26FC-46E8-AE07-C90F6ED39ECCQ36620857-61FD8BEB-F9CC-4000-965D-561CE113035CQ36713158-8A8C9DA9-6152-4C0F-878F-1B3BA8BC2CB9Q36818005-7764CC0D-19FD-4B33-802C-87766FA21796Q37963311-74E63844-B33D-4409-B47B-EA6BA6A3CC37Q38078918-D2AE2074-DE4B-4161-A454-F3F23C4E5862Q38669072-5A45E7D0-9704-4A1C-90D1-4BA7B7624D13Q38686579-6B3328F4-532A-4049-96E4-9F9B6BC9DA65Q38790824-3ACDF104-A7FD-4A73-8A6E-477651BA52DBQ40775991-F8A8F462-E9C6-4493-8582-DB9BBD373C14Q42847643-286EB2C2-BF8F-485C-9BCB-CAEFB88302BDQ44094350-A7CB1FA7-5FFF-4AF2-9C0D-B5BBBDE2C67BQ45019137-344F2328-1A49-4334-89A9-965ABADC0FD9Q46416731-651580ED-4F28-4B70-A670-5587238FA6A1Q55177198-0D08A2F3-B2C5-4550-9D64-E4EFF6453656
P2860
Molecular and cellular pathogenesis of hemoglobin SC disease.
description
1982 nî lūn-bûn
@nan
1982年の論文
@ja
1982年学术文章
@wuu
1982年学术文章
@zh-cn
1982年学术文章
@zh-hans
1982年学术文章
@zh-my
1982年学术文章
@zh-sg
1982年學術文章
@yue
1982年學術文章
@zh
1982年學術文章
@zh-hant
name
Molecular and cellular pathogenesis of hemoglobin SC disease.
@ast
Molecular and cellular pathogenesis of hemoglobin SC disease.
@en
type
label
Molecular and cellular pathogenesis of hemoglobin SC disease.
@ast
Molecular and cellular pathogenesis of hemoglobin SC disease.
@en
prefLabel
Molecular and cellular pathogenesis of hemoglobin SC disease.
@ast
Molecular and cellular pathogenesis of hemoglobin SC disease.
@en
P2093
P2860
P356
P1476
Molecular and cellular pathogenesis of hemoglobin SC disease.
@en
P2093
Hofrichter J
Noguchi CT
Schechter AN
Schechter GP
P2860
P304
P356
10.1073/PNAS.79.23.7527
P407
P577
1982-12-01T00:00:00Z