Hb Fort Worth or alpha2 27(B8)Glu----Gly beta2 in a black family from Canada

Endothelial ENaC as a repressor of oxidative stress and a guardian of lung capillary barrier function in bacterial and viral pneumonia.

Frontiers in physiology·2025

The clinical spectrum of HbSC sickle cell disease-not a benign condition.

British journal of haematology·2024

Evaluating the implementation of a multi-level mHealth study to improve hydroxyurea utilization in sickle cell disease.

Frontiers in health services·2023

A new sickling variant 'Hb S-Wake β[(Glu6Val-Asn139 Ser)]' found in a compound heterozygote with Hb S β(Glu6Val) coinherited with homozygous α-thalassemia-2: phenotype and molecular characteristics.

Acta haematologica·2010

Hb M Dothan [beta 25/26 (B7/B8)/(GGT/GAG-->GAG//Gly/Glu-->Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics.

Blood cells, molecules & diseases·2009

Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.

The pharmacogenomics journal·2007

Endocrine Complications in Patients with Congenital Dyserythropoietic Anemia: A Single-Center Cohort Study.

Hemoglobin·2026

Metabolomic and Proteomic Profiling of Vaso-Occlusive Crises in Sickle Cell Disease: Current Evidence and Future Perspectives.

Hemoglobin·2026

Evaluation of a Customized RDB-FTH Panel for β-Globin Variants in a Malaysian Tertiary Center.

Hemoglobin·2026

CRISPR-Based Mediated Reactivation of Fetal Hemoglobin as a Therapeutic Strategy for Hemoglobinopathies: Evidence from Preclinical to Clinical Trials in Sickle Cell Disease and β-Thalassemia.

Hemoglobin·2026

Genotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia.

Hemoglobin·2026

Mapping the Management-to-Cure Transition in Thalassemia Research: Semantic Topic Modeling of 17,651 Publications Across Three Decades.

Hemoglobin·2026

BBS10-related Bardet-Biedl syndrome with an atypical presentation of diabetes mellitus: A case report.

Experimental and therapeutic medicine·2026

Clinic-Based Proportion of Psoriatic Arthritis and HLA-B27 Distribution in Korean Psoriasis Patients: A Retrospective Study.

Annals of dermatology·2026

Amyloid-β plaque diversity across brain regions in Alzheimer's disease and its relation to major clinicopathological traits.

Acta neuropathologica·2026

Asthma: From Phenotypes to Endotypes-Beyond Type 2 Inflammation.

Respirology (Carlton, Vic.)·2026

Sample size effects on allele diversity, rare-allele recovery, and forensic parameters of 22 autosomal STRs in a cohort of 8,237 Argentines.

International journal of legal medicine·2026

Low-BMI sarcopenic obesity in adults with profound intellectual and multiple disabilities: A body composition analysis using bioelectrical impedance analysis and CT.

Brain & development·2026

Related Experiment Videos

Hb Fort Worth or alpha2 27(B8)Glu----Gly beta2 in a black family from Canada

Related Concept Videos

Endothelial ENaC as a repressor of oxidative stress and a guardian of lung capillary barrier function in bacterial and viral pneumonia.

The clinical spectrum of HbSC sickle cell disease-not a benign condition.

Evaluating the implementation of a multi-level mHealth study to improve hydroxyurea utilization in sickle cell disease.

A new sickling variant 'Hb S-Wake β[(Glu6Val-Asn139 Ser)]' found in a compound heterozygote with Hb S β(Glu6Val) coinherited with homozygous α-thalassemia-2: phenotype and molecular characteristics.

Hb M Dothan [beta 25/26 (B7/B8)/(GGT/GAG-->GAG//Gly/Glu-->Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics.

Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.

Endocrine Complications in Patients with Congenital Dyserythropoietic Anemia: A Single-Center Cohort Study.

Metabolomic and Proteomic Profiling of Vaso-Occlusive Crises in Sickle Cell Disease: Current Evidence and Future Perspectives.

Evaluation of a Customized RDB-FTH Panel for β-Globin Variants in a Malaysian Tertiary Center.

CRISPR-Based Mediated Reactivation of Fetal Hemoglobin as a Therapeutic Strategy for Hemoglobinopathies: Evidence from Preclinical to Clinical Trials in Sickle Cell Disease and β-Thalassemia.

Genotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia.

Mapping the Management-to-Cure Transition in Thalassemia Research: Semantic Topic Modeling of 17,651 Publications Across Three Decades.

BBS10-related Bardet-Biedl syndrome with an atypical presentation of diabetes mellitus: A case report.

Clinic-Based Proportion of Psoriatic Arthritis and HLA-B27 Distribution in Korean Psoriasis Patients: A Retrospective Study.

Amyloid-β plaque diversity across brain regions in Alzheimer's disease and its relation to major clinicopathological traits.

Asthma: From Phenotypes to Endotypes-Beyond Type 2 Inflammation.

Sample size effects on allele diversity, rare-allele recovery, and forensic parameters of 22 autosomal STRs in a cohort of 8,237 Argentines.

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Related Experiment Videos

Hb Fort Worth or alpha2 27(B8)Glu----Gly beta2 in a black family from Canada

Related Concept Videos

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