Hb Olomouc or alpha 2 beta 2(86)(F2)Ala----Asp, a new high oxygen affinity variant

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

Screening for the 'Silent' Burden of Menstrual and Mental Health Among Women with Sickle Cell Disease: A Prospective Study.

Hemoglobin·2026

Precision Medicine in Transfusion-Dependent and Non-Transfusion-Dependent β-Thalassemia: Toward Personalized Diagnosis and Therapy.

Hemoglobin·2026

The Silent Epidemic: A Scoping Review of Chronic Pain Etiology and Management Strategies in Transfusion-Dependent Thalassemia.

Hemoglobin·2026

Low Prevalence of the HBB c.20A > T (HbS) Allele in a Turkish Cypriot Cohort: A Molecular Screening Study.

Hemoglobin·2026

Identification of a Novel Compound Heterozygous SEC23B in a Chinese Child with Congenital Dyserythropoietic Anemia Type II.

Hemoglobin·2026

Compound Heterozygosity for Hb Port Phillip and the -α3.7 Deletion Leads to Persistent Hypoxemia in a Chinese Pediatric Family.

Hemoglobin·2026

Retraction notice to "Free convective oscillatory flow due to inclined perpendicular shield subject to the thermos-diffusion and suction effects" [Heliyon 9 (2023) e14781].

Heliyon·2026

Revisiting orientational relaxation in bulk water: Observation and mechanistic understanding of an intermediate time scale (around 1 ps).

The Journal of chemical physics·2026

High-altitude hyperuricemia: a double-edged sword of adaptation and maladaptation.

Frontiers in public health·2026

Pumping technique of elite iQfoil windsurfers in ecological settings.

Sports biomechanics·2026

Displacive Quantum Critical Point in Superconducting Hydrides: The Case of H_{3}S.

Physical review letters·2026

Ontogenetic Development of Hyperostosis in the Crevalle Jack Caranx hippos (Linnaeus, 1766) and New Records of Affected Bone Regions.

Journal of fish diseases·2026

Related Experiment Videos

Hb Olomouc or alpha 2 beta 2(86)(F2)Ala----Asp, a new high oxygen affinity variant

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.

Screening for the 'Silent' Burden of Menstrual and Mental Health Among Women with Sickle Cell Disease: A Prospective Study.

Precision Medicine in Transfusion-Dependent and Non-Transfusion-Dependent β-Thalassemia: Toward Personalized Diagnosis and Therapy.

The Silent Epidemic: A Scoping Review of Chronic Pain Etiology and Management Strategies in Transfusion-Dependent Thalassemia.

Low Prevalence of the HBB c.20A > T (HbS) Allele in a Turkish Cypriot Cohort: A Molecular Screening Study.

Identification of a Novel Compound Heterozygous SEC23B in a Chinese Child with Congenital Dyserythropoietic Anemia Type II.

Compound Heterozygosity for Hb Port Phillip and the -α3.7 Deletion Leads to Persistent Hypoxemia in a Chinese Pediatric Family.

Retraction notice to "Free convective oscillatory flow due to inclined perpendicular shield subject to the thermos-diffusion and suction effects" [Heliyon 9 (2023) e14781].

Revisiting orientational relaxation in bulk water: Observation and mechanistic understanding of an intermediate time scale (around 1 ps).

High-altitude hyperuricemia: a double-edged sword of adaptation and maladaptation.

Pumping technique of elite iQfoil windsurfers in ecological settings.

Displacive Quantum Critical Point in Superconducting Hydrides: The Case of H_{3}S.

Ontogenetic Development of Hyperostosis in the Crevalle Jack Caranx hippos (Linnaeus, 1766) and New Records of Affected Bone Regions.

Related Experiment Videos

Hb Olomouc or alpha 2 beta 2(86)(F2)Ala----Asp, a new high oxygen affinity variant

Related Concept Videos

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