Hb Le Lamentin or alpha 2 20(B1)His----GLN beta 2 found in a Spanish family

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

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

Uncovering the True Genotype: Unusually Severe Sickle Cell Disease in a Child with an Initial HbSC Diagnosis.

Hemoglobin·2026

Ocular Complications Among Patients with Beta-Thalassaemia Major and Intermedia: A Comparative Study from Pakistan.

Hemoglobin·2026

Psychometric Performance of the Adult Sickle Cell Quality-of-Life Measurement Information System (ASCQ-Me) in Jamaicans with Sickle Cell Disease.

Hemoglobin·2026

Co-Heredity of (-α)20.5 Deletion and IVS I-1 G > A (HBB: C.92 + 1 G > A) Mutations in a Pediatric Patient: A Cause of Moderate Anemia Phenotype?

Hemoglobin·2026

A novel de novo multi-exon deletion of SYT1 in a child with Baker-Gordon syndrome.

BMC pediatrics·2026

Locus-specific stratification and prioritization unveil genetic risk mechanism underlying complex diseases.

Nature communications·2026

Genome-wide pQTL mapping in human skin identifies specific genetic regulators and mechanistic links to skin disorders.

Nature communications·2026

Determinants of functional burden pleiotropy and gene dosage responses across human traits.

Nature communications·2026

Discovering common and population-specific QTLs for leaf rust resistance in different Barley populations.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2026

A Normal Phenotype Case of a Small Supernumerary Marker Chromosome Chimeric Carrier with 12p11.21p11.21 Duplication.

Clinical laboratory·2026

Related Experiment Videos

Hb Le Lamentin or alpha 2 20(B1)His----GLN beta 2 found in a Spanish family

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.

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.

Uncovering the True Genotype: Unusually Severe Sickle Cell Disease in a Child with an Initial HbSC Diagnosis.

Ocular Complications Among Patients with Beta-Thalassaemia Major and Intermedia: A Comparative Study from Pakistan.

Psychometric Performance of the Adult Sickle Cell Quality-of-Life Measurement Information System (ASCQ-Me) in Jamaicans with Sickle Cell Disease.

Co-Heredity of (-α)20.5 Deletion and IVS I-1 G > A (HBB: C.92 + 1 G > A) Mutations in a Pediatric Patient: A Cause of Moderate Anemia Phenotype?

A novel de novo multi-exon deletion of SYT1 in a child with Baker-Gordon syndrome.

Locus-specific stratification and prioritization unveil genetic risk mechanism underlying complex diseases.

Genome-wide pQTL mapping in human skin identifies specific genetic regulators and mechanistic links to skin disorders.

Determinants of functional burden pleiotropy and gene dosage responses across human traits.

Discovering common and population-specific QTLs for leaf rust resistance in different Barley populations.

A Normal Phenotype Case of a Small Supernumerary Marker Chromosome Chimeric Carrier with 12p11.21p11.21 Duplication.

Related Experiment Videos

Hb Le Lamentin or alpha 2 20(B1)His----GLN beta 2 found in a Spanish family

Related Concept Videos

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