Review of hemoglobin variants studied in Southwestern U.S.A

Involvement of His HC3 (146) beta in the Bohr effect of human hemoglobin. Studies of native and N-ethylmaleimide-treated hemoglobin A and hemoglobin Cowtown (beta 146 His replaced by Leu).

The Journal of biological chemistry·1984

Hb S Mobile: a new genetic combination.

Hemoglobin·1983

Globin chain synthesis in haemoglobin New York (beta 113 replaced by glutamic acid).

British journal of haematology·1980

Hemoglobin Ohio (beta 142 Ala replaced by): a new abnormal hemoglobin with high oxygen affinity and erythrocytosis.

Blood·1980

HbE-beta-thalassemia associated with G6PD deficiency.

Southern medical journal·1980

Biosynthesis of hemoglobin F Malta-I in culture by adult circulating erythropoietic precursors.

Blood·1980

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

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

Rationale and Design of the Atherosclerosis Risk in Communities Generation 2 (ARIC Gen2) Study.

American journal of epidemiology·2026

High-resolution spatial transcriptomic atlas of mouse soleus muscle: Unveiling single cell and subcellular heterogeneity in health and denervation.

The FEBS journal·2026

Investigating the Association of Genetic Markers, Previously Identified by Genome-Wide Association Studies, With ACL Rupture in Multiple Cohorts.

Journal of orthopaedic research : official publication of the Orthopaedic Research Society·2026

Copy Number Variant Detection by Exome/Genome Sequencing Versus Chromosomal Microarray: A Comparative Study of Over 9,000 Clinical Cases.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Connective tissue and genetics in the pathogenesis of rectal prolapse: A scoping review.

Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland·2026

tidyGenR: tidy multilocus amplicon genotypes in R.

PeerJ·2026

Related Experiment Videos

Review of hemoglobin variants studied in Southwestern U.S.A

Related Concept Videos

Involvement of His HC3 (146) beta in the Bohr effect of human hemoglobin. Studies of native and N-ethylmaleimide-treated hemoglobin A and hemoglobin Cowtown (beta 146 His replaced by Leu).

Hb S Mobile: a new genetic combination.

Globin chain synthesis in haemoglobin New York (beta 113 replaced by glutamic acid).

Hemoglobin Ohio (beta 142 Ala replaced by): a new abnormal hemoglobin with high oxygen affinity and erythrocytosis.

HbE-beta-thalassemia associated with G6PD deficiency.

Biosynthesis of hemoglobin F Malta-I in culture by adult circulating erythropoietic precursors.

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.

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.

Rationale and Design of the Atherosclerosis Risk in Communities Generation 2 (ARIC Gen2) Study.

High-resolution spatial transcriptomic atlas of mouse soleus muscle: Unveiling single cell and subcellular heterogeneity in health and denervation.

Investigating the Association of Genetic Markers, Previously Identified by Genome-Wide Association Studies, With ACL Rupture in Multiple Cohorts.

Copy Number Variant Detection by Exome/Genome Sequencing Versus Chromosomal Microarray: A Comparative Study of Over 9,000 Clinical Cases.

Connective tissue and genetics in the pathogenesis of rectal prolapse: A scoping review.

tidyGenR: tidy multilocus amplicon genotypes in R.

Related Experiment Videos

Review of hemoglobin variants studied in Southwestern U.S.A

Related Concept Videos

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