A new informative family for the close linkage between the structural beta and delta human hemoglobin genes

Butyrylcholinesterase and obesity in individuals with the CHE2 C5+ and CHE2 C5- phenotypes.

International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity·2003

Studies on a heterologous complex formed by human butyrylcholinesterase.

Biochemical genetics·2003

The X-X-/E+E+ genotype of the XbaI/EcoRI polymorphisms of the apolipoprotein B gene as a marker of coronary artery disease in a Brazilian sample.

Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas·2003

Butyrylcholinesterase activity and risk factors for coronary artery disease.

Scandinavian journal of clinical and laboratory investigation·2002

Association of the CHE2 locus with body mass index and butyrylcholinesterase activity.

Human biology·2001

Frequencies of the butyrylcholinesterase K mutation in Brazilian populations of European and African origin.

Human biology·1998

Hemoglobin E Associated with Hemoglobin Constant Spring: Diagnostic Challenges in Heterozygous and Homozygous States.

Hemoglobin·2026

An Unusual Presentation of Erythrocytosis Resulting in the Identification of a Novel Unstable Hemoglobin Variant: Hb Koskullskulle HBB: C.311T > C (p.Phe104Ser).

Hemoglobin·2026

Hematologic Indices of Hemoglobin D Co-Inheritance with α and β Thalassemia: A Comparative Study of 202 Patients.

Hemoglobin·2026

The Efficiency of Capillarys 2 Flex Piercing, Premier Resolution-HPLC, and VARIANT II-HPLC for Hemoglobin Constant Spring Detection.

Hemoglobin·2026

Tailoring Genetic Approaches for Easier Detection of Anti-3.7 Alpha-Globin Gene Triplication in the Iranian Population.

Hemoglobin·2026

Microcytic Anemia with Low HbA2 and Normal HbA: Two Cases of Rare Thalassemia.

Hemoglobin·2026

Whole-Exome Sequencing in a Consanguinity-Enriched South Indian Retinitis Pigmentosa Cohort: Diagnostic Yield and Molecular Spectrum.

Ophthalmology science·2026

Genetic analysis, reproductive decision-making, and pregnancy outcomes in 51 Chinese osteogenesis imperfecta families.

Journal of assisted reproduction and genetics·2026

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

American journal of human genetics·2026

Natural variation in SL6 determines fatty acid components and seed longevity in rice.

Science advances·2026

Genetic architecture of endometriosis: risk factors, comorbidities and clinical implications.

Human reproduction update·2026

Comprehensive analysis of non-synonymous single-nucleotide polymorphism of human TSC1 and TSC2 genes: An in silico approach.

PloS one·2026

Related Experiment Videos

A new informative family for the close linkage between the structural beta and delta human hemoglobin genes

Related Concept Videos

Butyrylcholinesterase and obesity in individuals with the CHE2 C5+ and CHE2 C5- phenotypes.

Studies on a heterologous complex formed by human butyrylcholinesterase.

The X-X-/E+E+ genotype of the XbaI/EcoRI polymorphisms of the apolipoprotein B gene as a marker of coronary artery disease in a Brazilian sample.

Butyrylcholinesterase activity and risk factors for coronary artery disease.

Association of the CHE2 locus with body mass index and butyrylcholinesterase activity.

Frequencies of the butyrylcholinesterase K mutation in Brazilian populations of European and African origin.

Hemoglobin E Associated with Hemoglobin Constant Spring: Diagnostic Challenges in Heterozygous and Homozygous States.

An Unusual Presentation of Erythrocytosis Resulting in the Identification of a Novel Unstable Hemoglobin Variant: Hb Koskullskulle HBB: C.311T > C (p.Phe104Ser).

Hematologic Indices of Hemoglobin D Co-Inheritance with α and β Thalassemia: A Comparative Study of 202 Patients.

The Efficiency of Capillarys 2 Flex Piercing, Premier Resolution-HPLC, and VARIANT II-HPLC for Hemoglobin Constant Spring Detection.

Tailoring Genetic Approaches for Easier Detection of Anti-3.7 Alpha-Globin Gene Triplication in the Iranian Population.

Microcytic Anemia with Low HbA2 and Normal HbA: Two Cases of Rare Thalassemia.

Whole-Exome Sequencing in a Consanguinity-Enriched South Indian Retinitis Pigmentosa Cohort: Diagnostic Yield and Molecular Spectrum.

Genetic analysis, reproductive decision-making, and pregnancy outcomes in 51 Chinese osteogenesis imperfecta families.

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

Natural variation in SL6 determines fatty acid components and seed longevity in rice.

Genetic architecture of endometriosis: risk factors, comorbidities and clinical implications.

Comprehensive analysis of non-synonymous single-nucleotide polymorphism of human TSC1 and TSC2 genes: An in silico approach.

Related Experiment Videos

A new informative family for the close linkage between the structural beta and delta human hemoglobin genes

Related Concept Videos

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