Genetically determined electrophoretic variants of human red cell NADH diaphorase

Regulation of clustered gene expression by cofactor of BRCA1 (COBRA1) in breast cancer cells.

Oncogene·2006

The canine homeobox gene MSX2: sequence, chromosome assignment and genetic analysis in dogs of different breeds.

Animal genetics·2001

Identification and characterisation of polymorphisms in human phosphoglucomutase (PGM1).

Annals of human genetics·2000

Mapping recombination hotspots in human phosphoglucomutase (PGM1).

Human molecular genetics·1999

A phylogenetic approach to the identification of phosphoglucomutase genes.

Molecular biology and evolution·1998

Molecular and cytological investigations of phosphoglucomutase (PGM1) in the K562 cell line.

Annals of human genetics·1997

Ancestry-Stratified Variant Classification in Monogenic Diabetes Genes: Annotation Coverage and Differential Curation Burden.

Annals of human genetics·2026

Population-Level Nucleotide Diversity and Genetic Differentiation at SOD1 Across Global Human Populations.

Annals of human genetics·2026

Structural Variations of Alu Elements in the Kuwaiti Population: Laying the Foundations for Forensic Medicine.

Annals of human genetics·2026

Trans-Ancestry Psychiatric Genomics in Admixed Populations: Advances, Challenges, and Future Directions.

Annals of human genetics·2026

Evidence of a Protective Effect of Metformin on Abdominal Aortic Aneurysm Risk: Insights From an Observational Study and Mendelian Randomisation Analysis Using Putative Metformin Targets.

Annals of human genetics·2026

Utility of Urine-Derived Cells for Characterizing Aberrant Splicing Caused by a Novel Deep Intronic L1CAM Variant.

Annals of human genetics·2026

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

Pharmacology & therapeutics·2026

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Related Experiment Videos

Genetically determined electrophoretic variants of human red cell NADH diaphorase

Related Concept Videos

Regulation of clustered gene expression by cofactor of BRCA1 (COBRA1) in breast cancer cells.

The canine homeobox gene MSX2: sequence, chromosome assignment and genetic analysis in dogs of different breeds.

Identification and characterisation of polymorphisms in human phosphoglucomutase (PGM1).

Mapping recombination hotspots in human phosphoglucomutase (PGM1).

A phylogenetic approach to the identification of phosphoglucomutase genes.

Molecular and cytological investigations of phosphoglucomutase (PGM1) in the K562 cell line.

Ancestry-Stratified Variant Classification in Monogenic Diabetes Genes: Annotation Coverage and Differential Curation Burden.

Population-Level Nucleotide Diversity and Genetic Differentiation at SOD1 Across Global Human Populations.

Structural Variations of Alu Elements in the Kuwaiti Population: Laying the Foundations for Forensic Medicine.

Trans-Ancestry Psychiatric Genomics in Admixed Populations: Advances, Challenges, and Future Directions.

Evidence of a Protective Effect of Metformin on Abdominal Aortic Aneurysm Risk: Insights From an Observational Study and Mendelian Randomisation Analysis Using Putative Metformin Targets.

Utility of Urine-Derived Cells for Characterizing Aberrant Splicing Caused by a Novel Deep Intronic L1CAM Variant.

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

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Related Experiment Videos

Genetically determined electrophoretic variants of human red cell NADH diaphorase

Related Concept Videos

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