Further studies on the distribution of erythrocyte enzyme types in Japanese

A de novo recombination in the ABO blood group gene and evidence for the occurence of recombination products.

Human genetics·1997

Novel polymorphisms and haplotypes in the human coagulation factor XIII A-subunit gene.

Human genetics·1996

Orosomucoid system: 17 additional orosomucoid variants and proposal for a new nomenclature.

Vox sanguinis·1993

Venous occlusion plethysmography reduces arterial diameter and flow velocity.

Journal of applied physiology (Bethesda, Md. : 1985)·1989

A case of paternity testing influenced by the silent allele of Rh erythrocyte groups.

Journal of forensic sciences·1987

A field study of infection with human T-cell leukemia virus among asian primates.

Microbiology and immunology·1985

Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

Rapid detection of a point mutation in thyroid-stimulating hormone beta-subunit gene causing congenital isolated thyroid-stimulating hormone deficiency.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

Biochemical characteristics of glucose-6-phosphate dehydrogenase variants among the Malays of Singapore with report of a new non-deficient (GdSingapore) and three deficient variants.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

Similar proportion of sporadic cases in cytochrome b558 negative chronic granulomatous disease and Duchenne muscular dystrophy.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

The MspI restriction fragment length polymorphism of human aldolase B gene on chromosome 9q21.3-q22.2.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

The prevalence at birth of cogenital malformations at a maternity hospital in Osaka City, 1948-1990.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

Mucopolysaccharidosis type IIIC diagnosed at the age of 12 years: Why was the disease diagnosed so late?

Pediatric endocrinology, diabetes, and metabolism·2026

Comprehensive Approach to Detect Liver Fibrosis by Indirect Serum Biomarkers.

The Journal of the Association of Physicians of India·2026

Parkinson's disease LRRK2 mutations dysregulate iron homeostasis and promote oxidative stress and ferroptosis in human neurons and astrocytes.

Molecular neurodegeneration·2026

Standardization of the Monocyte Monolayer Assay: Lessons Learned From Laboratory Optimization and Literature Review.

Journal of clinical laboratory analysis·2026

Back to the Basics: Mid-Year Risk Management Reset.

Innovations in clinical neuroscience·2026

Hepatic biomarker trajectories and mortality in septic adults with type 2 diabetes and recorded dipeptidyl peptidase-4 inhibitor exposure versus metformin-based therapy: A propensity-score-matched cohort study.

Metabolism open·2026

Related Experiment Videos

Further studies on the distribution of erythrocyte enzyme types in Japanese

Related Concept Videos

A de novo recombination in the ABO blood group gene and evidence for the occurence of recombination products.

Novel polymorphisms and haplotypes in the human coagulation factor XIII A-subunit gene.

Orosomucoid system: 17 additional orosomucoid variants and proposal for a new nomenclature.

Venous occlusion plethysmography reduces arterial diameter and flow velocity.

A case of paternity testing influenced by the silent allele of Rh erythrocyte groups.

A field study of infection with human T-cell leukemia virus among asian primates.

Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.

Rapid detection of a point mutation in thyroid-stimulating hormone beta-subunit gene causing congenital isolated thyroid-stimulating hormone deficiency.

Biochemical characteristics of glucose-6-phosphate dehydrogenase variants among the Malays of Singapore with report of a new non-deficient (GdSingapore) and three deficient variants.

Similar proportion of sporadic cases in cytochrome b558 negative chronic granulomatous disease and Duchenne muscular dystrophy.

The MspI restriction fragment length polymorphism of human aldolase B gene on chromosome 9q21.3-q22.2.

The prevalence at birth of cogenital malformations at a maternity hospital in Osaka City, 1948-1990.

Mucopolysaccharidosis type IIIC diagnosed at the age of 12 years: Why was the disease diagnosed so late?

Comprehensive Approach to Detect Liver Fibrosis by Indirect Serum Biomarkers.

Parkinson's disease LRRK2 mutations dysregulate iron homeostasis and promote oxidative stress and ferroptosis in human neurons and astrocytes.

Standardization of the Monocyte Monolayer Assay: Lessons Learned From Laboratory Optimization and Literature Review.

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Further studies on the distribution of erythrocyte enzyme types in Japanese

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