Complement receptor 1 (CR1) on erythrocytes of patients with systemic lupus erythematosus

Clathrin is involved in organization of mitotic spindle and phragmoplast as well as in endocytosis in tobacco cell cultures.

Protoplasma·2007

Possible association of actin filaments with chloroplasts of spinach mesophyll cells in vivo and in vitro.

Protoplasma·2006

Possible involvement of energy metabolism in the change of cytoplasm organization induced by a protein phosphatase inhibitor, calyculin A, in root hair cells of Limnobium stoloniferum.

Protoplasma·2003

Calcium-calmodulin suppresses the filamentous actin-binding activity of a 135-kilodalton actin-bundling protein isolated from lily pollen tubes.

Plant physiology·2000

Regulation of cytoplasmic pH under extreme acid conditions in suspension cultured cells of Catharanthus roseus: a possible role of inorganic phosphate.

Plant & cell physiology·2000

Direct observation of processive movement by individual myosin V molecules.

Biochemical and biophysical research communications·2000

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

Platelet indices and incident hypertension: effect modification by body mass index in a Chinese cohort.

Journal of global health·2026

Advancements in CRISPR-based in vivo gene therapy for hemophilia.

Frontiers in genome editing·2026

Assessing intra- and inter-analyser imprecision in automated hematological laboratories.

Journal of medical biochemistry·2026

Treatment of Deep Vein Thrombosis in Congenital Factor VII Deficiency: A Case Report and Literature Review.

Clinical case reports·2026

Intermittent Hematuria and Shock due to Uretero-Arterial Fistula Diagnosed by Provocative Angiography.

Annals of vascular diseases·2026

Complement diagnostics and therapeutics for the pediatric population: early successes and opportunities for further advancement.

Frontiers in pharmacology·2026

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Complement receptor 1 (CR1) on erythrocytes of patients with systemic lupus erythematosus

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Clathrin is involved in organization of mitotic spindle and phragmoplast as well as in endocytosis in tobacco cell cultures.

Possible association of actin filaments with chloroplasts of spinach mesophyll cells in vivo and in vitro.

Possible involvement of energy metabolism in the change of cytoplasm organization induced by a protein phosphatase inhibitor, calyculin A, in root hair cells of Limnobium stoloniferum.

Calcium-calmodulin suppresses the filamentous actin-binding activity of a 135-kilodalton actin-bundling protein isolated from lily pollen tubes.

Regulation of cytoplasmic pH under extreme acid conditions in suspension cultured cells of Catharanthus roseus: a possible role of inorganic phosphate.

Direct observation of processive movement by individual myosin V molecules.

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.

Platelet indices and incident hypertension: effect modification by body mass index in a Chinese cohort.

Advancements in CRISPR-based in vivo gene therapy for hemophilia.

Assessing intra- and inter-analyser imprecision in automated hematological laboratories.

Treatment of Deep Vein Thrombosis in Congenital Factor VII Deficiency: A Case Report and Literature Review.

Intermittent Hematuria and Shock due to Uretero-Arterial Fistula Diagnosed by Provocative Angiography.

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