[The molecular basis of the thalassemia syndromes (author's transl)]

Expression and localization of bone morphogenetic proteins (BMPs) and BMP receptors in ossification of the ligamentum flavum.

Bone·1997

Procedural memory in patients with mild Alzheimer's disease.

Dementia and geriatric cognitive disorders·1997

The disturbances of object vision and spatial vision in Alzheimer's disease.

Dementia and geriatric cognitive disorders·1997

Activation of blood coagulation factor X by arginine-specific cysteine proteinases (gingipain-Rs) from Porphyromonas gingivalis.

The Journal of biological chemistry·1997

Overexpression of resistance-related proteins (metallothioneins, glutathione-S-transferase pi, heat shock protein 27, and lung resistance-related protein) in osteosarcoma. Relationship with poor prognosis.

Cancer·1997

Selective determination of amitriptyline and nortriptyline in human plasma by HPLC with ultraviolet and particle beam mass spectrometry.

Journal of analytical toxicology·1997

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

Pan-genomic analysis of alternative polyadenylation reveals a 3'UTR remodeling regulatory layer controlling salt tolerance in rice.

Journal of integrative plant biology·2026

PRMT1-SFPQ regulates intron retention to control matrix gene expression during craniofacial development.

eLife·2026

Atypical Age-Related Patterns of Neural Signal Complexity in Autism Spectrum Disorder.

CNS neuroscience & therapeutics·2026

Who Are We Missing: Examining Health Insurance Coverage for Expanded Carrier Screening.

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

Goltz Syndrome With Large Esophageal Squamous Papillomas-A Unique Cause of Dysphagia Amenable to Endoscopic Treatment.

ACG case reports journal·2026

Characteristics of gut microbiota dysbiosis in patients with depression: a visual analysis of knowledge maps.

Frontiers in microbiology·2026

Related Experiment Videos

[The molecular basis of the thalassemia syndromes (author's transl)]

Related Concept Videos

Expression and localization of bone morphogenetic proteins (BMPs) and BMP receptors in ossification of the ligamentum flavum.

Procedural memory in patients with mild Alzheimer's disease.

The disturbances of object vision and spatial vision in Alzheimer's disease.

Activation of blood coagulation factor X by arginine-specific cysteine proteinases (gingipain-Rs) from Porphyromonas gingivalis.

Overexpression of resistance-related proteins (metallothioneins, glutathione-S-transferase pi, heat shock protein 27, and lung resistance-related protein) in osteosarcoma. Relationship with poor prognosis.

Selective determination of amitriptyline and nortriptyline in human plasma by HPLC with ultraviolet and particle beam mass spectrometry.

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.

Pan-genomic analysis of alternative polyadenylation reveals a 3'UTR remodeling regulatory layer controlling salt tolerance in rice.

PRMT1-SFPQ regulates intron retention to control matrix gene expression during craniofacial development.

Atypical Age-Related Patterns of Neural Signal Complexity in Autism Spectrum Disorder.

Who Are We Missing: Examining Health Insurance Coverage for Expanded Carrier Screening.

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[The molecular basis of the thalassemia syndromes (author's transl)]

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