[Molecular genetics of brain diseases]

Quantitation of heteroplasmy of mitochondrial tRNA(Leu(UUR)) gene using PCR-SSCP.

Muscle & nerve·1995

[Auditory comprehension in transcortical motor aphasia due to a medial lesions of the left frontal lobe].

No to shinkei = Brain and nerve·1995

Molecular cloning of a full-length cDNA for dentatorubral-pallidoluysian atrophy and regional expressions of the expanded alleles in the CNS.

American journal of human genetics·1995

A developmentally regulated member of the sialyltransferase family (ST8Sia II, STX) is a polysialic acid synthase.

FEBS letters·1995

Does homozygosity advance the onset of dentatorubral-pallidoluysian atrophy?

Neurology·1995

Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease.

Nature genetics·1995

[Japan-multimodal intervention trial for prevention of dementia (J-MINT) and its societal implementation: Concepts, challenges, and future directions].

Nihon Ronen Igakkai zasshi. Japanese journal of geriatrics·2026

[Mild cognitive impairment and interest in health among community-dwelling older adults: A cross-sectional analysis of the Wako Cohort Study].

Nihon Ronen Igakkai zasshi. Japanese journal of geriatrics·2026

[The factors influencing the progression of locomotive syndrome in community-dwelling older adults: focusing on a decline in muscular endurance].

Nihon Ronen Igakkai zasshi. Japanese journal of geriatrics·2026

[Association between tongue pressure and nutritional status assessed by multiple indicators in community-dwelling older adults: A cross-sectional study].

Nihon Ronen Igakkai zasshi. Japanese journal of geriatrics·2026

[Relationship between the frequency of participation in a preventive care exercise program and physical and mental health among older residents in the community].

Nihon Ronen Igakkai zasshi. Japanese journal of geriatrics·2026

[Development and evaluation of a dementia and delirium nursing education program using workshops and regular case conferences in acute-care hospitals].

Nihon Ronen Igakkai zasshi. Japanese journal of geriatrics·2026

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

American journal of medical genetics. Part A·2026

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

International journal of molecular sciences·2026

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

International journal of molecular sciences·2026

4-Phenylbutyrate Rescue in GABRA1 Variants Associated with Developmental Epileptic Encephalopathies: From Cell and Mouse Models to Humans.

Cells·2026

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Journal of medical genetics·2026

Ultrasound-guided renal artery administration of angiopoietin-1 RNA therapy slows the progression of preclinical WT1 glomerular disease.

Science translational medicine·2026

Related Experiment Videos

[Molecular genetics of brain diseases]

Related Concept Videos

Quantitation of heteroplasmy of mitochondrial tRNA(Leu(UUR)) gene using PCR-SSCP.

[Auditory comprehension in transcortical motor aphasia due to a medial lesions of the left frontal lobe].

Molecular cloning of a full-length cDNA for dentatorubral-pallidoluysian atrophy and regional expressions of the expanded alleles in the CNS.

A developmentally regulated member of the sialyltransferase family (ST8Sia II, STX) is a polysialic acid synthase.

Does homozygosity advance the onset of dentatorubral-pallidoluysian atrophy?

Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease.

[Japan-multimodal intervention trial for prevention of dementia (J-MINT) and its societal implementation: Concepts, challenges, and future directions].

[Mild cognitive impairment and interest in health among community-dwelling older adults: A cross-sectional analysis of the Wako Cohort Study].

[The factors influencing the progression of locomotive syndrome in community-dwelling older adults: focusing on a decline in muscular endurance].

[Association between tongue pressure and nutritional status assessed by multiple indicators in community-dwelling older adults: A cross-sectional study].

[Relationship between the frequency of participation in a preventive care exercise program and physical and mental health among older residents in the community].

[Development and evaluation of a dementia and delirium nursing education program using workshops and regular case conferences in acute-care hospitals].

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

4-Phenylbutyrate Rescue in GABRA1 Variants Associated with Developmental Epileptic Encephalopathies: From Cell and Mouse Models to Humans.

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Ultrasound-guided renal artery administration of angiopoietin-1 RNA therapy slows the progression of preclinical WT1 glomerular disease.

Related Experiment Videos

[Molecular genetics of brain diseases]

Related Concept Videos

Related Articles