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Last Updated: 10/31/2025

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Found 137 publications

Application of optical genome mapping technology for the detection of chromosomal structural variations

Application of optical genome mapping technology for the detection of chromosomal structural variations

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: March 06, 2024

I123-FP-CIT (DaTSCAN) SPECT beyond the Most Common Causes of Parkinsonism: A Systematic Review.

I123-FP-CIT (DaTSCAN) SPECT beyond the Most Common Causes of Parkinsonism: A Systematic Review.

Journal: Movement disorders clinical practice
Published: November 14, 2023

Growth retardation and congenital heart disease in a boy with a ring chromosome 6 of maternal origin.

Growth retardation and congenital heart disease in a boy with a ring chromosome 6 of maternal origin.

Journal: Molecular cytogenetics
Published: November 30, 2021

Restrictive cardiomyopathy with ring chromosome 6 anomaly in a child.

Restrictive cardiomyopathy with ring chromosome 6 anomaly in a child.

Journal: Anatolian journal of cardiology
Published: October 08, 2021

GWAS and genomic prediction of milk urea nitrogen in Australian and New Zealand dairy cattle.

GWAS and genomic prediction of milk urea nitrogen in Australian and New Zealand dairy cattle.

Journal: Genetics, selection, evolution : GSE
Published: June 30, 2021

Older-onset levodopa-responsive parkinsonism with normal DAT-SPECT and pterin hypometabolism.

Older-onset levodopa-responsive parkinsonism with normal DAT-SPECT and pterin hypometabolism.

Journal: BMJ case reports
Published: May 08, 2021

A 2.09 Mb fragment translocation on chromosome 6 causes abnormalities during meiosis and leads to less seed watermelon.

A 2.09 Mb fragment translocation on chromosome 6 causes abnormalities during meiosis and leads to less seed watermelon.

Journal: Horticulture research
Published: March 28, 2021

GCH1 mutations in hereditary spastic paraplegia.

GCH1 mutations in hereditary spastic paraplegia.

Journal: Clinical genetics
Published: January 06, 2021

A selective NLRP3 inflammasome inhibitor attenuates behavioral deficits and neuroinflammation in a mouse model of Parkinson's disease.

A selective NLRP3 inflammasome inhibitor attenuates behavioral deficits and neuroinflammation in a mouse model of Parkinson's disease.

Journal: Journal of neuroimmunology
Published: November 04, 2020

Identification of Genetic Factors Underlying the Association between Sodium Intake Habits and Hypertension Risk.

Identification of Genetic Factors Underlying the Association between Sodium Intake Habits and Hypertension Risk.

Journal: Nutrients
Published: August 05, 2020

Monascin exhibits neuroprotective effects in rotenone model of Parkinson's disease via antioxidation and anti-neuroinflammation.

Monascin exhibits neuroprotective effects in rotenone model of Parkinson's disease via antioxidation and anti-neuroinflammation.

Journal: Neuroreport
Published: May 20, 2020

GCH-1 genetic variant may cause Parkinsonism by unmasking the subclinical nigral pathology.

GCH-1 genetic variant may cause Parkinsonism by unmasking the subclinical nigral pathology.

Journal: Journal of neurology
Published: February 24, 2020
Showing 1-12 of 137

Last Updated: 10/31/2025