New method for identifying genetic variants of human proalbumin

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Increased blood-oxygen binding affinity in Tibetan and Han Chinese residents at 4200 m.

Experimental physiology·2014

Intranasally-administered deferoxamine mitigates toxicity of 6-OHDA in a rat model of Parkinson׳s disease.

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Removal of sedimentation decreases relative deposition of coarse particles in the lung periphery.

Journal of applied physiology (Bethesda, Md. : 1985)·2013

Intranasal deferoxamine improves performance in radial arm water maze, stabilizes HIF-1α, and phosphorylates GSK3β in P301L tau transgenic mice.

Experimental brain research·2012

Production and fate of the sea lamprey migratory pheromone.

Fish physiology and biochemistry·2010

Genetic Investigation of X-Linked Defects with Optimized Targeted Long-Read Sequencing.

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Extending Quality Control Procedures for Multiplexed Clinical Assays.

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Biological Variation of Adrenal-Related Endocrine Biomarkers Used for Investigation of Secondary Hypertension.

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Clinical chemistry·2026

Wilson disease associated with a novel variant in the ATP7B gene.

Frontiers in neurology·2026

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Scientific reports·2026

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Journal of genetics and genomics = Yi chuan xue bao·2026

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Clinica chimica acta; international journal of clinical chemistry·2026

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

Brain & development·2026

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

The Journal of heredity·2026

Related Experiment Videos

New method for identifying genetic variants of human proalbumin

Related Concept Videos

Intranasal deferoxamine affects memory loss, oxidation, and the insulin pathway in the streptozotocin rat model of Alzheimer's disease.

Increased blood-oxygen binding affinity in Tibetan and Han Chinese residents at 4200 m.

Intranasally-administered deferoxamine mitigates toxicity of 6-OHDA in a rat model of Parkinson׳s disease.

Removal of sedimentation decreases relative deposition of coarse particles in the lung periphery.

Intranasal deferoxamine improves performance in radial arm water maze, stabilizes HIF-1α, and phosphorylates GSK3β in P301L tau transgenic mice.

Production and fate of the sea lamprey migratory pheromone.

Genetic Investigation of X-Linked Defects with Optimized Targeted Long-Read Sequencing.

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Distinguishing Acute Myocardial Infarction from Other Forms of Cardiac Injury with the Cardiac Troponin Long-T ITC Complex and High-Sensitivity Troponin I and T in Patients with Suspected Acute Coronary Syndrome: MERITnI Substudy.

Biological Variation of Adrenal-Related Endocrine Biomarkers Used for Investigation of Secondary Hypertension.

Enriching Microbial Cell-Free DNA in Clinical Metagenomics Using Epigenetic Filters.

Wilson disease associated with a novel variant in the ATP7B gene.

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

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Related Experiment Videos

New method for identifying genetic variants of human proalbumin

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