Ran Zhang
Qingdao, China
Last Updated: 09/26/2026
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Found 8 publications
Identified five variants in CFTR gene that alter RNA splicing by minigene assay.
Journal: Frontiers in genetics
Published: December 11, 2024
Identifying six single nucleotide variants in the COL17A1 gene that alter RNA splicing: database analysis and minigene assays.
Journal: Scientific reports
Published: August 12, 2024
Complex phenotype in Fanconi renotubular syndrome type 1: Hypophosphatemic rickets as the predominant presentation.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: May 07, 2024
Minigene-based splice assays provide new insights on intronic variants of the PKHD1 gene.
Journal: Human genomics
Published: May 03, 2024
Identification of seven variants in the col4a1 gene that alter RNA splicing by minigene assay.
Journal: Clinical genetics
Published: February 26, 2024
A novel heterozygous variant of the SALL1 gene with atypical Townes-Brocks syndrome phenotypes in Chinese family.
Journal: Nephrology (Carlton, Vic.)
Published: December 14, 2023
Three exonic variants in the COL4A5 gene alter RNA splicing in a minigene assay.
Journal: Molecular genetics & genomic medicine
Published: September 05, 2023
Single nucleotide polymorphisms in the upstream regulatory region alter the expression of myostatin.
Single nucleotide polymorphisms in the upstream regulatory region alter the expression of myostatin.
Journal: In vitro cellular & developmental biology. Animal
Published: January 10, 2013
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Last Updated: 09/26/2026