Minjing Zou
Riyadh, 11211, Saudi Arabia
Last Updated: 09/26/2026
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Found 27 publications
SGK3 promoter deletion in late-onset hypophosphatemic rickets, a possible genetic cause of the disease.
Journal: Orphanet journal of rare diseases
Published: March 05, 2025
Identification of novel prognostic biomarkers for thyroid cancer by integrated transcriptome analysis of metastasis-associated genes.
Journal: Frontiers in oncology
Published: November 28, 2024
Genome-wide transcriptome analysis and drug target discovery reveal key genes and pathways in thyroid cancer metastasis.
Journal: Frontiers in endocrinology
Published: October 20, 2024
β-catenin attenuation leads to up-regulation of activating NKG2D ligands and tumor regression in BrafV600E-driven thyroid cancer cells.
Journal: Frontiers in immunology
Published: February 22, 2023
Insights of Noncanonical Splice-site Variants on RNA Splicing in Patients With Congenital Hypothyroidism.
Journal: The Journal of clinical endocrinology and metabolism
Published: May 30, 2021
β-Catenin Attenuation Inhibits Tumor Growth and Promotes Differentiation in a BRAFV600E-Driven Thyroid Cancer Animal Model.
Journal: Molecular cancer therapeutics
Published: January 13, 2021
Molecular Analysis of CYP27B1 Mutations in Vitamin D-Dependent Rickets Type 1A: c.590G > A (p.G197D) Missense Mutation Causes a RNA Splicing Error.
Journal: Frontiers in genetics
Published: September 17, 2020
Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostoses.
Journal: Orphanet journal of rare diseases
Published: August 12, 2020
NOVEL VDR MUTATIONS IN PATIENTS WITH VITAMIN D-DEPENDENT RICKETS TYPE 2A: A MILD DISEASE PHENOTYPE CAUSED BY A NOVEL CANONICAL SPLICE-SITE MUTATION.
Journal: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
Published: September 27, 2019
Mutation of SGK3, a Novel Regulator of Renal Phosphate Transport, Causes Autosomal Dominant Hypophosphatemic Rickets.
Journal: The Journal of clinical endocrinology and metabolism
Published: July 02, 2019
Phenotype heterogeneity of congenital adrenal hyperplasia due to genetic mosaicism and concomitant nephrogenic diabetes insipidus in a sibling.
Journal: BMC medical genetics
Published: January 16, 2018
Last Updated: 09/26/2026