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Yufei Shi

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Molecular Cancer Therapeutics|July 5, 2021

β-Catenin Attenuation Inhibits Tumor Growth and Promotes Differentiation in a BRAF<sup>V600E</sup>-Driven Thyroid Cancer Animal ModelMinjing Zou, Huda A BinEssa, Yousif H Al-Malki, et al.

The Journal of Clinical Endocrinology and Metabolism|March 17, 2018

Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid DyshormonogenesisMinjing Zou, Ali S Alzahrani, Ali Al-Odaib, et al.

Journal of the Endocrine Society|February 2, 2026

Molecular Genetics of 1α-Hydroxylase Deficiency in the Saudi PopulationBassam Bin-Abbas, Afaf Alsagheir, Balgees Alghamdi, et al.

Plos One|March 6, 2018

Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3Sezer Acar, Huda A BinEssa, Korcan Demir, et al.

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Search research articles

Showing results (121-130 of 124) with videos related to

Sort By:

Pageof 13

You have reached the last page of results.This site can display upto 124 results.

Molecular Cancer Therapeutics|July 5, 2021

β-Catenin Attenuation Inhibits Tumor Growth and Promotes Differentiation in a BRAF<sup>V600E</sup>-Driven Thyroid Cancer Animal ModelMinjing Zou, Huda A BinEssa, Yousif H Al-Malki, et al.

The Journal of Clinical Endocrinology and Metabolism|March 17, 2018

Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid DyshormonogenesisMinjing Zou, Ali S Alzahrani, Ali Al-Odaib, et al.

Journal of the Endocrine Society|February 2, 2026

Molecular Genetics of 1α-Hydroxylase Deficiency in the Saudi PopulationBassam Bin-Abbas, Afaf Alsagheir, Balgees Alghamdi, et al.

Plos One|March 6, 2018

Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3Sezer Acar, Huda A BinEssa, Korcan Demir, et al.

Pageof 13