H. BinEssa

发表

β-Catenin Attenuation Inhibits Tumor Growth and Promotes Differentiation in a BRAFV600E-Driven Thyroid Cancer Animal Model

M. Zou, K. Khabar, Yufei Shi, 2021, Molecular Cancer Therapeutics.

KRASG12D-mediated oncogenic transformation of thyroid follicular cells requires long-term TSH stimulation and is regulated by SPRY1

C. Pritchard, M. Zou, Yufei Shi, 2015, Laboratory Investigation.

Mutation of SGK3, a novel regulator of renal phosphate transport, causes autosomal dominant hypophosphatemic rickets.

M. Zou, Yufei Shi, E. Cavalier, 2019, The Journal of clinical endocrinology and metabolism.

Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3

M. Zou, Yufei Shi, B. Meyer, 2018, PloS one.

Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets

M. Zou, N. Kaya, Yufei Shi, 2017, Clinical endocrinology.

Spectrum of the Genetic Defects in Hypophosphatemic Rickets in A Group of Turkish Children

M. Zou, Yufei Shi, B. Meyer, 2016 .

Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis

M. Zou, Yufei Shi, E. Baitei, 2018, The Journal of clinical endocrinology and metabolism.

TSH overcomes BrafV600E-induced senescence to promote tumor progression via downregulation of p53 expression in papillary thyroid cancer

C. Pritchard, M. Zou, Y. Shi, 2016, Oncogene.

Cyp24a1 Attenuation Limits Progression of BrafV600E -Induced Papillary Thyroid Cancer Cells and Sensitizes Them to BRAFV600E Inhibitor PLX4720.

C. Pritchard, M. Zou, Yufei Shi, 2017, Cancer research.

Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic rickets.

M. Zou, Yufei Shi, B. Meyer, 2019, Bone.

Hypophosphatemic rickets caused by a novel splice donor site mutation and activation of two cryptic splice donor sites in the PHEX gene

M. Zou, Yufei Shi, B. Meyer, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A

M. Zou, Yufei Shi, B. Özkan, 2015, PloS one.

Molecular Analysis of CYP27B1 Mutations in Vitamin D-Dependent Rickets Type 1A: c.590G > A (p.G197D) Missense Mutation Causes a RNA Splicing Error

M. Zou, Yufei Shi, A. Guven, 2020, Frontiers in Genetics.

Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostoses

M. Zou, Yufei Shi, B. Meyer, 2021, Orphanet Journal of Rare Diseases.