Yucui Zang

发表

Mutations in ASH1L confer susceptibility to Tourette syndrome

F. Yu, Jinchuan Xing, C. Schaaf, 2019, Molecular Psychiatry.

Identification of a novel TSHR mutation from a Chinese baby with congenital hypothyroidism due to ectopy

Shiguo Liu, Bin Kong, Yucui Zang, 2015 .

Identification of Two Missense Mutations in DUOX1 (p.R1307Q) and DUOXA1 (p.R56W) That Can Cause Congenital Hypothyroidism Through Impairing H2O2 Generation

Shiguo Liu, Xu Ma, Hongwei Zang, 2019, Front. Endocrinol..

Association between polymorphisms rs2228001 and rs2228000 in XPC and genetic susceptibility to preeclampsia: a case control study

Jing-li Wang, C. Guan, S. Piao, 2021, BMC Pregnancy and Childbirth.

Genetic screening of solute carrier family 5 member 5 (SLC5A5) gene in Chinese Han congenital hypothyroidism patients with goiter

Shiguo Liu, F. Wang, Wenxiu Han, 2016 .

Study on DEHAL1 Mutations in Patients with Congenital Hypothyroidism and Thyroid Goiter

Shiguo Liu, Hongwei Zang, Wenxiu Han, 2016 .

Genetic Testing of PAX8 Mutations Associated with Thyroid Dysgenesis in Chinese Congenital Hypothyroidism Patients.

Shiguo Liu, Wenmiao Wang, Dehua Zhao, 2020, Endokrynologia Polska.

Novel THRB mutation analysis in congenital hypothyroidism with thyroid dysgenesis

Fuyan Lv, Shiguo Liu, Hongwei Zang, 2018, Journal of cellular biochemistry.

DUOX2 and DUOXA2 Variants Confer Susceptibility to Thyroid Dysgenesis and Gland-in-situ With Congenital Hypothyroidism

Shiguo Liu, Yangang Wang, Xiao-long Yu, 2020, Frontiers in Endocrinology.