Fei Gao

The Wilms tumor gene, Wt1, is required for Sox9 expression and maintenance of tubular architecture in the developing testis

Fei Gao, Florian Guillou, Richard R Behringer, 2006, Proceedings of the National Academy of Sciences.

The Wt1+/R394W Mouse Displays Glomerulosclerosis and Early-Onset Renal Failure Characteristic of Human Denys-Drash Syndrome

F. Gao, J. Deng, R. Behringer, 2004, Molecular and Cellular Biology.

The Wilms Tumor Gene, Wt1, Is Critical for Mouse Spermatogenesis via Regulation of Sertoli Cell Polarity and Is Associated with Non-Obstructive Azoospermia in Humans

T. Jiang, Zhi-mao Jiang, Jun Xie, 2013, PLoS genetics.

Wt1 negatively regulates β-catenin signaling during testis development

Hao Chang, R. Behringer, M. Taketo, 2008, Development.

Wt1 functions in ovarian follicle development by regulating granulosa cell differentiation.

Jun-ling Yang, Yi-Xun Liu, Dahua Chen, 2014, Human molecular genetics.

Wt1 ablation and Igf2 upregulation in mice result in Wilms tumors with elevated ERK1/2 phosphorylation.

Fei Gao, Richard R Behringer, L. Strong, 2011, The Journal of clinical investigation.

Wt 1 ablation and Igf 2 upregulation in mice result in Wilms tumors with elevated ERK 1 / 2 phosphorylation

L. Strong, R. Behringer, W. Tian, 2010 .

Identification of the mutation causing progressive retinal atrophy in Old Danish Pointing Dog

M. Fredholm, P. Karlskov-Mortensen, F. Gao, 2018, Animal genetics.