Lijuan Liu

Therapeutic potential and mechanism of kinetin as a treatment for the human splicing disease familial dysautonomia

M. Hims, J. Gusella, C. Lázaro, 2007, Journal of Molecular Medicine.

Loss of Mouse Ikbkap, a Subunit of Elongator, Leads to Transcriptional Deficits and Embryonic Lethality That Can Be Rescued by Human IKBKAP

M. Hims, M. Leyne, J. Mull, 2008, Molecular and Cellular Biology.

Mutation screening of crystallin genes in Chinese families with congenital cataracts

Zongfu Cao, Juhua Yang, Lijuan Liu, 2019, Molecular vision.

A humanized IKBKAP transgenic mouse models a tissue-specific human splicing defect.

M. Hims, J. Gusella, M. Leyne, 2007, Genomics.

Novel mutations in HSF4 cause congenital cataracts in Chinese families

Zongfu Cao, Juhua Yang, Lijuan Liu, 2018, BMC Medical Genetics.

Confirmation of the mitochondrial ND1 gene mutation G3635A as a primary LHON mutation.

Juhua Yang, Lijuan Liu, Xu Ma, 2009, Biochemical and biophysical research communications.

Transcriptome signatures reveal candidate key genes in the whole blood of patients with lumbar disc prolapse

Lijuan Liu, Yi Wang, Ling Jiang, 2019, Experimental and therapeutic medicine.