Lisha Yang

发表

A Novel Variant of the FZD4 Gene in a Chinese Family Causes Autosomal Dominant Familial Exudative Vitreoretinopathy

Jingliang Cheng, Junjiang Fu, Lisha Yang, 2018, Cellular Physiology and Biochemistry.

A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree

Jingliang Cheng, Junjiang Fu, M. Khan, 2019, Journal of cellular and molecular medicine.

Genetic identification and molecular modeling characterization reveal a novel PROM1 mutation in Stargardt4-like macular dystrophy

Jingliang Cheng, Yumei Li, Rui Chen, 2017, Oncotarget.

Prognostic value of systemic hemato-immunological indices in uterine cervical cancer: A systemic review, meta-analysis, and meta-regression of observational studies.

S. Fu, S. Imani, Lisha Yang, 2020, Gynecologic oncology.

Diagnostic value of a combination of next-generation sequencing, chorioretinal imaging and metabolic analysis: lessons from a consanguineous Chinese family with gyrate atrophy of the choroid and retina stemming from a novel OAT variant

Yumei Li, Rui Chen, Junjiang Fu, 2018, British Journal of Ophthalmology.

Evaluation of amplification refractory mutation system (ARMS) technique for quick and accurate prenatal gene diagnosis of CHM variant in choroideremia

Jingliang Cheng, Junjiang Fu, M. Khan, 2017, The application of clinical genetics.

Novel, heterozygous, pathogenic variant (c.4272delA: p.I1426Ffs*2) for the NF1 gene in a large Chinese family with neurofibromatosis type 1

Junjiang Fu, Lisha Yang, Jiewen Fu, 2022, Molecular Biology Reports.

Identification of a novel RPGRIP1 mutation in an Iranian family with leber congenital amaurosis by exome sequencing

Mohammad Hossein Khosravi, Jingliang Cheng, Yumei Li, 2017, Journal of cellular and molecular medicine.

Novel compound heterozygous EYS variants may be associated with arRP in a large Chinese pedigree

Lisha Yang, Jiewen Fu, Chunli Wei, 2020, Bioscience reports.

Novel splicing variant c. 208+2T>C in BBS5 segregates with Bardet–Biedl syndrome in an Iranian family by targeted exome sequencing

Jingliang Cheng, Junjiang Fu, S. Imani, 2019, Bioscience reports.

A novel, homozygous nonsense variant of the CDHR1 gene in a Chinese family causes autosomal recessive retinal dystrophy by NGS‐based genetic diagnosis

Jingliang Cheng, Rui Chen, Junjiang Fu, 2018, Journal of cellular and molecular medicine.

A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing

Jingliang Cheng, Yumei Li, Rui Chen, 2018, BMC Medical Genetics.

Comprehensive analysis, immune, and cordycepin regulation for SOX9 expression in pan-cancers and the matched healthy tissues

Lisha Yang, Jiewen Fu, Chunli Wei, 2023, Frontiers in Immunology.

Thymoquinone Inhibits the Migration and Invasive Characteristics of Cervical Cancer Cells SiHa and CaSki In Vitro by Targeting Epithelial to Mesenchymal Transition Associated Transcription Factors Twist1 and Zeb1

Jingliang Cheng, Junjiang Fu, Lisha Yang, 2017, Molecules.

Novel, heterozygous, de novo pathogenic variant (c.4963delA: p.Thr1656Glnfs*42) of the NF1 gene in a Chinese family with neurofibromatosis type 1

Lisha Yang, Jiewen Fu, Junjiang Fu, 2023, BMC Medical Genomics.

Abstract 2039: Cordycepin inhibits breast cancer migration and invasion by targeting epithelial to mesenchymal transition-inducing transcription factors (EMT-TFs)

Jingliang Cheng, Junjiang Fu, H. Zou, 2018, Tumor Biology.

Genetic Polymorphism and Population Genetic Structure Analysis of 21 Autosomal STR Loci for a Han-Chinese Population from Luzhou of Southwest China

Lisha Yang, Jiewen Fu, Junjiang Fu, 2023, Genes.

Novel, pathogenic insertion variant of GSDME associates with autosomal dominant hearing loss in a large Chinese pedigree.

Lisha Yang, Jiewen Fu, Shangyi Fu, 2023, Journal of cellular and molecular medicine.