S. Lian

发表

A novel frameshift mutation of the NF1 gene in a Chinese pedigree with neurofibromatosis type 1

Xuefei Lin, Hui Chen, Wei Zhu, 2017, Indian journal of dermatology, venereology and leprology.

The first case report of a Chinese Hermansky-Pudlak syndrome patient with a novel mutation on HPS1 gene.

S. Lian, Lejin Wang, A. Wei, 2009, Journal of dermatological science.

N-terminal 5-mer peptide analog P165 of amyloid precursor protein inhibits UVA-induced MMP-1 expression by suppressing the MAPK pathway in human dermal fibroblasts.

Hui Chen, Wei Zhu, S. Lian, 2014, European journal of pharmacology.

Photoprotective effect of the N‐terminal 5‐mer peptide analog P165 of amyloid precursor protein in human dermal fibroblasts

Hui Chen, Wei Zhu, S. Lian, 2014, Chinese medical journal.

Genetic analyses of Chinese patients with digenic oculocutaneous albinism.

S. Lian, A. Wei, Wei Li, 2013, Chinese medical journal.

Sun‐exposure knowledge and protection behavior in a North Chinese population: a questionnaire‐based study

Fan Zhang, S. Lian, Shujuan Li, 2010, Photodermatology, photoimmunology & photomedicine.

Genome-wide association study of chronic spontaneous urticaria reveals genetic overlap with autoimmune diseases, not atopic diseases.

Wei Huang, Wei Zhu, S. Lian, 2022, The Journal of investigative dermatology.

Reverse line blot hybridization and DNA sequencing studies of the 16S-23S rRNA gene intergenic spacer regions of five emerging pathogenic Nocardia species.

T. Sorrell, V. Sintchenko, S. Lian, 2010, Journal of medical microbiology.

Epstein–Barr Virus‐Associated Hydroa Vacciniforme‐like Cutaneous Lymphoma in Seven Chinese Children

S. Lian, Zigang Xu, 2010, Pediatric dermatology.

Downregulation of PTEN expression in psoriatic lesions

S. Lian, X. Man, Xiaoyan Zhang, 2014, International journal of dermatology.

Identification of a Novel Mutation in a Chinese Family with X-Linked Ocular Albinism

S. Lian, Y. Wang, A. Wei, 2009, European journal of ophthalmology.

Novel nonsense mutation of the TSC2 gene in a case of tuberous sclerosis complex

Xuefei Lin, Hui Chen, Wei Zhu, 2016, European Journal of Dermatology.

Dry skin : Specific features in chinese women

Wei Zhu, S. Lian, Hong-Duo Chen, 2005 .

Mucocutaneous manifestations of HIV‐infected patients in the era of HAART in Guangxi Zhuang Autonomous Region, China

S. Lian, Z. Meng, W. Lun, 2013, Journal of the European Academy of Dermatology and Venereology : JEADV.

MiR-203 inhibits melanoma invasive and proliferative abilities by targeting the polycomb group gene BMI1.

Wei Zhu, S. Lian, Yong Sun, 2015, Biochemical and biophysical research communications.

Four novel mutations of TYR gene in Chinese OCA1 patients.

Wei Li, Yu Wang, S. Lian, 2009, Journal of dermatological science.

A comprehensive analysis reveals mutational spectra and common alleles in Chinese patients with oculocutaneous albinism.

Wei Li, Wei Zhu, S. Lian, 2010, The Journal of investigative dermatology.

The Impact of microRNA Regulation on Immune Recovery in HIV-1-Infected Patients Treated during Acute Infection: A Pilot Study

S. Lian, Hao Wu, B. Su, 2020, BioMed research international.

Longitudinal changes in total, 2-LTR circular, and integrated HIV-1 DNA during the first year of HIV-1 infection in CD4Low and CD4High patient groups with HIV-1 subtype AE.

S. Lian, Wei-jun Zhu, Hao Wu, 2014, Viral immunology.

Sensitization of melanoma cells to temozolomide by overexpression of microRNA 203 through direct targeting of glutaminase‐mediated glutamine metabolism

S. Lian, W. Zhu, X. Chang, 2017, Clinical and experimental dermatology.

Implementation of an optimized strategy for genetic testing of the Chinese patients with oculocutaneous albinism.

Wei Li, S. Lian, A. Wei, 2011, Journal of dermatological science.

IgE and IgG Anti-Thyroid Autoantibodies in Chinese Patients With Chronic Spontaneous Urticaria and a Literature Review.

Wei Zhu, S. Lian, R. Qi, 2022, Allergy, asthma & immunology research.

WW domain-containing E3 ubiquitin protein ligase 1 depletion evokes antitumor effect in cutaneous squamous cell carcinoma by inhibiting signal transducer and activator of transcription 3 signaling pathway

Wei Zhu, S. Lian, Yong-hua Xia, 2018, The Journal of international medical research.

Aberrant expression of Fas and FasL pro‐apoptotic proteins in basal cell and squamous cell carcinomas

S. Lian, X. Wang, R. Zhang, 2011, Clinical and experimental dermatology.

Clinical manifestations and neurofibromatosis type 1 gene mutations of 25 patients with neurofibromatosis type 1 from 10 Chinese pedigrees

Xuefei Lin, Hui Chen, Wei Zhu, 2020, Zhōnghuá Pífūkē Yīxué Zázhì.

Neurofibromatosis type 1 and X-linked ichthyosis in a patient with a novel frameshift mutation in the NF1 gene

Xuefei Lin, Hui Chen, Wei Zhu, 2016, European Journal of Dermatology.

Potential Application of MicroRNA Profiling to the Diagnosis and Prognosis of HIV-1 Infection

S. Lian, Haoquan Wu, Hao Wu, 2018, Front. Microbiol..

A comprehensive study of oculocutaneous albinism type 1 reveals three previously unidentified alleles on the TYR gene

Wei Zhu, S. Lian, A. Wei, 2014, European Journal of Dermatology.

A novel missense mutation of the ECM1 gene in a Chinese patient with lipoid proteinosis

S. Lian, W. Xu, X. Yang, 2012, Clincal and Experimental Dermatology.

miR-137 suppresses tumor growth of malignant melanoma by targeting aurora kinase A.

Wei Zhu, S. Lian, X. Chang, 2016, Biochemical and biophysical research communications.

Longitudinal changes in total, 2-LTR circular, and integrated HIV-1 DNA during the first year of HIV-1 infection in CD4Low and CD4High patient groups with HIV-1 subtype AE.

S. Lian, Wei-jun Zhu, Hao Wu, 2014, Viral immunology.