W. Xiong

发表

miR-33a functions as a tumor suppressor in melanoma by targeting HIF-1α

Jianda Zhou, Rui Liu, Xiang Chen, 2015, Cancer biology & therapy.

CD71-Specific Aptamer Conjugated with Monomethyl Auristatin E for the Treatment of Uveal Melanoma.

Y. Liu, Mao Ye, Lin Zhang, 2021, ACS applied materials & interfaces.

Human Genetic Diseases

P. Riederer, W. Le, H. Deng, 2015, BioMed research international.

Different iron deposition patterns in akinetic/rigid-dominant and tremor-dominant Parkinson's disease

Ji-feng Guo, Ling Huang, Bei-sha Tang, 2020, Clinical Neurology and Neurosurgery.

A BRCA1 Splice Site Variant Responsible for Familial Ovarian Cancer in a Han-Chinese Family

H. Deng, W. Xiong, Lamei Yuan, 2022, Current Medical Science.

Gastric Polyposis Syndromes

Lik Hang Lee, W. Xiong, Kenrry Chiu, 2019, AJSP: Reviews and Reports.

Homozygous loss‐of‐function mutation of the LEPREL1 gene causes severe non‐syndromic high myopia with early‐onset cataract

Y. Zheng, K. Xia, Q. Pan, 2014, Clinical genetics.

Identification of a PRX variant in a Chinese family with congenital cataract by exome sequencing.

H. Xu, H. Deng, W. Xiong, 2016, QJM : monthly journal of the Association of Physicians.

Enhanced SOX2 expression in retinoblastoma tissues and peripheral blood is associated with the clinicopathological characteristics of the disease

W. Xiong, Bo-ding Tong, Yujie Wu, 2015, Oncology letters.

A novel splice‐site mutation in the ATP2C1 gene of a Chinese family with Hailey‐Hailey disease

Heng Xiao, Xiang Chen, H. Deng, 2018, Journal of cellular biochemistry.

Genetic analysis of a Chinese Han family with multiple endocrine neoplasia type 2A.

K. Gao, H. Deng, Zi-qiang Luo, 2013, Indian journal of biochemistry & biophysics.

A novel locus for primary focal hyperhidrosis mapped on chromosome 2q31.1

Z. Cao, J. Chen, W. Xiong, 2015, The British journal of dermatology.

Epigenetics effect on pathogenesis of thyroid-associated ophthalmopathy.

W. Xiong, Shichu Hou, X. Qi, 2021, International journal of ophthalmology.

A novel FN1 variant associated with familial hematuria: TBMN?

H. Deng, W. Xiong, Yuzhou Huang, 2016, Clinical biochemistry.

Identification of a Novel GJA3 Mutation in Congenital Nuclear Cataract

Jianguo Zhang, H. Deng, W. Xiong, 2015, Optometry and vision science : official publication of the American Academy of Optometry.

SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia

Liangdan Sun, Xuejun Zhang, K. Xia, 2014, Journal of Medical Genetics.

Genetic analysis of PITX3 variants in patients with essential tremor

L. Gong, H. Deng, Z. Song, 2017, Acta neurologica Scandinavica.

Association of the MTHFR rs1801131 and rs1801133 variants in sporadic Parkinson’s disease patients

H. Deng, Zhi Song, W. Xiong, 2016, Neuroscience Letters.

Genetic analysis of the S100B gene in Chinese patients with Parkinson disease

H. Deng, Zhi Song, W. Xiong, 2013, Neuroscience Letters.

Overview of Graves Ophthalmopathy Literature From 1999 to 2019: Bibliometric Analysis

W. Xiong, Shiying Hou, Yu Chen, 2020, Interactive journal of medical research.

Identification of a frame shift mutation in the CCDC151 gene in a Han-Chinese family with Kartagener syndrome

H. Deng, W. Xiong, S. Deng, 2020, Bioscience reports.

Examination of the MASH1 gene in patients with Parkinson's disease.

J. Jankovic, W. Le, H. Deng, 2010, Biochemical and biophysical research communications.

The risk factors for Graves’ ophthalmopathy

Chen Ma, W. Xiong, Yuhe Su, 2021, Graefe's Archive for Clinical and Experimental Ophthalmology.

Genetic analysis of TREM2 variants in Chinese Han patients with sporadic Parkinson’s disease

H. Deng, Zhi Song, W. Xiong, 2016, Neuroscience Letters.

Genetic Analysis and Literature Review of SNCA Variants in Parkinson's Disease

H. Deng, Wen Zheng, Zhi Song, 2021, Frontiers in Aging Neuroscience.

A novel heterozygous COL4A4 missense mutation in a Chinese family with focal segmental glomerulosclerosis

H. Deng, W. Xiong, P. Hu, 2016, Journal of cellular and molecular medicine.

Genetic analysis of SNCA coding mutation in Chinese Han patients with Parkinson disease

H. Deng, Zhi Song, W. Xiong, 2015, Acta Neurologica Belgica.

SLC6A3 rs28363170 and rs3836790 variants in Han Chinese patients with sporadic Parkinson’s disease

Hongwei Lu, H. Deng, Zhi Song, 2016, Neuroscience Letters.

Identification of a CNGB1 Frameshift Mutation in a Han Chinese Family with Retinitis Pigmentosa.

Y. Li, H. Deng, W. Xiong, 2018, Optometry and vision science : official publication of the American Academy of Optometry.

Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia

Y. Li, K. Xia, Q. Pan, 2015, Genetics in Medicine.

A homozygous MYO7A mutation associated to Usher syndrome and unilateral auditory neuropathy spectrum disorder.

H. Deng, W. Xiong, P. Hu, 2017, Molecular medicine reports.

Genetic analysis of the fused in sarcoma gene in Chinese Han patients with Parkinson's disease.

K. Gao, H. Deng, Wen Zheng, 2014, Parkinsonism & related disorders.

Compound heterozygous GJB2 mutations associated to a consanguineous Han family with autosomal recessive non-syndromic hearing loss

H. Deng, W. Xiong, Zhijian Yang, 2016, Acta oto-laryngologica.

Discovery of Aptamers and the Acceleration of the Development of Targeting Research in Ophthalmology

W. Xiong, Feng Zhang, Jiamin Cao, 2023, International journal of nanomedicine.

Association of the MTHFR rs1801131 and rs1801133 variants in sporadic Parkinson’s disease patients

H. Deng, Zhi Song, W. Xiong, 2016, Neuroscience Letters.

High monoamine oxidase a expression predicts poor prognosis for prostate cancer patients

Wei He, W. Xiong, Lingxiao Chen, 2023, BMC Urology.