Shu-shan Sang

发表

Nitroproteins in Human Astrocytomas Discovered by Gel Electrophoresis and Tandem Mass Spectrometry

Xuejun Li, D. Desiderio, X. Zhan, 2015, Journal of The American Society for Mass Spectrometry.

Downregualtion of dynamin-related protein 1 attenuates glutamate-induced excitotoxicity via regulating mitochondrial function in a calcium dependent manner in HT22 cells.

Qing Liu, Jun Su, Xiang-yu Wang, 2014, Biochemical and biophysical research communications.

Clinical Long-Term Follow-Up Evaluation of Functional Neuronavigation in Adult Cerebral Gliomas.

Siyi Wanggou, Xuejun Li, Ningrong Ye, 2018, World neurosurgery.

Neuroprotective and anti-apoptotic effects of valproic acid on adult rat cerebral cortex through ERK and Akt signaling pathway at acute phase of traumatic brain injury

Qing Liu, Jun Su, Xiang-yu Wang, 2014, Brain Research.

Corrigendum to “Neuroprotective and anti-apoptotic effects of valproic acid on adult rat cerebral cortex through ERK and Akt signaling pathway at acute phase of traumatic brain injury” [Brain Res.1555 (2014, Mar. 25) 1–9]

Qing Liu, Jun Su, Shu-shan Sang, 2016, Brain Research.

Next-generation sequencing-based mutation analysis of genes associated with enlarged vestibular aqueduct in Chinese families

Yong Feng, Shu-shan Sang, L. Mei, 2020, European Archives of Oto-Rhino-Laryngology.

Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families

Yong Feng, Jing Liu, Shu-shan Sang, 2019, Front. Genet..

Anti-Cancer Effect of Metabotropic Glutamate Receptor 1 Inhibition in Human Glioma U87 Cells: Involvement of PI3K/Akt/mTOR Pathway

Qing Liu, Jun Su, Shu-shan Sang, 2015, Cellular Physiology and Biochemistry.

Impact of GBA variants on longitudinal freezing of gait progression in early Parkinson’s disease

Hong Lu, Shu-shan Sang, Jingtao Wang, 2023, Journal of Neurology.

A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum review.

X. Liu, Yong Feng, Jing Liu, 2019, Gene.

A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family

Yong Feng, Shu-shan Sang, Zhijie Niu, 2018, Journal of Human Genetics.

Mutations in TMEM43 cause autosomal dominant auditory neuropathy spectrum disorder via interaction with connexin-mediated passive conductance channels

W. Park, Eunyoung Yi, S. Blanton, 2020, bioRxiv.

Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families.

M. Li, Yong Feng, Shu-shan Sang, 2018, International journal of pediatric otorhinolaryngology.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

X. Liu, M. Li, D. Yan, 2018, Human Genetics.

A nonsense TMEM43 variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder

W. Park, Eunyoung Yi, S. Blanton, 2021, Proceedings of the National Academy of Sciences.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

X. Liu, M. Li, D. Yan, 2018, Human Genetics.