about
Application of next generation sequencing technology in Mendelian movement disordersIdentification of TMEM230 mutations in familial Parkinson's diseaseThe EIF4G1 gene and Parkinson's diseaseTAp63 suppress metastasis via miR-133b in colon cancer cells.Compound heterozygous POMT1 mutations in a Chinese family with autosomal recessive muscular dystrophy-dystroglycanopathy C1.A functional variant of the dopamine D3 receptor is associated with risk and age-at-onset of essential tremor.LPLUNC1 inhibits nasopharyngeal carcinoma cell growth via down-regulation of the MAP kinase and cyclin D1/E2F pathwaysAdvances in the Molecular Genetics of Non-syndromic Syndactyly.Acute myelitis in a patient with vogt-koyanagi-harada disease: case report and review of the literature.Novel CLCN7 mutation identified in a Han Chinese family with autosomal dominant osteopetrosis-2.Upregulated long non-coding RNA LINC00152 expression is associated with progression and poor prognosis of tongue squamous cell carcinoma.The molecular biology of genetic-based epilepsies.Genetics, molecular biology, and phenotypes of x-linked epilepsy.Molecular genetics of congenital nuclear cataract.Genetic variants and animal models in SNCA and Parkinson disease.Integrating ChIP-sequencing and digital gene expression profiling to identify BRD7 downstream genes and construct their regulating network.Advances in the molecular genetics of non-syndromic polydactyly.Effects and mechanisms of action of SARI on androgen-independent prostate cancer (DU145) cells.TSC22D2 interacts with PKM2 and inhibits cell growth in colorectal cancer.An integrative transcriptomic analysis reveals p53 regulated miRNA, mRNA, and lncRNA networks in nasopharyngeal carcinoma.AFAP1-AS1, a long noncoding RNA upregulated in lung cancer and promotes invasion and metastasis.Molecular genetics of the COL2A1-related disorders.MicroRNA‑133b inhibits connective tissue growth factor in colorectal cancer and correlates with the clinical stage of the disease.The role of the ATP2C1 gene in Hailey-Hailey disease.Genetic analysis of PITX3 variants in patients with essential tremor.Identification of a novel GJA3 mutation in congenital nuclear cataract.Response to comment on 'TAp63 suppress metastasis via miR-133b in colon cancer cells'.Extended study of A265G variant of HS1BP3 in essential tremor and Parkinson disease.Gene polymorphism of rs556621 but Not rs11984041 is associated with the risk of large artery atherosclerotic stroke in a Xinjiang Uyghur population.EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson disease.Role of sphingosine-1-phosphate receptor 1 and sphingosine-1-phosphate receptor 2 in hyperglycemia-induced endothelial cell dysfunction.Identification of a Novel Mutation in the ABCA4 Gene in a Chinese Family with Retinitis Pigmentosa Using Exome Sequencing.No evidence of association between the LINGO4 gene and essential tremor in Chinese Han patients.Identification of a novel PHEX mutation in a Chinese family with X-linked hypophosphatemic rickets using exome sequencing.Identification of a novel COL4A5 mutation in a Chinese family with X-linked Alport syndrome using exome sequencing.Identification of a missense HOXD13 mutation in a Chinese family with syndactyly type I-c using exome sequencing.Identification of a missense mutation in the tyrosinase gene in a Chinese family with oculocutaneous albinism type 1.Role of metabolism in cancer cell radioresistance and radiosensitization methods.PINK1 p.K520RfsX3 mutation identified in a Chinese family with early-onset Parkinson's disease.Identification of a GNE homozygous mutation in a Han-Chinese family with GNE myopathy
P50
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P50
description
researcher
@en
հետազոտող
@hy
name
Hao Deng
@ast
Hao Deng
@en
Hao Deng
@es
Hao Deng
@nl
type
label
Hao Deng
@ast
Hao Deng
@en
Hao Deng
@es
Hao Deng
@nl
prefLabel
Hao Deng
@ast
Hao Deng
@en
Hao Deng
@es
Hao Deng
@nl
P108
P1053
O-6340-2017
P106
P1153
26643632600
P31
P4012
P496
0000-0003-3240-4352