Xinjian Wang

Institutes of Brain Science, Fudan University

Research Area

Developmental Biology

Biography

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title	2017

Other Publications

Article	Year
[Inhibitory effects of genistein on the synthesis of DNA and the protein expression of cyclin D1 in human gastric carcinoma cell-line]. Wei sheng yan jiu = Journal of hygiene research\| PubMed ID: 12561543	2002
Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations. American journal of human genetics\| PubMed ID: 16826519	2006
Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation. Gene\| PubMed ID: 17341440	2007
The mitochondrial tRNA(Glu) A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber's hereditary optic neuropathy. Biochemical and biophysical research communications\| PubMed ID: 17434142	2007
The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss. Biochemical and biophysical research communications\| PubMed ID: 17434445	2007
Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss. Biochemical and biophysical research communications\| PubMed ID: 17659260	2007
Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss. Biochemical and biophysical research communications\| PubMed ID: 17698030	2007
Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees. Gene\| PubMed ID: 17698299	2007
Deletion of the MTO2 gene related to tRNA modification causes a failure in mitochondrial RNA metabolism in the yeast Saccharomyces cerevisiae. FEBS letters\| PubMed ID: 17706197	2007
The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family. Biochemical and biophysical research communications\| PubMed ID: 17723226	2007
Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three... American journal of medical genetics. Part A\| PubMed ID: 18386806	2008
Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss. Mitochondrion\| PubMed ID: 18639500	2008
Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families. Pharmacogenetics and genomics\| PubMed ID: 18820594	2008
Mutation in MTO1 involved in tRNA modification impairs mitochondrial RNA metabolism in the yeast Saccharomyces cerevisiae. Mitochondrion\| PubMed ID: 19460296	2009
Combination of the loss of cmnm5U34 with the lack of s2U34 modifications of tRNALys, tRNAGlu, and tRNAGln altered mitochondrial biogenesis and respiration. Journal of molecular biology\| PubMed ID: 20004207	2010
Effects of Taishan Pinus massoniana pollen polysaccharide on immune response of rabbit haemorrhagic disease tissue inactivated vaccine and on production performance of Rex rabbits. Vaccine\| PubMed ID: 21295100	2011
Geographical patterns based on faunal types of breeding birds and mammals in China. Integrative zoology\| PubMed ID: 21396078	2008
Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAIle gene in a large Han Chinese family. Circulation research\| PubMed ID: 21454794	2011
Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene. Journal of medical genetics\| PubMed ID: 21931169	2011
Coronary heart disease is associated with a mutation in mitochondrial tRNA. Human molecular genetics\| PubMed ID: 23736300	2013
Seroprevalence of pertussis in China: need to improve vaccination strategies. Human vaccines & immunotherapeutics\| PubMed ID: 24018405	2014
A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential. Nucleic acids research\| PubMed ID: 24920829	2014
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome. PLoS genetics\| PubMed ID: 25807530	2015
Phenotypic and functional characterization of Bst+/- mouse retina. Disease models & mechanisms\| PubMed ID: 26035379	2015
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder. Nature genetics\| PubMed ID: 26168012	2015
Metabolic rescue in pluripotent cells from patients with mtDNA disease. Nature\| PubMed ID: 26176921	2015
5-Hydroxy-3,6,7,8,3',4'-hexamethoxyflavone, a polymethoxyflavone, exerts antitumor effect on PI3K/Akt signaling pathway in human gastric cancer cell BGC-7901. Journal of receptor and signal transduction research\| PubMed ID: 26671739	2016
Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules. Human pathology\| PubMed ID: 26826406	2016
Age-Related Accumulation of Somatic Mitochondrial DNA Mutations in Adult-Derived Human iPSCs. Cell stem cell\| PubMed ID: 27151456	2016
Deep Sequencing Reveals Novel Genetic Variants in Children with Acute Liver Failure and Tissue Evidence of Impaired Energy Metabolism. PloS one\| PubMed ID: 27483465	2016
Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations. Nature\| PubMed ID: 27919073	2016