Hu J - Search Results

1

Recent advances in nanoadjuvant-triggered STING activation for enhanced cancer immunotherapy.

Xu Z, Wu Y, Hu J, Mei Z, Zhao Y, Yang K, Shi Y, Xu X. Xu Z, et al. Among authors: hu j. Heliyon. 2024 Oct 5;10(20):e38900. doi: 10.1016/j.heliyon.2024.e38900. eCollection 2024 Oct 30. Heliyon. 2024. PMID: 39640775 Free PMC article. Review.

2

A pretreatment transcriptomic signature that predicts outcomes of immunotherapy in melanoma.

Hu J, Liu B, Hu W, Yang Y. Hu J, et al. Among authors: hu w. Heliyon. 2022 Dec 23;8(12):e12648. doi: 10.1016/j.heliyon.2022.e12648. eCollection 2022 Dec. Heliyon. 2022. PMID: 36619423 Free PMC article.

3

Case report: Prenatal diagnosis of Kagami-Ogata syndrome in a Chinese family.

Hu J, Zhang Y, Yang Y, Wang L, Sun Y, Dong M. Hu J, et al. Front Genet. 2022 Aug 11;13:959666. doi: 10.3389/fgene.2022.959666. eCollection 2022. Front Genet. 2022. PMID: 36035167 Free PMC article.

4

Hypoxia Confers Tumor with a Higher Immune Infiltration but Lower Mutation Burden in Gastrointestinal Cancer.

Hu J, Hu W, Yang Y. Hu J, et al. Among authors: hu w. J Oncol. 2022 Sep 12;2022:4965167. doi: 10.1155/2022/4965167. eCollection 2022. J Oncol. 2022. PMID: 36131795 Free PMC article.

5

[Application of single nucleotide polymorphism microarray in clinical diagnosis of intellectual disability or retardation].

Hu J, Qian Y, Sun Y, Yu J, Luo Y, Dong M. Hu J, et al. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2019 Jun 25;48(4):420-428. doi: 10.3785/j.issn.1008-9292.2019.08.12. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2019. PMID: 31901047 Free PMC article. Chinese.

6

Case Report: De novo DDX3X mutation caused intellectual disability in a female with skewed X-chromosome inactivation on the mutant allele.

Sun Y, Qian Y, Sun HX, Chen M, Luo Y, Xu X, Yan K, Wang L, Hu J, Dong M. Sun Y, et al. Among authors: hu j. Front Genet. 2022 Oct 10;13:999442. doi: 10.3389/fgene.2022.999442. eCollection 2022. Front Genet. 2022. PMID: 36299587 Free PMC article.

7

[Genetic analysis of a fetus with multiple malformations caused by complex translocations of four chromosomes].

Luo Y, Shen M, Sun Y, Qian Y, Wang L, Yu J, Hu J, Jin F, Dong M. Luo Y, et al. Among authors: hu j. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2019 Jun 25;48(4):397-402. doi: 10.3785/j.issn.1008-9292.2019.08.08. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2019. PMID: 31901043 Free PMC article. Chinese.

8

Advances of targeting the YAP/TAZ-TEAD complex in the hippo pathway for the treatment of cancers.

Luo M, Xu Y, Chen H, Wu Y, Pang A, Hu J, Dong X, Che J, Yang H. Luo M, et al. Among authors: hu j. Eur J Med Chem. 2022 Dec 15;244:114847. doi: 10.1016/j.ejmech.2022.114847. Epub 2022 Oct 13. Eur J Med Chem. 2022. PMID: 36265280 Review.

9

[Single nucleotide polymorphism microarray in prenatal diagnosis of fetuses with absent nasal bone].

Yu J, Sun Y, Hu J, Qian Y, Luo Y, Dong M. Yu J, et al. Among authors: hu j. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2019 Jun 25;48(4):414-419. doi: 10.3785/j.issn.1008-9292.2019.08.11. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2019. PMID: 31901046 Free PMC article. Chinese.

10

Prenatal diagnosis of trisomy 8 mosaicism, initially identified by cffDNA screening.

Hu J, Yan K, Jin P, Yang Y, Sun Y, Dong M. Hu J, et al. Mol Cytogenet. 2022 Sep 1;15(1):39. doi: 10.1186/s13039-022-00616-y. Mol Cytogenet. 2022. PMID: 36050777 Free PMC article.

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