Wu N - Search Results

1

Filamin B: The next hotspot in skeletal research?

Xu Q, Wu N, Cui L, Wu Z, Qiu G. Xu Q, et al. Among authors: wu n, wu z. J Genet Genomics. 2017 Jul 20;44(7):335-342. doi: 10.1016/j.jgg.2017.04.007. Epub 2017 Jul 6. J Genet Genomics. 2017. PMID: 28739045 Review.

2

[Advances in congenital vertebral malformation caused by genomic copy number variation].

Liu Z, Wu N, Wu Z, Zuo Y, Qiu G. Liu Z, et al. Among authors: wu n, wu z. Zhonghua Wai Ke Za Zhi. 2016 Apr 1;54(4):313-6. doi: 10.3760/cma.j.issn.0529-5815.2016.04.017. Zhonghua Wai Ke Za Zhi. 2016. PMID: 27029207 Chinese.

3

The genetic landscape and clinical implications of vertebral anomalies in VACTERL association.

Chen Y, Liu Z, Chen J, Zuo Y, Liu S, Chen W, Liu G, Qiu G, Giampietro PF, Wu N, Wu Z. Chen Y, et al. Among authors: wu n, wu z. J Med Genet. 2016 Jul;53(7):431-7. doi: 10.1136/jmedgenet-2015-103554. Epub 2016 Apr 15. J Med Genet. 2016. PMID: 27084730 Free PMC article. Review.

4

Progress and perspective of TBX6 gene in congenital vertebral malformations.

Chen W, Liu J, Yuan D, Zuo Y, Liu Z, Liu S, Zhu Q, Qiu G, Huang S, Giampietro PF, Zhang F, Wu N, Wu Z. Chen W, et al. Among authors: wu n, wu z. Oncotarget. 2016 Aug 30;7(35):57430-57441. doi: 10.18632/oncotarget.10619. Oncotarget. 2016. PMID: 27437870 Free PMC article. Review.

5

CRISPR/Cas9 in zebrafish: an efficient combination for human genetic diseases modeling.

Liu J, Zhou Y, Qi X, Chen J, Chen W, Qiu G, Wu Z, Wu N. Liu J, et al. Among authors: wu n, wu z. Hum Genet. 2017 Jan;136(1):1-12. doi: 10.1007/s00439-016-1739-6. Epub 2016 Nov 2. Hum Genet. 2017. PMID: 27807677 Free PMC article. Review.

6

Molecular therapeutic strategies for FGFR3 gene-related skeletal dysplasia.

Chen J, Liu J, Zhou Y, Liu S, Liu G, Zuo Y, Wu Z, Wu N, Qiu G. Chen J, et al. Among authors: wu n, wu z. J Mol Med (Berl). 2017 Dec;95(12):1303-1313. doi: 10.1007/s00109-017-1602-9. Epub 2017 Oct 23. J Mol Med (Berl). 2017. PMID: 29063142 Review.

7

Comparative analysis of the two extremes of FLNB-mutated autosomal dominant disease spectrum: from clinical phenotypes to cellular and molecular findings.

Xu Q, Wu N, Cui L, Lin M, Thirumal Kumar D, George Priya Doss C, Wu Z, Shen J, Song X, Qiu G. Xu Q, et al. Among authors: wu n, wu z. Am J Transl Res. 2018 May 15;10(5):1400-1412. eCollection 2018. Am J Transl Res. 2018. PMID: 29887954 Free PMC article.

8

The Progress of CRISPR/Cas9-Mediated Gene Editing in Generating Mouse/Zebrafish Models of Human Skeletal Diseases.

Wu N, Liu B, Du H, Zhao S, Li Y, Cheng X, Wang S, Lin J, Zhou J; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study; Qiu G, Wu Z, Zhang J. Wu N, et al. Among authors: wu z. Comput Struct Biotechnol J. 2019 Jun 13;17:954-962. doi: 10.1016/j.csbj.2019.06.006. eCollection 2019. Comput Struct Biotechnol J. 2019. PMID: 31360334 Free PMC article. Review.

9

A Recurrent Rare SOX9 Variant (M469V) is Associated with Congenital Vertebral Malformations.

Wu N, Wang L, Hu J, Zhao S, Liu B, Li Y, Du H, Zhang Y, Li X, Yan Z, Wang S, Wang Y, Zhang J, Wu Z, Disco Deciphering Disorders Involving Scoliosis Comorbidities Study Group, Qiu G. Wu N, et al. Among authors: wu z. Curr Gene Ther. 2019;19(4):242-247. doi: 10.2174/1566523219666190924120307. Curr Gene Ther. 2019. PMID: 31549955

10

Adiponectin receptor 1 mediates the difference in adiponectin- induced prostaglandin E2 production in rheumatoid arthritis and osteoarthritis synovial fibroblasts.

Zuo W, Wu ZH, Wu N, Duan YH, Wu JT, Wang H, Qiu GX. Zuo W, et al. Among authors: wu zh, wu n, wu jt. Chin Med J (Engl). 2011 Dec;124(23):3919-24. Chin Med J (Engl). 2011. PMID: 22340319

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