Jiang YL - Search Results

1

Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient.

Zhao ZY, Jiang YL, Li BR, Yang F, Li J, Jin XW, Ning SB, Sun SH. Zhao ZY, et al. Among authors: jiang yl. BMC Med Genet. 2017 Nov 15;18(1):130. doi: 10.1186/s12881-017-0471-y. BMC Med Genet. 2017. PMID: 29141581 Free PMC article.

2

[Analysis of STK11 gene variants among 64 patients with Peutz-Jeghers syndrome].

Li M, Sun T, Jiang Y, Li J, Ning S, Zhou P. Li M, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Sep 10;36(9):862-865. doi: 10.3760/cma.j.issn.1003-9406.2019.09.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31515776 Chinese.

3

A 23-Nucleotide Deletion in STK11 Gene Causes Peutz-Jeghers Syndrome and Malignancy in a Chinese Patient Without a Positive Family History.

Zhao ZY, Jiang YL, Li BR, Yang F, Li J, Jin XW, Ning SB, Sun SH. Zhao ZY, et al. Among authors: jiang yl. Dig Dis Sci. 2017 Nov;62(11):3014-3020. doi: 10.1007/s10620-017-4741-5. Epub 2017 Oct 6. Dig Dis Sci. 2017. PMID: 28986664

4

A novel germline mutation (c.A527G) in STK11 gene causes Peutz-Jeghers syndrome in a Chinese girl: A case report.

Zhao ZY, Jiang YL, Li BR, Yang F, Li J, Jin XW, Sun SH, Ning SB. Zhao ZY, et al. Among authors: jiang yl. Medicine (Baltimore). 2017 Dec;96(49):e8591. doi: 10.1097/MD.0000000000008591. Medicine (Baltimore). 2017. PMID: 29245219 Free PMC article.

5

A novel mutation (c.855delG) in STK11 gene is associated with Peutz-Jeghers syndrome in a Chinese family.

Zhao ZY, Jiang YL, Li BR, Yu ED, Ning SB. Zhao ZY, et al. Among authors: jiang yl. Dig Liver Dis. 2018 Mar;50(3):312-314. doi: 10.1016/j.dld.2017.12.007. Epub 2017 Dec 19. Dig Liver Dis. 2018. PMID: 29301733 No abstract available.

6

Close and regular surveillance is key to prevent severe complications for Peutz-Jeghers syndrome patients without gastrointestinal polyps: case report of a novel STK11 mutation (c.471_472delCT) in a Chinese girl.

Zhao ZY, Jiang YL, Li BR, Li J, Jin XW, Yu ED, Ning SB. Zhao ZY, et al. Among authors: jiang yl. BMC Surg. 2018 Apr 23;18(1):24. doi: 10.1186/s12893-018-0357-8. BMC Surg. 2018. PMID: 29685139 Free PMC article.

7

A novel STK11 missense mutation (c.346G > T) causing Peutz-Jeghers syndrome in a Chinese male with a negative family history.

Zhao ZY, Jiang YL, Li BR, Yu ED, Ning SB. Zhao ZY, et al. Among authors: jiang yl. Dig Liver Dis. 2018 Aug;50(8):864-866. doi: 10.1016/j.dld.2018.05.020. Epub 2018 Jun 4. Dig Liver Dis. 2018. PMID: 29921539 No abstract available.

8

The altered activity of P53 signaling pathway by STK11 gene mutations and its cancer phenotype in Peutz-Jeghers syndrome.

Jiang YL, Zhao ZY, Li BR, Yang F, Li J, Jin XW, Wang H, Yu ED, Sun SH, Ning SB. Jiang YL, et al. BMC Med Genet. 2018 Aug 9;19(1):141. doi: 10.1186/s12881-018-0626-5. BMC Med Genet. 2018. PMID: 30092773 Free PMC article.

9

STK11 gene analysis reveals a significant number of splice mutations in Chinese PJS patients.

Jiang YL, Zhao ZY, Li BR, Wang H, Yu ED, Ning SB. Jiang YL, et al. Cancer Genet. 2019 Jan;230:47-57. doi: 10.1016/j.cancergen.2018.11.008. Epub 2018 Nov 30. Cancer Genet. 2019. PMID: 30528796

10

Early screening the small bowel is key to protect Peutz-Jeghers syndrome patients from surgery: a novel mutation c.243delG in STK11 gene.

Jiang YL, Zhao ZY, Li BR, Li J, Jin XW, Yu ED, Xu XD, Ning SB. Jiang YL, et al. BMC Gastroenterol. 2019 May 9;19(1):70. doi: 10.1186/s12876-019-0987-z. BMC Gastroenterol. 2019. PMID: 31072341 Free PMC article.

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