Jin P - Search Results

1

Identification of Novel Variants in MEN1: A Study Conducted with Four Multiple Endocrine Neoplasia Type 1 Patients.

Hu WM, Zhang Q, Huang LH, Mo ZH, Long XD, Yang YB, Yang WJ, Liu J, Jin P. Hu WM, et al. Among authors: jin p. Horm Metab Res. 2020 Nov;52(11):788-795. doi: 10.1055/a-1147-1375. Epub 2020 Apr 16. Horm Metab Res. 2020. PMID: 32299109

2

Overexpression of Insig-1 protects β cell against glucolipotoxicity via SREBP-1c.

Chen K, Jin P, He HH, Xie YH, Xie XY, Mo ZH. Chen K, et al. Among authors: jin p. J Biomed Sci. 2011 Aug 16;18(1):57. doi: 10.1186/1423-0127-18-57. J Biomed Sci. 2011. PMID: 21843373 Free PMC article.

3

A 3' splice site mutation of IDS gene in a Chinese family with mucopolysaccharidosis type II.

Jin P, Hao JW, Chen K, Dong CS, Yang YB, Mo ZH. Jin P, et al. Gene. 2013 Oct 10;528(2):236-40. doi: 10.1016/j.gene.2013.06.084. Epub 2013 Jul 16. Gene. 2013. PMID: 23867855

4

A novel mutation in autoimmune regulator gene causes autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy.

Jin P, Zhang Q, Dong CS, Zhao SL, Mo ZH. Jin P, et al. J Endocrinol Invest. 2014 Oct;37(10):941-8. doi: 10.1007/s40618-014-0120-7. Epub 2014 Jul 27. J Endocrinol Invest. 2014. PMID: 25064028

5

[Van Wyk-Grumbach syndrome: A case report and  literature review].

Jin P, Zhang Q, Mo Z, Yang F, Xie Y. Jin P, et al. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2016 Dec 28;41(12):1366-1370. doi: 10.11817/j.issn.1672-7347.2016.12.020. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2016. PMID: 28070054 Free article. Chinese.

6

Extensive ARMC5 genetic variance in primary bilateral macronodular adrenal hyperplasia that started with exophthalmos: a case report.

Jin P, Janjua MU, Zhang Q, Dong CS, Yang Y, Mo ZH. Jin P, et al. J Med Case Rep. 2018 Jan 18;12(1):13. doi: 10.1186/s13256-017-1529-3. J Med Case Rep. 2018. PMID: 29343284 Free PMC article.

7

Association of medullary sponge kidney and hyperparathyroidism with RET G691S/S904S polymorphism: a case report.

Janjua MU, Long XD, Mo ZH, Dong CS, Jin P. Janjua MU, et al. Among authors: jin p. J Med Case Rep. 2018 Jul 9;12(1):197. doi: 10.1186/s13256-018-1736-6. J Med Case Rep. 2018. PMID: 29983117 Free PMC article.

8

Identification of a novel GNAS mutation in a case of pseudohypoparathyroidism type 1A with normocalcemia.

Long XD, Xiong J, Mo ZH, Dong CS, Jin P. Long XD, et al. Among authors: jin p. BMC Med Genet. 2018 Jul 30;19(1):132. doi: 10.1186/s12881-018-0648-z. BMC Med Genet. 2018. PMID: 30060753 Free PMC article.

9

[A case of growth hormone deficiency combined with neurofibromatosis Type 1 and its gene analysis].

Long X, Xiong J, Mo Z, Zhang Q, Jin P. Long X, et al. Among authors: jin p. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2018 Jul 28;43(7):811-815. doi: 10.11817/j.issn.1672-7347.2018.07.018. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2018. PMID: 30124220 Free article. Chinese.

10

[Two cases of primary hypertrophic osteoarthropathy with SLCO2A1 gene mutations].

Jin P, Zhang Q, He H, Zhu W, Long X, Mo Z. Jin P, et al. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2018 Jan 28;43(1):100-105. doi: 10.11817/j.issn.1672-7347.2018.01.016. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2018. PMID: 30154299 Free article. Chinese.

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