Similar articles for PMID: 17185897

Year	Number of Results
1997	2
1998	13
1999	14
2000	8
2001	3
2002	5
2003	4
2004	4
2005	5
2006	6
2007	7
2008	5
2009	5
2010	7
2011	7
2012	12
2013	4
2014	7
2015	5
2016	4
2017	7
2018	3
2019	2
2020	10
2021	8
2022	7
2024	0

1

New splicing mutation of MEN1 gene affecting the translocation of menin to the nucleus.

Tala HP, Carvajal CA, González AA, Garrido JL, Tobar J, Solar A, Campino C, Arteaga E, Fardella CE. Tala HP, et al. J Endocrinol Invest. 2006 Nov;29(10):888-93. doi: 10.1007/BF03349192. J Endocrinol Invest. 2006. PMID: 17185897

2

Novel intronic mutation of MEN1 gene causing familial isolated primary hyperparathyroidism.

Carrasco CA, González AA, Carvajal CA, Campusano C, Oestreicher E, Arteaga E, Wohllk N, Fardella CE. Carrasco CA, et al. J Clin Endocrinol Metab. 2004 Aug;89(8):4124-9. doi: 10.1210/jc.2003-032101. J Clin Endocrinol Metab. 2004. PMID: 15292357

3

Multiple endocrine neoplasia type 1 associated with a new germline Men1 mutation in a family with atypical tumor phenotype.

Perakakis N, Flohr F, Kayser G, Thomusch O, Parsons L, Billmann F, von Dobschuetz E, Rondot S, Seufert J, Laubner K. Perakakis N, et al. Hormones (Athens). 2016 Jan-Mar;15(1):113-7. doi: 10.14310/horm.2002.1626. Hormones (Athens). 2016. PMID: 26732163 Free article.

4

A novel intronic mutation and a missense mutation of MEN1 identified in two Chinese families with multiple endocrine neoplasia type 1.

Han B, Song ZY, Wu JJ, Liu W, Liu BL, Ye XP, Chen X, Pan CM, Xu HY, Li L, Zhu H, Lu YL, Wu WL, Chen MD, Song HD, Qiao J. Han B, et al. J Endocrinol Invest. 2013 Mar;36(3):162-7. doi: 10.3275/8336. Epub 2012 Apr 5. J Endocrinol Invest. 2013. PMID: 22522645

5

Impaired transforming growth factor-β (TGF-β) transcriptional activity and cell proliferation control of a menin in-frame deletion mutant associated with multiple endocrine neoplasia type 1 (MEN1).

Canaff L, Vanbellinghen JF, Kaji H, Goltzman D, Hendy GN. Canaff L, et al. J Biol Chem. 2012 Mar 9;287(11):8584-97. doi: 10.1074/jbc.M112.341958. Epub 2012 Jan 24. J Biol Chem. 2012. PMID: 22275377 Free PMC article. Clinical Trial.

6

Menin mutations in the diagnosis and prediction of multiple endocrine neoplasia type 1.

Karges W, Ludwig L, Kessler H, Wissmann A, Wagner PK, Boehm BO. Karges W, et al. Langenbecks Arch Surg. 1998 Apr;383(2):183-6. doi: 10.1007/s004230050115. Langenbecks Arch Surg. 1998. PMID: 9641896

7

MEN1 c.825‑1G>A mutation in a family with multiple endocrine neoplasia type 1: A case report.

Ning Z, Wang O, Meng X, Xing X, Xia W, Jiang Y, Li M, Xu Y. Ning Z, et al. Mol Med Rep. 2015 Oct;12(4):6152-6. doi: 10.3892/mmr.2015.4138. Epub 2015 Jul 29. Mol Med Rep. 2015. PMID: 26239674

8

Identification of a novel frameshift c.930delG MEN1 germline mutation (p.Glu273LysfsTer7) in a sporadic case of multiple endocrine neoplasia type 1: A case report.

Naruse H, Umemura H, Nakayama T. Naruse H, et al. Mol Med Rep. 2020 Dec;22(6):5423-5427. doi: 10.3892/mmr.2020.11596. Epub 2020 Oct 14. Mol Med Rep. 2020. PMID: 33173995

9

Mutation analysis in a Chinese family with multiple endocrine neoplasia type 1.

Zha BB, Liang W, Liu J, Cheng J, Hong XW, Liu J, Li YM, Ma D. Zha BB, et al. Chin Med J (Engl). 2010 Mar 5;123(5):569-73. Chin Med J (Engl). 2010. PMID: 20367983

10

Menin molecular interactions: insights into normal functions and tumorigenesis.

Agarwal SK, Kennedy PA, Scacheri PC, Novotny EA, Hickman AB, Cerrato A, Rice TS, Moore JB, Rao S, Ji Y, Mateo C, Libutti SK, Oliver B, Chandrasekharappa SC, Burns AL, Collins FS, Spiegel AM, Marx SJ. Agarwal SK, et al. Horm Metab Res. 2005 Jun;37(6):369-74. doi: 10.1055/s-2005-870139. Horm Metab Res. 2005. PMID: 16001329 Review.

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