PubMed for id: 7461

Year	Number of Results
1996	1
1997	1
1998	2
2001	1
2002	3
2003	1
2004	2
2005	1
2006	1
2010	2
2011	2
2012	2
2014	1
2015	3
2016	1
2017	2
2018	3
2019	1
2020	2
2021	2
2022	6
2023	3
2024	0

1

CILP-2 is a novel secreted protein and associated with insulin resistance.

Wu T, Zhang Q, Wu S, Hu W, Zhou T, Li K, Liu D, Gu HF, Zheng H, Zhu Z, Li L, Yang G. Wu T, et al. J Mol Cell Biol. 2019 Dec 19;11(12):1083-1094. doi: 10.1093/jmcb/mjz016. J Mol Cell Biol. 2019. PMID: 30896018 Free PMC article.

2

Integration of a radiation biomarker into modeling of thyroid carcinogenesis and post-Chernobyl risk assessment.

Kaiser JC, Meckbach R, Eidemüller M, Selmansberger M, Unger K, Shpak V, Blettner M, Zitzelsberger H, Jacob P. Kaiser JC, et al. Carcinogenesis. 2016 Dec;37(12):1152-1160. doi: 10.1093/carcin/bgw102. Epub 2016 Oct 11. Carcinogenesis. 2016. PMID: 27729373 Free PMC article.

3

Dose-dependent expression of CLIP2 in post-Chernobyl papillary thyroid carcinomas.

Selmansberger M, Kaiser JC, Hess J, Güthlin D, Likhtarev I, Shpak V, Tronko M, Brenner A, Abend M, Blettner M, Unger K, Jacob P, Zitzelsberger H. Selmansberger M, et al. Carcinogenesis. 2015 Jul;36(7):748-56. doi: 10.1093/carcin/bgv043. Epub 2015 May 8. Carcinogenesis. 2015. PMID: 25957251 Free PMC article.

4

CLIP2 as radiation biomarker in papillary thyroid carcinoma.

Selmansberger M, Feuchtinger A, Zurnadzhy L, Michna A, Kaiser JC, Abend M, Brenner A, Bogdanova T, Walch A, Unger K, Zitzelsberger H, Hess J. Selmansberger M, et al. Oncogene. 2015 Jul 23;34(30):3917-25. doi: 10.1038/onc.2014.311. Epub 2014 Oct 6. Oncogene. 2015. PMID: 25284583

5

Gain of chromosome band 7q11 in papillary thyroid carcinomas of young patients is associated with exposure to low-dose irradiation.

Hess J, Thomas G, Braselmann H, Bauer V, Bogdanova T, Wienberg J, Zitzelsberger H, Unger K. Hess J, et al. Proc Natl Acad Sci U S A. 2011 Jun 7;108(23):9595-600. doi: 10.1073/pnas.1017137108. Epub 2011 May 23. Proc Natl Acad Sci U S A. 2011. PMID: 21606360 Free PMC article.

6

The murine CYLN2 gene: genomic organization, chromosome localization, and comparison to the human gene that is located within the 7q11.23 Williams syndrome critical region.

Hoogenraad CC, Eussen BH, Langeveld A, van Haperen R, Winterberg S, Wouters CH, Grosveld F, De Zeeuw CI, Galjart N. Hoogenraad CC, et al. Genomics. 1998 Nov 1;53(3):348-58. doi: 10.1006/geno.1998.5529. Genomics. 1998. PMID: 9799601

7

Whole exome sequencing identifies three novel gene mutations in patients with the triad of diabetic ketoacidosis, hypertriglyceridemia, and acute pancreatitis.

Huang Z, Xu Z, Xu R, Huang L, Xu X, Lai X. Huang Z, et al. J Diabetes. 2021 Mar;13(3):200-210. doi: 10.1111/1753-0407.13100. Epub 2020 Sep 20. J Diabetes. 2021. PMID: 32734598

8

The contribution of CLIP2 haploinsufficiency to the clinical manifestations of the Williams-Beuren syndrome.

Vandeweyer G, Van der Aa N, Reyniers E, Kooy RF. Vandeweyer G, et al. Am J Hum Genet. 2012 Jun 8;90(6):1071-8. doi: 10.1016/j.ajhg.2012.04.020. Epub 2012 May 17. Am J Hum Genet. 2012. PMID: 22608712 Free PMC article.

9

Targeted mutation of Cyln2 in the Williams syndrome critical region links CLIP-115 haploinsufficiency to neurodevelopmental abnormalities in mice.

Hoogenraad CC, Koekkoek B, Akhmanova A, Krugers H, Dortland B, Miedema M, van Alphen A, Kistler WM, Jaegle M, Koutsourakis M, Van Camp N, Verhoye M, van der Linden A, Kaverina I, Grosveld F, De Zeeuw CI, Galjart N. Hoogenraad CC, et al. Nat Genet. 2002 Sep;32(1):116-27. doi: 10.1038/ng954. Epub 2002 Aug 26. Nat Genet. 2002. PMID: 12195424

10

Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy.

Evgrafov OV, Mersiyanova I, Irobi J, Van Den Bosch L, Dierick I, Leung CL, Schagina O, Verpoorten N, Van Impe K, Fedotov V, Dadali E, Auer-Grumbach M, Windpassinger C, Wagner K, Mitrovic Z, Hilton-Jones D, Talbot K, Martin JJ, Vasserman N, Tverskaya S, Polyakov A, Liem RK, Gettemans J, Robberecht W, De Jonghe P, Timmerman V. Evgrafov OV, et al. Nat Genet. 2004 Jun;36(6):602-6. doi: 10.1038/ng1354. Epub 2004 May 2. Nat Genet. 2004. PMID: 15122254

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