PubMed for id: 113707

Year	Number of Results
1996	3
1997	10
1998	4
1999	9
2000	9
2001	11
2002	7
2003	14
2004	11
2005	7
2006	4
2007	10
2008	7
2009	7
2010	10
2011	18
2012	9
2013	6
2024	0

1

BIN1 gene rs744373 polymorphism contributes to Alzheimer's disease in East Asian population.

Liu G, Zhang S, Cai Z, Li Y, Cui L, Ma G, Jiang Y, Zhang L, Feng R, Liao M, Chen Z, Zhao B, Li K. Liu G, et al. Neurosci Lett. 2013 Jun 7;544:47-51. doi: 10.1016/j.neulet.2013.02.075. Epub 2013 Apr 6. Neurosci Lett. 2013. PMID: 23570733

2

The BAR domain of amphiphysin is required for cleavage furrow tip-tubule formation during cellularization in Drosophila embryos.

Su J, Chow B, Boulianne GL, Wilde A. Su J, et al. Mol Biol Cell. 2013 May;24(9):1444-53. doi: 10.1091/mbc.E12-12-0878. Epub 2013 Feb 27. Mol Biol Cell. 2013. PMID: 23447705 Free PMC article.

3

Bin1 attenuation suppresses experimental colitis by enforcing intestinal barrier function.

Chang MY, Boulden J, Valenzano MC, Soler AP, Muller AJ, Mullin JM, Prendergast GC. Chang MY, et al. Dig Dis Sci. 2012 Jul;57(7):1813-21. doi: 10.1007/s10620-012-2147-y. Epub 2012 Apr 18. Dig Dis Sci. 2012. PMID: 22526583 Free PMC article.

4

Characterization of bridging integrator 1 (BIN1) as a potential tumor suppressor and prognostic marker in hepatocellular carcinoma.

Pan K, Liang XT, Zhang HK, Zhao JJ, Wang DD, Li JJ, Lian Q, Chang AE, Li Q, Xia JC. Pan K, et al. Mol Med. 2012 May 9;18(1):507-18. doi: 10.2119/molmed.2011.00319. Mol Med. 2012. PMID: 22281836 Free PMC article.

5

Disrupted membrane structure and intracellular Ca²⁺ signaling in adult skeletal muscle with acute knockdown of Bin1.

Tjondrokoesoemo A, Park KH, Ferrante C, Komazaki S, Lesniak S, Brotto M, Ko JK, Zhou J, Weisleder N, Ma J. Tjondrokoesoemo A, et al. PLoS One. 2011;6(9):e25740. doi: 10.1371/journal.pone.0025740. Epub 2011 Sep 30. PLoS One. 2011. PMID: 21984944 Free PMC article.

6

Identification of a novel effector domain of BIN1 for cancer suppression.

Lundgaard GL, Daniels NE, Pyndiah S, Cassimere EK, Ahmed KM, Rodrigue A, Kihara D, Post CB, Sakamuro D. Lundgaard GL, et al. J Cell Biochem. 2011 Oct;112(10):2992-3001. doi: 10.1002/jcb.23222. J Cell Biochem. 2011. PMID: 21678469 Free PMC article.

7

Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease.

Hu X, Pickering E, Liu YC, Hall S, Fournier H, Katz E, Dechairo B, John S, Van Eerdewegh P, Soares H; Alzheimer's Disease Neuroimaging Initiative. Hu X, et al. PLoS One. 2011 Feb 24;6(2):e16616. doi: 10.1371/journal.pone.0016616. PLoS One. 2011. PMID: 21390209 Free PMC article.

8

Replication of BIN1 association with Alzheimer's disease and evaluation of genetic interactions.

Carrasquillo MM, Belbin O, Hunter TA, Ma L, Bisceglio GD, Zou F, Crook JE, Pankratz VS, Sando SB, Aasly JO, Barcikowska M, Wszolek ZK, Dickson DW, Graff-Radford NR, Petersen RC, Morgan K, Younkin SG. Carrasquillo MM, et al. J Alzheimers Dis. 2011;24(4):751-8. doi: 10.3233/JAD-2011-101932. J Alzheimers Dis. 2011. PMID: 21321396 Free PMC article.

9

Case report of intrafamilial variability in autosomal recessive centronuclear myopathy associated to a novel BIN1 stop mutation.

Böhm J, Yiş U, Ortaç R, Cakmakçı H, Kurul SH, Dirik E, Laporte J. Böhm J, et al. Orphanet J Rare Dis. 2010 Dec 3;5:35. doi: 10.1186/1750-1172-5-35. Orphanet J Rare Dis. 2010. PMID: 21129173 Free PMC article. Review.

10

Defects in amphiphysin 2 (BIN1) and triads in several forms of centronuclear myopathies.

Toussaint A, Cowling BS, Hnia K, Mohr M, Oldfors A, Schwab Y, Yis U, Maisonobe T, Stojkovic T, Wallgren-Pettersson C, Laugel V, Echaniz-Laguna A, Mandel JL, Nishino I, Laporte J. Toussaint A, et al. Acta Neuropathol. 2011 Feb;121(2):253-66. doi: 10.1007/s00401-010-0754-2. Epub 2010 Oct 7. Acta Neuropathol. 2011. PMID: 20927630

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