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Items: 1 to 20 of 29

1.

Predominant expression of Alzheimer's disease-associated BIN1 in mature oligodendrocytes and localization to white matter tracts.

De Rossi P, Buggia-Prévot V, Clayton BL, Vasquez JB, van Sanford C, Andrew RJ, Lesnick R, Botté A, Deyts C, Salem S, Rao E, Rice RC, Parent A, Kar S, Popko B, Pytel P, Estus S, Thinakaran G.

Mol Neurodegener. 2016 Aug 3;11(1):59. doi: 10.1186/s13024-016-0124-1.

2.

Structural insights into the centronuclear myopathy-associated functions of BIN1 and dynamin 2.

Hohendahl A, Roux A, Galli V.

J Struct Biol. 2016 Oct;196(1):37-47. doi: 10.1016/j.jsb.2016.06.015.

3.

AD genetic risk factors and tau spreading.

Avila J, Gómez-Ramos A, Bolós M.

Front Aging Neurosci. 2015 May 21;7:99. doi: 10.3389/fnagi.2015.00099. No abstract available.

4.

Regulation of E2F1-induced apoptosis by poly(ADP-ribosyl)ation.

Kumari A, Iwasaki T, Pyndiah S, Cassimere EK, Palani CD, Sakamuro D.

Cell Death Differ. 2015 Feb;22(2):311-22. doi: 10.1038/cdd.2014.146.

5.
6.

Bridging integrator 1 (Bin1) deficiency in zebrafish results in centronuclear myopathy.

Smith LL, Gupta VA, Beggs AH.

Hum Mol Genet. 2014 Jul 1;23(13):3566-78. doi: 10.1093/hmg/ddu067.

7.

In silico to in vivo splicing analysis using splicing code models.

Gazzara MR, Vaquero-Garcia J, Lynch KW, Barash Y.

Methods. 2014 May 1;67(1):3-12. doi: 10.1016/j.ymeth.2013.11.006.

8.

Altered splicing of the BIN1 muscle-specific exon in humans and dogs with highly progressive centronuclear myopathy.

Böhm J, Vasli N, Maurer M, Cowling BS, Shelton GD, Kress W, Toussaint A, Prokic I, Schara U, Anderson TJ, Weis J, Tiret L, Laporte J.

PLoS Genet. 2013 Jun;9(6):e1003430. doi: 10.1371/journal.pgen.1003430. Erratum in: PLoS Genet. 2013 Jun;9(6). doi:10.1371/annotation/22ca13f1-1ce9-4bb5-9c9e-98670f7c4240. Cowling, Belinda [corrected to Cowling, Belinda S].

9.
10.

Defective membrane remodeling in neuromuscular diseases: insights from animal models.

Cowling BS, Toussaint A, Muller J, Laporte J.

PLoS Genet. 2012;8(4):e1002595. doi: 10.1371/journal.pgen.1002595. Review.

11.

Plasma BIN1 correlates with heart failure and predicts arrhythmia in patients with arrhythmogenic right ventricular cardiomyopathy.

Hong TT, Cogswell R, James CA, Kang G, Pullinger CR, Malloy MJ, Kane JP, Wojciak J, Calkins H, Scheinman MM, Tseng ZH, Ganz P, De Marco T, Judge DP, Shaw RM.

Heart Rhythm. 2012 Jun;9(6):961-7. doi: 10.1016/j.hrthm.2012.01.024.

12.
13.

The association between a polygenic Alzheimer score and cortical thickness in clinically normal subjects.

Sabuncu MR, Buckner RL, Smoller JW, Lee PH, Fischl B, Sperling RA; Alzheimer's Disease Neuroimaging Initiative..

Cereb Cortex. 2012 Nov;22(11):2653-61. doi: 10.1093/cercor/bhr348.

14.

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.

PLoS One. 2011;6(9):e25740. doi: 10.1371/journal.pone.0025740.

15.

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.

J Cell Biochem. 2011 Oct;112(10):2992-3001. doi: 10.1002/jcb.23222.

16.

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..

PLoS One. 2011 Feb 24;6(2):e16616. doi: 10.1371/journal.pone.0016616.

17.

Identification of an alternate splice form of tapasin in human melanoma.

Belicha-Villanueva A, Golding M, McEvoy S, Sarvaiya N, Cresswell P, Gollnick SO, Bangia N.

Hum Immunol. 2010 Oct;71(10):1018-26. doi: 10.1016/j.humimm.2010.05.019.

18.

Genetic variation and neuroimaging measures in Alzheimer disease.

Biffi A, Anderson CD, Desikan RS, Sabuncu M, Cortellini L, Schmansky N, Salat D, Rosand J; Alzheimer's Disease Neuroimaging Initiative (ADNI)..

Arch Neurol. 2010 Jun;67(6):677-85. doi: 10.1001/archneurol.2010.108.

19.

Genome-wide analysis of genetic loci associated with Alzheimer disease.

Seshadri S, Fitzpatrick AL, Ikram MA, DeStefano AL, Gudnason V, Boada M, Bis JC, Smith AV, Carassquillo MM, Lambert JC, Harold D, Schrijvers EM, Ramirez-Lorca R, Debette S, Longstreth WT Jr, Janssens AC, Pankratz VS, Dartigues JF, Hollingworth P, Aspelund T, Hernandez I, Beiser A, Kuller LH, Koudstaal PJ, Dickson DW, Tzourio C, Abraham R, Antunez C, Du Y, Rotter JI, Aulchenko YS, Harris TB, Petersen RC, Berr C, Owen MJ, Lopez-Arrieta J, Varadarajan BN, Becker JT, Rivadeneira F, Nalls MA, Graff-Radford NR, Campion D, Auerbach S, Rice K, Hofman A, Jonsson PV, Schmidt H, Lathrop M, Mosley TH, Au R, Psaty BM, Uitterlinden AG, Farrer LA, Lumley T, Ruiz A, Williams J, Amouyel P, Younkin SG, Wolf PA, Launer LJ, Lopez OL, van Duijn CM, Breteler MM; CHARGE Consortium.; GERAD1 Consortium.; EADI1 Consortium..

JAMA. 2010 May 12;303(18):1832-40. doi: 10.1001/jama.2010.574.

20.

Bin1 SRC homology 3 domain acts as a scaffold for myofiber sarcomere assembly.

Fernando P, Sandoz JS, Ding W, de Repentigny Y, Brunette S, Kelly JF, Kothary R, Megeney LA.

J Biol Chem. 2009 Oct 2;284(40):27674-86. doi: 10.1074/jbc.M109.029538.

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