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Dynamic regulation of dynein localization revealed by small molecule inhibitors of ubiquitination enzymes.

Monda JK, Cheeseman IM.

Open Biol. 2018 Sep 26;8(9). pii: 180095. doi: 10.1098/rsob.180095.


Comprehensive genotype-phenotype correlation in lissencephaly.

Tan AP, Chong WK, Mankad K.

Quant Imaging Med Surg. 2018 Aug;8(7):673-693. doi: 10.21037/qims.2018.08.08. Review.


A pilot Indian family-based association study between dyslexia and Reelin pathway genes, DCDC2 and ROBO1, identifies modest association with a triallelic unit TAT in the gene RELN.

Devasenapathy S, Midha R, Naskar T, Mehta A, Prajapati B, Ummekulsum M, Sagar R, Singh NC, Sinha S.

Asian J Psychiatr. 2018 Aug 25;37:121-129. doi: 10.1016/j.ajp.2018.08.020. [Epub ahead of print]


Clinical Phenotypes Associated to Engrailed 2 Gene Alterations in a Series of Neuropediatric Patients.

Carratala-Marco F, Andreo-Lillo P, Martinez-Morga M, Escamez-Martínez T, Botella-López A, Bueno C, Martinez S.

Front Neuroanat. 2018 Aug 10;12:61. doi: 10.3389/fnana.2018.00061. eCollection 2018.


Familial dominant epilepsy and mild pachygyria associated with a constitutional LIS1 mutation.

De Vita D, Mei D, Rutigliano D, Bartalucci N, Cinnante CM, Parrini E, Dilena R, Guerrini R.

Am J Med Genet A. 2018 Dec;176(12):2808-2812. doi: 10.1002/ajmg.a.40503. Epub 2018 Aug 25.


Nde1 promotes diverse dynein functions through differential interactions and exhibits an isoform-specific proteasome association.

Monda JK, Cheeseman IM.

Mol Biol Cell. 2018 Sep 15;29(19):2336-2345. doi: 10.1091/mbc.E18-07-0418. Epub 2018 Jul 19.


Mechanisms underlying the role of DISC1 in synaptic plasticity.

Tropea D, Hardingham N, Millar K, Fox K.

J Physiol. 2018 Jul;596(14):2747-2771. doi: 10.1113/JP274330.


Coupling of microtubule motors with AP-3 generated organelles in axons by NEEP21 family member calcyon.

Shi L, Hines T, Bergson C, Smith D.

Mol Biol Cell. 2018 Aug 15;29(17):2055-2068. doi: 10.1091/mbc.E18-01-0007. Epub 2018 Jun 27.


LINC complex-Lis1 interplay controls MT1-MMP matrix digest-on-demand response for confined tumor cell migration.

Infante E, Castagnino A, Ferrari R, Monteiro P, Agüera-González S, Paul-Gilloteaux P, Domingues MJ, Maiuri P, Raab M, Shanahan CM, Baffet A, Piel M, Gomes ER, Chavrier P.

Nat Commun. 2018 Jun 22;9(1):2443. doi: 10.1038/s41467-018-04865-7.


Comparative Pathologic Analysis of Breast Cancers Classified as HER2/neu-Amplified by FISH Using a Standard HER2/CEP17 Dual Probe and an Alternative Chromosome 17 Control Probe.

Zare S, Lin L, Alghamdi AG, Daehne S, Roma AA, Hasteh F, Dell'Aquila M, Fadare O.

Am J Surg Pathol. 2018 Sep;42(9):1208-1215. doi: 10.1097/PAS.0000000000001106.


Case Report of Proliferative Peripheral Retinopathy in Two Familial Lissencephaly Infants with Miller-Dieker Syndrome.

Shoukfeh O, Richards AB, Prouty LA, Hinrichsen J, Spencer WR, Langford MP.

J Pediatr Genet. 2018 Jun;7(2):86-91. doi: 10.1055/s-0037-1612638. Epub 2017 Dec 29.


Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1.

Brock S, Stouffs K, Scalais E, D'Hooghe M, Keymolen K, Guerrini R, Dobyns WB, Di Donato N, Jansen AC.

Eur J Hum Genet. 2018 Aug;26(8):1132-1142. doi: 10.1038/s41431-018-0146-y. Epub 2018 Apr 30.


Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly.

Di Donato N, Timms AE, Aldinger KA, Mirzaa GM, Bennett JT, Collins S, Olds C, Mei D, Chiari S, Carvill G, Myers CT, Rivière JB, Zaki MS; University of Washington Center for Mendelian Genomics, Gleeson JG, Rump A, Conti V, Parrini E, Ross ME, Ledbetter DH, Guerrini R, Dobyns WB.

Genet Med. 2018 Nov;20(11):1354-1364. doi: 10.1038/gim.2018.8. Epub 2018 Apr 19.


Neurodevelopmental Genetic Diseases Associated With Microdeletions and Microduplications of Chromosome 17p13.3.

Blazejewski SM, Bennison SA, Smith TH, Toyo-Oka K.

Front Genet. 2018 Mar 23;9:80. doi: 10.3389/fgene.2018.00080. eCollection 2018. Review.


GDNF-expressing macrophages mitigate loss of dopamine neurons and improve Parkinsonian symptoms in MitoPark mice.

Chen C, Li X, Ge G, Liu J, Biju KC, Laing SD, Qian Y, Ballard C, He Z, Masliah E, Clark RA, O'Connor JC, Li S.

Sci Rep. 2018 Apr 3;8(1):5460. doi: 10.1038/s41598-018-23795-4.


The LIS1/NDE1 Complex Is Essential for FGF Signaling by Regulating FGF Receptor Intracellular Trafficking.

Liu L, Lu J, Li X, Wu A, Wu Q, Zhao M, Tang N, Song H.

Cell Rep. 2018 Mar 20;22(12):3277-3291. doi: 10.1016/j.celrep.2018.02.077.


NudCD1 affects renal cell carcinoma through regulating LIS1/Dynein signaling pathway.

He H, Dai J, Wang X, Qian X, Zhao J, Wang H, Xu D.

Am J Transl Res. 2018 Feb 15;10(2):519-524. eCollection 2018.


Hepatic loss of Lissencephaly 1 (Lis1) induces fatty liver and accelerates liver tumorigenesis in mice.

Li X, Liu L, Li R, Wu A, Lu J, Wu Q, Jia J, Zhao M, Song H.

J Biol Chem. 2018 Apr 6;293(14):5160-5171. doi: 10.1074/jbc.RA117.001474. Epub 2018 Feb 23.


Lis1 dysfunction leads to traction force reduction and cytoskeletal disorganization during cell migration.

Jheng GW, Hur SS, Chang CM, Wu CC, Cheng JS, Lee HH, Chung BC, Wang YK, Lin KH, Del Álamo JC, Chien S, Tsai JW.

Biochem Biophys Res Commun. 2018 Mar 11;497(3):869-875. doi: 10.1016/j.bbrc.2018.02.151. Epub 2018 Feb 20.


An Essential Postdevelopmental Role for Lis1 in Mice.

Hines TJ, Gao X, Sahu S, Lange MM, Turner JR, Twiss JL, Smith DS.

eNeuro. 2018 Feb 2;5(1). pii: ENEURO.0350-17.2018. doi: 10.1523/ENEURO.0350-17.2018. eCollection 2018 Jan-Feb.

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