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Items: 1 to 50 of 191

1.

Society of Interventional Radiology Consensus Guidelines for the Periprocedural Management of Thrombotic and Bleeding Risk in Patients Undergoing Percutaneous Image-Guided Interventions-Part II: Recommendations: Endorsed by the Canadian Association for Interventional Radiology and the Cardiovascular and Interventional Radiological Society of Europe.

Patel IJ, Rahim S, Davidson JC, Hanks SE, Tam AL, Walker TG, Wilkins LR, Sarode R, Weinberg I.

J Vasc Interv Radiol. 2019 Jun 19. pii: S1051-0443(19)30407-5. doi: 10.1016/j.jvir.2019.04.017. [Epub ahead of print] No abstract available.

PMID:
31229333
3.

Identification of new Wilms tumour predisposition genes: an exome sequencing study.

Mahamdallie S, Yost S, Poyastro-Pearson E, Holt E, Zachariou A, Seal S, Elliott A, Clarke M, Warren-Perry M, Hanks S, Anderson J, Bomken S, Cole T, Farah R, Furtwaengler R, Glaser A, Grundy R, Hayden J, Lowis S, Millot F, Nicholson J, Ronghe M, Skeen J, Williams D, Yeomanson D, Ruark E, Rahman N.

Lancet Child Adolesc Health. 2019 May;3(5):322-331. doi: 10.1016/S2352-4642(19)30018-5. Epub 2019 Mar 16.

4.

Correction: Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height.

Tatton-Brown K, Hanks S, Ruark E, Zachariou A, Del Vecchio Duarte S, Ramsay E, Snape K, Murray A, Perdeaux ER, Seal S, Loveday C, Banka S, Clericuzio C, Flinter F, Magee A, McConnell V, Patton M, Raith W, Rankin J, Splitt M, Strenger V, Taylor C, Wheeler P, Temple IK, Cole T; Childhood Overgrowth Collaboration, Douglas J, Rahman N.

Oncotarget. 2018 Nov 30;9(94):36719. doi: 10.18632/oncotarget.26429. eCollection 2018 Nov 30.

5.

ADIPOR1 is essential for vision and its RPE expression is lost in the Mfrprd6 mouse.

Sluch VM, Banks A, Li H, Crowley MA, Davis V, Xiang C, Yang J, Demirs JT, Vrouvlianis J, Leehy B, Hanks S, Hyman AM, Aranda J, Chang B, Bigelow CE, Rice DS.

Sci Rep. 2018 Sep 25;8(1):14339. doi: 10.1038/s41598-018-32579-9.

6.

Prepared for practice and equipped for employment: what do dental foundation trainers think of their trainees?

Hanks S, Coelho C, Coster R.

Br Dent J. 2018 Sep 28;225(6):549-555. doi: 10.1038/sj.bdj.2018.756. Epub 2018 Sep 7. No abstract available.

PMID:
30191902
7.

The Discovery of N-(1-Methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-5-((6- ((methylamino)methyl)pyrimidin-4-yl)oxy)-1H-indole-1-carboxamide (Acrizanib), a VEGFR-2 Inhibitor Specifically Designed for Topical Ocular Delivery, as a Therapy for Neovascular Age-Related Macular Degeneration.

Adams CM, Anderson K, Artman G 3rd, Bizec JC, Cepeda R, Elliott J, Fassbender E, Ghosh M, Hanks S, Hardegger LA, Hosagrahara VP, Jaffee B, Jendza K, Ji N, Johnson L, Lee W, Liu D, Liu F, Long D, Ma F, Mainolfi N, Meredith EL, Miranda K, Peng Y, Poor S, Powers J, Qiu Y, Rao C, Shen S, Sivak JM, Solovay C, Tarsa P, Woolfenden A, Zhang C, Zhang Y.

J Med Chem. 2018 Feb 22;61(4):1622-1635. doi: 10.1021/acs.jmedchem.7b01731. Epub 2018 Feb 5.

PMID:
29400470
8.

Structural and functional insights into the interaction between the Cas family scaffolding protein p130Cas and the focal adhesion-associated protein paxillin.

Zhang C, Miller DJ, Guibao CD, Donato DM, Hanks SK, Zheng JJ.

J Biol Chem. 2017 Nov 3;292(44):18281-18289. doi: 10.1074/jbc.M117.807271. Epub 2017 Aug 31.

9.

ARHGAP42 is activated by Src-mediated tyrosine phosphorylation to promote cell motility.

Luo W, Janoštiak R, Tolde O, Ryzhova LM, Koudelková L, Dibus M, Brábek J, Hanks SK, Rosel D.

J Cell Sci. 2017 Jul 15;130(14):2382-2393. doi: 10.1242/jcs.197434. Epub 2017 Jun 5.

10.

Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation.

Yost S, de Wolf B, Hanks S, Zachariou A, Marcozzi C, Clarke M, de Voer R, Etemad B, Uijttewaal E, Ramsay E, Wylie H, Elliott A, Picton S, Smith A, Smithson S, Seal S, Ruark E, Houge G, Pines J, Kops GJPL, Rahman N.

Nat Genet. 2017 Jul;49(7):1148-1151. doi: 10.1038/ng.3883. Epub 2017 May 29.

11.

Collecting student feedback: a whole-school approach.

Collett T, Hanks S, Watson H, Davies T.

Med Educ. 2017 May;51(5):547-548. doi: 10.1111/medu.13303. No abstract available.

PMID:
28394052
12.

Long-acting protein drugs for the treatment of ocular diseases.

Ghosh JG, Nguyen AA, Bigelow CE, Poor S, Qiu Y, Rangaswamy N, Ornberg R, Jackson B, Mak H, Ezell T, Kenanova V, de la Cruz E, Carrion A, Etemad-Gilbertson B, Caro RG, Zhu K, George V, Bai J, Sharma-Nahar R, Shen S, Wang Y, Subramanian KK, Fassbender E, Maker M, Hanks S, Vrouvlianis J, Leehy B, Long D, Prentiss M, Kansara V, Jaffee B, Dryja TP, Roguska M.

Nat Commun. 2017 Mar 23;8:14837. doi: 10.1038/ncomms14837.

13.

Signaling by two-component system noncognate partners promotes intrinsic tolerance to polymyxin B in uropathogenic Escherichia coli.

Guckes KR, Breland EJ, Zhang EW, Hanks SC, Gill NK, Algood HM, Schmitz JE, Stratton CW, Hadjifrangiskou M.

Sci Signal. 2017 Jan 10;10(461). pii: eaag1775. doi: 10.1126/scisignal.aag1775.

14.

Reflections on learning and enhancing communication skills through community engagement: a student perspective.

Hanks S, Marples C, Wall E.

Br Dent J. 2016 Jul 22;221(2):81-5. doi: 10.1038/sj.bdj.2016.527.

PMID:
27444599
15.

When I say … capability.

Neve H, Hanks S.

Med Educ. 2016 Jun;50(6):610-1. doi: 10.1111/medu.12956. No abstract available.

PMID:
27170079
16.

Podosome dynamics and location in vascular smooth muscle cells require CLASP-dependent microtubule bending.

Zhu X, Efimova N, Arnette C, Hanks SK, Kaverina I.

Cytoskeleton (Hoboken). 2016 Jun;73(6):300-15. doi: 10.1002/cm.21302. Epub 2016 May 20.

17.

Corrigendum: Mutations in the transcriptional repressor REST predispose to Wilms tumor.

Mahamdallie SS, Hanks S, Karlin KL, Zachariou A, Perdeaux ER, Ruark E, Shaw CA, Renwick A, Ramsay E, Yost S, Elliott A, Birch J, Capra M, Gray J, Hale J, Kingston J, Levitt G, McLean T, Sheridan E, Renwick A, Seal S, Stiller C, Sebire N, Westbrook TF, Rahman N.

Nat Genet. 2016 Apr;48(4):473. doi: 10.1038/ng0329-473d. No abstract available.

PMID:
27023775
18.

The ICR142 NGS validation series: a resource for orthogonal assessment of NGS analysis.

Ruark E, Renwick A, Clarke M, Snape K, Ramsay E, Elliott A, Hanks S, Strydom A, Seal S, Rahman N.

Version 2. F1000Res. 2016 Mar 22 [revised 2018 Jan 1];5:386. doi: 10.12688/f1000research.8219.2. eCollection 2016.

19.

The ICR1000 UK exome series: a resource of gene variation in an outbred population.

Ruark E, Münz M, Renwick A, Clarke M, Ramsay E, Hanks S, Mahamdallie S, Elliott A, Seal S, Strydom A, Gerton L, Rahman N.

F1000Res. 2015 Sep 22;4:883. doi: 10.12688/f1000research.7049.1. eCollection 2015.

20.

Discovery of Oral VEGFR-2 Inhibitors with Prolonged Ocular Retention That Are Efficacious in Models of Wet Age-Related Macular Degeneration.

Meredith EL, Mainolfi N, Poor S, Qiu Y, Miranda K, Powers J, Liu D, Ma F, Solovay C, Rao C, Johnson L, Ji N, Artman G, Hardegger L, Hanks S, Shen S, Woolfenden A, Fassbender E, Sivak JM, Zhang Y, Long D, Cepeda R, Liu F, Hosagrahara VP, Lee W, Tarsa P, Anderson K, Elliott J, Jaffee B.

J Med Chem. 2015 Dec 10;58(23):9273-86. doi: 10.1021/acs.jmedchem.5b01227. Epub 2015 Nov 30.

PMID:
26568411
21.

Mutations in the transcriptional repressor REST predispose to Wilms tumor.

Mahamdallie SS, Hanks S, Karlin KL, Zachariou A, Perdeaux ER, Ruark E, Shaw CA, Renwick A, Ramsay E, Yost S, Elliott A, Birch J, Capra M, Gray J, Hale J, Kingston J, Levitt G, McLean T, Sheridan E, Renwick A, Seal S, Stiller C, Sebire N, Westbrook TF, Rahman N.

Nat Genet. 2015 Dec;47(12):1471-4. doi: 10.1038/ng.3440. Epub 2015 Nov 9. Erratum in: Nat Genet. 2016 Apr;48(4):473.

PMID:
26551668
22.

AAV-mediated RLBP1 gene therapy improves the rate of dark adaptation in Rlbp1 knockout mice.

Choi VW, Bigelow CE, McGee TL, Gujar AN, Li H, Hanks SM, Vrouvlianis J, Maker M, Leehy B, Zhang Y, Aranda J, Bounoutas G, Demirs JT, Yang J, Ornberg R, Wang Y, Martin W, Stout KR, Argentieri G, Grosenstein P, Diaz D, Turner O, Jaffee BD, Police SR, Dryja TP.

Mol Ther Methods Clin Dev. 2015 Jul 8;2:15022. doi: 10.1038/mtm.2015.22. eCollection 2015.

23.

Reliability of the mouse model of choroidal neovascularization induced by laser photocoagulation.

Poor SH, Qiu Y, Fassbender ES, Shen S, Woolfenden A, Delpero A, Kim Y, Buchanan N, Gebuhr TC, Hanks SM, Meredith EL, Jaffee BD, Dryja TP.

Invest Ophthalmol Vis Sci. 2014 Sep 9;55(10):6525-34. doi: 10.1167/iovs.14-15067.

PMID:
25205860
24.

Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour.

Hanks S, Perdeaux ER, Seal S, Ruark E, Mahamdallie SS, Murray A, Ramsay E, Del Vecchio Duarte S, Zachariou A, de Souza B, Warren-Perry M, Elliott A, Davidson A, Price H, Stiller C, Pritchard-Jones K, Rahman N.

Nat Commun. 2014 Aug 7;5:4398. doi: 10.1038/ncomms5398.

25.

Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability.

Tatton-Brown K, Seal S, Ruark E, Harmer J, Ramsay E, Del Vecchio Duarte S, Zachariou A, Hanks S, O'Brien E, Aksglaede L, Baralle D, Dabir T, Gener B, Goudie D, Homfray T, Kumar A, Pilz DT, Selicorni A, Temple IK, Van Maldergem L, Yachelevich N; Childhood Overgrowth Consortium, van Montfort R, Rahman N.

Nat Genet. 2014 Apr;46(4):385-8. doi: 10.1038/ng.2917. Epub 2014 Mar 9. Erratum in: Nat Genet. 2014 Jun;46(6):657.

26.

The Health Sciences and Technology Academy: an educational pipeline to address health care disparities in West Virginia.

McKendall SB, Kasten K, Hanks S, Chester A.

Acad Med. 2014 Jan;89(1):37-42. doi: 10.1097/ACM.0000000000000047.

27.

Global phosphotyrosine proteomics identifies PKCδ as a marker of responsiveness to Src inhibition in colorectal cancer.

McKinley ET, Liu H, McDonald WH, Luo W, Zhao P, Coffey RJ, Hanks SK, Manning HC.

PLoS One. 2013 Nov 8;8(11):e80207. doi: 10.1371/journal.pone.0080207. eCollection 2013.

28.

Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype.

Tatton-Brown K, Murray A, Hanks S, Douglas J, Armstrong R, Banka S, Bird LM, Clericuzio CL, Cormier-Daire V, Cushing T, Flinter F, Jacquemont ML, Joss S, Kinning E, Lynch SA, Magee A, McConnell V, Medeira A, Ozono K, Patton M, Rankin J, Shears D, Simon M, Splitt M, Strenger V, Stuurman K, Taylor C, Titheradge H, Van Maldergem L, Temple IK, Cole T, Seal S; Childhood Overgrowth Consortium, Rahman N.

Am J Med Genet A. 2013 Dec;161A(12):2972-80. doi: 10.1002/ajmg.a.36229. Epub 2013 Nov 8.

29.

Exact solution and high-temperature series expansion study of the one-fifth-depleted square-lattice Ising model.

Hanks S, Datta T, Oitmaa J.

Phys Rev E Stat Nonlin Soft Matter Phys. 2013 Jun;87(6):062143. Epub 2013 Jun 28.

PMID:
23848663
30.

Long distance bicycle riding causes prostate-specific antigen to increase in men aged 50 years and over.

Mejak SL, Bayliss J, Hanks SD.

PLoS One. 2013;8(2):e56030. doi: 10.1371/journal.pone.0056030. Epub 2013 Feb 13.

31.

Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer.

Ruark E, Snape K, Humburg P, Loveday C, Bajrami I, Brough R, Rodrigues DN, Renwick A, Seal S, Ramsay E, Duarte Sdel V, Rivas MA, Warren-Perry M, Zachariou A, Campion-Flora A, Hanks S, Murray A, Ansari Pour N, Douglas J, Gregory L, Rimmer A, Walker NM, Yang TP, Adlard JW, Barwell J, Berg J, Brady AF, Brewer C, Brice G, Chapman C, Cook J, Davidson R, Donaldson A, Douglas F, Eccles D, Evans DG, Greenhalgh L, Henderson A, Izatt L, Kumar A, Lalloo F, Miedzybrodzka Z, Morrison PJ, Paterson J, Porteous M, Rogers MT, Shanley S, Walker L, Gore M, Houlston R, Brown MA, Caufield MJ, Deloukas P, McCarthy MI, Todd JA; Breast and Ovarian Cancer Susceptibility Collaboration; Wellcome Trust Case Control Consortium, Turnbull C, Reis-Filho JS, Ashworth A, Antoniou AC, Lord CJ, Donnelly P, Rahman N.

Nature. 2013 Jan 17;493(7432):406-10. doi: 10.1038/nature11725. Epub 2012 Dec 16.

32.

A genome-wide association study identifies susceptibility loci for Wilms tumor.

Turnbull C, Perdeaux ER, Pernet D, Naranjo A, Renwick A, Seal S, Munoz-Xicola RM, Hanks S, Slade I, Zachariou A, Warren-Perry M, Ruark E, Gerrard M, Hale J, Hewitt M, Kohler J, Lane S, Levitt G, Madi M, Morland B, Neefjes V, Nicholson J, Picton S, Pizer B, Ronghe M, Stevens M, Traunecker H, Stiller CA, Pritchard-Jones K, Dome J, Grundy P, Rahman N.

Nat Genet. 2012 Apr 29;44(6):681-4. doi: 10.1038/ng.2251. Erratum in: Nat Genet. 2013 Aug;45(8):962.

33.

Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer.

Snape K, Ruark E, Tarpey P, Renwick A, Turnbull C, Seal S, Murray A, Hanks S, Douglas J, Stratton MR, Rahman N.

Breast Cancer Res Treat. 2012 Jul;134(1):429-33. doi: 10.1007/s10549-012-2057-x. Epub 2012 Apr 18.

34.

Crk1/2-dependent signaling is necessary for podocyte foot process spreading in mouse models of glomerular disease.

George B, Verma R, Soofi AA, Garg P, Zhang J, Park TJ, Giardino L, Ryzhova L, Johnstone DB, Wong H, Nihalani D, Salant DJ, Hanks SK, Curran T, Rastaldi MP, Holzman LB.

J Clin Invest. 2012 Feb;122(2):674-92. doi: 10.1172/JCI60070. Epub 2012 Jan 17.

35.

Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height.

Tatton-Brown K, Hanks S, Ruark E, Zachariou A, Duarte Sdel V, Ramsay E, Snape K, Murray A, Perdeaux ER, Seal S, Loveday C, Banka S, Clericuzio C, Flinter F, Magee A, McConnell V, Patton M, Raith W, Rankin J, Splitt M, Strenger V, Taylor C, Wheeler P, Temple KI, Cole T; Childhood Overgrowth Collaboration, Douglas J, Rahman N.

Oncotarget. 2011 Dec;2(12):1127-33. Erratum in: Oncotarget. 2018 Nov 30;9(94):36719.

36.

Tyrosine phosphorylation within the SH3 domain regulates CAS subcellular localization, cell migration, and invasiveness.

Janoštiak R, Tolde O, Brůhová Z, Novotný M, Hanks SK, Rösel D, Brábek J.

Mol Biol Cell. 2011 Nov;22(22):4256-67. doi: 10.1091/mbc.E11-03-0207. Epub 2011 Sep 21.

37.

Mutations in CEP57 cause mosaic variegated aneuploidy syndrome.

Snape K, Hanks S, Ruark E, Barros-Núñez P, Elliott A, Murray A, Lane AH, Shannon N, Callier P, Chitayat D, Clayton-Smith J, Fitzpatrick DR, Gisselsson D, Jacquemont S, Asakura-Hay K, Micale MA, Tolmie J, Turnpenny PD, Wright M, Douglas J, Rahman N.

Nat Genet. 2011 Jun;43(6):527-9. doi: 10.1038/ng.822. Epub 2011 May 8.

38.

DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome.

Slade I, Bacchelli C, Davies H, Murray A, Abbaszadeh F, Hanks S, Barfoot R, Burke A, Chisholm J, Hewitt M, Jenkinson H, King D, Morland B, Pizer B, Prescott K, Saggar A, Side L, Traunecker H, Vaidya S, Ward P, Futreal PA, Vujanic G, Nicholson AG, Sebire N, Turnbull C, Priest JR, Pritchard-Jones K, Houlston R, Stiller C, Stratton MR, Douglas J, Rahman N.

J Med Genet. 2011 Apr;48(4):273-8. doi: 10.1136/jmg.2010.083790. Epub 2011 Jan 25.

PMID:
21266384
39.

Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma.

Slade I, Murray A, Hanks S, Kumar A, Walker L, Hargrave D, Douglas J, Stiller C, Izatt L, Rahman N.

Fam Cancer. 2011 Jun;10(2):337-42. doi: 10.1007/s10689-010-9411-0.

PMID:
21188540
40.

KSR1 is a functional protein kinase capable of serine autophosphorylation and direct phosphorylation of MEK1.

Goettel JA, Liang D, Hilliard VC, Edelblum KL, Broadus MR, Gould KL, Hanks SK, Polk DB.

Exp Cell Res. 2011 Feb 15;317(4):452-63. doi: 10.1016/j.yexcr.2010.11.018. Epub 2010 Dec 7.

41.

Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesis.

Gisselsson D, Jin Y, Lindgren D, Persson J, Gisselsson L, Hanks S, Sehic D, Mengelbier LH, Øra I, Rahman N, Mertens F, Mitelman F, Mandahl N.

Proc Natl Acad Sci U S A. 2010 Nov 23;107(47):20489-93. doi: 10.1073/pnas.1006829107. Epub 2010 Nov 8.

42.

A phase II study of radiotherapy and concurrent paclitaxel chemotherapy in breast-conserving treatment for node-positive breast cancer.

Chen WC, Kim J, Kim E, Silverman P, Overmoyer B, Cooper BW, Anthony S, Shenk R, Leeming R, Hanks SH, Lyons JA.

Int J Radiat Oncol Biol Phys. 2012 Jan 1;82(1):14-20. doi: 10.1016/j.ijrobp.2010.08.051. Epub 2010 Oct 29.

PMID:
21035961
43.

P130Cas Src-binding and substrate domains have distinct roles in sustaining focal adhesion disassembly and promoting cell migration.

Meenderink LM, Ryzhova LM, Donato DM, Gochberg DF, Kaverina I, Hanks SK.

PLoS One. 2010 Oct 18;5(10):e13412. doi: 10.1371/journal.pone.0013412.

44.

Molecular causes for BUBR1 dysfunction in the human cancer predisposition syndrome mosaic variegated aneuploidy.

Suijkerbuijk SJ, van Osch MH, Bos FL, Hanks S, Rahman N, Kops GJ.

Cancer Res. 2010 Jun 15;70(12):4891-900. doi: 10.1158/0008-5472.CAN-09-4319. Epub 2010 Jun 1.

45.

Dynamics and mechanism of p130Cas localization to focal adhesions.

Donato DM, Ryzhova LM, Meenderink LM, Kaverina I, Hanks SK.

J Biol Chem. 2010 Jul 2;285(27):20769-79. doi: 10.1074/jbc.M109.091207. Epub 2010 Apr 29.

46.

Transportation of peripheral blood progenitor cell products: effect of ambient temperature.

Jansen J, Nolan PL, Reeves MI, Morgan JA, Akard LP, Thompson JM, Dugan MJ, Hanks SG.

Cytotherapy. 2010 Nov;12(7):919-23. doi: 10.3109/14653240903580288.

PMID:
20429789
47.

Focal adhesion kinase-dependent regulation of adhesive forces involves vinculin recruitment to focal adhesions.

Dumbauld DW, Michael KE, Hanks SK, García AJ.

Biol Cell. 2010 Jan 14;102(4):203-213. doi: 10.1042/BC20090104.

48.

Donor-site complications of autogenous nonvascularized fibula strut graft harvest for anterior cervical corpectomy and fusion surgery: experience with 163 consecutive cases.

Nassr A, Khan MH, Ali MH, Espiritu MT, Hanks SE, Lee JY, Donaldson WF, Kang JD.

Spine J. 2009 Nov;9(11):893-8. doi: 10.1016/j.spinee.2009.04.020. Epub 2009 Jun 13.

PMID:
19525152
49.
50.

Focal adhesion kinase modulates cell adhesion strengthening via integrin activation.

Michael KE, Dumbauld DW, Burns KL, Hanks SK, García AJ.

Mol Biol Cell. 2009 May;20(9):2508-19. doi: 10.1091/mbc.E08-01-0076. Epub 2009 Mar 18.

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