Phase II Trial of Neoadjuvant Exemestane in Combination With Celecoxib in Postmenopausal Women Who Have Breast Cancer von Lustberg, Maryam B, Povoski, Stephen P, Zhao, Weiqiang, Ziegler, Rebecca M, Sugimoto, Yasuro, Ruppert, Amy S, Lehman, Amy M, Shiels, Donna R, Mrozek, Ewa, Ramaswamy, Bhuvaneswari, Layman, Rachel M, Brueggemeier, Robert W, Shapiro, Charles L

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Phase I/II trial of non-cytotoxic suramin in combination with weekly paclitaxel in metastatic breast cancer treated with prior taxanes von Lustberg, Maryam B., Pant, Shubham, Ruppert, Amy S., Shen, Tong, Wei, Yong, Chen, Ling, Brenner, Lisa, Shiels, Donna, Jensen, Rhonda R., Berger, Michael, Mrozek, Ewa, Ramaswamy, Bhuvaneswari, Grever, Michael, Au, Jessie L., Wientjes, M. Guillaume, Shapiro, Charles L.

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Trends in hepatocellular carcinoma and viral hepatitis treatment in older Americans von Jiang, Joy, Shiels, Meredith S, Rivera, Donna, Ghany, Marc G, Engels, Eric A, O'Brien, Thomas R

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Exome Sequencing Identifies a Missense Variant in EFEMP1 Co-Segregating in a Family with Autosomal Dominant Primary Open-Angle Glaucoma von Mackay, Donna S, Bennett, Thomas M, Shiels, Alan

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Mutation of the melastatin-related cation channel, TRPM3, underlies inherited cataract and glaucoma von Bennett, Thomas M, Mackay, Donna S, Siegfried, Carla J, Shiels, Alan

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Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21q von Mackay, Donna S, Andley, Usha P, Shiels, Alan

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Definitive percutaneous treatment of lymphatic malformations of the trunk and extremities von Shiels, William E, Kenney, Brian D, Caniano, Donna A, Besner, Gail E

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A Missense Mutation in the Human Connexin50 Gene ( GJA8) Underlies Autosomal Dominant “Zonular Pulverulent” Cataract, on Chromosome 1q von Shiels, Alan, Mackay, Donna, Ionides, Alexander, Berry, Vanita, Moore, Anthony, Bhattacharya, Shomi

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Exome sequencing identifies novel and recurrent mutations in GJA8 and CRYGD associated with inherited cataract von Mackay, Donna S, Bennett, Thomas M, Culican, Susan M, Shiels, Alan

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Connexin46 Mutations in Autosomal Dominant Congenital Cataract von Mackay, Donna, Ionides, Alexander, Kibar, Zoha, Rouleau, Guy, Berry, Vanita, Moore, Anthony, Shiels, Alan, Bhattacharya, Shomi

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Refractive Defects and Cataracts in Mice Lacking Lens Intrinsic Membrane Protein-2 von Shiels, Alan, King, Jennifer M, Mackay, Donna S, Bassnett, Steven

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A Nonsense Mutation in CRYBB1 Associated with Autosomal Dominant Cataract Linked to Human Chromosome 22q von Mackay, Donna S., Boskovska, Olivera B., Knopf, Harry L.S., Lampi, Kirsten J., Shiels, Alan

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A cross-sectional mixed methods study protocol to generate learning from patient safety incidents reported from general practice von Carson-Stevens, Andrew, Hibbert, Peter, Avery, Anthony, Butlin, Amy, Carter, Ben, Cooper, Alison, Evans, Huw Prosser, Gibson, Russell, Luff, Donna, Makeham, Meredith, McEnhill, Paul, Panesar, Sukhmeet S, Parry, Gareth, Rees, Philippa, Shiels, Emma, Sheikh, Aziz, Ward, Hope Olivia, Williams, Huw, Wood, Fiona, Donaldson, Liam, Edwards, Adrian

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Difficult central venous access removal: case reports of the use of endovascular snare shearing of endothelialized tetherings von Teeple, Erin A, Shiels, William E, Nwomeh, Benedict C, Rocourt, Dorothy V, Caniano, Donna A

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Clinical and genetic heterogeneity in autosomal dominant cataract von Ionides, Alexander, Francis, Peter, Berry, Vanita, Mackay, Donna, Bhattacharya, Shomi, Shiels, Alan, Moore, Anthony

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Disruption of lens fiber cell architecture in mice expressing a chimeric AQP0‐LTR protein von Shiels, Alan, Mackay, Donna, Bassnett, Steven, Al‐Ghoul, Kristin, Kuszak, Jer

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Exome sequencing identifies novel and recurrent mutations in GJA8 and CRYGDassociated with inherited cataract von Mackay, Donna S, Bennett, Thomas M, Culican, Susan M, Shiels, Alan

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Connexin46 mutations linked to congenital cataract show loss of gap junction channel function von Pal, Jay D, Liu, Xiaoqin, Mackay, Donna, Shiels, Alan, Berthoud, Viviana M, Beyer, Eric C, Ebihara, Lisa

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A cross-sectional mixed methods study protocol to generate learning from patient safety incidents reported from general practice von Carson-Stevens, Andrew, Hibbert, Peter, Avery, Anthony, Butlin, Amy, Carter, Ben, Cooper, Alison, Evans, Huw Prosser, Gibson, Russell, Luff, Donna, Makeham, Meredith, McEnhill, Paul, Panesar, Sukhmeet S, Parry, Gareth, Rees, Philippa, Shiels, Emma, Sheikh, Aziz, Ward, Hope Olivia, Williams, Huw, Wood, Fiona, Donaldson, Liam, Edwards, Adrian

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Mutation of the Melastatin-Related Cation Channel, TRPM3, Underlies Inherited Cataract and Glaucoma: e104000 von Bennett, Thomas M, Mackay, Donna S, Siegfried, Carla J, Shiels, Alan

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