GATA4 sequence variants in patients with congenital heart disease von Tomita-Mitchell, A, Maslen, C L, Morris, C D, Garg, V, Goldmuntz, E

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Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene von Dietz, Harry C, Cutting, Carry R, Pyeritz, Reed E, Maslen, Cheryl L, Sakai, Lynn Y, Corson, Glen M, Puffenberger, Erik G, Hamosh, Ada, Nanthakumar, Elizabeth J, Curristin, Sheila M, Stetten, Gail, Meyers, Deborah A, Francomano, Clair A

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A Dense Corpus Study of Past Tense and Plural Overregularization in English von Maslen, Robert J. C, Theakston, Anna L, Lieven, Elena V. M, Tomasello, Michael

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Type VI Collagen Anchors Endothelial Basement Membranes by Interacting with Type IV Collagen von Kuo, Huey-Ju, Maslen, Cheryl L., Keene, Douglas R., Glanville, Robert W.

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CLINICAL CHARACTERISTICS OF AORTIC DISSECTION IN BICUSPID AORTIC VALVE DISEASE; PRELIMINARY DATA FROM THE GENTAC REGISTRY von Booher, Anna M, Devereux, R.B, Basson, C, Holmes, K.W, Lemaire, S.A, Tolunay, E, Maslen, C, Pyeritz, R, Kroner, B.L, Eagle, K.A

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Partial sequence of a candidate gene for the Marfan syndrome von Maslen, Cheryl L, Corson, Glen M, Maddox, B. Kerry, Glanville, Robert W, Sakai, Lynn Y

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The discovery of RPR 200765A, a p38 MAP kinase inhibitor displaying a good oral anti-arthritic efficacy von MCLAY, Lain M, HALLEY, Frank, FOSTER, Martyn, HELE, David, JAYYOSI, Zaid, KELLEY, Mike, MASLEN, Chris, MILLER, Glen, OULDELHKIM, Marie-Claude, PAGE, Kenneth, PHIPPS, Simon, POLLOCK, Kenneth, SOUNESS, John E, PORTER, Barry, RATCLIFFE, Andrew J, REDFORD, Elisabeth J, WEBBER, Stephen, SLATER, Bryan, THYBAUD, Veronique, WILSHER, Nicola, MCKENNA, Jeffrey, BENNING, Veronique, BIRRELL, Mark, BURTON, Brenda, BELVISI, Maria, COLLIS, Alan, CONSTAN, Alex

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PTPN11 mutations play a minor role in isolated congenital heart disease von Weismann, Constance G., Hager, A., Kaemmerer, H., Maslen, C. L., Morris, Cynthia D., Schranz, D., Kreuder, J., Gelb, B.D.

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MARFAN PHENOTYPE VARIABILITY IN A FAMILY SEGREGATING A MISSENSE MUTATION IN THE EPIDERMAL GROWTH-FACTOR LIKE MOTIF OF THE FIBRILLIN GENE von DIETZ, HC, PYERITZ, RE, PUFFENBERGER, EG, KENDZIOR, RJ, CORSON, GM, MASLEN, CL, SAKAI, LY, FRANCOMANO, CA, CUTTING, GR

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Evidence that cyclic AMP phosphodiesterase inhibitors suppress TNFα generation from human monocytes by interacting with a ‘low‐affinity’ phosphodiesterase 4 conformer von Souness, John E., Griffin, Miriam, Maslen, Christopher, Ebsworth, Karen, Scott, Lisa C., Pollock, Kenneth, Palfreyman, Malcolm N., Karlsson, Jan‐Anders

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A single mutation that results in an Asp to His substitution and partial exon skipping in a family with congenital contractural arachnodactyly von BABCOCK, D, GASNER, C, FRANCKE, U, MASLEN, C

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Prenatal ultrasound findings in a fetus with congenital contractural arachnodactyly von Kölble, N., Wisser, J., Babcock, D., Maslen, C., Huch, R., Steinmann, B.

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Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1 von Magenis, R.Ellen, Maslen, Cheryl L., Smith, Leslie, Allen, Leland, Sakai, Lynn Y.

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Calcium binding, hydroxylation, and glycosylation of the precursor epidermal growth factor-like domains of fibrillin-1, the Marfan gene protein von Glanville, R W, Qian, R Q, McClure, D W, Maslen, C L

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LB VPP - 840: Digital Health Interventions for Osteoporosis and Post-Fragility Fracture Care von Gupta, A, Maslen, C, Vindlacheruvu, M, Abel, R, Bhattacharya, P, Bromiley, P, Clark, E, Compston, J, Crabtree, N, Gregory, J, Kairki, E, Harvey, N, McCloskey, E, Ward, K, Poole, K

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Suppression of eosinophil function by RP 73401, a potent and selective inhibitor of cyclic AMP‐specific phosphodiesterase: comparison with rolipram von Soilness, John E., Maslen, Christopher, Webber, Stephen, Foster, Martyn, Raeburn, David, Palfreyman, Malcolm N., Ashton, Michael J., Karlsson, Jan‐Anders

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Angiotensin-converting enzyme DD genotype and cardiovascular disease in heterozygous familial hypercholesterolemia von O'Malley, J P, Maslen, C L, Illingworth, D R

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A NICE example? Variation in provision of bariatric surgery in England von Owen-Smith, Amanda, Kipping, Ruth, Donovan, Jenny, Hine, Christine, Maslen, Christina, Coast, Joanna

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Occurrence of a mutation associated with Wolman disease in a family with cholesteryl ester storage disease von Maslen, C. L., Babcock, D., Illingworth, D. R.

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Missense Mutations in CRELD1 Are Associated with Cardiac Atrioventricular Septal Defects von Robinson, Susan W., Morris, Cynthia D., Goldmuntz, Elizabeth, Reller, Mark D., Jones, Melanie A., Steiner, Robert D., Maslen, Cheryl L.

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