Development of the Human Pancreas From Foregut to Endocrine Commitment von JENNINGS, Rachel E, BERRY, Andrew A, KIRKWOOD-WILSON, Rebecca, ROBERTS, Neil A, HEARN, Thomas, SALISBURY, Rachel J, BLAYLOCK, Jennifer, HANLEY, Karen Piper, HANLEY, Neil A

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Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6 von Ratbi, Ilham, Falkenberg, Kim D., Sommen, Manou, Al-Sheqaih, Nada, Guaoua, Soukaina, Vandeweyer, Geert, Urquhart, Jill E., Chandler, Kate E., Williams, Simon G., Roberts, Neil A., El Alloussi, Mustapha, Black, Graeme C., Ferdinandusse, Sacha, Ramdi, Hind, Heimler, Audrey, Fryer, Alan, Lynch, Sally-Ann, Cooper, Nicola, Ong, Kai Ren, Smith, Claire E.L., Inglehearn, Christopher F., Mighell, Alan J., Elcock, Claire, Poulter, James A., Tischkowitz, Marc, Davies, Sally J., Sefiani, Abdelaziz, Mironov, Aleksandr A., Newman, William G., Waterham, Hans R., Van Camp, Guy

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Human HPSE2 gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndrome von Lopes, Filipa M, Grenier, Celine, Jarvis, Benjamin W, Al Mahdy, Sara, Lène-McKay, Adrian, Gurney, Alison M, Newman, William G, Waddington, Simon N, Woolf, Adrian S, Roberts, Neil A

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Experimental long-term diabetes mellitus alters the transcriptome and biomechanical properties of the rat urinary bladder von Hindi, Emad A., Williams, Craig J., Zeef, Leo A. H., Lopes, Filipa M., Newman, Katie, Davey, Martha M. M., Hodson, Nigel W., Hilton, Emma N., Huang, Jennifer L., Price, Karen L., Roberts, Neil A., Long, David A., Woolf, Adrian S., Gardiner, Natalie J.

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Congenital Disorders of the Human Urinary Tract: Recent Insights From Genetic and Molecular Studies von Woolf, Adrian S, Lopes, Filipa M, Ranjzad, Parisa, Roberts, Neil A

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Expanding the HPSE2 Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary Bladder von Beaman, Glenda M, Lopes, Filipa M, Hofmann, Aybike, Roesch, Wolfgang, Promm, Martin, Bijlsma, Emilia K, Patel, Chirag, Akinci, Aykut, Burgu, Berk, Knijnenburg, Jeroen, Ho, Gladys, Aufschlaeger, Christina, Dathe, Sylvia, Voelckel, Marie Antoinette, Cohen, Monika, Yue, Wyatt W, Stuart, Helen M, Mckenzie, Edward A, Elvin, Mark, Roberts, Neil A, Woolf, Adrian S, Newman, William G

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ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder von Cuvertino, Sara, Stuart, Helen M., Chandler, Kate E., Roberts, Neil A., Armstrong, Ruth, Bernardini, Laura, Bhaskar, Sanjeev, Callewaert, Bert, Clayton-Smith, Jill, Davalillo, Cristina Hernando, Deshpande, Charu, Devriendt, Koenraad, Digilio, Maria C., Dixit, Abhijit, Edwards, Matthew, Friedman, Jan M., Gonzalez-Meneses, Antonio, Joss, Shelagh, Kerr, Bronwyn, Lampe, Anne Katrin, Langlois, Sylvie, Lennon, Rachel, Loget, Philippe, Ma, David Y.T., McGowan, Ruth, Des Medt, Maryse, O’Sullivan, James, Odent, Sylvie, Parker, Michael J., Pebrel-Richard, Céline, Petit, Florence, Stark, Zornitza, Stockler-Ipsiroglu, Sylvia, Tinschert, Sigrid, Vasudevan, Pradeep, Villa, Olaya, White, Susan M., Zahir, Farah R., Woolf, Adrian S., Banka, Siddharth

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Dysfunctional bladder neurophysiology in urofacial syndrome Hpse2 mutant mice von Manak, Imerjit, Gurney, Alison M., McCloskey, Karen D., Woolf, Adrian S., Roberts, Neil A.

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Overactivity or blockade of transforming growth factor‐β each generate a specific ureter malformation von Lopes, Filipa M, Roberts, Neil A, Zeef, Leo AH, Gardiner, Natalie J, Woolf, Adrian S

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Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladder von Roberts, Neil A., Hilton, Emma N., Lopes, Filipa M., Singh, Subir, Randles, Michael J., Gardiner, Natalie J., Chopra, Karl, Coletta, Riccardo, Bajwa, Zunera, Hall, Robert J., Yue, Wyatt W., Schaefer, Franz, Weber, Stefanie, Henriksson, Roger, Stuart, Helen M., Hedman, Håkan, Newman, William G., Woolf, Adrian S.

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Envisioning treating genetically-defined urinary tract malformations with viral vector-mediated gene therapy von Lopes, Filipa M., Woolf, Adrian S., Roberts, Neil A.

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From gene discovery to new biological mechanisms: heparanases and congenital urinary bladder disease von Roberts, Neil A, Hilton, Emma N, Woolf, Adrian S

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Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus von Roberts, Neil A, Woolf, Adrian S, Stuart, Helen M, Thuret, Raphaël, McKenzie, Edward A, Newman, William G, Hilton, Emma N

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A Political Companion to Frederick Douglass von Roberts, Neil

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Exogenous transforming growth factor‐β1 enhances smooth muscle differentiation in embryonic mouse jejunal explants von Coletta, Riccardo, Roberts, Neil A., Randles, Michael J., Morabito, Antonino, Woolf, Adrian S.

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Urinary tract effects of HPSE2 mutations von Stuart, Helen M, Roberts, Neil A, Hilton, Emma N, McKenzie, Edward A, Daly, Sarah B, Hadfield, Kristen D, Rahal, Jeffery S, Gardiner, Natalie J, Tanley, Simon W, Lewis, Malcolm A, Sites, Emily, Angle, Brad, Alves, Cláudia, Lourenço, Teresa, Rodrigues, Márcia, Calado, Angelina, Amado, Marta, Guerreiro, Nancy, Serras, Inês, Beetz, Christian, Varga, Rita-Eva, Silay, Mesrur Selcuk, Darlow, John M, Dobson, Mark G, Barton, David E, Hunziker, Manuela, Puri, Prem, Feather, Sally A, Goodship, Judith A, Goodship, Timothy H J, Lambert, Heather J, Cordell, Heather J, Saggar, Anand, Kinali, Maria, Lorenz, Christian, Moeller, Kristina, Schaefer, Franz, Bayazit, Aysun K, Weber, Stefanie, Newman, William G, Woolf, Adrian S

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Urofacial syndrome: a genetic and congenital disease of aberrant urinary bladder innervation von Woolf, Adrian S., Stuart, Helen M., Roberts, Neil A., McKenzie, Edward A., Hilton, Emma N., Newman, William G.

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Regulation of protein kinase D activity in adult myocardium: Novel counter-regulatory roles for protein kinase Cε and protein kinase A von Haworth, Robert S, Roberts, Neil A, Cuello, Friederike, Avkiran, Metin

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Neurogenic Defects Occur in LRIG2-Associated Urinary Bladder Disease von Grenier, Celine, Lopes, Filipa M., Cueto-González, Anna M., Rovira-Moreno, Eulàlia, Gander, Romy, Jarvis, Benjamin W., McCloskey, Karen D., Gurney, Alison M., Beaman, Glenda M., Newman, William G., Woolf, Adrian S., Roberts, Neil A.

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Bridging the gap: functional healing of embryonic small intestine ex vivo von Coletta, Riccardo, Roberts, Neil A., Oltrabella, Francesca, Khalil, Basem A., Morabito, Antonino, Woolf, Adrian S.

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