Risultati della ricerca - Budd, Peter
- Mostra 1 - 14 risultati su 14
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Novel Mixed Matrix Membranes Based on Polymer of Intrinsic Microporosity PIM-1 Modified with Metal-Organic Frameworks for Removal of Heavy Metal Ions and Food Dyes by Nanofiltratio... di Kuzminova, Anna, Dmitrenko, Mariia, Zolotarev, Andrey, Korniak, Aleksandra, Poloneeva, Daria, Selyutin, Artem, Emeline, Alexei, Yushkin, Alexey, Foster, Andrew, Budd, Peter, Ermakov, Sergey
Pubblicazione 2021testo -
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Enhancement of CO(2) Affinity in a Polymer of Intrinsic Microporosity by Amine Modification di Mason, Christopher R., Maynard-Atem, Louise, Heard, Kane W. J., Satilmis, Bekir, Budd, Peter M., Friess, Karel, Lanc̆, Marek, Bernardo, Paola, Clarizia, Gabriele, Jansen, Johannes C.
Pubblicazione 2014testo -
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The unique calcium chelation property of poly(vinyl phosphonic acid‐co‐acrylic acid) and effects on osteogenesis in vitro di Wang, Qi Guang, Wimpenny, Ian, Dey, Rebecca E., Zhong, Xia, Youle, Peter J., Downes, Sandra, Watts, David C., Budd, Peter M., Hoyland, Judith A., Gough, Julie E.
Pubblicazione 2017testo -
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Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1R in Human Fetal Development di Kinsler, Veronica A, Abu-Amero, Sayeda, Budd, Peter, Jackson, Ian J, Ring, Susan M, Northstone, Kate, Atherton, David J, Bulstrode, Neil W, Stanier, Philip, Hennekam, Raoul C, Sebire, Neil J, Moore, Gudrun E, Healy, Eugene
Pubblicazione 2012testo -
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Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function di Findlay, Amy S., Carter, Roderick N., Starbuck, Becky, McKie, Lisa, Nováková, Klára, Budd, Peter S., Keighren, Margaret A., Marsh, Joseph A., Cross, Sally H., Simon, Michelle M., Potter, Paul K., Morton, Nicholas M., Jackson, Ian J.
Pubblicazione 2018testo -
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Human and Mouse Mutations in WDR35 Cause Short-Rib Polydactyly Syndromes Due to Abnormal Ciliogenesis di Mill, Pleasantine, Lockhart, Paul J., Fitzpatrick, Elizabeth, Mountford, Hayley S., Hall, Emma A., Reijns, Martin A.M., Keighren, Margaret, Bahlo, Melanie, Bromhead, Catherine J., Budd, Peter, Aftimos, Salim, Delatycki, Martin B., Savarirayan, Ravi, Jackson, Ian J., Amor, David J.
Pubblicazione 2011testo -
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PLAA Mutations Cause a Lethal Infantile Epileptic Encephalopathy by Disrupting Ubiquitin-Mediated Endolysosomal Degradation of Synaptic Proteins di Hall, Emma A., Nahorski, Michael S., Murray, Lyndsay M., Shaheen, Ranad, Perkins, Emma, Dissanayake, Kosala N., Kristaryanto, Yosua, Jones, Ross A., Vogt, Julie, Rivagorda, Manon, Handley, Mark T., Mali, Girish R., Quidwai, Tooba, Soares, Dinesh C., Keighren, Margaret A., McKie, Lisa, Mort, Richard L., Gammoh, Noor, Garcia-Munoz, Amaya, Davey, Tracey, Vermeren, Matthieu, Walsh, Diana, Budd, Peter, Aligianis, Irene A., Faqeih, Eissa, Quigley, Alan J., Jackson, Ian J., Kulathu, Yogesh, Jackson, Mandy, Ribchester, Richard R., von Kriegsheim, Alex, Alkuraya, Fowzan S., Woods, C. Geoffrey, Maher, Eamonn R., Mill, Pleasantine
Pubblicazione 2017testo