Protein kinase C: a worthwhile target for anticancer drugs? von Caponigro, Francesco, French, Raymond C., Kaye, Stan B.

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Protein kinase C: a worthwhile target for anticancer drugs? von Caponigro, Francesco, French, Raymond C, Kaye, Stan B

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Chromatographic characterisation of six human metabolites of the new anticancer drug GR63 178A von Cummings, Jeffrey, French, Raymond C., MacLellan, Alex, Smyth, John F.

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Effect of Human Recombinant Interferon-α on the Activity of cis-Diamminedichloroplatinum(II) in Human Non-Small Cell Lung Cancer Xenografts von French, Raymond C., Bowman, Angela, MacLeod, Kenneth G., Ritchie, Alison A., Cummings, Jeffrey, Smyth, John F.

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The comparative disposition of the pyrolloquinone GR63178A and its 9-hydroxy metabolite GR54374X in sensitive and resistant mouse colon adenocarcinoma von French, R C, Cummings, J, MacLellan, A, MacPherson, J S, Ritchie, A A, Smyth, J F

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Metabolic activation of diethylstilbestrol by stimulated human leukocytes von Eastmond, David A., French, Raymond C., Ross, David, Smith, Martyn T.

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METHOD OF ATTACHING KEY FACINGS AND APPARATUS THEREFOR von RAYMOND C. FRENCH

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Apparatus for making piano damper blocks and similar parts von FRENCH RAYMOND C

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Method of manufacturing key levers for musical instruments von FRENCH RAYMOND C

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Metabolic activation of 1-naphthol and phenol by a simple superoxide-generating system and human leukocytes von Eastmond, David A., French, Raymond C., Ross, David, Smith, Martyn T.

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Application of high-performance liquid chromatography for recognition of covalent nucleic acid modification with anticancer drugs von Cummings, Jeffrey, French, Raymond C., Smyth, John F.

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Survival in incident and prevalent cohorts of patients with pulmonary arterial hypertension von Humbert, M, Sitbon, O, Yaïci, A, Montani, D, O'Callaghan, D S, Jaïs, X, Parent, F, Savale, L, Natali, D, Günther, S, Chaouat, A, Chabot, F, Cordier, J-F, Habib, G, Gressin, V, Jing, Z-C, Souza, R, Simonneau, G

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Baicalein Targets GTPase‐Mediated Autophagy to Eliminate Liver Tumor–Initiating Stem Cell–Like Cells Resistant to mTORC1 Inhibition von Wu, Raymond, Murali, Ramachandran, Kabe, Yasuaki, French, Samuel W., Chiang, Yi‐Ming, Liu, Siyu, Sher, Linda, Wang, Clay C., Louie, Stan, Tsukamoto, Hidekazu

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Cerebellar Purkinje cells control eye movements with a rapid rate code that is invariant to spike irregularity von Payne, Hannah L, French, Ranran L, Guo, Christine C, Nguyen-Vu, Td Barbara, Manninen, Tiina, Raymond, Jennifer L

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Mast cells' involvement in inflammation pathways linked to depression: evidence in mastocytosis von Georgin-Lavialle, S, Moura, D S, Salvador, A, Chauvet-Gelinier, J-C, Launay, J-M, Damaj, G, Côté, F, Soucié, E, Chandesris, M-O, Barète, S, Grandpeix-Guyodo, C, Bachmeyer, C, Alyanakian, M-A, Aouba, A, Lortholary, O, Dubreuil, P, Teyssier, J-R, Trojak, B, Haffen, E, Vandel, P, Bonin, B, Hermine, O, Gaillard, R

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Characterization of long G4-rich enhancer-associated genomic regions engaging in a novel loop:loop ‘G4 Kissing’ interaction von Williams, Jonathan D, Houserova, Dominika, Johnson, Bradley R, Dyniewski, Brad, Berroyer, Alexandra, French, Hannah, Barchie, Addison A, Bilbrey, Dakota D, Demeis, Jeffrey D, Ghee, Kanesha R, Hughes, Alexandra G, Kreitz, Naden W, McInnis, Cameron H, Pudner, Susanna C, Reeves, Monica N, Stahly, Ashlyn N, Turcu, Ana, Watters, Brianna C, Daly, Grant T, Langley, Raymond J, Gillespie, Mark N, Prakash, Aishwarya, Larson, Erik D, Kasukurthi, Mohan V, Huang, Jingshan, Jinks-Robertson, Sue, Borchert, Glen M

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De Novo VPS4A Mutations Cause Multisystem Disease with Abnormal Neurodevelopment von Rodger, Catherine, Flex, Elisabetta, Allison, Rachel J., Sanchis-Juan, Alba, Hasenahuer, Marcia A., Cecchetti, Serena, French, Courtney E., Edgar, James R., Carpentieri, Giovanna, Ciolfi, Andrea, Pantaleoni, Francesca, Bruselles, Alessandro, Onesimo, Roberta, Zampino, Giuseppe, Marcon, Francesca, Siniscalchi, Ester, Lees, Melissa, Krishnakumar, Deepa, McCann, Emma, Yosifova, Dragana, Jarvis, Joanna, Kruer, Michael C., Marks, Warren, Campbell, Jonathan, Allen, Louise E., Gustincich, Stefano, Raymond, F. Lucy, Tartaglia, Marco, Reid, Evan

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Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders von Sanchis-Juan, Alba, Megy, Karyn, Stephens, Jonathan, Armirola Ricaurte, Camila, Dewhurst, Eleanor, Low, Kayyi, French, Courtney E., Grozeva, Detelina, Stirrups, Kathleen, Erwood, Marie, McTague, Amy, Penkett, Christopher J., Shamardina, Olga, Tuna, Salih, Daugherty, Louise C., Gleadall, Nicholas, Duarte, Sofia T., Hedrera-Fernández, Antonio, Vogt, Julie, Ambegaonkar, Gautam, Chitre, Manali, Josifova, Dragana, Kurian, Manju A., Parker, Alasdair, Rankin, Julia, Reid, Evan, Wakeling, Emma, Wassmer, Evangeline, Woods, C. Geoffrey, Raymond, F. Lucy, Carss, Keren J.

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Skin cancer classification via convolutional neural networks: systematic review of studies involving human experts von Haggenmüller, Sarah, Maron, Roman C., Hekler, Achim, Utikal, Jochen S., Barata, Catarina, Barnhill, Raymond L., Beltraminelli, Helmut, Berking, Carola, Betz-Stablein, Brigid, Blum, Andreas, Braun, Stephan A., Carr, Richard, Combalia, Marc, Fernandez-Figueras, Maria-Teresa, Ferrara, Gerardo, Fraitag, Sylvie, French, Lars E., Gellrich, Frank F., Ghoreschi, Kamran, Goebeler, Matthias, Guitera, Pascale, Haenssle, Holger A., Haferkamp, Sebastian, Heinzerling, Lucie, Heppt, Markus V., Hilke, Franz J., Hobelsberger, Sarah, Krahl, Dieter, Kutzner, Heinz, Lallas, Aimilios, Liopyris, Konstantinos, Llamas-Velasco, Mar, Malvehy, Josep, Meier, Friedegund, Müller, Cornelia S.L., Navarini, Alexander A., Navarrete-Dechent, Cristián, Perasole, Antonio, Poch, Gabriela, Podlipnik, Sebastian, Requena, Luis, Rotemberg, Veronica M., Saggini, Andrea, Sangueza, Omar P., Santonja, Carlos, Schadendorf, Dirk, Schilling, Bastian, Schlaak, Max, Schlager, Justin G., Sergon, Mildred, Sondermann, Wiebke, Soyer, H. Peter, Starz, Hans, Stolz, Wilhelm, Vale, Esmeralda, Weyers, Wolfgang, Zink, Alexander, Krieghoff-Henning, Eva, Kather, Jakob N., von Kalle, Christof, Lipka, Daniel B., Fröhling, Stefan, Hauschild, Axel, Kittler, Harald, Brinker, Titus J.

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Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children von French, Courtney E., Delon, Isabelle, Dolling, Helen, Sanchis-Juan, Alba, Shamardina, Olga, Mégy, Karyn, Abbs, Stephen, Austin, Topun, Bowdin, Sarah, Branco, Ricardo G., Firth, Helen, Rowitch, David H., Raymond, F. Lucy

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