Attachment an interpersonal processes in hearing voices von Robson, GE

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Vegetative incompatibility and the mating-type locus in the cellular slime mold Dictyostelium discoideum [Fungi] von Robson, G.E, Williams, K.L

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mating system of the cellular slime mould Dictyostelium discoideum von Robson, G.E, Williams, K.L

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Chromosome fragments in [the cellular slime mold] Dictyostelium discoideum obtained from parasexual crosses between strains of different genetic background von Williams, K.L, Robson, G.E, Welker, D.L

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Quantitative Analysis of Macrocyst Formation in Dictyostelium discoideum von ROBSON, G. E., WILLIAMS, K. L.

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The Caves of Sof Omar von Robson, G. E.

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Whole-exome sequencing reveals the origin and evolution of hepato-cholangiocarcinoma von Wang, Anqiang, Wu, Liangcai, Lin, Jianzhen, Han, Longzhe, Bian, Jin, Wu, Yan, Robson, Simon C., Xue, Lai, Ge, Yunxia, Sang, Xinting, Wang, Wenze, Zhao, Haitao

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Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania von Parks, Tom, Mirabel, Mariana M., Kado, Joseph, Auckland, Kathryn, Nowak, Jaroslaw, Rautanen, Anna, Mentzer, Alexander J., Marijon, Eloi, Jouven, Xavier, Perman, Mai Ling, Cua, Tuliana, Kauwe, John K., Allen, John B., Taylor, Henry, Robson, Kathryn J., Deane, Charlotte M., Steer, Andrew C., Hill, Adrian V. S.

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Expression of angiogenic growth factors by uterine natural killer cells during early pregnancy von Lash, Gendie E., Schiessl, Barbara, Kirkley, Maureen, Innes, Barbara A., Cooper, Alix, Searle, Roger F., Robson, Stephen C., Bulmer, Judith N.

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Biallelic Mutation of BEST1 Causes a Distinct Retinopathy in Humans von Burgess, Rosemary, Millar, Ian D., Leroy, Bart P., Urquhart, Jill E., Fearon, Ian M., De Baere, Elfrida, Brown, Peter D., Robson, Anthony G., Wright, Genevieve A., Kestelyn, Philippe, Holder, Graham E., Webster, Andrew R., Manson, Forbes D.C., Black, Graeme C.M.

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The Negative ERG: Clinical Phenotypes and Disease Mechanisms of Inner Retinal Dysfunction von Audo, Isabelle, MD, PhD, Robson, Anthony G., PhD, Holder, Graham E., PhD, Moore, Anthony T., MA, FRCS, FRCOphth, F MedSci

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Molecular and Clinical Findings in Patients With Knobloch Syndrome von Hull, Sarah, Arno, Gavin, Ku, Cristy A, Ge, Zhongqi, Waseem, Naushin, Chandra, Aman, Webster, Andrew R, Robson, Anthony G, Michaelides, Michel, Weleber, Richard G, Davagnanam, Indran, Chen, Rui, Holder, Graham E, Pennesi, Mark E, Moore, Anthony T

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Interferon-γ inhibits extravillous trophoblast cell invasion by a mechanism that involves both changes in apoptosis and protease levels von Lash, Gendie E, Otun, Harry A, Innes, Barbara A, Kirkley, Maureen, De Oliveira, Leandro, Searle, Roger F, Robson, Stephen C, Bulmer, Judith N

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Molecular Dynamics Reveals Complex Compensatory Effects of Ionic Strength on the Severe Acute Respiratory Syndrome Coronavirus 2 Spike/Human Angiotensin-Converting Enzyme 2 Interac... von Silva de Souza, Anacleto, Rivera, Jose David, Almeida, Vitor Medeiros, Ge, Pingju, de Souza, Robson Francisco, Farah, Chuck Shaker, Ulrich, Henning, Marana, Sandro Roberto, Salinas, Roberto Kopke, Guzzo, Cristiane Rodrigues

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CdSe Nano-tetrapods:  Controllable Synthesis, Structure Analysis, and Electronic and Optical Properties von Pang, Qi, Zhao, Lijuan, Cai, Yuan, Nguyen, Duc Phuong, Regnault, Nicolas, Wang, Ning, Yang, Shihe, Ge, Weikun, Ferreira, Robson, Bastard, Gerald, Wang, Jiannong

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Inhibition of Trophoblast Cell Invasion by TGFB1, 2, and 3 Is Associated with a Decrease in Active Proteases von Lash, Gendie E, Otun, Harry A, Innes, Barbara A, Bulmer, Judith N, Searle, Roger F, Robson, Stephen C

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Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity von Robson, A G, Saihan, Z, Jenkins, S A, Fitzke, F W, Bird, A C, Webster, A R, Holder, G E

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Abstract PD6-06: Impact of BRCA mutations on chemotherapy-induced loss of ovarian reserve: A prospective longitudinal study von Oktay, K, Bedoschi, G, Goldfarb, SB, Taylan, E, Titus, S, Palomaki, GE, Cigler, T, Robson, M, Dickler, MN

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Mutations in the Gene KCNV2 Encoding a Voltage-Gated Potassium Channel Subunit Cause “Cone Dystrophy with Supernormal Rod Electroretinogram” in Humans von Wu, Huimin, Cowing, Jill A., Michaelides, Michel, Wilkie, Susan E., Jeffery, Glen, Jenkins, Sharon A., Mester, Viktoria, Bird, Alan C., Robson, Anthony G., Holder, Graham E., Moore, Anthony T., Hunt, David M., Webster, Andrew R.

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Electrophysiological characterisation and monitoring in the management of birdshot chorioretinopathy von Holder, G E, Robson, A G, Pavesio, C, Graham, E M

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