نتائج البحث - Spasic‐Boskovic, Olivera

Clinico-pathological co-occurrence of Fahr’s disease and dementia with Lewy bodies حسب Jensen, Melanie P., Spasic-Boskovic, Olivera, Rowe, James B., Galton, Clare, Allinson, Kieren S. J.

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Trophoblastic Oxidative Stress and the Release of Cell-Free Feto-Placental DNA حسب Tjoa, May Lee, Cindrova-Davies, Tereza, Spasic-Boskovic, Olivera, Bianchi, Diana W., Burton, Graham J.

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Nuclear Factor-κB, p38, and Stress-Activated Protein Kinase Mitogen-Activated Protein Kinase Signaling Pathways Regulate Proinflammatory Cytokines and Apoptosis in Human Placental... حسب Cindrova-Davies, Tereza, Spasic-Boskovic, Olivera, Jauniaux, Eric, Charnock-Jones, D. Stephen, Burton, Graham J.

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Discovery of a novel dominant mutation in the REN gene after forty years of renal disease: a case report حسب Clissold, Rhian L., Clarke, Helen C., Spasic-Boskovic, Olivera, Brugger, Kim, Abbs, Stephen, Bingham, Coralie, Shaw-Smith, Charles

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Mosaicism for a pathogenic MFN2 mutation causes minimal clinical features of CMT2A in the parent of a severely affected child حسب Schon, Katherine, Spasic-Boskovic, Olivera, Brugger, Kim, Graves, Tracey D., Abbs, Stephen, Park, Soo-Mi, Ambegaonkar, Gautam, Armstrong, Ruth

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Oxidative Stress, Gene Expression, and Protein Changes Induced in the Human Placenta during Labor حسب Cindrova-Davies, Tereza, Yung, Hong-Wa, Johns, Jemma, Spasic-Boskovic, Olivera, Korolchuk, Svitlana, Jauniaux, Eric, Burton, Graham J., Charnock-Jones, D. Stephen

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The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription حسب Steffan, Joan S., Kazantsev, Aleksey, Spasic-Boskovic, Olivera, Greenwald, Marilee, Zhu, Ya-Zhen, Gohler, Heike, Wanker, Erich E., Bates, Gillian P., Housman, David E., Thompson, Leslie M.

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Rare Genetic Variation in 135 Families With Family History Suggestive of X-Linked Intellectual Disability حسب Sanchis-Juan, Alba, Bitsara, Christina, Low, Kay Yi, Carss, Keren J., French, Courtney E., Spasic-Boskovic, Olivera, Jarvis, Joanna, Field, Michael, Raymond, F. Lucy, Grozeva, Detelina

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De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability حسب Grozeva, Detelina, Carss, Keren, Spasic-Boskovic, Olivera, Parker, Michael J., Archer, Hayley, Firth, Helen V., Park, Soo-Mi, Canham, Natalie, Holder, Susan E., Wilson, Meredith, Hackett, Anna, Field, Michael, Floyd, James A.B., Hurles, Matthew, Raymond, F. Lucy

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Targeted Next‐Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability حسب Grozeva, Detelina, Carss, Keren, Spasic‐Boskovic, Olivera, Tejada, Maria‐Isabel, Gecz, Jozef, Shaw, Marie, Corbett, Mark, Haan, Eric, Thompson, Elizabeth, Friend, Kathryn, Hussain, Zaamin, Hackett, Anna, Field, Michael, Renieri, Alessandra, Stevenson, Roger, Schwartz, Charles, Floyd, James A.B., Bentham, Jamie, Cosgrove, Catherine, Keavney, Bernard, Bhattacharya, Shoumo, Hurles, Matthew, Raymond, F. Lucy

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Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability حسب Bengani, Hemant, Grozeva, Detelina, Moyon, Lambert, Bhatia, Shipra, Louros, Susana R., Hope, Jilly, Jackson, Adam, Prendergast, James G., Owen, Liusaidh J., Naville, Magali, Rainger, Jacqueline, Grimes, Graeme, Halachev, Mihail, Murphy, Laura C., Spasic-Boskovic, Olivera, van Heyningen, Veronica, Kind, Peter, Abbott, Catherine M., Osterweil, Emily, Raymond, F. Lucy, Roest Crollius, Hugues, FitzPatrick, David R.

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