Search Results - Spasic‐Boskovic, Olivera

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  1. 1
    Clinico-pathological co-occurrence of Fahr’s disease and dementia with Lewy bodies

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

    Published 2020
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  2. 2
    Trophoblastic Oxidative Stress and the Release of Cell-Free Feto-Placental DNA

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

    Published 2006
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  3. 3
    Nuclear Factor-κB, p38, and Stress-Activated Protein Kinase Mitogen-Activated Protein Kinase Signaling Pathways Regulate Proinflammatory Cytokines and Apoptosis in Human Placental Explants in Response to Oxidative Stress: Effects of Antioxidant Vitamins

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

    Published 2007
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  4. 4
    Discovery of a novel dominant mutation in the REN gene after forty years of renal disease: a case report

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

    Published 2017
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  5. 5
    Mosaicism for a pathogenic MFN2 mutation causes minimal clinical features of CMT2A in the parent of a severely affected child

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

    Published 2017
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  6. 6
    Oxidative Stress, Gene Expression, and Protein Changes Induced in the Human Placenta during Labor

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

    Published 2007
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  7. 7
    The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription

    The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription by 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.

    Published 2000
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  8. 8
    Rare Genetic Variation in 135 Families With Family History Suggestive of X-Linked Intellectual Disability

    Rare Genetic Variation in 135 Families With Family History Suggestive of X-Linked Intellectual Disability by 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

    Published 2019
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  9. 9
    De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability

    De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability by 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

    Published 2014
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  10. 10
    Targeted Next‐Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability

    Targeted Next‐Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability by 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

    Published 2015
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  11. 11
    Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability

    Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability by 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.

    Published 2021
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