Hasil Pencarian - Adam Giess

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  1. 1
    Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of severe chronic fatigue

    Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of severe chronic fatigue oleh Julia Oakley, Martin Hill, Adam Giess, Mélanie Tanguy, Greg Elgar

    Diterbitkan 2023-11-01
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  2. 2
    Ribosome signatures aid bacterial translation initiation site identification

    Ribosome signatures aid bacterial translation initiation site identification oleh Adam Giess, Veronique Jonckheere, Elvis Ndah, Katarzyna Chyżyńska, Petra Van Damme, Eivind Valen

    Diterbitkan 2017-08-01
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  3. 3
    Profiling of Small Ribosomal Subunits Reveals Modes and Regulation of Translation Initiation

    Profiling of Small Ribosomal Subunits Reveals Modes and Regulation of Translation Initiation oleh Adam Giess, Yamila N. Torres Cleuren, Håkon Tjeldnes, Maximilian Krause, Teshome Tilahun Bizuayehu, Senna Hiensch, Aniekan Okon, Carston R. Wagner, Eivind Valen

    Diterbitkan 2020-04-01
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  4. 4
    Characterisation of Invasive Streptococcus pneumoniae Isolated from Cambodian Children between 2007 - 2012.

    Characterisation of Invasive Streptococcus pneumoniae Isolated from Cambodian Children between 2007 - 2012. oleh Catrin E Moore, Adam Giess, Sona Soeng, Poda Sar, Varun Kumar, Pheakdey Nhoung, Rachel Bousfield, Paul Turner, Nicole Stoesser, Nicholas P J Day, Christopher M Parry

    Diterbitkan 2016-01-01
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  5. 5
    Low Dose Iron Treatments Induce a DNA Damage Response in Human Endothelial Cells within Minutes.

    Low Dose Iron Treatments Induce a DNA Damage Response in Human Endothelial Cells within Minutes. oleh Inês G Mollet, Dilipkumar Patel, Fatima S Govani, Adam Giess, Koralia Paschalaki, Manikandan Periyasamy, Elaine C Lidington, Justin C Mason, Michael D Jones, Laurence Game, Simak Ali, Claire L Shovlin

    Diterbitkan 2016-01-01
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  6. 6
    Copy-number analysis from genome sequencing data of 11,754 rare-disease parent-child trios: A model for identifying autosomal recessive human gene knockouts including a novel gene for autosomal recessive retinopathy

    Copy-number analysis from genome sequencing data of 11,754 rare-disease parent-child trios: A model for identifying autosomal recessive human gene knockouts including a novel gene... oleh Eric Olinger, Ian J. Wilson, Sarah Orr, Miguel Barroso-Gil, Ruxandra Neatu, Denize Atan, John A. Sayer, John C. Ambrose, Prabhu Arumugam, Roel Bevers, Marta Bleda, Freya Boardman-Pretty, Christopher R. Boustred, Helen Brittain, Mark J. Caulfield, Georgia C. Chan, Greg Elgar, Tom Fowler, Adam Giess, Angela Hamblin, Shirley Henderson, Tim J.P. Hubbard, Rob Jackson, Louise J. Jones, Dalia Kasperaviciute, Melis Kayikci, Athanasios Kousathanas, Lea Lahnstein, Sarah E.A. Leigh, Ivonne U.S. Leong, Javier F. Lopez, Fiona Maleady-Crowe, Meriel McEntagart, Federico Minneci, Loukas Moutsianas, Michael Mueller, Nirupa Murugaesu, Anna C. Need, Peter O’Donovan, Chris A. Odhams, Christine Patch, Mariana Buongermino Pereira, Daniel Perez-Gil, John Pullinger, Tahrima Rahim, Augusto Rendon, Tim Rogers, Kevin Savage, Kushmita Sawant, Richard H. Scott, Afshan Siddiq, Alexander Sieghart, Samuel C. Smith, Alona Sosinsky, Alexander Stuckey, Mélanie Tanguy, Ana Lisa Taylor Tavares, Ellen R.A. Thomas, Simon R. Thompson, Arianna Tucci, Matthew J. Welland, Eleanor Williams, Katarzyna Witkowska, Suzanne M. Wood

    Diterbitkan 2024-01-01
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