Výsledky vyhledávání - Richard Festenstein

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  1. 1
    Gene regulation and epigenetics in Friedreich's ataxia

    Gene regulation and epigenetics in Friedreich's ataxia Autor Cihangir Yandım, Theona Natisvili, Richard Festenstein

    Vydáno 2013
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    Revisão
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  2. 2
    Evidence for Distinct CD4 Silencer Functions at Different Stages of Thymocyte Differentiation

    Evidence for Distinct CD4 Silencer Functions at Different Stages of Thymocyte Differentiation Autor Ichiro Taniuchi, Mary Jean Sunshine, Richard Festenstein, Dan R. Littman

    Vydáno 2002
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    Artigo
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  3. 3
    Transcription Elongation and Tissue-Specific Somatic CAG Instability

    Transcription Elongation and Tissue-Specific Somatic CAG Instability Autor Agathi-Vasiliki Goula, Agnieszka Styś, Jackson Ping Kei Chan, Yvon Trottier, Richard Festenstein, Karine Mérienne

    Vydáno 2012
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  4. 4
    Sexual Dimorphism in Mammalian Autosomal Gene Regulation Is Determined Not Only by Sry but by Sex Chromosome Complement As Well

    Sexual Dimorphism in Mammalian Autosomal Gene Regulation Is Determined Not Only by Sry but by Sex Chromosome Complement As Well Autor Patrick J. Wijchers, Cihangir Yandım, Eleni Panousopoulou, Mushfika Ahmad, Nicky Harker, Alexander Saveliev, Paul S. Burgoyne, Richard Festenstein

    Vydáno 2010
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  5. 5
    H3 Lysine 4 Is Acetylated at Active Gene Promoters and Is Regulated by H3 Lysine 4 Methylation

    H3 Lysine 4 Is Acetylated at Active Gene Promoters and Is Regulated by H3 Lysine 4 Methylation Autor Benoît Guillemette, Paul Drogaris, Hsiu-Hsu Sophia Lin, Harry Armstrong, Kyoko Hiragami-Hamada, Axel Imhof, Éric Bonneil, Pierre Thibault, Alain Verreault, Richard Festenstein

    Vydáno 2011
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  6. 6
    A wearable motion capture suit and machine learning predict disease progression in Friedreich’s ataxia

    A wearable motion capture suit and machine learning predict disease progression in Friedreich’s ataxia Autor Balasundaram Kadirvelu, Constantinos Gavriel, Sathiji Nageshwaran, Jackson Ping Kei Chan, Suran Nethisinghe, Stavros Athanasopoulos, Valeria Ricotti, Thomas Voit, Paola Giunti, Richard Festenstein, A. Aldo Faisal

    Vydáno 2023
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  7. 7
    Heterochromatinization induced by GAA-repeat hyperexpansion in Friedreich's ataxia can be reduced upon HDAC inhibition by vitamin B3

    Heterochromatinization induced by GAA-repeat hyperexpansion in Friedreich's ataxia can be reduced upon HDAC inhibition by vitamin B3 Autor Paul K.S. Chan, Raul M. Torres, Cihangir Yandım, Pui Pik Law, Sanjay Khadayate, Marta Mauri, Crina Groşan, Nadine Chapman‐Rothe, Paola Giunti, Mark A. Pook, Richard Festenstein

    Vydáno 2013
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  8. 8
    Continuous Histone Replacement by Hira Is Essential for Normal Transcriptional Regulation and De Novo DNA Methylation during Mouse Oogenesis

    Continuous Histone Replacement by Hira Is Essential for Normal Transcriptional Regulation and De Novo DNA Methylation during Mouse Oogenesis Autor Buhe Nashun, Peter W. S. Hill, Sébastien A. Smallwood, Gopuraja Dharmalingam, Rachel Amouroux, Stephen J. Clark, Vineet K. Sharma, Elodie Ndjetehe, Paweł Pelczar, Richard Festenstein, Gavin Kelsey, Petra Hájková

    Vydáno 2015
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  9. 9
    Epigenetic and neurological effects and safety of high-dose nicotinamide in patients with Friedreich's ataxia: an exploratory, open-label, dose-escalation study

    Epigenetic and neurological effects and safety of high-dose nicotinamide in patients with Friedreich's ataxia: an exploratory, open-label, dose-escalation study Autor Vincenzo Libri, Cihangir Yandım, Stavros Athanasopoulos, Naomi Loyse, Theona Natisvili, Pui Pik Law, Ping Kei Chan, Tariq Mohammad, Marta Mauri, Kin Tung Tam, James Leiper, Sophie Piper, Aravind Ramesh, Michael Parkinson, Les Huson, Paola Giunti, Richard Festenstein

    Vydáno 2014
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  10. 10
    Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study

    Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study Autor Katherine Schon, Rita Horváth, Wei Wei, Claudia Calabrese, Arianna Tucci, Kristina Ibáñez, Thiloka Ratnaike, Robert D. S. Pitceathly, Enrico Bugiardini, Rosaline C. M. Quinlivan, Michael G. Hanna, Emma Clement, Emma Ashton, John A. Sayer, Paul M. Brennan, Dragana Josifova, Louise Izatt, Carl Fratter, Victoria Nesbitt, Timothy Barrett, Dominic J McMullen, Audrey Smith, Charulata Deshpande, Sarah Smithson, Richard Festenstein, Natalie Canham, Mark J. Caulfield, Henry Houlden, Shamima Rahman, Patrick F. Chinnery

    Vydáno 2021
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  11. 11
    Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study

    Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study Autor Kristina Ibáñez, James M. Polke, R. Tanner Hagelstrom, Egor Dolzhenko, Dorota Pasko, Ellen Thomas, Louise C. Daugherty, Dalia Kasperavičiūtė, Katherine R. Smith, Zandra C. Deans, Sue Hill, Tom Fowler, Richard H. Scott, John Hardy, Patrick F. Chinnery, Henry Houlden, Augusto Rendon, Mark J. Caulfield, Michael A. Eberle, Ryan J. Taft, Arianna Tucci, Ellen M. McDonagh, Antonio Rueda, Dimitris Polychronopoulos, G. C. Chan, Heather Angus‐Leppan, Kailash P. Bhatia, James Davison, Richard Festenstein, Pietro Fratta, Paola Giunti, Robin Howard, Laxmi Venkata, Matilde Laurá, Meriel McEntagart, Lara Menzies, Huw R. Morris, Mary M. Reilly, Robert Robinson, Elisabeth Rosser, Francesca Faravelli, Anette Schrag, Jonathan M. Schott, Thomas T. Warner, Nicholas Wood, David Bourn, Kelly Eggleton, Robyn Labrum, Philip Twiss, Stephen Abbs, Liana Santos, Ghareesa Almheiri, Isabella Sheikh, Jana Vandrovcová, Christine Patch, Ana Lisa Taylor Tavares, Zerin Hyder, Anna C. Need, Helen Brittain, Emma L. Baple, Loukas Moutsianas, Viraj Deshpande, Denise Perry, Subramanian S. Ajay, Aditi Chawla, Vani Rajan, Kathryn Oprych, Patrick F. Chinnery, Angela Douglas, Gill Wilson, Sian Ellard, I. Karen Temple, Andrew Mumford, Dom McMullan, Kikkeri N. Naresh, Frances Flinter, Jenny C. Taylor, Lynn Greenhalgh, William G. Newman, Paul M. Brennan, John A. Sayer, F. Lucy Raymond, Lyn S. Chitty, John C. Ambrose, Prabhu Arumugam, Marta Bleda, F. Boardman-Pretty, Jeanne M. Boissiere, C. R. Boustred, C. E. H. Craig, Anna de Burca, A. Devereau, Greg Elgar, Rebecca E. Foulger, Pedro Furió‐Tarí, Joanne Hackett, Dina Halai, Angela Hamblin, Shirley Henderson, James Holman

    Vydáno 2022
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