Bilaketaren emaitzak - Alan Hodgkinson

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  1. 1
    Human Triallelic Sites: Evidence for a New Mutational Mechanism?

    Human Triallelic Sites: Evidence for a New Mutational Mechanism? nork Alan Hodgkinson, Adam Eyre‐Walker

    Argitaratua 2009
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  2. 2
    Cryptic Variation in the Human Mutation Rate

    Cryptic Variation in the Human Mutation Rate nork Alan Hodgkinson, Emmanuel D. Ladoukakis, Adam Eyre‐Walker

    Argitaratua 2009
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  3. 3
    Nuclear genetic regulation of the human mitochondrial transcriptome

    Nuclear genetic regulation of the human mitochondrial transcriptome nork Aminah T. Ali, Lena Boehme, Guillermo Carbajosa, Vlad C. Seitan, Kerrin S. Small, Alan Hodgkinson

    Argitaratua 2019
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  4. 4
    Recombination affects accumulation of damaging and disease-associated mutations in human populations

    Recombination affects accumulation of damaging and disease-associated mutations in human populations nork Julie Hussin, Alan Hodgkinson, Youssef Idaghdour, Jean‐Christophe Grenier, Jean-Philippe Goulet, Elias Gbeha, Elodie Hip-Ki, Philip Awadalla

    Argitaratua 2015
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  5. 5
    Relaxed Selection During a Recent Human Expansion

    Relaxed Selection During a Recent Human Expansion nork Stephan Peischl, Isabelle Dupanloup, Adrien Foucal, Michèle Jomphe, Vanessa Bruat, Jean‐Christophe Grenier, Alexandre Gouy, Kimberly J. Gilbert, Elias Gbeha, Lars Bosshard, Elodie Hip-Ki, Mawussé Agbessi, Alan Hodgkinson, Hélène Vézina, Philip Awadalla, Laurent Excoffier

    Argitaratua 2017
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  6. 6
    Genetic variation at mouse and human ribosomal DNA influences associated epigenetic states

    Genetic variation at mouse and human ribosomal DNA influences associated epigenetic states nork Francisco Rodríguez-Algarra, Robert A. Seaborne, Amy F. Danson, Selin Yildizoglu, Harunori Yoshikawa, Pui Pik Law, Zakaryya Ahmad, Victoria A. Maudsley, Ama Brew, Nadine Holmes, Mateus Ochôa, Alan Hodgkinson, Sarah J. Marzi, Madapura M. Pradeepa, Matthew Loose, Michelle L. Holland, Vardhman K. Rakyan

    Argitaratua 2022
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  7. 7
    Exome sequencing identifies mutations in the gene<i>TTC7A</i>in French-Canadian cases with hereditary multiple intestinal atresia

    Exome sequencing identifies mutations in the gene<i>TTC7A</i>in French-Canadian cases with hereditary multiple intestinal atresia nork Mark E. Samuels, Jacek Majewski, Najmeh Alirezaie, Isabel Fernández, Ferrán Casals, Natalie Patey, Hélène Decaluwe, Isabelle Gosselin, Élie Haddad, Alan Hodgkinson, Youssef Idaghdour, Valérie Marchand, Jacques L. Michaud, Marc‐André Rodrigue, Sylvie Desjardins, Stéphane Dubois, Françoise Le Deist, Philip Awadalla, Vincent Raymond, Bruno Maranda

    Argitaratua 2013
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  8. 8
    Whole-Exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans

    Whole-Exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans nork Ferrán Casals, Alan Hodgkinson, Julie Hussin, Youssef Idaghdour, Vanessa Bruat, Thibault de Maillard, Jean‐Christophe Grenier, Elias Gbeha, Fadi F. Hamdan, Simon Girard, Jean-François Spinella, Mathieu Larivière, Virginie Saillour, Jasmine Healy, Isabel Fernández, Daniel Sinnett, Jacques L. Michaud, Guy A. Rouleau, Élie Haddad, Françoise Le Deist, Philip Awadalla

    Argitaratua 2013
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  9. 9
    Genetically encoded impairment of neuronal <scp>KCC</scp> 2 cotransporter function in human idiopathic generalized epilepsy

    Genetically encoded impairment of neuronal <scp>KCC</scp> 2 cotransporter function in human idiopathic generalized epilepsy nork Kristopher T. Kahle, Nancy D. Merner, Perrine Friedel, Liliya Silayeva, Bo Liang, Arjun Khanna, Yuze Shang, Pamela Lachance‐Touchette, Cynthia V. Bourassa, Annie Levert, Patrick A. Dion, Brian P. Walcott, Dan Spiegelman, Alexandre Dionne‐Laporte, Alan Hodgkinson, Philip Awadalla, Hamid Nikbakht, Jacek Majewski, Patrick Cossette, Tarek Z. Deeb, Stephen J. Moss, Igor Medina, Guy A. Rouleau

    Argitaratua 2014
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