Rezultati - Jesper Graakjær

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  1. 1
    The relative lengths of individual telomeres are defined in the zygote and strictly maintained during life

    The relative lengths of individual telomeres are defined in the zygote and strictly maintained during life od Jesper Graakjær, Leigh Pascoe, Héra Der‐Sarkissian, Anthony J. Gill, Steen Kølvraa, Kaare Christensen, Arturo Londoño‐Vallejo

    Izdano 2004
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  2. 2
    The Heritability of Telomere Length Among the Elderly and Oldest-Old

    The Heritability of Telomere Length Among the Elderly and Oldest-Old od Claus Bischoff, Jesper Graakjær, Hans Petersen, Jacob Hjelmborg, James W. Vaupel, Vilhelm A. Bohr, Steen Koelvraa, Kaare Christensen

    Izdano 2005
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  3. 3
    The Werner Syndrome Helicase and Exonuclease Cooperate to Resolve Telomeric D Loops in a Manner Regulated by TRF1 and TRF2

    The Werner Syndrome Helicase and Exonuclease Cooperate to Resolve Telomeric D Loops in a Manner Regulated by TRF1 and TRF2 od Patricia L. Opresko, Marit Otterlei, Jesper Graakjær, Per Bruheim, Lale Dawut, Steen Kølvraa, Alfred May, Michael M. Seidman, Vilhem A Bohr

    Izdano 2004
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  4. 4
    No Association Between Telomere Length and Survival Among the Elderly and Oldest Old

    No Association Between Telomere Length and Survival Among the Elderly and Oldest Old od Claus Bischoff, Hans Petersen, Jesper Graakjær, Karen Andersen‐Ranberg, James W. Vaupel, Vilhelm A. Bohr, Steen K oslash lvraa, Kaare Christensen

    Izdano 2006
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  5. 5
    Perturbations in RhoA signalling cause altered migration and impaired neuritogenesis in human iPSC-derived neural cells with PARK2 mutation

    Perturbations in RhoA signalling cause altered migration and impaired neuritogenesis in human iPSC-derived neural cells with PARK2 mutation od Helle Bogetofte, Pia Jensen, Justyna Okarmus, Sissel Ida Schmidt, Mikkel Agger, Matias Ryding, Peter Nørregaard, Christina Fenger, Xianmin Zeng, Jesper Graakjær, Brent J. Ryan, Richard Wade‐Martins, Martin R. Larsen, Morten Meyer

    Izdano 2019
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  6. 6
    Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes

    Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes od Claudia M.B. Carvalho, Shivakumar Vasanth, Marwan Shinawi, Chad Russell, Melissa B. Ramocki, Chester Brown, Jesper Graakjær, Anne‐Bine Skytte, Angela Maria Vianna‐Morgante, Ana Cristina Victorino Krepischi, Gayle Patel, LaDonna Immken, Kyrieckos A. Aleck, Cynthia Lim, S.W. Cheung, Carla Rosenberg, Nicholas Katsanis, James R. Lupski

    Izdano 2014
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  7. 7
    The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes

    The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes od Cynthia J. Curry, Jill A. Rosenfeld, Erica T. Grant, Karen W. Gripp, Carol E. Anderson, Arthur S. Aylsworth, Taha Ben Saad, Victor V. Chizhikov, Giedre Dybose, Christina Fagerberg, M. Falco, Christina Fels, Marco Fichera, Jesper Graakjær, Donatella Greco, Jennifer Hair, Elizabeth Hopkins, Marlene J. Huggins, Roger L. Ladda, Chumei Li, John B. Moeschler, Małgorzata J.M. Nowaczyk, Jillian R. Ozmore, S Reitano, Corrado Romano, Laura Roos, Rhonda E. Schnur, Susan L. Sell, Pim Suwannarat, Dea Svaneby, Marta Szybowska, Mark A. Tarnopolsky, Raymond C. Tervo, Anne Chun‐Hui Tsai, Megan Tucker, Stephanie E. Vallee, Ferrin C. Wheeler, Dina J. Zand, A. James Barkovich, Swaroop Aradhya, Lisa G. Shaffer, William B. Dobyns

    Izdano 2013
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