Search Results - North, Kathryn N.

Refine Results
  1. 1
    Phylogenetic analysis of ferlin genes reveals ancient eukaryotic origins

    Phylogenetic analysis of ferlin genes reveals ancient eukaryotic origins by Lek, Angela, Lek, Monkol, North, Kathryn N, Cooper, Sandra T

    Published 2010
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  2. 2
    Phylogenetic Analysis of Gene Structure and Alternative Splicing in α-Actinins

    Phylogenetic Analysis of Gene Structure and Alternative Splicing in α-Actinins by Lek, Monkol, MacArthur, Daniel G., Yang, Nan, North, Kathryn N.

    Published 2010
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  3. 3
    Loss of α-actinin-3 confers protection from eccentric contraction damage in fast-twitch EDL muscles from aged mdx dystrophic mice by reducing pathological fibre branching

    Loss of α-actinin-3 confers protection from eccentric contraction damage in fast-twitch EDL muscles from aged mdx dystrophic mice by reducing pathological fibre branching by Kiriaev, Leonit, Houweling, Peter J, North, Kathryn N, Head, Stewart I

    Published 2021
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  4. 4
    T2 hyperintensities in children with neurofibromatosis type 1 and their relationship to cognitive functioning

    T2 hyperintensities in children with neurofibromatosis type 1 and their relationship to cognitive functioning by Hyman, Shelley L, Gill, Deepak S, Shores, Edwin Arthur, Steinberg, Adam, North, Kathryn N

    Published 2007
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  5. 5
    Mild Functional Differences of Dynamin 2 Mutations Associated to Centronuclear Myopathy and Charcot-Marie-Tooth Peripheral Neuropathy

    Mild Functional Differences of Dynamin 2 Mutations Associated to Centronuclear Myopathy and Charcot-Marie-Tooth Peripheral Neuropathy by Koutsopoulos, Olga S., Koch, Catherine, Tosch, Valerie, Böhm, Johann, North, Kathryn N., Laporte, Jocelyn

    Published 2011
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  6. 6
    The genetic and neuroanatomical basis of social dysfunction: Lessons from neurofibromatosis type 1

    The genetic and neuroanatomical basis of social dysfunction: Lessons from neurofibromatosis type 1 by Pride, Natalie A., Korgaonkar, Mayuresh S., Barton, Belinda, Payne, Jonathan M., Vucic, Steve, North, Kathryn N.

    Published 2013
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  7. 7
    A transformative translational change programme to introduce genomics into healthcare: a complexity and implementation science study protocol

    A transformative translational change programme to introduce genomics into healthcare: a complexity and implementation science study protocol by Taylor, Natalie, Best, Stephanie, Martyn, Melissa, Long, Janet C, North, Kathryn N, Braithwaite, Jeffrey, Gaff, Clara

    Published 2019
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  8. 8
    Lifespan Analysis of Dystrophic mdx Fast-Twitch Muscle Morphology and Its Impact on Contractile Function

    Lifespan Analysis of Dystrophic mdx Fast-Twitch Muscle Morphology and Its Impact on Contractile Function by Kiriaev, Leonit, Kueh, Sindy, Morley, John W., North, Kathryn N., Houweling, Peter J., Head, Stewart I.

    Published 2021
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  9. 9
    Increased connective tissue growth factor associated with cardiac fibrosis in the mdx mouse model of dystrophic cardiomyopathy

    Increased connective tissue growth factor associated with cardiac fibrosis in the mdx mouse model of dystrophic cardiomyopathy by Au, Carol G, Butler, Tanya L, Sherwood, Megan C, Egan, Jonathan R, North, Kathryn N, Winlaw, David S

    Published 2011
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  10. 10
    Myoblast sensitivity and fibroblast insensitivity to osteogenic conversion by BMP-2 correlates with the expression of Bmpr-1a

    Myoblast sensitivity and fibroblast insensitivity to osteogenic conversion by BMP-2 correlates with the expression of Bmpr-1a by Liu, Renjing, Ginn, Samantha L, Lek, Monkol, North, Kathryn N, Alexander, Ian E, Little, David G, Schindeler, Aaron

    Published 2009
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  11. 11
    ACTN3 Allele Frequency in Humans Covaries with Global Latitudinal Gradient

    ACTN3 Allele Frequency in Humans Covaries with Global Latitudinal Gradient by Friedlander, Scott M., Herrmann, Amanda L., Lowry, Daniel P., Mepham, Emily R., Lek, Monkol, North, Kathryn N., Organ, Chris L.

    Published 2013
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  12. 12
    A Novel Syndrome of Episodic Muscle Weakness Maps to Xp22.3

    A Novel Syndrome of Episodic Muscle Weakness Maps to Xp22.3 by Ryan, Monique M., Taylor, Peter, Donald, Jennifer A., Ouvrier, Robert A., Morgan, Graeme, Danta, Gytis, Buckley, Michael F., North, Kathryn N.

    Published 1999
    Get full text Get full text
    Text
    Save to List
    Saved in:
  13. 13
    UDP-N-Acetylglucosamine 2-Epimerase/N-Acetylmannosamine Kinase (GNE) Binds to Alpha-Actinin 1: Novel Pathways in Skeletal Muscle?

    UDP-N-Acetylglucosamine 2-Epimerase/N-Acetylmannosamine Kinase (GNE) Binds to Alpha-Actinin 1: Novel Pathways in Skeletal Muscle? by Amsili, Shira, Zer, Hagit, Hinderlich, Stephan, Krause, Sabine, Becker-Cohen, Michal, MacArthur, Daniel G., North, Kathryn N., Mitrani-Rosenbaum, Stella

    Published 2008
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  14. 14
    Altered Ca(2+) Kinetics Associated with α-Actinin-3 Deficiency May Explain Positive Selection for ACTN3 Null Allele in Human Evolution

    Altered Ca(2+) Kinetics Associated with α-Actinin-3 Deficiency May Explain Positive Selection for ACTN3 Null Allele in Human Evolution by Head, Stewart I., Chan, Stephen, Houweling, Peter J., Quinlan, Kate G. R., Murphy, Robyn, Wagner, Sören, Friedrich, Oliver, North, Kathryn N.

    Published 2015
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  15. 15
    Absence of the Z-disc protein α-actinin-3 impairs the mechanical stability of Actn3KO mouse fast-twitch muscle fibres without altering their contractile properties or twitch kinetics

    Absence of the Z-disc protein α-actinin-3 impairs the mechanical stability of Actn3KO mouse fast-twitch muscle fibres without altering their contractile properties or twitch kineti... by Haug, Michael, Reischl, Barbara, Nübler, Stefanie, Kiriaev, Leonit, Mázala, Davi A. G., Houweling, Peter J., North, Kathryn N., Friedrich, Oliver, Head, Stewart I.

    Published 2022
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  16. 16
    Reduced Plasma Membrane Expression of Dysferlin Mutants Is Attributed to Accelerated Endocytosis via a Syntaxin-4-associated Pathway

    Reduced Plasma Membrane Expression of Dysferlin Mutants Is Attributed to Accelerated Endocytosis via a Syntaxin-4-associated Pathway by Evesson, Frances J., Peat, Rachel A., Lek, Angela, Brilot, Fabienne, Lo, Harriet P., Dale, Russell C., Parton, Robert G., North, Kathryn N., Cooper, Sandra T.

    Published 2010
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  17. 17
    Evidence Based Selection of Commonly Used RT-qPCR Reference Genes for the Analysis of Mouse Skeletal Muscle

    Evidence Based Selection of Commonly Used RT-qPCR Reference Genes for the Analysis of Mouse Skeletal Muscle by Thomas, Kristen C., Zheng, Xi Fiona, Garces Suarez, Francia, Raftery, Joanna M., Quinlan, Kate G. R., Yang, Nan, North, Kathryn N., Houweling, Peter J.

    Published 2014
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  18. 18
    Disease Severity and Thin Filament Regulation in M9R TPM3 Nemaline Myopathy

    Disease Severity and Thin Filament Regulation in M9R TPM3 Nemaline Myopathy by Ilkovski, Biljana, Mokbel, Nancy, Lewis, Raymond A., Walker, Kendall, Nowak, Kristen J., Domazetovska, Ana, Laing, Nigel G., Fowler, Velia M., North, Kathryn N., Cooper, Sandra T.

    Published 2008
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  19. 19
    Exclusion of biglycan mutations in a cohort of patients with neuromuscular disorders

    Exclusion of biglycan mutations in a cohort of patients with neuromuscular disorders by Peat, Rachel A., Gécz, Jozef, Fallon, Justin R., Tarpey, Patrick S., Smith, Raffaella, Futreal, Andrew, Stratton, Michael R., Lamandé, Shireen R., Yang, Nan, North, Kathryn N.

    Published 2008
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  20. 20
    Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy

    Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy by Hogarth, Marshall W., Houweling, Peter J., Thomas, Kristen C., Gordish-Dressman, Heather, Bello, Luca, Pegoraro, Elena, Hoffman, Eric P., Head, Stewart I., North, Kathryn N.

    Published 2017
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:

Search Tools: