Ngā hua rapu kaituhi

1

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

I whakaputaina 2010

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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2

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

I whakaputaina 2010

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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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 mā Kiriaev, Leonit, Houweling, Peter J, North, Kathryn N, Head, Stewart I

I whakaputaina 2021

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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4

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

I whakaputaina 2007

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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5

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

I whakaputaina 2011

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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6

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

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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7

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

I whakaputaina 2019

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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8

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

I whakaputaina 2021

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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9

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

I whakaputaina 2011

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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10

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

I whakaputaina 2009

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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11

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

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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12

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

I whakaputaina 1999

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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13

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

I whakaputaina 2008

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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14

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

I whakaputaina 2015

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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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 kineti... mā Haug, Michael, Reischl, Barbara, Nübler, Stefanie, Kiriaev, Leonit, Mázala, Davi A. G., Houweling, Peter J., North, Kathryn N., Friedrich, Oliver, Head, Stewart I.

I whakaputaina 2022

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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16

Reduced Plasma Membrane Expression of Dysferlin Mutants Is Attributed to Accelerated Endocytosis via a Syntaxin-4-associated Pathway mā 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.

I whakaputaina 2010

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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17

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

I whakaputaina 2014

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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18

Disease Severity and Thin Filament Regulation in M9R TPM3 Nemaline Myopathy mā 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.

I whakaputaina 2008

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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19

Exclusion of biglycan mutations in a cohort of patients with neuromuscular disorders mā 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.

I whakaputaina 2008

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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20

Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy mā 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.

I whakaputaina 2017

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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Ngā hua rapu - North, Kathryn N

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

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

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 mā Kiriaev, Leonit, Houweling, Peter J, North, Kathryn N, Head, Stewart I

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

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

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

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

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

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

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

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

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

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

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

Reduced Plasma Membrane Expression of Dysferlin Mutants Is Attributed to Accelerated Endocytosis via a Syntaxin-4-associated Pathway mā 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.

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

Disease Severity and Thin Filament Regulation in M9R TPM3 Nemaline Myopathy mā 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.

Exclusion of biglycan mutations in a cohort of patients with neuromuscular disorders mā 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.

Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy mā 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.

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