Results
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102.
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103.
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104.
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Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy. [electronic resource] by
- Bäumer, Dirk
- Lee, Sheena
- Nicholson, George
- Davies, Joanna L
- Parkinson, Nicholas J
- Murray, Lyndsay M
- Gillingwater, Thomas H
- Ansorge, Olaf
- Davies, Kay E
- Talbot, Kevin
Producer: 20100402
In:
PLoS genetics vol. 5
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105.
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106.
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107.
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Micro-utrophin Improves Cardiac and Skeletal Muscle Function of Severely Affected D2/ [electronic resource] by
- Kennedy, Tahnee L
- Guiraud, Simon
- Edwards, Ben
- Squire, Sarah
- Moir, Lee
- Babbs, Arran
- Odom, Guy
- Golebiowski, Diane
- Schneider, Joel
- Chamberlain, Jeffrey S
- Davies, Kay E
Publication details: Molecular therapy. Methods & clinical development Dec 2018
In:
Molecular therapy. Methods & clinical development vol. 11
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108.
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Mouse models of dominant ACTA1 disease recapitulate human disease and provide insight into therapies. [electronic resource] by
- Ravenscroft, Gianina
- Jackaman, Connie
- Bringans, Scott
- Papadimitriou, John M
- Griffiths, Lisa M
- McNamara, Elyshia
- Bakker, Anthony J
- Davies, Kay E
- Laing, Nigel G
- Nowak, Kristen J
Producer: 20110701
In:
Brain : a journal of neurology vol. 134
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109.
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Novel markers reveal subpopulations of subplate neurons in the murine cerebral cortex. [electronic resource] by
- Hoerder-Suabedissen, Anna
- Wang, Wei Zhi
- Lee, Sheena
- Davies, Kay E
- Goffinet, André M
- Rakić, Sonja
- Parnavelas, John
- Reim, Kerstin
- Nicolić, Margareta
- Paulsen, Ole
- Molnár, Zoltán
Producer: 20090916
In:
Cerebral cortex (New York, N.Y. : 1991) vol. 19
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110.
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Abnormal cardiac morphology, function and energy metabolism in the dystrophic mdx mouse: an MRI and MRS study. [electronic resource] by
- Zhang, Wen
- ten Hove, Michiel
- Schneider, Jürgen E
- Stuckey, Daniel J
- Sebag-Montefiore, Liam
- Bia, Britta L
- Radda, George K
- Davies, Kay E
- Neubauer, Stefan
- Clarke, Kieran
Producer: 20090122
In:
Journal of molecular and cellular cardiology vol. 45
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112.
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Current status of pharmaceutical and genetic therapeutic approaches to treat DMD. [electronic resource] by
- Pichavant, Christophe
- Aartsma-Rus, Annemieke
- Clemens, Paula R
- Davies, Kay E
- Dickson, George
- Takeda, Shin'ichi
- Wilton, Steve D
- Wolff, Jon A
- Wooddell, Christine I
- Xiao, Xiao
- Tremblay, Jacques P
Producer: 20111102
In:
Molecular therapy : the journal of the American Society of Gene Therapy vol. 19
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113.
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A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouse. [electronic resource] by
- Jeans, Alexander F
- Oliver, Peter L
- Johnson, Reuben
- Capogna, Marco
- Vikman, Jenny
- Molnár, Zoltán
- Babbs, Arran
- Partridge, Christopher J
- Salehi, Albert
- Bengtsson, Martin
- Eliasson, Lena
- Rorsman, Patrik
- Davies, Kay E
Producer: 20070517
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 104
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114.
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Circadian profiling in two mouse models of lysosomal storage disorders; Niemann Pick type-C and Sandhoff disease. [electronic resource] by
- Richardson, Katie
- Livieratos, Achilleas
- Dumbill, Richard
- Hughes, Steven
- Ang, Gauri
- Smith, David A
- Morris, Lauren
- Brown, Laurence A
- Peirson, Stuart N
- Platt, Frances M
- Davies, Kay E
- Oliver, Peter L
Producer: 20160920
In:
Behavioural brain research vol. 297
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115.
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Utrophin up-regulation by an artificial transcription factor in transgenic mice. [electronic resource] by
- Mattei, Elisabetta
- Corbi, Nicoletta
- Di Certo, Maria Grazia
- Strimpakos, Georgios
- Severini, Cinzia
- Onori, Annalisa
- Desantis, Agata
- Libri, Valentina
- Buontempo, Serena
- Floridi, Aristide
- Fanciulli, Maurizio
- Baban, Dilair
- Davies, Kay E
- Passananti, Claudio
Producer: 20100312
In:
PloS one vol. 2
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116.
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A functional genetic link between distinct developmental language disorders. [electronic resource] by
- Vernes, Sonja C
- Newbury, Dianne F
- Abrahams, Brett S
- Winchester, Laura
- Nicod, Jérôme
- Groszer, Matthias
- Alarcón, Maricela
- Oliver, Peter L
- Davies, Kay E
- Geschwind, Daniel H
- Monaco, Anthony P
- Fisher, Simon E
Producer: 20081204
In:
The New England journal of medicine vol. 359
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117.
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Compensation for dystrophin-deficiency: ADAM12 overexpression in skeletal muscle results in increased alpha 7 integrin, utrophin and associated glycoproteins. [electronic resource] by
- Moghadaszadeh, Behzad
- Albrechtsen, Reidar
- Guo, Ling T
- Zaik, Michaela
- Kawaguchi, Nobuko
- Borup, Rehannah H
- Kronqvist, Pauliina
- Schroder, Henrik D
- Davies, Kay E
- Voit, Thomas
- Nielsen, Finn C
- Engvall, Eva
- Wewer, Ulla M
Producer: 20040519
In:
Human molecular genetics vol. 12
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118.
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Actin nemaline myopathy mouse reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression. [electronic resource] by
- Ravenscroft, Gianina
- Jackaman, Connie
- Sewry, Caroline A
- McNamara, Elyshia
- Squire, Sarah E
- Potter, Allyson C
- Papadimitriou, John
- Griffiths, Lisa M
- Bakker, Anthony J
- Davies, Kay E
- Laing, Nigel G
- Nowak, Kristen J
Producer: 20120423
In:
PloS one vol. 6
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119.
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Absent sleep EEG spindle activity in GluA1 (Gria1) knockout mice: relevance to neuropsychiatric disorders. [electronic resource] by
- Ang, Gauri
- McKillop, Laura E
- Purple, Ross
- Blanco-Duque, Cristina
- Peirson, Stuart N
- Foster, Russell G
- Harrison, Paul J
- Sprengel, Rolf
- Davies, Kay E
- Oliver, Peter L
- Bannerman, David M
- Vyazovskiy, Vladyslav V
Producer: 20190304
In:
Translational psychiatry vol. 8
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120.
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Hsp72 preserves muscle function and slows progression of severe muscular dystrophy. [electronic resource] by
- Gehrig, Stefan M
- van der Poel, Chris
- Sayer, Timothy A
- Schertzer, Jonathan D
- Henstridge, Darren C
- Church, Jarrod E
- Lamon, Severine
- Russell, Aaron P
- Davies, Kay E
- Febbraio, Mark A
- Lynch, Gordon S
Producer: 20120525
In:
Nature vol. 484
Availability: No items available.
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