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Dystrophin and utrophin "double knockout" dystrophic mice exhibit a spectrum of degenerative musculoskeletal abnormalities
Dystrophin and utrophin "double knockout" dystrophic mice exhibit a spectrum of degenerative musculoskeletal abnormalities
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Dystrophin and utrophin "double knockout" dystrophic mice exhibit a spectrum of degenerative musculoskeletal abnormalities

Isaac, Christian ; Wright, Adam ; Usas, Arvydas ; Li, Hongshuai ; Tang, Ying ; Mu, Xiaodong ; Greco, Nicholas ; Dong, Qing ; Vo, Nam ; Kang, James ; Wang, Bing ; Huard, Johnny

Journal of orthopaedic research, 2013-03, Vol.31 (3), p.343-349 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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2
Skin biopsy findings in megaconial congenital muscular dystrophy with psoriasiform lesions due to variants in CHKB
Skin biopsy findings in megaconial congenital muscular dystrophy with psoriasiform lesions due to variants in CHKB
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Skin biopsy findings in megaconial congenital muscular dystrophy with psoriasiform lesions due to variants in CHKB

Gong, Zhuoqing ; Chen, Kai ; Xu, Zhe ; Yang, Zhou ; Wang, Huijun ; Lin, Zhimiao

Journal of the European Academy of Dermatology and Venereology, 2024-04, Vol.38 (4), p.e323-e325 [Periódico revisado por pares]

England

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3
Enhanced in vivo delivery of antisense oligonucleotides to restore dystrophin expression in adult mdx mouse muscle
Enhanced in vivo delivery of antisense oligonucleotides to restore dystrophin expression in adult mdx mouse muscle
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Enhanced in vivo delivery of antisense oligonucleotides to restore dystrophin expression in adult mdx mouse muscle

Wells, K.E. ; Fletcher, S. ; Mann, C.J. ; Wilton, S.D. ; Wells, D.J.

FEBS letters, 2003-09, Vol.552 (2), p.145-149 [Periódico revisado por pares]

England: Elsevier B.V

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4
Alternative utrophin mRNAs contribute to phenotypic differences between dystrophin‐deficient mice and Duchenne muscular dystrophy
Alternative utrophin mRNAs contribute to phenotypic differences between dystrophin‐deficient mice and Duchenne muscular dystrophy
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Alternative utrophin mRNAs contribute to phenotypic differences between dystrophin‐deficient mice and Duchenne muscular dystrophy

Perkins, Kelly J. ; Davies, Kay E.

FEBS letters, 2018-06, Vol.592 (11), p.1856-1869 [Periódico revisado por pares]

England: John Wiley and Sons Inc

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5
Label‐free 3D characterization of cardiac fibrosis in muscular dystrophy using SHG imaging of cleared tissue
Label‐free 3D characterization of cardiac fibrosis in muscular dystrophy using SHG imaging of cleared tissue
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Label‐free 3D characterization of cardiac fibrosis in muscular dystrophy using SHG imaging of cleared tissue

Pichon, Julien ; Ledevin, Mireille ; Larcher, Thibaut ; Jamme, Frédéric ; Rouger, Karl ; Dubreil, Laurence

Biology of the cell, 2022-03, Vol.114 (3), p.91-103 [Periódico revisado por pares]

England: Wiley

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6
Disruption of perlecan binding and matrix assembly by post-translational or genetic disruption of dystroglycan function
Disruption of perlecan binding and matrix assembly by post-translational or genetic disruption of dystroglycan function
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Disruption of perlecan binding and matrix assembly by post-translational or genetic disruption of dystroglycan function

Kanagawa, Motoi ; Michele, Daniel E. ; Satz, Jakob S. ; Barresi, Rita ; Kusano, Hajime ; Sasaki, Takako ; Timpl, Rupert ; Henry, Michael D. ; Campbell, Kevin P.

FEBS letters, 2005-08, Vol.579 (21), p.4792-4796 [Periódico revisado por pares]

England: Elsevier B.V

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7
Structural analysis of emerin, an inner nuclear membrane protein mutated in X-linked Emery–Dreifuss muscular dystrophy
Structural analysis of emerin, an inner nuclear membrane protein mutated in X-linked Emery–Dreifuss muscular dystrophy
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Structural analysis of emerin, an inner nuclear membrane protein mutated in X-linked Emery–Dreifuss muscular dystrophy

Wolff, Nicolas ; Gilquin, Bernard ; Courchay, Karine ; Callebaut, Isabelle ; Worman, Howard J. ; Zinn-Justin, Sophie

FEBS letters, 2001-07, Vol.501 (2), p.171-176 [Periódico revisado por pares]

England: Elsevier B.V

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8
The caveolin‐3 P104L mutation in LGMD‐1C patients inhibits non‐insulin‐stimulated glucose metabolism and growth but promotes myocyte proliferation
The caveolin‐3 P104L mutation in LGMD‐1C patients inhibits non‐insulin‐stimulated glucose metabolism and growth but promotes myocyte proliferation
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The caveolin‐3 P104L mutation in LGMD‐1C patients inhibits non‐insulin‐stimulated glucose metabolism and growth but promotes myocyte proliferation

Shang, Lina ; Chen, Tingting ; Xian, Jing ; Deng, Yufeng ; Huang, Yiyuan ; Zhao, Qiwei ; Liang, Guining ; Liang, Zhifeng ; Lian, Fang ; Wei, Hongqiao ; Huang, Qin

Cell biology international, 2019-06, Vol.43 (6), p.669-677 [Periódico revisado por pares]

England: Wiley Subscription Services, Inc

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9
Systemic human minidystrophin gene transfer improves functions and life span of dystrophin and dystrophin/utrophin-deficient mice
Systemic human minidystrophin gene transfer improves functions and life span of dystrophin and dystrophin/utrophin-deficient mice
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Systemic human minidystrophin gene transfer improves functions and life span of dystrophin and dystrophin/utrophin-deficient mice

Wang, Bing ; Li, Juan ; Fu, Freddie H. ; Xiao, Xiao

Journal of orthopaedic research, 2009-04, Vol.27 (4), p.421-426 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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10
Human ϵ-sarcoglycan is highly related to α-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene
Human ϵ-sarcoglycan is highly related to α-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene
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Human ϵ-sarcoglycan is highly related to α-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene

McNally, Elizabeth M ; Ly, Chantal T ; Kunkel, Louis M

FEBS letters, 1998-01, Vol.422 (1), p.27-32 [Periódico revisado por pares]

England: Elsevier B.V

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