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1
Cell surface and gene expression regulation molecules in dystrophinopathy: mdx vs. Duchenne
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Artigo
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Cell surface and gene expression regulation molecules in dystrophinopathy: mdx vs. Duchenne

Fadic, Ricardo

Biological research, 2005, Vol.38 (4), p.375-380 [Periódico revisado por pares]

England: Sociedad de Biología de Chile

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2
Genetic testing for Duchenne/Becker muscular dystrophy in Johannesburg, South Africa
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Artigo
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Genetic testing for Duchenne/Becker muscular dystrophy in Johannesburg, South Africa

Kerr, Robyn ; Robinson, Carol ; Essop, Fahmida B ; Krause, Amanda

SAMJ: South African Medical Journal, 2013-12, Vol.103 (12 Suppl 1), p.999-1004 [Periódico revisado por pares]

South Africa: Health & Medical Publishing Group

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3
Protein defects in neuromuscular diseases
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Artigo
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Protein defects in neuromuscular diseases

Vainzof, M ; Zatz, M

Brazilian journal of medical and biological research, 2003-05, Vol.36 (5), p.543-555 [Periódico revisado por pares]

Brazil: Associação Brasileira de Divulgação Científica

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4
The dystrophinopathies in Costa Rica
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The dystrophinopathies in Costa Rica

Azofeifa, Jorge

Revista de biología tropical, 2004-09, Vol.52 (3), p.485-490 [Periódico revisado por pares]

Costa Rica: Universidad de Costa Rica

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5
iPSCs ameliorate hypoxia-induced autophagy and atrophy in C2C12 myotubes via the AMPK/ULK1 pathway
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Artigo
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iPSCs ameliorate hypoxia-induced autophagy and atrophy in C2C12 myotubes via the AMPK/ULK1 pathway

Cen, Haimei ; Fan, Pin ; Ding, Yuting ; Luo, Bin ; Luo, Hong ; Chen, Menglong ; Zhang, Yu

Biological research, 2023-06, Vol.56 (1), p.29-29, Article 29 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
Erythropoietin reduces the expression of myostatin in mdx dystrophic mice
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Artigo
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Erythropoietin reduces the expression of myostatin in mdx dystrophic mice

Feder, D ; Rugollini, M ; Santomauro, Jr, A ; Oliveira, L P ; Lioi, V P ; Santos, R dos ; Ferreira, L G ; Nunes, M T ; Carvalho, M H ; Delgado, P O ; Carvalho, A A S ; Fonseca, F L A

Brazilian journal of medical and biological research, 2014-11, Vol.47 (11), p.966-971 [Periódico revisado por pares]

Brazil: Associacao Brasileira de Divulgacao Cientifica (ABDC)

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7
A novel FKRP-related muscular dystrophy founder mutation in South African Afrikaner patients with a phenotype suggestive of a dystrophinopathy
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Artigo
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A novel FKRP-related muscular dystrophy founder mutation in South African Afrikaner patients with a phenotype suggestive of a dystrophinopathy

Mudau, M.M. ; Essop, F. ; Krause, A.

SAMJ: South African Medical Journal, 2017-01, Vol.107 (1), p.80-82 [Periódico revisado por pares]

Health and Medical Publishing Group (HMPG)

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8
A South African family with oculopharyngeal muscular dystrophy: Clinical and molecular genetic characteristics
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Artigo
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A South African family with oculopharyngeal muscular dystrophy: Clinical and molecular genetic characteristics

Schutte, Clara Maria ; Dorfling, Cecelia M ; van Coller, Riaan ; Honey, Engela M ; van Rensburg, Elizabeth Jansen

SAMJ: South African Medical Journal, 2015-07, Vol.105 (7), p.540-543 [Periódico revisado por pares]

South Africa: Health & Medical Publishing Group

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9
Duchenne muscular dystrophy: High-resolution melting curve analysis as an affordable diagnostic mutation scanning tool in a South African cohort
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Artigo
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Duchenne muscular dystrophy: High-resolution melting curve analysis as an affordable diagnostic mutation scanning tool in a South African cohort

Esterhuizen, A I ; Wilmshurst, J M ; Goliath, R G ; Greenberg, L J

SAMJ: South African Medical Journal, 2014-11, Vol.104 (11), p.779-784 [Periódico revisado por pares]

South Africa: Health & Medical Publishing Group

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10
Muscle cell outside and inside: the nascent approach of a clinician
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Artigo
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Muscle cell outside and inside: the nascent approach of a clinician

Fadic, R

Biological research, 2001, Vol.34 (2), p.129-134 [Periódico revisado por pares]

England: Sociedad de Biología de Chile

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