Your search returned 798 results.

Results
	241.	Enhancing muscle membrane repair by gene delivery of MG53 ameliorates muscular dystrophy and heart failure in δ-Sarcoglycan-deficient hamsters. [electronic resource] by He, Bo Tang, Ru-hang Weisleder, Noah Xiao, Bin Yuan, Zhenhua Cai, Chuanxi Zhu, Hua Lin, Peihui Qiao, Chunping Li, Jianbin Mayer, Christina Li, Juan Ma, Jianjie Xiao, Xiao Producer: 20130220 In: Molecular therapy : the journal of the American Society of Gene Therapy vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	242.	The CC genotype of the delta-sarcoglycan gene polymorphism rs13170573 is associated with obstructive sleep apnea in the Chinese population. [electronic resource] by Ye, Rensong Yang, Wenlan Yuan, Yiming Deng, Xingqi Producer: 20150731 In: PloS one vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	243.	Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. [electronic resource] by Moreira, E S Vainzof, M Suzuki, O T Pavanello, R C M Zatz, M Passos-Bueno, M R Producer: 20030310 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	244.	Immunofluorescence study of a muscle biopsy from a 1-year-old patient with Walker-Warburg syndrome. [electronic resource] by Villanova, M Sabatelli, P He, Y Malandrini, A Petrini, S Maraldi, N M Merlini, L Producer: 19990222 In: Acta neuropathologica vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	245.	Complete fatty degeneration of lumbar erector spinae muscles caused by a primary dysferlinopathy. [electronic resource] by Seror, P Krahn, M Laforet, P Leturcq, F Maisonobe, T Producer: 20080502 In: Muscle & nerve vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	246.	Ringo: discordance between the molecular and clinical manifestation in a golden retriever muscular dystrophy dog. [electronic resource] by Zucconi, Eder Valadares, Marcos Costa Vieira, Natássia M Bueno, Carlos R Secco, Mariane Jazedje, Tatiana da Silva, Helga Cristina Almeida Vainzof, Mariz Zatz, Mayana Producer: 20100420 In: Neuromuscular disorders : NMD vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	247.	Overexpression of Myostatin2 in zebrafish reduces the expression of dystrophin associated protein complex (DAPC) which leads to muscle dystrophy. [electronic resource] by Amali, Aseervatham Anusha Lin, Cliff Ji-Fan Chen, Yi-Hsuan Wang, Wei-Lun Gong, Hong-Yi Rekha, Ravikumar Deepa Lu, Jenn-Kan Chen, Thomas T Wu, Jen-Leih Producer: 20081203 In: Journal of biomedical science vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	248.	Novel DYT11 gene mutation in patients without dopaminergic deficit (SWEDD) screened for dystonia. [electronic resource] by Cilia, Roberto Reale, Chiara Castagna, Anna Nasca, Alessia Muzi-Falconi, Marco Barzaghi, Chiara Marzegan, Alberto Granata, Magda Marotta, Giorgio Sacilotto, Giorgio Vallauri, Davide Pezzoli, Gianni Goldwurm, Stefano Garavaglia, Barbara Producer: 20141125 In: Neurology vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	249.	Biochemical and Functional Comparisons of mdx and Sgcg(-/-) Muscular Dystrophy Mouse Models. [electronic resource] by Roberts, Nathan W Holley-Cuthrell, Jenan Gonzalez-Vega, Magdalis Mull, Aaron J Heydemann, Ahlke Producer: 20160310 In: BioMed research international vol. 2015 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	250.	Isolated loss of gamma-sarcoglycan: diagnostic implications in autosomal recessive limb-girdle muscular dystrophies. [electronic resource] by Vorgerd, M Gencik, M Mortier, J Epplen, J T Malin, J P Mortier, W Producer: 20010607 In: Muscle & nerve vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	251.	A novel paradigm for therapeutic basis of advanced heart failure--assessment by gene therapy. [electronic resource] by Kawada, Tomie Masui, Fujiko Kumagai, Hiroyuki Koshimizu, Miki Nakazawa, Mikio Toyo-Oka, Teruhiko Producer: 20051005 In: Pharmacology & therapeutics vol. 107 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	252.	Sarcoglycanopathies and the risk of undetected deletion alleles in diagnosis. [electronic resource] by White, Stefan J Uitte de Willige, Shirley Verbove, Dennis Politano, Luisa Ginjaar, Ieke Breuning, Martijn H den Dunnen, Johan T Producer: 20060913 In: Human mutation vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	253.	Processing and assembly of the dystrophin glycoprotein complex. [electronic resource] by Allikian, Michael J McNally, Elizabeth M Producer: 20070827 In: Traffic (Copenhagen, Denmark) vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	254.	Fusion of bone marrow-derived stem cells with striated muscle may not be sufficient to activate muscle genes. [electronic resource] by Cossu, Giulio Producer: 20050208 In: The Journal of clinical investigation vol. 114 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	255.	Autosomal dominant myoclonus-dystonia and Tourette syndrome in a family without linkage to the SGCE gene. [electronic resource] by Orth, Michael Djarmati, Ana Bäumer, Tobias Winkler, Susan Grünewald, Anne Lohmann-Hedrich, Katja Kabakci, Kemal Hagenah, Johann Klein, Christine Münchau, Alexander Producer: 20080201 In: Movement disorders : official journal of the Movement Disorder Society vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	256.	Cleavage of β-dystroglycan occurs in sarcoglycan-deficient skeletal muscle without MMP-2 and MMP-9. [electronic resource] by Fukai, Yuta Ohsawa, Yutaka Ohtsubo, Hideaki Nishimatsu, Shin-Ichiro Hagiwara, Hiroki Noda, Makoto Sasaoka, Toshikuni Murakami, Tatsufumi Sunada, Yoshihide Producer: 20170925 In: Biochemical and biophysical research communications vol. 492 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	257.	Genetic manipulation of CCN2/CTGF unveils cell-specific ECM-remodeling effects in injured skeletal muscle. [electronic resource] by Petrosino, Jennifer M Leask, Andrew Accornero, Federica Producer: 20190805 In: FASEB journal : official publication of the Federation of American Societies for Experimental Biology vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	258.	Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy. [electronic resource] by Zatz, M Matsumura, K Vainzof, M Passos-Bueno, M R Pavanello, R C Marie, S K Campbell, K P Producer: 19940919 In: Journal of the neurological sciences vol. 123 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	259.	Immunogold localization of adhalin, alpha-dystroglycan and laminin in normal and dystrophic skeletal muscle. [electronic resource] by Cullen, M J Walsh, J Roberds, S L Campbell, K P Producer: 19961216 In: Biochemical Society transactions vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	260.	The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted. [electronic resource] by Grabowski, Monika Zimprich, Alexander Lorenz-Depiereux, Bettina Kalscheuer, Vera Asmus, Friedrich Gasser, Thomas Meitinger, Thomas Strom, Tim M Producer: 20030916 In: European journal of human genetics : EJHG vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 798 results.