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Summary Expression Phenotypes Gene Literature (36) GO Terms (0) Nucleotides (24) Proteins (7) Interactants (268) Wiki

Papers associated with dmd.2

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2 paper(s) referencing morpholinos

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Microfluidic encapsulation of Xenopus laevis cell-free extracts using hydrogel photolithography., Geisterfer ZM, Oakey J, Gatlin JC., STAR Protoc. December 18, 2020; 1 (3): 100221.        

S-nitrosylation of connexin43 hemichannels elicits cardiac stress-induced arrhythmias in Duchenne muscular dystrophy mice., Lillo MA, Himelman E, Shirokova N, Xie LH, Fraidenraich D, Contreras JE., JCI Insight. January 1, 2019; 4 (24):

The interplay between voluntary food intake, dietary carbohydrate-lipid ratio and nutrient metabolism in an amphibian, (Xenopus laevis)., Brenes-Soto A, Dierenfeld ES, Janssens GPJ., PLoS One. January 1, 2018; 13 (12): e0208445.        

Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy., Freyermuth F, Rau F, Kokunai Y, Linke T, Sellier C, Nakamori M, Kino Y, Arandel L, Jollet A, Thibault C, Philipps M, Vicaire S, Jost B, Udd B, Day JW, Duboc D, Wahbi K, Matsumura T, Fujimura H, Mochizuki H, Deryckere F, Kimura T, Nukina N, Ishiura S, Lacroix V, Campan-Fournier A, Navratil V, Chautard E, Auboeuf D, Horie M, Imoto K, Lee KY, Swanson MS, de Munain AL, Inada S, Itoh H, Nakazawa K, Ashihara T, Wang E, Zimmer T, Furling D, Takahashi MP, Charlet-Berguerand N., Nat Commun. April 11, 2016; 7 11067.              

Gene expression profiles in Rana pirica tadpoles following exposure to a predation threat., Mori T, Yanagisawa Y, Kitani Y, Sugiyama M, Kishida O, Nishimura K., BMC Genomics. April 2, 2015; 16 258.                

Stoichiometry and specific assembly of Best ion channels., Bharill S, Fu Z, Palty R, Isacoff EY., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6491-6.

M-cadherin-mediated intercellular interactions activate satellite cell division., Marti M, Montserrat N, Pardo C, Mulero L, Miquel-Serra L, Rodrigues AM, Andrés Vaquero J, Kuebler B, Morera C, Barrero MJ, Izpisua Belmonte JC., J Cell Sci. November 15, 2013; 126 (Pt 22): 5116-31.    

Ordered disorder of the astrocytic dystrophin-associated protein complex in the norm and pathology., Na I, Redmon D, Kopa M, Qin Y, Xue B, Uversky VN., PLoS One. January 1, 2013; 8 (8): e73476.                      

Skeletal muscle regeneration in Xenopus tadpoles and zebrafish larvae., Rodrigues AM, Christen B, Martí M, Izpisúa Belmonte JC., BMC Dev Biol. December 17, 2012; 12 9.                  

Muscular dystrophy begins early in embryonic development deriving from stem cell loss and disrupted skeletal muscle formation., Merrick D, Stadler LK, Larner D, Smith J., Dis Model Mech. July 1, 2009; 2 (7-8): 374-88.

Loss of REEP4 causes paralysis of the Xenopus embryo., Argasinska J, Rana AA, Gilchrist MJ, Lachani K, Young A, Smith JC., Int J Dev Biol. January 1, 2009; 53 (1): 37-43.          

Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides., Rana AA, Collart C, Gilchrist MJ, Smith JC., PLoS Genet. November 17, 2006; 2 (11): e193.                                    

HGF induction of postsynaptic specializations at the neuromuscular junction., Madhavan R, Peng HB., J Neurobiol. February 5, 2006; 66 (2): 134-47.

Formation of multiple complexes between beta-dystroglycan and dystrophin family products., Royuela M, Chazalette D, Hugon G, Paniagua R, Guerlavais V, Fehrentz JA, Martinez J, Labbe JP, Rivier F, Mornet D., J Muscle Res Cell Motil. January 1, 2003; 24 (7): 387-97.

Molecular cloning and expression analysis of dystroglycan during Xenopus laevis embryogenesis., Lunardi A, Dente L., Mech Dev. December 1, 2002; 119 Suppl 1 S49-54.      

Chimeric snRNA molecules carrying antisense sequences against the splice junctions of exon 51 of the dystrophin pre-mRNA induce exon skipping and restoration of a dystrophin synthesis in Delta 48-50 DMD cells., De Angelis FG, Sthandier O, Berarducci B, Toso S, Galluzzi G, Ricci E, Cossu G, Bozzoni I., Proc Natl Acad Sci U S A. July 9, 2002; 99 (14): 9456-61.

The 3''-untranslated region of the dystrophin gene - conservation and consequences of loss., Greener MJ, Sewry CA, Muntoni F, Roberts RG., Eur J Hum Genet. July 1, 2002; 10 (7): 413-20.

Changes in mechanosensitive channel gating following mechanical stimulation in skeletal muscle myotubes from the mdx mouse., Franco-Obregón A, Lansman JB., J Physiol. March 1, 2002; 539 (Pt 2): 391-407.

Dystroglycan overexpression in vivo alters acetylcholine receptor aggregation at the neuromuscular junction., Heathcote RD, Ekman JM, Campbell KP, Godfrey EW., Dev Biol. November 15, 2000; 227 (2): 595-605.              

In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide., Bartlett RJ, Stockinger S, Denis MM, Bartlett WT, Inverardi L, Le TT, thi Man N, Morris GE, Bogan DJ, Metcalf-Bogan J, Kornegay JN., Nat Biotechnol. June 1, 2000; 18 (6): 615-22.

The relationship between perlecan and dystroglycan and its implication in the formation of the neuromuscular junction., Peng HB, Ali AA, Daggett DF, Rauvala H, Hassell JR, Smalheiser NR., Cell Adhes Commun. September 1, 1998; 5 (6): 475-89.

In vitro genetic analysis of the RNA binding site of vigilin, a multi-KH-domain protein., Kanamori H, Dodson RE, Shapiro DJ., Mol Cell Biol. July 1, 1998; 18 (7): 3991-4003.

Dystrophins in vertebrates and invertebrates., Roberts RG, Bobrow M., Hum Mol Genet. April 1, 1998; 7 (4): 589-95.

Dystrophin is replaced by utrophin in frog heart; implications for muscular dystrophy., Morris GE., Neuromuscul Disord. December 1, 1997; 7 (8): 493-8.

Laminin-induced clustering of dystroglycan on embryonic muscle cells: comparison with agrin-induced clustering., Cohen MW, Jacobson C, Yurchenco PD, Morris GE, Carbonetto S., J Cell Biol. March 10, 1997; 136 (5): 1047-58.                                              

Smoothelin, a novel cytoskeletal protein specific for smooth muscle cells., van der Loop FT, Schaart G, Timmer ED, Ramaekers FC, van Eys GJ., J Cell Biol. July 1, 1996; 134 (2): 401-11.    

Apo-dystrophins (Dp140 and Dp71) and dystrophin splicing isoforms in developing brain., Morris GE, Simmons C, Nguyen TM., Biochem Biophys Res Commun. October 4, 1995; 215 (1): 361-7.

Toward the therapeutic editing of mutated RNA sequences., Woolf TM, Chase JM, Stinchcomb DT., Proc Natl Acad Sci U S A. August 29, 1995; 92 (18): 8298-302.

Expression of the 43 kDa dystrophin-associated glycoprotein in human neuromuscular disease., Helliwell TR, Nguyen TM, Morris GE., Neuromuscul Disord. March 1, 1994; 4 (2): 101-13.

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin., Ervasti JM, Campbell KP., J Cell Biol. August 1, 1993; 122 (4): 809-23.

Use of epitope libraries to identify exon-specific monoclonal antibodies for characterization of altered dystrophins in muscular dystrophy., Nguyen TM, Morris GE., Am J Hum Genet. June 1, 1993; 52 (6): 1057-66.

Monoclonal antibodies for dystrophin analysis. Epitope mapping and improved binding to SDS-treated muscle sections., Nguyen TM, Ginjaar IB, van Ommen GJ, Morris GE., Biochem J. December 1, 1992; 288 ( Pt 2) 663-8.

Induction of dystrophin localization in cultured Xenopus muscle cells by latex beads., Peng HB, Chen Q., J Cell Sci. October 1, 1992; 103 ( Pt 2) 551-63.                

Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in proliferating brain cell lines., Nguyen TM, Ellis JM, Love DR, Davies KE, Gatter KC, Dickson G, Morris GE., J Cell Biol. December 1, 1991; 115 (6): 1695-700.

Localization of dystrophin relative to acetylcholine receptor domains in electric tissue and adult and cultured skeletal muscle., Sealock R, Butler MH, Kramarcy NR, Gao KX, Murnane AA, Douville K, Froehner SC., J Cell Biol. June 1, 1991; 113 (5): 1133-44.

Dystrophin as a focal adhesion protein. Collocalization with talin and the Mr 48,000 sarcolemmal protein in cultured Xenopus muscle., Kramarcy NR, Sealock R., FEBS Lett. November 12, 1990; 274 (1-2): 171-4.

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