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Papers associated with
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Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates.
, Baxi AB,
Nemes P
,
Moody SA
.,
iScience. September 15, 2023; 26 (9): 107665.
Microfluidic encapsulation of Xenopus laevis cell-free extracts using hydrogel photolithography.
, Geisterfer ZM, Oakey J,
Gatlin JC
.,
STAR Protoc. October 31, 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. December 19, 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. December 7, 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.
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. January 1, 2009; 2 (7-8): 374-88.
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.
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.
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.
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