Bioprocessing technology of muscle stem cells: Implications for cultured meat
Muscle stem cells (MuSCs) are essential for the growth, maintenance, and repair of skeletal
muscle. In the emerging area of cultured meat, meat products are manufactured with MuSCs …
muscle. In the emerging area of cultured meat, meat products are manufactured with MuSCs …
The hallmarks of myotonic dystrophy type 1 muscle dysfunction
LL Ozimski, M Sabater‐Arcis, A Bargiela… - Biological …, 2021 - Wiley Online Library
ABSTRACT Myotonic dystrophy type 1 (DM1) is the most prevalent form of muscular
dystrophy in adults and yet there are currently no treatment options. Although this disease …
dystrophy in adults and yet there are currently no treatment options. Although this disease …
Immortalized bovine satellite cells for cultured meat applications
AJ Stout, MJ Arnett, K Chai, T Guo, L Liao… - ACS synthetic …, 2023 - ACS Publications
For cultured meat to succeed at scale, muscle cells from food-relevant species must be
expanded in vitro in a rapid and reliable manner to produce millions of metric tons of …
expanded in vitro in a rapid and reliable manner to produce millions of metric tons of …
[HTML][HTML] Peptide-conjugated oligonucleotides evoke long-lasting myotonic dystrophy correction in patient-derived cells and mice
AF Klein, MA Varela, L Arandel… - The Journal of …, 2019 - Am Soc Clin Investig
Antisense oligonucleotides (ASOs) targeting pathologic RNAs have shown promising
therapeutic corrections for many genetic diseases including myotonic dystrophy (DM1) …
therapeutic corrections for many genetic diseases including myotonic dystrophy (DM1) …
Precise small-molecule cleavage of an r (CUG) repeat expansion in a myotonic dystrophy mouse model
AJ Angelbello, SG Rzuczek… - Proceedings of the …, 2019 - National Acad Sciences
Myotonic dystrophy type 1 (DM1) is an incurable neuromuscular disorder caused by an
expanded CTG repeat that is transcribed into r (CUG) exp. The RNA repeat expansion …
expanded CTG repeat that is transcribed into r (CUG) exp. The RNA repeat expansion …
Transcriptome-Wide Studies of RNA-Targeted Small Molecules Provide a Simple and Selective r(CUG)exp Degrader in Myotonic Dystrophy
QMR Gibaut, JA Bush, Y Tong, JT Baisden… - ACS Central …, 2023 - ACS Publications
Myotonic dystrophy type 1 (DM1) is caused by a highly structured RNA repeat expansion, r
(CUG) exp, harbored in the 3′ untranslated region (3′ UTR) of dystrophia myotonica …
(CUG) exp, harbored in the 3′ untranslated region (3′ UTR) of dystrophia myotonica …
Study of an RNA-focused DNA-encoded library informs design of a degrader of ar (CUG) repeat expansion
QMR Gibaut, Y Akahori, JA Bush… - Journal of the …, 2022 - ACS Publications
A solid-phase DNA-encoded library (DEL) was studied for binding the RNA repeat
expansion r (CUG) exp, the causative agent of the most common form of adult-onset …
expansion r (CUG) exp, the causative agent of the most common form of adult-onset …
[HTML][HTML] RNA-binding proteins in the post-transcriptional control of skeletal muscle development, regeneration and disease
DL Shi, R Grifone - Frontiers in Cell and Developmental Biology, 2021 - frontiersin.org
Embryonic myogenesis is a temporally and spatially regulated process that generates
skeletal muscle of the trunk and limbs. During this process, mononucleated myoblasts …
skeletal muscle of the trunk and limbs. During this process, mononucleated myoblasts …
Reversal of RNA toxicity in myotonic dystrophy via a decoy RNA-binding protein with high affinity for expanded CUG repeats
L Arandel, M Matloka, AF Klein, F Rau… - Nature Biomedical …, 2022 - nature.com
Abstract Myotonic dystrophy type 1 (DM1) is an RNA-dominant disease whose pathogenesis
stems from the functional loss of muscleblind-like RNA-binding proteins (RBPs), which …
stems from the functional loss of muscleblind-like RNA-binding proteins (RBPs), which …
[HTML][HTML] Molecular therapies for myotonic dystrophy type 1: from small drugs to gene editing
M Izzo, J Battistini, C Provenzano, F Martelli… - International journal of …, 2022 - mdpi.com
Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy affecting many
different body tissues, predominantly skeletal and cardiac muscles and the central nervous …
different body tissues, predominantly skeletal and cardiac muscles and the central nervous …