496 related articles for article (PubMed ID: 34740639)
1. Defining and identifying satellite cell-opathies within muscular dystrophies and myopathies.
Ganassi M; Muntoni F; Zammit PS
Exp Cell Res; 2022 Feb; 411(1):112906. PubMed ID: 34740639
[TBL] [Abstract][Full Text] [Related]
2. Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies.
Ganassi M; Zammit PS
Eur J Transl Myol; 2022 Mar; 32(1):. PubMed ID: 35302338
[TBL] [Abstract][Full Text] [Related]
3. Direct effects of the pathogenic mutation on satellite cell function in muscular dystrophy.
Morgan JE; Zammit PS
Exp Cell Res; 2010 Nov; 316(18):3100-8. PubMed ID: 20546725
[TBL] [Abstract][Full Text] [Related]
4. Biallelic variants in the transcription factor PAX7 are a new genetic cause of myopathy.
Feichtinger RG; Mucha BE; Hengel H; Orfi Z; Makowski C; Dort J; D'Anjou G; Nguyen TTM; Buchert R; Juenger H; Freisinger P; Baumeister S; Schoser B; Ahting U; Keimer R; Nguyen CE; Fabre P; Gauthier J; Miguet M; Lopes F; AlHakeem A; AlHashem A; Tabarki B; Kandaswamy KK; Bauer P; Steinbacher P; Prokisch H; Sturm M; Strom TM; Ellezam B; Mayr JA; Schöls L; Michaud JL; Campeau PM; Haack TB; Dumont NA
Genet Med; 2019 Nov; 21(11):2521-2531. PubMed ID: 31092906
[TBL] [Abstract][Full Text] [Related]
5. ATOH8: a novel marker in human muscle fiber regeneration.
Güttsches AK; Balakrishnan-Renuka A; Kley RA; Tegenthoff M; Brand-Saberi B; Vorgerd M
Histochem Cell Biol; 2015 May; 143(5):443-52. PubMed ID: 25514850
[TBL] [Abstract][Full Text] [Related]
6. Barx2 is expressed in satellite cells and is required for normal muscle growth and regeneration.
Meech R; Gonzalez KN; Barro M; Gromova A; Zhuang L; Hulin JA; Makarenkova HP
Stem Cells; 2012 Feb; 30(2):253-65. PubMed ID: 22076929
[TBL] [Abstract][Full Text] [Related]
7. Muscle satellite cells and impaired late stage regeneration in different murine models for muscular dystrophies.
Ribeiro AF; Souza LS; Almeida CF; Ishiba R; Fernandes SA; Guerrieri DA; Santos ALF; Onofre-Oliveira PCG; Vainzof M
Sci Rep; 2019 Aug; 9(1):11842. PubMed ID: 31413358
[TBL] [Abstract][Full Text] [Related]
8. A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss.
Servián-Morilla E; Takeuchi H; Lee TV; Clarimon J; Mavillard F; Area-Gómez E; Rivas E; Nieto-González JL; Rivero MC; Cabrera-Serrano M; Gómez-Sánchez L; Martínez-López JA; Estrada B; Márquez C; Morgado Y; Suárez-Calvet X; Pita G; Bigot A; Gallardo E; Fernández-Chacón R; Hirano M; Haltiwanger RS; Jafar-Nejad H; Paradas C
EMBO Mol Med; 2016 Nov; 8(11):1289-1309. PubMed ID: 27807076
[TBL] [Abstract][Full Text] [Related]
9. Muscular dystrophies and other genetic myopathies.
Shieh PB
Neurol Clin; 2013 Nov; 31(4):1009-29. PubMed ID: 24176421
[TBL] [Abstract][Full Text] [Related]
10. Targeted massively parallel sequencing and histological assessment of skeletal muscles for the molecular diagnosis of inherited muscle disorders.
Nishikawa A; Mitsuhashi S; Miyata N; Nishino I
J Med Genet; 2017 Feb; 54(2):104-110. PubMed ID: 27600705
[TBL] [Abstract][Full Text] [Related]
11. Does satellite cell dysfunction contribute to disease progression in Emery-Dreifuss muscular dystrophy?
Gnocchi VF; Ellis JA; Zammit PS
Biochem Soc Trans; 2008 Dec; 36(Pt 6):1344-9. PubMed ID: 19021553
[TBL] [Abstract][Full Text] [Related]
12. Satellite cell-specific deletion of Cipc alleviates myopathy in mdx mice.
Zheng J; Lou J; Li Y; Qian P; He W; Hao Y; Xue T; Li Y; Song YH
Cell Rep; 2022 Jun; 39(11):110939. PubMed ID: 35705041
[TBL] [Abstract][Full Text] [Related]
13. G-CSF supports long-term muscle regeneration in mouse models of muscular dystrophy.
Hayashiji N; Yuasa S; Miyagoe-Suzuki Y; Hara M; Ito N; Hashimoto H; Kusumoto D; Seki T; Tohyama S; Kodaira M; Kunitomi A; Kashimura S; Takei M; Saito Y; Okata S; Egashira T; Endo J; Sasaoka T; Takeda S; Fukuda K
Nat Commun; 2015 Apr; 6():6745. PubMed ID: 25865621
[TBL] [Abstract][Full Text] [Related]
14. Megf10 deficiency impairs skeletal muscle stem cell migration and muscle regeneration.
Li C; Vargas-Franco D; Saha M; Davis RM; Manko KA; Draper I; Pacak CA; Kang PB
FEBS Open Bio; 2021 Jan; 11(1):114-123. PubMed ID: 33159715
[TBL] [Abstract][Full Text] [Related]
15. MicroRNA-431 accelerates muscle regeneration and ameliorates muscular dystrophy by targeting Pax7 in mice.
Wu R; Li H; Zhai L; Zou X; Meng J; Zhong R; Li C; Wang H; Zhang Y; Zhu D
Nat Commun; 2015 Jul; 6():7713. PubMed ID: 26151913
[TBL] [Abstract][Full Text] [Related]
16. The molecular regulation of muscle stem cell function.
Rudnicki MA; Le Grand F; McKinnell I; Kuang S
Cold Spring Harb Symp Quant Biol; 2008; 73():323-31. PubMed ID: 19329572
[TBL] [Abstract][Full Text] [Related]
17. Engineered matrices for skeletal muscle satellite cell engraftment and function.
Han WM; Jang YC; García AJ
Matrix Biol; 2017 Jul; 60-61():96-109. PubMed ID: 27269735
[TBL] [Abstract][Full Text] [Related]
18. Congenital myopathies and muscular dystrophies.
Gilbreath HR; Castro D; Iannaccone ST
Neurol Clin; 2014 Aug; 32(3):689-703, viii. PubMed ID: 25037085
[TBL] [Abstract][Full Text] [Related]
19. Severe Neonatal RYR1 Myopathy With Pathological Features of Congenital Muscular Dystrophy.
Helbling DC; Mendoza D; McCarrier J; Vanden Avond MA; Harmelink MM; Barkhaus PE; Basel D; Lawlor MW
J Neuropathol Exp Neurol; 2019 Mar; 78(3):283-287. PubMed ID: 30715496
[TBL] [Abstract][Full Text] [Related]
20. Concise Review: Epigenetic Regulation of Myogenesis in Health and Disease.
Sincennes MC; Brun CE; Rudnicki MA
Stem Cells Transl Med; 2016 Mar; 5(3):282-90. PubMed ID: 26798058
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]