Results 1 to 10 of about 8,131 (149)

Progression and Differentiation of Alveolar Rhabdomyosarcoma Is Regulated by PAX7 Transcription Factor—Significance of Tumor Subclones [PDF]

open access: yesCells, 2021
Rhabdomyosarcoma (RMS), is the most frequent soft tissue tumor in children that originates from disturbances in differentiation process. Mechanisms leading to the development of RMS are still poorly understood. Therefore, by analysis of two RMS RH30 cell
Klaudia Skrzypek   +4 more
doaj   +7 more sources

Expression patterns of FSHD-causing DUX4 and myogenic transcription factors PAX3 and PAX7 are spatially distinct in differentiating human stem cell cultures [PDF]

open access: yesSkeletal Muscle, 2017
Background Facioscapulohumeral muscular dystrophy (FSHD) is most commonly inherited in an autosomal dominant pattern and caused by the abnormal expression of DUX4 in skeletal muscle.
Premi Haynes   +3 more
doaj   +3 more sources

Regulation of the development of tectal neurons and their projections by transcription factors Brn3a and Pax7

open access: yesDevelopmental Biology, 2008
The rostral part of the dorsal midbrain, known as the superior colliculus in mammals or the optic tectum in birds, receives a substantial retinal input and plays a diverse and important role in sensorimotor integration. However, little is known about the development of specific subtypes of neurons in the tectum, particularly those which contribute ...
Eric E Turner, Lely Quina
exaly   +3 more sources

Pathomechanisms and biomarkers in facioscapulohumeral muscular dystrophy: roles of DUX4 and PAX7

open access: yesEMBO Molecular Medicine, 2021
Facioscapulohumeral muscular dystrophy (FSHD) is characterised by progressive skeletal muscle weakness and wasting. FSHD is linked to epigenetic derepression of the subtelomeric D4Z4 macrosatellite at chromosome 4q35.
Christopher R S Banerji, Peter S Zammit
doaj   +2 more sources

Pax7 reporter mouse models: a pocket guide for satellite cell research

open access: yesEuropean Journal of Translational Myology, 2023
Since their discovery, satellite cells have showcased their need as primary contributors to skeletal muscle maintenance and repair. Satellite cells lay dormant, but when needed, activate, differentiate, fuse to fibres and self-renew, that has bestowed ...
Huascar Pedro Ortuste Quiroga   +2 more
doaj   +1 more source

Pax7 is necessary and sufficient for the myogenic specification of CD45+:Sca1+ stem cells from injured muscle. [PDF]

open access: yesPLoS Biology, 2004
CD45(+):Sca1(+) adult stem cells isolated from uninjured muscle do not display any myogenic potential, whereas those isolated from regenerating muscle give rise to myoblasts expressing the paired-box transcription factor Pax7 and the bHLH factors Myf5 ...
Patrick Seale   +3 more
doaj   +1 more source

Satellite cell-specific deletion of Cipc alleviates myopathy in mdx mice

open access: yesCell Reports, 2022
Summary: Skeletal muscle regeneration relies on satellite cells that can proliferate, differentiate, and form new myofibers upon injury. Emerging evidence suggests that misregulation of satellite cell fate and function influences the severity of Duchenne
Jiqing Zheng   +8 more
doaj   +1 more source

Ck2-Dependent Phosphorylation Is Required to Maintain Pax7 Protein Levels in Proliferating Muscle Progenitors. [PDF]

open access: yesPLoS ONE, 2016
Skeletal muscle regeneration and long term maintenance is directly link to the balance between self-renewal and differentiation of resident adult stem cells known as satellite cells.
Natalia González   +6 more
doaj   +1 more source

c-Abl Kinase Is Required for Satellite Cell Function Through Pax7 Regulation

open access: yesFrontiers in Cell and Developmental Biology, 2021
Satellite cells (SCs) are tissue-specific stem cells responsible for adult skeletal muscle regeneration and maintenance. SCs function is critically dependent on two families of transcription factors: the paired box (Pax) involved in specification and ...
Fabián Montecino   +6 more
doaj   +1 more source

Pax7 haploinsufficiency impairs muscle stem cell function in Cre-recombinase mice and underscores the importance of appropriate controls

open access: yesStem Cell Research & Therapy, 2023
Ever since its introduction as a genetic tool, the Cre-lox system has been widely used for molecular genetic studies in vivo in the context of health and disease, as it allows time- and cell-specific gene modifications.
Despoina Mademtzoglou   +3 more
doaj   +1 more source

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