| scholarly article | Q13442814 |
| P50 | author | Alessandro Rosa | Q41002249 |
| P2093 | author name string | Riccardo De Santis | |
| Irene Bozzoni | |||
| Cristina Limatola | |||
| Silvia Di Angelantonio | |||
| Francesca Pagani | |||
| Jessica Lenzi | |||
| P2860 | cites work | Skeletal Muscle Is a Primary Target of SOD1G93A-Mediated Toxicity | Q62397259 |
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| State of play in amyotrophic lateral sclerosis genetics | Q26864816 | ||
| Pathways disrupted in human ALS motor neurons identified through genetic correction of mutant SOD1. | Q27303723 | ||
| Efficient and reproducible myogenic differentiation from human iPS cells: prospects for modeling Miyoshi Myopathy in vitro | Q27324593 | ||
| Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis | Q28131805 | ||
| Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons | Q28298056 | ||
| Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons | Q29616199 | ||
| Onset and progression in inherited ALS determined by motor neurons and microglia | Q29619515 | ||
| Overexpression of human wild-type FUS causes progressive motor neuron degeneration in an age- and dose-dependent fashion | Q30532680 | ||
| Epigenetic reprogramming of human embryonic stem cells into skeletal muscle cells and generation of contractile myospheres. | Q30538794 | ||
| Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic mice | Q33832905 | ||
| miR-373 is regulated by TGFβ signaling and promotes mesendoderm differentiation in human Embryonic Stem Cells. | Q33844889 | ||
| Modeling ALS with iPSCs reveals that mutant SOD1 misregulates neurofilament balance in motor neurons | Q34503763 | ||
| Gene transfer demonstrates that muscle is not a primary target for non-cell-autonomous toxicity in familial amyotrophic lateral sclerosis | Q35540066 | ||
| A functionally characterized test set of human induced pluripotent stem cells | Q35588556 | ||
| ALS mutant FUS proteins are recruited into stress granules in induced pluripotent stem cell-derived motoneurons | Q35802889 | ||
| Mutant induced pluripotent stem cell lines recapitulate aspects of TDP-43 proteinopathies and reveal cell-specific vulnerability | Q35889309 | ||
| Mutant SOD1 in cell types other than motor neurons and oligodendrocytes accelerates onset of disease in ALS mice. | Q36677109 | ||
| TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration | Q37733168 | ||
| Understanding ALS: new therapeutic approaches. | Q38065343 | ||
| Human TDP-43 and FUS selectively affect motor neuron maturation and survival in a murine cell model of ALS by non-cell-autonomous mechanisms | Q38853070 | ||
| Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons | Q39007648 | ||
| Human embryonic stem cell-derived motor neurons are sensitive to the toxic effect of glial cells carrying an ALS-causing mutation | Q39910909 | ||
| Fusion-independent expression of functional ACh receptors in mouse mesoangioblast stem cells contacting muscle cells | Q40524044 | ||
| Myogenic differentiation of muscular dystrophy-specific induced pluripotent stem cells for use in drug discovery | Q41956611 | ||
| Derivation of Skeletal Myogenic Precursors from Human Pluripotent Stem Cells Using Conditional Expression of PAX7. | Q42181288 | ||
| A regulatory circuitry comprised of miR-302 and the transcription factors OCT4 and NR2F2 regulates human embryonic stem cell differentiation | Q42578044 | ||
| Transplantation of genetically corrected human iPSC-derived progenitors in mice with limb-girdle muscular dystrophy. | Q42819955 | ||
| Drug screening for ALS using patient-specific induced pluripotent stem cells | Q42820289 | ||
| Wild-Type Nonneuronal Cells Extend Survival of SOD1 Mutant Motor Neurons in ALS Mice | Q46254778 | ||
| Rodent models of amyotrophic lateral sclerosis. | Q51822707 | ||
| Directed Myogenic Differentiation of Human Induced Pluripotent Stem Cells. | Q53506908 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 1 | |
| P921 | main subject | amyotrophic lateral sclerosis | Q206901 |
| skeletal muscle cell | Q66505052 | ||
| P304 | page(s) | 140-147 | |
| P577 | publication date | 2016-06-08 | |
| P1433 | published in | Stem Cell Research | Q15762171 |
| P1476 | title | Differentiation of control and ALS mutant human iPSCs into functional skeletal muscle cells, a tool for the study of neuromuscolar diseases | |
| P478 | volume | 17 |
| Q94487112 | Acute conversion of patient-derived Duchenne muscular dystrophy iPSC into myotubes reveals constitutive and inducible over-activation of TGFβ-dependent pro-fibrotic signaling |
| Q92794366 | C9ORF72-related cellular pathology in skeletal myocytes derived from ALS-patient induced pluripotent stem cells |
| Q47680582 | FUS Mutant Human Motoneurons Display Altered Transcriptome and microRNA Pathways with Implications for ALS Pathogenesis. |
| Q99637145 | Functional skeletal muscle model derived from SOD1-mutant ALS patient iPSCs recapitulates hallmarks of disease progression |
| Q38429049 | In Vitro Innervation as an Experimental Model to Study the Expression and Functions of Acetylcholinesterase and Agrin in Human Skeletal Muscle |
| Q41230060 | Mechanically patterned neuromuscular junctions-in-a-dish have improved functional maturation |
| Q52585184 | Messenger RNA Delivery for Tissue Engineering and Regenerative Medicine Applications. |
| Q38430493 | Modelling FUS Mislocalisation in an In Vitro Model of Innervated Human Muscle. |
| Q64238282 | Quantification of human neuromuscular function through optogenetics |
| Q92747686 | iPSCs: A powerful tool for skeletal muscle tissue engineering |
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