Cell-based technologies for Huntington's disease

scientific article

Cell-based technologies for Huntington's disease is …
instance of (P31):
scholarly articleQ13442814
review articleQ7318358

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P356DOI10.1590/S1980-5764-2016DN1004006
P932PMC publication ID5619267
P698PubMed publication ID29213471

P2093author name stringIrina Kerkis
Celine Pompeia
Cristiane Valverde Wenceslau
Mônica Santoro Haddad
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Susceptibility-weighted imaging changes suggesting brain iron accumulation in Huntington's disease: an epiphenomenon which causes diagnostic difficultyQ45297881
Technical factors that influence neural transplant safety in Huntington's disease.Q45299664
Survival, neuronal differentiation, and fiber outgrowth of propagated human neural precursor grafts in an animal model of Huntington's disease.Q45300235
Mesenchymal stem cell transplantation and DMEM administration in a 3NP rat model of Huntington's disease: morphological and behavioral outcomesQ45300522
Transplanted adult neural progenitor cells survive, differentiate and reduce motor function impairment in a rodent model of Huntington's disease.Q45300810
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Age-dependent vulnerability of the striatum to the mitochondrial toxin 3-nitropropionic acid.Q48365871
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The anti-apoptotic gene survivin contributes to teratoma formation by human embryonic stem cells.Q51791870
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Malignant tumor formation after transplantation of short-term cultured bone marrow mesenchymal stem cells in experimental myocardial infarction and diabetic neuropathy.Q35030040
Adult stem cells for tissue repair - a new therapeutic concept?Q35194623
Stem cell technology for neurodegenerative diseases.Q35224202
Transplanted fetal striatum in Huntington's disease: phenotypic development and lack of pathologyQ35579484
Review: mesenchymal stem cells: cell-based reconstructive therapy in orthopedicsQ36249852
Astrocytes generated from patient induced pluripotent stem cells recapitulate features of Huntington's disease patient cellsQ36423519
Equine-Induced Pluripotent Stem Cells Retain Lineage Commitment Toward Myogenic and Chondrogenic FatesQ36480691
Role of brain-derived neurotrophic factor in Huntington's diseaseQ36767260
Striatal progenitors derived from human ES cells mature into DARPP32 neurons in vitro and in quinolinic acid-lesioned rats.Q36954944
Mesenchymal stem cells: revisiting history, concepts, and assays.Q37036368
The psychopathology of Huntington's diseaseQ37079566
A patient with Huntington's disease and long-surviving fetal neural transplants that developed mass lesionsQ37178480
Progress in restorative neurosurgery: human fetal striatal transplantation in Huntington's disease. Review.Q37971315
A systematic review of the intergenerational aspects and the diverse genetic profiles of Huntington's diseaseQ38126446
Choosing an animal model for the study of Huntington's diseaseQ38139868
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Neuronal properties, in vivo effects, and pathology of a Huntington's disease patient-derived induced pluripotent stem cellsQ38462208
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Feeder-free derivation of induced pluripotent stem cells from human immature dental pulp stem cellsQ39764925
Slowed progression in models of Huntington disease by adipose stem cell transplantationQ39770706
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Human embryonic stem cell-derived neural precursor transplants attenuate apomorphine-induced rotational behavior in rats with unilateral quinolinic acid lesionsQ40099462
Proactive transplantation of human neural stem cells prevents degeneration of striatal neurons in a rat model of Huntington diseaseQ40543499
Neural stem cells constitutively secrete neurotrophic factors and promote extensive host axonal growth after spinal cord injuryQ40643190
Embryonic stem cell-derived glial precursors: a source of myelinating transplantsQ40938819
Human neural stem cell transplants improve motor function in a rat model of Huntington's diseaseQ42463574
fMRI biomarker of early neuronal dysfunction in presymptomatic Huntington's Disease.Q42471124
Comparison of transplant efficiency between spontaneously derived and noggin-primed human embryonic stem cell neural precursors in the quinolinic acid rat model of Huntington's diseaseQ43115809
Mitochondrial calcium, oxidative stress and apoptosis in a neurodegenerative disease model induced by 3-nitropropionic acidQ44792354
Mesenchymal stem cells that produce neurotrophic factors reduce ischemic damage in the rat middle cerebral artery occlusion modelQ45178238
Neuroprotective effects and magnetic resonance imaging of mesenchymal stem cells labeled with SPION in a rat model of Huntington's diseaseQ45289124
Development of human striatal anlagen after transplantation in a patient with Huntington's diseaseQ45289953
Histological findings on fetal striatal grafts in a Huntington's disease patient early after transplantationQ45292873
Early striatal dendrite deficits followed by neuron loss with advanced age in the absence of anterograde cortical brain-derived neurotrophic factor.Q45293425
Neuropsychological functioning following fetal striatal transplantation in Huntington's chorea: three case presentationsQ45294365
Safety of intrastriatal neurotransplantation for Huntington's disease patientsQ45295583
P433issue4
P921main subjectHuntington's diseaseQ190564
P304page(s)287-295
P577publication date2016-10-01
P1433published inDementia & neuropsychologiaQ27725091
P1476titleCell-based technologies for Huntington's disease
P478volume10

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cites work (P2860)
Q64077907Application of PMCA to screen for prion infection in a human cell line used to produce biological therapeutics
Q90662510Recent Overview of the Use of iPSCs Huntington's Disease Modeling and Therapy

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