Genetically modified pig models for neurodegenerative disorders

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Genetically modified pig models for neurodegenerative disorders is …
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scholarly articleQ13442814

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P356DOI10.1002/PATH.4654
P698PubMed publication ID26446984

P50authorYonglun LuoQ68703561
P2093author name stringAage Kristian Olsen Alstrup
Ida E Holm
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Aclarubicin treatment restores SMN levels to cells derived from type I spinal muscular atrophy patientsQ28209134
Use of the CRISPR/Cas9 system to produce genetically engineered pigs from in vitro-derived oocytes and embryosQ28245450
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Inactivation of the mouse Huntington's disease gene homolog HdhQ28509662
Amino-terminal fragments of mutant huntingtin show selective accumulation in striatal neurons and synaptic toxicityQ28513938
Inactivation of Hdh in the brain and testis results in progressive neurodegeneration and sterility in miceQ28594828
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Expression of mutant huntingtin in mouse brain astrocytes causes age-dependent neurological symptomsQ30492587
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Animal models of neurodegenerative diseases.Q45293452
ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.Q46135324
Neuroimaging of the vesicular acetylcholine transporter by a novel 4-[18F]fluoro-benzoyl derivative of 7-hydroxy-6-(4-phenyl-piperidin-1-yl)-octahydro-benzo[1,4]oxazines.Q46139745
Synthesis and cerebral uptake of 1-(1-[(11)C]methyl-1H-pyrrol-2-yl)-2-phenyl-2-(1-pyrrolidinyl)ethanone, a novel tracer for positron emission tomography studies of monoamine oxidase type A.Q46728257
Effect of monoamine oxidase inhibition on amphetamine-evoked changes in dopamine receptor availability in the living pig: a dual tracer PET study with [11C]harmine and [11C]racloprideQ46950279
Inverse correlation between SMN1 and SMN2 copy numbers: evidence for gene conversion from SMN2 to SMN1.Q47996236
Hippocampus of the domestic pig: a stereological study of subdivisional volumes and neuron numbersQ48184432
The use of pigs in neuroscience: modeling brain disordersQ48195971
Serotonergic modulation of receptor occupancy in rats treated with L-DOPA after unilateral 6-OHDA lesioningQ48210282
A PET study of effects of chronic 3,4-methylenedioxymethamphetamine (MDMA, "ecstasy") on serotonin markers in Göttingen minipig brainQ48212891
MPTP-induced Parkinsonism in minipigs: A behavioral, biochemical, and histological studyQ48245796
Imaging imidazoline-I2 binding sites in porcine brain using 11C-BU99008.Q48261312
Statistical mapping of effects of middle cerebral artery occlusion (MCAO) on blood flow and oxygen consumption in porcine brainQ48356823
In vivo estimation of cerebral blood flow, oxygen consumption and glucose metabolism in the pig by [15O]water injection, [15O]oxygen inhalation and dual injections of [18F]fluorodeoxyglucose.Q48518620
Tau proteins of Alzheimer paired helical filaments: abnormal phosphorylation of all six brain isoformsQ48571996
MR-based statistical atlas of the Göttingen minipig brainQ48719637
MRI protocol for in vivo visualization of the Göttingen minipig brain improves targeting in experimental functional neurosurgeryQ48772422
Histochemical demonstration of zinc in the hippocampal region of the domestic pig: II. Subiculum and hippocampusQ48788634
Ataxia telangiectasia: new neurons and ATM.Q48865724
Object recognition as a measure of memory in 1-2 years old transgenic minipigs carrying the APPsw mutation for Alzheimer's disease.Q50803794
Foreword: neurodegenerative diseases: challenges and opportunities.Q51563574
Generation of CRISPR/Cas9-mediated gene-targeted pigs via somatic cell nuclear transfer.Q52423182
Targeted disruption of Ataxia-telangiectasia mutated gene in miniature pigs by somatic cell nuclear transfer.Q52653447
An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondriaQ54965159
Molecular analysis of spinal muscular atrophy and modification of the phenotype by SMN2.Q55035683
Juvenile Huntington's disease: does a dosage-effect pathogenic mechanism differ from the classical adult disease?Q36308082
Efficient TALEN-mediated gene knockout in livestockQ36378266
Current approaches to the treatment of Parkinson's diseaseQ36876438
Disruption of the CFTR gene produces a model of cystic fibrosis in newborn pigsQ36944556
Genetic manipulations of mutant huntingtin in mice: new insights into Huntington's disease pathogenesisQ37165188
Effects of anesthesia and species on the uptake or binding of radioligands in vivo in the Göttingen minipigQ37191041
Rodent genetic models of Huntington diseaseQ37220633
Derivation of induced pluripotent stem cells from pig somatic cellsQ37233718
Generation of induced pluripotent stem cell lines from Tibetan miniature pig.Q37285271
PiB Fails to Map Amyloid Deposits in Cerebral Cortex of Aged Dogs with Canine Cognitive DysfunctionQ37417915
ALS-associated mutation FUS-R521C causes DNA damage and RNA splicing defectsQ37609639
Perspectives and diagnostic considerations in spinal muscular atrophyQ37670613
Species-dependent neuropathology in transgenic SOD1 pigsQ37684257
Genetic animal models of Parkinson's diseaseQ37765030
Cognitive testing of pigs (Sus scrofa) in translational biobehavioral researchQ37765677
The association between infectious burden and Parkinson's disease: A case-control study.Q37840384
TAL effectors: customizable proteins for DNA targetingQ37940951
Recent rodent models for Alzheimer's disease: clinical implications and basic researchQ37956513
Genetically modified pigs for biomedical research.Q37997627
Therapeutic interventions targeting Beta amyloid pathogenesis in an aging dog modelQ38015346
Three repeat isoforms of tau inhibit assembly of four repeat tau filamentsQ33593147
Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's diseaseQ33682442
Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick?Q33785933
An ovine transgenic Huntington's disease modelQ33815561
Phylogenetic diversity of the expression of the microtubule-associated protein tau: implications for neurodegenerative disordersQ33861704
Focal loss of the glutamate transporter EAAT2 in a transgenic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS).Q34010341
Antisense correction of SMN2 splicing in the CNS rescues necrosis in a type III SMA mouse modelQ34030144
Comparison of gene expression and genome-wide DNA methylation profiling between phenotypically normal cloned pigs and conventionally bred controlsQ34055767
Juvenile onset Huntington's disease--clinical and research perspectives.Q34091006
A good practice guide to the administration of substances and removal of blood, including routes and volumesQ34141695
Determination of Odor Detection Threshold in the Gottingen MinipigQ34145250
Expression of Huntington's disease protein results in apoptotic neurons in the brains of cloned transgenic pigsQ34163091
A humanized Smn gene containing the SMN2 nucleotide alteration in exon 7 mimics SMN2 splicing and the SMA disease phenotypeQ34184793
Proposed Motor Scoring System in a Porcine Model of Parkinson's Disease induced by Chronic Subcutaneous Injection of MPTP.Q34241599
A polymorphic DNA marker genetically linked to Huntington's diseaseQ34255139
Neuropathology of amyotrophic lateral sclerosis with extra-motor system degeneration: characteristics and differences in the molecular pathology between ALS with dementia and Guamanian ALS.Q34315764
Efficient bi-allelic gene knockout and site-specific knock-in mediated by TALENs in pigsQ34452907
Genetically engineered mouse models of neurodegenerative diseasesQ34708236
Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosisQ34718757
Transgenic mouse models of neurodegenerative disease: opportunities for therapeutic developmentQ34778122
Hemizygous minipigs produced by random gene insertion and handmade cloning express the Alzheimer's disease-causing dominant mutation APPswQ34934330
The ΔF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigsQ35056880
Long-term accumulation of amyloid-beta, beta-secretase, presenilin-1, and caspase-3 in damaged axons following brain traumaQ35103035
Compensatory mechanisms in genetic models of neurodegeneration: are the mice better than humans?Q35153576
Mutations in DJ-1 are rare in familial Parkinson diseaseQ35231079
Clinical utility of cerebrospinal fluid biomarkers in the diagnosis of early Alzheimer's diseaseQ35284971
Huntington's disease in Chinese: a hypothesis of its originQ35351538
A guide to neurotoxic animal models of Parkinson's diseaseQ35603488
Traumatic brain injury in later life increases risk for Parkinson diseaseQ35661022
Disruption of the Survival Motor Neuron (SMN) gene in pigs using ssDNA.Q35683524
Genetically engineered pig models for human diseasesQ35700104
Splicing variants of porcine synphilin-1Q35745078
In vivo interrogation of gene function in the mammalian brain using CRISPR-Cas9Q35820051
Changing metabolic signatures of amino acids and lipids during the prediabetic period in a pig model with impaired incretin function and reduced β-cell massQ36109246
P433issue2
P921main subjectneurodegenerationQ1755122
P304page(s)267-287
P577publication date2015-10-08
P1433published inJournal of PathologyQ400296
P1476titleGenetically modified pig models for neurodegenerative disorders
P478volume238

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