-
1
-
-
84954377568
-
Molecular neuropathology of the synapse in sheep with CLN5 Batten disease
-
PID: 26664787
-
Amorim IS et al (2015) Molecular neuropathology of the synapse in sheep with CLN5 Batten disease. Brain Behav 5(11):e00401. doi:10.1002/brb3.401
-
(2015)
Brain Behav
, vol.5
, Issue.11
-
-
Amorim, I.S.1
-
2
-
-
15844426692
-
Atm-deficient mice: a paradigm of ataxia telangiectasia
-
COI: 1:CAS:528:DyaK28XktlGnsbc%3D, PID: 8689683
-
Barlow C et al (1996) Atm-deficient mice: a paradigm of ataxia telangiectasia. Cell 86(1):159–171
-
(1996)
Cell
, vol.86
, Issue.1
, pp. 159-171
-
-
Barlow, C.1
-
3
-
-
0024954987
-
MPTP-induced Parkinson-like disease in sheep: clinical and pathologic findings
-
COI: 1:CAS:528:DyaK3MXlslSmsg%3D%3D, PID: 2637935
-
Beale AM et al (1989) “MPTP-induced Parkinson-like disease in sheep: clinical and pathologic findings”. J Environ Pathol Toxicol Oncol 9(5–6):417–428
-
(1989)
J Environ Pathol Toxicol Oncol
, vol.9
, Issue.5-6
, pp. 417-428
-
-
Beale, A.M.1
-
4
-
-
84937758654
-
Paving the path to HIV neurotherapy: Predicting SIV CNS disease
-
COI: 1:CAS:528:DC%2BC2MXls1Wqu7k%3D, PID: 25818747
-
Beck SE et al (2015) Paving the path to HIV neurotherapy: Predicting SIV CNS disease. Eur J Pharmacol 759:303–312
-
(2015)
Eur J Pharmacol
, vol.759
, pp. 303-312
-
-
Beck, S.E.1
-
5
-
-
84949032534
-
A novel porcine model of ataxia telangiectasia reproduces neurological features and motor deficits of human disease
-
COI: 1:CAS:528:DC%2BC28XntVWjt70%3D, PID: 26374845
-
Beraldi R et al (2015) A novel porcine model of ataxia telangiectasia reproduces neurological features and motor deficits of human disease. Hum Mol Genet 24(22):6473–6484
-
(2015)
Hum Mol Genet
, vol.24
, Issue.22
, pp. 6473-6484
-
-
Beraldi, R.1
-
6
-
-
2942597781
-
Regional and cellular neuropathology in the palmitoyl protein thioesterase-1 null mutant mouse model of infantile neuronal ceroid lipofuscinosis
-
COI: 1:CAS:528:DC%2BD2cXkvVegsbc%3D, PID: 15193291
-
Bible E et al (2004) Regional and cellular neuropathology in the palmitoyl protein thioesterase-1 null mutant mouse model of infantile neuronal ceroid lipofuscinosis. Neurobiol Dis 16(2):346–359
-
(2004)
Neurobiol Dis
, vol.16
, Issue.2
, pp. 346-359
-
-
Bible, E.1
-
7
-
-
84941254141
-
Increasing disparities between resource inputs and outcomes, as measured by certain health deliverables, in biomedical research
-
COI: 1:CAS:528:DC%2BC2MXhtlCgs7vJ, PID: 26283360
-
Bowen A, Casadevall A (2015) Increasing disparities between resource inputs and outcomes, as measured by certain health deliverables, in biomedical research. Proc Natl Acad Sci USA 112(36):11335–11340
-
(2015)
Proc Natl Acad Sci USA
, vol.112
, Issue.36
, pp. 11335-11340
-
-
Bowen, A.1
Casadevall, A.2
-
8
-
-
84939781588
-
Of mice and monkeys: can animal models be utilized to study neurological consequences of pediatric HIV-1 infection?
-
COI: 1:CAS:528:DC%2BC2MXptlOgs7g%3D, PID: 26034832
-
Carryl H, et al (2015). Of mice and monkeys: can animal models be utilized to study neurological consequences of pediatric HIV-1 infection? ACS Chem Neurosci 6(8):1276–1289
-
(2015)
ACS Chem Neurosci
, vol.6
, Issue.8
, pp. 1276-1289
-
-
Carryl, H.1
-
9
-
-
84897382112
-
Target cell availability, rather than breast milk factors, dictates mother-to-infant transmission of SIV in sooty mangabeys and rhesus macaques
-
PID: 24604066
-
Chahroudi A et al (2014) Target cell availability, rather than breast milk factors, dictates mother-to-infant transmission of SIV in sooty mangabeys and rhesus macaques. PLoS Pathog 10(3):e1003958
-
(2014)
PLoS Pathog
, vol.10
, Issue.3
-
-
Chahroudi, A.1
-
10
-
-
84929222865
-
Transgenic animal models for study of the pathogenesis of Huntington’s disease and therapy
-
Chang R et al (2015) Transgenic animal models for study of the pathogenesis of Huntington’s disease and therapy. Drug Des Dev Ther 9:2179–2188
-
(2015)
Drug Des Dev Ther
, vol.9
, pp. 2179-2188
-
-
Chang, R.1
-
11
-
-
84992561435
-
Ten-year follow-up of two cohorts with an increased risk of variant CJD: donors to individuals who later developed variant CJD and other recipients of these at-risk donors
-
COI: 1:CAS:528:DC%2BC28XhvVymtr%2FM, PID: 27432362
-
Checchi M et al (2016) Ten-year follow-up of two cohorts with an increased risk of variant CJD: donors to individuals who later developed variant CJD and other recipients of these at-risk donors. Vox Sang 111(4):325–332
-
(2016)
Vox Sang
, vol.111
, Issue.4
, pp. 325-332
-
-
Checchi, M.1
-
12
-
-
84908463972
-
Genetics of Alzheimer’s disease
-
COI: 1:CAS:528:DC%2BC28XhsFGjsLrL, PID: 25311924
-
Chouraki V, Seshadri S (2014) Genetics of Alzheimer’s disease. Adv Genet 87:245–294
-
(2014)
Adv Genet
, vol.87
, pp. 245-294
-
-
Chouraki, V.1
Seshadri, S.2
-
13
-
-
77953666105
-
Genetic animal models of Parkinson’s disease
-
COI: 1:CAS:528:DC%2BC3cXnvFaksb4%3D, PID: 20547124
-
Dawson TM et al (2010) Genetic animal models of Parkinson’s disease. Neuron 66(5):646–661
-
(2010)
Neuron
, vol.66
, Issue.5
, pp. 646-661
-
-
Dawson, T.M.1
-
14
-
-
84959378242
-
Animal and human mucosal tissue models to study HIV biomedical interventions: can we predict success?
-
PID: 26530077
-
Dezzutti CS (2015) Animal and human mucosal tissue models to study HIV biomedical interventions: can we predict success? J Int AIDS Soc 18:20301
-
(2015)
J Int AIDS Soc
, vol.18
, pp. 20301
-
-
Dezzutti, C.S.1
-
15
-
-
84912051121
-
Pig models of neurodegenerative disorders: Utilization in cell replacement-based preclinical safety and efficacy studies
-
PID: 24610493
-
Dolezalova D et al (2014) Pig models of neurodegenerative disorders: Utilization in cell replacement-based preclinical safety and efficacy studies. J Comp Neurol 522(12):2784–2801
-
(2014)
J Comp Neurol
, vol.522
, Issue.12
, pp. 2784-2801
-
-
Dolezalova, D.1
-
16
-
-
84923771867
-
A large animal model of spinal muscular atrophy and correction of phenotype
-
COI: 1:CAS:528:DC%2BC2MXjtlSltLs%3D, PID: 25516063
-
Duque SI et al (2015) A large animal model of spinal muscular atrophy and correction of phenotype. Ann Neurol 77(3):399–414
-
(2015)
Ann Neurol
, vol.77
, Issue.3
, pp. 399-414
-
-
Duque, S.I.1
-
17
-
-
84921842338
-
HIV-associated neurocognitive disorders (HAND)
-
PID: 25739180
-
Elbirt D et al (2015) HIV-associated neurocognitive disorders (HAND). Isr Med Assoc J 17(1):54–59
-
(2015)
Isr Med Assoc J
, vol.17
, Issue.1
, pp. 54-59
-
-
Elbirt, D.1
-
18
-
-
36048948687
-
Nonhuman primate models of Parkinson’s disease
-
COI: 1:CAS:528:DC%2BD2sXhtVSns73E, PID: 17712221
-
Emborg ME (2007) Nonhuman primate models of Parkinson’s disease. ILAR J 48(4):339–355
-
(2007)
ILAR J
, vol.48
, Issue.4
, pp. 339-355
-
-
Emborg, M.E.1
-
19
-
-
0032129737
-
Transmissible spongiform encephalopathies: transmission, mechanism of disease, and persistence
-
COI: 1:STN:280:DyaK1M7osFanug%3D%3D, PID: 10066515
-
Foster J, Hunter N (1998) Transmissible spongiform encephalopathies: transmission, mechanism of disease, and persistence. Curr Opin Microbiol 1(4):442–447
-
(1998)
Curr Opin Microbiol
, vol.1
, Issue.4
, pp. 442-447
-
-
Foster, J.1
Hunter, N.2
-
20
-
-
0028918337
-
Alterations in dopamine uptake sites and D1 and D2 receptors in cats symptomatic for and recovered from experimental parkinsonism
-
COI: 1:CAS:528:DyaK2MXjt1OntLk%3D, PID: 7709343
-
Frohna PA et al (1995) Alterations in dopamine uptake sites and D1 and D2 receptors in cats symptomatic for and recovered from experimental parkinsonism. Synapse 19(1):46–55
-
(1995)
Synapse
, vol.19
, Issue.1
, pp. 46-55
-
-
Frohna, P.A.1
-
21
-
-
84978877889
-
Understanding the molecular consequences of inherited muscular dystrophies: advancements through proteomic experimentation
-
COI: 1:CAS:528:DC%2BC28XhtFahsLrJ, PID: 27329572
-
Fuller HR et al (2016) Understanding the molecular consequences of inherited muscular dystrophies: advancements through proteomic experimentation. Expert Rev Proteomics 13(7):659–671
-
(2016)
Expert Rev Proteomics
, vol.13
, Issue.7
, pp. 659-671
-
-
Fuller, H.R.1
-
22
-
-
84928176699
-
The significance of meaning: why do over 90% of behavioral neuroscience results fail to translate to humans, and what can we do to fix it?
-
COI: 1:CAS:528:DC%2BC28Xht1Wqt7zI, PID: 25541546
-
Garner JP (2014) The significance of meaning: why do over 90% of behavioral neuroscience results fail to translate to humans, and what can we do to fix it?” ILAR J 55(3):438–456
-
(2014)
ILAR J
, vol.55
, Issue.3
, pp. 438-456
-
-
Garner, J.P.1
-
23
-
-
84966440677
-
Moving towards effective therapeutic strategies for Neuronal Ceroid Lipofuscinosis
-
PID: 27083890
-
Geraets RD, et al (2016) Moving towards effective therapeutic strategies for Neuronal Ceroid Lipofuscinosis. Orphanet J Rare Dis 11:40
-
(2016)
Orphanet J Rare Dis
, vol.11
, pp. 40
-
-
Geraets, R.D.1
-
24
-
-
84873355257
-
Systematic reviews of animal models: methodology versus epistemology
-
PID: 23372426
-
Greek R, Menache A (2013) Systematic reviews of animal models: methodology versus epistemology. Int J Med Sci 10(3):206–221
-
(2013)
Int J Med Sci
, vol.10
, Issue.3
, pp. 206-221
-
-
Greek, R.1
Menache, A.2
-
25
-
-
84986573166
-
Advantages of nonhuman primates as preclinical models for evaluating stem cell-based therapies for Parkinson’s disease
-
COI: 1:CAS:528:DC%2BC28XhsV2rt7rN, PID: 27622596
-
Grow DA et al (2016) Advantages of nonhuman primates as preclinical models for evaluating stem cell-based therapies for Parkinson’s disease. Stem Cell Res 17(2):352–366
-
(2016)
Stem Cell Res
, vol.17
, Issue.2
, pp. 352-366
-
-
Grow, D.A.1
-
26
-
-
84943379725
-
Impaired APP activity and altered Tau splicing in embryonic stem cell-derived astrocytes obtained from an APPsw transgenic minipig
-
COI: 1:CAS:528:DC%2BC28XhsVWgtrjM, PID: 26398935
-
Hall VJ et al (2015) Impaired APP activity and altered Tau splicing in embryonic stem cell-derived astrocytes obtained from an APPsw transgenic minipig. Dis Model Mech 8(10):1265–1278
-
(2015)
Dis Model Mech
, vol.8
, Issue.10
, pp. 1265-1278
-
-
Hall, V.J.1
-
27
-
-
84857126830
-
Nonhuman primates of Alzheimer-like cerebral proteopathy
-
COI: 1:CAS:528:DC%2BC38XlvVSqt78%3D, PID: 22288403
-
Heuer E et al (2012) Nonhuman primates of Alzheimer-like cerebral proteopathy. Curr Pharm Des 18(8):1159–1169
-
(2012)
Curr Pharm Des
, vol.18
, Issue.8
, pp. 1159-1169
-
-
Heuer, E.1
-
28
-
-
84951299418
-
Genetically modified pig models for neurodegenerative disorders
-
COI: 1:CAS:528:DC%2BC28XitVCgtg%3D%3D, PID: 26446984
-
Holm IE et al (2016) Genetically modified pig models for neurodegenerative disorders. J Pathol 238(2):267–287
-
(2016)
J Pathol
, vol.238
, Issue.2
, pp. 267-287
-
-
Holm, I.E.1
-
29
-
-
58149378573
-
Prion diseases are efficiently transmitted by blood transfusion in sheep
-
COI: 1:CAS:528:DC%2BD1cXhsVCltbjJ, PID: 18647958
-
Houston F et al (2008)“Prion diseases are efficiently transmitted by blood transfusion in sheep. Blood 112(12):4739–4745
-
(2008)
Blood
, vol.112
, Issue.12
, pp. 4739-4745
-
-
Houston, F.1
-
30
-
-
84907939186
-
Mind the gap: models in multiple species needed for therapeutic development in Huntington’s disease
-
PID: 25155258
-
Howland DS, Munoz-Sanjuan I (2014) Mind the gap: models in multiple species needed for therapeutic development in Huntington’s disease. Mov Disord 29(11):1397–1403
-
(2014)
Mov Disord
, vol.29
, Issue.11
, pp. 1397-1403
-
-
Howland, D.S.1
Munoz-Sanjuan, I.2
-
31
-
-
0036843096
-
Transmission of prion diseases by blood transfusion
-
COI: 1:CAS:528:DC%2BD38XosF2jtrY%3D, PID: 12388826
-
Hunter N et al (2002) Transmission of prion diseases by blood transfusion. J Gen Virol 83(Pt 11):2897–2905
-
(2002)
J Gen Virol
, vol.83
, Issue.11
, pp. 2897-2905
-
-
Hunter, N.1
-
32
-
-
85016017024
-
Restoration of SMN in Schwann cells reverses myelination defects and improves neuromuscular function in spinal muscular atrophy
-
COI: 1:CAS:528:DC%2BC2sXhvVClsro%3D, PID: 27170316
-
Hunter G et al (2016) Restoration of SMN in Schwann cells reverses myelination defects and improves neuromuscular function in spinal muscular atrophy. Hum Mol Genet 25(13):2853–2861
-
(2016)
Hum Mol Genet
, vol.25
, Issue.13
, pp. 2853-2861
-
-
Hunter, G.1
-
33
-
-
84883350837
-
Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases
-
COI: 1:CAS:528:DC%2BC3sXhsVKksLrP, PID: 23959875
-
Jackson WS et al (2013) Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases. Proc Natl Acad Sci USA 110(36):14759–14764
-
(2013)
Proc Natl Acad Sci USA
, vol.110
, Issue.36
, pp. 14759-14764
-
-
Jackson, W.S.1
-
34
-
-
84958035386
-
Evaluation of Models of Parkinson’s Disease
-
PID: 26834536
-
Jagmag SA et al (2015) Evaluation of Models of Parkinson’s Disease. Front Neurosci 9:503
-
(2015)
Front Neurosci
, vol.9
, pp. 503
-
-
Jagmag, S.A.1
-
35
-
-
84991717315
-
Putting the “Biology” Back into “Neurobiology”: The Strength of Diversity in Animal Model Systems for Neuroscience Research
-
PID: 27597819
-
Keifer J, Summers CH (2016) Putting the “Biology” Back into “Neurobiology”: The Strength of Diversity in Animal Model Systems for Neuroscience Research. Front Syst Neurosci 10:69
-
(2016)
Front Syst Neurosci
, vol.10
, pp. 69
-
-
Keifer, J.1
Summers, C.H.2
-
36
-
-
84863100006
-
Influence of species differences on the neuropathology of transgenic Huntington’s disease animal models
-
COI: 1:CAS:528:DC%2BC38Xht1Kktr7I
-
Li XJ, Li S (2012) Influence of species differences on the neuropathology of transgenic Huntington’s disease animal models. J Genet Genom 39(6):239–245
-
(2012)
J Genet Genom
, vol.39
, Issue.6
, pp. 239-245
-
-
Li, X.J.1
Li, S.2
-
37
-
-
84942576224
-
A review of the human vs. porcine female genital tract and associated immune system in the perspective of using minipigs as a model of human genital Chlamydia infection
-
PID: 26411309
-
Lorenzen E et al (2015) A review of the human vs. porcine female genital tract and associated immune system in the perspective of using minipigs as a model of human genital Chlamydia infection. Vet Res 46:116
-
(2015)
Vet Res
, vol.46
, pp. 116
-
-
Lorenzen, E.1
-
38
-
-
84929145979
-
Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy
-
COI: 1:CAS:528:DC%2BC2MXlt1Kjur4%3D, PID: 25740330
-
McGreevy JW et al (2015) “Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy”. Dis Model Mech 8(3):195–213
-
(2015)
Dis Model Mech
, vol.8
, Issue.3
, pp. 195-213
-
-
McGreevy, J.W.1
-
39
-
-
0033031162
-
MPTP-induced Parkinsonism in minipigs: A behavioral, biochemical, and histological study
-
COI: 1:CAS:528:DyaK1MXitVSrtLk%3D, PID: 10192277
-
Mikkelsen M et al (1999) MPTP-induced Parkinsonism in minipigs: A behavioral, biochemical, and histological study. Neurotoxicol Teratol 21(2):169–175
-
(1999)
Neurotoxicol Teratol
, vol.21
, Issue.2
, pp. 169-175
-
-
Mikkelsen, M.1
-
40
-
-
79551643723
-
Executive decision-making in the domestic sheep
-
COI: 1:CAS:528:DC%2BC3MXhvFaitLk%3D, PID: 21305061
-
Morton AJ, Avanzo L (2011) Executive decision-making in the domestic sheep”. PLoS ONE 6(1):e15752
-
(2011)
PLoS ONE
, vol.6
, Issue.1
-
-
Morton, A.J.1
Avanzo, L.2
-
41
-
-
84902329646
-
Early and progressive circadian abnormalities in Huntington’s disease sheep are unmasked by social environment
-
Morton AJ et al (2013) Early and progressive circadian abnormalities in Huntington’s disease sheep are unmasked by social environment. Hum Mol Genet 23(13):3375–3383
-
(2013)
Hum Mol Genet
, vol.23
, Issue.13
, pp. 3375-3383
-
-
Morton, A.J.1
-
42
-
-
84878765869
-
The wobbler mouse, an ALS animal model
-
COI: 1:CAS:528:DC%2BC3sXot1ektbo%3D
-
Moser JM et al (2013) The wobbler mouse, an ALS animal model. Mol Genet Genom 288(5–6):207–229
-
(2013)
Mol Genet Genom
, vol.288
, Issue.5-6
, pp. 207-229
-
-
Moser, J.M.1
-
43
-
-
84885547156
-
Label-free proteomics identifies Calreticulin and GRP75/Mortalin as peripherally accessible protein biomarkers for spinal muscular atrophy
-
PID: 24134804
-
Mutsaers CA et al (2013) Label-free proteomics identifies Calreticulin and GRP75/Mortalin as peripherally accessible protein biomarkers for spinal muscular atrophy. Genome Med 5(10):95
-
(2013)
Genome Med
, vol.5
, Issue.10
, pp. 95
-
-
Mutsaers, C.A.1
-
44
-
-
84940793201
-
Recent studies of ovine neuronal ceroid lipofuscinoses from BARN, the Batten Animal Research Network
-
COI: 1:CAS:528:DC%2BC2MXhtVWqs73N, PID: 26073432
-
Palmer DN et al (2015) Recent studies of ovine neuronal ceroid lipofuscinoses from BARN, the Batten Animal Research Network. Biochim Biophys Acta 1852(10 Pt B):2279–2286
-
(2015)
Biochim Biophys Acta
, vol.1852
, pp. 2279-2286
-
-
Palmer, D.N.1
-
45
-
-
84975764350
-
Mechanisms of muscle denervation in aging: insights from a mouse model of amyotrophic lateral sclerosis
-
Park, K. H. (2015). Mechanisms of muscle denervation in aging: insights from a mouse model of amyotrophic lateral sclerosis. Aging Dis 6(5):380–389
-
(2015)
Aging Dis
, vol.6
, Issue.5
, pp. 380-389
-
-
Park, K.H.1
-
46
-
-
84860996856
-
Simian retroviruses in African apes
-
COI: 1:STN:280:DC%2BC38rmt1OrtQ%3D%3D, PID: 22515409
-
Peeters M, Delaporte E (2012) Simian retroviruses in African apes. Clin Microbiol Infect 18(6):514–520
-
(2012)
Clin Microbiol Infect
, vol.18
, Issue.6
, pp. 514-520
-
-
Peeters, M.1
Delaporte, E.2
-
47
-
-
84949228570
-
Rodent models of amyotrophic lateral sclerosis
-
Philips T, Rothstein JD (2015) Rodent models of amyotrophic lateral sclerosis. Curr Protoc Pharmacol 69:5.67.1–5.67.21. doi:10.1002/0471141755.ph0567s69
-
(2015)
Curr Protoc Pharmacol
, vol.69
, pp. 5.67.1-5.67.21
-
-
Philips, T.1
Rothstein, J.D.2
-
48
-
-
84940570535
-
Large animal models of rare genetic disorders: sheep as phenotypically relevant models of human genetic disease
-
PID: 26329332
-
Pinnapureddy AR et al (2015) Large animal models of rare genetic disorders: sheep as phenotypically relevant models of human genetic disease. Orphanet J Rare Dis 10:107
-
(2015)
Orphanet J Rare Dis
, vol.10
, pp. 107
-
-
Pinnapureddy, A.R.1
-
49
-
-
27744565604
-
Δex7/8 knock-in mouse model of Batten disease
-
COI: 1:CAS:528:DC%2BD2MXht1egsbzL, PID: 16006136
-
Δex7/8 knock-in mouse model of Batten disease. Neurobiol Dis 20(3):823–836
-
(2005)
Neurobiol Dis
, vol.20
, Issue.3
, pp. 823-836
-
-
Pontikis, C.C.1
-
50
-
-
84884537922
-
Choosing an animal model for the study of Huntington’s disease
-
COI: 1:CAS:528:DC%2BC3sXhsVynurvO, PID: 24052178
-
Pouladi MA et al (2013) Choosing an animal model for the study of Huntington’s disease. Nat Rev Neurosci 14(10):708–721
-
(2013)
Nat Rev Neurosci
, vol.14
, Issue.10
, pp. 708-721
-
-
Pouladi, M.A.1
-
51
-
-
0032491494
-
Genetic neurodegenerative diseases: the human illness and transgenic models
-
COI: 1:CAS:528:DyaK1cXntlaksr0%3D, PID: 9804539
-
Price DL et al (1998) Genetic neurodegenerative diseases: the human illness and transgenic models. Science 282(5391):1079–1083
-
(1998)
Science
, vol.282
, Issue.5391
, pp. 1079-1083
-
-
Price, D.L.1
-
53
-
-
36049044225
-
Animal models of Huntington’s disease
-
COI: 1:CAS:528:DC%2BD2sXhtVSns73F, PID: 17712222
-
Ramaswamy S et al (2007) Animal models of Huntington’s disease. ILAR J 48(4):356–373
-
(2007)
ILAR J
, vol.48
, Issue.4
, pp. 356-373
-
-
Ramaswamy, S.1
-
54
-
-
84899647552
-
Single App knock-in mouse models of Alzheimer’s disease
-
COI: 1:CAS:528:DC%2BC2cXmtlWjsbs%3D, PID: 24728269
-
Saito T et al (2014) Single App knock-in mouse models of Alzheimer’s disease. Nat Neurosci 17(5):661–663
-
(2014)
Nat Neurosci
, vol.17
, Issue.5
, pp. 661-663
-
-
Saito, T.1
-
55
-
-
84923195380
-
Unraveling the swine genome: implications for human health
-
COI: 1:CAS:528:DC%2BC2MXlvVWmtLc%3D, PID: 25689318
-
Schook LB et al (2015) Unraveling the swine genome: implications for human health. Annu Rev Anim Biosci 3:219–244
-
(2015)
Annu Rev Anim Biosci
, vol.3
, pp. 219-244
-
-
Schook, L.B.1
-
56
-
-
84861730516
-
Disease phenotype in sheep after infection with cloned murine scrapie strains
-
COI: 1:CAS:528:DC%2BC38XhtFSru77P, PID: 22421207
-
Siso S et al (2012) Disease phenotype in sheep after infection with cloned murine scrapie strains. Prion 6(2):174–183
-
(2012)
Prion
, vol.6
, Issue.2
, pp. 174-183
-
-
Siso, S.1
-
57
-
-
79953093064
-
Drugs and clinical trials in neurodegenerative diseases
-
PID: 21430339
-
Stanzione P, Tropepi D (2011) Drugs and clinical trials in neurodegenerative diseases. Ann Ist Super Sanita 47(1):49–54
-
(2011)
Ann Ist Super Sanita
, vol.47
, Issue.1
, pp. 49-54
-
-
Stanzione, P.1
Tropepi, D.2
-
58
-
-
84863471166
-
Does Alzheimer’s disease exist in all primates? Alzheimer pathology in non-human primates and its pathophysiological implications
-
COI: 1:STN:280:DC%2BC38zptlaitA%3D%3D, PID: 22197064
-
Toledano A et al (2012) Does Alzheimer’s disease exist in all primates? Alzheimer pathology in non-human primates and its pathophysiological implications. Neurologia 27(6):354–369
-
(2012)
Neurologia
, vol.27
, Issue.6
, pp. 354-369
-
-
Toledano, A.1
-
59
-
-
84872115824
-
Time to diagnosis in young-onset dementia as compared with late-onset dementia
-
PID: 22640548
-
van Vliet D et al (2013) Time to diagnosis in young-onset dementia as compared with late-onset dementia. Psychol Med 43(2):423–432
-
(2013)
Psychol Med
, vol.43
, Issue.2
, pp. 423-432
-
-
van Vliet, D.1
-
60
-
-
84957592496
-
One-step generation of triple gene-targeted pigs using CRISPR/Cas9 system
-
COI: 1:CAS:528:DC%2BC28Xitlymurs%3D, PID: 26857844
-
Wang X, et al (2016) One-step generation of triple gene-targeted pigs using CRISPR/Cas9 system. Sci Rep 6:20620
-
(2016)
Sci Rep
, vol.6
, pp. 20620
-
-
Wang, X.1
-
61
-
-
84883734645
-
Large animal models for Batten disease: a review
-
PID: 24014507
-
Weber K, Pearce DA (2013) Large animal models for Batten disease: a review. J Child Neurol 28(9):1123–1127
-
(2013)
J Child Neurol
, vol.28
, Issue.9
, pp. 1123-1127
-
-
Weber, K.1
Pearce, D.A.2
-
62
-
-
84951310011
-
Engineering large animal models of human disease
-
PID: 26414877
-
Whitelaw CB et al (2016) Engineering large animal models of human disease. J Pathol 238(2):247–256
-
(2016)
J Pathol
, vol.238
, Issue.2
, pp. 247-256
-
-
Whitelaw, C.B.1
-
63
-
-
84866175104
-
Combining comparative proteomics and molecular genetics uncovers regulators of synaptic and axonal stability and degeneration in vivo
-
COI: 1:CAS:528:DC%2BC38XhtlSjsr3J, PID: 22952455
-
Wishart TM et al (2012) Combining comparative proteomics and molecular genetics uncovers regulators of synaptic and axonal stability and degeneration in vivo. PLoS Genet 8(8):e1002936
-
(2012)
PLoS Genet
, vol.8
, Issue.8
-
-
Wishart, T.M.1
-
64
-
-
84897548490
-
Dysregulation of ubiquitin homeostasis and beta-catenin signaling promote spinal muscular atrophy
-
COI: 1:CAS:528:DC%2BC2cXmtVGgtbk%3D, PID: 24590288
-
Wishart TM et al (2014) Dysregulation of ubiquitin homeostasis and beta-catenin signaling promote spinal muscular atrophy. J Clin Invest 124(4):1821–1834
-
(2014)
J Clin Invest
, vol.124
, Issue.4
, pp. 1821-1834
-
-
Wishart, T.M.1
-
65
-
-
77957732707
-
Expression of Huntington’s disease protein results in apoptotic neurons in the brains of cloned transgenic pigs
-
COI: 1:CAS:528:DC%2BC3cXht1eqtLzF, PID: 20660116
-
Yang D et al (2010) Expression of Huntington’s disease protein results in apoptotic neurons in the brains of cloned transgenic pigs. Hum Mol Genet 19(20):3983–3994
-
(2010)
Hum Mol Genet
, vol.19
, Issue.20
, pp. 3983-3994
-
-
Yang, D.1
-
66
-
-
84898033899
-
Species-dependent neuropathology in transgenic SOD1 pigs
-
COI: 1:CAS:528:DC%2BC2cXjvV2hsro%3D, PID: 24577199
-
Yang H et al (2014) Species-dependent neuropathology in transgenic SOD1 pigs. Cell Res 24(4):464–481
-
(2014)
Cell Res
, vol.24
, Issue.4
, pp. 464-481
-
-
Yang, H.1
-
67
-
-
84947936455
-
Overexpression of α-synuclein simultaneously increases glutamate NMDA receptor phosphorylation and reduces glucocerebrosidase activity
-
COI: 1:CAS:528:DC%2BC2MXhvFantbvO, PID: 26610904
-
Yang J et al (2016) Overexpression of α-synuclein simultaneously increases glutamate NMDA receptor phosphorylation and reduces glucocerebrosidase activity. Neurosci Lett 611:51–58
-
(2016)
Neurosci Lett
, vol.611
, pp. 51-58
-
-
Yang, J.1
-
68
-
-
0031855367
-
Prions: properties, occurrence, modes of transmission and relevance for blood transfusion and blood derivatives
-
COI: 1:CAS:528:DyaK1cXkvFCisr4%3D, PID: 9704435
-
Yap PL et al (1998) Prions: properties, occurrence, modes of transmission and relevance for blood transfusion and blood derivatives. Vox Sang 74(Suppl 2):131–134
-
(1998)
Vox Sang
, vol.74
, pp. 131-134
-
-
Yap, P.L.1
-
69
-
-
85006448388
-
Modeling Parkinson’s disease in the common marmoset (Callithrix jacchus): overview of models, methods, and animal care
-
PID: 26755918
-
Yun JW et al (2015) Modeling Parkinson’s disease in the common marmoset (Callithrix jacchus): overview of models, methods, and animal care. Lab Anim Res 31(4):155–165
-
(2015)
Lab Anim Res
, vol.31
, Issue.4
, pp. 155-165
-
-
Yun, J.W.1
-
70
-
-
84924249888
-
More than a FAD: the in vivo effects of disease-linked presenilin-1 mutations
-
COI: 1:CAS:528:DC%2BC2MXktFehtrY%3D, PID: 25741717
-
Zahs KR, Ashe KH (2015) More than a FAD: the in vivo effects of disease-linked presenilin-1 mutations. Neuron 85(5):893–895
-
(2015)
Neuron
, vol.85
, Issue.5
, pp. 893-895
-
-
Zahs, K.R.1
Ashe, K.H.2
|