Detalhe da pesquisa
1.
Heteroplasmy of mouse mtDNA is genetically unstable and results in altered behavior and cognition.
Cell
; 151(2): 333-343, 2012 Oct 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-23063123
2.
Cystatin F attenuates neuroinflammation and demyelination following murine coronavirus infection of the central nervous system.
J Neuroinflammation
; 21(1): 157, 2024 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38879499
3.
Sex-specific associations between AD genotype and the microbiome of human amyloid beta knock-in (hAß-KI) mice.
Alzheimers Dement
; 2024 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38572865
4.
Genetic diversity promotes resilience in a mouse model of Alzheimer's disease.
Alzheimers Dement
; 20(4): 2794-2816, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38426371
5.
The Abca7V1613M variant reduces Aß generation, plaque load, and neuronal damage.
Alzheimers Dement
; 2024 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38506634
6.
BIN1K358R suppresses glial response to plaques in mouse model of Alzheimer's disease.
Alzheimers Dement
; 20(4): 2922-2942, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38460121
7.
Dual roles of myocardial mitochondrial AKT on diabetic cardiomyopathy and whole body metabolism.
Cardiovasc Diabetol
; 22(1): 294, 2023 10 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37891673
8.
Tubular mitochondrial AKT1 is activated during ischemia reperfusion injury and has a critical role in predisposition to chronic kidney disease.
Kidney Int
; 99(4): 870-884, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33316281
9.
Miles to go (mtgo) encodes FNDC3 proteins that interact with the chaperonin subunit CCT3 and are required for NMJ branching and growth in Drosophila.
Dev Biol
; 445(1): 37-53, 2019 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30539716
10.
Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction.
Biochim Biophys Acta
; 1857(8): 1203-1212, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27048932
11.
Cell-specific deletion of C1qa identifies microglia as the dominant source of C1q in mouse brain.
J Neuroinflammation
; 14(1): 48, 2017 03 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28264694
12.
BMP signaling is required for cell cleavage in preimplantation-mouse embryos.
Dev Biol
; 397(1): 45-55, 2015 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25446538
13.
Mouse mtDNA mutant model of Leber hereditary optic neuropathy.
Proc Natl Acad Sci U S A
; 109(49): 20065-70, 2012 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-23129651
14.
APOE Christchurch enhances a disease-associated microglial response to plaque but suppresses response to tau pathology.
bioRxiv
; 2024 Jun 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38895362
15.
Single cell spatial transcriptomics reveals distinct patterns of dysregulation in non-neuronal and neuronal cells induced by the Trem2R47H Alzheimer's risk gene mutation.
Res Sq
; 2023 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38106071
16.
A Trem2R47H mouse model without cryptic splicing drives age- and disease-dependent tissue damage and synaptic loss in response to plaques.
Mol Neurodegener
; 18(1): 12, 2023 02 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36803190
17.
Comparison of male chimeric mice generated from microinjection of JM8.N4 embryonic stem cells into C57BL/6J and C57BL/6NTac blastocysts.
Transgenic Res
; 21(6): 1149-58, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22422470
18.
Interneuron Dysfunction in a New Mouse Model of SCN1A GEFS.
eNeuro
; 8(2)2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33658306
19.
Systematic phenotyping and characterization of the 5xFAD mouse model of Alzheimer's disease.
Sci Data
; 8(1): 270, 2021 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34654824
20.
Systematic Phenotyping and Characterization of the 3xTg-AD Mouse Model of Alzheimer's Disease.
Front Neurosci
; 15: 785276, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35140584