Detalhe da pesquisa
1.
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.
PLoS Genet
; 16(12): e1009190, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33370286
2.
INFRAFRONTIER quality principles in systemic phenotyping.
Mamm Genome
; 33(1): 120-122, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34328547
3.
Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration.
PLoS Genet
; 14(5): e1007383, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29746474
4.
FTO demethylase activity is essential for normal bone growth and bone mineralization in mice.
Biochim Biophys Acta Mol Basis Dis
; 1864(3): 843-850, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29203346
5.
Early embryonic lethality in complex I associated p.L104P Nubpl mutant mice.
Orphanet J Rare Dis
; 17(1): 386, 2022 10 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-36280881
6.
Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes.
Dis Model Mech
; 14(10)2021 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34477842
7.
Phenotype of a transient neonatal diabetes point mutation (SUR1-R1183W) in mice.
Wellcome Open Res
; 5: 15, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-34368464
8.
Human and mouse essentiality screens as a resource for disease gene discovery.
Nat Commun
; 11(1): 655, 2020 01 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-32005800
9.
A refinement to the formalin test in mice.
F1000Res
; 8: 891, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31489182
10.
Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.
Commun Biol
; 2: 97, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30854487
11.
Assessing mouse behaviour throughout the light/dark cycle using automated in-cage analysis tools.
J Neurosci Methods
; 300: 37-47, 2018 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28456660
12.
A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways.
Cell Rep
; 25(12): 3315-3328.e6, 2018 12 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-30566859
13.
Identification of genes required for eye development by high-throughput screening of mouse knockouts.
Commun Biol
; 1: 236, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30588515
14.
A scoring system for the evaluation of the mutated Crb1/rd8-derived retinal lesions in C57BL/6N mice.
F1000Res
; 6: 404, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28928942
15.
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.
Nat Commun
; 8(1): 886, 2017 10 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29026089
16.
An in vitro model of traumatic brain injury utilising two-dimensional stretch of organotypic hippocampal slice cultures.
J Neurosci Methods
; 150(2): 192-201, 2006 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-16098599
17.
Temporal development of hippocampal cell death is dependent on tissue strain but not strain rate.
J Biomech
; 39(15): 2810-8, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16289515
18.
Exploring the Lean Phenotype of Glutathione-Depleted Mice: Thiol, Amino Acid and Fatty Acid Profiles.
PLoS One
; 11(10): e0163214, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27788147
19.
Analysis of Individual Mouse Activity in Group Housed Animals of Different Inbred Strains using a Novel Automated Home Cage Analysis System.
Front Behav Neurosci
; 10: 106, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27375446
20.
A SLM2 Feedback Pathway Controls Cortical Network Activity and Mouse Behavior.
Cell Rep
; 17(12): 3269-3280, 2016 12 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-28009295