Detalhe da pesquisa
1.
Genome-wide screening reveals the genetic basis of mammalian embryonic eye development.
BMC Biol
; 21(1): 22, 2023 02 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36737727
2.
Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.
Mamm Genome
; 34(2): 180-199, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37294348
3.
Corrigendum: High-throughput discovery of novel developmental phenotypes.
Nature
; 551(7680): 398, 2017 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-29144450
4.
High-throughput discovery of novel developmental phenotypes.
Nature
; 537(7621): 508-514, 2016 09 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-27626380
5.
Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay.
Genet Med
; 23(4): 661-668, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33420346
6.
Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.
Pain
; 163(6): 1139-1157, 2022 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35552317
7.
Supplier-origin mouse microbiomes significantly influence locomotor and anxiety-related behavior, body morphology, and metabolism.
Commun Biol
; 4(1): 716, 2021 06 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34112927
8.
A metabolome atlas of the aging mouse brain.
Nat Commun
; 12(1): 6021, 2021 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34654818
9.
Experiments from unfinished Registered Reports in the Reproducibility Project: Cancer Biology.
Elife
; 102021 12 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34874009
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.
A Population Study of Common Ocular Abnormalities in C57BL/6N rd8 Mice.
Invest Ophthalmol Vis Sci
; 59(6): 2252-2261, 2018 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29847629
12.
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
13.
Identification of genetic elements in metabolism by high-throughput mouse phenotyping.
Nat Commun
; 9(1): 288, 2018 01 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-29348434
14.
Arap1 Deficiency Causes Photoreceptor Degeneration in Mice.
Invest Ophthalmol Vis Sci
; 58(3): 1709-1718, 2017 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28324111
15.
Prevalence of sexual dimorphism in mammalian phenotypic traits.
Nat Commun
; 8: 15475, 2017 06 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-28650954
16.
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
17.
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.
Nat Genet
; 49(8): 1231-1238, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28650483