Detalhe da pesquisa
1.
The Regulatory Factor ZFHX3 Modifies Circadian Function in SCN via an AT Motif-Driven Axis.
Cell
; 162(3): 607-21, 2015 Jul 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-26232227
2.
Cleft palate and minor metabolic disturbances in a mouse global Arl15 gene knockout.
FASEB J
; 37(11): e23211, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37773757
3.
Genic constraint against nonsynonymous variation across the mouse genome.
BMC Genomics
; 24(1): 562, 2023 Sep 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37736706
4.
Mouse genomic and cellular annotations.
Mamm Genome
; 33(1): 19-30, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35124726
5.
Modelling the genetic aetiology of complex disease: human-mouse conservation of noncoding features and disease-associated loci.
Biol Lett
; 18(3): 20210630, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35317627
6.
Sizing, stabilising, and cloning repeat-expansions for gene targeting constructs.
Methods
; 191: 15-22, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32721467
7.
A holistic view of mouse enhancer architectures reveals analogous pleiotropic effects and correlation with human disease.
BMC Genomics
; 21(1): 754, 2020 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33138777
8.
A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways.
PLoS Genet
; 13(8): e1006969, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28806779
9.
Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants.
BMC Biol
; 16(1): 70, 2018 06 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-29925374
10.
Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutations.
PLoS Genet
; 9(1): e1003219, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23382690
11.
Current strategies for mutation detection in phenotype-driven screens utilising next generation sequencing.
Mamm Genome
; 26(9-10): 486-500, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26449678
12.
High throughput sequencing approaches to mutation discovery in the mouse.
Mamm Genome
; 23(9-10): 499-513, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22991087
13.
Making sense of the linear genome, gene function and TADs.
Epigenetics Chromatin
; 15(1): 4, 2022 01 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35090532
14.
Genomic Mutation Identification in Mice Using Illumina Sequencing and Linux-Based Computational Methods.
Curr Protoc Mouse Biol
; 9(3): e64, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31532925
15.
Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis.
J Bone Miner Res
; 34(7): 1324-1335, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30830987
16.
An N-Ethyl-N-Nitrosourea (ENU)-Induced Tyr265Stop Mutation of the DNA Polymerase Accessory Subunit Gamma 2 (Polg2) Is Associated With Renal Calcification in Mice.
J Bone Miner Res
; 34(3): 497-507, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30395686
17.
Clarin-2 is essential for hearing by maintaining stereocilia integrity and function.
EMBO Mol Med
; 11(9): e10288, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31448880
18.
Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function.
Dis Model Mech
; 11(12)2018 12 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-30478029
19.
An N-Ethyl-N-Nitrosourea (ENU) Mutagenized Mouse Model for Autosomal Dominant Nonsyndromic Kyphoscoliosis Due to Vertebral Fusion.
JBMR Plus
; 2(3): 154-163, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30283900
20.
Author Correction: Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition.
Nat Genet
; 50(9): 1342, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30087441