Detalhe da pesquisa
1.
An interactive resource to identify cancer genetic and lineage dependencies targeted by small molecules.
Cell
; 154(5): 1151-1161, 2013 Aug 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-23993102
2.
Long-read sequencing for fast and robust identification of correct genome-edited alleles: PCR-based and Cas9 capture methods.
PLoS Genet
; 20(3): e1011187, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38457464
3.
An animal model for Pierpont syndrome: a mouse bearing the Tbl1xr1Y446C/Y446C mutation.
Hum Mol Genet
; 31(17): 2951-2963, 2022 08 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35416977
4.
Ap2s1 mutation causes hypercalcaemia in mice and impairs interaction between calcium-sensing receptor and adaptor protein-2.
Hum Mol Genet
; 30(10): 880-892, 2021 05 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33729479
5.
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
6.
Inhibition of Pro-apoptotic BAX by a noncanonical interaction mechanism.
Mol Cell
; 57(5): 873-886, 2015 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25684204
7.
Genomic discovery of an evolutionarily programmed modality for small-molecule targeting of an intractable protein surface.
Proc Natl Acad Sci U S A
; 117(29): 17195-17203, 2020 07 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32606248
8.
An Improved Method for Growing Primary Neurons on Electron Microscopy Grids Co-Cultured with Astrocytes.
Int J Mol Sci
; 24(20)2023 Oct 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37894872
9.
Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis.
EMBO J
; 37(11)2018 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29764981
10.
Correction: Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons.
PLoS Biol
; 17(10): e3000520, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31593567
11.
Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons.
PLoS Biol
; 17(9): e3000414, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31479441
12.
Risk, rights and deservedness: Navigating the tensions of Gladue, Fetal Alcohol Spectrum Disorder and settler colonialism in Canadian courts.
Behav Sci Law
; 40(1): 14-30, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34708434
13.
Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy.
N Engl J Med
; 379(11): 1007-1016, 2018 Sep 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30145929
14.
A novel knockout mouse for the small EDRK-rich factor 2 (Serf2) showing developmental and other deficits.
Mamm Genome
; 32(2): 94-103, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33713180
15.
A genetic modifier suggests that endurance exercise exacerbates Huntington's disease.
Hum Mol Genet
; 27(10): 1723-1731, 2018 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29509900
16.
Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy.
Am J Hum Genet
; 98(6): 1249-1255, 2016 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27236917
17.
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
18.
Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration.
Hum Mol Genet
; 25(2): 291-307, 2016 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26604141
19.
Estimating the global prevalence of transthyretin familial amyloid polyneuropathy.
Muscle Nerve
; 57(5): 829-837, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29211930
20.
Analysing the outcome of CRISPR-aided genome editing in embryos: Screening, genotyping and quality control.
Methods
; 121-122: 68-76, 2017 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28363792