Detalhe da pesquisa
1.
Early embryonic mutations reveal dynamics of somatic and germ cell lineages in mice.
Genome Res
; 32(5): 945-955, 2022 05.
Artigo
Inglês
| MEDLINE | ID: mdl-35534232
2.
Mitochondrial Electron Transport Chain Complex II Dysfunction Causes Premature Aging of Hematopoietic Stem Cells.
Stem Cells
; 41(1): 39-49, 2023 01 30.
Artigo
Inglês
| MEDLINE | ID: mdl-36219686
3.
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
Inglês
| MEDLINE | ID: mdl-29764981
4.
Depression-like behaviors induced by defective PTPRT activity through dysregulated synaptic functions and neurogenesis.
J Cell Sci
; 133(20)2020 10 21.
Artigo
Inglês
| MEDLINE | ID: mdl-32938684
5.
Establishment of mouse line showing inducible priapism-like phenotypes.
Reprod Med Biol
; 21(1): e12472, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35765371
6.
Involvement of Rev1 in alkylating agent-induced loss of heterozygosity in Oryzias latipes.
Genes Cells
; 25(2): 124-138, 2020 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-31917895
7.
Crim1C140S mutant mice reveal the importance of cysteine 140 in the internal region 1 of CRIM1 for its physiological functions.
Mamm Genome
; 30(11-12): 329-338, 2019 12.
Artigo
Inglês
| MEDLINE | ID: mdl-31776724
8.
The linear ubiquitin-specific deubiquitinase gumby regulates angiogenesis.
Nature
; 498(7454): 318-24, 2013 Jun 20.
Artigo
Inglês
| MEDLINE | ID: mdl-23708998
9.
Mouse models for ROS1-fusion-positive lung cancers and their application to the analysis of multikinase inhibitor efficiency.
Carcinogenesis
; 37(5): 452-60, 2016 05.
Artigo
Inglês
| MEDLINE | ID: mdl-26964870
10.
Degradation of Stop Codon Read-through Mutant Proteins via the Ubiquitin-Proteasome System Causes Hereditary Disorders.
J Biol Chem
; 290(47): 28428-28437, 2015 Nov 20.
Artigo
Inglês
| MEDLINE | ID: mdl-26442586
11.
Novel allelic mutations in murine Serca2 induce differential development of squamous cell tumors.
Biochem Biophys Res Commun
; 476(4): 175-182, 2016 08 05.
Artigo
Inglês
| MEDLINE | ID: mdl-27131742
12.
Bcl11b prevents the intrathymic development of innate CD8 T cells in a cell intrinsic manner.
Int Immunol
; 27(4): 205-15, 2015 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-25422283
13.
Bcl11b SWI/SNF-complex subunit modulates intestinal adenoma and regeneration after γ-irradiation through Wnt/ß-catenin pathway.
Carcinogenesis
; 36(6): 622-31, 2015 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-25827435
14.
Defective craniofacial development and brain function in a mouse model for depletion of intracellular inositol synthesis.
J Biol Chem
; 289(15): 10785-10796, 2014 Apr 11.
Artigo
Inglês
| MEDLINE | ID: mdl-24554717
15.
Novel retinoblastoma mutation abrogating the interaction to E2F2/3, but not E2F1, led to selective suppression of thyroid tumors.
Cancer Sci
; 105(10): 1360-8, 2014 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-25088905
16.
Effects of background mutations and single nucleotide polymorphisms (SNPs) on the Disc1 L100P behavioral phenotype associated with schizophrenia in mice.
Behav Brain Funct
; 10: 45, 2014 Dec 08.
Artigo
Inglês
| MEDLINE | ID: mdl-25487992
17.
Trends in large-scale mouse mutagenesis: from genetics to functional genomics.
Nat Rev Genet
; 9(10): 803-10, 2008 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-18781157
18.
Novel mouse model for Gardner syndrome generated by a large-scale N-ethyl-N-nitrosourea mutagenesis program.
Cancer Sci
; 104(7): 937-44, 2013 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-23551873
19.
DETECTION OF TRANSGENERATIONAL GENETIC EFFECTS BASED ON WHOLE-GENOME SEQUENCING IN THE MOUSE MODEL.
Radiat Prot Dosimetry
; 198(13-15): 1137-1142, 2022 Sep 09.
Artigo
Inglês
| MEDLINE | ID: mdl-36083724
20.
Assessing reproducibility of inherited variants detected with short-read whole genome sequencing.
Genome Biol
; 23(1): 2, 2022 01 03.
Artigo
Inglês
| MEDLINE | ID: mdl-34980216