Detalhe da pesquisa
1.
Genetic deletion of a short fragment of glucokinase in rabbit by CRISPR/Cas9 leading to hyperglycemia and other typical features seen in MODY-2.
Cell Mol Life Sci
; 77(16): 3265-3277, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-31720743
2.
The disrupted balance between hair follicles and sebaceous glands in Hoxc13-ablated rabbits.
FASEB J
; 33(1): 1226-1234, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30125135
3.
The minimal promoter (P1) of Xist is non-essential for X chromosome inactivation.
RNA Biol
; 17(5): 623-629, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32036747
4.
CRISPR/Cas9-mediated mutation of PHEX in rabbit recapitulates human X-linked hypophosphatemia (XLH).
Hum Mol Genet
; 25(13): 2661-2671, 2016 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27126636
5.
Efficient dual sgRNA-directed large gene deletion in rabbit with CRISPR/Cas9 system.
Cell Mol Life Sci
; 73(15): 2959-68, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26817461
6.
α-Gal antigen-deficient rabbits with GGTA1 gene disruption via CRISPR/Cas9.
BMC Genom Data
; 23(1): 54, 2022 07 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35820824
7.
LMNA-mutated Rabbits: A Model of Premature Aging Syndrome with Muscular Dystrophy and Dilated Cardiomyopathy.
Aging Dis
; 10(1): 102-115, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30705772
8.
Generation and Phenotype Identification of PAX4 Gene Knockout Rabbit by CRISPR/Cas9 System.
G3 (Bethesda)
; 8(8): 2833-2840, 2018 07 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-29950431
9.
Highly efficient RNA-guided base editing in rabbit.
Nat Commun
; 9(1): 2717, 2018 07 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30006570
10.
CRISPR-induced exon skipping is dependent on premature termination codon mutations.
Genome Biol
; 19(1): 164, 2018 10 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-30333044
11.
Functional validation of the albinism-associated tyrosinase T373K SNP by CRISPR/Cas9-mediated homology-directed repair (HDR) in rabbits.
EBioMedicine
; 36: 517-525, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30274819
12.
Multiple homologous genes knockout (KO) by CRISPR/Cas9 system in rabbit.
Gene
; 647: 261-267, 2018 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-29339069
13.
CRISPR/Cas9-mediated mosaic mutation of SRY gene induces hermaphroditism in rabbits.
Biosci Rep
; 38(2)2018 04 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-29439141
14.
Truncated C-terminus of fibrillin-1 induces Marfanoid-progeroid-lipodystrophy (MPL) syndrome in rabbit.
Dis Model Mech
; 11(4)2018 04 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29666143
15.
Mutation of the Sp1 binding site in the 5' flanking region of SRY causes sex reversal in rabbits.
Oncotarget
; 8(24): 38176-38183, 2017 Jun 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-28445127
16.
CRISPR/Cas9-mediated mutation of tyrosinase (Tyr) 3' UTR induce graying in rabbit.
Sci Rep
; 7(1): 1569, 2017 05 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28484254
17.
CRISPR/Cas9-Mediated Mutation of αA-Crystallin Gene Induces Congenital Cataracts in Rabbits.
Invest Ophthalmol Vis Sci
; 58(6): BIO34-BIO41, 2017 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28475701
18.
Identification of differentially methylated regions (DMRs) of neuronatin in mice.
Springerplus
; 5(1): 2018, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27994995
19.
Efficient Generation of Myostatin Gene Mutated Rabbit by CRISPR/Cas9.
Sci Rep
; 6: 25029, 2016 04 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-27113799
20.
CRISPR/Cas9-mediated GJA8 knockout in rabbits recapitulates human congenital cataracts.
Sci Rep
; 6: 22024, 2016 Feb 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-26912477