Detalhe da pesquisa
1.
Syndromic immune disorder caused by a viable hypomorphic allele of spliceosome component Snrnp40.
Nat Immunol
; 20(10): 1322-1334, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31427773
2.
NLRP3 activation and mitosis are mutually exclusive events coordinated by NEK7, a new inflammasome component.
Nat Immunol
; 17(3): 250-8, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26642356
3.
RNPS1 inhibits excessive tumor necrosis factor/tumor necrosis factor receptor signaling to support hematopoiesis in mice.
Proc Natl Acad Sci U S A
; 119(18): e2200128119, 2022 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35482923
4.
De novo germline mutation in the dual specificity phosphatase 10 gene accelerates autoimmune diabetes.
Proc Natl Acad Sci U S A
; 118(47)2021 11 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34782469
5.
Thousands of induced germline mutations affecting immune cells identified by automated meiotic mapping coupled with machine learning.
Proc Natl Acad Sci U S A
; 118(28)2021 07 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-34260399
6.
Dominant atopy risk mutations identified by mouse forward genetic analysis.
Allergy
; 76(4): 1095-1108, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32810290
7.
Adjuvant effect of the novel TLR1/TLR2 agonist Diprovocim synergizes with anti-PD-L1 to eliminate melanoma in mice.
Proc Natl Acad Sci U S A
; 115(37): E8698-E8706, 2018 09 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30150374
8.
IgD class switching is initiated by microbiota and limited to mucosa-associated lymphoid tissue in mice.
Proc Natl Acad Sci U S A
; 114(7): E1196-E1204, 2017 02 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-28137874
9.
Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5.
Proc Natl Acad Sci U S A
; 114(26): E5197-E5206, 2017 06 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-28607088
10.
Real-time resolution of point mutations that cause phenovariance in mice.
Proc Natl Acad Sci U S A
; 112(5): E440-9, 2015 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-25605905
11.
Genetic determinants of blood pressure and heart rate identified through ENU-induced mutagenesis with automated meiotic mapping.
Sci Adv
; 10(9): eadj9797, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38427739
12.
Modulation of autoimmune diabetes by N-ethyl-N-nitrosourea- induced mutations in non-obese diabetic mice.
Dis Model Mech
; 15(6)2022 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35502705
13.
Obesity caused by an OVOL2 mutation reveals dual roles of OVOL2 in promoting thermogenesis and limiting white adipogenesis.
Cell Metab
; 34(11): 1860-1874.e4, 2022 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36228616
14.
N4BP1 negatively regulates NF-κB by binding and inhibiting NEMO oligomerization.
Nat Commun
; 12(1): 1379, 2021 03 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33654074
15.
SLFN2 protection of tRNAs from stress-induced cleavage is essential for T cell-mediated immunity.
Science
; 372(6543)2021 05 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-33986151
16.
Mutual inhibition between Prkd2 and Bcl6 controls T follicular helper cell differentiation.
Sci Immunol
; 5(43)2020 01 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-31980486
17.
Probability of phenotypically detectable protein damage by ENU-induced mutations in the Mutagenetix database.
Nat Commun
; 9(1): 441, 2018 01 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-29382827
18.
HCFC2 is needed for IRF1- and IRF2-dependent Tlr3 transcription and for survival during viral infections.
J Exp Med
; 214(11): 3263-3277, 2017 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28970238