Detalhe da pesquisa
1.
Screen for alterations of iron related parameters in N-ethyl-N-nitrosourea-treated mice identified mutant lines with increased plasma ferritin levels.
Biometals
; 28(2): 293-306, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25636453
2.
New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.
Mamm Genome
; 23(7-8): 416-30, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22527485
3.
A novel N-ethyl-N-nitrosourea-induced mutation in phospholipase Cγ2 causes inflammatory arthritis, metabolic defects, and male infertility in vitro in a murine model.
Arthritis Rheum
; 63(5): 1301-11, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21305534
4.
Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse lines.
Eur J Oral Sci
; 120(4): 269-77, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22813216
5.
New C3H KitN824K/WT cancer mouse model develops late-onset malignant mammary tumors with high penetrance.
Sci Rep
; 12(1): 19793, 2022 11 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36396684
6.
Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in hematological parameters.
Mamm Genome
; 22(9-10): 495-505, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21553221
7.
Mutation of the Na(+)-K(+)-2Cl(-) cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia.
Am J Physiol Renal Physiol
; 298(6): F1405-15, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20219826
8.
Mutation in Bmpr1b Leads to Optic Disc Coloboma and Ventral Retinal Gliosis in Mice.
Invest Ophthalmol Vis Sci
; 61(2): 44, 2020 02 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32106289
9.
Novel missense mutation of uromodulin in mice causes renal dysfunction with alterations in urea handling, energy, and bone metabolism.
Am J Physiol Renal Physiol
; 297(5): F1391-8, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19692485
10.
Genome-wide search for genes that modulate inflammatory arthritis caused by Ali18 mutation in mice.
Mamm Genome
; 20(3): 152-61, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19238339
11.
Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in plasma enzyme activities as novel organ-specific disease models.
Exp Physiol
; 94(4): 412-21, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19151073
12.
A genetic screen for modifiers of the delta1-dependent notch signaling function in the mouse.
Genetics
; 175(3): 1451-63, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17179084
13.
Defective immuno- and thymoproteasome assembly causes severe immunodeficiency.
Sci Rep
; 8(1): 5975, 2018 04 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-29654304
14.
ARTS: a web-based tool for the set-up of high-throughput genome-wide mapping panels for the SNP genotyping of mouse mutants.
Nucleic Acids Res
; 33(Web Server issue): W496-500, 2005 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-15980520
15.
New mutation in the mouse Xpd/Ercc2 gene leads to recessive cataracts.
PLoS One
; 10(5): e0125304, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25951169
16.
Features and strategies of ENU mouse mutagenesis.
Curr Pharm Biotechnol
; 10(2): 198-213, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19199953
17.
Reduced corneal thickness and enlarged anterior chamber in a novel ColVIIIa2G257D mutant mouse.
Invest Ophthalmol Vis Sci
; 50(12): 5653-61, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19578028
18.
Targeted inactivation of the murine Abca3 gene leads to respiratory failure in newborns with defective lamellar bodies.
Biochem Biophys Res Commun
; 359(4): 947-51, 2007 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-17577581
19.
Screening for increased plasma urea levels in a large-scale ENU mouse mutagenesis project reveals kidney disease models.
Am J Physiol Renal Physiol
; 292(5): F1560-7, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17264314
20.
Dominant-negative effects of a novel mutated Ins2 allele causes early-onset diabetes and severe beta-cell loss in Munich Ins2C95S mutant mice.
Diabetes
; 56(5): 1268-76, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17303807