Search details
1.
The chemerin knockout rat reveals chemerin dependence in female, but not male, experimental hypertension.
FASEB J
; : fj201800479, 2018 Jun 15.
Article
in English
| MEDLINE | ID: mdl-29906243
2.
A novel intergenic ETnII-ß insertion mutation causes multiple malformations in polypodia mice.
PLoS Genet
; 9(12): e1003967, 2013.
Article
in English
| MEDLINE | ID: mdl-24339789
3.
Blood vascular abnormalities in Rasa1(R780Q) knockin mice: implications for the pathogenesis of capillary malformation-arteriovenous malformation.
Am J Pathol
; 184(12): 3163-9, 2014 Dec.
Article
in English
| MEDLINE | ID: mdl-25283357
4.
Development of a C3 Humanized Rat as a New Model for Evaluating Novel C3 Inhibitors.
J Innate Immun
; 16(1): 56-65, 2024.
Article
in English
| MEDLINE | ID: mdl-38035563
5.
An inactivating caspase 11 passenger mutation originating from the 129 murine strain in mice targeted for c-IAP1.
Biochem J
; 443(2): 355-9, 2012 Apr 15.
Article
in English
| MEDLINE | ID: mdl-22332634
6.
Angiogenesis depends upon EPHB4-mediated export of collagen IV from vascular endothelial cells.
JCI Insight
; 7(4)2022 02 22.
Article
in English
| MEDLINE | ID: mdl-35015735
7.
Genetic analysis of SH2D4A, a novel adapter protein related to T cell-specific adapter and adapter protein in lymphocytes of unknown function, reveals a redundant function in T cells.
J Immunol
; 181(3): 2019-27, 2008 Aug 01.
Article
in English
| MEDLINE | ID: mdl-18641339
8.
Mice hypomorphic for Atr have increased DNA damage and abnormal checkpoint response.
Mamm Genome
; 20(6): 375-85, 2009 Jun.
Article
in English
| MEDLINE | ID: mdl-19504344
9.
Next Generation Transgenic Rat Model Production.
Methods Mol Biol
; 2018: 97-114, 2019.
Article
in English
| MEDLINE | ID: mdl-31228153
10.
Knock-In Rat Lines with Cre Recombinase at the Dopamine D1 and Adenosine 2a Receptor Loci.
eNeuro
; 6(5)2019.
Article
in English
| MEDLINE | ID: mdl-31451604
11.
Generation of mice with a conditional allele of the p120 Ras GTPase-activating protein.
Genesis
; 45(12): 762-7, 2007 Dec.
Article
in English
| MEDLINE | ID: mdl-18064675
12.
Hair Cell Loss, Spiral Ganglion Degeneration, and Progressive Sensorineural Hearing Loss in Mice with Targeted Deletion of Slc44a2/Ctl2.
J Assoc Res Otolaryngol
; 16(6): 695-712, 2015 Dec.
Article
in English
| MEDLINE | ID: mdl-26463873
13.
Normal TCR signal transduction in mice that lack catalytically active PTPN3 protein tyrosine phosphatase.
J Immunol
; 178(6): 3680-7, 2007 Mar 15.
Article
in English
| MEDLINE | ID: mdl-17339465
14.
Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell line.
Mamm Genome
; 18(8): 549-58, 2007 Aug.
Article
in English
| MEDLINE | ID: mdl-17828574
15.
Beta-mannosidosis mice: a model for the human lysosomal storage disease.
Hum Mol Genet
; 15(3): 493-500, 2006 Feb 01.
Article
in English
| MEDLINE | ID: mdl-16377659
16.
Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.
Hum Mol Genet
; 12(16): 2049-61, 2003 Aug 15.
Article
in English
| MEDLINE | ID: mdl-12913076
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