Search details
1.
Limb development genes underlie variation in human fingerprint patterns.
Cell
; 185(1): 95-112.e18, 2022 01 06.
Article
in English
| MEDLINE | ID: mdl-34995520
2.
Pleiotropic Impacts of Macrophage and Microglial Deficiency on Development in Rats with Targeted Mutation of the Csf1r Locus.
J Immunol
; 201(9): 2683-2699, 2018 11 01.
Article
in English
| MEDLINE | ID: mdl-30249809
3.
Ectodysplasin signalling deficiency in mouse models of hypohidrotic ectodermal dysplasia leads to middle ear and nasal pathology.
Hum Mol Genet
; 25(16): 3564-3577, 2016 08 15.
Article
in English
| MEDLINE | ID: mdl-27378689
4.
Macrophage colony-stimulating factor increases hepatic macrophage content, liver growth, and lipid accumulation in neonatal rats.
Am J Physiol Gastrointest Liver Physiol
; 314(3): G388-G398, 2018 03 01.
Article
in English
| MEDLINE | ID: mdl-29351395
5.
Correction: Pleiotropic Impacts of Macrophage and Microglial Deficiency on Development in Rats with Targeted Mutation of the Csf1r Locus.
J Immunol
; 202(11): 3334-3335, 2019 Jun 01.
Article
in English
| MEDLINE | ID: mdl-31028122
6.
Otitis media in the Tgif knockout mouse implicates TGFß signalling in chronic middle ear inflammatory disease.
Hum Mol Genet
; 22(13): 2553-65, 2013 Jul 01.
Article
in English
| MEDLINE | ID: mdl-23459932
7.
KATNAL1 regulation of sertoli cell microtubule dynamics is essential for spermiogenesis and male fertility.
PLoS Genet
; 8(5): e1002697, 2012.
Article
in English
| MEDLINE | ID: mdl-22654668
8.
Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb.
Hum Mol Genet
; 21(8): 1706-24, 2012 Apr 15.
Article
in English
| MEDLINE | ID: mdl-22199023
9.
EVI1 acts as an inducible negative-feedback regulator of NF-κB by inhibiting p65 acetylation.
J Immunol
; 188(12): 6371-80, 2012 Jun 15.
Article
in English
| MEDLINE | ID: mdl-22581859
10.
Oxr1 is essential for protection against oxidative stress-induced neurodegeneration.
PLoS Genet
; 7(10): e1002338, 2011 Oct.
Article
in English
| MEDLINE | ID: mdl-22028674
11.
HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutants.
PLoS Genet
; 7(10): e1002336, 2011 Oct.
Article
in English
| MEDLINE | ID: mdl-22028672
12.
Surveying the Down syndrome mouse model resource identifies critical regions responsible for chronic otitis media.
Mamm Genome
; 24(11-12): 439-45, 2013 Dec.
Article
in English
| MEDLINE | ID: mdl-24068166
13.
A mutation in the mitochondrial fission gene Dnm1l leads to cardiomyopathy.
PLoS Genet
; 6(6): e1001000, 2010 Jun 24.
Article
in English
| MEDLINE | ID: mdl-20585624
14.
The Comparative Pathology Workbench: Interactive visual analytics for biomedical data.
J Pathol Inform
; 14: 100328, 2023.
Article
in English
| MEDLINE | ID: mdl-37693862
15.
Static respiratory cilia associated with mutations in Dnahc11/DNAH11: a mouse model of PCD.
Hum Mutat
; 33(3): 495-503, 2012 Mar.
Article
in English
| MEDLINE | ID: mdl-22102620
16.
Loss of mitogen-activated protein kinase kinase kinase 4 (MAP3K4) reveals a requirement for MAPK signalling in mouse sex determination.
PLoS Biol
; 7(9): e1000196, 2009 Sep.
Article
in English
| MEDLINE | ID: mdl-19753101
17.
Trans-cortical vessels in the mouse temporal bulla bone are a means to recruit myeloid cells in chronic otitis media and limit peripheral leukogram changes.
Front Genet
; 13: 985214, 2022.
Article
in English
| MEDLINE | ID: mdl-36246635
18.
The EDA-deficient mouse has Zymbal's gland hypoplasia and acute otitis externa.
Dis Model Mech
; 15(3)2022 03 01.
Article
in English
| MEDLINE | ID: mdl-35107126
19.
Disparities in Air Pollutants Across Racial, Ethnic, and Poverty Groups at US Public Schools.
Geohealth
; 6(12): e2022GH000672, 2022 Dec.
Article
in English
| MEDLINE | ID: mdl-36467256
20.
Unraveling the genetics of otitis media: from mouse to human and back again.
Mamm Genome
; 22(1-2): 66-82, 2011 Feb.
Article
in English
| MEDLINE | ID: mdl-21107580