Mutation of the BiP/GRP78 gene causes axon outgrowth and fasciculation defects in the thalamocortical connections of the mammalian forebrain.
The Journal of comparative neurology
, 2013 Feb 15: 521(3)677-96
Loss of the ciliary kinase Nek8 causes left-right asymmetry defects.
Journal of the American Society of Nephrology : JASN
, 2013 Jan: 24(1)100-12
Mutation mapping and identification by whole-genome sequencing.
Genome research
, 2012 Aug: 22(8)1541-8
The IFT-A complex regulates Shh signaling through cilia structure and membrane protein trafficking.
The Journal of cell biology
, 2012 Jun 11: 197(6)789-800
Cholesterol metabolism is required for intracellular hedgehog signal transduction in vivo.
PLoS genetics
, 2011 Sep: 7(9)e1002224
The naive airway hyperresponsiveness of the A/J mouse is Kit-mediated.
Proceedings of the National Academy of Sciences of the United States of America
, 2011 Aug 2: 108(31)12787-92
A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype.
Neural development
, 2011 Jan 7: 63
A transient transgenic RNAi strategy for rapid characterization of gene function during embryonic development.
PloS one
, 2010 Dec 16: 5(12)e14375
Genome-wide identification of mouse congenital heart disease loci.
Human molecular genetics
, 2010 Aug 15: 19(16)3105-13
Prdm16 is required for normal palatogenesis in mice.
Human molecular genetics
, 2010 Mar 1: 19(5)774-89
Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210.
The New England journal of medicine
, 2010 Jan 21: 362(3)206-16
THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia.
Nature genetics
, 2008 Apr: 40(4)403-10
Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.
Genome research
, 2006 Mar: 16(3)436-40
Fog2 is required for normal diaphragm and lung development in mice and humans.
PLoS genetics
, 2005 Jul: 1(1)58-65
Interacting genetic loci cause airway hyperresponsiveness.
Physiological genomics
, 2005 Mar 21: 21(1)105-11
A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish.
Development (Cambridge, England)
, 2002 Dec: 129(24)5839-46
Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis.
Nature genetics
, 2002 Feb: 30(2)185-9