Publications Page - The Jackson Laboratory

Publications

The following list of citations contains links to NCBI where abstracts and full text version of research articles may be found.

Fairfield H et al. 2011. Mutation discovery in mice by whole exome sequencing. Genome Biol. 12(9):R86. PMCID: PMCJournal - In Process.
Keane TM et al. 2011. Mouse genomic variation and its effect on phenotypes and gene regulation. Nature 477:289-294. PMCID: PMC3276836.
Hochheiser H et al. 2011. The FaceBase Consortium: A Comprehensive Program to Facilitate Craniofacial Research. Developmental Biology 355(2):175-82. NIHMSID: 296937.
Pratt CH, Curtain M, Donahue LR, Shopland LS. 2011. Mitotic Defects Lead to Pervasive Aneuploidy and Accompany Loss of RB1 Activity in Mouse LmnaDhe Dermal Fibroblasts. PLoS ONE 6(3): e18065. PMCID: PMC3064591.
Murray SA. 2011. Mouse resources for craniofacial research. Genesis 49(4):190-9. PMC Journal – In Process; NIHMSID 360634.
Odgren PR, Pratt CH, Mackay CA, Mason-Savas A , Curtain M, Shopland L, Ichicki T, Sundberg JP , Donahue LR. 2010. Disheveled hair and ear (Dhe), a spontaneous mouse Lmna mutation modeling human laminopathies. PLoS One Apr1:5(4):e9959.PMCID:2848607.
Mao M, Thedens DR, Chang B, Harris BS, Zheng QY, Johnson KR, Donahue LR, Anderson MG. 2009. The podosomal-adaptor protein SH3PXD2B is essential for normal postnatal development. Mamm Genome 20(8):462-75. PMCID: PMC2759419 .
Davisson MT. Discovery Genetics: Serendipity in Basic Research. 2005. ILAR J 46(4):338-344.
Lorenz-Depiereux B, Guido VE, Johnson KR, Zheng QY, Gagnon LH, Bauschatz JD, Davisson MT, Washburn LL, Donahue LR, Strom TM, Eicher EM. 2004. New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice. Mamm Genome. 15(3):151-61.
Bauschatz JD, Curtain MM, Davisson MT, Lane PW, Donahue LR. 2003. In collaboration: The Jackson Laboratory Craniofacial Resource. Crit Rev Eukaryot Gene Expr. 13(2-4):107-8.
Donahue LR, Chang B, Mohan S, Miyakoshi N, Wergedal JE, Baylink DJ, Hawes NL, Rosen CJ, Ward-Bailey P, Zheng QY, Bronson RT, Johnson KR, Davisson MT. 2003. A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis. J Bone Miner Res. 18(9):1612-21.

The following contains links to published Craniofacial Resource research articles. Web publication of short research articles, containing preliminary phenotypic characterization and mapping, allows us to provide basic information on mutations to the scientific community more rapidly.

Title	Author	Year
An Ear Pinna Mutation in Fgfr1	Kane, C. et al	2012
An Ear Pinna Mutation in the Mouse on Chromosome Two	Curtain, M. et al	2011
A Mouse Mutation in Lrp4 missing digits 2 Jackson	Curtain, M. et al	2011
A mouse mutation in the Large gene with muscular dystrophy and retinoschisis	Curtain, M. et al	2010
A mutation in the Arsb gene; a mouse model that resembles Mucopolysaccharidosis Type VI (MPS VI, also known as Maroteaux-Lamy syndrome	Curtain, M. et al	2009
A Hydrocephalus Mutation with Rhinitis on Mouse Chromosome Eight	Dionne, L. et al	2008
Stunted; A Short Face Mutation on Chromosome 19 in the Mouse	Curtain, M. et. al.	2008
A Spontaneous Mouse Strain with Cryptophthalmos	Curtain, M. et. al.	2008
Froggy;a new mutation on Chromosome 13 affecting skull shape and body size	Marden, C. et al	2008
Sharkey, a new mutation in the Sostdc1 gene	Curtain, M. et. al.	2007
Helicopter ears: A structural mutation	Curtain, M. et. al.	2007
A short face mutation on Chromosome 11	Curtain, M. et. al.	2007
A New Spontaneous Mutation Causing Corneal Opacity.	Giggey, J. et. al.	2007
A New Semi-Dominant Short Nose Mutation.	Giggey, J. et. al.	2006
A Remutation to Cauliflower Ear.	Curtain, M. et. al.	2006
A cauliflower remutation to Bmp5.	Giggey, J. et. al.	2006
Cauliflower ear, a remutation to Bmp5.	Giggey, J. et. al.	2005
Snubnose-like (snol), a new spontaneous skeletal mutation on Chromosome 4 in the mouse	Ward-Bailey, P.F. et. al.	2003
Preliminary skull characterization and comparison of C57BL/6J, C3H/HeSnJ, BALB/cByJ and DBA/2J inbred mice.	Bauschatz, J.D. et. al.	2001
Preliminary characterization of the craniofacial morphology of the B6C3Fe a/a-din/+ mouse strain	Bauschatz, J.D. et. al.	2001

Last Modified: March 23, 2012

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