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Found 14 results
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2012
Lichius A, Lord KM, Jeffree CE, Oborny R, Boonyarungsrit P, Read ND.  2012.  Importance of MAP kinases during protoperithecial morphogenesis in Neurospora crassa.PLoS One. 7(8):e42565.
2011
Sprooten E, Sussmann JE, Moorhead TW, Whalley HC, ffrench-Constant C, Blumberg HP, Bastin ME, Hall J, Lawrie SM, McIntosh AM.  2011.  Association of white matter integrity with genetic variation in an exonic DISC1 SNP.Mol Psychiatry. 16(7):685,688-9.
2008
Crisan M, Deasy B, Gavina M, Zheng B, Huard J, Lazzari L, Péault B.  2008.  Purification and long-term culture of multipotent progenitor cells affiliated with the walls of human blood vessels: myoendothelial cells and pericytes.Methods Cell Biol. 86:295-309.
2005
Ramos-Mejía V, Escalante-Alcalde D, Kunath T, Ramírez L, Gertsenstein M, Nagy A, Lomelí H.  2005.  Phenotypic analyses of mouse embryos with ubiquitous expression of Oct4: effects on mid-hindbrain patterning and gene expression.Dev Dyn. 232(1):180-90.
2004
Mesli S, Javorschi S, Bérard AM, Landry M, Priddle H, Kivlichan D, Smith AG, Yen FT, Bihain BE, Darmon M.  2004.  Distribution of the lipolysis stimulated receptor in adult and embryonic murine tissues and lethality of LSR-/- embryos at 12.5 to 14.5 days of gestation.Eur J Biochem. 271(15):3103-14.
Tse E, Smith AG, Hunt S, Lavenir I, Forster A, Warren AJ, Grutz G, Foroni L, Carlton MBL, Colledge WH et al..  2004.  Null mutation of the Lmo4 gene or a combined null mutation of the Lmo1/Lmo3 genes causes perinatal lethality, and Lmo4 controls neural tube development in mice.Mol Cell Biol. 24(5):2063-73.
2003
Meunier D, Aubin J, Jeannotte L.  2003.  Perturbed thyroid morphology and transient hypothyroidism symptoms in Hoxa5 mutant mice.Dev Dyn. 227(3):367-78.
2001
Hendrich B, Guy J, Ramsahoye B, Wilson V, Bird A.  2001.  Closely related proteins MBD2 and MBD3 play distinctive but interacting roles in mouse development.Genes Dev. 15(6):710-23.
Gordon J, Bennett AR, C Blackburn C, Manley NR.  2001.  Gcm2 and Foxn1 mark early parathyroid- and thymus-specific domains in the developing third pharyngeal pouch.Mech Dev. 103(1-2):141-3.
Loh NY, Nebenuis-Oosthuizen D, Blake DJ, Smith AG, Davies KE.  2001.  Role of beta-dystrobrevin in nonmuscle dystrophin-associated protein complex-like complexes in kidney and liver.Mol Cell Biol. 21(21):7442-8.
1997
Sharp MG, Kantachuvesiri S, Mullins JJ.  1997.  Genotype and cardiovascular phenotype: lessons from genetically manipulated animals and diseased humans.Curr Opin Nephrol Hypertens. 6(1):51-7.
1994
de Silva R, Ironside JW, McCardle L, Esmonde T, Bell J, Will R, Windl O, Dempster M, Estibeiro P, Lathe R.  1994.  Neuropathological phenotype and 'prion protein' genotype correlation in sporadic Creutzfeldt-Jakob disease.Neurosci Lett. 179(1-2):50-2.
1992
Dorin JR, Dickinson P, Alton EW, Smith SN, Geddes DM, Stevenson BJ, Kimber WL, Fleming S, Clarke AR, Hooper ML.  1992.  Cystic fibrosis in the mouse by targeted insertional mutagenesis.Nature. 359(6392):211-5.
1991
Ganten D, Takahashi S, Lindpaintner K, Mullins JJ.  1991.  Genetic basis of hypertension. The renin-angiotensin paradigm.Hypertension. 18(5 Suppl):III109-14.