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Page 1
The Centre for Modeling Human Disease Gene Trap resource.
To C, Epp T, Reid T, Lan Q, Yu M, Li CY, Ohishi M, Hant P, Tsao N, Casallo G, Rossant J, Osborne LR, Stanford WL. To C, et al. Among authors: rossant j. Nucleic Acids Res. 2004 Jan 1;32(Database issue):D557-9. doi: 10.1093/nar/gkh106. Nucleic Acids Res. 2004. PMID: 14681480 Free PMC article.
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
Flenniken AM, Osborne LR, Anderson N, Ciliberti N, Fleming C, Gittens JE, Gong XQ, Kelsey LB, Lounsbury C, Moreno L, Nieman BJ, Peterson K, Qu D, Roscoe W, Shao Q, Tong D, Veitch GI, Voronina I, Vukobradovic I, Wood GA, Zhu Y, Zirngibl RA, Aubin JE, Bai D, Bruneau BG, Grynpas M, Henderson JE, Henkelman RM, McKerlie C, Sled JG, Stanford WL, Laird DW, Kidder GM, Adamson SL, Rossant J. Flenniken AM, et al. Among authors: rossant j. Development. 2005 Oct;132(19):4375-86. doi: 10.1242/dev.02011. Development. 2005. PMID: 16155213
Lunatic Fringe-mediated Notch signaling is required for lung alveogenesis.
Xu K, Nieuwenhuis E, Cohen BL, Wang W, Canty AJ, Danska JS, Coultas L, Rossant J, Wu MY, Piscione TD, Nagy A, Gossler A, Hicks GG, Hui CC, Henkelman RM, Yu LX, Sled JG, Gridley T, Egan SE. Xu K, et al. Among authors: rossant j. Am J Physiol Lung Cell Mol Physiol. 2010 Jan;298(1):L45-56. doi: 10.1152/ajplung.90550.2008. Epub 2009 Nov 6. Am J Physiol Lung Cell Mol Physiol. 2010. PMID: 19897741 Free PMC article.
A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis.
Hughes MR, Anderson N, Maltby S, Wong J, Berberovic Z, Birkenmeier CS, Haddon DJ, Garcha K, Flenniken A, Osborne LR, Adamson SL, Rossant J, Peters LL, Minden MD, Paulson RF, Wang C, Barber DL, McNagny KM, Stanford WL. Hughes MR, et al. Among authors: rossant j. Exp Hematol. 2011 Mar;39(3):305-20, 320.e1-2. doi: 10.1016/j.exphem.2010.12.009. Epub 2010 Dec 28. Exp Hematol. 2011. PMID: 21193012 Free PMC article.
The Sweet Pee model for Sglt2 mutation.
Ly JP, Onay T, Sison K, Sivaskandarajah G, Sabbisetti V, Li L, Bonventre JV, Flenniken A, Paragas N, Barasch JM, Adamson SL, Osborne L, Rossant J, Schnermann J, Quaggin SE. Ly JP, et al. Among authors: rossant j. J Am Soc Nephrol. 2011 Jan;22(1):113-23. doi: 10.1681/ASN.2010080888. J Am Soc Nephrol. 2011. PMID: 21209254 Free PMC article.
426 results