Periderm Fate during Palatogenesis: TGF-β and Periderm Dedifferentiation von Saroya, G., Hu, J., Hu, M., Panaretos, C., Mann, J., Kim, S., Bush, J.O., Kaartinen, V.

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Functional Redundancy of TGF-beta Family Type I Receptors and Receptor-Smads in Mediating Anti-Müllerian Hormone-Induced Müllerian Duct Regression in the Mouse von Orvis, G.D, Jamin, S.P, Kwan, K.M, Mishina, Y, Kaartinen, V.M, Huang, S, Roberts, A.B, Umans, L, Huylebroeck, D, Zwijsen, A, Wang, D, Martin, J.F, Behringer, R.R

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Abnormal function of astroglia lacking Abr and Bcr RacGAPs von Kaartinen, Vesa, Gonzalez-Gomez, Ignacio, Voncken, Jan Willem, Haataja, Leena, Faure, Emmanuelle, Nagy, Andre, Groffen, John, Heisterkamp, Nora

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Abr and Bcr are Multifunctional Regulators of the Rho GTP-Binding Protein Family von T.-H. Chuang, Xu, X., Kaartinen, V., Heisterkamp, N., Groffen, J., Bokoch, G. M.

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BCR/ABL P210 and P190 Cause Distinct Leukemia in Transgenic Mice von Voncken, Jan Willem, Kaartinen, Vesa, Pattengale, Paul K., Germeraad, Wilfred T.V., Groffen, John, Heisterkamp, Nora

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proBDNF and p75NTR Control Excitability and Persistent Firing of Cortical Pyramidal Neurons von Gibon, Julien, Buckley, Shannon M, Unsain, Nicolas, Kaartinen, Vesa, Séguéla, Philippe, Barker, Philip A

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Tgf- beta 3-induced palatal fusion is mediated by Alk-5/Smad pathway von Dudas, M, Nagy, A, Laping, N J, Moustakas, A, Kaartinen, V

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Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction von Kaartinen, V, Voncken, J W, Shuler, C, Warburton, D, Bu, D, Heisterkamp, N, Groffen, J

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Abnormal lung development and cleft palate in mice lacking TGF–β3 indicates defects of epithelial–mesenchymal interaction von Kaartinen, Vesa, Voncken, Jan Willem, Shuler, Charles, Warburton, David, Bu, Ding, Heisterkamp, Nora, Groffen, John

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TGF-β3-induced Palatogenesis Requires Matrix Metalloproteinases von Blavier, Laurence, Lazaryev, Alisa, Groffen, John, Heisterkamp, Nora, DeClerck, Yves A., Kaartinen, Vesa

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A Fluorometric Assay for Glycosylasparaginase Activity and Detection of Aspartylglycosaminuria von Mononen, I.T., Kaartinen, V.M., Williams, J.C.

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Glycosaparaginase from human leukocytes. Inactivation and covalent modification with diazo-oxonorvaline von Kaartinen, V, Williams, J C, Tomich, J, Yates, J R, Hood, L E, Mononen, I

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Removal of the floxed neo gene from a conditional knockout allele by the adenoviral Cre recombinase in vivo von Kaartinen, Vesa, Nagy, Andre

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Substrate specificity and reaction mechanism of human glycoasparaginase. The N-glycosidic linkage of various glycoasparagines is cleaved through a reaction mechanism similar to L-a... von Kaartinen, V, Mononen, T, Laatikainen, R, Mononen, I

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Phosphorylation substrates and altered signalling in leukemias caused by BCR/ABL von Groffen, J, de Jong, R, Haataja, L, Kaartinen, V, Heisterkamp, N

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Assay of aspartylglycosylaminase by high-performance liquid chromatography von Kaartinen, V., Mononen, I.

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Aspartylglycosaminuria in the Finnish Population: Identification of Two Point Mutations in the Heavy Chain of Glycoasparaginase von Mononen, Ilkka, Heisterkamp, Nora, Kaartinen, Vesa, Williams, Julian C., Yates, John R., Griffin, Patrick R., Hood, Leroy E., Groffen, John

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Notch Signaling Prevents Mucous Metaplasia in Mouse Conducting Airways during Postnatal Development von Tsao, P -N, Wei, S -C, Wu, M -F, Huang, M -T, Lin, H -Y, Lee, M -C, Lin, K M -C, Wang, I -J, Kaartinen, V, Yang, L -T, Cardoso, W V

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Phenotypic characterization of mice with targeted disruption of glycosylasparaginase gene: A mouse model for aspartylglycosaminuria von Kaartinen, V., Mononen, I., Gonzales‐Gomez, I., Noronkoski, T., Heisterkamp, N., Groffen, J.

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Enzyme replacement therapy in a mouse model of aspartylglycosaminuria von Dunder, Ulla, Kaartinen, Vesa, Valtonen, Pirjo, VÄÄnÄnen, Eira, Kosma, Veli-Matti, Heisterkamp, Nora, Groffen, John, Mononen, Ilkka

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