Human Immunodeficiency Virus Type 1 Nef Selectively Associates with a Catalytically Active Subpopulation of p21-Activated Kinase 2 (PAK2) Independently of PAK2 Binding to Nck or...

Por Renkema, G. Herma, Manninen, Aki, Saksela, Kalle
Publicado em 2001

Cdc42/Rac1-Mediated Activation Primes PAK2 for Superactivation by Tyrosine Phosphorylation

Por Renkema, G. Herma, Pulkkinen, Kati, Saksela, Kalle
Publicado em 2002

Nef Associates with p21-Activated Kinase 2 in a p21-GTPase-Dependent Dynamic Activation Complex within Lipid Rafts

Por Pulkkinen, Kati, Renkema, G. Herma, Kirchhoff, Frank, Saksela, Kalle
Publicado em 2004

Activation of NFAT-Dependent Gene Expression by Nef: Conservation among Divergent Nef Alleles, Dependence on SH3 Binding and Membrane Association, and Cooperation with Protein Ki...

Por Manninen, Aki, Huotari, Päivi, Hiipakka, Marita, Renkema, G. Herma, Saksela, Kalle
Publicado em 2001

Identification of preferred protein interactions by phage-display of the human Src homology-3 proteome

Por Kärkkäinen, Satu, Hiipakka, Marita, Wang, Jing-Huan, Kleino, Iivari, Vähä-Jaakkola, Marika, Renkema, G Herma, Liss, Michael, Wagner, Ralf, Saksela, Kalle
Publicado em 2006

A Raft-derived, Pak1-regulated Entry Participates in α2β1 Integrin-dependent Sorting to Caveosomes

Por Karjalainen, Mikko, Kakkonen, Elina, Upla, Paula, Paloranta, Heli, Kankaanpää, Pasi, Liberali, Prisca, Renkema, G. Herma, Hyypiä, Timo, Heino, Jyrki, Marjomäki, Varpu
Publicado em 2008

Nef Proteins from Simian Immunodeficiency Virus-Infected Chimpanzees Interact with p21-Activated Kinase 2 and Modulate Cell Surface Expression of Various Human Receptors

Por Kirchhoff, Frank, Schindler, Michael, Bailer, Nicola, Renkema, G. Herma, Saksela, Kalle, Knoop, Volker, Müller-Trutwin, Michaela C., Santiago, Mario L., Bibollet-Ruche, Frederic, Dittmar, Matthias T., Heeney, Jonathan L., Hahn, Beatrice H., Münch, Jan
Publicado em 2004

SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors

Por Renkema, G Herma, Wortmann, Saskia B, Smeets, Roel J, Venselaar, Hanka, Antoine, Marion, Visser, Gepke, Ben-Omran, Tawfeg, van den Heuvel, Lambert P, Timmers, Henri J L M, Smeitink, Jan A, Rodenburg, Richard J T
Publicado no Eur J Hum Genet (2015)

Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extra-oral halitosis

Por Pol, Arjan, Renkema, G. Herma, Tangerman, Albert, Winkel, Edwin G., Engelke, Udo F., de Brouwer, Arjan P. M., Lloyd, Kent C., Araiza, Renee S., van den Heuvel, Lambert, Omran, Heymut, Olbrich, Heike, Elberink, Marijn Oude, Gilissen, Christian, Rodenburg, Richard J., Sass, Jörn Oliver, Schwab, K. Otfried, Schäfer, Hendrik, Venselaar, Hanka, Sequeira, J. Silvia, Op den Camp, Huub J.M., Wevers, Ron A.
Publicado no Nat Genet (2017)

CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder

Por Wortmann, Saskia B., Ziętkiewicz, Szymon, Kousi, Maria, Szklarczyk, Radek, Haack, Tobias B., Gersting, Søren W., Muntau, Ania C., Rakovic, Aleksandar, Renkema, G. Herma, Rodenburg, Richard J., Strom, Tim M., Meitinger, Thomas, Rubio-Gozalbo, M. Estela, Chrusciel, Elzbieta, Distelmaier, Felix, Golzio, Christelle, Jansen, Joop H., van Karnebeek, Clara, Lillquist, Yolanda, Lücke, Thomas, Õunap, Katrin, Zordania, Riina, Yaplito-Lee, Joy, van Bokhoven, Hans, Spelbrink, Johannes N., Vaz, Frédéric M., Pras-Raves, Mia, Ploski, Rafal, Pronicka, Ewa, Klein, Christine, Willemsen, Michel A.A.P., de Brouwer, Arjan P.M., Prokisch, Holger, Katsanis, Nicholas, Wevers, Ron A.
Publicado no Am J Hum Genet (2015)