Role of prolyl hydroxylation in the molecular interactions of collagens

par Rappu, Pekka, Salo, Antti M., Myllyharju, Johanna, Heino, Jyrki
Publié dans Essays Biochem (2019)

Expression and Roles of Individual HIF Prolyl 4-Hydroxylase Isoenzymes in the Regulation of the Hypoxia Response Pathway along the Murine Gastrointestinal Epithelium

par Dengler, Franziska, Sova, Sofia, Salo, Antti M., Mäki, Joni M., Koivunen, Peppi, Myllyharju, Johanna
Publié dans Int J Mol Sci (2021)

A Connective Tissue Disorder Caused by Mutations of the Lysyl Hydroxylase 3 Gene

par Salo, Antti M., Cox, Helen, Farndon, Peter, Moss, Celia, Grindulis, Helen, Risteli, Maija, Robins, Simon P., Myllylä, Raili
Publié 2008

Proline hydroxylation in collagen supports integrin binding by two distinct mechanisms

par Sipilä, Kalle H., Drushinin, Kati, Rappu, Pekka, Jokinen, Johanna, Salminen, Tiina A., Salo, Antti M., Käpylä, Jarmo, Myllyharju, Johanna, Heino, Jyrki
Publié dans J Biol Chem (2018)

Reduction of Lysyl Hydroxylase 3 Causes Deleterious Changes in the Deposition and Organization of Extracellular Matrix

par Risteli, Maija, Ruotsalainen, Heli, Salo, Antti M., Sormunen, Raija, Sipilä, Laura, Baker, Naomi L., Lamandé, Shireen R., Vimpari-Kauppinen, Leena, Myllylä, Raili
Publié 2009

Type I and type V procollagen triple helix uses different subsets of the molecular ensemble for lysine posttranslational modifications in the rER

par Ishikawa, Yoshihiro, Taga, Yuki, Zientek, Keith, Mizuno, Nobuyo, Salo, Antti M., Semenova, Olesya, Tufa, Sara F., Keene, Douglas R., Holden, Paul, Mizuno, Kazunori, Gould, Douglas B., Myllyharju, Johanna, Bächinger, Hans Peter
Publié dans J Biol Chem (2021)

Severe Extracellular Matrix Abnormalities and Chondrodysplasia in Mice Lacking Collagen Prolyl 4-Hydroxylase Isoenzyme II in Combination with a Reduced Amount of Isoenzyme I

par Aro, Ellinoora, Salo, Antti M., Khatri, Richa, Finnilä, Mikko, Miinalainen, Ilkka, Sormunen, Raija, Pakkanen, Outi, Holster, Tiina, Soininen, Raija, Prein, Carina, Clausen-Schaumann, Hauke, Aszódi, Attila, Tuukkanen, Juha, Kivirikko, Kari I., Schipani, Ernestina, Myllyharju, Johanna
Publié dans J Biol Chem (2015)

The glucose-sensing transcription factor ChREBP is targeted by proline hydroxylation

par Heidenreich, Steffi, Weber, Pamela, Stephanowitz, Heike, Petricek, Konstantin M., Schütte, Till, Oster, Moritz, Salo, Antti M., Knauer, Miriam, Goehring, Isabel, Yang, Na, Witte, Nicole, Schumann, Anne, Sommerfeld, Manuela, Muenzner, Matthias, Myllyharju, Johanna, Krause, Eberhard, Schupp, Michael
Publié dans J Biol Chem (2020)

Wnt5a Deficiency Leads to Anomalies in Ureteric Tree Development, Tubular Epithelial Cell Organization and Basement Membrane Integrity Pointing to a Role in Kidney Collecting Duct...

par Pietilä, Ilkka, Prunskaite-Hyyryläinen, Renata, Kaisto, Susanna, Tika, Elisavet, van Eerde, Albertien M., Salo, Antti M., Garma, Leonardo, Miinalainen, Ilkka, Feitz, Wout F., Bongers, Ernie M. H. F., Juffer, André, Knoers, Nine V. A. M., Renkema, Kirsten Y., Myllyharju, Johanna, Vainio, Seppo J.
Publié dans PLoS One (2016)

P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eye

par Zou, Yaqun, Donkervoort, Sandra, Salo, Antti M., Foley, A. Reghan, Barnes, Aileen M., Hu, Ying, Makareeva, Elena, Leach, Meganne E., Mohassel, Payam, Dastgir, Jahannaz, Deardorff, Matthew A., Cohn, Ronald D., DiNonno, Wendy O., Malfait, Fransiska, Lek, Monkol, Leikin, Sergey, Marini, Joan C., Myllyharju, Johanna, Bönnemann, Carsten G.
Publié dans Hum Mol Genet (2017)