Works by Myllyharju, Johanna


Results: 43
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    PHD1 regulates p53-mediated colorectal cancer chemoresistance.

    Published in:
    EMBO Molecular Medicine, 2015, v. 7, n. 10, p. 1350, doi. 10.15252/emmm.201505492
    By:
    • Deschoemaeker, Sofie;
    • Di Conza, Giusy;
    • Lilla, Sergio;
    • Martín‐Pérez, Rosa;
    • Mennerich, Daniela;
    • Boon, Lise;
    • Hendrikx, Stefanie;
    • Maddocks, Oliver DK;
    • Marx, Christian;
    • Radhakrishnan, Praveen;
    • Prenen, Hans;
    • Schneider, Martin;
    • Myllyharju, Johanna;
    • Kietzmann, Thomas;
    • Vousden, Karen H;
    • Zanivan, Sara;
    • Mazzone, Massimiliano
    Publication type:
    Article
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    Loss of Cln5 leads to altered Gad1 expression and deficits in interneuron development in mice.

    Published in:
    Human Molecular Genetics, 2019, v. 28, n. 19, p. 3309, doi. 10.1093/hmg/ddz165
    By:
    • Singh, Yajuvinder;
    • Leinonen, Henri;
    • Fazaludeen, Feroze;
    • Jaronen, Merja;
    • Guest, Debbie;
    • Buckley, Noel;
    • Byts, Nadiya;
    • Oksa, Petra;
    • Jalkanen, Kari;
    • Iqbal, Imran;
    • Huuskonen, Mikko;
    • Savchenko, Ekaterina;
    • Keksa-Goldsteine, Velta;
    • Chew, Sweelin;
    • Myllyharju, Johanna;
    • Tanila, Heikki;
    • Ooi, Lezanne;
    • Koistinaho, Jari;
    • Kanninen, Katja M;
    • Malm, Tarja
    Publication type:
    Article
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    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 Patterning.

    Published in:
    PLoS ONE, 2016, v. 11, n. 1, p. 1, doi. 10.1371/journal.pone.0147171
    By:
    • 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.
    Publication type:
    Article
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    Metabolic characteristics of transmembrane prolyl 4-hydroxylase (P4H-TM) deficient mice.

    Published in:
    Pflügers Archiv: European Journal of Physiology, 2024, v. 476, n. 9, p. 1339, doi. 10.1007/s00424-024-02920-5
    By:
    • Ala-Nisula, Tuulia;
    • Halmetoja, Riikka;
    • Leinonen, Henri;
    • Kurkela, Margareta;
    • Lipponen, Henna-Riikka;
    • Sakko, Samuli;
    • Karpale, Mikko;
    • Salo, Antti M.;
    • Sissala, Niina;
    • Röning, Tapio;
    • Raza, Ghulam S.;
    • Mäkelä, Kari A.;
    • Thevenot, Jérôme;
    • Herzig, Karl-Heinz;
    • Serpi, Raisa;
    • Myllyharju, Johanna;
    • Tanila, Heikki;
    • Koivunen, Peppi;
    • Dimova, Elitsa Y.
    Publication type:
    Article
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    Characterization of two carnation petal prolyl 4 hydroxylases.

    Published in:
    Physiologia Plantarum, 2010, v. 140, n. 2, p. 199, doi. 10.1111/j.1399-3054.2010.01390.x
    By:
    • Vlad, Florina;
    • Tiainen, Päivi;
    • Owen, Carolyn;
    • Spano, Thodhoraq;
    • Daher, Firas Bou;
    • Oualid, Fatiha;
    • Senol, Namik Ozer;
    • Vlad, Daniela;
    • Myllyharju, Johanna;
    • Kalaitzis, Panagiotis
    Publication type:
    Article
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    Structural basis of homo- and heterotrimerization of collagen I.

    Published in:
    Nature Communications, 2017, v. 8, n. 3, p. 14671, doi. 10.1038/ncomms14671
    By:
    • Sharma, Urvashi;
    • Carrique, Loïc;
    • Vadon-Le Goff, Sandrine;
    • Mariano, Natacha;
    • Georges, Rainier-Numa;
    • Delolme, Frederic;
    • Koivunen, Peppi;
    • Myllyharju, Johanna;
    • Moali, Catherine;
    • Aghajari, Nushin;
    • Hulmes, David J. S.
    Publication type:
    Article
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    Prolyl 4-hydroxylation regulates Argonaute 2 stability.

    Published in:
    Nature, 2008, v. 455, n. 7211, p. 421, doi. 10.1038/nature07186
    By:
    • Qi, Hank H.;
    • Ongusaha, Pat P.;
    • Myllyharju, Johanna;
    • Dongmei Cheng;
    • Pakkanen, Outi;
    • Yujiang Shi;
    • Lee, Sam W.;
    • Junmin Peng;
    • Yang Shi
    Publication type:
    Article
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    P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eye.

    Published in:
    Human Molecular Genetics, 2017, v. 26, n. 12, p. 2207, doi. 10.1093/hmg/ddx110
    By:
    • Yaqun Zou;
    • Donkervoort, Sandra;
    • Salo, Antti M.;
    • Foley, A. Reghan;
    • Barnes, Aileen M.;
    • Ying Hu;
    • 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.
    Publication type:
    Article
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    Lack of P4H-TM in mice results in age-related retinal and renal alterations.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 17, p. 3810, doi. 10.1093/hmg/ddw228
    By:
    • Leinonen, Henri;
    • Rossi, Maarit;
    • Salo, Antti M.;
    • Tiainen, Päaivi;
    • Hyväarinen, Jaana;
    • Pitkäanen, Marja;
    • Sormunen, Raija;
    • Miinalainen, Ilkka;
    • Chi Zhang;
    • Soininen, Raija;
    • Kivirikko, Kari I.;
    • Koskelainen, Ari;
    • Tanila, Heikki;
    • Myllyharju, Johanna;
    • Koivunen, Peppi
    Publication type:
    Article
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