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Items: 25

1.

Alternative oxidase-mediated respiration prevents lethal mitochondrial cardiomyopathy.

Rajendran J, Purhonen J, Tegelberg S, Smolander OP, Mörgelin M, Rozman J, Gailus-Durner V, Fuchs H, Hrabe de Angelis M, Auvinen P, Mervaala E, Jacobs HT, Szibor M, Fellman V, Kallijärvi J.

EMBO Mol Med. 2019 Jan;11(1). pii: e9456. doi: 10.15252/emmm.201809456.

2.

NAD+ repletion produces no therapeutic effect in mice with respiratory chain complex III deficiency and chronic energy deprivation.

Purhonen J, Rajendran J, Tegelberg S, Smolander OP, Pirinen E, Kallijärvi J, Fellman V.

FASEB J. 2018 May 21:fj201800090R. doi: 10.1096/fj.201800090R. [Epub ahead of print]

PMID:
29782205
3.

Ret receptor tyrosine kinase sustains proliferation and tissue maturation in intestinal epithelia.

Perea D, Guiu J, Hudry B, Konstantinidou C, Milona A, Hadjieconomou D, Carroll T, Hoyer N, Natarajan D, Kallijärvi J, Walker JA, Soba P, Thapar N, Burns AJ, Jensen KB, Miguel-Aliaga I.

EMBO J. 2017 Oct 16;36(20):3029-3045. doi: 10.15252/embj.201696247. Epub 2017 Sep 12.

4.

Zebrafish GDNF and its co-receptor GFRα1 activate the human RET receptor and promote the survival of dopaminergic neurons in vitro.

Saarenpää T, Kogan K, Sidorova Y, Mahato AK, Tascón I, Kaljunen H, Yu L, Kallijärvi J, Jurvansuu J, Saarma M, Goldman A.

PLoS One. 2017 May 3;12(5):e0176166. doi: 10.1371/journal.pone.0176166. eCollection 2017.

5.

Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model.

Tegelberg S, Tomašić N, Kallijärvi J, Purhonen J, Elmér E, Lindberg E, Nord DG, Soller M, Lesko N, Wedell A, Bruhn H, Freyer C, Stranneheim H, Wibom R, Nennesmo I, Wredenberg A, Eklund EA, Fellman V.

Orphanet J Rare Dis. 2017 Apr 20;12(1):73. doi: 10.1186/s13023-017-0624-2.

6.

Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation.

Purhonen J, Rajendran J, Mörgelin M, Uusi-Rauva K, Katayama S, Krjutskov K, Einarsdottir E, Velagapudi V, Kere J, Jauhiainen M, Fellman V, Kallijärvi J.

Sci Rep. 2017 Apr 19;7(1):957. doi: 10.1038/s41598-017-01109-4.

7.

COX7A2L/SCAFI and Pre-Complex III Modify Respiratory Chain Supercomplex Formation in Different Mouse Strains with a Bcs1l Mutation.

Davoudi M, Kotarsky H, Hansson E, Kallijärvi J, Fellman V.

PLoS One. 2016 Dec 20;11(12):e0168774. doi: 10.1371/journal.pone.0168774. eCollection 2016.

8.

Effect of High-Carbohydrate Diet on Plasma Metabolome in Mice with Mitochondrial Respiratory Chain Complex III Deficiency.

Rajendran J, Tomašić N, Kotarsky H, Hansson E, Velagapudi V, Kallijärvi J, Fellman V.

Int J Mol Sci. 2016 Nov 1;17(11). pii: E1824.

9.

Exploring the Conserved Role of MANF in the Unfolded Protein Response in Drosophila melanogaster.

Lindström R, Lindholm P, Kallijärvi J, Palgi M, Saarma M, Heino TI.

PLoS One. 2016 Mar 14;11(3):e0151550. doi: 10.1371/journal.pone.0151550. eCollection 2016.

10.

Suppression of RNAi by dsRNA-degrading RNaseIII enzymes of viruses in animals and plants.

Weinheimer I, Jiu Y, Rajamäki ML, Matilainen O, Kallijärvi J, Cuellar WJ, Lu R, Saarma M, Holmberg CI, Jäntti J, Valkonen JP.

PLoS Pathog. 2015 Mar 6;11(3):e1004711. doi: 10.1371/journal.ppat.1004711. eCollection 2015 Mar.

11.

A mouse model of mitochondrial complex III dysfunction induced by myxothiazol.

Davoudi M, Kallijärvi J, Marjavaara S, Kotarsky H, Hansson E, Levéen P, Fellman V.

Biochem Biophys Res Commun. 2014 Apr 18;446(4):1079-84. doi: 10.1016/j.bbrc.2014.03.058. Epub 2014 Mar 21.

PMID:
24661880
12.

Characterization of the structural and functional determinants of MANF/CDNF in Drosophila in vivo model.

Lindström R, Lindholm P, Kallijärvi J, Yu LY, Piepponen TP, Arumäe U, Saarma M, Heino TI.

PLoS One. 2013 Sep 3;8(9):e73928. doi: 10.1371/journal.pone.0073928. eCollection 2013.

13.

Characterization of Drosophila GDNF receptor-like and evidence for its evolutionarily conserved interaction with neural cell adhesion molecule (NCAM)/FasII.

Kallijärvi J, Stratoulias V, Virtanen K, Hietakangas V, Heino TI, Saarma M.

PLoS One. 2012;7(12):e51997. doi: 10.1371/journal.pone.0051997. Epub 2012 Dec 20.

14.

Gynecological tumors in Mulibrey nanism and role for RING finger protein TRIM37 in the pathogenesis of ovarian fibrothecomas.

Karlberg S, Lipsanen-Nyman M, Lassus H, Kallijärvi J, Lehesjoki AE, Butzow R.

Mod Pathol. 2009 Apr;22(4):570-8. doi: 10.1038/modpathol.2009.13. Epub 2009 Mar 27.

15.

RNAi screening for kinases and phosphatases identifies FoxO regulators.

Mattila J, Kallijärvi J, Puig O.

Proc Natl Acad Sci U S A. 2008 Sep 30;105(39):14873-8. doi: 10.1073/pnas.0803022105. Epub 2008 Sep 24.

16.

Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism.

Hämäläinen RH, Mowat D, Gabbett MT, O'brien TA, Kallijärvi J, Lehesjoki AE.

Clin Genet. 2006 Dec;70(6):473-9.

PMID:
17100991
17.

Tissue expression of the mulibrey nanism-associated Trim37 protein in embryonic and adult mouse tissues.

Kallijärvi J, Hämäläinen RH, Karlberg N, Sainio K, Lehesjoki AE.

Histochem Cell Biol. 2006 Sep;126(3):325-34. Epub 2006 Mar 3.

PMID:
16514549
18.

Characterisation of the mulibrey nanism-associated TRIM37 gene: transcription initiation, promoter region and alternative splicing.

Hämäläinen RH, Joensuu T, Kallijärvi J, Lehesjoki AE.

Gene. 2006 Jan 17;366(1):180-8. Epub 2005 Nov 28.

PMID:
16310976
19.

Insulin resistance syndrome in subjects with mutated RING finger protein TRIM37.

Karlberg N, Jalanko H, Kallijärvi J, Lehesjoki AE, Lipsanen-Nyman M.

Diabetes. 2005 Dec;54(12):3577-81.

20.

TRIM37 defective in mulibrey nanism is a novel RING finger ubiquitin E3 ligase.

Kallijärvi J, Lahtinen U, Hämäläinen R, Lipsanen-Nyman M, Palvimo JJ, Lehesjoki AE.

Exp Cell Res. 2005 Aug 1;308(1):146-55.

PMID:
15885686
21.

Novel mutations in the TRIM37 gene in Mulibrey Nanism.

Hämäläinen RH, Avela K, Lambert JA, Kallijärvi J, Eyaid W, Gronau J, Ignaszewski AP, McFadden D, Sorge G, Lipsanen-Nyman M, Lehesjoki AE.

Hum Mutat. 2004 May;23(5):522.

PMID:
15108285
22.

Mulibrey nanism--a novel peroxisomal disorder.

Kallijärvi J, Lehesjoki AE, Lipsanen-Nyman M.

Adv Exp Med Biol. 2003;544:31-7. Review. No abstract available.

PMID:
14713209
23.

The TRIM37 gene encodes a peroxisomal RING-B-box-coiled-coil protein: classification of mulibrey nanism as a new peroxisomal disorder.

Kallijärvi J, Avela K, Lipsanen-Nyman M, Ulmanen I, Lehesjoki AE.

Am J Hum Genet. 2002 May;70(5):1215-28. Epub 2002 Apr 5.

25.

Apolipoprotein E includes a binding site which is recognized by several amyloidogenic polypeptides.

Baumann MH, Kallijärvi J, Lankinen H, Soto C, Haltia M.

Biochem J. 2000 Jul 1;349(Pt 1):77-84.

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