S. Kärkkäinen

发表

Serum Lipidomics Meets Cardiac Magnetic Resonance Imaging: Profiling of Subjects at Risk of Dilated Cardiomyopathy

J. Lötjönen, M. Orešič, J. Kuusisto, 2011, PloS one.

Respiratory motion reduction with a dual gating approach in myocardial perfusion SPECT: Effect on left ventricular functional parameters

Matti J Kortelainen, M. Vauhkonen, M. Kortelainen, 2018, Journal of Nuclear Cardiology.

A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy.

M. Laakso, M. Nieminen, J. Kuusisto, 2004, European heart journal.

Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy

J. Lötjönen, J. Kuusisto, J. Koikkalainen, 2011, Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance.

Arachidonic acid increases matrix metalloproteinase 9 secretion and expression in human monocytic MonoMac 6 cells

S. Kärkkäinen, S. Nikkari, T. Solakivi, 2009, Lipids in Health and Disease.

A novel mutation, Arg71Thr, in the delta-sarcoglycan gene is associated with dilated cardiomyopathy.

M. Laakso, M. Nieminen, J. Kuusisto, 2003, Journal of molecular medicine.

A novel mutation, Arg71Thr, in the δ-sarcoglycan gene is associated with dilated cardiomyopathy

M. Laakso, M. Nieminen, J. Kuusisto, 2003, Journal of Molecular Medicine.

Threonine phosphorylation sites in the beta 2 and beta 7 leukocyte integrin polypeptides.

C. Gahmberg, S. Kärkkäinen, L. Valmu, 2003, Journal of immunology.

Genetics of dilated cardiomyopathy

K. Peuhkurinen, S. Kärkkäinen, 2007, Annals of medicine.

POSH2 is a RING finger E3 ligase with Rac1 binding activity through a partial CRIB domain

S. Kärkkäinen, G. Renkema, M. van der Linden, 2010, FEBS letters.

Cardiac Autonomic Control in Relation to Other Prognostic Markers in Idiopathic Dilated Cardiomyopathy

E. Vanninen, J. Kuusisto, J. Fedačko, 2015 .

Early familial dilated cardiomyopathy: identification with determination of disease state parameter from cine MR image data.

M. Laakso, M. Nieminen, J. Lötjönen, 2008, Radiology.

Hereditary hemochromatosis gene (HFE) mutations C282Y, H63D and S65C in patients with idiopathic dilated cardiomyopathy

M. Nieminen, P. Nieminen, M. Kaartinen, 2004, European journal of heart failure.

Idiopathic dilated cardiomyopathy and chronic atrial fibrillation

E. Vanninen, J. Kuusisto, J. Fedačko, 2014, Clinical physiology and functional imaging.

Increased ventilatory response to exercise in symptomatic and asymptomatic LMNA mutation carriers: a follow‐up study

P. Piirilä, J. Kuusisto, M. Kaartinen, 2017, Clinical physiology and functional imaging.

Pregnancy and childbirth in carriers of the lamin A/C‐gene mutation

J. Kuusisto, M. Kaartinen, S. Kärkkäinen, 2010, European journal of heart failure.

Characterization of familial and sporadic arrhythmogenic right ventricular cardiomyopathy in Finland

L. Toivonen, M. Kaartinen, S. Kärkkäinen, 2007, Annals of medicine.

Novel mutations in the lamin A/C gene in heart transplant recipients with end stage dilated cardiomyopathy

M. Laakso, M. Nieminen, J. Kuusisto, 2005, Heart.

Two novel mutations in the β‐myosin heavy chain gene associated with dilated cardiomyopathy

M. Laakso, M. Nieminen, J. Kuusisto, 2004, European journal of heart failure.

Leukocyte Integrin Polypeptides 7 b and 2 b Threonine Phosphorylation Sites in the

C. Gahmberg, S. Kärkkäinen, L. Valmu, 2003 .

Supplemental Data High-Throughput Phosphotyrosine Profiling Using SH 2 Domains

T. Pawson, M. Schiller, B. Mayer, 2007 .

Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland

I. Vauhkonen, M. Laakso, S. Heikkinen, 2002, Journal of Molecular Medicine.

High-throughput phosphotyrosine profiling using SH2 domains.

Tony Pawson, Dong-Guk Shin, Martin R Schiller, 2007, Molecules and Cells.

Lamin A/C mutation affecting primarily the right side of the heart

E. Widén, J. Kuusisto, M. Kaartinen, 2013 .

A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy

M. Laakso, M. Nieminen, J. Kuusisto, 2014, Annals of medicine.

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

Michael Liss, R. Wagner, S. Kärkkäinen, 2006, EMBO reports.

Threonine Phosphorylation Sites in the β2 and β7 Leukocyte Integrin Polypeptides1

C. Gahmberg, S. Kärkkäinen, L. Valmu, 2003, The Journal of Immunology.

No variants in the cardiac actin gene in Finnish patients with dilated or hypertrophic cardiomyopathy.

M. Laakso, J. Kuusisto, R. Miettinen, 2002, American heart journal.

Left Atrial Appendage Volume Increased in More Than Half of Patients with Cryptogenic Stroke

R. Vanninen, P. Jäkälä, T. Tapiola, 2013, PloS one.

Clinical disease presentation and ECG characteristics of LMNA mutation carriers

P. Piirilä, J. Kuusisto, K. Nikus, 2017, Open Heart.