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Eino Palin
Eino Palin
Postdoctoral researcher, University of Helsinki
Verified email at helsinki.fi - Homepage
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Cited by
Cited by
Year
Genetic basis of severe childhood-onset cardiomyopathies
C Vasilescu, TH Ojala, V Brilhante, S Ojanen, HM Hinterding, E Palin, ...
Journal of the American College of Cardiology 72 (19), 2324-2338, 2018
822018
Phosphorylation of Parkin at serine 65 is essential for its activation in vivo
TG McWilliams, E Barini, R Pohjolan-Pirhonen, SP Brooks, F Singh, ...
Royal Society Open Biology 8 (11), 180108, 2018
692018
ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia
HM Cooper, Y Yang, E Ylikallio, R Khairullin, R Woldegebriel, KL Lin, ...
Human molecular genetics 26 (8), 1432-1443, 2017
662017
Clustering of Alpers disease mutations and catalytic defects in biochemical variants reveal new features of molecular mechanism of the human mitochondrial replicase, Pol γ
L Euro, GA Farnum, E Palin, A Suomalainen, LS Kaguni
Nucleic acids research 39 (21), 9072-9084, 2011
522011
Mesencephalic complex I deficiency does not correlate with parkinsonism in mitochondrial DNA maintenance disorders
EJH Palin, A Paetau, A Suomalainen
Brain 136 (8), 2379-2392, 2013
452013
The variant p.(Arg183Trp) in SPTLC2 causes late-onset hereditary sensory neuropathy
S Suriyanarayanan, M Auranen, J Toppila, A Paetau, M Shcherbii, E Palin, ...
Neuromolecular medicine 18 (1), 81-90, 2016
202016
Mitochondrial recessive ataxia syndrome mimicking dominant spinocerebellar ataxia
EJH Palin, AH Hakonen, M Korpela, A Paetau, A Suomalainen
Journal of the neurological sciences 315 (1-2), 160-163, 2012
162012
Functional analysis of H. sapiens DNA polymerase γ spacer mutation W748S with and without common variant E1143G
EJH Palin, A Lesonen, CL Farr, L Euro, A Suomalainen, LS Kaguni
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1802 (6), 545-551, 2010
132010
SNCA mutation p. Ala53Glu is derived from a common founder in the Finnish population
P Pasanen, E Palin, R Pohjolan-Pirhonen, M Pöyhönen, JO Rinne, ...
Neurobiology of Aging 50, 168. e5-168. e8, 2017
122017
Genetic background of ataxia in children younger than 5 years in Finland
E Ignatius, P Isohanni, M Pohjanpelto, P Lahermo, S Ojanen, V Brilhante, ...
Neurology Genetics 6 (4), 2020
62020
Elucidating the genetic background of childhood-onset ataxias
E Ignatius, P Isohanni, M Pohjanpelto, E Palin, V Brilhante, S Ojanen, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1417-1417, 2019
2019
ATPase-deficient ATAD3A alters mitochondrial dynamics in hereditary spastic paraplegia
RA Woldegebriel, HM Cooper, EA Ylikallio, R Khairullin, K Lin, L Euro, ...
European Journal of Human Genetics 26, 111-112, 2018
2018
Disorders of mitochondrial DNA polymerase: a clinical, biochemical and structural study
E Palin
Helsingin yliopisto, 2013
2013
Biochemical Genetics of the Mitochondrial Replicase: Clustering of Pathogenic Mutations into Five Functional Modules in Human DNA Polymerase γ
LS Kaguni, GA Farnum, L Euro, E Palin, A Wartiovaara
The FASEB Journal 26, 739.5-739.5, 2012
2012
Molecular background of mitochondrial recessive ataxia syndrome, MIRAS
EJ Palin, A Hakonen, S Heiskanen, V Juvonen, B Udd, LA Bindoff, ...
The FASEB Journal 20 (5), A920-A920, 2006
2006
Genetic basis of severe childhood-onset cardiomyopathies: high prevalence of family-specific and de novo pathogenic variants Short title: Genetics of severe childhood …
C Vasilescu, TH Ojala, V Brilhante, S Ojanen, HM Hinterding, E Palin, ...
SURVEY AND SUMMARY Clustering of Alpers disease mutations and catalytic defects in biochemical variants reveal new features of molecular mechanism of the human mitochondrial …
L Euro, GA Farnum, E Palin, A Suomalainen, LS Kaguni
ATpase-deficient mitochondrial inner membrane protein ATAD3a disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia
R Khairullin, L Euro, R Woldegebriel, S Kaakkola, K Lin, E Ylikallio, ...
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