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European Journal of Neurology
|
December 4, 2008
Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration
J Krüger, A-L Kaivorinne, B Udd, et al.
Journal of Neurology
|
October 15, 2013
Variations of mitochondrial DNA polymerase γ in patients with Parkinson's disease
S Ylönen, P Ylikotila, A Siitonen, et al.
Life Sciences
|
January 1, 1996
Increase of blood NAD+ and attenuation of lactacidemia during nicotinamide treatment of a patient with the MELAS syndrome
K Majamaa, H Rusanen, A M Remes, et al.
European Journal of Neurology
|
April 24, 2010
Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients
A-L Kaivorinne, J Krüger, B Udd, et al.
Human Genetics
|
May 31, 2001
Hearing impairment in patients with 3243A-->G mtDNA mutation: phenotype and rate of progression
S Uimonen, J S Moilanen, M Sorri, et al.
The Journal of Biological Chemistry
|
May 10, 1984
Ascorbate is consumed stoichiometrically in the uncoupled reactions catalyzed by prolyl 4-hydroxylase and lysyl hydroxylase
R Myllylä, K Majamaa, V Günzler, et al.
Luminescence : the Journal of Biological and Chemical Luminescence
|
December 13, 2000
Time-resolved fluorometry (TRF)-based immunoassay concept for rapid and quantitative determination of biochemical myocardial infarction markers from whole blood, serum and plasma
K Pettersson, T Katajamäki, K Irjala, et al.
Biochimica Et Biophysica Acta
|
August 24, 1999
Increase of collagen synthesis and deposition in the arachnoid and the dura following subarachnoid hemorrhage in the rat
J Sajanti, A S Björkstrand, S Finnilä, et al.
The Journal of Biological Chemistry
|
June 15, 1986
Partial identity of the 2-oxoglutarate and ascorbate binding sites of prolyl 4-hydroxylase
K Majamaa, V Günzler, H M Hanauske-Abel, et al.
Genomics
|
April 1, 1993
Kearns-Sayre syndrome case presenting a mitochondrial DNA deletion with unusual direct repeats and a rudimentary RNAase mitochondrial ribonucleotide processing target sequence
A M Remes, K J Peuhkurinen, R Herva, et al.
Page
of 7
Search research articles
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Showing results (41-50 of 67) with videos related to
Sort By:
Page
of 7
European Journal of Neurology
|
December 4, 2008
Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration
J Krüger, A-L Kaivorinne, B Udd, et al.
Journal of Neurology
|
October 15, 2013
Variations of mitochondrial DNA polymerase γ in patients with Parkinson's disease
S Ylönen, P Ylikotila, A Siitonen, et al.
Life Sciences
|
January 1, 1996
Increase of blood NAD+ and attenuation of lactacidemia during nicotinamide treatment of a patient with the MELAS syndrome
K Majamaa, H Rusanen, A M Remes, et al.
European Journal of Neurology
|
April 24, 2010
Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients
A-L Kaivorinne, J Krüger, B Udd, et al.
Human Genetics
|
May 31, 2001
Hearing impairment in patients with 3243A-->G mtDNA mutation: phenotype and rate of progression
S Uimonen, J S Moilanen, M Sorri, et al.
The Journal of Biological Chemistry
|
May 10, 1984
Ascorbate is consumed stoichiometrically in the uncoupled reactions catalyzed by prolyl 4-hydroxylase and lysyl hydroxylase
R Myllylä, K Majamaa, V Günzler, et al.
Luminescence : the Journal of Biological and Chemical Luminescence
|
December 13, 2000
Time-resolved fluorometry (TRF)-based immunoassay concept for rapid and quantitative determination of biochemical myocardial infarction markers from whole blood, serum and plasma
K Pettersson, T Katajamäki, K Irjala, et al.
Biochimica Et Biophysica Acta
|
August 24, 1999
Increase of collagen synthesis and deposition in the arachnoid and the dura following subarachnoid hemorrhage in the rat
J Sajanti, A S Björkstrand, S Finnilä, et al.
The Journal of Biological Chemistry
|
June 15, 1986
Partial identity of the 2-oxoglutarate and ascorbate binding sites of prolyl 4-hydroxylase
K Majamaa, V Günzler, H M Hanauske-Abel, et al.
Genomics
|
April 1, 1993
Kearns-Sayre syndrome case presenting a mitochondrial DNA deletion with unusual direct repeats and a rudimentary RNAase mitochondrial ribonucleotide processing target sequence
A M Remes, K J Peuhkurinen, R Herva, et al.
Page
of 7