Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticus.
- Published in:
- Epilepsia (Series 4), 2008, v. 49, n. 6, p. 1038, doi. 10.1111/j.1528-1167.2008.01544.x
- By:
- Publication type:
- Article
Works by Hassinen, Ilmo
Results: 15
1
2
Myocardial glucose uptake in patients with the m.3243A > G mutation in mitochondrial DNA.
- Published in:
- Journal of Inherited Metabolic Disease, 2016, v. 39, n. 1, p. 67, doi. 10.1007/s10545-015-9865-1
- By:
- Publication type:
- Article
3
Hearing impairment in patients with 3243A→G mtDNA mutation: phenotype and rate of progression.
- Published in:
- Human Genetics, 2001, v. 108, n. 4, p. 284, doi. 10.1007/s004390100475
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- Publication type:
- Article
4
Sequence analysis of nuclear genes encoding functionally important complex I subunits in children with encephalomyopathy.
- Published in:
- Journal of Molecular Medicine, 2005, v. 83, n. 10, p. 786, doi. 10.1007/s00109-005-0712-y
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- Publication type:
- Article
5
A new endogenous ATP analog (ApppI) inhibits the mitochondrial adenine nucleotide translocase (ANT) and is responsible for the apoptosis induced by nitrogen-containing bisphosphonates.
- Published in:
- British Journal of Pharmacology, 2006, v. 147, n. 4, p. 437, doi. 10.1038/sj.bjp.0706628
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- Publication type:
- Article
6
POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype.
- Published in:
- BMC Neurology, 2010, v. 10, p. 29, doi. 10.1186/1471-2377-10-29
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- Publication type:
- Article
7
From identification of fluorescent flavoproteins to mitochondrial redox indicators in intact tissues.
- Published in:
- Journal of Innovative Optical Health Sciences, 2014, v. 7, n. 2, p. -1, doi. 10.1142/S1793545813500582
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- Publication type:
- Article
8
Oxygen and substrate dependence of hepatic cellular respiration: Sinusoidal oxygen gradient and effects of ethanol in isolated perfused liver and hepatocytes.
- Published in:
- Journal of Cellular Physiology, 1987, v. 133, n. 1, p. 119, doi. 10.1002/jcp.1041330115
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- Publication type:
- Article
9
Effect of Acute Pancreatitis on Porcine Intestine: A Morphological Study.
- Published in:
- Ultrastructural Pathology, 2013, v. 37, n. 2, p. 127, doi. 10.3109/01913123.2012.745638
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- Publication type:
- Article
10
Frequency of mitochondrial DNA point mutations among patients with familial sensorineural hearing impairment.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 4, p. 315, doi. 10.1038/sj.ejhg.5200455
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- Publication type:
- Article
11
The MELAS mutations 3946 and 3949 perturb the critical structure in a conserved loop of the ND1 subunit of mitochondrial complex I.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 17, p. 2543, doi. 10.1093/hmg/ddl176
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- Publication type:
- Article
12
Myocardial Overexpression of Mecr, a Gene of Mitochondrial FAS II Leads to Cardiac Dysfunction in Mouse.
- Published in:
- PLoS ONE, 2009, v. 4, n. 5, p. 1, doi. 10.1371/journal.pone.0005589
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- Publication type:
- Article
13
Ischaemic preconditioning and a mitochondrial K<sub>ATP</sub> channel opener both produce cardioprotection accompanied by F<sub>1</sub>F<sub>0</sub>-ATPase inhibition in early ischaemia.
- Published in:
- Basic Research in Cardiology, 2003, v. 98, n. 4, p. 250, doi. 10.1007/s00395-003-0413-z
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- Publication type:
- Article
14
Association between mitochondrial DNA haplogroups J and K, serum branched-chain amino acids and lowered capability for endurance exercise.
- Published in:
- BMC Sports Science, Medicine & Rehabilitation, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13102-022-00485-3
- By:
- Publication type:
- Article
15
Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.
- Published in:
- BMC Cardiovascular Disorders, 2002, v. 2, p. 12, doi. 10.1186/1471-2261-2-12
- By:
- Publication type:
- Article