Denna sida på svenska

Anna Wredenberg

Gruppledare

Publications

Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy
Haack Tb, Ignatius E, Calvo-garrido J, Iuso A, Isohanni P, Maffezzini C, et al
American journal of human genetics 2016;99(3):735-43

Mitochondrial Polyadenylation Is a One-Step Process Required for mRNA Integrity and tRNA Maturation
Bratic A, Clemente P, Calvo-garrido J, Maffezzini C, Felser A, Wibom R, et al
PLoS genetics 2016;12(5):e1006028-

Complementation between polymerase- and exonuclease-deficient mitochondrial DNA polymerase mutants in genomically engineered flies
Bratic A, Kauppila Te, Macao B, Grönke S, Siibak T, Stewart Jb, et al
Nature communications 2015;6():8808-

Cyclophilin D, a target for counteracting skeletal muscle dysfunction in mitochondrial myopathy
Gineste C, Hernandez A, Ivarsson N, Cheng Aj, Naess K, Wibom R, et al
Human molecular genetics 2015;24(23):6580-7

Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26
Kishita Y, Pajak A, Bolar Na, Marobbio Cm, Maffezzini C, Miniero Dv, et al
American journal of human genetics 2015;97(5):761-8

Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4-dihydroxybensoic acid
Freyer C, Stranneheim H, Naess K, Mourier A, Felser A, Maffezzini C, et al
Journal of medical genetics 2015;52(11):779-83

SUV3 helicase is required for correct processing of mitochondrial transcripts
Clemente P, Pajak A, Laine I, Wibom R, Wedell A, Freyer C, et al
Nucleic acids research 2015;43(15):7398-413

Neu-Laxova syndrome is a heterogeneous metabolic disorder caused by defects in enzymes of the L-serine biosynthesis pathway
Acuna-hidalgo R, Schanze D, Kariminejad A, Nordgren A, Kariminejad Mh, Conner P, et al
American journal of human genetics 2014;95(3):285-93

Rapid pulsed whole genome sequencing for comprehensive acute diagnostics of inborn errors of metabolism
Stranneheim H, Engvall M, Naess K, Lesko N, Larsson P, Dahlberg M, et al
BMC genomics 2014;15():1090-

MTERF3 regulates mitochondrial ribosome biogenesis in invertebrates and mammals
Wredenberg A, Lagouge M, Bratic A, Metodiev Md, Spåhr H, Mourier A, et al
PLoS genetics 2013;9(1):e1003178-

LRPPRC is necessary for polyadenylation and coordination of translation of mitochondrial mRNAs
Ruzzenente B, Metodiev Md, Wredenberg A, Bratic A, Park Cb, Camara Y, et al
EMBO JOURNAL 2012;31(2):443-56

The Bicoid Stability Factor Controls Polyadenylation and Expression of Specific Mitochondrial mRNAs in Drosophila melanogaster
Bratic A, Wredenberg A, Gronke S, Stewart Jb, Mourier A, Ruzzenente B, et al
PLOS GENETICS 2011;7(10):e1002324-

Increased mitochondrial Ca2+ and decreased sarcoplasmic reticulum Ca2+ in mitochondrial myopathy
Aydin J, Andersson Dc, Hanninen Sl, Wredenberg A, Tavi P, Park Cb, et al
HUMAN MOLECULAR GENETICS 2009;18(2):278-88

Random Point Mutations with Major Effects on Protein-Coding Genes Are the Driving Force behind Premature Aging in mtDNA Mutator Mice
Edgar D, Shabalina I, Camara Y, Wredenberg A, Calvaruso Ma, Nijtmans L, et al
CELL METABOLISM 2009;10(2):131-8

Strong purifying selection in transmission of mammalian mitochondrial DNA
Stewart Jb, Freyer C, Elson Jl, Wredenberg A, Cansu Z, Trifunovic A, et al
PLOS BIOLOGY 2008;6(1):e10-

Respiratory chain dysfunction in skeletal muscle does not cause insulin resistance
Wredenberg A, Freyer C, Sandstrom Me, Katz A, Wibom R, Westerblad H, et al
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 2006;350(1):202-7

Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production
Trifunovic A, Hansson A, Wredenberg A, Rovio At, Dufour E, Khvorostov I, et al
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 2005;102(50):17993-8

Premature ageing in mice expressing defective mitochondrial DNA polymerase
Trifunovic A, Wredenberg A, Falkenberg M, Spelbrink Jn, Rovio At, Bruder Ce, et al
NATURE 2004;429(6990):417-23

Increased mitochondrial mass in mitochondrial myopathy mice
Wredenberg A, Wibom R, Wilhelmsson H, Graff C, Wiener Hh, Burden Sj, et al
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 2002;99(23):15066-71

Complex genetic counselling and prenatal analysis in a woman with external ophthalmoplegia and deleted mtDNA
Graff C, Wredenberg A, Silva Jp, Bui Th, Borg K, Larsson Ng
PRENATAL DIAGNOSIS 2000;20(5):426-31

Effects of high resistance training in patients with myotonic dystrophy
Tollback A, Eriksson S, Wredenberg A, Jenner G, Vargas R, Borg K, et al
SCANDINAVIAN JOURNAL OF REHABILITATION MEDICINE 1999;31(1):9-16

Show all publications