P. H. Backe

发表

Structural insight into repair of alkylated DNA by a new superfamily of DNA glycosylases comprising HEAT-like repeats

T. Rognes, B. Dalhus, M. Bjørås, 2007, Nucleic acids research.

Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis

P. Sowa, J. Koht, M. D. Vigeland, 2019, Brain : a journal of neurology.

A new family of proteins related to the HEAT-like repeat DNA glycosylases with affinity for branched DNA structures.

T. Rognes, A. Kolstø, B. Dalhus, 2013, Journal of structural biology.

Structural basis for substrate and product recognition in human phosphoglucomutase-1 (PGM1) isoform 2, a member of the α-d-phosphohexomutase superfamily

B. Dalhus, M. Bjørås, J. K. Laerdahl, 2020, Scientific Reports.

Biallelic variants in KIF14 cause intellectual disability with microcephaly

Kiely N. James, J. Lupski, S. Jhangiani, 2018, European Journal of Human Genetics.

In situ cofactor regeneration enables selective CO2 reduction in a stable and efficient enzymatic photoelectrochemical cell

Kaiqi Xu, F. Rise, Junwang Tang, 2021 .

PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia.

Ankita Patel, J. Lupski, R. Gibbs, 2014, American journal of human genetics.

Novel mutations in the HADHB gene causing a mild phenotype of mitochondrial trifunctional protein (MTP) deficiency

K. Ørstavik, P. Mathisen, T. Tangeraas, 2022, JIMD reports.

Crystallization, microPIXE and preliminary crystallographic analysis of the complex between the third KH domain of hnRNP K and single-stranded DNA.

S. Cusack, R. Ravelli, E. Garman, 2004, Acta crystallographica. Section D, Biological crystallography.

Publisher Correction: Impaired oxidative stress response characterizes HUWE1-promoted X-linked intellectual disability

Enni Markkanen, G. Dianov, F. Raymond, 2018, Scientific Reports.

Molecular Characterization of Two Homozygous Factor VII Variants Associated with Intracranial Bleeding.

Elisabeth Andersen, E. Skarpen, B. Thiede, 2021, Thrombosis and haemostasis.

ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequences

D. Misceo, C. Venditti, R. Wevers, 2022, Brain : a journal of neurology.

The Chromatin Remodeling Factor SMARCB1 Forms a Complex with Human Cytomegalovirus Proteins UL114 and UL44

H. Rollag, M. Bjørås, L. Luna, 2012, PloS one.

Four novel mutations identified in Norwegian patients result in intermittent maple syrup urine disease when combined with the R301C mutation.

H. Rootwelt, M. Bjørås, A. Lund, 2010, Molecular genetics and metabolism.

L-isoleucyl-L-asparagine 1.094-hydrate: a hybrid hydrogen-bonding pattern.

P. H. Backe, C. Görbitz, 2010, Acta crystallographica. Section C, Crystal structure communications.

DNA base repair--recognition and initiation of catalysis.

B. Dalhus, M. Bjørås, J. K. Laerdahl, 2009, FEMS microbiology reviews.

Hereditary tyrosinaemia type I in Norway: Incidence and three novel small deletions in the fumarylacetoacetase gene

H. Rootwelt, B. Woldseth, P. H. Backe, 2012, Scandinavian journal of clinical and laboratory investigation.

Biallelic variants in KIF14 cause intellectual disability with microcephaly

Kiely N. James, J. Lupski, S. Jhangiani, 2018, European Journal of Human Genetics.

Novel UCHL1 mutations reveal new insights into ubiquitin processing

Z. Iqbal, M. Bjørås, G. Slupphaug, 2016, Human molecular genetics.

Novel UCHL1 mutations reveal new insights into ubiquitin processing.

Z. Iqbal, M. Bjørås, G. Slupphaug, 2017, Human molecular genetics.

A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T‐cell dysfunction

J. Lupski, R. Gibbs, D. Muzny, 2016, Molecular genetics & genomic medicine.

Separation-of-function mutants unravel the dual-reaction mode of human 8-oxoguanine DNA glycosylase.

Magnar Bjørås, Bjørn Dalhus, B. Dalhus, 2011, Structure.

Structures of endonuclease V with DNA reveal initiation of deaminated adenine repair

J. Tainer, Weiguo Cao, B. Dalhus, 2009, Nature Structural &Molecular Biology.

Identification and Characterization of Novel Mutations in the Human Gene Encoding the Catalytic Subunit Calpha of Protein Kinase A (PKA)

M. Bjørås, J. K. Laerdahl, T. Jahnsen, 2012, PloS one.

The SH3 domains of the protein kinases ITK and LCK compete for adjacent sites on T cell–specific adapter protein

A. Andreotti, S. Boyken, A. Spurkland, 2019, The Journal of Biological Chemistry.

A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge–Weber syndrome

N. Matsumoto, J. Pevsner, Roar Fjær, 2021, Human molecular genetics.

Structure and function of the human sperm-specific isoform of protein kinase A (PKA) catalytic subunit Cα2.

C. Scheich, K. Rosendal, M. Bjørås, 2012, Journal of structural biology.

X-ray crystallographic and NMR studies of the third KH domain of hnRNP K in complex with single-stranded nucleic acids.

S. Cusack, R. Ravelli, M. Sattler, 2005, Structure.

Hallmarks of Processivity in Glycoside Hydrolases from Crystallographic and Computational Studies of the Serratia marcescens Chitinases

Christina M. Payne, G. Beckham, B. Dalhus, 2012, The Journal of Biological Chemistry.

Human OXR1 maintains mitochondrial DNA integrity and counteracts hydrogen peroxide-induced oxidative stress by regulating antioxidant pathways involving p21.

M. Bjørås, N. Danbolt, L. Luna, 2014, Free radical biology & medicine.

Molecular Characterization of Two Homozygous Factor VII Variants Associated with Intracranial Bleeding

Elisabeth Andersen, E. Skarpen, B. Thiede, 2020, Thrombosis and Haemostasis.

Molecular Analysis of the GJB2 Gene in Iraqi Patients with Sensorineural Non-Syndromic Hearing Loss

F. Alzoubi, P. H. Backe, S. Jaradat, 2016 .

Generalized epilepsy in a family with basal ganglia calcifications and mutations in SLC20A2 and CHRNB2.

E. Brodtkorb, K. Kvistad, M. D. Vigeland, 2015, European journal of medical genetics.

Novel Deletion Mutation Identified in a Patient with Late-Onset Combined Methylmalonic Acidemia and Homocystinuria, cblC Type.

H. Rootwelt, M. Bjørås, Å. Røhr, 2013, JIMD reports.

Susceptibility to infections, without concomitant hyper-IgE, reported in 1976, is caused by hypomorphic mutation in the phosphoglucomutase 3 (PGM3) gene

L. Moens, K. E. Lundin, M. Bjørås, 2015, Clinical immunology.

In situ cofactor regeneration enables selective CO 2 reduction in a stable and efficient enzymatic photoelectrochemical cell Applied Catalysis B: Environmental

F. Rise, Junwang Tang, T. Norby, 2021 .

Impaired oxidative stress response characterizes HUWE1-promoted X-linked intellectual disability

Enni Markkanen, G. Dianov, F. Raymond, 2017, Scientific Reports.

BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening.

A. Ormazabal, R. Artuch, M. Dixon, 2023, Brain : a journal of neurology.

Non-flipping DNA glycosylase AlkD scans DNA without formation of a stable interrogation complex

K. Glette, J. Tørresen, B. Dalhus, 2021, Communications biology.

Molecular analysis of maple syrup urine disease in Jordanian families

P. H. Backe, S. Jaradat, Wajdi Amayreh, 2016 .

X-ray crystallographic and NMR studies of the third KH domain of hnRNP K in complex with single-stranded nucleic acids.

S. Cusack, R. Ravelli, M. Sattler, 2005, Structure.

A new family of proteins related to the HEAT-like repeat DNA glycosylases with affinity for branched DNA structures.

A. Kolstø, B. Dalhus, M. Bjørås, 2013, Journal of structural biology.

High performance and toxicity assessment of Ta3N5 nanotubes for photoelectrochemical water splitting

Kaiqi Xu, M. Bjørås, T. Norby, 2021 .