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Splicing factor 1 modulates dietary restriction and TORC1 pathway longevity in C. elegans

Nature (London), 2017-01, Vol.541 (7635), p.102-106

2017

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Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate disposition

Genome research, 2012-01, Vol.22 (1), p.1

2012

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Global identification of hnRNP A1 binding sites for SSO-based splicing modulation

BMC biology, 2016-07, Vol.14 (1), p.54-54, Article 54

2016

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Influence of polymorphic OATP1B-type carriers on the disposition of docetaxel

Clinical cancer research, 2012-08, Vol.18 (16), p.4433-4440

2012

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Treatment of deep caries lesions in adults: randomized clinical trials comparing stepwise vs. direct complete excavation, and direct pulp capping vs. partial pulpotomy

European journal of oral sciences, 2010-06, Vol.118 (3), p.290-297

2010

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Down-regulation of CK2α correlates with decreased expression levels of DNA replication minichromosome maintenance protein complex (MCM) genes

Scientific reports, 2019-10, Vol.9 (1), p.14581-16, Article 14581

2019

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A synonymous polymorphic variation in ACADM exon 11 affects splicing efficiency and may affect fatty acid oxidation

Molecular genetics and metabolism, 2013-09, Vol.110 (1-2), p.122-128

2013

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Healthcare practices that increase the quality of care in cancer trajectories from a general practice perspective: a scoping review

Scandinavian journal of primary health care, 2022-03, Vol.40 (1), p.11-28

2022

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Blocking of an intronic splicing silencer completely rescues IKBKAP exon 20 splicing in familial dysautonomia patient cells

Nucleic acids research, 2018-09, Vol.46 (15), p.7938

2018

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Revisiting the symptom iceberg based on the Danish symptom cohort – Symptom experiences and healthcare-seeking behaviour in the general Danish population in 2022

Heliyon, 2024-05, Vol.10 (10), p.e31090-e31090, Article e31090

2024

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The ETFDH c.158A>G Variation Disrupts the Balanced Interplay of ESE- and ESS-Binding Proteins thereby Causing Missplicing and Multiple Acyl-CoA Dehydrogenation Deficiency

Human mutation, 2014-01, Vol.35 (1), p.86-95

2014

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Candidate genes and sequence variants for susceptibility to mycobacterial infection identified by whole-exome sequencing

Frontiers in genetics, 2022-10, Vol.13, p.969895-969895

2022

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Splice-shifting oligonucleotide (SSO) mediated blocking of an exonic splicing enhancer (ESE) created by the prevalent c.903+469T>C MTRR mutation corrects splicing and restores enzyme activity in patient cells

Nucleic acids research, 2015-05, Vol.43 (9), p.4627

2015

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Adeno-associated virus-delivered polycistronic microRNA-clusters for knockdown of vascular endothelial growth factor in vivo

The journal of gene medicine, 2012-05, Vol.14 (5), p.328-338

2012

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RNA-sequencing of a mouse-model of spinal muscular atrophy reveals tissue-wide changes in splicing of U12-dependent introns

Nucleic acids research, 2017-01, Vol.45 (1), p.395

2017

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Randomized Clinical Trials on Deep Carious Lesions: 5-Year Follow-up

Journal of dental research, 2017-07, Vol.96 (7), p.747-753

2017

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A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1

Scientific reports, 2019-01, Vol.9 (1), p.645-645, Article 645

2019

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An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency

Molecular genetics and metabolism, 2017-12, Vol.122 (4), p.182-188

2017

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The prevalent deep intronic c. 639+919 G>A GLA mutation causes pseudoexon activation and Fabry disease by abolishing the binding of hnRNPA1 and hnRNP A2/B1 to a splicing silencer

Molecular genetics and metabolism, 2016-11, Vol.119 (3), p.258-269

2016

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Long-term biopsychosocial issues and health-related quality of life in young adolescents and adults treated for childhood Complex Regional Pain Syndrome, type 1

Scandinavian journal of pain, 2022-07, Vol.22 (3), p.473-482

2022

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Corrigendum: Splicing factor 1 modulates dietary restriction and TORC1 pathway longevity in C. elegans

Nature (London), 2017-07, Vol.547 (7664), p.476

2017

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Erratum: Corrigendum: Splicing factor 1 modulates dietary restriction and TORC1 pathway longevity in C. elegans

Nature (London), 2017-07, Vol.547 (7664), p.476-476

2017

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Structured intervention for management of pain following day surgery in children

Pediatric anesthesia, 2016-02, Vol.26 (2), p.151-157

2016

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Behandling af profund caries - baseret på evidens fra nyere kliniske undersøgelser

Den Norske tannlaegeforenings tidende, 2013, Vol.123 (8)

2013

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Consultation expectations among patients with respiratory tract infection symptoms

Danish medical journal, 2017-06, Vol.64 (6)

2017

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Splicing factor 1 modulates dietary restriction and TORC1 pathway longevity in C. elegans

Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate disposition

Global identification of hnRNP A1 binding sites for SSO-based splicing modulation

Influence of polymorphic OATP1B-type carriers on the disposition of docetaxel

Treatment of deep caries lesions in adults: randomized clinical trials comparing stepwise vs. direct complete excavation, and direct pulp capping vs. partial pulpotomy

Down-regulation of CK2α correlates with decreased expression levels of DNA replication minichromosome maintenance protein complex (MCM) genes

A synonymous polymorphic variation in ACADM exon 11 affects splicing efficiency and may affect fatty acid oxidation

Healthcare practices that increase the quality of care in cancer trajectories from a general practice perspective: a scoping review

Blocking of an intronic splicing silencer completely rescues IKBKAP exon 20 splicing in familial dysautonomia patient cells

Revisiting the symptom iceberg based on the Danish symptom cohort – Symptom experiences and healthcare-seeking behaviour in the general Danish population in 2022

The ETFDH c.158A>G Variation Disrupts the Balanced Interplay of ESE- and ESS-Binding Proteins thereby Causing Missplicing and Multiple Acyl-CoA Dehydrogenation Deficiency

Candidate genes and sequence variants for susceptibility to mycobacterial infection identified by whole-exome sequencing

Splice-shifting oligonucleotide (SSO) mediated blocking of an exonic splicing enhancer (ESE) created by the prevalent c.903+469T>C MTRR mutation corrects splicing and restores enzyme activity in patient cells

Adeno-associated virus-delivered polycistronic microRNA-clusters for knockdown of vascular endothelial growth factor in vivo

RNA-sequencing of a mouse-model of spinal muscular atrophy reveals tissue-wide changes in splicing of U12-dependent introns

Randomized Clinical Trials on Deep Carious Lesions: 5-Year Follow-up

A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1

An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency

The prevalent deep intronic c. 639+919 G>A GLA mutation causes pseudoexon activation and Fabry disease by abolishing the binding of hnRNPA1 and hnRNP A2/B1 to a splicing silencer

Long-term biopsychosocial issues and health-related quality of life in young adolescents and adults treated for childhood Complex Regional Pain Syndrome, type 1

Corrigendum: Splicing factor 1 modulates dietary restriction and TORC1 pathway longevity in C. elegans

Erratum: Corrigendum: Splicing factor 1 modulates dietary restriction and TORC1 pathway longevity in C. elegans

Structured intervention for management of pain following day surgery in children

Behandling af profund caries - baseret på evidens fra nyere kliniske undersøgelser

Consultation expectations among patients with respiratory tract infection symptoms

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