Publications by authors named "Marit Nielsen"

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E
Effects of mindfulness-based stress reduction on neuropeptide Y plasma levels in stressed individuals.
Helle Degnbol Østergaard, Karen Johanne Pallesen, Marit Nyholm Nielsen, Lone Fjorback, Lise Juul

J Psychiatr Res· January 2025

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Exploring the sortilin related receptor, SorLA, in depression.
Henriette N Buttenschøn, Betina Elfving, Marit Nielsen, Sune Skeldal, Mathias Kaas

J Affect Disord· May 2018

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Investigation of serum levels of sortilin in response to antidepressant treatment.
Henriette Nørmølle Buttenschøn, Marit Nielsen, Simon Glerup, Ole Mors

Acta Neuropsychiatr· April 2018

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Progranulin gene variation affects serum progranulin levels differently in Danish bipolar individuals compared with healthy controls.
Henriette N Buttenschøn, Marit N Nielsen, Gangadaar Thotakura, Chris W Lee, Anders Nykjær

Psychiatr Genet· June 2017

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Association analyses of depression and genes in the hypothalamus-pituitary-adrenal axis.
Henrietta Nørmølle Buttenschøn, Jesper Krogh, Marit Nyholm Nielsen, Linda Kaerlev, Merete Nordentoft

Acta Neuropsychiatr· February 2017

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Association between genes on chromosome 19p13.2 and panic disorder.
Noomi O Gregersen, Henriette N Buttenschøn, Anne Hedemand, Marit N Nielsen, Hans A Dahl

Psychiatr Genet· December 2016

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Heterozygosity for an in-frame deletion causes glutaryl-CoA dehydrogenase deficiency in a patient detected by newborn screening: investigation of the effect of the mutant allele.
Peter Bross, Jane B Frederiksen, Anne S Bie, Jakob Hansen, Johan Palmfeldt, Marit N Nielsen

J Inherit Metab Dis· September 2012

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Inactivation of the hereditary spastic paraplegia-associated Hspd1 gene encoding the Hsp60 chaperone results in early embryonic lethality in mice.
Jane H Christensen, Marit N Nielsen, Jakob Hansen, Annette Füchtbauer, Ernst-Martin Füchtbauer

Cell Stress Chaperones· November 2010

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Periostin is a collagen associated bone matrix protein regulated by parathyroid hormone.
Dario Fortunati, Sjur Reppe, Ase-Karine Fjeldheim, Marit Nielsen, Vigdis T Gautvik

Matrix Biol· September 2010

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Calmodulin-dependent kinase 1beta is expressed in the epiphyseal growth plate and regulates proliferation of mouse calvarial osteoblasts in vitro.
Mona E Pedersen, Dario Fortunati, Marit Nielsen, Sverre-Henning Brorson, Tove Lekva

Bone· October 2008

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The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo.
Peter Bross, Søren Naundrup, Jakob Hansen, Marit Nyholm Nielsen, Jane Hvarregaard Christensen, Kåre Lehmann Nielsen

J Biol Chem· June 2008

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A novel mutation in the HSPD1 gene in a patient with hereditary spastic paraplegia.
Jakob Hansen, Kirsten Svenstrup, Debbie Ang, Marit N Nielsen, Jane H Christensen, Jørgen E Nielsen

J Neurol· July 2007

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Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential.
Peter Bross, Zhijie Li, Jakob Hansen, Jens Jacob Hansen, Marit Nyholm Nielsen

J Hum Genet· March 2007

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Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter.
Jens J Hansen, Peter Bross, Majken Westergaard, Marit Nielsen, Hans Eiberg

Hum Genet· April 2003

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Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter.
Jens J Hansen, Peter Bross, Majken Westergaard, Marit Nyholm Nielsen, Hans Eiberg

Hum Genet· January 2003

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Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60.
Jens Jacob Hansen, Alexandra Dürr, Isabelle Cournu-Rebeix, Costa Georgopoulos, Debbie Ang, Marit Nyholm Nielsen

Am J Hum Genet· May 2002

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