Jane H Christensen

Jane H Christensen

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Jane H Christensen

Jane H Christensen

Publications by authors named "Jane H Christensen"

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The effect of hypoxia on ZEB1 expression in a mimetic system of the blood-brain barrier.

Microvasc Res 2019 03 23;122:131-135. Epub 2018 Aug 23.

Department of Biomedicine, Aarhus University, Aarhus, Denmark; iPSYCH, the Lundbeck Foundation Initiative for Integrative Psychiatric Research, Denmark; iSEQ, Centre for Integrative Sequencing, Aarhus University, Aarhus, Denmark. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00262862183005
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http://dx.doi.org/10.1016/j.mvr.2018.08.004DOI Listing
March 2019

Identification of common genetic risk variants for autism spectrum disorder.

Nat Genet 2019 03 25;51(3):431-444. Epub 2019 Feb 25.

The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, Denmark.

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http://dx.doi.org/10.1038/s41588-019-0344-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454898PMC
March 2019

Determination of the renal concentration capacity following intravenous administration of dDAVP in healthy humans.

Scand J Clin Lab Invest 2018 Feb - Apr;78(1-2):114-119. Epub 2018 Jan 23.

a Department of Pediatrics , Aarhus University Hospital , Aarhus , Denmark.

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http://dx.doi.org/10.1080/00365513.2017.1420215DOI Listing
September 2018

Voluntary Physical Exercise Induces Expression and Epigenetic Remodeling of VegfA in the Rat Hippocampus.

Mol Neurobiol 2018 01 14;55(1):567-582. Epub 2016 Dec 14.

Department of Biomedicine, Aarhus University, 8000, Aarhus C, Denmark.

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http://dx.doi.org/10.1007/s12035-016-0344-yDOI Listing
January 2018

The Effects of Voluntary Physical Exercise-Activated Neurotrophic Signaling in Rat Hippocampus on mRNA Levels of Downstream Signaling Molecules.

J Mol Neurosci 2017 Jun 24;62(2):142-153. Epub 2017 Apr 24.

Department of Biomedicine, Aarhus University, 8000, Aarhus C, Denmark.

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http://dx.doi.org/10.1007/s12031-017-0918-9DOI Listing
June 2017

Mice heterozygous for an inactivated allele of the schizophrenia associated Brd1 gene display selective cognitive deficits with translational relevance to schizophrenia.

Neurobiol Learn Mem 2017 May 21;141:44-52. Epub 2017 Mar 21.

Department of Biomedicine, Aarhus University, Denmark; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Denmark; Centre for Integrative Sequencing, iSEQ, Aarhus University, Denmark. Electronic address:

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http://dx.doi.org/10.1016/j.nlm.2017.03.009DOI Listing
May 2017

Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq.

BMC Genomics 2015 Jul 25;16:548. Epub 2015 Jul 25.

Department of Biomedicine, Aarhus University, 6, Bartholins Allé, Aarhus C, Aarhus, 8000, Denmark.

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http://dx.doi.org/10.1186/s12864-015-1767-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4515013PMC
July 2015

Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder.

Bipolar Disord 2015 Mar 23;17(2):205-11. Epub 2014 Jul 23.

Department of Biomedicine, Institute of Human Genetics, Aarhus University, Aarhus, Denmark; Translational Neuropsychiatry Unit, Department of Clinical Medicine, Aarhus University, Risskov, Denmark; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, Denmark; Centre for Integrative Sequencing, iSEQ, Aarhus University, Aarhus, Denmark.

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http://dx.doi.org/10.1111/bdi.12239DOI Listing
March 2015

A novel variation in the AVP gene resulting in familial neurohypophyseal diabetes insipidus in a large Italian kindred.

Pituitary 2013 Jun;16(2):152-7

Department of Pediatrics, Aarhus University Hospital, Brendstrupgaardsvej 100, 8200 Aarhus, Denmark.

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http://dx.doi.org/10.1007/s11102-012-0392-xDOI Listing
June 2013

Late onset motoneuron disorder caused by mitochondrial Hsp60 chaperone deficiency in mice.

Neurobiol Dis 2013 Jun 4;54:12-23. Epub 2013 Mar 4.

Research Unit for Molecular Medicine, Department of Clinical Medicine, Health Aarhus University Hospital and Aarhus University, Aarhus, Denmark.

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http://dx.doi.org/10.1016/j.nbd.2013.02.012DOI Listing
June 2013

Homozygosity for a mutation in the CYP11B2 gene in an infant with congenital corticosterone methyl oxidase deficiency type II.

Acta Paediatr 2012 Nov;101(11):e519-25

Pediatric Research Laboratory, Aarhus University Hospital, Denmark.

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http://dx.doi.org/10.1111/j.1651-2227.2012.02823.xDOI Listing
November 2012

Late-onset familial neurohypophyseal diabetes insipidus due to a novel mutation in the AVP gene.

Clin Endocrinol (Oxf) 2012 Oct;77(4):586-92

School of Health and Medical Sciences, Örebro University, Örebro, Sweden.

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http://dx.doi.org/10.1111/j.1365-2265.2012.04417.xDOI Listing
October 2012

A novel variation in the AVP gene resulting in familial neurohypophyseal diabetes insipidus in a large Italian kindred.

Pituitary 2013 Jun;16(2):152-7

Department of Pediatrics, Aarhus University Hospital, Brendstrupgaardsvej 100, 8200 Aarhus, Denmark.

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http://dx.doi.org/10.1007/s11102-012-0392-xDOI Listing
June 2013

Skewed X-chromosome inactivation causing diagnostic misinterpretation in congenital nephrogenic diabetes insipidus.

Scand J Urol Nephrol 2010 Nov 12;44(5):324-30. Epub 2010 May 12.

Department of Human Genetics, Aarhus University, Aarhus University Hospital, Aarhus N, Denmark.

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http://dx.doi.org/10.3109/00365599.2010.482946DOI Listing
November 2010

Diverse vasopressin V2 receptor functionality underlying partial congenital nephrogenic diabetes insipidus.

Am J Physiol Renal Physiol 2009 Dec 7;297(6):F1518-25. Epub 2009 Oct 7.

Department of Pediatrics, Aarhus University Hospital, Skejby, Denmark.

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http://dx.doi.org/10.1152/ajprenal.00331.2009DOI Listing
December 2009

Protein misfolding and human disease.

Annu Rev Genomics Hum Genet 2006 ;7:103-24

Research Unit for Molecular Medicine, Institute of Clinical Medicine, Aarhus University Hospital and Faculty of Health Sciences, University of Aarhus, Skejby Sygehus, 8200 Aarhus N, Denmark.

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http://www.annualreviews.org/doi/10.1146/annurev.genom.7.080
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http://dx.doi.org/10.1146/annurev.genom.7.080505.115737DOI Listing
April 2008

A novel mutation in the HSPD1 gene in a patient with hereditary spastic paraplegia.

J Neurol 2007 Jul 10;254(7):897-900. Epub 2007 Apr 10.

Research Unit for Molecular Medicine, Faculty of Health Sciences Aarhus University Hospital , Skejby Sygehus, Brendstrupgaardsvej, 8200, Aarhus N, Denmark,

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http://link.springer.com/content/pdf/10.1007/s00415-006-0470
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http://link.springer.com/10.1007/s00415-006-0470-y
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http://dx.doi.org/10.1007/s00415-006-0470-yDOI Listing
July 2007

Familial neurohypophyseal diabetes insipidus--an update.

Semin Nephrol 2006 May;26(3):209-23

Research Unit for Molecular Medicine, Aarhus University Hospital, Skejby Sygehus, Aarhus, Denmark.

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http://dx.doi.org/10.1016/j.semnephrol.2006.03.003DOI Listing
May 2006

[Congenital nephrogenic diabetes insipidus. A four-month-old girl with delayed psychomotor development].

Ugeskr Laeger 2005 Apr;167(16):1759-61

Arhus Universitetshospital, Skejby Sygehus, Børneafdeling A.

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April 2005

Autosomal dominant familial neurohypophyseal diabetes insipidus.

APMIS Suppl 2003 (109):92-5

Department of Pediatrics, Aarhus University Hospital, Skejby Sygehus, Brendstrupgaardsvej, DK-8200 Aarhus N, Denmark.

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August 2003