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

BMC genomics, 2015-07, Vol.16 (1), p.548-548, Article 548

2015

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Leptin regulation of Hsp60 impacts hypothalamic insulin signaling

The Journal of clinical investigation, 2013-11, Vol.123 (11), p.4667-4680

2013

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Protein misfolding and human disease

Annual review of genomics and human genetics, 2006-01, Vol.7 (1), p.103-124

2006

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DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele

PloS one, 2017-01, Vol.12 (1), p.e0170121-e0170121

2017

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

Neurobiology of disease, 2013-06, Vol.54, p.12-23

2013

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Inactivation of the hereditary spastic paraplegia-associated Hspd1 gene encoding the Hsp60 chaperone results in early embryonic lethality in mice

Cell stress & chaperones, 2010-11, Vol.15 (6), p.851-863

2010

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A Novel Synonymous Variant in the AVP Gene Associated with Autosomal Dominant Familial Neurohypophyseal Diabetes Insipidus Causes Partial RNA Missplicing

Neuroendocrinology, 2018-01, Vol.107 (2), p.167-180

2018

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Modeling the cooperativity of schizophrenia risk genes

Nature genetics, 2019-10, Vol.51 (10), p.1434-1436

2019

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Induced pluripotent stem cells derived from a patient with autosomal dominant familial neurohypophyseal diabetes insipidus caused by a variant in the AVP gene

Stem cell research, 2017-03, Vol.19, p.37-42

2017

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Partial nephrogenic diabetes insipidus caused by a novel AQP2 variation impairing trafficking of the aquaporin-2 water channel

BMC nephrology, 2015-12, Vol.16 (208), p.217-217, Article 217

2015

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Diverse vasopressin V2 receptor functionality underlying partial congenital nephrogenic diabetes insipidus

American journal of physiology. Renal physiology, 2009-12, Vol.297 (6), p.F1518-F1525

2009

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

Molecular neurobiology, 2018-01, Vol.55 (1), p.567-582

2018

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Partial nephrogenic diabetes insipidus caused by a novel mutation in the AVPR2 gene

Clinical endocrinology (Oxford), 2008-03, Vol.68 (3), p.395-403

2008

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The Novel Ser18del AVP Variant Causes Inherited Neurohypophyseal Diabetes Insipidus by Mechanisms Shared with Other Signal Peptide Variants

Neuroendocrinology, 2018-02, Vol.106 (2), p.167-186

2018

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Mitochondrial proteomics on human fibroblasts for identification of metabolic imbalance and cellular stress

Proteome science, 2009-05, Vol.7 (20), p.20-20

2009

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Brain volumetric alterations accompanied with loss of striatal medium-sized spiny neurons and cortical parvalbumin expressing interneurons in Brd1 +/- mice

Scientific reports, 2018-11, Vol.8 (1), p.16486-12, Article 16486

2018

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

Neurobiology of learning and memory, 2017-05, Vol.141, p.44-52

2017

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

Microvascular research, 2019-03, Vol.122, p.131-135

2019

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Familial Neurohypophyseal Diabetes Insipidus—An Update

Seminars in nephrology, 2006-05, Vol.26 (3), p.209-223

2006

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Reduced Brd1 expression leads to reversible depression-like behaviors and gene-expression changes in female mice

Translational psychiatry, 2020-07, Vol.10 (1), p.239, Article 239

2020

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

Journal of molecular neuroscience, 2017-06, Vol.62 (2), p.142-153

2017

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

Scandinavian journal of clinical and laboratory investigation, 2018-02, Vol.78 (1-2), p.114-119

2018

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Identification of genetic loci associated with nocturnal enuresis: a genome-wide association study

The lancet child & adolescent health, 2021-03, Vol.5 (3), p.201-209

2021

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Identification of the BRD1 interaction network and its impact on mental disorder risk

Genome medicine, 2016-05, Vol.8 (1), p.53-53, Article 53

2016

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

Clinical endocrinology (Oxford), 2012-10, Vol.77 (4), p.586-592

2012

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

Leptin regulation of Hsp60 impacts hypothalamic insulin signaling

Protein misfolding and human disease

DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele

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

Inactivation of the hereditary spastic paraplegia-associated Hspd1 gene encoding the Hsp60 chaperone results in early embryonic lethality in mice

A Novel Synonymous Variant in the AVP Gene Associated with Autosomal Dominant Familial Neurohypophyseal Diabetes Insipidus Causes Partial RNA Missplicing

Modeling the cooperativity of schizophrenia risk genes

Induced pluripotent stem cells derived from a patient with autosomal dominant familial neurohypophyseal diabetes insipidus caused by a variant in the AVP gene

Partial nephrogenic diabetes insipidus caused by a novel AQP2 variation impairing trafficking of the aquaporin-2 water channel

Diverse vasopressin V2 receptor functionality underlying partial congenital nephrogenic diabetes insipidus

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

Partial nephrogenic diabetes insipidus caused by a novel mutation in the AVPR2 gene

The Novel Ser18del AVP Variant Causes Inherited Neurohypophyseal Diabetes Insipidus by Mechanisms Shared with Other Signal Peptide Variants

Mitochondrial proteomics on human fibroblasts for identification of metabolic imbalance and cellular stress

Brain volumetric alterations accompanied with loss of striatal medium-sized spiny neurons and cortical parvalbumin expressing interneurons in Brd1 +/- mice

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

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

Familial Neurohypophyseal Diabetes Insipidus—An Update

Reduced Brd1 expression leads to reversible depression-like behaviors and gene-expression changes in female mice

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

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

Identification of genetic loci associated with nocturnal enuresis: a genome-wide association study

Identification of the BRD1 interaction network and its impact on mental disorder risk

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

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