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A case of bipolar I disorder with a loss‐of‐function variant of schizophrenia risk gene SETD1A: possible expansion of the relevant clinical spectrum supported by a meta‐analysis

Psychiatry and clinical neurosciences, 2024-06, Vol.78 (6), p.374-375

2024

Volltextzugriff (PDF)

Systematic analysis of exonic germline and postzygotic de novo mutations in bipolar disorder

Nature communications, 2021-06, Vol.12 (1), p.3750-3750, Article 3750

2021

Volltextzugriff (PDF)

Loss of function mutations in ATP2A2 and psychoses: A case report and literature survey

Psychiatry and clinical neurosciences, 2016-08, Vol.70 (8), p.342-350

2016

Volltextzugriff (PDF)

Exome sequencing in the knockin mice generated using the CRISPR/Cas system

Scientific reports, 2016-10, Vol.6 (1), p.34703, Article 34703

2016

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Identification of mitochondrial DNA polymorphisms that alter mitochondrial matrix pH and intracellular calcium dynamics

PLoS genetics, 2006-08, Vol.2 (8), p.e128-e128

2006

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Proteomic analysis of lymphoblastoid cells derived from monozygotic twins discordant for bipolar disorder: a preliminary study

PloS one, 2013-02, Vol.8 (2), p.e53855

2013

Volltextzugriff (PDF)

Suppression of inflammatory and neuropathic pain symptoms in mice lacking the N-type Ca2+ channel

The EMBO journal, 2001-05, Vol.20 (10), p.2349-2356

2001

Volltextzugriff (PDF)

Deep exome sequencing identifies enrichment of deleterious mosaic variants in neurodevelopmental disorder genes and mitochondrial tRNA regions in bipolar disorder

Molecular psychiatry, 2023-10, Vol.28 (10), p.4294-4306

2023

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Topologically associating domains define the impact of de novo promoter variants on autism spectrum disorder risk

Cell genomics, 2024-02, Vol.4 (2), p.100488-100488, Article 100488

2024

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Mitochondrial DNA haplogroup analysis in patients with bipolar disorder

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2009-03, Vol.150B (2), p.243-247

2009

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Mitochondrial DNA sequence analysis of patients with ‘atypical psychosis’

Psychiatry and clinical neurosciences, 2005-08, Vol.59 (4), p.497-503

2005

Volltextzugriff (PDF)

Intact LTP and Fear Memory but Impaired Spatial Memory in Mice Lacking Cav2.3 (αIE) Channel

Biochemical and biophysical research communications, 2001-03, Vol.282 (1), p.242-248

2001

Volltextzugriff (PDF)

A 3-bp deletion of mitochondrial DNA tRNALys observed in lymphoblastoid cells

Journal of human genetics, 2009-10, Vol.54 (10), p.612-613

2009

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Mitochondrial DNA-dependent effects of valproate on mitochondrial calcium levels in transmitochondrial cybrids

The international journal of neuropsychopharmacology, 2008-02, Vol.11 (1), p.71-78

2008

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Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder in Japanese and the National Institute of Mental Health pedigrees

Biological psychiatry (1969), 2004-10, Vol.56 (7), p.483-489

2004

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Relationships between mitochondrial DNA subhaplogroups and intracellular calcium dynamics

Mitochondrion, 2008-03, Vol.8 (2), p.164-169

2008

Volltextzugriff (PDF)

A 3-bp deletion of mitochondrial DNA tRNA observed in lymphoblastoid cells

Journal of human genetics, 2009-10, Vol.54 (10), p.612-613

2009

Volltextzugriff (PDF)

Altered cerebellar function in mice lacking CaV2.3 Ca2+ channel

Biochemical and biophysical research communications, 2006-06, Vol.344 (3), p.920-925

2006

Volltextzugriff (PDF)

Altered pain responses in mice lacking α1E subunit of the voltage-dependent Ca2+ channel

Proceedings of the National Academy of Sciences - PNAS, 2000-05, Vol.97 (11), p.6132-6137

2000

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Altered cerebellar function in mice lacking CaV2.3 Ca2+ channel

Biochemical and biophysical research communications, 2006-06, Vol.344 (3), p.920-925

2006

Volltextzugriff (PDF)

Altered cerebellar function in mice lacking Ca V2.3 Ca 2+ channel

Biochemical and biophysical research communications, 2006, Vol.344 (3), p.920-925

2006

Volltextzugriff (PDF)

A case of bipolar I disorder with a loss-of-function variant of schizophrenia risk gene SETD1A: possible expansion of the relevant clinical spectrum supported by a meta-analysis

Psychiatry and clinical neurosciences, 2024, Vol.78 (6), p.374-375

2024

Volltextzugriff (PDF)

Suppression of inflammatory and neuropathic pain symptoms in mice lacking the N-type Ca 2+ channel

The EMBO journal, 2001-05, Vol.20 (10), p.2349-2356

2001

Volltextzugriff (PDF)

Intact LTP and Fear Memory but Impaired Spatial Memory in Mice Lacking Ca sub(v)2.3 ( alpha sub(IE)) Channel

Biochemical and biophysical research communications, 2001-03, Vol.282 (1), p.242-248

2001

Volltextzugriff (PDF)

Regular Article: Mitochondrial DNA sequence analysis of patients with 'atypical psychosis'

Psychiatry and clinical neurosciences, 2005-08, Vol.59 (4), p.497-503

2005

Volltextzugriff (PDF)

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A case of bipolar I disorder with a loss‐of‐function variant of schizophrenia risk gene SETD1A: possible expansion of the relevant clinical spectrum supported by a meta‐analysis

Systematic analysis of exonic germline and postzygotic de novo mutations in bipolar disorder

Loss of function mutations in ATP2A2 and psychoses: A case report and literature survey

Exome sequencing in the knockin mice generated using the CRISPR/Cas system

Identification of mitochondrial DNA polymorphisms that alter mitochondrial matrix pH and intracellular calcium dynamics

Proteomic analysis of lymphoblastoid cells derived from monozygotic twins discordant for bipolar disorder: a preliminary study

Suppression of inflammatory and neuropathic pain symptoms in mice lacking the N-type Ca2+ channel

Deep exome sequencing identifies enrichment of deleterious mosaic variants in neurodevelopmental disorder genes and mitochondrial tRNA regions in bipolar disorder

Topologically associating domains define the impact of de novo promoter variants on autism spectrum disorder risk

Mitochondrial DNA haplogroup analysis in patients with bipolar disorder

Mitochondrial DNA sequence analysis of patients with ‘atypical psychosis’

Intact LTP and Fear Memory but Impaired Spatial Memory in Mice Lacking Cav2.3 (αIE) Channel

A 3-bp deletion of mitochondrial DNA tRNALys observed in lymphoblastoid cells

Mitochondrial DNA-dependent effects of valproate on mitochondrial calcium levels in transmitochondrial cybrids

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder in Japanese and the National Institute of Mental Health pedigrees

Relationships between mitochondrial DNA subhaplogroups and intracellular calcium dynamics

A 3-bp deletion of mitochondrial DNA tRNA observed in lymphoblastoid cells

Altered cerebellar function in mice lacking CaV2.3 Ca2+ channel

Altered pain responses in mice lacking α1E subunit of the voltage-dependent Ca2+ channel

Altered cerebellar function in mice lacking CaV2.3 Ca2+ channel

Altered cerebellar function in mice lacking Ca V2.3 Ca 2+ channel

A case of bipolar I disorder with a loss-of-function variant of schizophrenia risk gene SETD1A: possible expansion of the relevant clinical spectrum supported by a meta-analysis

Suppression of inflammatory and neuropathic pain symptoms in mice lacking the N-type Ca 2+ channel

Intact LTP and Fear Memory but Impaired Spatial Memory in Mice Lacking Ca sub(v)2.3 ( alpha sub(IE)) Channel

Regular Article: Mitochondrial DNA sequence analysis of patients with 'atypical psychosis'

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