(Q39463718)

12 September 2017

title

Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia (English)

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12 September 2017

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B Alexandrov

11

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Bharti Morar

B Morar

13

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Stuart Macgregor

S MacGregor

28

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Aleksandra Filipovska

A Filipovska

15

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Alan R. Bishop

17

A R Bishop

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12 September 2017

Cynthia Shannon Weickert

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C S Weickert

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12 September 2017

A Jablensky

1

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12 September 2017

D Angelicheva

2

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M Cruickshank

4

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D N Azmanov

5

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A McRae

7

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K W Carter

9

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D Chandler

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A Usheva

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P L Verbrugghe

14

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K Ø Rasmussen

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M Dragovic

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M Phillips

21

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J Badcock

22

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E Bramon-Bosch

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O P Almeida

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L Flicker

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L Kalaydjieva

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12 September 2017

language of work or name

English

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publication date

4 October 2011

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12 September 2017

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12 September 2017

volume

17

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12 September 2017

issue

12

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12 September 2017

page(s)

1328-1339

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https://scigraph.springernature.com/pub.10.1038/mp.2011.129

12 September 2017

exact match

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cites work

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Systemic hypotheses for generalized cognitive deficits in schizophrenia: a new take on an old problem

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Mathematical typology: a grade of membership technique for obtaining disease definition

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Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficit

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Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

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Perturbation in mitochondrial network dynamics and in complex I dependent cellular respiration in schizophrenia

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SNPExpress: integrated visualization of genome-wide genotypes, copy numbers and gene expression levels

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Transcriptome analysis of male-female differences in prefrontal cortical development.

21 January 2018

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SimHap GUI: an intuitive graphical user interface for genetic association analysis

21 January 2018

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A nonlinear dynamic model of DNA with a sequence-dependent stacking term

21 January 2018

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DNA dynamics play a role as a basal transcription factor in the positioning and regulation of gene transcription initiation

21 January 2018

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Toward a detailed description of the thermally induced dynamics of the core promoter

21 January 2018

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The joint WAIS-III and WMS-III factor structure: development and cross-validation of a six-factor model of cognitive functioning

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Aminoacyl tRNA synthetases and their connections to disease

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The role of aminoacyl-tRNA synthetases in genetic diseases

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The Nfs1 interacting protein Isd11 has an essential role in Fe/S cluster biogenesis in mitochondria

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Essential role of Isd11 in mitochondrial iron-sulfur cluster synthesis on Isu scaffold proteins

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Function and biogenesis of iron-sulphur proteins

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Human frataxin is an allosteric switch that activates the Fe-S cluster biosynthetic complex

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Verbal and visual memory: characterizing the clinical and intermediate phenotype in schizophrenia

21 January 2018

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Dominant mutations in the tyrosyl-tRNA synthetase gene recapitulate in Drosophila features of human Charcot-Marie-Tooth neuropathy

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21 January 2018

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Splice mutation in the iron-sulfur cluster scaffold protein ISCU causes myopathy with exercise intolerance

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The pathogenesis of Friedreich ataxia and the structure and function of frataxin

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Understanding the molecular mechanisms of Friedreich's ataxia to develop therapeutic approaches.

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Mitochondrial frataxin interacts with ISD11 of the NFS1/ISCU complex and multiple mitochondrial chaperones.

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Human ISD11 is essential for both iron-sulfur cluster assembly and maintenance of normal cellular iron homeostasis

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Mitochondrial dysfunction in schizophrenia: evidence for compromised brain metabolism and oxidative stress

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2011.129

Alterations in oligodendrocyte proteins, calcium homeostasis and new potential markers in schizophrenia anterior temporal lobe are revealed by shotgun proteome analysis

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https://api.crossref.org/works/10.1038%2FMP.2011.129

The role of energy metabolism dysfunction and oxidative stress in schizophrenia revealed by proteomics

21 January 2018

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Hypofrontality in unmedicated schizophrenia patients studied with PET during performance of a serial verbal learning task

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7 January 2021

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Myopathy with lactic acidosis is linked to chromosome 12q23.3-24.11 and caused by an intron mutation in the ISCU gene resulting in a splicing defect

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https://api.crossref.org/works/10.1038%2FMP.2011.129

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Reduced phosphodiesters and high-energy phosphates in the frontal lobe of schizophrenic patients: a (31)P chemical shift spectroscopic-imaging study

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7 January 2021

Identifiers

DOI

10.1038/MP.2011.129

1 reference

Dimensions Publication ID

12 September 2017

1025562394

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Fatcat ID

release_ucodlmoplrauhd7v2g7v5lmiwy

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1 reference