Incomplete penetrance of NRXN1 deletions in families with schizophrenia.

Incomplete penetrance of NRXN1 deletions in families with schizophrenia.

Item
http://www.wikidata.org/entity/Q45797750
Identification of aberrant gene expression associated with aberrant promoter methylation in primordial germ cells between E13 and E16 rat F3 generation vinclozolin lineageTet3 regulates synaptic transmission and homeostatic plasticity via DNA oxidation and repairOne CNV Discordance in NRXN1 Observed Upon Genome-wide Screening in 38 Pairs of Adult Healthy Monozygotic Twins.Neurexin 1 (NRXN1) splice isoform expression during human neocortical development and aging.Genetic Relationship between Schizophrenia and Nicotine Dependence.When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations.Altering the course of schizophrenia: progress and perspectives.Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.Explaining the variable penetrance of CNVs: Parental intelligence modulates expression of intellectual impairment caused by the 22q11.2 deletion.Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1.Synaptic Neurexin Complexes: A Molecular Code for the Logic of Neural Circuits.Association study between the neurexin-1 gene and tardive dyskinesia.Convergent roles of de novo mutations and common variants in schizophrenia in tissue-specific and spatiotemporal co-expression network.
P2860

Incomplete penetrance of NRXN1 deletions in families with schizophrenia.

Item
http://www.wikidata.org/entity/Q45797750
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh-hant
name
Incomplete penetrance of NRXN1 deletions in families with schizophrenia.
@en
Incomplete penetrance of NRXN1 deletions in families with schizophrenia.
@nl
type
label
Incomplete penetrance of NRXN1 deletions in families with schizophrenia.
@en
Incomplete penetrance of NRXN1 deletions in families with schizophrenia.
@nl
prefLabel
Incomplete penetrance of NRXN1 deletions in families with schizophrenia.
@en
Incomplete penetrance of NRXN1 deletions in families with schizophrenia.
@nl
P1433
P1476
P2093
P304
P31
P356
P407
P433
P478
P50
P577
P698
P921
P356
P1433
P1476
Incomplete penetrance of NRXN1 deletions in families with schizophrenia.
@en
P2093
P304
P31
P356
10.1016/J.SCHRES.2014.02.023
P407
P433
P478
P50
P577
P698
P921