Javascript must be enabled to continue!
Analysis of DEXI/<i>Dexi</i> refines the organization of the mouse 7C and human 15q11→q13 imprinting clusters
View through CrossRef
Identification of imprinted genes in the Prader-Willi/Angelman syndrome deletion region is complicated by the presence of large flanking repeats. While inactive copies of DEXI are located within the repeats, we have now localized the active DEXI gene to 15q11→q13 outside the PWS/AS deletion and <i>Dexi</i> to mouse chromosome 16, suggesting complex evolution of this genomic region in both species.
Title: Analysis of DEXI/<i>Dexi</i> refines the organization of the mouse 7C and human 15q11→q13 imprinting clusters
Description:
Identification of imprinted genes in the Prader-Willi/Angelman syndrome deletion region is complicated by the presence of large flanking repeats.
While inactive copies of DEXI are located within the repeats, we have now localized the active DEXI gene to 15q11→q13 outside the PWS/AS deletion and <i>Dexi</i> to mouse chromosome 16, suggesting complex evolution of this genomic region in both species.
.
Related Results
Numerical Study on the Optimization of Roll-to-Roll Ultraviolet Imprint Lithography
Numerical Study on the Optimization of Roll-to-Roll Ultraviolet Imprint Lithography
Roll-to-roll ultraviolet (R2R-UV) imprinting is a low-cost and high-throughput method that includes the manufacturing of large-area functional films. However, the quality of the fi...
The Significance of Genomic Imprinting for Brain Development and Behaviour
The Significance of Genomic Imprinting for Brain Development and Behaviour
Professor Barry Keverne FRS, FMedSci – Behavioural Neuroscience, King's College, Cambridge, described how genomic imprinting provides for co-adaptation of mother and fetus, for mat...
Characterization of imprinted genes in rice reveals post-fertilization regulation and conservation at some loci of imprinting in plant species
Characterization of imprinted genes in rice reveals post-fertilization regulation and conservation at some loci of imprinting in plant species
Abstract
Genomic imprinting is an epigenetic phenomenon by which certain genes display monoallelic expression in a parent-of-origin-dependent man...
Dexi
disruption depletes gut microbial metabolites and accelerates autoimmune diabetes
Dexi
disruption depletes gut microbial metabolites and accelerates autoimmune diabetes
Abstract
Non-coding genetic variants in the CLEC16A gene on human chromosome 16p13.13 are associated with risk of autoimmune diseases, including ...
DNA methylation as an epigenetic biomarker in imprinting
disorders
DNA methylation as an epigenetic biomarker in imprinting
disorders
Epigenetic modifications control gene expression and enable the same genotype to lead
to various phenotypes, thus exhibiting extensive variability in human cells function.
DNA meth...
Efficacy and Safety of Supraciliary Dexamethasone Implantation in Patients with Macular Edema: Preliminary and Comparative Study
Efficacy and Safety of Supraciliary Dexamethasone Implantation in Patients with Macular Edema: Preliminary and Comparative Study
Abstract
Purpose
To investigate the efficacy and safety of dexamethasone implantation (DEXI) in the supraciliary (SC) region, a potential new implantation site, compared t...
Abstract 5051: RenMab Mouse: A leading platform for fully human antibody generation
Abstract 5051: RenMab Mouse: A leading platform for fully human antibody generation
Abstract
With the development of immune-oncology, therapeutic antibodies have been proven to be extraordinarily effective for cancer treatment. Conventional human an...
The psychiatric phenotype of 15q11.2-q13.3 duplications
The psychiatric phenotype of 15q11.2-q13.3 duplications
Introduction15q11.2-q13.3 region is prone to genomic rearrangements leading to both deletions and duplications. A wide spectrum of neuropsychiatric conditions, such as developmenta...

