Mobile Elements in the Human Genome: Implications for Disease

about

Mobile Elements in the Human Genome: Implications for Disease

Item

http://www.wikidata.org/entity/Q56992548

description

wetenschappelijk artikel

@nl

наукова стаття, опублікована в грудні 2017

@uk

name

Mobile Elements in the Human Genome: Implications for Disease

@en

Mobile Elements in the Human Genome: Implications for Disease

@nl

type

Item

label

Mobile Elements in the Human Genome: Implications for Disease

@en

Mobile Elements in the Human Genome: Implications for Disease

@nl

prefLabel

Mobile Elements in the Human Genome: Implications for Disease

@en

Mobile Elements in the Human Genome: Implications for Disease

@nl

P1476

Mobile Elements in the Human Genome: Implications for Disease

@en

P2860

Initial sequencing and analysis of the human genome

The impact of retrotransposons on human genome evolution

Structure and distribution of an Alu-type deletion mutation in Sandhoff disease

The role of transposable elements in health and diseases of the central nervous system

Molecular genetics of the LDL receptor gene in familial hypercholesterolemia

The Opitz syndrome gene Mid1 is transcribed from a human endogenous retroviral promoter

Repetitive elements may comprise over two-thirds of the human genome

A de novo Alu insertion results in neurofibromatosis type 1

DNA transposons and the evolution of eukaryotic genomes

Landscape of somatic retrotransposition in human cancers

P304

1-9

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/9780470015902.A0024377

http://www.w3.org/2001/XMLSchema#string

P50

Benoît Chénais

P577

2017-12-15T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime