Landmarks in the Evolution of (t)-RNAs from the Origin of Life up to Their Present Role in Human Cognition

about

Landmarks in the Evolution of (t)-RNAs from the Origin of Life up to Their Present Role in Human Cognition

Item

http://www.wikidata.org/entity/Q26771990

description

2015 nî lūn-bûn

@nan

2015 թուականին հրատարակուած գիտական յօդուած

@hyw

2015 թվականին հրատարակված գիտական հոդված

@hy

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

name

Landmarks in the Evolution of ...... resent Role in Human Cognition

@ast

Landmarks in the Evolution of ...... resent Role in Human Cognition

@en

Landmarks in the Evolution of ...... resent Role in Human Cognition

@nl

type

Item

label

Landmarks in the Evolution of ...... resent Role in Human Cognition

@ast

Landmarks in the Evolution of ...... resent Role in Human Cognition

@en

Landmarks in the Evolution of ...... resent Role in Human Cognition

@nl

prefLabel

Landmarks in the Evolution of ...... resent Role in Human Cognition

@ast

Landmarks in the Evolution of ...... resent Role in Human Cognition

@en

Landmarks in the Evolution of ...... resent Role in Human Cognition

@nl

P1476

Landmarks in the Evolution of ...... resent Role in Human Cognition

@en

P2093

Andreas Kuss

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

Darko Balke

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

P2860

An integrated encyclopedia of DNA elements in the human genome

Origin of life: The RNA world

The X-linked mental retardation gene SMCX/JARID1C defines a family of histone H3 lysine 4 demethylases

Methylation of tRNAAsp by the DNA methyltransferase homolog Dnmt2

Identification of human tRNA:m5C methyltransferase catalysing intron-dependent m5C formation in the first position of the anticodon of the pre-tRNA Leu (CAA)

Topology of the human and mouse m6A RNA methylomes revealed by m6A-seq

Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation.

Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation.

MRM2 encodes a novel yeast mitochondrial 21S rRNA methyltransferase.

Dnmt2 is not required for de novo and maintenance methylation of viral DNA in embryonic stem cells

P304

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

P31

scholarly article

P356

10.3390/LIFE6010001

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

P407

English

P433

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

P478

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

P50

Sabine Müller

P577

2015-12-23T00:00:00Z

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

P5875

288020344

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

P698

26703740

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

P932

4810232

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