Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution - sprookjes - yvandenbroek - TriplyDB

Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution

Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution

http://www.wikidata.org/entity/Q21092496

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Krüppel-like factors: three fingers in control Critical evaluation of imprinted gene expression by RNA-Seq: a new perspective New role for Kruppel-like factor 14 as a transcriptional activator involved in the generation of signaling lipids Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis Mammalian Krüppel-like factors in health and diseases New common variants affecting susceptibility to basal cell carcinoma Epigenetic principles and mechanisms underlying nervous system functions in health and disease A new family of predicted Krüppel-like factor genes and pseudogenes in placental mammals RNA-based gene duplication: mechanistic and evolutionary insights The emergence of human-evolutionary medical genomics Novel retrotransposed imprinted locus identified at human 6p25 Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7.The Missing lnc(RNA) between the pancreatic β-cell and diabetes The evolution of genomic imprinting: theories, predictions and empirical tests.Different yet similar: evolution of imprinting in flowering plants and mammals.A survey for novel imprinted genes in the mouse placenta by mRNA-seq The role of imprinted genes in fetal growth abnormalities.Tissue-specific alternative polyadenylation at the imprinted gene Mest regulates allelic usage at Copg2 KLF/SP Transcription Factor Family Evolution: Expansion, Diversification, and Innovation in Eukaryotes.DLX5 expression is monoallelic and Dlx5 is up-regulated in the Mecp2-null frontal cortex.Molecular correlates of fat mass expansion in C57BL/6J mice after short-term exposure to dietary fat.The human imprintome: regulatory mechanisms, methods of ascertainment, and roles in disease susceptibility Parental origin of sequence variants associated with complex diseases Investigation of parent-of-origin effect in comitant strabismus using MOD score analysis Age-related epigenetic drift in the pathogenesis of MDS and AML.Retrotransposition as a source of new promoters.Krüppel-like factors in mammalian stem cells and development.Genetics of Type 2 Diabetes: It Matters From Which Parent We Inherit the Risk.Non-linear patterns in age-related DNA methylation may reflect CD4+ T cell differentiation.Association of the KLF14 rs4731702 SNP and serum lipid levels in the Guangxi Mulao and Han populations.Genome-wide open chromatin regions and their effects on the regulation of silk protein genes in Bombyx mori Conducting the metabolic syndrome orchestra.The KLF14 transcription factor regulates hepatic gluconeogenesis in mice.Population diversity and adaptive evolution in keratinization genes: impact of environment in shaping skin phenotypes.Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition.Krüppel-like factors: Crippling and un-crippling metabolic pathways.

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Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution

http://www.wikidata.org/entity/Q21092496

description

2007 nî lūn-bûn

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2007 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2007 թվականի մայիսին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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Identification of the imprinte ...... specific accelerated evolution

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Identification of the imprinte ...... specific accelerated evolution

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Identification of the imprinte ...... specific accelerated evolution

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Identification of the imprinte ...... specific accelerated evolution

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Identification of the imprinte ...... specific accelerated evolution

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Identification of the imprinte ...... specific accelerated evolution

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Charles Lee

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George H Perry

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Gudrun E Moore

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Hiroyuki Sasaki

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Kazuhiko Nakabayashi

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Keiko Kobayashi

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Layla Parker-Katiraee

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Makiko Meguro-Horike

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Sayeda N Abu-Amero

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Detecting recent positive selection in the human genome from haplotype structure

Identification of microcephalin, a protein implicated in determining the size of the human brain

Human PEG1/MEST, an imprinted gene on chromosome 7

Statistical method for testing the neutral mutation hypothesis by DNA polymorphism

Statistical tests of neutrality of mutations.

Allele-specific histone lysine methylation marks regulatory regions at imprinted mouse genes.

Hitchhiking under positive Darwinian selection

A conserved alpha-helical motif mediates the interaction of Sp1-like transcriptional repressors with the corepressor mSin3A

Human chromosome 7: DNA sequence and biology

Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia

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10.1371/JOURNAL.PGEN.0030065

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Masahiro Kaneda

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