Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene - Wikidata - awgldk - TriplyDB

Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene

Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene

http://www.wikidata.org/entity/Q24555185

about

Gene losses during human origins Mobile DNA and the TE-Thrust hypothesis: supporting evidence from the primates Sequencing the chimpanzee genome: insights into human evolution and disease Inactivation of CMP-N-acetylneuraminic acid hydroxylase occurred prior to brain expansion during human evolution Fixation of the human-specific CMP-N-acetylneuraminic acid hydroxylase pseudogene and implications of haplotype diversity for human evolution Colloquium paper: uniquely human evolution of sialic acid genetics and biology Reconstructing phylogenies and phenotypes: a molecular view of human evolution Analysis of the human Alu Ye lineage Modeling the amplification dynamics of human Alu retrotransposons.Sialic acids as link to Japanese scientists Gut microbiota elicits a protective immune response against malaria transmission Oxidative stress and ROS metabolism via down-regulation of sirtuin 3 expression in Cmah-null mice affect hearing loss Gene expression and pathway analysis of effects of the CMAH deactivation on mouse lung, kidney and heart.Ancient human sialic acid variant restricts an emerging zoonotic malaria parasite Loss of gene function and evolution of human phenotypes Genetic basis for the lack of N-glycolylneuraminic acid expression in human tissues and its implication to human evolution LINE-1 elements in structural variation and disease Transposable element insertions have strongly affected human evolution INDELSCAN: a web server for comparative identification of species-specific and non-species-specific insertion/deletion events Alu-mediated 100-kb deletion in the primate genome: the loss of the agouti signaling protein gene in the lesser apes CMP-Neu5Ac Hydroxylase Null Mice as a Model for Studying Metabolic Disorders Caused by the Evolutionary Loss of Neu5Gc in Humans.MicroRNA dysregulation in liver and pancreas of CMP-Neu5Ac hydroxylase null mice disrupts insulin/PI3K-AKT signaling Racotumomab: an anti-idiotype vaccine related to N-glycolyl-containing gangliosides - preclinical and clinical data Why Is N-Glycolylneuraminic Acid Rare in the Vertebrate Brain?RISCI--Repeat Induced Sequence Changes Identifier: a comprehensive, comparative genomics-based, in silico subtractive hybridization pipeline to identify repeat induced sequence changes in closely related genomes Multiple fates of L1 retrotransposition intermediates in cultured human cells.NGcGM3 ganglioside: a privileged target for cancer vaccines Interaction of platelet endothelial cell adhesion molecule (PECAM) with α2,6-sialylated glycan regulates its cell surface residency and anti-apoptotic role.Rescuing Alu: recovery of new inserts shows LINE-1 preserves Alu activity through A-tail expansion Impact of transposable elements on the evolution of mammalian gene regulation.Human genomic deletions mediated by recombination between Alu elements.A human-specific mutation limits nonhuman primate efficacy in preclinical xenotransplantation studies.Species-specific exon loss in human transcriptomes Duplication, coclustering, and selection of human Alu retrotransposons Metabolism of vertebrate amino sugars with N-glycolyl groups: mechanisms underlying gastrointestinal incorporation of the non-human sialic acid xeno-autoantigen N-glycolylneuraminic acid.Reverse transcription in genome evolution.The glycans of stem cells.Molecular characterization of the pericentric inversion that causes differences between chimpanzee chromosome 19 and human chromosome 17 Linear decay of retrotransposon antisense bias across genes is contingent upon tissue specificity.Evidence for a novel human-specific xeno-auto-antibody response against vascular endothelium.

P2860

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P2860

Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene

http://www.wikidata.org/entity/Q24555185

description

2001 nî lūn-bûn

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2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2001 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2001年の論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年论文

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name

Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene

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Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene

@en

Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene

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type

label

Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene

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Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene

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Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene

@nl

prefLabel

Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene

@ast

Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene

@en

Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene

@en

P2093

Gagneux P

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

Hayakawa T

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Takahata N

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Varki A

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P2860

Initial sequencing and analysis of the human genome

Molecular phylogeny of the hominoids: inferences from multiple independent DNA sequence data sets

A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence

Genomic divergences between humans and other hominoids and the effective population size of the common ancestor of humans and chimpanzees.

The consensus sequence of a major Alu subfamily contains a functional retinoic acid response element

The neighbor-joining method: a new method for reconstructing phylogenetic trees

Human L1 retrotransposon encodes a conserved endonuclease required for retrotransposition

The DNA sequence of human chromosome 22

The DNA sequence of human chromosome 21

Human type I hair keratin pseudogene phihHaA has functional orthologs in the chimpanzee and gorilla: evidence for recent inactivation of the human gene after the Pan-Homo divergence

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11399-11404

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10.1073/PNAS.191268198

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98

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