(Q44738240)

English

Nonrandom intragenic variations in patterns of codon bias implicate a sequential interplay between transitional genetic drift and functional amino acid selection

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scholarly article

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Europe PubMed Central

PubMed publication ID

5 December 2017

Nonrandom intragenic variations in patterns of codon bias implicate a sequential interplay between transitional genetic drift and functional amino acid selection (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

1 reference

based on heuristic

inferred from title

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based on heuristic

inferred from title

Prasanna R. Kolatkar

3

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Europe PubMed Central

PubMed publication ID

5 December 2017

author name string

K Lin

1

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Europe PubMed Central

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5 December 2017

S B Tan

2

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Europe PubMed Central

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5 December 2017

R J Epstein

4

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Europe PubMed Central

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5 December 2017

publication date

1 November 2003

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Europe PubMed Central

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5 December 2017

Journal of Molecular Evolution

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Europe PubMed Central

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5 December 2017

57

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Europe PubMed Central

PubMed publication ID

5 December 2017

5

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Europe PubMed Central

PubMed publication ID

5 December 2017

538-545

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Europe PubMed Central

PubMed publication ID

5 December 2017

https://scigraph.springernature.com/pub.10.1007/s00239-003-2507-5

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The human genome: organization and evolutionary history

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

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Methylation status of the 3rd exon of the c-MYC oncogene in B-cell malignancies

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https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylation of coding region alone inhibits gene expression in plant protoplasts

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https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

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Synonymous codon usage in Drosophila melanogaster: natural selection and translational accuracy.

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https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

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DNA methylation represses transcription in vivo.

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https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

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Methylation similarities of two CpG sites within exon 5 of human H19 between normal tissues and testicular germ cell tumours of adolescents and adults, without correlation with allelic and total level of expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

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Altered chromatin structure associated with methylation-induced gene silencing in cancer cells: correlation of accessibility, methylation, MeCP2 binding and acetylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

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High fidelity of guanine translation in a plasmid-directed in vitro system.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

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Carcinogen-induced de novo methylation in c-myc exon I.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

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Local DNA demethylation in vertebrates: how could it be performed and targeted?

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https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

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A method for detecting positive selection at single amino acid sites

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Do essential genes evolve slowly?

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

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Amino acid and nucleotide recurrence in aligned sequences: synonymous substitution patterns in association with global and local base compositions

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

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Disease-causing mutations in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Site and sequence specific DNA methylation in the neurofibromatosis (NF1) gene includes C5839T: the site of the recurrent substitution mutation in exon 31

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytosine methylation and the fate of CpG dinucleotides in vertebrate genomes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A functional significance for codon third bases

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

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Single base-pair substitutions in pathology and evolution: two sides to the same coin.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

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Methylation of exon 2 of p16 is associated with late stage oesophageal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

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Identification and characterization of a family of mammalian methyl-CpG binding proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Significant differences between the G+C content of synonymous codons in orthologous genes and the genomic G+C content

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA methylation of coding and non-coding regions of the human H-RAS gene in normal and tumor tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylation of CpG sites in exon 2 of the bcl-2 gene occurs in colorectal carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylation of histone H3 Lys 4 in coding regions of active genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A methylation-responsive MDBP/RFX site is in the first exon of the collagen alpha2(I) promoter

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The influence of nearest neighbors on the rate and pattern of spontaneous point mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two human gene families display preferences for different nucleotides and have distinct codon usage patterns

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A model for the correlation of mutation rate with GC content and the origin of GC-rich isochores.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selective constraints, amino acid composition, and the rate of protein evolution

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detecting recent positive selection in the human genome from haplotype structure

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

5-Methylcytosine as an Endogenous Mutagen in the Human LDL Receptor and p53 Genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intragenic variation of synonymous substitution rates is caused by nonrandom mutations at methylated CpG

1 reference

https://pubmed.ncbi.nlm.nih.gov/14738312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00239-003-2507-5

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

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