| case report | Q2782326 |
| scholarly article | Q13442814 |
| P2093 | author name string | Jacek Majewski | |
| P2860 | cites work | The human genome browser at UCSC | Q24672361 |
| Evolution of synonymous codon usage in metazoans | Q28214982 | ||
| Asymmetric substitution patterns in the two DNA strands of bacteria | Q29618276 | ||
| HugeIndex: a database with visualization tools for high-density oligonucleotide array data from normal human tissues | Q30667277 | ||
| A set of 840 mouse oocyte genes with well-matched human homologues | Q30991002 | ||
| Asymmetric substitution patterns: a review of possible underlying mutational or selective mechanisms | Q33778360 | ||
| Illegitimate transcription: transcription of any gene in any cell type | Q33849869 | ||
| A compendium of gene expression in normal human tissues | Q34107680 | ||
| Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genes | Q34386556 | ||
| Distribution and characterization of regulatory elements in the human genome | Q35807015 | ||
| Transcription-induced mutations: increase in C to T mutations in the nontranscribed strand during transcription in Escherichia coli | Q35937258 | ||
| Transcription-associated mutational asymmetry in mammalian evolution | Q44337576 | ||
| Preferential repair of DNA damage on the transcribed strand of the human metallothionein genes requires RNA polymerase II. | Q46636730 | ||
| Intra-strand biases in bacteriophage T4 genome. | Q52173061 | ||
| Intrastrand parity rules of DNA base composition and usage biases of synonymous codons. | Q52209838 | ||
| Inequality in mutation rates of the two strands of DNA. | Q52849056 | ||
| Wide variations in neighbor-dependent substitution rates. | Q52883096 | ||
| Patterns of nucleotide substitution in pseudogenes and functional genes | Q59204189 | ||
| Strand symmetry of mutation rates in theβ-globin region | Q67828695 | ||
| Neighboring base effects on substitution rates in pseudogenes | Q68690598 | ||
| Strand asymmetry in human mitochondrial DNA mutations | Q72371606 | ||
| Structure and function of nucleic acids as cell constituents | Q75888908 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 688-692 | |
| P577 | publication date | 2003-07-24 | |
| P1433 | published in | American Journal of Human Genetics | Q4744249 |
| P1476 | title | Dependence of mutational asymmetry on gene-expression levels in the human genome | |
| P478 | volume | 73 |
| Q25255969 | A third approach to gene prediction suggests thousands of additional human transcribed regions |
| Q33963920 | Abasic sites in the transcribed strand of yeast DNA are removed by transcription-coupled nucleotide excision repair |
| Q34267941 | Abrupt onset of mutations in a developmentally regulated gene during terminal differentiation of post-mitotic photoreceptor neurons in mice |
| Q53188446 | Are Synonymous Sites in Primates and Rodents Functionally Constrained? |
| Q43104534 | Characterization of intron loss events in mammals |
| Q24796884 | Comprehensive analysis of the base composition around the transcription start site in Metazoa |
| Q39642475 | Conservation of neutral substitution rate and substitutional asymmetries in mammalian genes |
| Q37319267 | Distinct contributions of replication and transcription to mutation rate variation of human genomes |
| Q53060381 | Distributions of selectively constrained sites and deleterious mutation rates in the hominid and murid genomes. |
| Q37508064 | Divergent transcription: a driving force for new gene origination? |
| Q35171468 | Does the genetic code have a eukaryotic origin? |
| Q24814018 | Evidence for selection on synonymous mutations affecting stability of mRNA secondary structure in mammals |
| Q33534685 | Evidence of genetic instability in tumors and normal nearby tissues |
| Q33633422 | Evidence that replication-associated mutation alone does not explain between-chromosome differences in substitution rates |
| Q24805194 | Evolutionary conservation and selection of human disease gene orthologs in the rat and mouse genomes |
| Q53241757 | Gene expression, nucleotide composition and codon usage bias of genes associated with human Y chromosome. |
| Q30481457 | Genomic DNA from animals shows contrasting strand bias in large and small subsequences |
| Q34239161 | Genomic signatures of germline gene expression |
| Q34485607 | Hearing silence: non-neutral evolution at synonymous sites in mammals |
| Q61761498 | Intron length and accelerated 3′ gene evolution |
| Q52710198 | Intronic AT Skew is a Defendable Proxy for Germline Transcription but does not Predict Crossing-Over or Protein Evolution Rates in Drosophila melanogaster |
| Q40062641 | Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distribution |
| Q33307007 | Large-scale genomic 2D visualization reveals extensive CG-AT skew correlation in bird genomes. |
| Q39273323 | Linking the DNA strand asymmetry to the spatio-temporal replication program. I. About the role of the replication fork polarity in genome evolution |
| Q33564395 | Mutation patterns in cancer genomes |
| Q41835481 | Mutational pattern and frequency of induced nucleotide changes in mouse ENU mutagenesis |
| Q40744789 | Occurrence and consequences of coding sequence insertions and deletions in Mammalian genomes |
| Q34114418 | Opposite GC skews at the 5' and 3' ends of genes in unicellular fungi |
| Q33258810 | Phylogenetic reconstruction of orthology, paralogy, and conserved synteny for dog and human |
| Q36766892 | Programmed genetic instability: a tumor-permissive mechanism for maintaining the evolvability of higher species through methylation-dependent mutation of DNA repair genes in the male germ line |
| Q35714487 | Replication-Associated Mutational Pressure (RMP) Governs Strand-Biased Compositional Asymmetry (SCA) and Gene Organization in Animal Mitochondrial Genomes |
| Q39582800 | Replication-associated mutational asymmetry in the human genome |
| Q34645301 | Selective and mutational patterns associated with gene expression in humans: influences on synonymous composition and intron presence |
| Q42173311 | Strand bias in complementary single-nucleotide polymorphisms of transcribed human sequences: evidence for functional effects of synonymous polymorphisms |
| Q33314636 | Strand bias structure in mouse DNA gives a glimpse of how chromatin structure affects gene expression |
| Q33281613 | Strand compositional asymmetries in vertebrate large genes |
| Q34151543 | Synonymous but not the same: the causes and consequences of codon bias |
| Q37319931 | The pendulum model for genome compositional dynamics: from the four nucleotides to the twenty amino acids |
| Q36268130 | The relation of codon bias to tissue-specific gene expression in Arabidopsis thaliana. |
| Q37319400 | The transcript-centric mutations in human genomes |
| Q36036444 | Transcription as a source of genome instability |
| Q36804846 | Transcription induces strand-specific mutations at the 5' end of human genes |
| Q93216537 | Transcription-coupled repair and mismatch repair contribute towards preserving genome integrity at mononucleotide repeat tracts |
| Q37347927 | Understanding what determines the frequency and pattern of human germline mutations |
| Q42692889 | Unexpected functional similarities between gatekeeper tumour suppressor genes and proto-oncogenes revealed by systems biology |
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