Pages that link to "Q24801512"

The following pages link to Noncoding DNA, isochores and gene expression: nucleosome formation potential (Q24801512):

Displaying 32 items.

• Both selective and neutral processes drive GC content evolution in the human genome (Q24655865) (← links)
• The evolution of intron size in amniotes: a role for powered flight? (Q28714241) (← links)
• The footprint of metabolism in the organization of mammalian genomes (Q28727949) (← links)
• Assignment of isochores for all completely sequenced vertebrate genomes using a consensus (Q30482794) (← links)
• In plants, expression breadth and expression level distinctly and non-linearly correlate with gene structure (Q30492350) (← links)
• Length and GC content variability of introns among teleostean genomes in the light of the metabolic rate hypothesis (Q30585912) (← links)
• Mice and men: their promoter properties (Q33242819) (← links)
• Chromatin structure and evolution in the human genome. (Q33284151) (← links)
• Effective transcription factor binding site prediction using a combination of optimization, a genetic algorithm and discriminant analysis to capture distant interactions. (Q33311392) (← links)
• The impact of recombination on nucleotide substitutions in the human genome (Q33332585) (← links)
• ContDist: a tool for the analysis of quantitative gene and promoter properties (Q33398148) (← links)
• Relationship between amino acid composition and gene expression in the mouse genome. (Q33805379) (← links)
• Chromatin organization in sperm may be the major functional consequence of base composition variation in the human genome (Q33872269) (← links)
• Nucleosome DNA sequence structure of isochores (Q33878965) (← links)
• Tandemly repeated DNA families in the mouse genome (Q34060742) (← links)
• Implications of human genome structural heterogeneity: functionally related genes tend to reside in organizationally similar genomic regions (Q34525787) (← links)
• The small introns of antisense genes are better explained by selection for rapid transcription than by "genomic design" (Q34587115) (← links)
• 'Genome design' model and multicellular complexity: golden middle (Q35128164) (← links)
• Developmental stage related patterns of codon usage and genomic GC content: searching for evolutionary fingerprints with models of stem cell differentiation (Q35794410) (← links)
• On the genome base composition of teleosts: the effect of environment and lifestyle (Q35943556) (← links)
• Genome Compositional Organization in Gars Shows More Similarities to Mammals than to Other Ray-Finned Fish (Q36236165) (← links)
• GC- and AT-rich chromatin domains differ in conformation and histone modification status and are differentially modulated by Rpd3p (Q36672405) (← links)
• Lifestyle and DNA base composition in polychaetes (Q39266216) (← links)
• NXSensor web tool for evaluating DNA for nucleosome exclusion sequences and accessibility to binding factors. (Q42552587) (← links)
• "Genome design" model: evidence from conserved intronic sequence in human-mouse comparison (Q43252160) (← links)
• DNA helix: the importance of being AT-rich. (Q47912883) (← links)
• Abundance of dinucleotide repeats and gene expression are inversely correlated: a role for gene function in addition to intron length. (Q54102312) (← links)
• Genome size and metabolic intensity in tetrapods: a tale of two lines. (Q55191645) (← links)
• COMPARING BITMAPPED MICRORNA STRUCTURE IMAGES USING MUTUAL SYMMETRY (Q56928938) (← links)
• Different functional classes of genes are characterized by different compositional properties (Q57951132) (← links)
• Comparative analysis of distinct non-coding characteristics potentially contributing to the divergence of human tissue-specific genes (Q82063567) (← links)
• GC-made protein disorder sheds new light on vertebrate evolution (Q85347814) (← links)