scholarly article | Q13442814 |
P2093 | author name string | Thaler DS | |
P2860 | cites work | The chemical basis of morphogenesis | Q769913 |
Role of DNA 5-methylcytosine transferase in cell transformation by fos | Q22008665 | ||
The neutral theory of molecular evolution: A review of recent evidence | Q22065260 | ||
Elevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2 | Q22248073 | ||
A theory of the epigenesis of neuronal networks by selective stabilization of synapses | Q24562900 | ||
p53, the cellular gatekeeper for growth and division | Q27860990 | ||
The transcriptional program of sporulation in budding yeast | Q27938344 | ||
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer | Q28256988 | ||
The clonal evolution of tumor cell populations | Q28271546 | ||
The origin of mutants | Q28288915 | ||
Evolution, development, and the units of selection | Q28775940 | ||
The significance of responses of the genome to challenge | Q28913697 | ||
Transcriptional activation by recruitment | Q29615048 | ||
Somatic generation of antibody diversity | Q29616439 | ||
RNA processing and the evolution of eukaryotes | Q33541973 | ||
Contingency loci, mutator alleles, and their interactions. Synergistic strategies for microbial evolution and adaptation in pathogenesis | Q33692357 | ||
Normal genetically mosaic mice produced from malignant teratocarcinoma cells | Q33883130 | ||
Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation | Q33886793 | ||
Transcriptional bias: a non-Lamarckian mechanism for substrate-induced mutations | Q34286408 | ||
The multistep nature of cancer | Q34366937 | ||
Genetic mechanisms of estrogen-independence in breast cancer | Q34403755 | ||
The mutation rate and cancer | Q34410886 | ||
Escherichia coli RNA and DNA polymerase bypass of dihydrouracil: mutagenic potential via transcription and replication | Q34660557 | ||
DNA hypomethylation leads to elevated mutation rates | Q34752442 | ||
Differentiation requires continuous regulation | Q35016700 | ||
The competence transcription factor of Bacillus subtilis recognizes short A/T-rich sequences arranged in a unique, flexible pattern along the DNA helix | Q35200591 | ||
Experimental control of neoplastic progression in cell populations: Foulds' rules revisited | Q35586746 | ||
Reversion rates in a leuB auxotroph of Escherichia coli K-12 correlate with ppGpp levels during exponential growth. | Q54570024 | ||
Adaptational origin of some purine-analogue resistant phenotypes in cultured mammalian cells | Q54588041 | ||
Frameshift mutator mutations | Q57978058 | ||
Fate of teratocarcinoma cells injected into early mouse embryos | Q59085799 | ||
A unicorn in the garden | Q59085860 | ||
Hormonally mediated inheritance of acquired characteristics in Mongolian gerbils | Q59093927 | ||
Nonadaptive mutations occur on the F' episome during adaptive mutation conditions in Escherichia coli | Q35620439 | ||
V(D)J recombinase induction in splenic B lymphocytes is inhibited by antigen-receptor signalling | Q35911221 | ||
In vitro V(D)J recombination: signal joint formation | Q35940601 | ||
Toward a resolution of the introns early/late debate: only phase zero introns are correlated with the structure of ancient proteins | Q36064406 | ||
Evidence for a methylation-blocking factor (mbf) locus involved in pap pilus expression and phase variation in Escherichia coli | Q36131735 | ||
Differential activity of a transposable element in Escherichia coli colonies | Q36184008 | ||
The effect of cells transferred into the mouse blastocyst on subsequent development | Q36273346 | ||
Oncogenes of RNA tumor viruses as determinants of cancer | Q36444186 | ||
Tumour heterogeneity of DNA cell cycle variables in breast cancer measured by flow cytometry | Q37225488 | ||
Selective stabilisation of developing synapses as a mechanism for the specification of neuronal networks | Q37298395 | ||
ENZYME INDUCTION AS AN ALL-OR-NONE PHENOMENON | Q37617203 | ||
Mutants in the Exo I motif of Escherichia coli dnaQ: defective proofreading and inviability due to error catastrophe | Q37678547 | ||
Neural edelmanism | Q38206664 | ||
Multiplex PCR/LDR for detection of K-ras mutations in primary colon tumors | Q38469522 | ||
Developmental selection and self-organization | Q38558464 | ||
The role of cell lineage in development | Q38684927 | ||
The multiple codes of nucleotide sequences | Q38687858 | ||
Relationship between differentiation and carcinogenesis | Q39646431 | ||
Special sites in generalized recombination | Q39854468 | ||
Specificity of SOS mutagenesis in native M13lacI phage | Q39958375 | ||
The origin of human cancers | Q40123412 | ||
SOS functions, cancer and inducible evolution | Q40313397 | ||
Mutation detection using immobilized mismatch binding protein (MutS). | Q40396149 | ||
The Directed Mutation Controversy and Neo-Darwinism | Q40484446 | ||
Somatic genetic changes in human breast cancer | Q40567907 | ||
Neural Darwinism: selection and reentrant signaling in higher brain function | Q40708418 | ||
The molecular biology of carcinogenesis | Q40826918 | ||
Molecular analysis of the t(8;14)(q24;q11) chromosomal breakpoint junctions in the T-cell leukemia line MOLT-16. | Q41074026 | ||
Conditional mutator phenotypes in hMSH2-deficient tumor cell lines | Q41091724 | ||
Histone H4 isoforms acetylated at specific lysine residues define individual chromosomes and chromatin domains in Drosophila polytene nuclei | Q41116253 | ||
The role of DNA methylation in cancer genetic and epigenetics | Q41291310 | ||
Does selective gene activation direct evolution? | Q41334517 | ||
A versatile mismatch recognition agent: specific cleavage of a plasmid DNA at a single base mispair | Q41645389 | ||
DNA transposition by the RAG1 and RAG2 proteins: a possible source of oncogenic translocations | Q47750695 | ||
Intricate combinatorial patterns of exon splicing generate multiple regulated troponin T isoforms from a single gene | Q48379485 | ||
The 5' hypermutation boundary of kappa chains is independent of local and neighbouring sequences and related to the distance from the initiation of transcription. | Q50111104 | ||
Evidence that gene amplification underlies adaptive mutability of the bacterial lac operon | Q50128814 | ||
Interspecies gene exchange in bacteria: the role of SOS and mismatch repair systems in evolution of species. | Q50144938 | ||
The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants | Q50192890 | ||
A Darwinian theory for the origin of cellular differentiation. | Q52194206 | ||
Microbial genetics. The tinkerer's evolving tool-box. | Q52262067 | ||
Is neural Darwinism Darwinism? | Q52284748 | ||
Counting and classifying attractors in high dimensional dynamical systems. | Q52288144 | ||
Propagating epigenetic states through meiosis: where Mendel's gene is more than a DNA moiety. | Q52565504 | ||
Role of mutator alleles in adaptive evolution. | Q54564129 | ||
P433 | issue | 2 | |
P304 | page(s) | 113-122 | |
P577 | publication date | 1999-09-01 | |
P1433 | published in | Evolution & Development | Q5418582 |
P1476 | title | Hereditary stability and variation in evolution and development. | |
P478 | volume | 1 |
Q25257146 | A Global Workspace perspective on mental disorders |
Q77384373 | Design for an aging brain |
Q51727179 | Evolutionary biology of cancer. |
Q36500617 | Positive selection in the evolution of cancer |
Q52138165 | The concept of developmental reprogramming and the quest for an inclusive theory of evolutionary mechanisms. |
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