scholarly article | Q13442814 |
P2093 | author name string | Wagner A | |
P2860 | cites work | Dollo's law and the death and resurrection of genes | Q22066216 |
Subtle Cerebellar Phenotype in Mice Homozygous for a Targeted Deletion of the En-2 Homeobox | Q24337933 | ||
Preservation of duplicate genes by complementary, degenerative mutations | Q24548042 | ||
Saccharomyces cerevisiae contains two functional genes encoding 3-hydroxy-3-methylglutaryl-coenzyme A reductase | Q27935656 | ||
Rescue of the En-1 mutant phenotype by replacement of En-1 with En-2 | Q28506189 | ||
Positive Darwinian selection after gene duplication in primate ribonuclease genes | Q29615093 | ||
The MyoD family and myogenesis: redundancy, networks, and thresholds | Q29618503 | ||
HedgehogandBmpGenes Are Coexpressed at Many Diverse Sites of Cell–Cell Interaction in the Mouse Embryo | Q29618704 | ||
Identification and molecular characterization of a yeast myosin I. | Q30193767 | ||
A myogenic factor from sea urchin embryos capable of programming muscle differentiation in mammalian cells | Q33648239 | ||
On the time for gene silencing at duplicate Loci. | Q33949675 | ||
Simulating evolution by gene duplication. | Q33952738 | ||
Recombination and the evolution of diploidy | Q33959654 | ||
mik1 and wee1 cooperate in the inhibitory tyrosine phosphorylation of cdc2. | Q34000451 | ||
Invasion and maintenance of a gene duplication | Q35146073 | ||
Functional redundancy: the respective roles of the two sloppy paired genes in Drosophila segmentation. | Q35568633 | ||
Redundant functions of the genes knirps and knirps-related for the establishment of anterior Drosophila head structures | Q35730691 | ||
Human BMP sequences can confer normal dorsal-ventral patterning in the Drosophila embryo | Q36205981 | ||
Drosophila abl and genetic redundancy in signal transduction | Q37061091 | ||
Fixation of a deleterious allele at one of two "duplicate" loci by mutation pressure and random drift | Q37333609 | ||
A rapidly evolving homeobox at the site of a hybrid sterility gene | Q38548882 | ||
Convergent evolution: the need to be explicit | Q40731512 | ||
Genome analysis with gene expression microarrays | Q40992214 | ||
Paralogous Hox genes: function and regulation | Q41291347 | ||
Evolutionary origins and maintenance of redundant gene expression during metazoan development | Q41587568 | ||
Evolution of the differential regulation of duplicate genes after polyploidization | Q41637382 | ||
Deleterious mutations and the origin of the meiotic ploidy cycle | Q41773451 | ||
Comparable rates of gene loss and functional divergence after genome duplications early in vertebrate evolution | Q41830334 | ||
Loss of duplicate gene expression after polyploidisation | Q43990337 | ||
Transition from haploidy to diploidy | Q44989990 | ||
Haploidy or diploidy: which is better? | Q45672766 | ||
Evolution of distinct developmental functions of three Drosophila genes by acquisition of different cis-regulatory regions | Q47069983 | ||
Subtype determination of Drosophila embryonic external sensory organs by redundant homeo box genes BarH1 and BarH2. | Q47071084 | ||
Molecular evolution of a duplication: the sex-peptide (Acp70A) gene region of Drosophila subobscura and Drosophila madeirensis | Q48028084 | ||
Phylogenetic reconstruction of vertebrate Hox cluster duplications | Q48046766 | ||
Enhancer detector analysis of the extent of genomic involvement in nervous system development in Drosophila melanogaster. | Q52224531 | ||
Current versus historical population sizes in vertebrate species with high gene flow: a comparison based on mitochondrial DNA lineages and inbreeding theory for neutral mutations | Q68472872 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | pleiotropy | Q1134884 |
P1104 | number of pages | 13 | |
P304 | page(s) | 1389-1401 | |
P577 | publication date | 2000-03-01 | |
P1433 | published in | Genetics | Q3100575 |
P1476 | title | The role of population size, pleiotropy and fitness effects of mutations in the evolution of overlapping gene functions | |
P478 | volume | 154 |
Q34791987 | A case of adaptation through a mutation in a tandem duplication during experimental evolution in Escherichia coli |
Q51942239 | A diffusion approach to approximating preservation probabilities for gene duplicates. |
Q40510242 | A global view of pleiotropy and phenotypically derived gene function in yeast |
Q27931126 | A highly redundant gene network controls assembly of the outer spore wall in S. cerevisiae |
Q46259830 | Bijective codon transformations show genetic code symmetries centered on cytosine's coding properties |
Q33758089 | Bioinformatics and expression analyses of the Ixodes scapularis tick cystatin family. |
Q28583715 | Canalization, developmental stability, and morphological integration in primate limbs |
Q42206086 | Combinatorial RNA interference in Caenorhabditis elegans reveals that redundancy between gene duplicates can be maintained for more than 80 million years of evolution |
Q21245217 | Degeneracy: a link between evolvability, robustness and complexity in biological systems |
Q79738436 | Duplicate genes and robustness to transient gene knock-downs in Caenorhabditis elegans |
Q28475317 | Evolution under fluctuating environments explains observed robustness in metabolic networks |
Q42059556 | Evolutionary framework for protein sequence evolution and gene pleiotropy |
Q33633613 | Evolutionary persistence of functional compensation by duplicate genes in Arabidopsis |
Q36439810 | Gene functional trade-offs and the evolution of pleiotropy. |
Q39686965 | GenomeHistory: a software tool and its application to fully sequenced genomes |
Q35730032 | Global eQTL mapping reveals the complex genetic architecture of transcript-level variation in Arabidopsis |
Q35786786 | Impact of the presence of paralogs on sequence divergence in a set of mouse-human orthologs |
Q33888869 | Mind the dbGAP: the application of data mining to identify biological mechanisms |
Q36993054 | Model-driven analysis of experimentally determined growth phenotypes for 465 yeast gene deletion mutants under 16 different conditions |
Q28768106 | Multiple mechanisms promote the retained expression of gene duplicates in the tetraploid frog Xenopus laevis |
Q24615100 | Networked buffering: a basic mechanism for distributed robustness in complex adaptive systems |
Q36837782 | Parasites lead to evolution of robustness against gene loss in host signaling networks |
Q36429411 | Patterns of Gene Conversion in Duplicated Yeast Histones Suggest Strong Selection on a Coadapted Macromolecular Complex |
Q42544122 | Pleiotropy can be effectively estimated without counting phenotypes through the rank of a genotype-phenotype map. |
Q39206189 | Quantitative trait loci from identification to exploitation for crop improvement. |
Q37242091 | Scan-o-matic: High-Resolution Microbial Phenomics at a Massive Scale. |
Q42231890 | Selection to minimise noise in living systems and its implications for the evolution of gene expression |
Q24542541 | The probability of preservation of a newly arisen gene duplicate |
Q30727697 | The zebrafish annexin gene family. |
Search more.