scholarly article | Q13442814 |
P2093 | author name string | David W Stock | |
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The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools | Q24248165 | ||
Genomic structure and functional control of the Dlx3-7 bigene cluster | Q24530533 | ||
The evolution of the vertebrate Dlx gene family | Q24600282 | ||
Were vertebrates octoploid? | Q24676010 | ||
MEGA2: molecular evolutionary genetics analysis software | Q27860788 | ||
The rapid generation of mutation data matrices from protein sequences | Q27860880 | ||
Genomic analysis of a new mammalian distal-less gene: Dlx7 | Q28115909 | ||
Developmental functions of the Distal-less/Dlx homeobox genes | Q28201148 | ||
Specification of jaw subdivisions by Dlx genes | Q28218878 | ||
Dlx genes encode DNA-binding proteins that are expressed in an overlapping and sequential pattern during basal ganglia differentiation | Q28589450 | ||
Evolution of Antennapedia-class homeobox genes | Q28769445 | ||
Diversification of the Wnt gene family on the ancestral lineage of vertebrates | Q28775842 | ||
Ancient genome duplications did not structure the human Hox-bearing chromosomes | Q28776444 | ||
Zebrafish hox clusters and vertebrate genome evolution | Q29616830 | ||
Hox cluster organization in the jawless vertebrate Petromyzon marinus | Q30830135 | ||
Genomic analysis of Hox clusters in the sea lamprey Petromyzon marinus | Q30830142 | ||
Numerous groups of chromosomal regional paralogies strongly indicate two genome doublings at the root of the vertebrates | Q30955958 | ||
Identification and developmental expression of three Distal-less homeobox containing genes in the ascidian Ciona intestinalis | Q30968718 | ||
Molecular evolution of two vertebrate aryl hydrocarbon (dioxin) receptors (AHR1 and AHR2) and the PAS family | Q33724237 | ||
Evidence for 14 homeobox gene clusters in human genome ancestry | Q33918402 | ||
Lamprey Dlx genes and early vertebrate evolution | Q34097483 | ||
The human Hox-bearing chromosome regions did arise by block or chromosome (or even genome) duplications | Q34162705 | ||
Evolution of the vertebrate genome as reflected in paralogous chromosomal regions in man and the house mouse | Q34364325 | ||
Hox cluster duplications and the opportunity for evolutionary novelties | Q34382145 | ||
Sequence, organization, and transcription of the Dlx-1 and Dlx-2 locus | Q34397850 | ||
The Hox Paradox: More complex(es) than imagined | Q34825209 | ||
Hox clusters and bilaterian phylogeny | Q34831880 | ||
The evolution of spliceosomal introns | Q34998373 | ||
PCR amplification of up to 35-kb DNA with high fidelity and high yield from lambda bacteriophage templates | Q35100239 | ||
Developmental roles of pufferfish Hox clusters and genome evolution in ray-fin fish | Q35125121 | ||
The role of gene duplication in the evolution and function of the vertebrate Dlx/distal-less bigene clusters | Q35167138 | ||
Dopamine receptors for every species: gene duplications and functional diversification in Craniates | Q35167141 | ||
Expansion of the Hox gene family and the evolution of chordates | Q36405626 | ||
Cloning of ascidian homeobox genes provides evidence for a primordial chordate cluster | Q36704390 | ||
Hox cluster genomics in the horn shark, Heterodontus francisci | Q37112239 | ||
Chromosomal localization of the proteasome Z subunit gene reveals an ancient chromosomal duplication involving the major histocompatibility complex | Q37385647 | ||
Regulatory roles of conserved intergenic domains in vertebrate Dlx bigene clusters. | Q38452651 | ||
Relationship between the Genomic Organization and the Overlapping Embryonic Expression Patterns of the ZebrafishdlxGenes | Q38463218 | ||
The evolution of the Hox cluster: insights from outgroups | Q38547851 | ||
Bichir HoxA cluster sequence reveals surprising trends in ray-finned fish genomic evolution. | Q40431580 | ||
Evolution of Hox genes | Q40614030 | ||
New evidence for genome-wide duplications at the origin of vertebrates using an amphioxus gene set and completed animal genomes | Q40829863 | ||
Gen(om)e duplications in the evolution of early vertebrates | Q41312106 | ||
Isolation of Dlx and Emx gene cognates in an agnathan species, Lampetra japonica, and their expression patterns during embryonic and larval development: conserved and diversified regulatory patterns of homeobox genes in vertebrate head evolution. | Q42648803 | ||
Evolution of a gene. Multiple genes for LDH isozymes provide a model of the evolution of gene structure, function and regulation | Q44888420 | ||
Evolutionary history of the enolase gene family. | Q45996024 | ||
A monophyletic origin of heart-predominant lactate dehydrogenase (LDH) isozymes of gnathostome vertebrates: evidence from the cDNA sequence of the spiny dogfish (Squalus acanthias) LDH-B | Q46677663 | ||
Homeotic genes of the Bithorax complex repress limb development in the abdomen of the Drosophila embryo through the target gene Distal-less | Q47072865 | ||
Lactate dehydrogenase (LDH) gene duplication during chordate evolution: the cDNA sequence of the LDH of the tunicate Styela plicata | Q48041614 | ||
Phylogenetic reconstruction of vertebrate Hox cluster duplications | Q48046766 | ||
Three neuropeptide Y receptor genes in the spiny dogfish, Squalus acanthias, support en bloc duplications in early vertebrate evolution | Q48244030 | ||
Analysis of lamprey and hagfish genes reveals a complex history of gene duplications during early vertebrate evolution | Q48285597 | ||
Heterotopic shift of epithelial-mesenchymal interactions in vertebrate jaw evolution. | Q48303673 | ||
Structural evolution of Otx genes in craniates. | Q48347889 | ||
Fin development in a cartilaginous fish and the origin of vertebrate limbs | Q52121697 | ||
2R or not 2R: testing hypotheses of genome duplication in early vertebrates | Q52608843 | ||
TaqStart Antibody: "hot start" PCR facilitated by a neutralizing monoclonal antibody directed against Taq DNA polymerase. | Q55065856 | ||
Independent Hox-cluster duplications in lampreys | Q56991607 | ||
The amphioxus Hox cluster: deuterostome posterior flexibility and Hox14 | Q58063323 | ||
Gene duplications and the origins of vertebrate development | Q58063347 | ||
Structure and Expression of Three Emx Genes in the Dogfish Scyliorhinus canicula: Functional and Evolutionary Implications | Q58456824 | ||
Phylogenetic analyses alone are insufficient to determine whether genome duplication(s) occurred during early vertebrate evolution | Q58482638 | ||
Erratum: Lamprey Hox genes and the origin of jaws | Q59093172 | ||
Gene loss and gain in the evolution of the vertebrates | Q71789873 | ||
Vertebrate evolution by interspecific hybridisation--are we polyploid? | Q72989525 | ||
Is tetralogy true? Lack of support for the "one-to-four rule" | Q73352636 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | leopard shark | Q1478899 |
P304 | page(s) | 807-817 | |
P577 | publication date | 2004-10-16 | |
P1433 | published in | Genetics | Q3100575 |
P1476 | title | The Dlx gene complement of the leopard shark, Triakis semifasciata, resembles that of mammals: implications for genomic and morphological evolution of jawed vertebrates | |
P478 | volume | 169 |
Q34124449 | A conserved cluster of three PRD-class homeobox genes (homeobrain, rx and orthopedia) in the Cnidaria and Protostomia |
Q39796959 | Ancestral and derived attributes of the dlx gene repertoire, cluster structure and expression patterns in an African cichlid fish |
Q33994038 | Annelid Distal-less/Dlx duplications reveal varied post-duplication fates |
Q28709673 | Developmental evidence for serial homology of the vertebrate jaw and gill arch skeleton |
Q42681078 | Direct evidence of allele equivalency at the Dlx5/6 locus |
Q51914503 | Evolution of oropharyngeal patterning mechanisms involving Dlx and endothelins in vertebrates. |
Q41941463 | Expression and function of Dlx genes in the osteoblast lineage |
Q33588101 | Functional conservation of a forebrain enhancer from the elephant shark (Callorhinchus milii ) in zebrafish and mice |
Q33457179 | Gene classification based on amino acid motifs and residues: the DLX (distal-less) test case |
Q28680815 | Heterogeneous conservation of Dlx paralog co-expression in jawed vertebrates |
Q35797868 | Molecular phylogeny of four homeobox genes from the purple sea star Pisaster ochraceus |
Q21563325 | Multiple chromosomal rearrangements structured the ancestral vertebrate Hox-bearing protochromosomes |
Q28709583 | Non-parsimonious evolution of hagfish Dlx genes |
Q34331978 | Pattern and polarity in the development and evolution of the gnathostome jaw: both conservation and heterotopy in the branchial arches of the shark, Scyliorhinus canicula. |
Q33370668 | Phylogenetic and chromosomal analyses of multiple gene families syntenic with vertebrate Hox clusters |
Q28272592 | Phylogeny of hammerhead sharks (Family Sphyrnidae) inferred from mitochondrial and nuclear genes |
Q28767452 | Reassessing the Dlx code: the genetic regulation of branchial arch skeletal pattern and development |
Q28742677 | The homology of odontodes in gnathostomes: insights from Dlx gene expression in the dogfish, Scyliorhinus canicula |
Q36203683 | The origin and diversification of the developmental mechanisms that pattern the vertebrate head skeleton. |
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