Image:DNA Overview.png
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[edit] Summary
An overview of the structure of DNA. Created by Michael Ströck (mstroeck) on February 8, 2006. Released under the GFDL.
[edit] FPC nomination
The end result of the nomination process for this image was that it was not promoted. There were some questions about the accuracy/design philosophy of the diagram. A modified version that addresses at least some of the concerns expressed in the nomination discussion would likely be promoted, judging by the comments. The utility of such a diagram is obvious. -- moondigger 16:36, 18 June 2006 (UTC)
[edit] Licensing
I, the creator of this work, hereby grant the permission to copy, distribute and/or modify this document under the terms of the GNU Free Documentation License, Version 1.2 or any later version published by the Free Software Foundation; with no Invariant Sections, no Front-Cover Texts, and no Back-Cover Texts.
Subject to disclaimers.
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- (del) (cur) 03:04, 8 February 2006 . . Mstroeck (Talk | contribs) . . 799×2000 (937,433 bytes) (An overview of the structure of DNA. Created by Michael Ströck (mstroeck) on February 8, 2006. Released under the GFDL.)
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File links
The following pages on the English Wikipedia link to this file (pages on other projects are not listed):
- Astrobiology
- DNA
- Retroposon
- XY sex-determination system
- Inverted repeat
- Phocomelia
- Warkany syndrome 2
- Monocistronic
- Gene pool
- CpG island
- Circular DNA
- Regulatory sequence
- GRK3
- Structural genomics
- Homologous chromosome
- Tietz syndrome
- Allen Brain Atlas
- Restriction modification system
- Classical genetics
- List of gene families
- Yeast artificial chromosome
- Genetic diversity
- Genetic program
- Gene knockdown
- Terminator (genetics)
- Polymorphism (biology)
- DNase footprinting assay
- Dyad symmetry
- DnaQ
- Okazaki fragment
- Genome (book)
- Gene family
- Naked DNA
- TATA box
- Activator (genetics)
- Canonical sequence
- Polycistronic
- Pribnow box
- Repeated sequence (DNA)
- Wobble base pair
- Replication fork
- Nucleotide salvage
- Frameshift mutation
- Structural inheritance
- Haldane's rule
- Human Genome Organisation
- Heredity (journal)
- Modifications (genetics)
- Daf-2
- Immediate early gene
- Phagemid
- Cosmid
- Evolvability
- Genome@home
- Integron
- Smart gene
- Parkin (ligase)
- Gene lethality
- Behavioural genetics
- Constitutive heterochromatin
- Trans-splicing
- Germline mutation
- The Institute for Genomic Research
- Serial clone
- Genetic determinism
- D-loop replication
- Internal transcribed spacer
- Conservation (genetics)
- J. Craig Venter Institute
- Tree breeding
- PGL2
- Monohybrid cross
- Bookmarking
- Non-mendelian inheritance
- Dosage compensation
- Megabase
- Genetic architecture
- Fitness (genetic algorithm)
- Identity by type
- De Finetti diagram
- Interferon Consensus Sequence-binding protein
- Smith-Waterman algorithm
- Giemsa
- Blending inheritance
- Genetic viability
- Gene conversion
- Restriction digest
- Intergenic region
- Complementation (genetics)
- Ecological Genetics (book)
- Sotos syndrome
- Tandem repeat locus
- Genetic marker
- Candidate gene
- Genetic insertion
- Fusion gene
- Repressor
- PGLO
- Multiple cloning site
- Underdominance
- FOXP3
- Dimple
- General transcription factor
- Synteny
- CAAT box
- Polygene
- Cassette (genetics)
- Anlage
- Synaptonemal complex
- Rat genome database
- Nick translation
- Vector DNA
- Amplified fragment length polymorphism
- Phenocopy
- Inbred backcross lines
- Human Genetics Commission
- Gene mapping
- Behavior Genetics Association
- Leucism
- Metagenics
- Gemmules
- Pathogenomics
- B chromosome
- Animal Genome Size Database
- UBE1
- Gene chip technology
- Depurination
- Imaging genetics
- Sox2
- Sim4
- Genetic distance
- VPg
- Tandemly arrayed genes
- Paramutation
- Genetic variability
- Phi-X174 phage
- Termination factor
- Locus (genetics)
- Dominant allele
- Y chromosome microdeletion
- Nick (DNA)
- Gene revolution
- Homeotic gene
- Restriction fragment
- TUNEL assay
- Dirty phenotypes
- Ectopic expression
- Ribosome shunting
- HER2/neu
- SLITRK1
- PBR322
- Reprimo
- Fragile sites
- Gene copy number
- Lck gene
- Test cross
- Template:Genetics-stub
- Chromosome 6 (human)
- Chromosome 13 (human)
- Chromosome 4 (human)
- Chromosome 8 (human)
- Chromosome 9 (human)
- Chromosome 10 (human)
- Chromosome 11 (human)
- Chromosome 12 (human)
- Chromosome 14 (human)
- Chromosome 16 (human)
- Chromosome 17 (human)
- Chromosome 18 (human)
- Chromosome 19 (human)
- Chromosome 20 (human)
- Annealing (biology)
- Reannealing
- Regulator gene
- Genetic discrimination
- Chromomere
- Molecular anatomy
- Gene product
- Phylogenomics
- Transmission disequilibrium test
- Mutational robustness
- Canalisation (genetics)
- HMOX1
- Recombination hotspot
- Mutator genotype
- Genetic Information Research Institute
- Ancestry-informative marker
- Gene map
- Phylogenetic network
- Theranostics
- Insertion sequence
- X hyperactivation
- X:A ratio
- SOS box
- Back mutation
- Bead theory
- Biparental zygote
- Spacer DNA
- Fluorescent green pig
- European Society of Gene Therapy
- American Society of Gene Therapy
- PBluescript
- PelB leader sequence
- Replicon (genetics)
- TCF21
- Acrocentric chromosome
- Avery Sandberg
- SOX genes
- Genetic equilibrium
- Ribotyping
- Shaker gene
- Homogeneously staining region
- Electrophoretic mobility shift assay
- Sp1
- Wikipedia:Featured picture candidates/DNA Overview
- Zinc finger protein
- MSin3 interaction domain
- Transcription Factor II D
- Coactivator (genetics)
- Cis-regulatory element
- Genotyping
- DNA Resequencer
- Kozak sequence
- Haplo-sufficiency
- Clan McWho
- Polybrene
- Nuclear gene
- AraB
- PComb3H
- Electroelution
- Haplogroup F (mtDNA)
- Haplogroup W (mtDNA)
- Haplogroup N (Y-DNA)
- Haplogroup O (Y-DNA)
- Haplogroup P (Y-DNA)
- Haplogroup Q (Y-DNA)
- Haplogroup Q3 (Y-DNA)
- Adapter (genetics)
- Mung bean exonuclease
- Haplogroup JT (mtDNA)
- NlaIII
- Active chromatin sequence
- Interlocus contest evolution
- List of Y-STR public databases
- MN gene
- Attenuator (genetics)
- MUT (zinc finger protein)
- Tn10
- Methylation specific oligonucleotide microarray
- Nature Via Nurture: Genes, Experience, and What Makes us Human
- Gene dosage
- HFE (gene)
- Kozak consensus sequence
- Overlap extension polymerase chain reaction
- Histone methylation
- Centromeric
- Vitellogenin
- Cre recombinase
- Pseudodiploid
- TNA (nucleic acid)
- GNA (nucleic acid)
- Directed mutagenesis
- Isopycnic centrifugation
- XPB
- Gene cassette
- Ori (genetics)
- RpoB
- Eukaryotic chromosome structure
- Eukaryotic intergenic DNA
- X0 sex-determination system
- ZW sex-determination system
- Haplodiploid sex-determination system
- Guide RNA
- Matrix attachment region
- Revertant
- DNA laddering
- HPRD
- Genetic divergence
- Satellite chromosome
- Short interspersed nuclear element
- Recombineering
- CYP1A1
- Miodrag Stojković
- ROR2
- Overlapping generations
- Ultrabithorax
- UvrABC endonuclease
- Cyclobutyl dimer
- Selective sweep
- Wikipedia:Featured picture candidates/June-2006
- Interkinesis
- Ka/Ks ratio
- GATTO
- Wikipedia:Featured picture candidates/DNA
- Exon shuffling
- Cadastral gene
- Neutral mutation
- Sense strand
- Trp operon
- Hypervariable region
- Structural Genomics Consortium
- Acycloguanosine
- Preimplantation Genetic Haplotyping
- Wikipedia:WikiProject Medicine/Stub sorting
- Splice site mutation
- International Congress of Human Genetics
- Stemcellomics
- Stem cell chip
- Microbial genetics
- Barbourin
- Concatomer
- Calcitriol receptor
- Subclade
- User:GAThrawn22/Sandbox2/wikiproject
- Bare lymphocyte syndrome 2
- Outcrossing
- Human artificial chromosome
- G banding
- High mobility group
- Probands
- Anticipation phenomenon
- COS cells
- FLP-FRT Recombination
- Locus Control Region
- Krüppel
- Gap gene
- Bare lymphocyte syndrome
- Polar overdominance
- Biological transmutation
- Eukaryotic gene example
- Human β-globin locus
- Synexpression
- Single Base Extension
- Noninvasive genotyping
- Extranuclear Inheritance
- Blue white screen
- Xq28
- Insertional mutagenesis
- Impalefection
- Charles Cantor
- Clastogenic
- Gene delivery
- FOXC2
- CIAS1
- Gene orders
- Neanderthal Genome Project
- CYP27A1
- KCNA1
- Recognition sequence
- P14arf
- P16INK4a
- Wikipedia talk:WikiProject Molecular and Cellular Biology/Discussion Archive
- 3'-Cluster
- SULT2A1
- Psychiatric genetics
- Founder mutation
- Gene cluster
- MGC8902
- KCNJ2
- KCNE1
- SLC12A3
- Genetics and violence
- Haplogroup O1 (Y-DNA)
- C-Fos
- Dyad (biology)
- Allosome
- Chromosomal duplication
- Core binding factor
- Homogametic sex
- Wikipedia:WikiProject Dentistry/Stub sorting
- General feature format
- Microsatellite instability
- Origin Recognition Complex Protein
- Haplogroup O2a (Y-DNA)
- Adenovirus E1B protein
- Haplogroup O2b (Y-DNA)
- Fosmid
- Suppressor mutation
- Polar effect (genetics)
- Oncogenomics
- Mixoploidy
- Falconer's formula
- NADH-Q
- Wikipedia:Today's featured article/February 2007
- Wikipedia:Today's featured article/February 13, 2007
- AmpliChip CYP450 Test
- Background selection
- Hybrid growth disorders
- Female Choice
- Bacteriophage MS2
- HIS3
- HisB
- Antitermination
- Haplogroup Y (mtDNA)
- Haplogroup Q (mtDNA)
- Haplogroup G (mtDNA)
- Haplogroup CZ (mtDNA)
- Introduction to evolution
- Interrupted gene
- Negative selection (natural selection)
- Introduction to genetics
- Palladin
- Balancer chromosome
- Caspase-9
- Luxury gene
- Cancer Genome Project
- ABCB5
- Vertical resistance
- Horizontal resistance
- Dynamic mutation
- Haplogroup P (mtDNA)
- DNA adduct
- KRAS
- Superman (gene)
- Bang senseless
- Fixation (population genetics)
- Allele chart
- AMELY
- Gametic phase
- ACGT
- Haplogroup DE (Y-DNA)
- MEF2A
- SLC30A8
- Photo 51
- Indy (gene)
- Mendelian error
- ERCC2 gene
- Derivative chromosome
- Ink4
- Translational Genomics Research Institute
- Gene trapping
- Winged-helix transcription factors
- Exonic splicing silencer
- Immunogenetics
- Xanthochromism
- Relative Synonymous Codon Usage
- Resistance mutation
