Pages that link to "Q34098904"
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The following pages link to Recent duplication, domain accretion and the dynamic mutation of the human genome (Q34098904):
Displaying 50 items.
- Fusion and fission of genes define a metric between fungal genomes (Q21092569) (← links)
- Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes (Q21145278) (← links)
- Duplication and relocation of the functional DPY19L2 gene within low copy repeats (Q21266579) (← links)
- Cloning and characterisation of hAps1 and hAps2, human diadenosine polyphosphate-metabolising Nudix hydrolases (Q21284394) (← links)
- Identification of TCP10L as primate-specific gene derived via segmental duplication and homodimerization of TCP10L through the leucine zipper motif (Q24300661) (← links)
- Expansion of the BPI family by duplication on human chromosome 20: characterization of the RY gene cluster in 20q11.21 encoding olfactory transporters/antimicrobial-like peptides (Q24306653) (← links)
- High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridization (Q24530660) (← links)
- The Tre2 (USP6) oncogene is a hominoid-specific gene (Q24554200) (← links)
- Complex genomic rearrangements lead to novel primate gene function (Q24556569) (← links)
- Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10p (Q24561591) (← links)
- DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage (Q24656170) (← links)
- Distinguishing protein-coding and noncoding genes in the human genome (Q24670087) (← links)
- Gene conversion homogenizes the CMT1A paralogous repeats (Q24797658) (← links)
- Finishing a whole-genome shotgun: release 3 of the Drosophila melanogaster euchromatic genome sequence (Q24803366) (← links)
- Functional evolution of ADAMTS genes: evidence from analyses of phylogeny and gene organization (Q24805033) (← links)
- The gentle art of gene arrangement: the meaning of gene clusters (Q24806567) (← links)
- The rarity of gene shuffling in conserved genes (Q24812477) (← links)
- Duplication processes in Saccharomyces cerevisiae haploid strains (Q24813575) (← links)
- Expression of evolutionarily novel genes in tumors (Q26738894) (← links)
- Genetic variation and the de novo assembly of human genomes (Q26786788) (← links)
- The mosaic that is our genome (Q28204607) (← links)
- The DNA sequence, annotation and analysis of human chromosome 3 (Q28236820) (← links)
- Segmental duplications and copy-number variation in the human genome (Q28253048) (← links)
- Repetitive elements may comprise over two-thirds of the human genome (Q28254709) (← links)
- TFG, a target of chromosome translocations in lymphoma and soft tissue tumors, fuses to GPR128 in healthy individuals (Q28260191) (← links)
- Punctuated emergences of genetic and phenotypic innovations in eumetazoan, bilaterian, euteleostome, and hominidae ancestors (Q28661921) (← links)
- Fusion transcripts and transcribed retrotransposed loci discovered through comprehensive transcriptome analysis using Paired-End diTags (PETs) (Q28757561) (← links)
- Rates and patterns of gene duplication and loss in the human genome (Q28766861) (← links)
- Evolutionary mechanisms shaping the genomic structure of the Williams-Beuren syndrome chromosomal region at human 7q11.23 (Q28769508) (← links)
- The evolutionary origin of human subtelomeric homologies--or where the ends begin (Q28776101) (← links)
- Major events in the genome evolution of vertebrates: paranome age and size differ considerably between ray-finned fishes and land vertebrates (Q28776288) (← links)
- Genome architecture, rearrangements and genomic disorders (Q29614721) (← links)
- Heterogeneity in gene loci associated with type 2 diabetes on human chromosome 20q13.1. (Q30438316) (← links)
- Vertebrate genome sequencing: building a backbone for comparative genomics (Q30803039) (← links)
- Evidence for a fast, intrachromosomal conversion mechanism from mapping of nucleotide variants within a homogeneous alpha-satellite DNA array (Q30872875) (← links)
- Duplicative and conservative transpositions of larval serum protein 1 genes in the genus Drosophila. (Q31117189) (← links)
- Complete physical map and gene content of the human NF1 tumor suppressor region in human and mouse (Q31138286) (← links)
- Use of fluorescent sequence-specific polyamides to discriminate human chromosomes by microscopy and flow cytometry (Q33183872) (← links)
- DNM1DN: a new class of paralogous genomic segments (duplicons) with highly conserved copies on chromosomes Y and 15. (Q33199120) (← links)
- Database of Trypanosoma cruzi repeated genes: 20,000 additional gene variants (Q33304033) (← links)
- Chromosomal evolution of the PKD1 gene family in primates (Q33372432) (← links)
- Evolutionary analysis of the highly dynamic CHEK2 duplicon in anthropoids (Q33373501) (← links)
- Large-scale inference of the point mutational spectrum in human segmental duplications (Q33401963) (← links)
- The apoptotic machinery as a biological complex system: analysis of its omics and evolution, identification of candidate genes for fourteen major types of cancer, and experimental validation in CML and neuroblastoma (Q33436471) (← links)
- Genome-wide computational prediction of tandem gene arrays: application in yeasts (Q33525699) (← links)
- A sensitive method for detecting variation in copy numbers of duplicated genes. (Q33679715) (← links)
- Pooled genomic indexing of rhesus macaque (Q33780853) (← links)
- Lineage-specific evolution of the vertebrate Otopetrin gene family revealed by comparative genomic analyses (Q33801727) (← links)
- Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7. (Q33883082) (← links)
- Short interspersed transposable elements (SINEs) are excluded from imprinted regions in the human genome (Q33897588) (← links)