mtDNA

Related by string. * * mitochondrial DNA mtDNA . Mitochondrial DNA mtDNA . mtDNA mutations . mtDNA sequences . mtDNA sequence *

Related by context. All words. (Click for frequent words.) 74 mitochondrial DNA 70 mitochondrial DNA mtDNA 68 #S rRNA 67 Mitochondrial DNA 67 mitochondrial genome 67 autosomal 65 alleles 65 haplotype 65 orthologs 65 chromosomal 64 haplotypes 64 maternal lineage 64 mutant alleles 64 allelic 63 haplogroups 63 Y chromosome 63 mitochondrial 63 mitochondrial genomes 62 nucleotide sequence 62 maternally inherited 62 genomic DNA 62 Y STR 62 VNTR 62 A. thaliana 62 cDNA 61 linkage disequilibrium 61 mutation 61 microsatellite markers 61 phylogeny 61 DNA sequences 61 paternally inherited 61 mRNA transcripts 61 segmental duplications 61 cytochrome b 61 mutations 60 Y chromosomal 60 paternal lineage 60 heterozygosity 60 mutant allele 60 CNVs 60 mtDNA sequences 60 clades 60 NF1 gene 60 Haplogroup 60 Alu elements 60 karyotype 60 gene 60 telomeric 60 X chromosome 60 genetic lineages 60 FMR1 gene 59 missense mutations 59 genomes 59 pseudogenes 59 lineages 59 gene expression profiles 59 mitochondrial gene 59 Y chromosomes 59 nucleotide sequences 59 #S rRNA gene 59 aneuploidy 59 mtDNA mutations 59 spontaneous mutations 59 genotypic 59 sporadic ALS 59 genetic 59 chromosomal aberrations 59 genes 59 loci 59 homozygosity 59 D. melanogaster 59 allele 59 chromosomal DNA 59 miRNAs 59 genetic markers 59 centromeres 59 mtDNA sequence 59 chromosomes 59 mosaicism 58 #S rDNA 58 haplogroup 58 gene expression patterns 58 MTHFR gene 58 phenotype 58 noncoding 58 nucleotide substitution 58 FMR1 58 #q# [001] 58 polymorphism 58 germline 58 gene amplification 58 phylogenetic 58 chromosome 58 indels 58 archaeal 58 mitochondrial DNA sequences 58 centromeric 58 CFTR gene 58 PTPN# 58 piRNAs 58 phylogenetic analysis 58 rRNA 58 gene expression 58 kilobase 58 allele frequencies 58 Neandertal 58 homologs 58 imprinted genes 58 phylogenies 58 Phylogenetic analysis 58 PALB2 58 rDNA 58 heterozygotes 58 #q#.# [001] 58 ribosomal DNA 58 phylogenetic analyzes 58 genes encoding 57 Neandertal DNA 57 S. cerevisiae 57 cDNA libraries 57 genotyped 57 RNA transcripts 57 mammalian genomes 57 DNA methylation 57 LIS1 57 genetic diversity 57 polymorphisms 57 nucleotide substitutions 57 Jhdm2a 57 STAT4 57 KIAA# 57 intronic 57 #p# [001] 57 SRY gene 57 organism genome 57 methylation 57 exon 57 chromosome #q 57 exome 57 methylated DNA 57 centrosome 57 miRNA expression 57 somatic mutations 57 telomere length 57 BARD1 57 methylation patterns 57 #q# [002] 57 nucleotide 57 ncRNAs 57 phylogenetically 57 genetic mutations 57 MLH1 57 virulence genes 57 DNA 57 phenotypic variation 57 intergenic 57 mammalian genome 57 coding sequences 57 kilobases 57 gene mutation 57 RNA sequences 57 microRNA expression 57 phenotypically 57 transcriptomes 57 phenotypic 57 MSH2 57 genotype 57 non coding RNA 57 cytoplasmic 57 miRNA 57 SNPs 56 eukaryotic 56 ribosomal RNA 56 GAPDH 56 heterozygous 56 genome 56 myostatin gene 56 genetic variant 56 intron 56 genotypes 56 mitochondrial genes 56 causative genes 56 yeast genome 56 CGG repeats 56 genomic instability 56 causal variants 56 gene duplications 56 amino acid sequences 56 tumor suppressor gene 56 Chromosomal 56 indel 56 diploid 56 cytogenetic 56 single nucleotide polymorphism 56 gene sequences 56 breast cancer genes BRCA1 56 splice junctions 56 genetic variation 56 proteomes 56 substrate specificity 56 alternatively spliced 56 HOTAIR 56 retrotransposon 56 blastomeres 56 PCR amplified 56 isotopic 56 microdeletions 56 MECP2 gene 56 vimentin 56 chromosomal regions 56 apoE 56 mutated gene 56 heterochromatin 56 monozygotic twins 56 HAR1 56 KLF4 56 mutated genes 56 radial glia 56 microdeletion 56 cohesin 56 chromosome #q# [001] 56 evolutionarily conserved 56 endogenous retroviruses 56 genomic sequence 56 CRISPR Cas 56 aneuploid 56 IGF2 56 mitochondrial proteins 55 Chromosome 55 cytosolic 55 subcellular localization 55 endogenous retrovirus 55 chromosome #q# [002] 55 mutational 55 prion gene 55 bacterial genomes 55 #q#.# [002] 55 Supplementary Fig 55 orthologous 55 mRNA expression 55 BRCA1 gene 55 primate genomes 55 eukaryote 55 inbred strains 55 genomic sequences 55 genomewide 55 sequenced genomes 55 Arabidopsis genome 55 genetically 55 X inactivation 55 transgene expression 55 Supplementary Table 55 ribosomal RNA rRNA 55 MLL gene 55 guanine G 55 mRNA 55 #p#.# [001] 55 aneuploidies 55 monophyletic 55 homozygous 55 methyltransferase 55 EBNA1 55 isotope ratios 55 chromosomal rearrangements 55 CCL#L# 55 IRAK1 55 evolutionary lineage 55 germline mutations 55 thymine 55 mRNAs 55 chromatid 55 MLL2 55 paternal ancestry 55 PCR RFLP 55 quantitative trait loci 55 sequence homology 55 suppressor gene 55 PTEN gene 55 chimp genomes 55 microsatellite loci 55 genetic sequences 55 genomic 55 transcriptome 55 CHD7 55 spontaneous mutation 55 H#K#me# 55 missense mutation 55 monozygotic 55 MYH9 gene 55 exons 55 somatic cells 55 cDNAs 55 histone modifications 55 N Myc 55 chromosomal translocations 55 genomic loci 54 microglial 54 cDNA library 54 unmethylated 54 karyotypes 54 VHL gene 54 isoform 54 Wwox 54 palladin 54 frameshift mutation 54 proband 54 genome rearrangements 54 gene encoding 54 autosomes 54 inherited maternally 54 PCR amplification 54 splice variant 54 BAC clones 54 At#g# 54 placental mammals 54 S#A# [002] 54 5 hmC 54 RBP4 54 EGFR gene 54 MeCP2 gene 54 telomere DNA 54 gene mutations 54 5 hydroxymethylcytosine 54 chimpanzee genomes 54 CTCF 54 abnormal chromosomes 54 chromosomal abnormalities 54 amplicons 54 KCNQ1 54 platypus genome 54 orthologous genes 54 BRCA2 54 ciliated 54 Mitochondrial 54 telomerase RNA 54 GSTP1 54 CAG repeats 54 ZNF# 54 SMN2 gene 54 genetic makeup 54 parkin gene 54 Sanger sequencing 54 isoforms 54 TAp# 54 S. pombe 54 genetically identical 54 chromatin structure 54 heterochromatic 54 genomic imprinting 54 de novo mutations 54 hypervariable 54 coexpression 54 Pol IV 54 plastid 54 PrP 54 ssDNA 54 glycoproteins 54 germline cells 54 genetic recombination 54 dizygotic twins 54 miRNA genes 54 mutant p# 54 cytosine methylation 54 rs# [002] 54 lysine residues 54 positional cloning 54 exonuclease 54 epistasis 54 Single Nucleotide Polymorphisms SNPs 54 CNTNAP2 54 penetrance 54 splice variants 54 fission yeast 54 noncoding RNAs 54 insertion deletion 54 uPAR 54 differentially expressed genes 54 epigenetic modification 54 DNA polymerases 54 BRCA2 gene 54 array CGH 54 fig. S1 54 morphological 54 PrPSc 54 differential gene expression 54 gene variants 54 TP# mutation 54 uniparental 54 Saccharomyces cerevisiae 54 vertebrate genomes 54 mitochondrial genome sequence 54 valine 54 p# mutations 54 Prox1 54 HFE gene 54 prion protein gene 53 major histocompatibility complex 53 RFLP 53 CDH1 53 constitutively 53 LRRK2 gene 53 chromosome #q#.# [001] 53 mutant gene 53 cis regulatory 53 HMGA2 53 somatic mutation 53 Neanderthal genes 53 meiotic 53 matrix metalloproteinase 53 Rap1 53 genetic ancestry 53 X. laevis 53 #p# [003] 53 RUNX3 53 lymphoblastoid cell lines 53 RT qPCR 53 ribonucleic acid RNA 53 phenotypes 53 centromere 53 IgA deficiency 53 number variation CNV 53 estrogen receptor alpha 53 heterodimers 53 intergenic regions 53 ADRB2 53 microRNA miR 53 quantitative RT PCR 53 Plasmodium 53 subfamilies 53 microcephalin 53 budding yeast 53 T. brucei 53 Homozygous 53 homozygotes 53 promoter methylation 53 centrosomes 53 phylogenetic trees 53 mRNA molecules 53 amplicon 53 genetic relatedness 53 genetic alteration 53 DNA deoxyribonucleic acid 53 ESR1 53 globin 53 overexpression 53 FLT3 53 Y Chromosome 53 HLA genes 53 genetic mutation 53 transcriptional activation 53 genetic variability 53 DGGE 53 MC1R gene 53 transposable elements 53 hierarchical clustering 53 HLA G 53 paralogs 53 segmental duplication 53 Dpp 53 messenger RNAs mRNAs 53 NFKBIA 53 lamin 53 MDM2 53 C. jejuni 53 transcriptional repression 53 susceptibility gene 53 taxa 53 nucleic acid sequence 53 DLC1 53 ribonucleoprotein 53 Western blotting 53 C#Y 53 coding genes 53 trimer 53 histone acetylation 53 ortholog 53 synuclein 53 viral genomes 53 epigenetic modifications 53 CHEK2 53 uracil 53 Cyclin D1 53 5 methylcytosine 53 chromosomal anomalies 53 tyrosine phosphorylation 53 subtype 53 Germline 53 Rb gene 53 p# mutation 53 trypanosome 53 DICER1 gene 53 Neanderthal DNA 53 parthenogenetic 53 P. falciparum 53 #BP# 53 APOE e4 53 colorectal tumor 53 KCNE2 53 paternal lineages 53 chromosomal deletions 53 amino acid residues 53 glycosylation 53 SMN1 53 chromosome #p# [001] 53 nucleosome positioning 53 neuroligins 53 miRNA sequences 53 haploid 53 homozygote 53 CNTNAP2 gene 53 chromosomal instability 53 colocalization 53 fig. S4 53 Cytogenetic 53 constitutively active 53 meiotic recombination 53 primordial germ cells 53 Prevotella 53 ncRNA 53 Hox gene 53 polyploidy 53 cyclin E 53 histone modification 53 PFGE 53 genetic abnormalities 53 Mutation 53 EGFP 53 acetylation 53 CagA 53 MMP# 53 mammary cells 53 epigenetic silencing 53 nucleolar 52 Haplotype 52 translocations 52 UTRs 52 ploidy 52 cybrid 52 deleterious mutations 52 sister chromatid 52 enzymatic activity 52 mutant genes 52 Transcriptome 52 ribozyme 52 bases adenine 52 transmembrane 52 M. pneumoniae 52 genetic loci 52 NR#A# 52 RNA binding 52 X chromosome inactivation 52 metazoan 52 TRIM5 52 morphogen 52 CDK4 52 H2AX 52 proteome 52 FGFR2 52 IKKa 52 epigenetically 52 lincRNA 52 phenotypic traits 52 neural crest 52 dinucleotide 52 cytosine 52 operon 52 gene locus 52 chromosome segregation 52 introns 52 RAR beta 52 CYP#D# gene 52 SLC#A# gene [001] 52 chordate 52 mutant protein 52 genome sequences 52 epigenetic changes 52 cell lysate 52 IKZF1 52 mitochondrial DNA sequence 52 #S ribosomal RNA 52 allelic variants 52 body louse genome 52 fungal genomes 52 gene expression microarrays 52 codons 52 serum samples 52 M. leprae 52 Fig. 1E 52 morphologic 52 contigs 52 micro RNAs 52 phytochrome 52 microarray experiments 52 NR#A# gene 52 MC1R 52 E cadherin 52 ramidus 52 granulocyte 52 evolutionary relatedness 52 subfamily 52 chromosome abnormalities 52 gDNA 52 APOL1 52 ultraconserved elements 52 Leptospira 52 estrogen receptor 52 MALAT1 52 PON1 52 polyploid 52 qRT PCR 52 TP# gene 52 Genotypic 52 Genetic variation 52 β amyloid 52 CpG 52 CYP#B# 52 BRAF protein 52 amino acid sequence 52 chloroplast DNA 52 Rad# 52 gut microbes 52 DEAR1 52 DNA rearrangements 52 taxon 52 proteolytic cleavage 52 endonuclease 52 inherited mutations 52 apoE4 52 clonally 52 MSH6 52 activating mutations 52 H#K# [002] 52 p# INK4a 52 cyclin 52 clade 52 cDNA microarray 52 protein phosphorylation 52 Phylogenetic 52 TACI mutations 52 viral nucleic acids 52 Fig. 1b 52 phylogenetic relationships 52 globin genes 52 E#F# 52 allelic variation 52 aY chromosome 52 HERV 52 ultrastructure 52 RNA ribonucleic acid 52 DNA methylation patterns 52 homology 52 ribosomal proteins 52 polynucleotide 52 ERBB2 52 recombination hotspots 52 medulloblastomas 52 alpha synuclein gene 52 MTHFR 52 NF1 52 dizygotic 52 introgression 52 microRNA 52 phylogenetic tree 52 functional polymorphism 52 T. gondii 52 PKD1 52 Rickettsia 52 M. genitalium 52 tRNA 52 clonal 52 miR #a [001] 52 CCR5 delta# 52 noncoding DNA 52 β1 52 rhesus 51 serologic 51 δ 51 dynamin 51 JAK2 mutation 51 genomic variation 51 #p#.# [002] 51 viral genome 51 tetramers 51 heritable traits 51 tumor suppressor protein 51 SGK1 51 TERT 51 allele frequency 51 genetic variants 51 lacZ 51 serine protease 51 transgenic mice expressing 51 Leydig cells 51 herpesviruses 51 coding exons 51 CD1d 51 IGFBP 51 genomic deletions 51 hepatoma 51 immunohistochemical 51 R#W [002] 51 CRISPR 51 MHC genes 51 haematopoietic 51 PGCs 51 recessive genes 51 Trypanosoma brucei 51 agouti gene 51 Immunohistochemical analysis 51 TRF1 51 beta subunit 51 PRNP 51 epigenomes 51 Hepatocyte 51 QTLs 51 APOE4 51 outer membrane proteins 51 microbiota 51 heterozygote 51 LMNA 51 olfactory receptor 51 epigenetic regulation 51 alanine 51 amino acid substitution 51 sCJD 51 maize genome 51 genetic polymorphisms 51 antibody antigen 51 ChIP 51 perilipin 51 ERK2 51 succinate dehydrogenase 51 fig. S# 51 chromosome aberrations 51 amyloid peptide 51 genotoxic stress 51 Akt1 51 mice lacking 51 Apobec3 51 TCF#L# gene 51 mammalian fatty acid 51 polyglutamine 51 heritable 51 protein isoforms 51 chimeric 51 CISH 51 HSCs 51 thymine T 51 telomere 51 nucleic acid fragments 51 OGG1 51 Typhi 51 histone H4 51 OCA2 gene 51 breast carcinomas 51 homologous 51 TIMP 51 euchromatin 51 MicroRNA 51 transmembrane protein 51 mutant mouse 51 Nup# 51 mutational analysis 51 sarcosine 51 miRNA expression profiles 51 ApoE gene 51 G6PD 51 COMT gene 51 polymerases 51 ChIP seq 51 HLA markers 51 hypermethylated 51 Notch signaling 51 gametophyte 51 SNP rs# [001] 51 fig. S2 51 Mendelian 51 IDH1 51 Chlamydomonas 51 Rh factor 51 methylation markers 51 untranslated regions 51 ChIP Seq 51 amino terminal 51 catenin 51 HbF 51 ectopic expression 51 #S rRNA genes 51 hair follicle stem cells 51 CpG islands 51 guanine 51 BRCA1 51 huntingtin 51 CD8 + 51 ALDH2 51 prion infection 51 genetic alterations 51 genes BRCA1 51 deleterious mutation 51 homologue 51 short hairpin RNA 51 Foxp3 51 multigene 51 MECP2 51 receptor gene 51 fluorescence intensity 51 ERCC1 51 antisense RNA 51 RCAN1 51 monocyte 51 chromosomal rearrangement 51 mitochondrial mutations 51 immunoreactivity 51 ataxin 51 RNA splicing 51 FUS protein 51 proteomic analysis 51 p# protein 51 mitochondrial DNA mutations 51 SIR2 51 deletion mutant 51 thymidine 51 rs# [004] 51 DISC1 51 wildtype 51 hippocampal neurons 51 cystatin C 51 HLA B 51 miR 51 non coding RNAs 51 Drosha 51 Phenotypic 51 TOP2A gene 51 Src 51 KRAS mutations 51 outbred 51 epigenetic marks 51 AFLP 51 P. patens 51 deoxyribonucleic acid 51 proteins encoded 51 nuclei 51 transcription elongation 51 metabolic enzymes 51 immunoglobulin genes 51 Neanderthal genome sequence 51 clusterin 51 activin 51 KRAS oncogene 51 HLA molecules 51 phosphorylate 51 chordates 51 telomere lengths 51 transcriptional regulation 51 eukaryotic cells 51 nucleic 51 Xenopus 51 autosomal recessive 51 TMEM#B 51 leukemic cell 51 human leukocyte antigen 51 BRCA2 mutation 51 glycosyltransferase 51 SMN2 51 membrane proximal 51 PTEN mutations 51 hTERT 51 immunohistochemical staining 51 Proteobacteria 51 maternal lineages 51 C#BL 6 51 NFAT 51 testis 51 viral RNA 51 genetically distinct 51 HLA B# 51 prokaryotic 51 Bacteroides 50 dopamine transporter gene 50 SATB1 50 hematopoietic cells 50 pseudogene 50 diploid genome 50 CYP#E# gene 50 LRAT 50 morphologically 50 chromatin immunoprecipitation ChIP 50 metazoans 50 selfing 50 FGFR2 gene 50 TCF4 50 transgene 50 susceptibility genes 50 androgen receptor 50 H#K# methylation 50 microRNAs 50 immunofluorescence 50 MAPK pathway 50 situ hybridization 50 karyotyping 50 hematopoetic stem cells 50 murine 50 HMGA2 gene 50 transmembrane receptor 50 rs# [003] 50 immunofluorescent 50 SCN5A 50 peripheral blood mononuclear 50 HLA typing 50 clade B 50 endosymbiosis 50 epigenetic markers 50 bilaterians 50 C. neoformans 50 histone H3 50 RNA Seq 50 TMPRSS2 ERG fusion 50 ubiquitylation 50 noncoding RNA 50 recessive mutation 50 ALK mutations 50 homodimer 50 RASSF1A 50 polyamines 50 alpha synuclein 50 Alleles 50 LPA gene 50 transgenic mice 50 HER2 gene 50 amphioxus 50 transfected 50 GBM tumors 50 Deoxyribonucleic acid DNA 50 lysates 50 EZH2 50 chromosome #q#.# [002] 50 GSTT1 50 odorant receptor 50 synthetase 50 protein kinases 50 sphingolipid 50 primate lineage 50 p# gene 50 APOC3 50 autism susceptibility genes 50 transcriptome sequencing 50 deacetylation 50 inhibin 50 disulfide bond 50 zebrafish genome 50 syngeneic 50 chaperone proteins 50 paraffin embedded tissue 50 protein encoded 50 lymphoid cells 50 coding RNA 50 lipoprotein 50 glycan 50 BDNF gene 50 unmutated 50 tRNA synthetase 50 chimerism 50 IL#B 50 iPS cell 50 cellularity 50 6S RNA 50 functional annotation 50 normal prion protein 50 epigenetic alterations 50 tumorigenicity 50 lymphoid 50 oocyte 50 distantly related species 50 binding affinity 50 genetic defects 50 heterozygosity LOH 50 RNAs 50 D. simulans 50 eukaryotic cell 50 defensin 50 microarray analysis 50 subcellular compartments 50 homodimers 50 hnRNP 50 multiprotein complex 50 Toxoplasma gondii 50 D#G 50 kinases 50 GNAQ 50 genetic heterogeneity 50 subcellular 50 mutant mice 50 c Myb 50 Dictyostelium 50 abnormal prions 50 gene variant 50 condensin 50 p# [001] 50 laforin

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