chromosome #q# [001]

Related by string. chromosome #q# [002] * Chromosome . Chromosomes . chromosomes : chromosome abnormalities . Y chromosome . inactive X chromosome . aY chromosome . chromosome aberrations . chromosome segregation . chromosome deletion / #Q# [001] . #Q# [005] . #q# [002] . #Q# [002] . #Q# [003] . #Q# [004] : #Q# EPS . #Q# YTD . #Q# #Q# Var . #Q# #Q# QoQ . Geography #Q# #Q# . * DisplaySearch #Q# * *

Related by context. All words. (Click for frequent words.) 80 chromosome #q# [002] 79 #q# [001] 78 chromosome #p# [001] 76 #p#.# [001] 75 rs# [002] 75 #q# [002] 74 rs# [004] 74 rs# [003] 74 #p# [001] 73 #p#.# [002] 73 chromosome #p#.# 72 microdeletions 72 PTPN# 72 chromosome #q#.# [001] 72 SNP rs# [001] 72 #q#.# [002] 72 chromosome #q#.# [002] 72 #q#.# [001] 72 TCF#L# gene 71 hypermethylated 71 #p# [003] 71 intronic 71 chromosome #q 70 susceptibility locus 70 chromosome #p# [002] 70 susceptibility gene 70 C#Y 70 haplotypes 69 ABCB1 69 germline mutations 69 haplotype 69 rs# [001] 69 VNTR 68 genetic loci 68 CDKN2A 68 orthologs 68 MLH1 68 DRB1 * 68 microcephalin 68 polymorphisms 68 MECP2 gene 68 susceptibility loci 68 functional polymorphism 67 #S rRNA 67 MYH9 gene 67 TCF#L# 67 orthologous 67 chromosomal regions 67 heterozygotes 67 KIAA# 67 single nucleotide polymorphism 67 SNP rs# [002] 66 loci 66 intergenic 66 GSTP1 66 allelic variants 66 GSTM1 66 ribosomal DNA 66 CHEK2 66 missense mutations 66 PRNP 66 somatic mutations 66 BRAF V#E 66 intergenic regions 66 BARD1 66 rs# rs# 66 microdeletion 66 monogenic 65 COL#A# 65 LPA gene 65 linkage disequilibrium 65 apolipoprotein E gene 65 SMAD4 65 FGFR2 65 gene polymorphisms 65 alleles 65 MSH2 65 ZNF# 65 indel 65 paternally inherited 65 Polymorphisms 65 ORMDL3 65 gene locus 65 KIF6 gene 65 5 HTTLPR 65 homozygosity 65 causal variants 65 trinucleotide 65 colorectal carcinoma 65 variant rs# 65 HLA DRB1 * 65 MTHFR 65 somatic mutation 65 EGFR gene 64 heterozygosity 64 apolipoprotein E 64 serine protease 64 autosomal 64 CCR5 delta# 64 HLA DRB1 64 cytochrome b 64 DQB1 * 64 LRRK2 gene 64 major histocompatibility complex 64 TSC1 64 Plasmodium vivax 64 APOE e4 64 BRCA1 BRCA2 64 quantitative trait loci 64 genes differentially expressed 64 promoter methylation 64 CDH1 64 indels 64 SHANK3 64 ankyrin repeat 64 haplogroups 64 HFE gene 64 PALB2 64 genes encoding 64 TP# mutations 64 genetic polymorphisms 64 KRAS oncogene 64 genetic variants associated 64 chromosomal aberrations 64 cagA 64 allelic 64 RRM1 64 virulence genes 64 APOL1 63 susceptibility genes 63 SLC#A# [001] 63 mitochondrial gene 63 CYP#A# [002] 63 dinucleotide 63 caveolin 63 apolipoprotein E APOE 63 ribosomal protein 63 Genotypes 63 segmental duplications 63 Clusterin 63 globin genes 63 IgA deficiency 63 UGT#A# * 63 GPC5 63 CYP#D# gene 63 caveolae 63 variant allele 63 NR#A# 63 gene MECP2 63 immunoreactive 63 intron 63 CDH# 63 constitutively expressed 63 MAPK pathway 63 Alu elements 63 gene polymorphism 63 homozygotes 63 de novo mutations 63 KCNQ1 63 ERBB2 63 nucleotide sequences 63 polymorphism 63 GSTT1 63 CNTNAP2 63 OCA2 63 hypermethylation 63 variant alleles 63 K ras mutations 63 DRD2 gene 63 HLA DQ2 63 ABCB1 gene 63 IKZF1 63 proto oncogene 63 QTLs 63 miRNA genes 63 UGT#B# 63 paralogs 63 IL#R 63 vitamin D receptor 63 subcellular localization 63 SNPs 63 CpG islands 63 apolipoprotein E4 63 phylogenetic analyzes 63 homolog 63 autism susceptibility genes 62 ADPKD 62 MTHFR gene 62 etiologic 62 lysine residues 62 splice junctions 62 PICALM 62 Mycoplasma pneumoniae 62 membrane proximal 62 differentially methylated 62 SCN5A 62 susceptibility alleles 62 NF1 gene 62 CAG repeats 62 CpG island 62 methylenetetrahydrofolate reductase 62 IL#B 62 airway hyperresponsiveness 62 mitochondrial DNA mtDNA 62 FMR1 62 causative mutations 62 mRNA expression 62 clade B 62 LRP5 62 genomic deletions 62 chromosomal deletions 62 nucleotide sequence 62 3'UTR 62 hypomethylation 62 MYBPC3 62 allele frequencies 62 p# mutation 62 genetic locus 62 C#T [002] 62 penetrance 62 TP# gene 62 homologues 62 neuroligins 62 TET2 62 CpG 62 sequence homology 62 GNAQ 62 cis regulatory 62 methylation patterns 62 dopamine transporter gene 62 cyclin E 62 cell adhesion molecule 62 Cathepsin B 62 receptor tyrosine kinase 62 heterozygous 62 genomewide 62 WNK1 62 chromosomal rearrangement 62 Microarray analysis 62 cytokeratin 62 D#N 62 BDNF gene 62 DRD2 62 protein tyrosine phosphatase 62 Genetic variants 62 microsatellite instability 62 alpha synuclein gene 62 JAK2 enzyme 62 proband 62 Leydig cells 62 sCJD 62 SLC#A# [002] 62 LIS1 62 serum antibodies 62 MC4R gene 62 proline rich 62 histone modifications 62 missense mutation 62 T#M 62 carboxy terminal 62 autosomal dominant disorder 62 FMR1 gene 62 Supplementary Fig 62 microsatellite markers 62 transmembrane domain 62 periventricular 62 mutant allele 62 microglial 62 ORFs 62 PTEN gene 62 LRAT 62 IDH1 gene 62 colocalization 61 amino terminal 61 ERK signaling 61 ataxias 61 SCN1A 61 lymph node metastasis 61 MLL2 61 R#W [002] 61 amino acid residues 61 hypoperfusion 61 apoE4 61 entorhinal cortex 61 Haplotype 61 KCNH2 61 catechol O methyltransferase 61 metalloprotease 61 transmembrane protein 61 Trichophyton rubrum 61 chromosomal rearrangements 61 CYP#B# 61 unmethylated 61 CagA 61 dysbindin 61 immunoblotting 61 MYH9 61 carcinoembryonic antigen 61 conserved sequences 61 mutated BRCA1 61 node metastases 61 mRNA transcripts 61 dopamine D4 receptor 61 TT genotype 61 monozygotic twins 61 protein encoded 61 kilobase 61 Wwox 61 Polymorphism 61 gene loci 61 heterozygote 61 noncoding 61 serine threonine kinase 61 Single Nucleotide Polymorphism 61 untranslated regions 61 atypical hyperplasia 61 chromosomal alterations 61 KRAS mutations 61 p# mutations 61 3' UTR 61 RNA binding 61 gene APOE 61 TMEM#B 61 extracellular domain 61 methyltransferase 61 Arabidopsis genome 61 c KIT 61 pathogenic mutations 61 non coding RNA 61 transcriptionally active 61 androgen receptor AR 61 AMACR 61 splice variants 61 glomerular 61 ESR1 61 BRAF protein 61 CC genotype 61 fig. S4 61 previously undescribed 61 CHD7 61 TTR gene 61 HLA genes 61 prostate cancer CaP 61 MLL gene 61 HER2 expression 61 human leukocyte antigen 61 frameshift mutation 61 carboxyl terminal 61 missense 61 gastric carcinoma 60 homologs 60 ADH1B * 60 karyotypes 60 STAT4 60 repeat allele 60 EphB4 60 V#F mutation 60 Prox1 60 aneuploidies 60 thyrotropin levels 60 Immunohistochemical analysis 60 situ LCIS 60 tau gene 60 nucleolar 60 LRRK2 mutation 60 insertions deletions 60 mesotheliomas 60 astrocytomas 60 karyotype 60 differentially expressed genes 60 SLC#A# gene [001] 60 B7 H3 60 familial pancreatic cancer 60 coding exons 60 transmembrane receptor 60 inherited mutations 60 polyadenylation 60 NAT2 60 parkinsonism 60 Supplementary Table 60 clusterin 60 HLA DR 60 breast carcinomas 60 CGG repeats 60 ADRB2 60 transgenic mouse model 60 APOC3 60 pheochromocytomas 60 microRNA expression 60 G allele 60 hepatocellular carcinomas 60 periodontal pathogens 60 epithelial tumors 60 immunoreactivity 60 hyperplastic 60 immunohistochemical 60 BMP2 60 homeobox gene 60 transmembrane 60 NFKBIA 60 At#g# 60 sporadic ALS 60 mitogen activated protein kinase 60 Dysregulation 60 epistasis 60 generalized vitiligo 60 CNTNAP2 gene 60 adenoma 60 PON1 60 CYP#A# gene 60 heterochromatic 60 evolutionarily conserved 60 cadherin 60 homozygote 60 androgen receptor gene 60 gene encoding 60 HepG2 cells 60 HG PIN 60 Upregulation 60 previously uncharacterized 60 phenotype 60 PIK3CA 60 TRAF1 C5 60 MGUS 60 perivascular 60 subfamily 60 colonic mucosa 60 genome rearrangements 60 miRNA expression 60 evolutionary conserved 60 forkhead 60 hepatic lipase 60 CFTR gene 60 G6PD 60 virulence determinants 60 thyrotropin 60 mosaicism 60 VKORC1 60 homodimer 60 prostate carcinoma 60 condensin 60 Activating mutations 60 germline mutation 60 SNCA 60 postsynaptic 60 subventricular zone 60 endonuclease 60 pDC 60 mutated K ras 60 neuritic 60 familial ALS 60 histone acetylation 60 epithelia 60 TOP2A gene 60 genes CYP#C# 60 distinct subtypes 60 genes predisposing 60 allele 60 UTRs 60 PON1 gene 60 hypogonadotropic hypogonadism 60 unmutated 60 EGF receptors 60 nucleoli 60 cytopathic 60 uPAR 60 genetic polymorphism 60 amino acid substitutions 60 MMP# 60 phenotypic variation 60 cytosine methylation 60 hyperhomocysteinemia 60 A. thaliana 60 cysteine residues 59 epigenetic modification 59 L#R 59 KLF4 59 myeloproliferative 59 K#N 59 H#K# [002] 59 aberrant methylation 59 CYP#C# [002] 59 G#S [002] 59 astrocytic 59 maternally inherited 59 Rap1 59 YKL 59 vacuolar 59 SLITRK1 59 LRP6 59 microbleeds 59 DNA methyltransferase 59 gene variants 59 tRNA synthetase 59 ALK mutations 59 coding sequences 59 HLA DRB1 SE 59 colorectal adenoma 59 C. neoformans 59 rRNA 59 5q 59 centromeric 59 inactive X chromosome 59 hamartomas 59 lung carcinomas 59 papillary renal cell carcinoma 59 RASSF1A 59 APOE4 59 CYP#E# gene 59 MEF2A 59 MECP2 59 genes BRCA1 59 DNA methylation patterns 59 telomeric 59 paraganglioma 59 PNET 59 FKBP# 59 Fas ligand 59 adipogenic 59 renal cysts 59 herpesviruses 59 assay detects 59 receptor gene 59 tryptophan hydroxylase 59 GLUT1 59 oxytocin receptor 59 ncRNA 59 lymphangiogenesis 59 progressive neurodegenerative disorder 59 HMGA1 59 cAMP signaling 59 Trypanosoma brucei 59 miRNAs miR 59 N. gonorrhoeae 59 amyloid deposition 59 archaeal 59 nucleotide substitutions 59 phosphorylates 59 fruitfly Drosophila 59 genetic variant 59 homodimers 59 cytoplasmic tail 59 #q# deletion 59 homologous genes 59 BMPR2 59 chemokine receptor 59 Ki# 59 Caenorhabditis 59 Apolipoprotein E 59 Lp PLA 2 59 cardioembolic stroke 59 kDa protein 59 KLF# 59 cysteines 59 mucinous 59 exfoliative glaucoma 59 histologic subtype 59 parkin gene 59 epigenetic alterations 59 null mice 59 NKX#.# 59 number variation CNV 59 ENPP1 59 CREBBP 59 airway responsiveness 59 autosomal recessive 59 Single Nucleotide Polymorphisms SNPs 59 cytoplasmic domain 59 metaplasia 59 TGFBR1 * 6A 59 PCR RFLP 59 FXTAS 59 clades 59 mtDNA mutations 59 APOE allele 59 APOE ε4 59 Haplogroup 59 #S rDNA 59 H#K#me# 59 hydrolase 59 Immunohistochemical staining 59 TOMM# 59 BRAF V#E mutation 59 TMPRSS2 ERG fusion 59 ALK gene 59 inducible nitric oxide synthase 59 Arrhythmogenic Right Ventricular Cardiomyopathy 59 arrhythmogenic 59 nicotine receptor 59 catenin 59 Drosophila genome 59 S#A# [002] 59 breast cancer genes BRCA1 59 basal forebrain 59 Elevated serum 59 gene APOE4 59 mutations 59 E selectin 59 WT1 59 ERalpha 59 pRb 59 E#F# 59 substrate specificity 59 extramedullary 59 aggrecan 59 infarcts 59 FUS1 59 PTEN mutations 59 Cx# [001] 59 ductal lobular 59 MC1R gene 59 matrix metalloproteinase 59 familial clustering 59 supratentorial 59 NPY gene 59 hydroxylase 59 A2 Lp PLA2 59 enolase 59 tumor suppressor protein 59 Genetic variation 59 subfamilies 59 prefrontal cortical 59 vimentin 59 5 HT1A 59 gastric adenocarcinoma 59 progranulin gene 59 gastrointestinal stromal tumors GISTs 59 FLT3 59 β1 59 nitrotyrosine 59 epigenetic changes 59 hypothalamic pituitary 59 Leydig cell 59 FGFR3 59 Chromosome 59 HLA alleles 58 ApoE gene 58 ependymomas 58 BRAF gene 58 tetramer 58 seropositivity 58 anogenital 58 C. pneumoniae 58 APOA5 58 transferase 58 IL8 58 bronchial epithelial cells 58 TCF4 58 RNA polymerases 58 prothrombotic 58 constitutively active 58 K#R [002] 58 coding genes 58 circadian genes 58 fig. S1 58 deacetylation 58 glutamic acid decarboxylase 58 hepatoma 58 colorectal neoplasms 58 CD#b 58 GATA4 58 CD# expression [001] 58 meiotic recombination 58 polyomavirus 58 C. trachomatis 58 MIF protein 58 codon 58 isotypes 58 adenocarcinomas 58 LMNA 58 number variations CNVs 58 dopamine receptor gene 58 fibrillin 1 58 striatal 58 phospho 58 CFH gene 58 MC1R 58 Hashimoto thyroiditis 58 acetylcholine receptor 58 causative genes 58 PCa 58 synuclein 58 PITX2 58 ADAMTS# 58 gene amplification 58 epigenetic silencing 58 PDZ domain 58 D. melanogaster 58 familial aggregation 58 proteolytic cleavage 58 Single Nucleotide Polymorphisms 58 TYMS 58 LKB1 58 Leukemias 58 #S rRNA gene 58 chromosomal translocations 58 HER2 receptor 58 HDL2 58 proapoptotic 58 noncoding RNAs 58 Chlamydia pneumoniae 58 CD1d 58 homology 58 p tau 58 selective antagonists 58 serous ovarian cancer 58 cytosine 58 SSc 58 Brugada syndrome 58 phenotypes 58 subgenual cingulate 58 differentially regulated 58 osteoblastic 58 lactate dehydrogenase 58 NKG2D 58 rDNA 58 TP# mutation 58 CNVs 58 clefting 58 ncRNAs 58 kinase domain 58 thymine T 58 isoenzyme 58 HLA B# 58 SPINK1 58 IRAK1 58 MDR1 58 site directed mutagenesis 58 dbSNP 58 radial glia 58 Chromosomal 58 exon 58 bacterial genomes 58 cytokine receptors 58 autosomal recessive disease 58 advanced adenoma 58 M. pneumoniae 58 linkage disequilibrium LD 58 urothelial 58 encodes protein 58 serine threonine 58 tyrosine kinase receptor 58 L. pneumophila 58 DLX5 58 Cytogenetic 58 CYP#D# 58 amino acid sequence 58 genotyping arrays 58 polyglutamine 58 clinicopathologic 58 HPV# 58 beta globin 58 proteinases 58 adenylate cyclase 58 Figure 1C 58 multivariate Cox 58 Phylogenetic analysis 58 hyperactivation 58 breast cancer subtypes 58 gene rearrangements 58 MAP#K# 58 immunohistochemical staining 58 transcriptional activation 58 ERBB4 58 Jhdm2a 58 succinate dehydrogenase 58 histologic subtypes 58 VIPR2 58 inactivating mutations 58 colorectal adenomas 58 DLC1 58 exon intron 58 trophoblast cells 58 PKD1 58 PLA2 58 RNA sequences 58 MSMB 58 Meckel Gruber 58 TIMP 58 RUNX3 58 methylated DNA 58 hereditary hemochromatosis 58 Chlamydophila pneumoniae 58 malignant prostate 58 dimeric 58 Histone 58 multigenic 58 sphingolipid 58 gene variant 58 esophageal squamous cell carcinoma 58 COMT gene 58 beta globin gene 58 beta1 integrin 58 LDL receptor 58 oligomerization 58 JAK2 mutation 58 ectodomain 58 genotypes 58 alternatively spliced 58 HER2 neu 58 nodal metastasis 58 FTLD 58 LVNC 58 serum BDNF 58 CCL#L# 58 Macrophage 58 IL #R 58 DNMT1 58 P cadherin 58 peroxisomal 58 clinicopathological 58 C1q 58 myeloperoxidase 58 amyloidogenic 58 ultrastructural 58 Asymptomatic 58 CDK4 58 breast carcinoma 58 coexpression 58 monophyletic 58 distinct lineages 58 Fig. 2b 58 genetic variants 58 spontaneous mutations 58 alpha2 58 catechol O methyltransferase COMT 58 mediated inhibition 58 CEACAM1 58 precursor lesions 58 lymphocytic 58 CALHM1 58 activating mutations 58 Cytotoxic T 58 mutated genes 58 downregulated 58 amplicons 58 posttranslational modifications 58 IgG4 58 chromosomal DNA 58 cardiac troponin T 58 surgically resected 58 differential gene expression 58 HbF 58 subclinical 58 Single nucleotide polymorphisms 58 contigs 58 cutaneous lesions 58 cTnI 58 WDR# 58 homologue 58 #S ribosomal RNA 58 COMT 58 Brain derived neurotrophic 58 PTP1B 58 Mutational 58 diagnostic biomarker 57 amino acid substitution 57 Sonic Hedgehog 57 CISH 57 Figure 2C 57 Sp1 57 PDE#A 57 hyperintense lesions 57 receptor kinase 57 SE alleles 57 protein isoforms 57 histological subtype 57 apo E 57 fronto temporal dementia 57 lipoxygenase 57 pseudogenes 57 CD# CD# 57 tetramers 57 chromosome rearrangements 57 T1D 57 neurexins 57 neuronal dysfunction 57 bcl 2 57 IPAH 57 Kir#.# 57 subcortical 57 codons 57 lung adenocarcinomas 57 cyclin dependent kinase 57 unmethylated DNA 57 P. gingivalis 57 alpha1 57 P aeruginosa 57 cM 57 homozygous 57 lymph node metastases 57 transcriptional repressor 57 lymphoid 57 CA1 57 hypervariable 57 Li Fraumeni 57 rCBF 57 Supplemental Figure 57 pancreatic endocrine 57 PPARg 57 APOE e4 allele 57 EGFR mutant 57 promoter polymorphism 57 outer membrane proteins 57 receptor molecule 57 neoplastic cells 57 perirhinal cortex 57 imprinted genes 57 C#Y mutation 57 paragangliomas 57 CYP#C# * 57 plasma adiponectin 57 testicular germ cell 57 colorectal polyp 57 IGFBP 57 atherothrombosis 57 gastric cardia 57 ectopic expression 57 virus XMRV 57 palladin 57 klotho 57 paramyxoviruses 57 micrometastases 57 HOTAIR 57 invasive carcinomas 57 ESBL producing 57 hypometabolism 57 tyrosine phosphorylation 57 presynaptic 57 melatonin receptor 57 arcuate nucleus 57 arterial calcification 57 myocardial fibrosis 57 CHRNA5 57 H#K# [001] 57 striata 57 normal karyotype 57 gastric carcinogenesis 57 proximal colon 57 morphologic 57 tryptase 57 alanine aminotransferase 57 endophenotypes 57 chronic myeloid 57 upregulated 57 schwannomas 57 thyroglobulin 57 synovial cells 57 cerebellar 57 ciliates 57 genotyped 57 EF Tu 57 subclinical hyperthyroidism 57 PCA3 gene 57 etiologic agent 57 thyroid hormone receptor 57 thyroid carcinoma 57 VEGF receptor 57 Phosphorylation 57 granulomatous 57 genomic rearrangement 57 N acetyltransferase 57 kilobases 57 Foxp2 57 TOP2A 57 clonally 57 papillomas 57 β amyloid 57 CYP#C# gene 57 cytosolic 57 ubiquitinated 57 gp# protein [002] 57 bronchoalveolar lavage fluid 57 P. ovale 57 Prevotella 57 adhesion molecule 57 neuroblastoma tumors 57 ortholog 57 telomere lengths 57 monozygotic 57 Kupffer cells 57 single nucleotide polymorphisms 57 metalloproteinase 57 picomolar 57 centromere 57 immunofluorescence 57 lymphoblastoid cell lines 57 mRNA encoding 57 molecular subtypes 57 endothelial activation 57 anterior pituitary 57 beta3 57 cTnT 57 superior temporal gyrus 57 IgG1 57 OGG1 57 TIMP 1 57 beta lactamases 57 SORL1

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