chromosomal regions

Related by string. * Chromosomal : chromosomal abnormalities . chromosomal instability . chromosomal aberrations . both genders chromosomal . chromosomal abnormality . chromosomal rearrangements / re gion . REGION . Regions . REGIONS . Re gion . Region : Great Lakes Region . Mid Atlantic Region . Class 5A Region . Class 4A Region . Geographic Region Percentage Breakdown . tribal regions * *

Related by context. All words. (Click for frequent words.) 75 genetic loci 71 #q#.# [002] 70 missense mutations 70 quantitative trait loci 70 susceptibility genes 70 #q# [001] 70 splice junctions 68 PTPN# 68 genetic variants associated 68 causal variants 68 neuroligins 68 loci 68 KIAA# 68 histone modifications 67 chromosome #q#.# [001] 67 microdeletions 67 LIS1 67 susceptibility loci 67 chromosome #q# [001] 67 #p#.# [001] 67 autism susceptibility genes 67 chromosomal DNA 67 molecular pathways 67 chromosome #q 67 histone modification 67 genetic polymorphisms 67 splice variants 67 gene locus 66 nucleotide sequence 66 gene loci 66 sporadic ALS 66 DNA methylation patterns 66 segmental duplications 66 paralogs 66 QTLs 66 alpha synuclein gene 66 miRNA expression 66 CNVs 66 phylogenetic analyzes 66 #p# [001] 66 mitochondrial gene 66 FGFs 66 genes encoding 66 somatic mutations 66 orthologs 66 #S rRNA 66 FGFR2 66 methylation patterns 65 causative genes 65 virulence genes 65 #p#.# [002] 65 modifier genes 65 spontaneous mutations 65 molecular abnormalities 65 ABCB1 65 MLH1 65 PALB2 65 rRNA 65 allelic 65 chromatin structure 65 chromosome #p#.# 65 chromosome #q# [002] 65 KLF4 65 p# mutations 65 microRNA molecules 65 susceptibility locus 65 non coding RNA 65 microdeletion 65 phenotypes 65 IL#R 65 genetic alterations 65 gene variants 65 polymorphisms 65 transcriptomes 65 gene polymorphisms 65 rs# [004] 65 p# activation 65 miRNA genes 65 susceptibility gene 65 transcriptional regulation 64 protein kinases 64 gene expression patterns 64 haplotypes 64 TSC1 64 HOTAIR 64 germline mutations 64 cellular pathways 64 chromosomal rearrangements 64 PICALM 64 vimentin 64 genetic variants 64 #q#.# [001] 64 heterozygosity 64 chromosomal translocations 64 genomic alterations 64 causative mutations 64 hypermethylation 64 genetic determinants 64 mRNA expression 64 biologic pathways 64 differentially expressed genes 64 Genetic variations 64 CDH1 64 CHD7 64 chromosomal instability 64 dysbindin 64 microRNA expression 64 Genetic variants 64 noncoding RNAs 64 apoE 64 chromosome #p# [001] 64 DQB1 * 64 miRNAs 64 epigenetic modification 64 APOE e4 64 mutated genes 64 inherited mutations 64 Genetic variation 64 drug metabolizing enzymes 64 MYH9 64 ribosomal proteins 64 circadian genes 64 #q# [002] 64 epigenetic mechanisms 63 uPAR 63 SNP rs# [001] 63 RNA sequences 63 rs# [003] 63 MAPK pathway 63 tyrosine phosphorylation 63 endophenotypes 63 pRb 63 secreted proteins 63 Clusterin 63 BARD1 63 HDACs 63 genetic locus 63 CNTNAP2 63 circadian clock genes 63 MSH2 63 tyrosine kinases 63 cyclin E 63 histone deacetylases 63 p#/CBP 63 PON1 63 ZNF# 63 mRNA transcripts 63 intron 63 PTEN mutations 63 linkage disequilibrium 63 SLC#A# [002] 63 neuropsychiatric diseases 63 TCF#L# 63 familial pancreatic cancer 63 signaling pathways 63 GPC5 63 gene expression profiles 63 CHI#L# 63 micro RNAs 63 mtDNA mutations 63 genetic polymorphism 63 TCF#L# gene 63 H#K#me# 63 cohesin 63 gene rearrangements 63 histone deacetylation 63 amino acid substitutions 63 genes 63 RNA binding 63 hypermethylated 63 ultraconserved elements 63 DLX5 63 intergenic regions 63 ncRNAs 62 phenotype 62 RUNX3 62 miR #b [002] 62 selective antagonists 62 Prox1 62 transcriptional activation 62 glycoproteins 62 #q# deletion 62 glycan 62 protein isoforms 62 sequence homology 62 phosphorylates 62 KLF# 62 SMAD4 62 DARPP 62 STAT4 62 Wnt signaling pathway 62 genomic loci 62 Wwox 62 epigenetic alterations 62 subcellular 62 epigenetic regulation 62 gene mutations 62 TAp# 62 MECP2 gene 62 cell signaling pathways 62 CDKN2A 62 glycolipids 62 kinase domain 62 mitochondrial DNA mtDNA 62 major histocompatibility complex 62 tumor suppressor protein 62 cofactors 62 COL#A# 62 PTEN gene 62 molecular subtypes 62 chromosome #q#.# [002] 62 haplotype 62 promoter methylation 62 apoE4 62 isoforms 62 microglial 62 molecular biomarkers 62 intergenic 62 functional polymorphism 62 A. thaliana 62 imprinted genes 62 metabolic abnormalities 62 centrosome 62 M. pneumoniae 62 signaling cascades 62 primate genomes 62 familial clustering 62 mutant allele 62 MTHFR 62 histone acetylation 62 gene duplications 62 SH#B# 62 K ras mutations 62 progranulin gene 62 tRNA synthetase 62 promoter hypermethylation 62 cysteine residues 62 primary cilia 62 HLA DRB1 62 proto oncogene 62 micro RNA 62 chromosome aberrations 62 GSTP1 62 serine protease 62 TMEM#B 62 homozygosity 62 PDGFR 62 intronic 62 perilipin 62 maternally inherited 62 Cathepsin B 62 chromosome rearrangements 62 tumor suppressor genes 61 CagA 61 deacetylation 61 virulence determinants 61 androgen receptor AR 61 ERK2 61 serine proteases 61 metabolic enzymes 61 PARP inhibition 61 dopamine D2 receptors 61 PIK3CA 61 mammary stem cells 61 yeast genome 61 HLA molecules 61 exons 61 c MET 61 herpesviruses 61 nucleotide sequences 61 untranslated regions 61 LRP5 61 metalloprotease 61 genotypes 61 miR #a [002] 61 LDL receptor 61 homologues 61 genetic mutations 61 de novo mutations 61 bacterial genomes 61 TGFBR1 * 6A 61 metabolizing enzymes 61 Alu elements 61 Dysregulation 61 miR #a [001] 61 phenotypic traits 61 biochemical pathways 61 GABAergic interneurons 61 potent inhibition 61 genetic aberrations 61 LRP6 61 FUS1 61 Transcription factors 61 rs# [001] 61 neurexins 61 operons 61 VNTR 61 SLITRK1 61 MLL gene 61 C#Y 61 monozygotic twins 61 receptor gamma 61 alleles 61 nicotinic receptors 61 FGFR3 61 enolase 61 chromosomal alterations 61 conserved sequences 61 ALK mutations 61 LPA gene 61 germline mutation 61 distinct subtypes 61 membrane proximal 61 HDAC enzymes 61 HER2 HER3 61 exomes 61 p# mutation 61 LRRK2 gene 61 mutations 61 substrate specificity 61 Drosophila genome 61 receptor gene 61 chromosomal rearrangement 61 neurexin 61 ApoE gene 61 indels 61 PPARg 61 NF kB pathway 61 vacuolar 61 inbred strains 61 DNA methyltransferases 61 narcolepsy cataplexy 61 ERBB2 61 CAG repeats 61 microRNAs miRNAs 61 transmembrane proteins 61 gastric carcinogenesis 61 genetic markers 61 palladin 61 genomic deletions 61 synuclein 61 UGT#B# 61 coding sequences 61 enterotypes 61 Kinases 61 constitutively expressed 61 previously uncharacterized 61 HLA DR 61 phenotypic variation 61 coding exons 61 lysine residues 61 aneuploidies 60 sphingolipid 60 CYP#C# [002] 60 amino acid sequences 60 receptor subtypes 60 caveolae 60 coding genes 60 NFKBIA 60 monogenic 60 DGAT1 60 transmembrane receptor 60 genotypic 60 outer membrane proteins 60 presynaptic 60 clefting 60 genomewide 60 heterologous expression 60 CYP#E# gene 60 mRNA molecules 60 amino acid residues 60 WNK1 60 HipA 60 chromatin remodeling 60 C. neoformans 60 ERK signaling 60 USP# 60 VHL gene 60 gene amplification 60 serotonin transporter 60 glutamate receptors 60 mutated protein 60 PPARγ 60 SNCA 60 CCL#L# 60 genome rearrangements 60 homologs 60 MYH9 gene 60 ortholog 60 uncharacterized genes 60 evolutionarily conserved 60 SIRT1 gene 60 SNPs 60 Smad3 60 heritable traits 60 E#F# 60 MDSCs 60 NPY gene 60 genomic instability 60 proteins misfold 60 etiologic 60 metabolic pathways 60 GABAB receptors 60 FTLD 60 protein tyrosine phosphatase 60 PKM2 60 differentially regulated 60 NR#A# 60 ALDH2 60 microRNA miR 60 WDR# 60 ABCB1 gene 60 CRISPR Cas 60 #p# [003] 60 E3 ligase 60 epigenetic silencing 60 ERK1 60 lipoxygenase 60 Jhdm2a 60 heterozygote 60 oncoprotein 60 breast cancer subtypes 60 ribosomal protein 60 gp# [002] 60 UTRs 60 biologic pathway 60 NKX#.# 60 caveolin 60 KRAS mutations 60 MeCP2 gene 60 gene expression 60 E1A 60 single nucleotide polymorphism 60 CYP#D# gene 60 chemokine receptors 60 missense mutation 60 Fibroblast Growth Factor Receptor 60 biochemical mechanisms 60 posttranslational modifications 60 sRNA 60 orthologous 60 BRAF protein 60 homodimers 60 FGFR1 60 PAK1 60 BDNF gene 60 Arp2 3 60 Polymorphisms 60 subcellular compartments 60 MEF2A 60 Skp2 60 anterior pituitary 60 epigenetic modifications 60 Wnt pathway 60 genetic variations 60 differential gene expression 60 pathogenic mechanisms 60 SIRT3 60 signaling molecules 60 NR2B 60 ubiquitin ligases 60 KCNQ1 60 HGPS 60 gene fusions 60 ankyrin repeat 60 autosomal 60 deleterious mutations 60 chromosomal anomalies 60 Microarray analysis 60 proteins 60 A3 adenosine receptor 60 mRNA sequences 60 molecular markers 60 oncogenic proteins 60 downregulation 60 neuroanatomical 60 mitogen activated protein kinase 60 molecular pathway 60 microRNAs 60 DNA demethylation 60 proteomes 60 proteolysis 60 mutant huntingtin protein 60 HNPCC 60 transmembrane domains 60 isotype 60 R#W [002] 60 KIBRA 60 mammalian genomes 60 clusterin 60 Haplotype 60 IGFBP2 60 TCF4 60 FLT3 60 IDH1 60 noncoding 60 proband 60 neuronal circuitry 60 causative mutation 60 RNA splicing 60 IKKß 60 underlying pathophysiology 60 rs# [002] 60 pathogenic mutations 60 multigene 59 BMAL1 59 genes differentially expressed 59 serine threonine kinase 59 glycosylation 59 causal pathways 59 microsatellite markers 59 gene encoding 59 prion strains 59 epigenetic marks 59 gene deletions 59 HLA genes 59 synaptic proteins 59 protein p# 59 cysteines 59 cDNA libraries 59 epigenetic markers 59 TTR gene 59 potent inhibitors 59 SNP rs# [002] 59 transmembrane 59 subcellular localization 59 CYP#B# 59 ADAM# 59 HER2 expression 59 MHC molecules 59 regulates gene expression 59 orthologous genes 59 5 hmC 59 cypin 59 isoenzymes 59 lincRNAs 59 MAP kinases 59 ncRNA 59 neurones 59 5 hydroxymethylcytosine 59 microcephalin 59 mammary cells 59 adaptive immunity 59 lipid rafts 59 RRM1 59 SOCS3 59 aldehyde dehydrogenase 59 Li Fraumeni 59 multigenic 59 tau protein 59 PKD1 59 phenotypic differences 59 nucleolar 59 C1q 59 endonuclease 59 alexithymia 59 SLC#A# [001] 59 V3 loop 59 prognostic markers 59 causative gene 59 messenger RNAs mRNAs 59 inactivating mutations 59 tumor suppressor gene 59 Immunohistochemical analysis 59 IGFBP 59 vasopressin receptors 59 somatic mutation 59 RNA transcripts 59 mucins 59 HepG2 cells 59 neurobiological mechanisms 59 chromosomal aberrations 59 CD# expression [001] 59 mitochondrial mutations 59 APOL1 59 microvesicles 59 4E BP1 59 transgenic mouse model 59 granzyme B 59 FMR1 gene 59 PITX2 59 abnormal prion protein 59 cell adhesion molecules 59 estrogen receptor alpha 59 S#A# [002] 59 apoptotic pathway 59 epigenetic changes 59 myoepithelial 59 granule cells 59 paxillin 59 Cyclin D1 59 cadherin 59 epithelial tumors 59 proteases 59 signal transduction pathways 59 methylated DNA 59 CXCL# 59 protein encoded 59 genes predisposing 59 transgene expression 59 genotype phenotype 59 Genotypes 59 cDNA microarray 59 DRD2 gene 59 MMP# 59 BRAF mutation 59 cytokine receptors 59 UCRs 59 miRs 59 SCN5A 59 pleiotropic effects 59 HLA DQ2 59 DNA sequences 59 DNA polymerases 59 JAK2 59 JNK1 59 c Myb 59 molecular mechanisms underlying 59 EphB4 59 protein kinase C 59 subtypes 59 epithelial tissues 59 GSTM1 59 EGFR mutations 59 transcription factors 59 GPR# [002] 59 telomere DNA 59 PML RARA 59 APOE genotype 59 cDNAs 59 DNA rearrangements 59 phosphatases 59 MAPK 59 protein ligand 59 genes encode proteins 59 mutant proteins 59 colonic mucosa 59 transcriptome 59 MDM2 59 striatal 59 intracellular bacteria 59 MLL2 59 TMPRSS2 ERG 59 CXCL5 59 DISC1 59 microarray experiments 59 LRAT 59 mutant SOD1 59 BRAF V#E 59 phosphate S1P 59 ribosomal RNA 59 operon 59 COMT gene 59 medial frontal cortex 59 medulloblastomas 59 vasopressin receptor 59 CDK8 59 At#g# 59 periodontal pathogens 59 Bacteroides 59 Arabidopsis genes 59 mosaicism 59 Rab# 59 beta1 integrin 59 VIPR2 59 clonally 59 vitamin D receptor 59 neurite outgrowth 59 previously undescribed 59 PIP3 59 positional cloning 59 synapse formation 59 astrocytic 59 DRD2 59 acetylcholine receptor 59 H#K# [002] 59 biosynthetic pathways 59 heterodimer 59 variant allele 59 EphA2 59 SWI SNF 59 Arabidopsis genome 59 CD1d 59 adipokines 59 GATA4 59 ApoE 59 mitochondrial metabolism 59 IgA deficiency 59 GABRA2 59 short hairpin RNAs 59 estrogen metabolism 59 NF1 gene 59 proteins encoded 59 VEGF receptor 59 acetylation 59 receptor ligand 59 cAMP signaling 59 cell adhesion molecule 59 IRAK1 58 IGF1 58 miRNA molecules 58 UGT#A# * 58 nicotinic receptor 58 presenilin 58 ribosomal DNA 58 phenotypic expression 58 oncogenic 58 gene 58 podocytes 58 H2AX 58 genes CYP#C# 58 CaM kinase II 58 motor neuron degeneration 58 MIF protein 58 OCT4 58 intracellular signaling 58 Notch signaling 58 tumor biopsies 58 genomic variation 58 paternally inherited 58 ERBB4 58 testicular germ cell 58 Vps# 58 CHEK2 58 lymphoid cells 58 Kv#.# 58 sCJD 58 etiologic factors 58 GSTT1 58 Wnt#b 58 Rap1 58 ORFs 58 lincRNA 58 FGF2 58 Leydig cell 58 eIF 4E 58 glucocorticoid receptors 58 CEACAM1 58 molecular underpinnings 58 colorectal tumor 58 genetic variation 58 copper zinc superoxide 58 HIP1 58 kinases 58 neurofibrillary tangles 58 histone H3 58 bile acid metabolism 58 cathepsins 58 #BP# 58 IKZF1 58 intracellular signaling pathways 58 radial glia 58 neuroligin 58 cis regulatory 58 nAChRs 58 neuropilin 58 AT1R 58 protein conformation 58 epitope 58 protein alpha synuclein 58 axon guidance 58 OGG1 58 cell nuclei 58 Transcriptome 58 lipid metabolism 58 Lp PLA 2 58 polymerases 58 APOE4 58 cyclic AMP cAMP 58 STK# [002] 58 ribosomal RNA rRNA 58 ligase 58 tumor subtypes 58 alpha synuclein protein 58 cytoskeletal 58 ataxias 58 EBNA1 58 T#M 58 MTHFR gene 58 intracellular proteins 58 tumor microenvironment 58 eukaryotic cells 58 JAK2 enzyme 58 epitopes 58 PAR1 58 NKG2D 58 activating mutations 58 Phylogenetic analysis 58 adhesion molecule 58 fatty acid synthase 58 Notch receptor 58 alternative splicing 58 c KIT 58 PI3K AKT 58 SIRT2 58 centromeres 58 synaptogenesis 58 Activating mutations 58 multiprotein complex 58 HLA antigens 58 Dpp 58 SPINK1 58 indel 58 CALHM1 58 androgen receptor gene 58 ciliated 58 IgG antibody 58 apolipoprotein E 58 MiRNAs 58 generalized vitiligo 58 P#X# 58 colocalization 58 S#P# 58 CCR5 delta# 58 heterodimers 58 GLUT1 58 mitochondrial proteins 58 signaling pathway 58 renal fibrosis 58 hippocampal cells 58 pDCs 58 forkhead 58 CDX2 58 CHRNA5 58 regulating gene expression 58 amino acid sequence 58 OPHN1 58 c Src 58 transgenic mouse models 58 extramedullary 58 eotaxin 58 picomolar 58 molecular biomarker 58 metazoan 58 nucleolin 58 chromatin remodeling complex 58 PKCi 58 5 HTTLPR 58 prefrontal cortical 58 NS5A 58 HCV replication 58 Trypanosoma brucei 58 biochemical signaling pathways 58 Epstein Barr virus EBV 58 MEF2D 58 non coding RNAs 58 synthases 58 TYMS 58 neuropathologic 58 ligases 58 familial ALS 58 HLA alleles 58 SE alleles 58 insulin receptors 58 TGF β 58 serum antibodies 58 TRAF1 C5 58 perivascular 58 S. maltophilia 58 Wnt proteins 58 p# MAPK 58 P. gingivalis 58 LRRK2 mutation 58 tropomyosin 58 allelic variants 58 histone H4 58 HOX genes 58 histone 58 intracellular protein 58 dopamine transporter 58 podocyte 58 ErbB2 58 transmembrane protein 58 biological pathways 58 structural rearrangements 58 hereditary predisposition 58 chromosomal deletions 58 CYP#A# [002] 58 RIP1 58 polyploid 58 glioblastoma cells 58 TEP1 58 druggable targets 58 hypomethylation 58 Htt 58 centromere 58 dopamine receptor 58 catechol O methyltransferase 58 transcriptional coactivator 58 misfolded protein 58 transgenic mice expressing 58 NS3 58 archaeal 58 chitinase 58 increased intestinal permeability 58 LRP1 58 receptor proteins 58 NEDD9 58 CCR3 58 EGFR gene 58 CREB protein 58 Fas ligand 58 telomere lengths 58 pleiotropic 58 methylation 58 chromosome #p# [002] 58 MetAP2 58 β amyloid 58 V#F mutation 58 alternatively spliced 58 c MYC 58 activin 58 EAAT2 58 DICER1 gene 58 TGF ß 58 HLA B# 58 caveolin 1 58 receptor molecule 58 oncoproteins 58 fungal genomes 58 HBx 58 G allele 58 Single Nucleotide Polymorphisms SNPs 58 atypical hyperplasia 58 INF2 58 genomic sequence 58 focal adhesions 58 MHC genes 58 phylogenetically 58 phenotypic 58 intestinal epithelium 58 telomere shortening 58 seminomas 58 Li Fraumeni syndrome 58 ultrastructural 58 excitatory synapses 58 glycosyltransferase 58 dimerization 58 T. brucei 58 serine threonine kinases 58 UCP2 58 NKT cell 58 Neuregulin 1 58 TrkB 58 clade B 58 Alleles 58 Drosha 58 allele frequencies 58 FGFR2 gene 58 HFE gene 58 histone methylation 57 EGFR signaling 57 aberrant activation 57 cyclin dependent kinase 57 abnormal methylation 57 genes BRCA1 57 glycans 57 metabolomic profiles 57 neuronal dysfunction 57 viral genomes 57 ribonucleic acids 57 AMACR 57 nAChR 57 ubiquitinated 57 sarcosine 57 allelic variation 57 endogenous ligands 57 oxidized phospholipids 57 ADAMTS# 57 sequenced genomes 57 matrix metalloproteinases 57 Eg5 57 GPNMB 57 IL #p# 57 ABCA1 57 urocortin 57 C. jejuni 57 inhibitory receptor 57 Chromosome 57 NR2B subunit 57 nucleoli 57 RNA polymerases 57 aberrant methylation 57 APOE allele 57 COMT 57 secreted protein 57 heterochromatic 57 GAGs 57 glucocorticoid receptor GR 57 S6K 57 H#K# [001] 57 dentate gyrus 57 susceptibility alleles 57 IKK beta 57 BRCA1 BRCA2 57 #S ribosomal RNA 57 IDH2 57 PTP1B 57 P cadherin

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