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(Click for frequent words.) 69 X chromosome 60 aY chromosome 59 mutated gene 58 alleles 58 imprinted genes 57 HLA genes 57 X inactivation 57 mutations 57 centrosomes 56 autosomes 56 mutation 56 allele 56 heterozygous 55 FMR1 gene 55 genes 55 SRY gene 55 recessive gene 55 mosaicism 54 germ cells 54 XY chromosome 54 defective gene 54 homologous chromosomes 53 NR#A# gene 53 chromosomes 53 XX chromosomes 53 chromosome 53 LIS1 53 neuroligins 53 mutant gene 53 recessive genes 53 MHC genes 53 Y chromosome 53 piRNAs 52 inherited mutations 52 BRCA1 gene 52 Neuregulin 1 52 gene 52 IGF2 52 homozygous 52 BRIP1 52 chromosomal 52 Pol IV 52 dizygotic 52 XY chromosomes 52 MLL gene 52 colocalization 52 D. melanogaster 51 thymine 51 thymocytes 51 premutation 51 homologs 51 haploid 51 FGFR2 51 MSH2 51 spontaneous mutations 51 genetic mutations 51 gene mutation 51 Klinefelter syndrome 51 FMR1 51 tumor suppressor gene 51 missense mutations 51 PALB2 51 genetic mutation 51 dizygotic twins 51 synapsis 51 genes predisposing 51 APOE4 51 mutant allele 51 DISC1 51 MHC molecules 51 germline stem cells 51 ERK2 51 germline cells 51 microdeletion 50 mutated genes 50 heterochromatin 50 recessive trait 50 chromosomal deletions 50 epigenetic silencing 50 heritable 50 FXTAS 50 estrogen receptor alpha 50 PTEN gene 50 epigenetically 50 prairie vole 50 blastomeres 50 diploid 50 MTHFR 50 germline 50 spontaneous mutation 50 de novo mutations 50 centromeres 50 mice lacking 50 Alu elements 50 Y chromosomes 50 BRCA gene mutation 50 chromosomal rearrangements 50 genes encoding 50 tRNAs 50 tyrosine phosphorylation 49 mutant genes 49 mutant alleles 49 presenilin 49 Rb gene 49 polymorphism 49 codons 49 olfactory receptor 49 tumor suppressor genes 49 RNA transcripts 49 ApoE 49 BRCA2 gene 49 unmethylated 49 homologues 49 nucleotide 49 frameshift mutation 49 meiosis 49 autosomal recessive 49 deleterious mutations 49 alanine 49 homodimers 49 gene mutations 49 divide asymmetrically 49 tetramers 49 genetic variant 49 heterozygotes 49 major histocompatibility complex 49 MeCP2 gene 49 Hsp# [001] 49 Vpu 49 Foxp3 49 centrosome 49 monozygotic twins 49 amino acid residues 49 HLA molecules 49 polymerases 49 sister chromatid 49 APOE4 gene 49 androgen receptor gene 49 phosphorylate 49 Fragile X gene 49 germline mutations 49 somatic cells 49 Oct4 49 paternally inherited 49 epigenetic changes 49 antisense RNA 48 protein encoded 48 eukaryotic cells 48 CDKN2A 48 polymorphisms 48 BRCA1 mutations 48 recombination 48 radial glia 48 odorant receptor 48 cohesin 48 Pax6 48 monozygotic 48 cyclin D1 48 mammary cells 48 fibroblast cells 48 SMN1 48 chromosomal abnormalities 48 X chromosome inactivation 48 p# mutation 48 autosomal dominant 48 constitutively 48 X chromosome genes 48 adrenal cortex 48 maternally inherited 48 sexually reproducing 48 IgA deficiency 48 mutated BRCA1 48 aneuploid 48 C#Y 48 RNA molecule 48 KCNQ1 48 breast cancer genes BRCA1 48 BARD1 48 OPRM1 gene 48 Or#b 48 microcephalin 48 BRCA2 48 protein p# 48 TAp# 48 Wolbachia 48 totipotent 48 homozygosity 48 vasopressin receptors 48 Yamanaka recipe 48 mutant mice 48 genetically identical 48 orthologs 48 DEC2 48 MC1R 48 parthenogenetic 48 ovules 48 DLX5 48 chromosomally 47 fertilized egg splits 47 VIPR2 47 leptin receptors 47 familial ALS 47 heterozygote 47 tRNA synthetase 47 gene encoding 47 sister chromatids 47 primordial germ cells 47 spermatogenesis 47 polycystic ovary syndrome PCOS 47 gametocytes 47 EZH2 47 ectopic expression 47 genetic loci 47 SORL1 47 CagA 47 PrP 47 TACI mutations 47 granule cells 47 mutant proteins 47 CCR5 delta# 47 c Myc 47 pre eclamptic 47 autosomal 47 MLH1 47 pathogenic mutations 47 sex hormone estrogen 47 CNVs 47 Hox gene 47 isoforms 47 phenotypically 47 mtDNA mutations 47 Math1 47 ovulate 47 genetic abnormality 47 selfing 47 BRCA mutation 47 fetal hemoglobin 47 KLF# 47 PTCHD1 gene 47 nucleus Chinnery 47 homolog 47 apoE4 47 genomic instability 47 micro RNAs 47 vasopressin 47 OCA2 47 enzymatic activity 47 APOE 47 Notch signaling 47 IKKa 47 SHANK3 47 SMN2 gene 47 microRNA molecules 47 FGF# 47 gametophyte 47 male prairie voles 47 aneuploidy 47 tau gene 47 Chromosomes 47 alpha amylase 47 G#S mutation 47 Leydig cells 47 BDNF gene 47 Hh 47 IL#R 47 serine 47 XPB 47 mRNA transcripts 47 LRAT 47 globin genes 47 premature ovarian 47 receptor molecule 47 cryptochrome 47 abnormal hemoglobin 47 non coding RNAs 47 NF1 47 BRCA1 47 inactive X chromosome 47 genomic imprinting 47 ovulates 47 klotho 47 prolactin 47 pseudogenes 47 amino acid substitution 47 miRNAs 47 pRb 47 ApoE4 47 DRD4 gene 47 Sox9 46 chromatid 46 ErbB4 46 MnSOD 46 BRCA1 mutation 46 p# MAPK 46 thyroid hormones 46 progranulin 46 p# mutations 46 transcriptional repression 46 EBNA1 46 methylation 46 KLF4 46 Dicer 46 exons 46 arrestin 46 phenotype 46 chromosome rearrangements 46 CCL#L# 46 endometrial cells 46 FANCD2 46 chaperone proteins 46 IFN gamma 46 virulence genes 46 Wwox 46 CAG repeats 46 kisspeptin 46 LKB1 46 ADAM# 46 chromosomal abnormality 46 IGF1 46 paralogs 46 glycosylation 46 VHL gene 46 E cadherin 46 mitochondrial dysfunction 46 ovulated 46 #q# [001] 46 CGG repeats 46 nestin 46 chromosome abnormalities 46 LDL receptor 46 c Myb 46 gene variant 46 MLL2 46 evolutionarily conserved 46 Skp2 46 Apobec3 46 FGFs 46 mitochondrial gene 46 apolipoprotein E 46 hyperactivation 46 TRIM5 46 unpaired 46 aromatase 46 ovarian hormones 46 centrioles 46 #BP# 46 MECP2 46 karyotype 46 introns 46 MECP2 gene 46 homozygotes 46 RPE# 46 fru 46 cytoplasmic 46 mammary cancers 46 Sonic hedgehog 46 CIB1 46 Mutations 46 HPRT gene 46 Wnt signaling 46 ribosomal proteins 46 ciliated 46 codon 46 gametes 46 abnormal chromosome 46 guanine 46 RCAN1 46 MDM2 46 SLC#A# [002] 46 var genes 46 SCN5A 46 gamete 46 methylated 46 rhesus 46 chromosomal alterations 46 beta globin 46 STAT3 46 defective mitochondria 46 doublesex 46 signaling molecules 46 FOXP2 gene 46 HLA B# 46 ApoE gene 46 C. neoformans 46 TMEM#B 46 monozygotic twin 46 CFTR gene 46 TSC1 46 prokaryote 46 morphogen 46 KCNE2 46 fertilized embryo 46 intron 46 SLC#A# gene [001] 46 heterosexual males 46 APOE ε4 46 non coding RNA 46 untranslated regions 46 CCR5 receptors 46 mutant flies 46 PTPN# 46 mtDNA 46 TEP1 46 HMGA2 46 chromosome segregation 46 hypermethylation 46 genetic defect 46 mitogen activated protein kinase 46 androgen receptor 46 pDCs 46 RhoA 46 seminiferous tubules 46 glucocorticoid receptor 46 transmembrane protein 46 abnormal prions 46 herpesviruses 46 metabolic enzymes 46 orthologous genes 46 holoprosencephaly 46 APOE gene 46 constitutively active 46 oocytes 46 eusociality 46 hermaphrodites 45 estrogen receptor 45 FADS2 45 recombination hotspots 45 #q#.# [002] 45 HLAs 45 CXCL# 45 Wnt1 45 maternal antibodies 45 missense mutation 45 allelic variants 45 exomes 45 p# gene 45 genetic rearrangements 45 overexpress 45 chromosome #q# [001] 45 gene variation 45 alpha synuclein gene 45 apolipoprotein E gene 45 multicellular organism 45 unfertilised egg 45 abnormal chromosomes 45 gene p# 45 epigenetic marks 45 JAK STAT 45 impregnate females 45 retinoic acid 45 Vangl2 45 oviducts 45 COMT gene 45 somatic stem cells 45 homologous recombination 45 UGT#B# 45 DSBs 45 GSTT1 45 anterior pituitary 45 cytosine 45 gut microbes 45 subunits 45 MC1R gene 45 guanine G 45 ovule 45 beta subunit 45 GPC5 45 helices 45 Genetic abnormalities 45 mouse embryos 45 ApoE4 gene 45 forebrain 45 indel 45 sporadic ALS 45 ovulations 45 chromosomal translocations 45 loci 45 reproductive glands 45 receptor gene 45 mRNAs 45 inbred strains 45 HOX genes 45 trisomy 45 mutational 45 corpus luteum 45 cadherins 45 ALDH2 45 M. pneumoniae 45 TIR1 45 helicase 45 myotonic dystrophy 45 microRNAs miRNAs 45 calcineurin 45 disulfide bond 45 phosphorylation 45 cyclins 45 glycoproteins 45 genetic variation 45 MAOA gene 45 L1s 45 catenin 45 epigenetic modifications 45 ARID1A 45 ambiguous genitalia 45 masculinization 45 autism susceptibility genes 45 myostatin gene 45 asexual reproduction 45 oncoproteins 45 CD8 cells 45 miRNA genes 45 GSTM1 45 RNAs 45 rhodopsin 45 TACI 45 Cx# [001] 45 gene variants 45 TP# mutation 45 IRAK1 45 Dpp 45 CETP VV 45 Beckwith Wiedemann syndrome 45 apoE 45 indels 45 overexpressed 45 alternative splicing 45 blastocyst 45 sexual dimorphism 45 lateralized 45 gene expression patterns 45 fruitflies 45 meiotic recombination 45 HSCs 45 mutant worms 45 susceptibility gene 45 MTHFR gene 45 eggs fertilized 45 excitatory synapses 45 Akt1 45 Aβ 45 granzyme B 45 microdeletions 45 endostatin 45 zygotes 45 CD1d 45 zebrafish genome 45 TP# mutations 45 genetic variants 45 chloroplasts 45 endogenous retroviruses 45 SATB1 45 CCR5 gene 45 APOE e4 45 mammalian cells 45 NF1 gene 45 CNTNAP2 45 caspases 45 G6PD 45 #p#.# [001] 45 SIRT6 45 pituitary hormone 45 ultraconserved elements 45 genetic abnormalities 45 mammary stem cells 44 membrane fusion 44 CYP#B# 44 insulin signaling pathway 44 PrPSc 44 undifferentiated cells 44 mitochondria 44 endosymbiosis 44 transcriptional repressor 44 SRY 44 laforin 44 Golgi apparatus 44 reproductive hormones 44 IKZF1 44 immature dendritic cells 44 endonuclease 44 olfactory neurons 44 postnatally 44 granulocytes 44 CHD7 44 follicle stimulating hormone FSH 44 neuronal progenitor cells 44 progranulin gene 44 masculinized 44 RNA molecules 44 RUNX3 44 SIRT3 44 ERK1 44 Smad3 44 prion gene 44 ubiquitylation 44 clonally 44 CYP#E# gene 44 nucleotide sequence 44 GFP gene 44 phosphatases 44 mammalian genome 44 karyotypes 44 antisense strand 44 GTPase 44 blastomere 44 CHEK2 gene 44 cortisol 44 TCF#L# gene 44 chromatin proteins 44 neuroblasts 44 tau protein 44 BRAF gene 44 S#K# 44 unfertilized egg 44 CFTR 44 genetic alterations 44 Transcription factors 44 suppressor gene 44 hybridizations 44 prairie voles 44 INF2 44 reproduce asexually 44 ubiquitination 44 X. laevis 44 NKT cells 44 huntingtin protein 44 NF2 44 apoptosis pathway 44 neuroligin 44 valine 44 FoxO3 44 eukaryote 44 progerin 44 narcolepsy cataplexy 44 p# activation 44 palladin 44 genotoxic stress 44 KRAS mutations 44 reproductively 44 HER2 receptor 44 MYH9 gene 44 pluripotent cells 44 multiprotein complex 44 female reproductive tract 44 acetylation 44 B lymphocytes 44 segmental duplications 44 costimulatory 44 GABAergic neurons 44 coding exons 44 Rh negative 44 activin 44 membrane protein 44 tRNA 44 susceptibility genes 44 transgenic mice 44 transgene 44 Treg cell 44 MHC dissimilar 44 demethylation 44 histone H4 44 C EBP alpha 44 serotonin transporter 44 symbiont 44 cysteines 44 synuclein 44 germline mutation 44 SOD1 protein 44 #S rRNA 44 5 hydroxymethylcytosine 44 MeCP2 44 oestradiol 44 melanocyte 44 histone modification 44 C1q 44 granulosa cells 44 phytochrome 44 WAGR syndrome 44 DLC1 44 ovarian follicles 44 ovaries 44 lipin 44 clade B 44 PAK1 44 M. genitalium 44 mitochondrial DNA mtDNA 44 vitamin D receptors 44 Heterozygous 44 H#K# [002] 44 subunit 44 kappa opioid receptor 44 5 HTTLPR 44 autosomal recessive disease 44 CDH1 44 transcriptional regulators 44 5 HTT gene 44 T lymphocytes 44 PKD1 44 Pten 44 chromosomal regions 44 BRAC2 44 SHBG 44 gamma globin gene 44 trophoblast 44 Sertoli cells 44 Rh factor 44 behavioral disinhibition 44 chromosome abnormality 44 asexuals 44 ES cells 44 APOE allele 44 chromosomal anomalies 44 transcriptional machinery 44 GPR# [002] 44 primary cilia 44 DNMT1 44 telomeric 44 downregulated 44 proto oncogene 44 protein kinases 44 duplicated chromosomes 44 SGK1 44 glucocorticoid receptors 44 genomic rearrangements 44 hair follicle stem cells 44 methylation patterns 44 cAMP 44 transcriptional activation 44 fibrillin 1 44 GNAQ 44 HSF1 44 isoform 44 lymphocyte 44 differentially methylated 44 causative genes 44 chromatids 44 bacterial genomes 44 phthalate syndrome 44 CD#c 44 allelic 44 mRNA molecules 44 tetramer 44 chromosome #q#.# [001] 44 chromosomal disorders 44 microglial cells 44 globin 43 mutant protein 43 epithelial tissues 43 genetically 43 hTERT 43 Th# cells 43 KIAA# 43 beta defensin 43 genotype 43 SMN1 gene 43 caveolin 43 homodimer 43 genotypes 43 Dictyostelium 43 Apert syndrome 43 causal variants 43 BRCA2 mutation 43 gastrulation 43 Pin1 43 parkin gene 43 miR #b [001] 43 HOTAIR 43 mutated protein 43 sequence homology 43 ncRNAs 43 neurogenesis 43 connexin 43 chordate 43 prion strains 43 BRCA mutations 43 promoter methylation 43 organism genome 43 Jhdm2a 43 transcription factors 43 conformational 43 oocyte 43 neural crest stem cells 43 genes BRCA1 43 outcrossing 43 polymerase 43 glutamate signaling 43 unicellular organism 43 estradiol 43 autoantibodies 43 SLC#A# [001] 43 short hairpin RNAs 43 stranded RNA oligonucleotides 43 cDNAs 43 topoisomerases 43 NF κB 43 Chromosome 43 Drosophila melanogaster 43 homozygote 43 viral genomes 43 EGFR gene 43 transactivation 43 Prox1 43 MAPK 43 genetic alteration 43 hippocampal neurons 43 microfilariae 43 5 methylcytosine 43 mitochondrial genomes 43 defensin 43 APOL1 43 hypermethylated 43 chromosomal aberrations 43 TRPV3 43 genetically programmed 43 antral follicles 43 SMAD4 43 brassinosteroid 43 TRP channels 43 LRP6 43 RAD# [001] 43 HLA antigens 43 mitochondrial mutations 43 heterozygosity 43 sickle hemoglobin 43 HbF 43 #q#.# deletion syndrome 43 epigenetic 43 protein fragment 43 microchimerism 43 dioecious 43 chromosome #q# [002] 43 D2 receptors 43 p# protein 43 TH# cells 43 nonidentical 43 epigenetic alterations 43 chromosomal defect 43 DICER1 43 familial pancreatic cancer 43 dimer 43 deuterostomes 43 signaling molecule 43 PGCs 43 haplotypes 43 HGPS 43 SMN2 43 recessive 43 CYP#D# gene 43 nonsense mutation 43 cultured cells 43 PIP3 43 mice genetically engineered 43 deacetylation 43 genetic trait 43 chromosome deletion 43 phenotypes 43 yeast cells 43 genetic defects 43 recessive mutations 43 platypus genome 43 coding genes 43 situs inversus 43 follicles 43 E4 variant 43 IRS1 43 C. elegans 43 JAK2 enzyme 43 somatic cell 43 sebaceous glands 43 telomeres shorten 43 gene encodes protein 43 somatic mutations 43 chromosome #q 43 nonhereditary 43 prion protein 43 chloroplast 43 translocations 43 pluripotent embryonic 43 IKK2 43 trypanosome 43 Smad7 43 tumor suppressor protein 43 receptor protein 43 primordial follicles 43 alternatively spliced 43 hormone estrogen 43 sexually dimorphic 43 HAR1 43 gonadotropins 43 brain hemispheres 43 PDGFR 43 CNTNAP2 gene 43 PON1 43 Dicer enzyme 43 uncharacterized 43 thrombospondin 43 recessive mutation 43 basal cell nevus syndrome 43 spermatozoa 43 recessive traits 43 NMDA receptors 43 TGF ß 43 adiponectin 43 PPAR alpha 43 myelination 43 endocrine glands 43 cytosolic 43 CFH gene 43 H#K# [001] 43 #S rRNA genes 43 prion protein gene 43 inhibitory receptor 43 transcription factor 43 estrogen 43 genetic recombination 43 Notch1 43 DNA rearrangements 43 mutated BRCA 43 H#K# methylation 43 phosphorylates 43 mitochondrial genome 43 Rh positive 43 Six3 43 severe congenital neutropenia 43 CHD5 43 S. cerevisiae 43 ALK gene 43 dedifferentiation 43 overexpression 43 neurones 43 IL# [001] 43 presynaptic 43 Nf1 43 tRNA synthetases 43 H2AX 43 LMNA gene 43 regulate gene expression 43 glutamate receptors 43 BRCA gene mutations 43 CHEK2 43 Cdc# 43 proteins 43 phenotypic expression 43 genetic makeups 43 dopamine transporter gene 43 inherited predisposition 43 osteoblast 43 bcl 2 43 uPAR 43 cardiac fibroblasts 43 androgen hormones 43 accomplice Hudgens 43 Helicobacter 43 amyloid precursor protein 43 mammalian genomes 43 mutant mouse 42 antigenic 42 ovum 42 gene MECP2 42 gene locus 42 cyclin 42 hormone receptors 42 sphingolipid 42 GBM tumors 42 dystrophin gene 42 methyltransferases 42 Sox2 42 ZNF# 42 embryonic tissues 42 CFTR protein 42 messenger RNAs mRNAs 42 MAPK pathway 42 RNA polymerase II 42 tau proteins 42 monoclonal antibodies aptamers 42 genetic predisposition 42 Cdk5 42 embryogenesis 42 XX chromosome 42 Cyclin D1 42 HER2 neu 42 DARPP 42 GSTM1 gene 42 dimers 42 tyrosine kinases 42 human leukocyte antigens 42 amino acid sequence 42 artificial chromosomes 42 IRF6 gene 42 PML RARA 42 CDH# 42 FOXP3 42 Bcl xL 42 subfertile 42 phenotypic variation 42 abnormal proteins 42 euchromatin 42 penetrance 42 Igf2 42 Aβ peptides