Related by context. All words. (Click for frequent words.) 68 sickle hemoglobin 65 progranulin gene 65 defective gene 64 WAGR syndrome 64 HFE gene 64 recessive trait 63 CFTR gene 62 MIF protein 62 vesicular stomatitis virus 62 missense mutation 62 FMR1 gene 62 autosomal recessive disease 61 recessive gene 61 melanin pigments 61 hemoglobin molecule 61 globin 61 RPE# gene 61 CHD7 61 LMNA 61 MYH9 gene 61 mutated gene 61 MTHFR 61 autosomal dominant disorder 60 VHL gene 60 HLA B# 60 glucocerebrosidase 60 huntingtin gene 60 secretase 60 SMN2 gene 60 Trypanosoma brucei 60 laforin 60 misshapen proteins 60 RPE# 60 Hutchinson Gilford progeria 60 protein encoded 60 Homozygous 60 SMN1 60 TEL AML1 60 SHANK3 59 NF1 gene 59 C#Y 59 de novo mutations 59 LIS1 59 enterotoxin 59 Fas ligand 59 CFTR cystic fibrosis transmembrane 59 TSLP 59 abnormal prions 59 SMN1 gene 59 DGAT1 59 autosomal recessive disorder 59 genetic defect 59 gene MECP2 59 progerin 59 Beta thalassemia 59 transcriptional repressor 59 CRISPR Cas 58 mutant gene 58 protein fragment 58 MLL2 58 GFP gene 58 mutated protein 58 MECP2 gene 58 Heterozygous 58 granzyme B 58 erythrocytes 58 MC1R 58 glycolipid 58 HLA molecules 58 constitutively 58 olfactory receptor 58 Rh factor 58 trypanosome 58 Oxidative stress 58 DICER1 gene 58 SMN protein 58 dystrophin gene 58 receptor molecule 58 haem 58 dystrophin protein 58 Genetic variation 58 heme oxygenase 1 58 beta globin gene 58 APOC3 58 cytochromes 58 beta globin 58 gene p# 58 holoprosencephaly 58 CYP#E# gene 58 IRAK1 58 Streptococcus agalactiae 58 lysine residues 58 Hemophilia B 58 recessive mutation 58 parasite Plasmodium falciparum 58 polycystin 58 Shiga toxin 58 leptin deficiency 58 neuroligins 58 MEF2A 58 dominantly inherited 57 Niemann Pick disease 57 TP# mutation 57 shiga toxin 57 filaggrin 57 parasite Trypanosoma cruzi 57 pRb 57 Salmonella typhi 57 BRIP1 57 activin 57 gene encodes protein 57 PHLPP 57 PrP 57 parkin gene 57 C1q 57 misfolded 57 TCF#L# gene 57 LRAT 57 SLC#A# [001] 57 molybdenum cofactor deficiency 57 apolipoprotein E gene 57 survival motor neuron 57 regulator CFTR gene 57 proteinase 57 WNK1 57 PTPN# 57 mosaicism 57 gene encodes 57 recessively inherited 57 peroxisome 57 severe congenital neutropenia 57 APOE gene 57 regulates gene expression 57 Entamoeba 57 BRCA2 gene 57 Brugada Syndrome 57 COL#A# 57 H. influenzae 57 Cockayne syndrome 57 klotho 57 normal prion protein 57 NFkB 57 huntingtin protein 57 MTHFR gene 57 progressive neurodegenerative disorder 57 IRS1 57 Dystrophin 57 desmin 57 meningococcus 57 genes predisposing 57 KCNE2 57 G6PD deficiency 57 inherited mutations 57 bacterium Mycobacterium tuberculosis 57 cytochrome c 57 ribosomal protein 57 JAK2 enzyme 57 Plasmodium parasite 57 Cystic fibrosis CF 57 cryopyrin 57 synuclein 57 Hemochromatosis 57 mycobacterium tuberculosis 57 MECP2 57 tuberculosis bacterium 57 Phenylalanine 57 CCR5 delta# 57 BRAF protein 56 C EBP alpha 56 pyogenes 56 IgA deficiency 56 HMGA2 56 anaerobic bacterium 56 R#W [002] 56 Rh positive 56 tiny roundworm 56 mRNA transcripts 56 chronic granulomatous disease 56 exocrine 56 nonsense mutation 56 trophoblasts 56 MC4R gene 56 Lafora disease 56 LKB1 56 SOD2 gene 56 von Willebrand factor 56 ADAMTS# 56 phosphorylates 56 prion protein PrP 56 Plasmodium parasites 56 fat soluble vitamin 56 telomere dysfunction 56 leptin receptor 56 dyskeratosis congenita 56 Cyclin D1 56 recombinantly 56 Kufs disease 56 aldehyde dehydrogenase 56 alternatively spliced 56 nonsense mutations 56 syntaxin 56 ApoE gene 56 TGF ß 56 chitinase 56 lysosomal enzyme 56 sortilin 56 ectopic expression 56 mice lacking 56 G#S mutation 56 amyloid peptide 56 p# mutation 56 Neuregulin 1 56 HLA DRB1 56 RCAN1 56 lung epithelial cells 56 intracellularly 56 Wwox 56 cystic fibrosis transmembrane conductance 56 PALB2 56 MC1R gene 56 TP# gene 56 autosomal recessive 56 Genetic mutation 56 flavin 56 bacterial enzyme 56 HLA G 56 inherited retinal degeneration 56 G#S [002] 56 TAp# 56 IGF2 56 APOE4 56 water soluble vitamin 56 SGK1 56 glutamic acid decarboxylase 56 BRAF gene 55 lysyl oxidase 55 apoE4 55 undergo apoptosis 55 HLA DQ2 55 HGPS 55 KCNQ1 55 synthetase 55 sporadic Creutzfeldt Jakob 55 chromosomal defect 55 monogenic 55 inherited neurological disorder 55 defective telomerase 55 ubiquitylation 55 podocytes 55 familial ALS 55 mtDNA mutations 55 receptor protein 55 NPC1 55 TGFBR1 55 bacterium Bacillus anthracis 55 asymptomatically 55 PON1 55 DLX5 55 HLA DRB1 * 55 chromatin structure 55 genetic abnormality 55 C. neoformans 55 endogenous ligands 55 Epstein Barr virus EBV 55 KIF6 gene 55 protein synthesis machinery 55 PGC 1α 55 TACI mutations 55 diffusible 55 ectodomain 55 GSNO 55 Monocyte 55 dynamin 55 muscular dystrophies 55 leucine zipper 55 mutated BRCA 55 transferase 55 fungus Aspergillus 55 bacteria Streptococcus pneumoniae 55 murine leukemia virus 55 primordial germ cells 55 pDC 55 LDL receptor 55 receptor gene 55 chromosome abnormality 55 disulfide bond 55 von Hippel Lindau 55 TNFAIP3 55 protein tau 55 apoE 55 PTEN gene 55 KIAA# 55 aspartate 55 tetramer 55 apoC III 55 parainfluenza virus 55 SCN5A 55 LRRK2 gene 55 LRP5 55 naturally occurring molecule 55 folic acid deficiency 55 deacetylation 55 adrenal cortex 55 glutamate signaling 55 autosomal dominant 55 polyglutamine diseases 55 histocompatibility 55 SHANK3 gene 55 BARD1 55 endogenous retroviruses 55 B. cepacia 55 thermophilum 55 Ferritin 55 Math1 55 recessive mutations 55 telomere DNA 55 mutant allele 55 genetic mutation 55 myotonic dystrophy 55 lamin 55 homocystinuria 55 glycosyltransferase 55 segmental duplications 55 susceptibility gene 55 hemoglobin molecules 55 transcriptional activation 55 Amino acid 55 anti microbial peptides 55 fertilized egg splits 55 cytokine receptor 55 CETP VV 55 Polycystic kidney disease 55 tumor suppressor p# 55 alpha Gal 55 epigenetic inheritance 55 ChR2 55 catenin 55 ADAM# 55 beta thalassemia 55 viral proteins 55 CYP #D# 55 PKD1 55 Clusterin 55 Spinal muscular atrophy 55 GPC5 55 chimeric mice 55 TCF4 55 chaperone proteins 55 MEF2C 55 chloroplasts 55 glucocerebroside primarily 55 MLL gene 55 plasmodium 55 congenital adrenal hyperplasia CAH 55 #p#.# [001] 55 homodimer 55 gamma globin gene 55 misregulation 55 peroxisomal 55 CFTR protein 55 CALHM1 55 Helicobacter 55 CDK4 55 Hsp# [001] 55 fronto temporal dementia 55 IL#R 55 SMN2 55 mitochondrial gene 55 N Myc 55 D. melanogaster 55 immunodeficiencies 55 c KIT 54 CDH1 54 V Leiden 54 APOL1 54 metabolizing enzyme 54 bacterium E. coli 54 inherited maternally 54 micro RNAs 54 SOD1 gene 54 TMEM#B 54 podocyte 54 Cryptococcus neoformans 54 BCR ABL protein 54 globin genes 54 LPA gene 54 caveolin 54 cell adhesion molecules 54 melanocyte 54 Hutchinson Gilford Progeria Syndrome 54 Von Willebrand 54 autophagic 54 lymphocyte activation 54 IFNg 54 ptau 54 number variants CNVs 54 glycated 54 MeCP2 gene 54 ciliated 54 AAT deficiency 54 Meckel Gruber 54 TIR1 54 medulloblastoma tumors 54 LMNA gene 54 chromosomal aberrations 54 Severe Combined Immunodeficiency 54 Glucocorticoids 54 phospholipase 54 constitutively active 54 HbF 54 hemolysin 54 MIF gene 54 plasminogen activator inhibitor 54 myelin fatty substance 54 Prevotella 54 Aplastic anemia 54 hepatoma 54 number variations CNVs 54 bacterium Escherichia coli 54 TB bacterium 54 insulin secreting islet cells 54 tau proteins 54 epigenetic modifications 54 ADPKD 54 Insulin resistance 54 abnormal prion protein 54 Autoimmune disorders 54 cytidine 54 mitochondrial dysfunction 54 Smad3 54 lung epithelium 54 naturally occurring enzyme 54 huntingtin 54 hemagglutinin H 54 chemokine receptor 54 presenilin 54 lipoxygenase 54 immature dendritic cells 54 uncoupling protein 54 gene mutation 54 microfilariae 54 mutant genes 54 abnormal proteins 54 Epidermolysis bullosa 54 defensin 54 protein clumps 54 misfolds 54 M. pneumoniae 54 ribonucleic acid RNA 54 thymidine kinase 54 transcriptionally active 54 virulence genes 54 p# mutations 54 SLC#A# gene [001] 54 piRNAs 54 GSTT1 54 epithelial cells lining 54 APOE e4 54 toxic amyloid beta 54 fetal hemoglobin 54 deaminase 54 fibrillin 1 54 transfusion syndrome 54 GPR# [002] 54 varicella zoster virus 54 melanin pigment 54 neuregulin 1 54 ectoderm 54 metabolic enzymes 54 M. capricolum 54 hydroxylation 54 Osteogenesis imperfecta 54 Foxp3 54 microcephalin 54 nasal epithelium 54 mutant protein 54 Hashimoto thyroiditis 54 mutation 54 D. simulans 54 condensin 54 TACI 54 acyl CoA 54 Smad7 54 mucus glands 54 mineralocorticoid receptor 54 transmembrane receptor 54 collagen VII 54 somatic mutation 54 Mycoplasma pneumoniae 54 Cathepsin B 54 replicase 54 pneumococci 54 hydrogenase 54 digesting enzyme 54 vacuolar 54 FMR1 54 cell adhesion molecule 54 recessive dystrophic epidermolysis bullosa 54 cell nuclei 54 Corynebacterium 54 NOTCH1 54 Oxidative 54 carboxy terminal 54 centrosome 54 debilitating neurodegenerative disorder 54 GNAQ 54 cybrid 54 NKX2 54 6 phosphate dehydrogenase 54 Aldosterone 54 Anencephaly 54 thyrotropin 54 beta defensin 54 clade C 54 MDMX 54 Deoxyribonucleic acid DNA 54 oxidized LDL 54 STAT4 54 uracil 54 EGFR protein 54 genotoxic stress 54 Variant Creutzfeldt Jakob 54 hydrolase 54 E#F# 54 cypin 54 NADPH 54 chromosome #q#.# [001] 54 mutant proteins 54 maternally inherited 54 Skp2 54 DUX4 54 Akt1 54 null mice 54 eosinophilic 54 hnRNP 54 Lymphocytic 54 chromosome #q#.# [002] 54 multigenic 54 coenzyme 54 SOD1 protein 54 proapoptotic 54 Human Leukocyte Antigen 54 rotaviruses 54 ABCB1 54 prodynorphin 54 enzyme deficiency 54 Rap1 54 Interferon gamma 54 transmembrane protein 53 reductase 53 caveolae 53 Myotonic dystrophy 53 vimentin 53 palmitate 53 hemochromatosis 53 Irs2 53 tubule 53 NFKBIA 53 Haemoglobin 53 spermidine 53 iNOS 53 Leptospira 53 regulated kinase ERK 53 vitamin B2 53 autoinflammatory 53 immunodeficiency disorder 53 haemochromatosis 53 RNA molecule 53 transcriptional repression 53 antisense RNA 53 skeletal muscle cells 53 haemagglutinin 53 secrete protein 53 prion gene 53 OCT4 53 telomerase gene 53 breast cancer genes BRCA1 53 clonally 53 PfEMP1 53 PrPSc 53 Hutchinson Gilford Progeria 53 Peptide YY 53 epigenetic regulation 53 transthyretin 53 PON1 gene 53 serovar 53 prostaglandin E2 53 genetic alteration 53 tetramers 53 autosomal 53 ryanodine receptor 53 NPHP 53 PB1 F2 53 CD1d 53 cytoplasmic domain 53 amino acid phenylalanine 53 Frizzled 53 titin 53 cardiac hypertrophy 53 apolipoprotein E4 53 MAP kinase 53 inflammatory demyelinating 53 Ras oncogene 53 #BP# 53 collagen VI 53 resistin 53 dysgenesis 53 androgen receptor AR 53 CXCL# 53 neuropeptide Y NPY 53 Rad# 53 dynactin 53 Sickle cell 53 Dynein 53 single celled parasite 53 anthrax bacterium 53 spontaneous mutation 53 NEIL1 53 S. pombe 53 MMP# 53 Cytotoxic T 53 genetic trait 53 Htt 53 paternally inherited 53 acetylcholine receptor 53 ENPP1 53 urease 53 non coding RNA 53 donor marrow 53 tetanus toxin 53 familial hypercholesterolemia 53 DHFR 53 phytoplasma 53 functional dystrophin protein 53 Genetic mutations 53 homozygosity 53 enzymatic activity 53 Rab5 53 drug metabolizing enzyme 53 Trichomonas vaginalis 53 platelet dysfunction 53 Tuberous sclerosis 53 PAK1 53 homolog 53 NAGS deficiency 53 ZNF# 53 Joubert syndrome 53 Vpu 53 OCA2 53 Fragile X mental retardation 53 Hemoglobin 53 neuromuscular junction 53 bronchoalveolar 53 GSTP1 53 pyrimidines 53 endonuclease 53 roseola 53 heterodimer 53 missense mutations 53 Catenin 53 acetyl CoA 53 ACE2 gene 53 Prion proteins 53 von Willebrand 53 Leukemias 53 Neutrophil 53 retinoblastoma protein 53 organelle 53 epigenetically 53 microdeletion 53 plastid 53 BCL#A 53 FUS1 53 ubiquinol 53 neurodegenerative disorder 53 Secretase 53 enzyme phenylalanine hydroxylase PAH 53 overactivation 53 serine threonine kinase 53 Fibrinogen 53 mutated genes 53 UGT#B# 53 Tay Sachs thalassemia 53 rRNA 53 immunodeficiency 53 virulence determinants 53 germline mutation 53 downregulates 53 Dilated cardiomyopathy 53 SMAD4 53 molecular mimicry 53 GRNOPC1 contains 53 FADS2 53 Systemic lupus erythematosus 53 Borrelia burgdorferi 53 pyrrolysine 53 Oncogenic 53 substrate specificity 53 Polymorphisms 53 Aromatase 53 incurable neurodegenerative disease 53 ADH1B * 53 VLDL 53 Thiamine 53 Soluble CD# 53 androgen receptor gene 53 CYP#D# gene 53 inherited gene mutation 53 Human cl 53 UCP1 53 RANTES 53 HMGCR 53 JAK STAT 53 genetic variant 53 histone modification 53 Holoprosencephaly 53 cause cardiac channelopathies 53 epigenetic silencing 53 hexose 53 cysteines 53 influenzae 53 GAPDH 53 tau protein 53 fibrodysplasia ossificans progressiva FOP 53 BDNF gene 53 Tubulin 53 bacterium Clostridium botulinum 53 insulin resistance syndrome 53 phenotypic variation 53 Sox9 53 adipose cells 53 CNTNAP2 gene 53 CAG repeats 53 Drp1 53 exotoxin 53 tau gene 53 Notch signaling 53 CCR5 gene 53 MMP9 53 seminiferous tubules 53 phenylalanine 53 Six3 53 toxic beta amyloid 53 Li Fraumeni syndrome 53 Pulmonary hypertension 53 Prolactin 53 MSH2 53 transplanted bone marrow 53 succinate dehydrogenase 52 Jakob Disease 52 GATA4 52 adipokine 52 outer membrane proteins 52 Ras pathway 52 CagA 52 Leishmania donovani 52 Eisenmenger syndrome 52 chromatid 52 flavivirus 52 proinsulin 52 β1 52 CYP#C# gene 52 epigenetic changes 52 secretory proteins 52 enzyme cytochrome 52 gene rearrangements 52 sulfatase 52 myostatin gene 52 CNTNAP2 52 galactose 52 deoxy 52 cardiac channelopathies 52 immunoglobulin G 52 P gp 52 hyperactivation 52 histone demethylase 52 Cx# [001] 52 glycogen synthase kinase 52 ANCA associated 52 transgene 52 tubercle bacillus 52 mutated BRCA1 52 GAB2 52 oxysterols 52 Myasthenia gravis 52 Alu RNA 52 neuroblastoma tumors 52 germline mutations 52 KRAS oncogene 52 B. fragilis 52 chromosomal DNA 52 causative genes 52 connexin 52 spinocerebellar ataxia 52 hereditary hemochromatosis 52 nitric oxide synthase NOS 52 Dental fluorosis 52 Cadherin 52 genetic polymorphism 52 pigment melanin 52 Rickettsia 52 DRB1 52 Fanconi Anemia 52 SORL1 52 lacZ 52 mutated K ras 52 hydrops 52 lipofuscin 52 Gastroparesis 52 UCP2 52 Propionibacterium 52 ferroportin 52 immunoadhesins 52 Epstein Barr Virus EBV 52 adenosine deaminase 52 Vangl2 52 human leukocyte antigens 52 periodontal infection 52 acinar cells 52 Pax3 52 Protein Kinase 52 familial adenomatous polyposis 52 Arrhythmogenic Right Ventricular Cardiomyopathy 52 B. henselae 52 Magnesium deficiency 52 protein tyrosine phosphatase 52 HLA DQ 52 vanA gene 52 nematode worm 52 Carcinoid tumors 52 rhodopsin 52 MyoD 52 abnormal chromosomes 52 encodes protein 52 proNGF 52 nerve degeneration 52 superoxide dismutase 52 gene encoding 52 human leukocyte antigen 52 iPSC lines 52 Klotho gene 52 Mitochondrial 52 phosphorylate 52 JAK2 mutation 52 HepG2 cells 52 human herpesvirus 52 transgenic rats 52 alleles 52 heterozygotes 52 histone methylation 52 microglial 52 chromosomal instability 52 Upregulation 52 CFH gene 52 extracellular matrix protein 52 copper zinc superoxide 52 genetic syndromes 52 Fatty liver 52 cerebri 52 cardiolipin 52 prion protein 52 c myc 52 glomerulonephritis 52 Angiotensin II 52 NKX#.# 52 inflammasome 52 lysosomal enzymes 52 protein ubiquitin 52 Oxidative damage 52 isoenzyme 52 trophoblast cells 52 Janus kinase 52 Bcr Abl 52 cytokines IL 52 Autoantibodies 52 gene 52 miRNA genes 52 germline cells 52 trypanosome parasite 52 misfolded protein 52 messenger RNAs mRNAs 52 DEAR1 52 Monoclonal 52 cytopathic 52 positional cloning 52 associated tremor ataxia 52 endosome 52 DUX4 gene 52 Factor NGF 52 Methionine 52 SWI SNF 52 mucins 52 IL# [001] 52 Creutzfeldt Jacob 52 FGFR2 52 viral genome 52 RNA ribonucleic acid 52 interleukins 52 vacuole 52 GABAergic neurons 52 CCR5 protein 52 globin gene 52 monocyte 52 Vitamin B# deficiency 52 pyloric stenosis 52 hydroxylase 52 beta islets 52 S#K# 52 dioxygenase 52 tyrosine 52 microscopic parasites 52 Factor XIII 52 MHC molecules 52 Endothelial 52 tyrosine phosphorylation 52 MYCN 52 normal prion proteins 52 gliosis 52 Fanconi anemia FA 52 PDZ domain 52 downregulation 52 eotaxin 52 fatty acid synthesis 52 CYP#A# gene 52 STAT1 52 channelopathies 52 rDNA 52 Ets2 52 transgenic mouse models 52 calcineurin 52 X chromosome 52 major histocompatibility complex 52 Ectodermal Dysplasia 52 Carnosine 52 aminopeptidase 52 mammary cells 52 bacterium Listeria 52 polynucleotide 52 NR#A# 52 Buckminsterfullerene 52 palladin 52 E. faecalis 52 RecA 52 multisystem disease 52 adenylyl cyclase 52 OGG1 52 p# gene 52 mutant alleles 52 GTPase 52 polypeptide 52 pyruvate kinase 52 Antigens 52 Igf2 52 hypertrophic cardiomyopathy HCM 52 Cancer cachexia 52 Bardet Biedl syndrome 52 proline rich 52 Diabetic Ketoacidosis 52 TRIM5 52 Nf1 52 phenotypic expression 52 retinal dystrophy 52 Creutzfeld Jakob disease 52 hereditary disorders 52 salmonella bacterium 52 Genetic Mutation 52 genes encoding 52 protein kinase C 52 ALK gene 52 sickle cell hemoglobin 52 monomeric 52 DISC1 gene 52 telomeres shorten 52 CIB1 52 Nedd4 52 S. cerevisiae 52 tryptase 52 ApoE4 52 tumor specific antigen 52 Sindbis 52 cystatin 52 Single Nucleotide Polymorphisms SNPs 52 Thorough cooking kills 52 GRK5 52 Dehydroepiandrosterone 52 adeno associated viruses 52 BMP4 52 differential gene expression 52 HMGA2 gene 52 Histone 52 thymine 52 typhimurium 52 familial hypercholesterolaemia 52 stilbene 52 nestin 52 cytochrome 52 H2AX 52 SOX3 gene 52 mitochondrial biogenesis