Williams Beuren syndrome

Related by string. * Wil liams . williams . WILLIAMS . WILLIAM . WIlliams : William H. . William H. Rehnquist . Defending champion Serena Williams . Mo Williams . Prince William / : Van Beuren . van Beuren / syndromes . Syndromes . SYNDROME . Syndrome : Severe Acute Respiratory Syndrome . Acquired Immune Deficiency Syndrome . Acquired Immune Deficiency Syndromes . chronic fatigue syndrome * *

Related by context. All words. (Click for frequent words.) 62 paraneoplastic 62 upregulates 62 dysgenesis 61 MSH2 60 cell adhesion molecule 60 phospholipase A2 60 von Hippel Lindau 60 de novo mutations 60 constitutively expressed 59 ABCB1 59 phosphatidylinositol 3 59 monogenic 59 hormone secretion 59 synaptogenesis 59 arcuate nucleus 59 Hypothalamic 59 CHEK2 59 lymphatic vessel 59 LPS induced 59 MEF2A 59 LRP5 59 mediated inhibition 59 COX2 59 PON1 59 motor neuron degeneration 59 downregulation 59 ERK signaling 59 lymphangiogenesis 59 SCN1A 59 steroidogenic 59 polyglutamine 59 metabolic abnormality 59 AT1R 59 MLH1 59 metalloproteinase 59 sphingolipid 58 murine model 58 HLA DQ2 58 CagA 58 Upregulation 58 Transcriptional 58 transcriptional activity 58 Spinal muscular atrophy 58 transgenic mouse models 58 metabolizing enzyme 58 MTHFR 58 Dehydrogenase 58 #β estradiol 58 hypothalamic pituitary adrenal axis 58 transthyretin 58 Inactivation 58 paraganglioma 58 HepG2 cells 58 leptin receptor 58 gene polymorphism 58 germline mutations 58 GABAergic interneurons 58 Akt signaling 58 Treg cell 58 pDC 58 Huntingtin 58 BMP signaling 58 cotransporter 58 upregulating 58 interstitial fibrosis 57 FGFs 57 IRF6 57 Polymorphisms 57 Xenopus laevis 57 hypothalamic pituitary 57 Phosphorylation 57 downregulates 57 Epstein Barr Virus EBV 57 missense mutations 57 protein secreted 57 #p#.# [002] 57 enterocolitis 57 KRAS oncogene 57 inherited mutations 57 mutant huntingtin protein 57 PTPN# 57 renal fibrosis 57 pulmonary hypoplasia 57 activated microglia 57 myopathies 57 functional polymorphism 57 druggable target 57 misregulation 57 Prox1 57 Thyroid hormone 57 Dysregulation 57 kinase pathway 57 ß1 57 kinase gene 57 Entamoeba histolytica 57 locus coeruleus 57 dorsal root ganglia 57 CHD7 57 TGF ß 57 serpin 57 extracellular signal 57 systemic amyloidosis 57 leukocyte adhesion 57 mosaicism 57 Factor VEGF 57 tumor suppressor protein 57 Elevated serum 57 Brain derived neurotrophic 57 calcium homeostasis 57 FGF2 57 basal forebrain 57 intracellular bacteria 57 Genetic variations 57 forkhead 57 microcephalin 57 etiologic factors 57 transgenic mice expressing 57 ductal adenocarcinoma 57 protein tyrosine phosphatase 57 ectopic expression 57 autosomal recessive disease 57 nitric oxide synthase 57 carboxyl terminal 57 circadian genes 56 SNP rs# [001] 56 BRCA1 BRCA2 56 Clusterin 56 regulates gene expression 56 susceptibility locus 56 prefrontal cortical 56 phosphorylates 56 allelic variants 56 endothelial activation 56 chemokine receptors 56 BCL#A 56 Apolipoprotein E 56 epigenetic alterations 56 proximal tubule 56 microdeletion 56 subcellular compartments 56 neurofibrillary 56 phenotypic expression 56 Osteopontin 56 haematopoietic 56 CNTNAP2 56 leucocytes 56 NQO1 56 Rho kinase 56 neuritic 56 podocyte 56 splenocytes 56 Myocarditis 56 acetylcholine receptor 56 fibrosing 56 Hh signaling 56 pRb 56 mutated K ras 56 amyloid deposition 56 potent inducer 56 transmembrane receptor 56 autosomal dominant inheritance 56 dominantly inherited 56 PC# cells 56 Genetic variation 56 syngeneic 56 neovascularisation 56 Leydig cell 56 KCNH2 56 autosomal dominant disorder 56 neuronal dysfunction 56 autophagic 56 striated muscle 56 hyperactivation 56 carbohydrate metabolism 56 deacetylation 56 striatal dopamine 56 glomerular 56 autosomal recessive genetic 56 demyelinating 56 caveolin 56 humoral responses 56 tyrosine hydroxylase 56 abnormal methylation 56 maternally transmitted 56 decarboxylase 56 inverse agonist 56 muscarinic receptors 56 Smad3 56 cyclin dependent kinase inhibitor 56 immunoregulatory 56 eotaxin 56 BCL2 56 colorectal adenoma 56 NR2B 56 neuroligins 56 membrane proximal 56 myo inositol 56 inhibitory neurotransmitters 56 SMN1 56 transcriptional activation 56 Li Fraumeni syndrome 56 hypothalamic 56 endocrine dysfunction 56 MELAS 56 proto oncogene 56 osteoprotegerin 56 mice lacking 56 Wnt signaling pathway 56 inducible nitric oxide synthase 56 glucocorticoid induced 56 MMP2 56 glycosyltransferase 56 apoE 56 causative genes 56 Dopaminergic 56 genes predisposing 56 FGFR3 55 PLA2 55 PTHrP 55 FGFR4 55 Inhibitory 55 phosphatase 55 arterial calcification 55 T1DM 55 hemoglobinopathies 55 transcriptional repressor 55 arachidonic acid AA 55 mineralocorticoid 55 NR#A# 55 Rap1 55 adenylate cyclase 55 circadian clock genes 55 breast cancer metastasis 55 fatty acid oxidation 55 COL#A# 55 regulator CFTR gene 55 airway hyperresponsiveness 55 GSTT1 55 excitotoxic 55 gene locus 55 IL#R 55 hyperinsulinism 55 metabolizing enzymes 55 apolipoprotein E APOE 55 TSH receptor 55 antiphospholipid syndrome 55 Overexpression 55 agonist induced 55 neurite outgrowth 55 noradrenergic 55 CYP#B# 55 TMEM#B 55 ADAMTS# 55 medium chain acyl 55 overactivation 55 CEACAM1 55 Sjögren syndrome 55 germline mutation 55 bone marrow mesenchymal stem 55 isoenzyme 55 alveolar epithelial cells 55 metalloprotease 55 prostaglandin synthesis 55 lipoxygenase 55 null mice 55 microglial 55 chromosome condensation 55 isoenzymes 55 virulence genes 55 CIAS1 55 NMDAR 55 aneuploidies 55 gene polymorphisms 55 Cadherin 55 polyamine 55 ERK1 2 55 chronic granulomatous disease 55 STAT4 55 amyloid peptide 55 AMPA receptor 55 5q 55 Macrophage 55 spontaneous mutation 55 neuroinflammation 55 PDGFRA 55 Kupffer cells 55 Angiotensin converting enzyme 55 Leukemias 55 atherogenesis 55 MMP# 55 GPC5 55 #q#.# [001] 55 neuro endocrine 55 neuroendocrine 55 tryptase 55 EP4 55 myeloproliferative 55 SSc 55 Meckel Gruber syndrome 55 methyltransferase 55 pancreatic endocrine 55 airway remodeling 55 genetic polymorphism 55 Wiskott Aldrich syndrome 55 PPAR γ 55 prostate carcinogenesis 55 GABAA receptors 55 Neurofibromatosis type 55 β1 55 cytochrome c oxidase 55 myocyte 55 TCF#L# gene 55 apoptosis pathways 55 plasma kallikrein 55 antibody mediated 55 gastric carcinogenesis 55 apolipoprotein E 55 lymphoid cells 55 regulated kinase ERK 55 acyl CoA 55 hypermethylation 55 Oxidative damage 55 elastase 55 Cryptococcus neoformans 55 dehydrogenase deficiency 55 glutamic acid decarboxylase 55 TrkB 55 KLF4 55 DAT1 55 polycystin 55 PB1 F2 55 #q# deletion 55 peroxisomal 55 #q# [001] 55 serine protease 55 tumorigenicity 55 oligomerization 55 TGF b 54 PARP1 54 fasting plasma 54 phosphatases 54 autosomal recessive 54 primary hyperparathyroidism 54 tumor suppressor PTEN 54 baroreceptor 54 #p# [001] 54 p# activation 54 dopamine signaling 54 autosomal dominant polycystic kidney 54 HbF 54 Hippocampal 54 retinol binding protein 54 Nf1 54 HIV reverse transcriptase 54 Kv#.# 54 Hereditary angioedema 54 FasL 54 human leukocyte antigen HLA 54 annexin 54 thrombospondin 54 thromboemboli 54 PGC 1b 54 4E BP1 54 P#X# receptor 54 CCR5 delta# 54 clostridium 54 beta1 integrin 54 cholesterol homeostasis 54 beta amyloid peptides 54 Fibroblast 54 TNF α 54 somatostatin 54 intraepithelial neoplasia 54 cytopathic 54 Neurofibromatosis Type 54 cAMP signaling 54 MYBPC3 54 bronchial epithelial cells 54 GSTP1 54 mGluR 54 Epstein Barr virus EBV 54 Chromosomal 54 hypermethylated 54 epigenetic modification 54 transcriptional regulation 54 ADPKD 54 Porphyromonas gingivalis 54 BRAF V#E 54 transcriptional repression 54 ribosomal protein 54 Cytotoxic T 54 osteoblast 54 synapse formation 54 granulosa cell 54 PPARγ 54 causative mutation 54 nonhereditary 54 vacuolar 54 chromosome #q 54 progressive neurodegenerative disorder 54 cyclic AMP cAMP 54 TXNIP 54 fibrillin 1 54 NAc 54 proteolysis 54 homeobox gene 54 KIBRA 54 WNK1 54 CDH1 54 #p#.# [001] 54 intestinal microbiota 54 Streptococcus agalactiae 54 hyperplastic 54 dysbindin 54 mediated apoptosis 54 parasitemia 54 TNFalpha 54 gastric adenocarcinoma 54 holoprosencephaly 54 Lymphocytic 54 gastric carcinoma 54 differentially regulated 54 antitrypsin 54 HLA DR4 54 MECP2 gene 54 APOC3 54 Wnt signaling 54 aberrantly activated 54 Amino acid 54 ERalpha 54 colony stimulating factor 54 renal tubular 54 neuronal apoptosis 54 Cockayne syndrome 54 proband 54 amyloid plaque formation 54 dysregulated 54 phosphorylated tau 54 1beta 54 Src kinase 54 Activating mutations 54 SOD2 54 hematopoiesis 54 CYP#A# [002] 54 JAK2 gene 54 hematopoietic progenitors 54 subcellular localization 54 colorectal carcinoma 54 gene MECP2 54 primary ciliary dyskinesia 54 β amyloid 54 raphe 54 fibrocytes 54 chromosomal regions 54 hepatoma 54 plasma lipids 54 ankyrin repeat 54 Ph + acute lymphoblastic 54 IPAH 54 MYCN amplification 54 paraoxonase 54 thyrotropin 54 monocyte chemotactic protein 54 motoneurons 54 capillary endothelial cells 54 Pten 54 p# MAPK 54 melanocyte 54 chromosome #q#.# [002] 54 Chlamydia pneumoniae 54 vasopressin receptor 54 chromosomal instability 54 APOL1 54 lipoprotein metabolism 54 proapoptotic 54 Hashimoto thyroiditis 53 hyperhomocysteinemia 53 channelopathies 53 overexpressing 53 predisposing factor 53 congenital deficiency 53 embryonic tissues 53 isolated perfused 53 53 pharmacological inhibition 53 hypomethylation 53 Neuroprotection 53 monocyte 53 essential thrombocythemia 53 post transplant lymphoproliferative 53 sporadic ALS 53 glycogen synthase 53 lysine residues 53 rotaviruses 53 lysosomal storage disease 53 5 hydroxytryptamine 53 BMP2 53 antiphospholipid antibodies 53 rs# [004] 53 intraventricular hemorrhage 53 γδ T cells 53 mTOR signaling 53 genetic polymorphisms 53 hypocretin neurons 53 beta globin gene 53 nicotinic receptor 53 downregulate 53 dorsal root ganglion 53 neurodegenerative disorder 53 CYP#C# [002] 53 Protein Kinase C 53 transient receptor 53 O methyltransferase 53 Oncogenic 53 immunopathology 53 G6PD 53 KIAA# 53 catenin 53 PDGFR 53 transcriptional regulator 53 Hedgehog signaling 53 ANCA associated 53 beta subunit 53 serotonin uptake 53 NF kB signaling 53 p# mitogen activated 53 SCD1 53 Cathepsin B 53 actinin 53 MYH9 gene 53 histone modification 53 pathophysiological 53 estrogen receptor alpha 53 neuroinflammatory 53 isomerase 53 1 proteinase inhibitor 53 adrenoceptor 53 muscarinic receptor 53 amyloid β 53 protein phosphatase 53 monocytes macrophages 53 chromosome #q#.# [001] 53 parkinsonism 53 mitochondrial enzyme 53 normal karyotype 53 hyperparathyroidism 53 transactivation 53 constitutively active 53 neural crest 53 Cytochrome P# 53 CALHM1 53 hydrolase 53 cell signaling pathways 53 genetic loci 53 transgenic mouse model 53 gene rearrangements 53 nNOS 53 transmembrane protein 53 DNA methyltransferase 53 plasminogen activator 53 leukoencephalopathy 53 enteroviral 53 nucleolar 53 uricase 53 mechanotransduction 53 V#F mutation 53 differential gene expression 53 apoE4 53 antiapoptotic 53 mevalonate 53 cyclin dependent kinase 53 ERBB2 53 replicase 53 receptor gene 53 Cerebellar 53 Purkinje cells 53 methylation patterns 53 subgenual cingulate 53 pathophysiological effects 53 enteropathy 53 CaM kinase II 53 tissue transglutaminase 53 PKC inhibitors 53 trisomic 53 ANGPTL4 53 etiologic 53 pathogenetic 53 striatal 53 E selectin 53 beta globin 53 53 ApoE 53 CD8 + 53 plasminogen activator inhibitor 53 podocytes 53 induced apoptosis 53 SIRT3 53 neurodevelopmental disorder 53 GABA receptor 53 Notch signaling 53 lymphocyte activation 53 conductance regulator 53 regulating gene expression 53 mRNA expression 53 receptor mediated endocytosis 53 dyskeratosis congenita 53 cyclin E 53 dopamine D2 receptor 53 huntingtin gene 53 haemolytic 53 SLC#A# [001] 53 caspase activation 53 CNTNAP2 gene 53 SLC#A# gene [002] 53 proinflammatory 53 hyperresponsiveness 53 eNOS 53 Extracellular 53 HLA DRB1 * 53 polyomavirus 53 paraventricular nucleus 53 diabetes mellitus DM 53 prognostic significance 53 artery stenosis 53 periventricular leukomalacia 53 microRNAs miRNAs 53 Placental 53 trophoblast cells 53 thyroid carcinoma 53 HLA DRB1 53 metabolic dysfunction 53 trinucleotide 53 MECP2 53 chitinase 53 FGF signaling 53 GluR1 53 neuronal synapses 53 lymphocytic 53 enterococcal 53 TYMS 53 apo E 53 SMAD4 53 secretase 53 immunoreactive 53 monocytic 53 acute myeloid 53 SLITRK1 53 idiopathic thrombocytopenic purpura 53 matrix metalloproteinase 53 pineal 53 fatty acid metabolism 53 SGPT 53 Hh 53 pleiotropic effects 53 ß amyloid 52 myeloperoxidase 52 DQB1 * 52 leptin signaling 52 transcriptional silencing 52 multisystemic 52 IGF1 52 pro angiogenic 52 susceptibility loci 52 carboxy terminal 52 adrenocortical 52 APOE e4 52 SOCS3 52 genus Plasmodium 52 idiopathic PAH 52 intestinal microflora 52 atherosclerotic lesions 52 Genetic variants 52 villous atrophy 52 Neutrophil 52 immunotoxin 52 perilipin 52 tuberous sclerosis complex 52 soluble fms 52 isotypes 52 LRRK2 gene 52 aggrecan 52 glutamatergic neurons 52 apo AI 52 G6PD deficiency 52 enkephalin 52 pseudotumor cerebri 52 Meckel Gruber 52 Alzheimer Disease AD 52 progerin 52 chorioamnionitis 52 apolipoprotein E4 52 thyroid hormone receptor 52 alpha1 antitrypsin deficiency 52 Borrelia burgdorferi 52 IL#B gene 52 c MYC 52 tumors secrete 52 hypoxia inducible factor 52 herpesviruses 52 coinfection 52 SMase 52 CYP #D# 52 aberrant activation 52 CFTR cystic fibrosis transmembrane 52 Polymorphism 52 tropomyosin 52 CIB1 52 tubule 52 necrotising enterocolitis 52 tumor infiltrating lymphocytes 52 chemokine receptor 52 gastric cardia 52 virus XMRV 52 apoA 52 SOD2 gene 52 p tau 52 receptor gamma 52 enzymatic pathways 52 LXRs 52 epigenetic mechanisms 52 cardiac myocytes 52 p# mutation 52 missense mutation 52 BARD1 52 RUNX3 52 multifactorial disease 52 Notch receptor 52 mRNA encoding 52 cofactors 52 Bardet Biedl syndrome 52 heterozygote 52 periventricular 52 multi factorial disease 52 Monocyte 52 overactivated 52 Glycosylation 52 metaplasia 52 Id1 52 RNA splicing 52 protein kinase C 52 cultured hippocampal neurons 52 Acidosis 52 neuronal plasticity 52 ovarian hormones 52 substrate specificity 52 neural cells 52 CAG repeats 52 SLC#A# [002] 52 MC4R gene 52 mitogen activated protein 52 #p# [003] 52 triiodothyronine 52 modulatory 52 LIS1 52 GPI anchored 52 umbilical artery 52 hippocampal neurons 52 primary effusion lymphoma 52 alpha defensin 52 BMAL1 52 iNOS 52 UCP2 52 chromosome #q# [002] 52 shorter telomere length 52 H#K# [001] 52 irreversible inhibitor 52 cytolytic 52 EGFR signaling 52 neurofibromatosis type 52 neuronal signaling 52 p#Kip# 52 prothrombotic 52 neuropathological 52 urinary excretion 52 synovial cells 52 vascular reactivity 52 Transcriptome 52 PI3K signaling 52 Escherichia coli Klebsiella pneumoniae 52 mTOR mammalian target 52 histone deacetylase 52 DNA methylation patterns 52 proinflammatory mediators 52 dysregulation 52 TRPV4 52 histologic subtype 52 proteinases 52 COUP TFII 52 nicotinamide 52 transiently transfected 52 antisense inhibitor 52 amyloidogenic 52 serum BDNF 52 chromosomal anomalies 52 non coding RNA 52 cerebellar 52 epigenetically 52 collagenous colitis 52 R#W [002] 52 receptor subtypes 52 catechol O methyltransferase 52 monocyte chemoattractant protein 52 histological subtype 52 hamartoma 52 generalized vitiligo 52 proteolytic cleavage 52 Fc receptor 52 progranulin gene 52 peptide CGRP 52 inhibitory antibodies 52 gene loci 52 susceptibility gene 52 myeloproliferative neoplasms 52 Propionibacterium acnes 52 MT1 MMP 52 lymphoblasts 52 cerebellar vermis 52 chromosomal alterations 52 MAPK pathway 52 IgG4 52 extracellular dopamine 52 PNET 52 postoperative delirium 52 hormone angiotensin II 52 Htt 52 guanine nucleotide exchange 52 cypin 52 Factor Receptor 52 proNGF 52 gonadotrophin releasing hormone 52 anaplastic lymphoma kinase 52 CC genotype 52 52 thyroid peroxidase 52 promoter polymorphism 52 evolutionarily conserved 52 RRM1 52 IgA deficiency 52 histone methylation 52 Ischemic 52 chromosome #q# [001] 52 Transcription Factor 52 tyrosine kinase receptor 52 arginase 52 humanized monoclonal 52 Transgenic Mice 52 Hcrt 52 capsular polysaccharide 52 protein misfolding 52 chromosomal aberrations 52 PTEN gene 52 oxidases 52 neoplasias 52 gene encoding 52 kinase domain 52 secretory pathway 52 hydroxylase 51 cholestasis 51 obesity insulin resistance 51 micronuclei 51 NKT cell 51 habenula 51 phospholipase 51 FMR1 gene 51 kDa protein 51 IgG1 51 paratuberculosis 51 genotoxic stress 51 Janus kinase 51 Diabetic nephropathy 51 neuro developmental disorders 51 SVZ 51 hyperphosphorylation 51 mitochondrial mutations 51 glycated 51 leukemic cell 51 Staphylococcus epidermidis 51 IFN γ 51 homozygosity 51 neuro protective 51 neuropeptide Y 51 homolog 51 renal cysts 51 potent inhibitors 51 FOXO 51 brain neurochemistry 51 N. gonorrhoeae 51 replicon 51 neuroligin 51 morphogenesis 51 innervation 51 cerevisiae 51 oncogenesis 51 focal segmental glomerulosclerosis FSGS 51 estrogen metabolism 51 mitotic progression 51 retinoid X 51 eicosanoids 51 Trichophyton rubrum 51 Catenin 51 SNP rs# [002] 51 Epithelial 51 synaptic transmission 51 alpha1 proteinase inhibitor 51 IL 1ß 51 transgene expression 51 potent stimulator 51 ciliated 51 HDAC enzymes 51 cytomegalovirus infection 51 IL6 51 PIK3CA 51 leukocyte counts 51 Progenitor Cells 51 microdeletions 51 NFkB 51 mitochondrial dysfunction 51 atrophic gastritis 51 lymphoproliferative disorders 51 Cowden syndrome 51 FOXO3a 51 Estrogen Receptor 51 androgen receptor AR 51 MnSOD 51 caveolae 51 ATPase 51 downregulated 51 Apc 51 anterior temporal 51 apolipoprotein E gene 51 myofibroblasts 51 Parkinson Disease PD 51 CD4 + CD8 + 51 inflammatory demyelinating 51 Cyclin D1 51 necrotizing 51 51 cystic fibrosis Duchenne muscular 51 CatB 51 XLHED 51 TGFß 51 encephalomyelitis 51 neuromuscular junction 51 Varicella zoster virus 51 dystroglycan 51 MSSE 51 Caveolin 1 51 toxic beta amyloid 51 Medulloblastoma 51 EBV infection 51 pertussis toxin 51 hypometabolism 51 dopamine transporter gene 51 integrin binding 51 cyclic adenosine monophosphate cAMP 51 Bordetella pertussis 51 BMPR2 51 mitochondrial metabolism 51 prion protein PrP 51 myeloproliferative diseases 51 underlying pathophysiology 51 Galectin 3 51 Notch signaling pathway 51 MLL gene 51 small molecule activator 51 hepatic lipase 51 FKBP# 51 tumorigenesis 51 phosphorylase 51 intracellular protein 51 Protease 51 inosine 51 #q# deletion syndrome 51 Diabetic neuropathy 51 miR# 51 cytomegalovirus CMV 51 nonalcoholic steatohepatitis 51 ABCB1 gene 51 Cx# [001] 51 epithelia 51 spontaneous mutations 51 glucocorticoid receptor 51 parietal cortices 51 potentiation 51 PDE5A 51 cAMP pathway 51 TMPRSS6 51 hypothalamus pituitary 51 malignant lymphomas 51 biogenesis 51 JAK2 V#F 51 Pathogenesis 51 γ secretase 51 osteoblast differentiation 51 MassGeneral Institute 51 neuropsychiatric diseases 51 choriocarcinoma 51 sequence homology 51 regulated kinase

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