Related by context. All words. (Click for frequent words.) 62 CHD7 62 phthalate syndrome 62 epigenetic changes 62 neuroligins 61 mitochondrial defects 61 phenotypic expression 61 developmental abnormalities 61 telomere DNA 60 prion gene 60 MECP2 gene 60 protein conformation 60 holoprosencephaly 60 mosaicism 60 Hutchinson Gilford progeria 60 Folic acid deficiency 60 Kufs disease 60 cnidarians 60 microdeletion 59 vertebrate embryos 59 motor neuron degeneration 59 Preimplantation Genetic Diagnosis PGD 59 persistent pulmonary hypertension 59 transfusion syndrome 59 inherited mutations 59 DNA methylation patterns 59 Genetic mutations 59 alpha synuclein protein 59 congenital disorders 59 infertility miscarriages 59 gastrulation 59 monozygotic twins 59 defective mitochondria 59 Nimbadon 59 gamma globin gene 59 vitro maturation 59 methylation patterns 59 mechanotransduction 59 genomic imprinting 59 acrosome reaction 59 epigenetic regulation 59 chromosome rearrangements 59 regulates gene expression 59 BARD1 59 fetu 58 aneuploidies 58 neurodevelopmental disorder 58 mitochondrial DNA mtDNA 58 epigenetic markers 58 chromatin structure 58 clefting 58 fetal chromosomal 58 Rb gene 58 fertilized egg splits 58 primordial germ cells 58 Chlamydia pneumoniae 58 germline cells 58 bilaterians 58 cloned primate 58 causative genes 58 filaggrin gene 58 neuropsychiatric disorder 58 epigenetic modification 58 microchimerism 58 JAK mutations 58 Bacterial vaginosis 58 aneuploid 58 conceptus 58 spontaneous miscarriages 58 Epstein Barr Virus EBV 58 multisensory integration 58 TCF#L# gene 58 Rh incompatibility 58 pancreatic endocrine 58 de novo mutations 58 genetic recombination 58 telomere dysfunction 58 Genetic variation 58 Fragile X gene 58 reproductive abnormalities 57 cystic fibrosis muscular dystrophy 57 spontaneously aborted 57 Meckel Gruber 57 Helicobacter infection 57 nongenetic 57 Klotho gene 57 MECP2 57 inhaled fibers 57 sexually dimorphic 57 embryological 57 spontaneous mutation 57 mitochondrial mutations 57 chromosomal imbalance 57 membrane fusion 57 totipotent 57 Induced pluripotent stem cells 57 piRNAs 57 KCNQ1 57 LIS1 57 STAT4 57 Single Nucleotide Polymorphisms SNPs 57 chromosomal anomalies 57 progranulin gene 57 folate metabolism 57 ovulatory cycles 57 MLL gene 57 epigenetic alterations 57 SRY gene 57 microRNA molecules 57 embryo clones 57 ovarian follicles 57 induced pluripotent cells 57 testicular dysgenesis syndrome 57 CNTNAP2 gene 57 IRAK1 57 cybrid 57 epigenetic inheritance 57 prion strains 57 TP# gene 57 recessive trait 57 Neuregulin 1 57 neural crest stem cells 57 synovial cells 57 Mycoplasma genitalium 57 chromosomal anomaly 57 abnormal chromosomes 57 connexin 57 Sexual arousal 57 CFTR gene 57 ectoderm 57 octuplets conceived 57 epigenetic reprogramming 57 teratogens 57 Male infertility 57 SHANK3 gene 57 STAT3 signaling 57 embryonal 57 IUGR 57 NKT cell 57 monozygotic 57 HGPS 57 copper zinc superoxide 57 blastomeres 57 neuro developmental disorder 57 coevolution 57 CNTNAP2 57 Brugada Syndrome 57 MeCP2 protein 57 Creutzfeld Jakob disease 57 incurable genetic 57 Leydig cells 56 trophoblast 56 Sporadic CJD 56 transgenic mice expressing 56 inherited retinal degeneration 56 aneuploidy 56 axon guidance 56 chromosome abnormality 56 eukaryote 56 Atopic eczema 56 DLX5 56 embryonic fetal 56 abnormal prions 56 FUS protein 56 HLA DRB1 56 severe congenital neutropenia 56 Apert syndrome 56 dizygotic twins 56 microcephalin 56 Beckwith Wiedemann syndrome 56 ontogenetic 56 FMR1 gene 56 HAR1 56 dizygotic 56 corpus luteum 56 chromosomal defect 56 normal prion protein 56 Genetic predisposition 56 #q# deletion 56 evolvability 56 granulosa cell 56 GPC5 56 androgen signaling 56 embryonic tissue 56 morphogenetic 56 BCL#A 56 intra cytoplasmic sperm 56 parthenogenetic 56 genetic loci 56 Thorough cooking kills 56 biomineralization 56 FGFR2 gene 56 cultured neurons 56 Pax3 56 aneuploid cells 56 embryonic tissues 56 apoE 56 olfactory receptor 56 neurodevelopmental disorders 56 hemolytic disease 56 sequence homology 56 ribonucleic acids 56 molar pregnancy 56 intracytoplasmic sperm injection ICSI 56 placental mammals 56 excitatory synapses 56 organogenesis 56 Ectopic pregnancy 56 proteoglycan 56 glycolipid 56 physiological characteristics 56 deformed fetuses dying 56 egg follicles 56 LMNA gene 56 Prion proteins 56 mammalian sperm 56 IgA deficiency 56 Oxidative stress 56 muscular dystrophy cystic fibrosis 56 maternally inherited 56 T. vaginalis 56 chick embryos 56 cohesin 56 DISC1 gene 56 PrPC 56 adult neurogenesis 56 neural crest cells 56 factor PlGF 56 multicellularity 55 hemoglobin molecule 55 nanobacteria 55 histone methylation 55 molecular etiology 55 Fragile X mental retardation 55 underlying pathophysiology 55 superfetation 55 placental cells 55 BRIP1 55 von Hippel Lindau 55 single celled microorganisms 55 fatal neurodegenerative 55 CYP#D# gene 55 LRAT 55 deuterostomes 55 GRNOPC1 contains 55 Kabuki syndrome 55 aetiological 55 MC1R 55 gene locus 55 remains mystery Yairi 55 Folate deficiency 55 intracellular signal transduction 55 autistic enterocolitis 55 neuropathologic 55 dedifferentiation 55 MLL2 55 evolutionary divergence 55 neurofibrillary 55 protein tau 55 insulin secreting cells 55 retinoid X 55 glia cells 55 imprinted genes 55 CYP#B# 55 β1 55 Thyroid hormone 55 reproduce asexually 55 placenta praevia 55 IDH mutations 55 multicellular animals 55 placental function 55 primitive vertebrates 55 pathophysiologic 55 epigenetic modifications 55 neurexins 55 TEL AML1 55 neural tube defect 55 haplotype map 55 mouse embryos 55 neuropsychiatric diseases 55 synaptic function 55 trophoblast cells 55 Hair follicles 55 fetal chromosomal abnormalities 55 unfertilised eggs 55 podocytes 55 lymphatic vasculature 55 SOD1 gene 55 fungal genomes 55 mRNA decay 55 MMP# 55 neuritic 55 excitotoxicity 55 axonal degeneration 55 embryoid bodies 55 genetic abnormalities 55 previously undescribed 55 GAB2 55 epiblast stem cells 55 #q#.# deletion syndrome 55 glial tumors 55 intracytoplasmic sperm injection 55 budding yeast Saccharomyces 55 called Abydosaurus mcintoshi 55 Bardet Biedl syndrome 55 nerve degeneration 55 neuroanatomical 55 Contagious yawning 55 #S ribosomal RNA 55 non coding RNA 55 autosomal 55 spontaneous mutations 55 M. genitalium 55 amniotic cavity 55 Hemangiomas 55 metabolomic profiles 55 mRNA transcripts 55 Polycomb proteins 55 microRNAs miRNAs 55 intercellular signaling 55 Sertoli cells 55 histone acetylation 55 Heterodontosaurus 55 metazoans 55 hepatic stellate cells 55 hydrops 55 PrPSc 55 genetically inherited 55 genetic polymorphisms 55 gut microbiota 55 chromosomal abnormalities 55 deriving stem cells 55 mitochondrial dysfunction 55 guinea pigs lubiprostone 55 Endometrial cancer 55 metabolomic profiling 55 Hox gene 55 cell nuclei 55 skeletal dysplasia 55 APOL1 55 airway remodeling 55 etiologic 55 KIAA# 55 fetal malformations 55 Spinal muscular atrophy 55 congenital toxoplasmosis 55 mitogen activated protein kinases 55 monogenic 55 cytoplasmic hybrids 55 chromosomal rearrangement 55 Wnt proteins 55 pluripotent embryonic 55 epigenetically 55 familial ALS 55 Umbilical cord stem cells 55 limb deformities 55 bronchopulmonary dysplasia BPD 55 normal prion proteins 55 granule cells 55 cellular prion protein 55 pituitary hormone 55 microbiome 55 neurogenetic 55 gamete formation 55 #beta HSD1 55 survival motor neuron 55 suppress ovulation 55 Wnt1 54 IL#R 54 endocasts 54 preimplantation genetic diagnosis PGD 54 SETDB1 54 neurobiological 54 sphingolipid 54 ovarian hormones 54 vacuolar 54 Laurean fathered 54 tiny roundworm 54 Proximate cause 54 sperm fertilizes 54 chordate 54 genetic susceptibility 54 cypin 54 evolutionary conserved 54 testicular germ cell 54 choroid plexus 54 CRISPR Cas 54 Genetic mutation 54 progerin 54 positional cloning 54 phenotypic differences 54 insulin secreting beta 54 X chromosome inactivation 54 recessive genes 54 Fetal heartbeats 54 differential gene expression 54 hippocampal function 54 gene rearrangements 54 placental tissue 54 unspecialized cells 54 Pseudomonas syringae 54 desmosomes 54 Peripheral nerves 54 vertebrate evolution 54 neuronal circuits 54 enterocolitis 54 pre eclamptic 54 spore formation 54 tumor suppressors cytokines 54 primate genomes 54 evolutionary origins 54 Parthenogenesis 54 primitive organisms 54 ependymomas 54 Peptide YY 54 exocrine 54 dysgenesis 54 prenatally diagnosed 54 prenatal exposures 54 fascin 54 neuronal migration 54 NOD2 54 X inactivation 54 Hh pathway 54 hyperactivated 54 misfolding 54 lung epithelium 54 bacterium Escherichia coli 54 beta globin gene 54 misfolds 54 metazoan 54 mitochondrial disorders 54 trophoblasts 54 RNA splicing 54 oncogenic transformation 54 pathogenic mechanisms 54 mutant huntingtin protein 54 unstable detrusor muscle 54 posttranslational modification 54 chemosignals 54 inherit predisposition 54 peroxisome 54 marsupial mammals 54 pathogenic mutations 54 muscular dystrophies 54 premature ovarian 54 MYH9 gene 54 myopathies 54 Genetic variations 54 MiRNAs 54 Ectopic pregnancies 54 Neural stem cells 54 fruitfly Drosophila 54 mammary tissue 54 ChR2 54 Mycoplasma capricolum 54 FGF signaling 54 progressive neurodegenerative disorder 54 phthalate exposure 54 lissencephaly 54 nanoparticle aggregates 54 pathophysiological mechanisms 54 RAD# gene 54 infertility miscarriage 54 trophoblastic 54 Polycystic ovarian syndrome 54 thyroid hormone deficiency 54 methylation markers 54 herpesviruses 54 chemically alters 54 Prevotella 54 histone demethylase 54 neuromuscular junction 54 MC4R gene 54 neural tube 54 hereditary deafness 54 mutant mouse 54 mammalian embryos 54 gonadotropins 54 Irritable bowel syndrome IBS 54 congenital anomalies 54 nematode worms 54 chromosome abnormalities 54 congenital brain tumor 54 podocyte 54 sporadic Creutzfeldt Jakob 54 jawed vertebrates 54 neonatal sepsis 54 heritable disorders 54 ribosomal RNA 54 Tammar wallaby 54 degenerative neurological diseases 54 LRP5 54 gene MECP2 54 miRNA genes 54 synaptogenesis 54 heritable variation 54 JAK2 enzyme 54 abnormal methylation 54 injection ICSI 54 #BP# 54 genital abnormalities 54 orofacial clefts 54 DEC2 54 birth asphyxia 54 female hormones estrogen 54 neural crest 54 MIF protein 54 amyloid plaque formation 54 platypus genome 54 eusociality 54 huntingtin protein 54 Südhof 54 male hormone androgen 54 tau protein 54 mammalian ancestor 54 non mammalian vertebrates 54 germline mutations 54 bacterium Mycobacterium tuberculosis 54 Gestational age 54 Helicobacter 54 neuro developmental disorders 54 Cryptococcus neoformans 54 congenital abnormalities 54 gliosis 54 Progenitor cells 54 Xenopus laevis 54 MeCP2 gene 54 missense mutations 54 Pseudomonas spp 54 neural cells 54 NF1 gene 54 mammary cells 54 Infant botulism 54 nephron 54 mouse mammary 54 virulence genes 54 male reproductive organs 54 cardiac fibrosis 54 deacetylation 54 histone code 54 thyroid hormone levels 54 ribonucleic acid RNA 54 exomes 54 archaic ungulates 54 neuronal synapses 54 Infectious prions 54 SCN5A 54 sensory receptors 54 Amyloid plaques 54 Transcriptome 54 Myotonic dystrophy 54 deafness neurological 54 IVF ICSI 54 achromatopsia 54 cerebro spinal fluid 54 SOX3 gene 54 plasma kallikrein 54 neuronal pathways 54 retinal pigment epithelium 54 cloned blastocysts 54 genomic rearrangements 54 Hirschsprung disease 54 myelomeningocele 54 Pelvic inflammatory 54 synapse formation 54 neuronal signaling 54 SOD1 protein 54 multicellular creatures 54 polyploid 54 Kirichok 53 enzymatic pathway 53 epistasis 53 blastomere 53 multiprotein complex 53 cytoplasmic hybrid 53 neurobiological underpinnings 53 FASEB advances 53 Hip dysplasia 53 Atlantic Multidecadal Oscillation AMO 53 congenital adrenal hyperplasia 53 Male pattern baldness 53 ORMDL3 53 mammalian brains 53 Neural tube defects 53 MAPKs 53 sonographic diagnosis 53 #p#.# [001] 53 lipofuscin 53 spontaneously abort 53 transcriptomics 53 retinal dysfunction 53 kidney urologic 53 species reproduce asexually 53 mammary gland tumors 53 evolutionary lineage 53 FGFs 53 obligate intracellular 53 VHL gene 53 neurofibroma 53 neurodegenerative disorder 53 germline stem cells 53 intra uterine 53 SLC#A# gene [001] 53 Entamoeba 53 disfigurations birthmarks 53 bioluminescence imaging 53 dimorphic 53 leiomyoma 53 pyelonephritis 53 IRS1 53 cybrids 53 vanA gene 53 amyloid proteins 53 causative gene 53 abnormal proteins 53 somites 53 hamartomas 53 microRNA expression 53 DNA demethylation 53 inheritable genetic 53 Hashimoto thyroiditis 53 zona pellucida 53 papillomaviruses 53 brassinosteroid 53 cause cardiac channelopathies 53 luteal cells 53 olfactory epithelium 53 facial clefts 53 autosomal recessive 53 neuronal dysfunction 53 DHFR 53 polyhydramnios 53 genetic alterations 53 ovulation fertilization 53 Shabaniyah festival marks 53 Physiology Seminar 53 Muscular dystrophies 53 Amborella 53 parasitic flatworms 53 mtDNA mutations 53 PHLPP 53 Neural tube 53 carbonate globules 53 chromosomal alterations 53 Preimplantation Factor 53 neurofibromas 53 placental tissues 53 polygenic 53 chorioamnionitis 53 Tor Bjerkedal report 53 mental retardation epilepsy 53 sCJD 53 Leydig cell 53 unfertilised egg 53 DNA rearrangements 53 Biliary atresia 53 LPA receptors 53 mucus clogs 53 dynamin 53 ABCB1 gene 53 Protein folding 53 CDK4 53 inherited maternally 53 oxidases 53 multi celled organisms 53 MEF2A 53 intestinal microbiota 53 channelopathies 53 Six3 53 neurological dysfunction 53 apolipoprotein E4 53 Uveal melanoma 53 fatty acid oxidation 53 prevent fertilized egg 53 dyskeratosis congenita 53 monozygotic twin 53 ADPKD 53 Spina bifida occurs 53 microbiomes 53 CCR5 delta# 53 HER2 neu 53 hormone FSH 53 HLA genes 53 multicellular organisms 53 reproductive endocrine 53 chemosensory 53 ZFN TM 53 Brugada syndrome 53 dominantly inherited 53 pAkt 53 pyrimidines 53 laforin 53 Hoxb8 53 unicellular organism 53 autosomal dominant disorder 53 NR#A# gene 53 astrocyte cells 53 FOXP2 gene 53 chromosomal aberrations 53 Cyclin D1 53 genome rearrangements 53 WDR# 53 BRAF protein 53 ovule 53 enucleated egg 53 Li Fraumeni syndrome 53 BRAF gene 53 LRRK2 gene 53 regenerating tissues 53 genetic 53 Dicer enzyme 53 metabonomics 53 Foxp2 53 singleton pregnancy 53 dysbindin gene 53 Thyroid hormones 53 thale cress Arabidopsis thaliana 53 undiagnosed celiac disease 53 intrauterine infection 53 adnexal mass 53 choriocarcinoma 53 brain lesions 53 Celiac sprue 53 mRNA sequences 53 fetal aneuploidy 53 cardiac progenitor cells 53 Selenium deficiency 53 oocyte maturation 53 Mycoplasma pneumoniae 53 Joubert syndromes 53 INF2 53 genomic variants 53 TMPRSS2 ERG fusion 53 Ichthyostega 53 allelic variation 53 oligodendrocyte progenitor cells 53 gametophyte 53 primordial follicles 53 olfactory receptors 53 microscopic single celled 53 African clawed frog 53 morphometrics 53 telomere maintenance 53 molecular mimicry 53 adrenal cortex 53 onset sepsis 53 congenital hypothyroidism 53 testicular tumors 53 maternal serum 53 Epileptic seizures 53 Wnt signaling pathway 53 Variant CJD 53 Chromosomal 53 PGD PGS 53 amyloid deposition 53 embyros 53 p# mutations 53 Neu5Gc 53 recessive genetic 53 noncoding RNA 53 innermost lining 53 Trichomonas 53 neural precursor 53 embryonic germ 53 prestin 53 HMGA2 53 Peritoneal mesothelioma 53 Prolactin 53 female hormone progesterone 53 transcriptional repressor 53 tumor suppressor protein 53 rhodopsin 53 Polycystic ovary syndrome PCOS 53 Chlamydia psittaci 53 Caenorhabditis 53 myostatin gene 53 intracytoplasmic 53 Skeletal muscles 53 underlying molecular mechanisms 53 sickle cell hemoglobin 53 Pten 53 apoE4 53 renal fibrosis 53 Evolutionarily speaking 53 protein misfolding 53 PCR RFLP 53 neonatal respiratory distress 53 epigenetic 53 fertilized embryo 53 spongiform encephalopathies 53 neurosensory 53 Xenopus 53 Urinary tract 53 Aromatase 53 thyroid dysfunction 53 posttranslational 53 schistosome 52 matrix metalloproteinases MMPs 52 transdifferentiation 52 fungal strains 52 estrous cycle 52 monoamine neurotransmitters 52 CDH# 52 human microbiome 52 clonally 52 endocrine glands 52 OPHN1 52 chromosomal disorders 52 parasite Plasmodium falciparum 52 Selembu shows 52 pathophysiological 52 transgenic rats 52 multi celled 52 transfer SCNT 52 enzymatic pathways 52 vomeronasal organ VNO 52 germ cells 52 chromosomal defects 52 haploid 52 Sertoli cell 52 amnion 52 chordates 52 CHEK2 52 neuronal degeneration 52 interferon pathway 52 Notch signaling 52 muscle dystrophies 52 peroxisomes 52 sporadic ALS 52 chromosomal translocations 52 histone modifications 52 Study Spacing 52 zebrafish embryo 52 Soluble CD# 52 neonatal encephalopathy 52 neuro degenerative disease 52 Wnts 52 transgene expression 52 dendritic spine 52 Mitochondrial diseases 52 prion disease 52 Telomere length 52 fertilized ovum 52 MAPCs 52 amino acid metabolism 52 TMEM#B 52 stress cardiomyopathy 52 hypogonadotropic hypogonadism 52 homochirality 52 promoter hypermethylation 52 Myocarditis 52 chromosome translocations 52 Neanderthals interbred 52 RUNX3 52 Molnar Szakacs 52 mutated protein 52 implantation genetic 52 neuroendocrine 52 beta1 integrin 52 biogenesis 52 bronchopulmonary dysplasia 52 gestational diabetes mellitus GDM 52 microdeletions 52 maize genome 52 modulatory 52 siRNA knockdown 52 genes BRCA1 52 Inhaled nitric oxide 52 gastric carcinoma 52 hypermethylated 52 embryogenesis 52 redox reactions 52 Streptococcus agalactiae 52 photoreceptor cell 52 follicular fluid 52 severe dehydrating diarrhea 52 GPIHBP1 52 H#K# [001] 52 WAGR syndrome 52 mitochondrial genomes 52 cathepsins 52 sumoylation 52 LMNA 52 chromosomal DNA 52 Spina bifida 52 Confocal microscopy 52 preeclamptic women 52 cystic fibrosis chronic pancreatitis 52 zebra finch 52 methyltransferase 52 Htt 52 SHANK3 52 maternally derived 52 indels 52 protein fragment 52 xenotropic murine leukemia 52 γ secretase 52 Severe Combined Immunodeficiency 52 Ectopia Cordis 52 environmental toxicants 52 inactive X chromosome 52 affective psychoses 52 Leptospira 52 transcriptional regulation 52 prematurity ROP 52 Heidi Rehm 52 budding yeast 52 singleton babies 52 autistic regression 52 Genetic variants 52 precancerous tumors 52 facioscapulohumeral muscular dystrophy 52 Matthew T. Carrano 52 nucleotide substitutions 52 pyloric stenosis 52 Sandhoff disease 52 pathogenic bacterium 52 myelogenous leukemia 52 protein coding RNAs 52 basal epithelial 52 oocyte retrieval 52 roundworm C. elegans 52 fungus Cryptococcus neoformans 52 fibroma 52 phenotypic variation 52 paternally inherited 52 tiny single celled 52 amyloid peptide 52 medulloblastoma tumors 52 Treg cell 52 electrophysiologic 52 planaria 52 primordia 52 Crouzon syndrome 52 klotho gene 52 Hox genes 52 neural underpinnings 52 Folate supplementation 52 Menkes disease 52 Sudden infant 52 familial clustering 52 protein clumps 52 zebrafish embryos 52 C1q 52 X. laevis 52 misregulation 52 #q#.# [002] 52 neuronal stem cells 52 tau mutation 52 Hypospadias 52 p# MAPK 52 hormones leptin 52 Sensorineural hearing loss 52 ductal breast cancer 52 monogenic diabetes 52 globin genes 52 dose ionizing radiation 52 antiphospholipid syndrome 52 autosomal recessive genetic 52 MGUS 52 MYH9 52 maturational 52 twin transfusion 52 embryo biopsy 52 coding exons 52 autoimmune encephalitis 52 C. neoformans 52 heritable diseases 52 potent inducer 52 alpha synuclein gene 52 inherited predisposition 52 genetic syndromes 52 infectious prion proteins 52 vermis 52 polycystic 52 umbilical hernias 52 recessive mutation 52 microglial 52 metabolic enzymes 52 IVF pregnancies 52 pigtail macaques 52 soluble proteins 52 autoinflammatory diseases 52 genomic instability 52 Nucleic acid 52 RNA sequences 52 PDZ domains 52 CYP#E# gene 52 genes predisposing 52 hermaphroditism 52 hormones neurotransmitters 52 penile spines 52 developmental plasticity 52 uterus fallopian tubes 52 neurodevelopment disorder 52 childhood disintegrative disorder 52 myofibroblasts 52 ERK signaling 52 gastric carcinomas