Pages that link to "Q46156066"
Jump to navigation
Jump to search
The following pages link to Neomorphic agouti mutations in obese yellow mice (Q46156066):
Displaying 50 items.
- Long-term effects of environmental endocrine disruptors on reproductive physiology and behavior (Q21129084) (← links)
- L1 antisense promoter drives tissue-specific transcription of human genes (Q21284466) (← links)
- The mouse mahogany locus encodes a transmembrane form of human attractin (Q22009076) (← links)
- Antagonism of central melanocortin receptors in vitro and in vivo by agouti-related protein (Q24314579) (← links)
- A longitudinal study of epigenetic variation in twins (Q24600673) (← links)
- Environmental studies of schizophrenia through the prism of epigenetics (Q24643547) (← links)
- Mouse U2af1-rs1 is a neomorphic imprinted gene (Q24647321) (← links)
- Epigenetics: a molecular link between environmental factors and type 2 diabetes (Q24652830) (← links)
- A natural allele of Nxf1 suppresses retrovirus insertional mutations (Q24658176) (← links)
- Transposable elements: targets for early nutritional effects on epigenetic gene regulation (Q24681243) (← links)
- Maternal nutrient supplementation counteracts bisphenol A-induced DNA hypomethylation in early development (Q24681489) (← links)
- Liver-specific expression of the agouti gene in transgenic mice promotes liver carcinogenesis in the absence of obesity and diabetes (Q24799830) (← links)
- Melanocortin 1 Receptor: Structure, Function, and Regulation (Q26745953) (← links)
- Obesity genetics in mouse and human: back and forth, and back again (Q26782027) (← links)
- Bisphenol A Effects on Mammalian Oogenesis and Epigenetic Integrity of Oocytes: A Case Study Exploring Risks of Endocrine Disrupting Chemicals (Q26784473) (← links)
- Maternal nutritional status, C(1) metabolism and offspring DNA methylation: a review of current evidence in human subjects (Q27015643) (← links)
- Epigenetics and life-long consequences of an adverse nutritional and diabetic intrauterine environment (Q27022688) (← links)
- Chromatin Modifications Associated With Diabetes and Obesity (Q27028212) (← links)
- Nxf1 natural variant E610G is a semi-dominant suppressor of IAP-induced RNA processing defects (Q27311325) (← links)
- A Novel Analytical Strategy to Identify Fusion Transcripts between Repetitive Elements and Protein Coding-Exons Using RNA-Seq (Q27334758) (← links)
- Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse (Q28248620) (← links)
- Targeted disruption of the melanocortin-4 receptor results in obesity in mice (Q28302831) (← links)
- Mechanisms of mutation induction in germ cells of the mouse as assessed by the specific locus test (Q28374123) (← links)
- Mvwf, a dominant modifier of murine von Willebrand factor, results from altered lineage-specific expression of a glycosyltransferase (Q28510698) (← links)
- DNA methylation is dispensable for suppression of the agouti viable yellow controlling element in murine embryonic stem cells (Q28542838) (← links)
- Transgenerational inheritance of epigenetic states at the murine Axin(Fu) allele occurs after maternal and paternal transmission (Q28588249) (← links)
- Deletion of eIF2beta suppresses testicular cancer incidence and causes recessive lethality in agouti-yellow mice (Q28592368) (← links)
- Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome (Q28593604) (← links)
- Chromosomal Rearrangements as Barriers to Genetic Homogenization between Archaic and Modern Humans (Q28596394) (← links)
- Measuring natural selection on genotypes and phenotypes in the wild (Q28659333) (← links)
- Transposable elements and viruses as factors in adaptation and evolution: an expansion and strengthening of the TE-Thrust hypothesis (Q28710587) (← links)
- Reactivation of L1 retrotransposon by benzo(a)pyrene involves complex genetic and epigenetic regulation (Q28740315) (← links)
- Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2 (Q29303884) (← links)
- Environmental epigenomics and disease susceptibility (Q29547452) (← links)
- Epigenetic inheritance at the agouti locus in the mouse (Q29617318) (← links)
- A B2 SINE insertion in the Comt1 gene (Comt1(B2i)) results in an overexpressing, behavior modifying allele present in classical inbred mouse strains (Q30476995) (← links)
- Gene-trap mutagenesis: past, present and beyond (Q30728811) (← links)
- A method to quantify mouse coat-color proportions (Q33436730) (← links)
- Fetal programming of adult glucose homeostasis in mice (Q33507523) (← links)
- CpG methylation of a silent controlling element in the murine Avy allele is incomplete and unresponsive to methyl donor supplementation (Q33530122) (← links)
- The role of agouti-related protein in regulating body weight (Q33656384) (← links)
- The agouti mouse model: an epigenetic biosensor for nutritional and environmental alterations on the fetal epigenome (Q33658173) (← links)
- Adaptive radiation-induced epigenetic alterations mitigated by antioxidants (Q33713388) (← links)
- Repression of chimeric transcripts emanating from endogenous retrotransposons by a sequence-specific transcription factor (Q33751768) (← links)
- Intracisternal A-particle element transposition into the murine beta-glucuronidase gene correlates with loss of enzyme activity: a new model for beta-glucuronidase deficiency in the C3H mouse (Q33781490) (← links)
- Complex patterns of inheritance of an imprinted murine transgene suggest incomplete germline erasure (Q33786662) (← links)
- An N-ethyl-N-nitrosourea screen for genes involved in variegation in the mouse (Q33836232) (← links)
- Genome-wide prediction of imprinted murine genes (Q33841575) (← links)
- piRNA pathway targets active LINE1 elements to establish the repressive H3K9me3 mark in germ cells. (Q33850547) (← links)
- Discordance between genetic and epigenetic defects in pseudohypoparathyroidism type 1b revealed by inconsistent loss of maternal imprinting at GNAS1 (Q33905190) (← links)