Pages that link to "Q36259490"
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The following pages link to Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation (Q36259490):
Displaying 50 items.
- Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals (Q22122053) (← links)
- Epigenetic regulation of CpG promoter methylation in invasive prostate cancer cells (Q24302022) (← links)
- Absence of methylation of a CpG-rich region at the 5' end of the MIC2 gene on the active X, the inactive X, and the Y chromosome (Q24652389) (← links)
- DNA methylation in mammals (Q26852141) (← links)
- Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome (Q27908479) (← links)
- Genome-wide epigenomic profiling for biomarker discovery (Q28080102) (← links)
- DNA methylation, its mediators and genome integrity (Q28080760) (← links)
- CpG-rich islands and the function of DNA methylation (Q28131800) (← links)
- LOT1 (PLAGL1/ZAC1), the candidate tumor suppressor gene at chromosome 6q24-25, is epigenetically regulated in cancer (Q28217017) (← links)
- Functions of DNA methylation: islands, start sites, gene bodies and beyond (Q29547260) (← links)
- Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer (Q29615066) (← links)
- The history of cancer epigenetics (Q29617273) (← links)
- Clonal analysis of focal nodular hyperplasia of the liver. (Q30445025) (← links)
- DNA methylation and differentiation (Q30498513) (← links)
- Asynchronous replication of homologous loci on human active and inactive X chromosomes (Q33579193) (← links)
- X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease (Q33594410) (← links)
- X inactivation patterns in females with Alport's syndrome: a means of selecting against a deleterious gene? (Q33594464) (← links)
- The short arm of chromosome 11 is a "hot spot" for hypermethylation in human neoplasia (Q33636876) (← links)
- Inactive X chromosome has the highest concentration of unmethylated Hha I sites (Q33655662) (← links)
- X chromosome-wide analyses of genomic DNA methylation states and gene expression in male and female neutrophils (Q33734823) (← links)
- Genome-wide binding of MBD2 reveals strong preference for highly methylated loci (Q33753555) (← links)
- Polymerase chain reaction-aided genomic sequencing of an X chromosome-linked CpG island: methylation patterns suggest clonal inheritance, CpG site autonomy, and an explanation of activity state stability (Q33859871) (← links)
- Comparison of factor IX methylation on human active and inactive X chromosomes: implications for X inactivation and transcription of tissue-specific genes (Q33880345) (← links)
- Differential X reactivation in human placental cells: implications for reversal of X inactivation (Q34021115) (← links)
- Variable escape from X-chromosome inactivation: identifying factors that tip the scales towards expression (Q34086589) (← links)
- Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation (Q34206865) (← links)
- DNA methylation stabilizes X chromosome inactivation in eutherians but not in marsupials: evidence for multistep maintenance of mammalian X dosage compensation (Q34343329) (← links)
- X Chromosome Inactivation Is Mediated by Xist RNA Stabilization (Q34439255) (← links)
- Low expression of human histocompatibility leukocyte antigen-DR is associated with hypermethylation of human histocompatibility leukocyte antigen-DR alpha gene regions in B cells from patients with systemic lupus erythematosus (Q34557472) (← links)
- Nonrandom X chromosome DNA methylation patterns in hemophiliac females (Q34571270) (← links)
- Stage-specific DNA methylation in a fungal plant pathogen (Q34684344) (← links)
- Fine structure of the human hypoxanthine phosphoribosyltransferase gene (Q34684524) (← links)
- Hypomethylation of serum blood clot DNA, but not plasma EDTA-blood cell pellet DNA, from vitamin B12-deficient subjects (Q34778660) (← links)
- Characterization of in vivo somatic mutations at the hypoxanthine phosphoribosyltransferase gene of a human control population (Q34844726) (← links)
- Role of the promoter in maintaining transcriptionally active chromatin structure and DNA methylation patterns in vivo (Q35019887) (← links)
- Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation (Q35094123) (← links)
- Presence of 5-methylcytosine in CpNpG trinucleotides in the human genome (Q35189916) (← links)
- Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation (Q35195259) (← links)
- Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency (Q35195669) (← links)
- Methylation status of genes flanking the fragile site in males with the fragile-X syndrome: a test of the imprinting hypothesis (Q35197941) (← links)
- Skewed X inactivation in a female MZ twin results in Duchenne muscular dystrophy (Q35197963) (← links)
- A restriction-fragment-length difference detected by the anonymous probe DXS199 exhibits non-Mendelian inheritance (Q35246171) (← links)
- Selection against lethal alleles in females heterozygous for incontinentia pigmenti (Q35247308) (← links)
- Genetic and epigenetic regulation of gene expression in fetal and adult human livers (Q35302040) (← links)
- Complete concordance between glucose-6-phosphate dehydrogenase activity and hypomethylation of 3' CpG clusters: implications for X chromosome dosage compensation (Q35482874) (← links)
- Methylation patterns in the gene for the alpha subunit of chorionic gonadotropin are inherited with variable fidelity in clonal lineages of human fibroblasts (Q35561800) (← links)
- Complete reactivation of X chromosomes from human chorionic villi with a switch to early DNA replication (Q35597782) (← links)
- Actively transcribed genes in the raf oncogene group, located on the X chromosome in mouse and human (Q35608836) (← links)
- A pooling-based approach to mapping genetic variants associated with DNA methylation (Q35614128) (← links)
- X inactivation in mouse ES cells: histone modifications and FISH. (Q35671815) (← links)