Expression of imprinted genes in human preimplantation development

Molecular and Cellular Endocrinology

Volumn 183, Issue SUPPL. 1, 2001, Pages

  Monk, Marilyn ^a   Salpekar, Ashreena ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Embryonic cDNA libraries; Embryonic imprinted gene expression; Human preimplantation embryos; Imprinted disease

Indexed keywords

COMPLEMENTARY DNA;

ANIMAL MODEL; ARTICLE; BECKWITH WIEDEMANN SYNDROME; BLASTOCYST; DNA LIBRARY; EGG; EMBRYO; EMBRYO DEVELOPMENT; GENE EXPRESSION; GENETIC ANALYSIS; GROWTH RETARDATION; HAPPY PUPPET SYNDROME; HUMAN; HUMAN CELL; MOUSE; NONHUMAN; OOCYTE; PRADER WILLI SYNDROME; PREIMPLANTATION EMBRYO; PRIORITY JOURNAL; SILVER RUSSELL SYNDROME; SPERM; ANIMAL; DNA METHYLATION; FEMALE; GENE AMPLIFICATION; GENE EXPRESSION REGULATION; GENETICS; GENOME IMPRINTING; MALE; PHYSIOLOGY; PREGNANCY; REVIEW;

ANIMAL; DNA METHYLATION; DNA, COMPLEMENTARY; FEMALE; GENE AMPLIFICATION; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENOMIC IMPRINTING; HUMAN; MALE; MICE; OOCYTES; PREGNANCY; PREIMPLANTATION PHASE;

EID: 0035935233     PISSN: 03037207     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0303-7207(01)00575-5     Document Type: Article

References (44)

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5. Parental-origin-specific epigenetic modification of the mouse H19 gene
6. Genomic imprinting: potential function and mechanism revealed by the Prader-Willi and Angelman syndromes
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8. Expression of an Xist promoter-luciferase construct during spermatogenesis and preimplantation embryos-regulation by DNA methylation
9. IGF-2 receptors are first expressed at the 2-cell stage of mouse development
10. Evolutionary conservation of possible functional domains of the human and murine XIST genes
11. A methylation-dependent DNA-binding activity recognising the methylated promoter region of the mouse Xist gene
12. Imprinted expression of SNRPN in human preimplantation embryos
13. Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridisation
14. Expression of Xist during mouse development suggests a role in the initiation of X chromosome inactivation
15. Imprinting and X chromosome counting mechanisms determine Xist expression in early mouse development
16. Human PEG1/MEST, an imprinted gene on chromosome 7
17. Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation
18. Epigenetic modification and imprinting of the mammalian genome during development
19. Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements
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23. IGF2 is parentally imprinted in human preimplantation embryos
24. The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse
25. Tissue-specific expression and cDNA cloning of small nuclear ribonucleoprotein-associated polypepetide N
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31. Insulin-like growth factor II acts through an endogenous growth pathway regulated by imprinting in early mouse embryos
32. XIST expression from the maternal X chromosome in human male preimplantation embryos at the blastocyst stage
33. The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain
34. The use of amplified cDNA to investigate the expression of seven imprinted genes in human oocytes and preimplantation embryos
35. Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene
36. Gene expression in pre-implantation mammalian embryos
37. Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal
38. Allele-specific expression and total expression levels of imprinted genes during early mouse development: implications for imprinting mechanisms
39. A paternal-specific methylation imprint marks the alleles of the mouse H19 gene
40. Zygotic expression of connexin 43 gene supplies subunits for gap junction assembly during mouse re-implantation development
41. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
42. Monoallelic expression of the human H19 gene
43. Methylation of the mouse Xist gene in sperm and eggs correlates with imprinted Xist expression and paternal X-inactivation