Pages that link to "Q34088761"
Jump to navigation
Jump to search
The following pages link to Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse (Q34088761):
Displaying 50 items.
- Detailed analysis of X chromosome inactivation in a 49,XXXXX pentasomy (Q21092940) (← links)
- The Demoiselle of X-Inactivation: 50 Years Old and As Trendy and Mesmerising As Ever (Q21144943) (← links)
- Tsix transcription across the Xist gene alters chromatin conformation without affecting Xist transcription: implications for X-chromosome inactivation (Q24529595) (← links)
- Regulation of X-chromosome inactivation in development in mice and humans (Q24548607) (← links)
- A sequence motif found in aDrosophilaheterochromatin protein is conserved in animals and plants (Q24633125) (← links)
- Evidence of Xist RNA-independent initiation of mouse imprinted X-chromosome inactivation (Q24644032) (← links)
- Mapping and identification of candidate loci responsible for Peromyscus hybrid overgrowth (Q24677395) (← links)
- The "lnc" between 3D chromatin structure and X chromosome inactivation (Q26750498) (← links)
- Long nonoding RNAs in the X-inactivation center (Q26853173) (← links)
- Long noncoding RNAs: past, present, and future (Q26991873) (← links)
- Imprinted silencing is extended over broad chromosomal domains in mouse extra-embryonic lineages (Q26999035) (← links)
- Histone H3.3 variant dynamics in the germline of Caenorhabditis elegans (Q27315564) (← links)
- Imprinted gene expression in hybrids: perturbed mechanisms and evolutionary implications. (Q27686892) (← links)
- Genetic and epigenetic incompatibilities underlie hybrid dysgenesis in Peromyscus (Q28143956) (← links)
- Epigenetic reprogramming in early embryonic development: effects of in-vitro production and somatic nuclear transfer (Q28241243) (← links)
- The evolution of heteromorphic sex chromosomes (Q28252276) (← links)
- The inheritance of acquired epigenetic variations (Q28261493) (← links)
- Essential role of the CUL4B ubiquitin ligase in extra-embryonic tissue development during mouse embryogenesis (Q28262931) (← links)
- Association of IGF2 and H19 imprinting with choriocarcinoma development (Q28305462) (← links)
- The role of epigenetic mechanisms and processes in autoimmune disorders (Q28389137) (← links)
- Plac1 (placenta-specific 1) is essential for normal placental and embryonic development (Q28507167) (← links)
- Choroideremia gene product affects trophoblast development and vascularization in mouse extra-embryonic tissues (Q28511845) (← links)
- X-inactivation is stably maintained in mouse embryos deficient for histone methyl transferase G9a (Q28589156) (← links)
- Cited1 is required in trophoblasts for placental development and for embryo growth and survival (Q28589675) (← links)
- Esx1 is an X-chromosome-imprinted regulator of placental development and fetal growth (Q28591932) (← links)
- X-inactivation analysis of embryonic lethality in Ocrl wt/-; Inpp5b-/- mice (Q28593005) (← links)
- Evolution from XIST-independent to XIST-controlled X-chromosome inactivation: epigenetic modifications in distantly related mammals (Q28740797) (← links)
- Two-step imprinted X inactivation: repeat versus genic silencing in the mouse (Q30495292) (← links)
- Mapping dysmorphic syndromes with the aid of the human/mouse homology map (Q30501668) (← links)
- The Polycomb group protein EED is dispensable for the initiation of random X-chromosome inactivation (Q30814417) (← links)
- X chromosome reactivation initiates in nascent primordial germ cells in mice (Q30833162) (← links)
- Differential pattern of Xist RNA accumulation in single blastomeres isolated from 8-cell stage mouse embryos following laser zona drilling (Q31117850) (← links)
- Heterogeneous X inactivation in trophoblastic cells of human full-term female placentas (Q33178120) (← links)
- Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues (Q33240549) (← links)
- The evolution of imprinting: chromosomal mapping of orthologues of mammalian imprinted domains in monotreme and marsupial mammals (Q33297805) (← links)
- The status of dosage compensation in the multiple X chromosomes of the platypus (Q33354959) (← links)
- Role of the transcriptional corepressor Bcor in embryonic stem cell differentiation and early embryonic development (Q33369857) (← links)
- Identification of regulatory elements flanking human XIST reveals species differences (Q33538340) (← links)
- Antisense transcription through the Xist locus mediates Tsix function in embryonic stem cells (Q33551220) (← links)
- Random X inactivation and extensive mosaicism in human placenta revealed by analysis of allele-specific gene expression along the X chromosome (Q33598339) (← links)
- Enzymatic amplification of a Y chromosome repeat in a single blastomere allows identification of the sex of preimplantation mouse embryos (Q33601734) (← links)
- PRC2 represses transcribed genes on the imprinted inactive X chromosome in mice (Q33634777) (← links)
- Genetic study of indirect inguinal hernia (Q33673499) (← links)
- Uniparental and functional X disomy in Turner syndrome patients with unexplained mental retardation and X derived marker chromosomes (Q33680960) (← links)
- Maternal bias and escape from X chromosome imprinting in the midgestation mouse placenta (Q33711072) (← links)
- Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster (Q33774256) (← links)
- Evidence for local regulatory control of escape from imprinted X chromosome inactivation. (Q33779627) (← links)
- Dosage compensation in the process of inactivation/reactivation during both germ cell development and early embryogenesis in mouse (Q33807862) (← links)
- RNF12 activates Xist and is essential for X chromosome inactivation (Q33813511) (← links)
- Genome-wide prediction of imprinted murine genes (Q33841575) (← links)