Pages that link to "Q24318274"
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The following pages link to The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis (Q24318274):
Displaying 50 items.
- Pleckstrin homology like domain family A member 2 (Q21122517) (← links)
- A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region (Q22009166) (← links)
- Inhibition of protein synthesis by the T cell receptor-inducible human TDAG51 gene product (Q24291248) (← links)
- Placental overgrowth in mice lacking the imprinted gene Ipl (Q24530568) (← links)
- Characterization of conserved and nonconserved imprinted genes in swine (Q24647126) (← links)
- Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples (Q24681580) (← links)
- Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting (Q24684284) (← links)
- TDAG51 is not essential for Fas/CD95 regulation and apoptosis in vivo (Q24746223) (← links)
- The origin and evolution of genomic imprinting and viviparity in mammals (Q27007861) (← links)
- Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting (Q28138506) (← links)
- Phosphoinositide binding by the pleckstrin homology domains of Ipl and Tih1 (Q28206637) (← links)
- Genes affecting the cell cycle, growth, maintenance, and drug sensitivity are preferentially regulated by anti-HER2 antibody through phosphatidylinositol 3-kinase-AKT signaling (Q28289659) (← links)
- Fetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndrome (Q28505485) (← links)
- The imprinted Phlda2 gene regulates extraembryonic energy stores (Q28512597) (← links)
- Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1 (Q28589840) (← links)
- The imprinted Phlda2 gene modulates a major endocrine compartment of the placenta to regulate placental demands for maternal resources (Q28593841) (← links)
- The history of cancer epigenetics (Q29617273) (← links)
- Antisense transcripts with FANTOM2 clone set and their implications for gene regulation (Q31147226) (← links)
- Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7. (Q33285306) (← links)
- Transcriptomic profiling of bovine IVF embryos revealed candidate genes and pathways involved in early embryonic development (Q33523184) (← links)
- Genomic imprinting: implications for human disease (Q33541538) (← links)
- Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome (Q33575632) (← links)
- Phosphatidylinositol 3 kinase modulation of trophoblast cell differentiation (Q33692490) (← links)
- Genomic imprinting and chromatin insulation in Beckwith-Wiedemann syndrome (Q33721384) (← links)
- Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster (Q33774256) (← links)
- Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways (Q33875930) (← links)
- Developmental stage-specific imprinting of IPL in domestic pigs (Sus scrofa). (Q33889437) (← links)
- Characterisation of marsupial PHLDA2 reveals eutherian specific acquisition of imprinting (Q33997704) (← links)
- Isolating the role of elevated Phlda2 in asymmetric late fetal growth restriction in mice (Q34241144) (← links)
- Death the Fas way: regulation and pathophysiology of CD95 and its ligand (Q34241318) (← links)
- Regulation of T-cell death-associated gene 51 (TDAG51) expression in human T-cells. (Q34303375) (← links)
- Epigenetic regulation of placental endocrine lineages and complications of pregnancy (Q34734556) (← links)
- Genomic imprinting: could the chromatin structure be the driving force? (Q35037387) (← links)
- Chromosome-wide analysis of parental allele-specific chromatin and DNA methylation. (Q35077074) (← links)
- An extended domain of Kcnq1ot1 silencing revealed by an imprinted fluorescent reporter (Q35096694) (← links)
- Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region (Q35806688) (← links)
- High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes (Q35814612) (← links)
- Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight (Q35877833) (← links)
- Lentivirus-mediated PHLDA2 overexpression inhibits trophoblast proliferation, migration and invasion, and induces apoptosis (Q35943539) (← links)
- Two distinct mechanisms of silencing by the KvDMR1 imprinting control region (Q36392021) (← links)
- Epigenetic and phenotypic consequences of a truncation disrupting the imprinted domain on distal mouse chromosome 7. (Q36421376) (← links)
- The maternally expressed gene Tssc3 regulates the expression of MASH2 transcription factor in mouse trophoblast stem cells through the AKT-Sp1 signaling pathway (Q36466639) (← links)
- Expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 and the methylation patterns at the KvDMR1 and H19/IGF2 imprinting control regions is conserved between human and bovine (Q36499262) (← links)
- Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction (Q36648088) (← links)
- Structure and sequence of the human fast skeletal troponin T (TNNT3) gene: insight into the evolution of the gene and the origin of the developmentally regulated isoforms. (Q36748462) (← links)
- Relationship between placental expression of the imprinted PHLDA2 gene, intrauterine skeletal growth and childhood bone mass (Q36852705) (← links)
- Gain of imprinting at chromosome 11p15: A pathogenetic mechanism identified in human hepatocarcinomas (Q36976941) (← links)
- The placental imprintome and imprinted gene function in the trophoblast glycogen cell lineage (Q37284688) (← links)
- New Perspectives on Genomic Imprinting, an Essential and Multifaceted Mode of Epigenetic Control in the Developing and Adult Brain (Q37445958) (← links)
- Paternally expressed, imprinted insulin-like growth factor-2 in chorionic villi correlates significantly with birth weight (Q37484070) (← links)