Pages that link to "Q48806810"
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The following pages link to Timing of establishment of paternal methylation imprints in the mouse (Q48806810):
Displaying 50 items.
- Dazl functions in maintenance of pluripotency and genetic and epigenetic programs of differentiation in mouse primordial germ cells in vivo and in vitro (Q21143776) (← links)
- Genomic imprinting in mammals: emerging themes and established theories (Q21145256) (← links)
- Epigenetics and male reproduction: the consequences of paternal lifestyle on fertility, embryo development, and children lifetime health (Q26777239) (← links)
- Genomic imprinting effects on complex traits in domesticated animal species (Q26824384) (← links)
- Regulatory non-coding transcripts in spermatogenesis: shedding light on 'dark matter' (Q26853399) (← links)
- Paternal alcohol exposure reduces alcohol drinking and increases behavioral sensitivity to alcohol selectively in male offspring (Q27324436) (← links)
- Male Germ Cell Apoptosis and Epigenetic Histone Modification Induced by Tripterygium wilfordii Hook F (Q28478589) (← links)
- DNA methyltransferase expression in the mouse germ line during periods of de novo methylation (Q28510173) (← links)
- Meiosis arrest female 1 (MARF1) has nuage-like function in mammalian oocytes (Q28511020) (← links)
- CRL4 complex regulates mammalian oocyte survival and reprogramming by activation of TET proteins (Q28586529) (← links)
- A tripartite paternally methylated region within the Gpr1-Zdbf2 imprinted domain on mouse chromosome 1 identified by meDIP-on-chip (Q28592430) (← links)
- Dynamic association rules for gene expression data analysis (Q31005000) (← links)
- Loss of spermatogonia and wide-spread DNA methylation defects in newborn male mice deficient in DNMT3L. (Q33299280) (← links)
- Widespread epigenetic abnormalities suggest a broad DNA methylation erasure defect in abnormal human sperm (Q33309935) (← links)
- Association of ATRX with pericentric heterochromatin and the Y chromosome of neonatal mouse spermatogonia (Q33325809) (← links)
- Global mapping of DNA methylation in mouse promoters reveals epigenetic reprogramming of pluripotency genes (Q33347134) (← links)
- Effects of ooplasm manipulation on DNA methylation and growth of progeny in mice (Q33586272) (← links)
- H19 imprinting control region methylation requires an imprinted environment only in the male germ line. (Q33648826) (← links)
- CTCF-dependent chromatin bias constitutes transient epigenetic memory of the mother at the H19-Igf2 imprinting control region in prospermatogonia. (Q33760850) (← links)
- Forced expression of DNA methyltransferases during oocyte growth accelerates the establishment of methylation imprints but not functional genomic imprinting (Q33784510) (← links)
- Epigenetic reprogramming in the porcine germ line (Q33830098) (← links)
- Genome-wide prediction of imprinted murine genes (Q33841575) (← links)
- Mammalian genomic imprinting. (Q34026917) (← links)
- Critical Period of Nonpromoter DNA Methylation Acquisition during Prenatal Male Germ Cell Development (Q34031268) (← links)
- Alterations in the developing testis transcriptome following embryonic vinclozolin exposure (Q34150133) (← links)
- Dynamic changes in DNA modification states during late gestation male germ line development in the rat (Q34178891) (← links)
- Sequences sufficient for programming imprinted germline DNA methylation defined. (Q34189788) (← links)
- An unbiased assessment of the role of imprinted genes in an intergenerational model of developmental programming. (Q34236638) (← links)
- Imprinting methylation errors in ART. (Q34277727) (← links)
- Culture of oocytes and risk of imprinting defects. (Q34305206) (← links)
- Testicular germ cells can colonize sexually undifferentiated embryonic gonad and produce functional eggs in fish (Q34479508) (← links)
- Modifiers of epigenetic reprogramming show paternal effects in the mouse. (Q34621450) (← links)
- Epigenetic events in mammalian germ-cell development: reprogramming and beyond (Q34736397) (← links)
- Identification of the mouse paternally expressed imprinted gene Zdbf2 on chromosome 1 and its imprinted human homolog ZDBF2 on chromosome 2. (Q34939534) (← links)
- Transcription driven somatic DNA methylation within the imprinted Gnas cluster (Q35057896) (← links)
- Cytological studies of human meiosis: sex-specific differences in recombination originate at, or prior to, establishment of double-strand breaks (Q35078534) (← links)
- DNA methylation dynamics at imprinted genes during bovine pre-implantation embryo development. (Q35186705) (← links)
- Timing and sequence requirements defined for embryonic maintenance of imprinted DNA methylation at Rasgrf1. (Q35221412) (← links)
- Genomic imprinting in mammals: its life cycle, molecular mechanisms and reprogramming (Q35347999) (← links)
- Epigenetic modifications and self-renewal regulation of mouse germline stem cells (Q35348735) (← links)
- Genes and Conditions Controlling Mammalian Pre- and Post-implantation Embryo Development (Q35548107) (← links)
- Differential histone modifications mark mouse imprinting control regions during spermatogenesis. (Q35629621) (← links)
- Coordinate regulation of DNA methyltransferase expression during oogenesis (Q35813658) (← links)
- Global profiling of DNA methylation erasure in mouse primordial germ cells (Q35864711) (← links)
- Establishment of paternal allele-specific DNA methylation at the imprinted mouseGtl2locus (Q35985459) (← links)
- Tet-mediated imprinting erasure in H19 locus following reprogramming of spermatogonial stem cells to induced pluripotent stem cells. (Q36017968) (← links)
- Origins of extreme sexual dimorphism in genomic imprinting. (Q36436505) (← links)
- The H19 gene: regulation and function of a non-coding RNA. (Q36436572) (← links)
- Importance of the matriline for genomic imprinting, brain development and behaviour (Q36515797) (← links)
- Severe impairment of male reproductive organ development in a low SMN expressing mouse model of spinal muscular atrophy (Q36528254) (← links)