Pages that link to "Q29949753"
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The following pages link to Anne Ferguson-Smith (Q29949753):
Displayed 50 items.
- Azim Surani (Q793786) (← links)
- Francis H. Ruddle (Q1441522) (← links)
- Malcolm Ferguson-Smith (Q15436161) (← links)
- A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints (Q24322379) (← links)
- Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignancies (Q24562340) (← links)
- Cognate homeo-box loci mapped on homologous human and mouse chromosomes (Q24628673) (← links)
- Novel Primate Model of Serotonin Transporter Genetic Polymorphisms Associated with Gene Expression, Anxiety and Sensitivity to Antidepressants (Q27310483) (← links)
- Gene dosage effects of the imprinted delta-like homologue 1 (dlk1/pref1) in development: implications for the evolution of imprinting (Q27312725) (← links)
- Considerations when investigating lncRNA function in vivo. (Q27691450) (← links)
- Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region (Q28202378) (← links)
- High-frequency generation of viable mice from engineered bi-maternal embryos (Q28241220) (← links)
- Isolation, chromosomal localization, and nucleotide sequence of the human HOX 1.4 homeobox (Q28257798) (← links)
- The Air noncoding RNA epigenetically silences transcription by targeting G9a to chromatin (Q28506981) (← links)
- L3mbtl, the mouse orthologue of the imprinted L3MBTL, displays a complex pattern of alternative splicing and escapes genomic imprinting (Q28589217) (← links)
- Mutation in folate metabolism causes epigenetic instability and transgenerational effects on development (Q28589368) (← links)
- Non-CG DNA methylation is a biomarker for assessing endodermal differentiation capacity in pluripotent stem cells (Q28601391) (← links)
- Relationship between DNA methylation, histone H4 acetylation and gene expression in the mouse imprinted Igf2-H19 domain. (Q31864191) (← links)
- Parental origin effects in human trisomy for chromosome 14q: implications for genomic imprinting. (Q33681378) (← links)
- Mammalian genomic imprinting. (Q34026917) (← links)
- Placental-specific IGF-II is a major modulator of placental and fetal growth. (Q34135795) (← links)
- Genomic imprinting and cancer; new paradigms in the genetics of neoplasia. (Q34232354) (← links)
- An unbiased assessment of the role of imprinted genes in an intergenerational model of developmental programming. (Q34236638) (← links)
- Epigenetic control of the genome-lessons from genomic imprinting (Q34347672) (← links)
- Distinct fibroblast lineages determine dermal architecture in skin development and repair. (Q34391786) (← links)
- Genomic imprinting variations in the mouse type 3 deiodinase gene between tissues and brain regions. (Q34422507) (← links)
- Silencing of miR-370 in human cholangiocarcinoma by allelic loss and interleukin-6 induced maternal to paternal epigenotype switch (Q34460281) (← links)
- DLK1/PREF1 regulates nutrient metabolism and protects from steatosis. (Q34526596) (← links)
- Comparative developmental anatomy of the murine and human definitive placentae. (Q34546263) (← links)
- DNMT1 and AIM1 Imprinting in human placenta revealed through a genome-wide screen for allele-specific DNA methylation. (Q35008254) (← links)
- Genomic imprinting--insights from studies in mice. (Q35043699) (← links)
- Regulation of supply and demand for maternal nutrients in mammals by imprinted genes. (Q35058363) (← links)
- Parent-of-origin effects implicate epigenetic regulation of experimental autoimmune encephalomyelitis and identify imprinted Dlk1 as a novel risk gene. (Q35133737) (← links)
- Nonallelic transcriptional roles of CTCF and cohesins at imprinted loci. (Q35139414) (← links)
- Roles for genomic imprinting and the zygotic genome in placental development. (Q35267816) (← links)
- In utero effects. In utero undernourishment perturbs the adult sperm methylome and intergenerational metabolism (Q35502732) (← links)
- Germline and somatic imprinting in the nonhuman primate highlights species differences in oocyte methylation. (Q35561940) (← links)
- CRISPR-Cas9-Mediated Genetic Screening in Mice with Haploid Embryonic Stem Cells Carrying a Guide RNA Library. (Q35689038) (← links)
- X inactivation: pre- or post-fertilisation turn-off? (Q35745790) (← links)
- Regulation of gene activity and repression: a consideration of unifying themes. (Q35749941) (← links)
- Allele-specific binding of ZFP57 in the epigenetic regulation of imprinted and non-imprinted monoallelic expression (Q35819244) (← links)
- Oxidative stress and the induction of cyclooxygenase enzymes and apoptosis in the murine placenta. (Q35849259) (← links)
- Imprinted gene dosage is critical for the transition to independent life. (Q35859500) (← links)
- A trans-homologue interaction between reciprocally imprinted miR-127 and Rtl1 regulates placenta development (Q35878122) (← links)
- Imprinted small RNA genes. (Q35954758) (← links)
- Imprinted X inactivation and reprogramming in the preimplantation mouse embryo. (Q36088945) (← links)
- Trim28 Haploinsufficiency Triggers Bi-stable Epigenetic Obesity. (Q36526377) (← links)
- Dlk1 is a negative regulator of emerging hematopoietic stem and progenitor cells. (Q36579049) (← links)
- Mechanisms regulating imprinted genes in clusters. (Q36805477) (← links)
- Evidence for transcriptional activity in the syncytiotrophoblast of the human placenta. (Q37015377) (← links)
- Intergenerational transmission of glucose intolerance and obesity by in utero undernutrition in mice. (Q37066931) (← links)