Genetic and epigenetic dysregulation of imprinted genes in the brain (Q37961799)

26 August 2017

title

Genetic and epigenetic dysregulation of imprinted genes in the brain (English)

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26 August 2017

Kristin D Kernohan

1

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26 August 2017

Nathalie G Bérubé

series ordinal

2

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26 August 2017

language of work or name

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1 December 2010

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26 August 2017

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26 August 2017

volume

2

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26 August 2017

issue

6

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26 August 2017

page(s)

743-763

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An ICE pattern crystallizes

26 August 2017

cites work

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A potential imprint control element: identification of a conserved 42 bp sequence upstream of H19.

21 January 2018

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A paternal-specific methylation imprint marks the alleles of the mouse H19 gene

21 January 2018

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A 5′ 2-Kilobase-Pair Region of the Imprinted Mouse H19 Gene Exhibits Exclusive Paternal Methylation throughout Development

21 January 2018

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Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2.

21 January 2018

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Parental-origin-specific epigenetic modification of the mouse H19 gene

21 January 2018

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Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.

21 January 2018

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Genomic imprinting recapitulated in the human beta-globin locus

21 January 2018

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The H19 differentially methylated region marks the parental origin of a heterologous locus without gametic DNA methylation

21 January 2018

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H19 imprinting control region methylation requires an imprinted environment only in the male germ line.

21 January 2018

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Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene

21 January 2018

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Role for DNA methylation in genomic imprinting

21 January 2018

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Modulation of Igf2 genomic imprinting in mice induced by 5-azacytidine, an inhibitor of DNA methylation

21 January 2018

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Allele-specific histone lysine methylation marks regulatory regions at imprinted mouse genes

21 January 2018

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Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes.

21 January 2018

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Active and repressive chromatin are interspersed without spreading in an imprinted gene cluster in the mammalian genome.

21 January 2018

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The transcriptional status but not the imprinting control region determines allele-specific histone modifications at the imprinted H19 locus

21 January 2018

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Differential histone modifications mark mouse imprinting control regions during spermatogenesis.

21 January 2018

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Genome-wide maps of chromatin state in pluripotent and lineage-committed cells

21 January 2018

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Regulated expression of two sets of paternally imprinted genes is necessary for mouse parthenogenetic development to term

21 January 2018

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Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation.

21 January 2018

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Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting

21 January 2018

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Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1

21 January 2018

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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

21 January 2018

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A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

21 January 2018

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A developmental window of opportunity for imprinted gene silencing mediated by DNA methylation and the Kcnq1ot1 noncoding RNA

21 January 2018

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Kcnq1ot1 antisense noncoding RNA mediates lineage-specific transcriptional silencing through chromatin-level regulation

21 January 2018

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G9a histone methyltransferase contributes to imprinting in the mouse placenta

21 January 2018

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Parental origin-specific expression of Mash2 is established at the time of implantation with its imprinting mechanism highly resistant to genome-wide demethylation.

21 January 2018

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Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster

21 January 2018

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Specific expression of long noncoding RNAs in the mouse brain

21 January 2018

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The function of non-coding RNAs in genomic imprinting

21 January 2018

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Non-coding RNAs in imprinted gene clusters

21 January 2018

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The imprinted Air ncRNA is an atypical RNAPII transcript that evades splicing and escapes nuclear export

21 January 2018

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The non-coding Air RNA is required for silencing autosomal imprinted genes

21 January 2018

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Imprinted silencing of Slc22a2 and Slc22a3 does not need transcriptional overlap between Igf2r and Air.

21 January 2018

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The Air noncoding RNA epigenetically silences transcription by targeting G9a to chromatin

21 January 2018

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Capturing chromosome conformation

21 January 2018

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Circular chromosome conformation capture (4C) uncovers extensive networks of epigenetically regulated intra- and interchromosomal interactions.

21 January 2018

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Chromosome Conformation Capture Carbon Copy (5C): a massively parallel solution for mapping interactions between genomic elements

21 January 2018

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ChIP-based methods for the identification of long-range chromatin interactions

21 January 2018

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Nuclear organization of active and inactive chromatin domains uncovered by chromosome conformation capture-on-chip (4C).

21 January 2018

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Comprehensive mapping of long-range interactions reveals folding principles of the human genome

21 January 2018

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Loss of IGF2 imprinting is associated with abrogation of long-range intrachromosomal interactions in human cancer cells

21 January 2018

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Cohesin is required for higher-order chromatin conformation at the imprinted IGF2-H19 locus

21 January 2018

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A complex deoxyribonucleic acid looping configuration associated with the silencing of the maternal Igf2 allele

21 January 2018

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Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops

21 January 2018

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CTCF regulates allelic expression of Igf2 by orchestrating a promoter-polycomb repressive complex 2 intrachromosomal loop

21 January 2018

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CTCF binding and higher order chromatin structure of the H19 locus are maintained in mitotic chromatin

21 January 2018

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CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2

21 January 2018

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Analysis of the H19ICR insulator

21 January 2018

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Integrative analysis of the cancer transcriptome

21 January 2018

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ATRX partners with cohesin and MeCP2 and contributes to developmental silencing of imprinted genes in the brain

21 January 2018

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CTCF is the master organizer of domain-wide allele-specific chromatin at the H19/Igf2 imprinted region

21 January 2018

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CTCF-dependent chromatin insulator is linked to epigenetic remodeling

21 January 2018

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Cohesins functionally associate with CTCF on mammalian chromosome arms

21 January 2018

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Cohesin mediates transcriptional insulation by CCCTC-binding factor

21 January 2018

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A direct link between sister chromatid cohesion and chromosome condensation revealed through the analysis of MCD1 in S. cerevisiae

21 January 2018

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Identification of Xenopus SMC protein complexes required for sister chromatid cohesion

21 January 2018

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Cohesins: chromosomal proteins that prevent premature separation of sister chromatids

21 January 2018

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Yeast cohesin complex requires a conserved protein, Eco1p(Ctf7), to establish cohesion between sister chromatids during DNA replication

21 January 2018

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Condensin and cohesin display different arm conformations with characteristic hinge angles

21 January 2018

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Chromosomal cohesin forms a ring

21 January 2018

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Completion of mouse embryogenesis requires both the maternal and paternal genomes

21 January 2018

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Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

21 January 2018

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The importance of imprinting in the human placenta.

21 January 2018

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Epigenetics in the placenta

21 January 2018

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Distribution of parthenogenetic cells in the mouse brain and their influence on brain development and behavior.

21 January 2018

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Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: implications for genetic imprinting

21 January 2018

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Genomic imprinting and the differential roles of parental genomes in brain development

21 January 2018

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Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein.

21 January 2018

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BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources

21 January 2018

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Imprinted gene expression in the brain

21 January 2018

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Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest

21 January 2018

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Regulation of maternal behavior and offspring growth by paternally expressed Peg3.

21 January 2018

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Expression patterns of the novel imprinted genes Nap1l5 and Peg13 and their non-imprinted host genes in the adult mouse brain.

21 January 2018

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Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain

21 January 2018

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Genome-wide atlas of gene expression in the adult mouse brain

21 January 2018

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Parental imprinting of the mouse H19 gene

21 January 2018

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Zim1, a maternally expressed mouse Kruppel-type zinc-finger gene located in proximal chromosome 7.

21 January 2018

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[The expression analysis of Grb10 during mouse embryonic development].

21 January 2018

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The spatial and temporal expression pattern of Nesp and its antisense Nespas, in mid-gestation mouse embryos

21 January 2018

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A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2

21 January 2018

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Expression pattern of the maternally imprinted gene Gtl2 in the forebrain during embryonic development and adulthood.

21 January 2018

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A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting.

21 January 2018

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Grb10 interacts with Bim L and inhibits apoptosis

21 January 2018

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Calcr, a brain-specific imprinted mouse calcitonin receptor gene in the imprinted cluster of the proximal region of chromosome 6

21 January 2018

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The Angelman syndrome candidate gene, UBE3AIE6-AP, is imprinted in brain

21 January 2018

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Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain

21 January 2018

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Parental imprinting of the mouse insulin-like growth factor II gene.

21 January 2018

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The mouse Murr1 gene is imprinted in the adult brain, presumably due to transcriptional interference by the antisense-oriented U2af1-rs1 gene.

21 January 2018

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Sex-specific parent-of-origin allelic expression in the mouse brain

21 January 2018

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High-resolution analysis of parent-of-origin allelic expression in the mouse brain

21 January 2018

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Activation of p53 by MEG3 non-coding RNA

21 January 2018

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Interneuron migration from basal forebrain to neocortex: dependence on Dlx genes

21 January 2018

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Evidence for uniparental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer

21 January 2018

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The GABAA receptor beta 3 subunit gene: characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7

21 January 2018

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GABAA receptor beta3 subunit gene-deficient heterozygous mice show parent-of-origin and gender-related differences in beta3 subunit levels, EEG, and behavior

21 January 2018

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21 January 2018

Chromosome territories

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Nuclear neighborhoods and gene expression

21 January 2018

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Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size.

21 January 2018

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DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

21 January 2018

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DLX5 expression is monoallelic and Dlx5 is up-regulated in the Mecp2-null frontal cortex

21 January 2018

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Chromosome loops, insulators, and histone methylation: new insights into regulation of imprinting in clusters.

21 January 2018

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Zac1 regulates an imprinted gene network critically involved in the control of embryonic growth

21 January 2018

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An imprinted gene network that controls mammalian somatic growth is down-regulated during postnatal growth deceleration in multiple organs

21 January 2018

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Temporal and spatial expression of a growth-regulated network of imprinted genes in growth plate.

21 January 2018

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CTCF mediates interchromosomal colocalization between Igf2/H19 and Wsb1/Nf1.

21 January 2018

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Nonallelic transvection of multiple imprinted loci is organized by the H19 imprinting control region during germline development

21 January 2018

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H19 acts as a trans regulator of the imprinted gene network controlling growth in mice

21 January 2018

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The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria

21 January 2018

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Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome

21 January 2018

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The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

21 January 2018

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Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

21 January 2018

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A mouse model for Prader-Willi syndrome imprinting-centre mutations

21 January 2018

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Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth

21 January 2018

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Developmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdin

21 January 2018

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Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons.

21 January 2018

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Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival

21 January 2018

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Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death

21 January 2018

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Necdin and TrkA contribute to modulation by p75NTR of resistance to oxidant stress.

21 January 2018

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Necdin downregulates CDC2 expression to attenuate neuronal apoptosis.

21 January 2018

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Necdin promotes GABAergic neuron differentiation in cooperation with Dlx homeodomain proteins.

21 January 2018

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Prediction of preadipocyte differentiation by gene expression reveals role of insulin receptor substrates and necdin

21 January 2018

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Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation

21 January 2018

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Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster

21 January 2018

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A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism

21 January 2018

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Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain

21 January 2018

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Small nucleolar RNAs direct site-specific synthesis of pseudouridine in ribosomal RNA

21 January 2018

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UBE3A/E6-AP mutations cause Angelman syndrome

21 January 2018

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De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome

21 January 2018

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The "happy puppet" syndrome

21 January 2018

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Distinct phenotypes distinguish the molecular classes of Angelman syndrome

21 January 2018

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Angelman syndrome 2005: updated consensus for diagnostic criteria.

21 January 2018

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Angelman syndrome: current understanding and research prospects.

21 January 2018

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Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons

21 January 2018

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The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology

21 January 2018

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Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a

21 January 2018

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Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome

21 January 2018

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Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn.

21 January 2018

1 reference

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

21 January 2018

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Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

21 January 2018

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MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression

21 January 2018

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The overlapping spectrum of rett and angelman syndromes: a clinical review

21 January 2018

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Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

21 January 2018

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Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice

21 January 2018

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Ube3a is required for experience-dependent maturation of the neocortex.

21 January 2018

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Genomic imprinting of experience-dependent cortical plasticity by the ubiquitin ligase gene Ube3a

21 January 2018

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Identification of HHR23A as a substrate for E6-associated protein-mediated ubiquitination.

21 January 2018

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Expression of the Rho-GEF Pbl/ECT2 is regulated by the UBE3A E3 ubiquitin ligase

21 January 2018

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E6AP promotes the degradation of the PML tumor suppressor.

21 January 2018

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The Angelman Syndrome protein Ube3A regulates synapse development by ubiquitinating arc.

21 January 2018

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Dosage-sensitive X-linked locus influences the development of amygdala and orbitofrontal cortex, and fear recognition in humans

21 January 2018

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Turner's syndrome in adulthood

21 January 2018

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The Turner syndrome: cognitive deficits, affective discrimination, and behavior problems

21 January 2018

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Use of estrogen in young girls with Turner syndrome: effects on memory.

21 January 2018

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Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

21 January 2018

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Distinctive patterns of memory function in subgroups of females with Turner syndrome: evidence for imprinted loci on the X-chromosome affecting neurodevelopment.

21 January 2018

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Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome

21 January 2018

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Amygdala and hippocampal volumes in Turner syndrome: a high-resolution MRI study of X-monosomy

21 January 2018

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Effects of X-monosomy and X-linked imprinting on superior temporal gyrus morphology in Turner syndrome

21 January 2018

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The 39,XO mouse as a model for the neurobiology of Turner syndrome and sex-biased neuropsychiatric disorders.

21 January 2018

1 reference

Identification of a cluster of X-linked imprinted genes in mice

21 January 2018

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Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice

21 January 2018

1 reference

A new gene family (FAM9) of low-copy repeats in Xp22.3 expressed exclusively in testis: implications for recombinations in this region

21 January 2018

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Cux1 and Cux2 regulate dendritic branching, spine morphology, and synapses of the upper layer neurons of the cortex

21 January 2018

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Xp deletions associated with autism in three females

21 January 2018

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Schizophrenia susceptibility gene locus at Xp22.3.

21 January 2018

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Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations

21 January 2018

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Neuropathology of Rett syndrome

21 January 2018

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

21 January 2018

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Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

21 January 2018

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Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA

21 January 2018

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MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions

21 January 2018

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Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.

21 January 2018

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Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

21 January 2018

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Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets

21 January 2018

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Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome

21 January 2018

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Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain

21 January 2018

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Mecp2-null mice provide new neuronal targets for Rett syndrome.

21 January 2018

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Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.

21 January 2018

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Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state.

21 January 2018

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Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

21 January 2018

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A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

21 January 2018

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Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

21 January 2018

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Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice

21 January 2018

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Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.

21 January 2018

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Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

21 January 2018

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Reversal of neurological defects in a mouse model of Rett syndrome

21 January 2018

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The odyssey of MeCP2 and parental imprinting

21 January 2018

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Ube3a expression is not altered in Mecp2 mutant mice

21 January 2018

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Chicken MAR-Binding Protein ARBP Is Homologous to Rat Methyl-CpG-Binding Protein MeCP2

21 January 2018

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MeCP2-dependent repression of an imprinted miR-184 released by depolarization

21 January 2018

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The methyl-CpG-binding protein MeCP2 links DNA methylation to histone methylation

21 January 2018

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Methylation-dependent silencing at the H19 imprinting control region by MeCP2

21 January 2018

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Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation

21 January 2018

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Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation

21 January 2018

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ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome

21 January 2018

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Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53.

21 January 2018

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Mutation in the 5' alternatively spliced region of the XNP/ATR-X gene causes Chudley-Lowry syndrome

21 January 2018

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Loss of ATRX leads to chromosome cohesion and congression defects

21 January 2018

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ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes

21 January 2018

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Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes

21 January 2018

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Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association

21 January 2018

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Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues

21 January 2018

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The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome

21 January 2018

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Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD.

21 January 2018

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Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD.

21 January 2018

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Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD.

21 January 2018

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The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder.

21 January 2018

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Transmission disequilibrium studies of the serotonin 5-HT2A receptor gene (HTR2A) in autism

21 January 2018

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Linkage and association of the glutamate receptor 6 gene with autism

21 January 2018

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Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder.

21 January 2018

1 reference

Dopamine D4 receptor and tyrosine hydroxylase genes in bipolar disorder: evidence for a role of DRD4.

21 January 2018

1 reference

Family-based association study of the serotonin-2A receptor gene (5-HT2A) and bipolar disorder

21 January 2018

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Maternal transmission disequilibrium of the glutamate receptor GRIK2 in schizophrenia.

21 January 2018

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Analysis of the linkage of the Taq1A and Taq1B loci of the dopamine D2 receptor gene with schizophrenia in patients and their siblings.

21 January 2018

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Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader–Willi syndromes

21 January 2018

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The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice

21 January 2018

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Imprinting in Angelman and Prader-Willi syndromes

21 January 2018

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Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

21 January 2018

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Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome

21 January 2018

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The imprinted gene Magel2 regulates normal circadian output.

21 January 2018

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Loss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice

21 January 2018

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SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice

21 January 2018

1 reference

Ear and hearing problems in 44 middle-aged women with Turner's syndrome

21 January 2018

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Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.

21 January 2018

1 reference

X-chromosome effects on female brain: a magnetic resonance imaging study of Turner's syndrome

21 January 2018

1 reference

Inability of mouse blastomere nuclei transferred to enucleated zygotes to support development in vitro

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.2217/EPI.10.61

1 reference

release_yfkidupz4nbvjbj4p2i7zqcjre

26 August 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/yfkidupz4nbvjbj4p2i7zqcjre

mapped directly with Wikidata item

24 November 2022

based on heuristic

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