(Q47638614)

4 February 2018

title

Analysis of imprinting in mice with uniparental duplication of proximal chromosomes 7 and 15 by use of a custom oligonucleotide microarray (English)

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4 February 2018

author

Jeff Longmate

2

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4 February 2018

author name string

Victoria L Buettner

1

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4 February 2018

Michael E Barish

3

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4 February 2018

Jeffrey R Mann

4

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4 February 2018

Judith Singer-Sam

5

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4 February 2018

publication date

1 March 2004

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4 February 2018

number of pages

11

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inferred from page(s)

published in

Mammalian Genome

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4 February 2018

volume

15

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4 February 2018

issue

3

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4 February 2018

page(s)

199-209

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4 February 2018

Genomic imprinting in the brain

cites work

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12 December 2020

Dissociation of IGF2 and H19 imprinting in human brain

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12 December 2020

Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse

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12 December 2020

The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

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12 December 2020

Analysis of parent-specific gene expression in early mouse embryos and embryonic stem cells using high-resolution two-dimensional electrophoresis of proteins.

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12 December 2020

Association between a GABRB3 polymorphism and autism.

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12 December 2020

GABAA receptor beta 3 subunit gene is possibly paternally imprinted in humans

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12 December 2020

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

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12 December 2020

Allele-specific expression and total expression levels of imprinted genes during early mouse development: implications for imprinting mechanisms

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12 December 2020

Mouse Peg9/Dlk1 and human PEG9/DLK1 are paternally expressed imprinted genes closely located to the maternally expressed imprinted genes: mouse Meg3/Gtl2 and human MEG3.

1 reference

12 December 2020

Microarray expression profiling of tissues from mice with uniparental duplications of chromosomes 7 and 11 to identify imprinted genes

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12 December 2020

The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse

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12 December 2020

Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype

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12 December 2020

Strain-dependent developmental relaxation of imprinting of an endogenous mouse gene, Kvlqt1.

1 reference

12 December 2020

Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse

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12 December 2020

Parental imprinting of the Mas protooncogene in mouse

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12 December 2020

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region

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12 December 2020

Tissue- and developmental stage-specific imprinting of the mouse proinsulin gene, Ins2.

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12 December 2020

Mouse models of Angelman syndrome, a neurodevelopmental disorder, display different brain regional GABA(A) receptor alterations

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12 December 2020

Distinct phenotypes distinguish the molecular classes of Angelman syndrome

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12 December 2020

Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization

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12 December 2020

Temporal and spatial regulation of H19 imprinting in normal and uniparental mouse embryos.

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12 December 2020

The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region

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12 December 2020

Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction

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12 December 2020

Genomic imprinting of Mash2, a mouse gene required for trophoblast development

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12 December 2020

Imprinted methylation and its effect on expression of the mouse Zfp127 gene

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12 December 2020

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region

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12 December 2020

A new imprinted gene cloned by a methylation-sensitive genome scanning method

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12 December 2020

Cloning the differences between two complex genomes

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12 December 2020

Imprinting of mouse Kvlqt1 is developmentally regulated.

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12 December 2020

A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression

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12 December 2020

The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region

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12 December 2020

Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.

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12 December 2020

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

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12 December 2020

The transition from oocyte-coded to embryo-coded glucose phosphate isomerase in the early mouse embryo

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12 December 2020

Dosage-dependent gene regulation in multicellular eukaryotes: implications for dosage compensation, aneuploid syndromes, and quantitative traits

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12 December 2020

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

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12 December 2020

Genome imprinting phenomena on mouse chromosome 7

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12 December 2020

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

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12 December 2020

Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region

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12 December 2020

Complementation studies with mouse translocations

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12 December 2020

10.1007/S00335-003-2322-8

Identifiers

DOI

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4 February 2018

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4 February 2018