Imprinting analysis of 10 genes and/or transcripts in a 1.5-Mb MEST-flanking region at human chromosome 7q32. (Q34298590)

1 August 2017

Imprinting analysis of 10 genes and/or transcripts in a 1.5-Mb MEST-flanking region at human chromosome 7q32. (English)

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1 August 2017

9

Hisanori Minakami

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1 August 2017

8

Hideto Yamada

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1 August 2017

Takahiro Yamada

1

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1 August 2017

Kohzoh Mitsuya

2

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1 August 2017

Tomohiko Kayashima

3

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1 August 2017

Kentaro Yamasaki

4

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1 August 2017

Tohru Ohta

5

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1 August 2017

Koh-ichiro Yoshiura

6

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1 August 2017

Naomichi Matsumoto

7

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1 August 2017

Mitsuo Oshimura

10

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1 August 2017

Norio Niikawa

11

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1 August 2017

Tatsuya Kishino

12

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1 August 2017

1 March 2004

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1 August 2017

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1 August 2017

83

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1 August 2017

402-412

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1 August 2017

3

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The sins of the fathers and mothers: genomic imprinting in mammalian development.

1 August 2017

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Human PEG1/MEST, an imprinted gene on chromosome 7

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

A catalogue of imprinted genes and parent-of-origin effects in humans and animals.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Construction of a physical and transcript map flanking the imprinted MEST/PEG1 region at 7q32

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

The novel gene, gamma2-COP (COPG2), in the 7q32 imprinted domain escapes genomic imprinting

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

The novel imprinted carboxypeptidase A4 gene ( CPA4) in the 7q32 imprinting domain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

The gene TSGA14, adjacent to the imprinted gene MEST, escapes genomic imprinting.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

An imprinted PEG1/MEST antisense expressed predominantly in human testis and in mature spermatozoa

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Genetic studies of autistic disorder and chromosome 7

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Assignment of growth factor receptor-bound protein 10 (GRB10) to human chromosome 7p11.2-p12

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Evidence against a major role of PEG1/MEST in Silver-Russell syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Evidence against GRB10 as the gene responsible for Silver-Russell syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Structure, expression, and chromosomal assignment of the human gene encoding nuclear respiratory factor 1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Prediction of the coding sequences of unidentified human genes. VI. The coding sequences of 80 new genes (KIAA0201-KIAA0280) deduced by analysis of cDNA clones from cell line KG-1 and brain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Identification and characterization of three members of the human metallocarboxypeptidase gene family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Carboxypeptidase A isoforms produced by distinct genes or alternative splicing in brain and other extrapancreatic tissues

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Construction of 700 human/mouse A9 monochromosomal hybrids and analysis of imprinted genes on human chromosome 6.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

A novel epigenetic control operating on Vme1+ locus leads to variegated monoallelic expression.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Characterization of the C3 YAC contig from proximal mouse chromosome 17 and analysis of allelic expression of genes flanking the imprinted Igf2r gene.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Bidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Chromatin modification and epigenetic reprogramming in mammalian development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

DNA demethylation reactivates a subset of imprinted genes in uniparental mouse embryonic fibroblasts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

Isoform-specific imprinting of the human PEG1/MEST gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.016

10.1016/J.YGENO.2003.08.016

7 January 2021

Identifiers

DOI

1 reference

1 August 2017

1 reference