Mit1/Lb9 and Copg2, new members of mouse imprinted genes closely linked to Peg1/Mest(1). (Q47864302)

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6 November 2019

title

Mit1/Lb9 and Copg2, new members of mouse imprinted genes closely linked to Peg1/Mest(1) (English)

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6 November 2019

3

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6 November 2019

author name string

Y J Lee

1

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6 November 2019

C W Park

2

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6 November 2019

J Park

4

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6 November 2019

J Lee

5

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6 November 2019

J H Yun

6

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6 November 2019

B Hyun

7

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6 November 2019

J H Chung

8

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6 November 2019

language of work or name

English

0 references

publication date

1 April 2000

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6 November 2019

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6 November 2019

volume

472

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6 November 2019

page(s)

230-234

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6 November 2019

issue

2-3

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Imprinting and the initiation of gene silencing in the germ line.

6 November 2019

cites work

1 reference

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

21 January 2018

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

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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Peg5/Neuronatin is an imprinted gene located on sub-distal chromosome 2 in the mouse.

21 January 2018

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Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene

21 January 2018

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Screening for imprinted genes by allelic message display: identification of a paternally expressed gene impact on mouse chromosome 18

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

21 January 2018

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Human PEG1/MEST, an imprinted gene on chromosome 7

21 January 2018

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The human homolog of a mouse-imprinted gene, Peg3, maps to a zinc finger gene-rich region of human chromosome 19q13.4

21 January 2018

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Cloning of human neuronatin gene and its localization to chromosome-20q 11.2-12: the deduced protein is a novel "proteolipid'

21 January 2018

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

21 January 2018

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Disruption of imprinting caused by deletion of the H19 gene region in mice

21 January 2018

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Imprinted expression of the Igf2r gene depends on an intronic CpG island.

21 January 2018

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Identification of a novel paternally expressed gene in the Prader-Willi syndrome region

21 January 2018

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LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

21 January 2018

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

21 January 2018

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Maternal uniparental disomy 7 in Silver-Russell syndrome

21 January 2018

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Paternally inherited deletion of CSH1 in a patient with Silver-Russell syndrome

21 January 2018

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Identification of the C-->T polymorphism in the +93 position of the apo(a) gene by mismatch PCR-mediated site-directed mutagenesis and restriction enzyme digestion

21 January 2018

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

7 January 2021

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