Human PEG1/MEST, an imprinted gene on chromosome 7 (Q24322948)

GOA release 2020-03-11

mesoderm development

1 reference

GOA release 2020-03-11

author name string

S Kobayashi

1

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T Kohda

2

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N Miyoshi

3

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Y Kuroiwa

4

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K Aisaka

5

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O Tsutsumi

6

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T Kaneko-Ishino

7

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F Ishino

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

8

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language of work or name

English

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publication date

May 1997

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published in

Human Molecular Genetics

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volume

6

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issue

5

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page(s)

781-6

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cites work

1 reference

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Genomic imprinting and genetic disorders in man.

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

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

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

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

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

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A genetic linkage map of the mouse: current applications and future prospects

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Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7

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Genomic imprinting and chromosomal localization of the human MEST gene

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Mosaic and polymorphic imprinting of the WT1 gene in humans.

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The 1993-94 Généthon human genetic linkage map

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Experimental embryological analysis of genetic imprinting in mouse development

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Three-generation dominant transmission of the Silver-Russell syndrome

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Reevaluation of Russell-Silver syndrome.

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Severe Silver-Russell syndrome and translocation (17;20) (q25;q13)

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Second observation of Silver-Russel syndrome in a carrier of a reciprocal translocation with one breakpoint at site 17q25

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7 January 2021

The non-viability of uniparental mouse conceptuses correlates with the loss of the products of imprinted genes

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7 January 2021

Integration of physical, genetic and cytogenetic maps of human chromosome 7: isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers

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7 January 2021

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

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Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis

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Phenotypic and genetic analysis of the Silver-Russell syndrome

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X-linked short stature with skin pigmentation: evidence for heterogeneity of the Russell-Silver syndrome

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