(Q51046179)

27 March 2018

title

Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies. (English)

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27 March 2018

author name string

Pàldi A

series ordinal

1

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27 March 2018

Gyapay G

series ordinal

2

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27 March 2018

Jami J

series ordinal

3

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27 March 2018

language of work or name

English

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publication date

1 September 1995

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27 March 2018

number of pages

6

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inferred from page(s)

published in

Current Biology

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27 March 2018

volume

5

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27 March 2018

page(s)

1030-1035

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27 March 2018

issue

9

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27 March 2018

A genetic linkage map of the human genome.

cites work

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Parental imprinting of autosomal mammalian genes

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Allele-specific replication timing of imprinted gene regions

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Functional imprinting and epigenetic modification of the human SNRPN gene

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Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome

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

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7 January 2021

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

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7 January 2021

Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting.

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

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Mosaic and polymorphic imprinting of the WT1 gene in humans.

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Functional Polymorphism in the Parental Imprinting of the Human IGF2R Gene

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Sex, maps, and imprinting

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7 January 2021

A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites

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A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene.

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Evolution of Insulin-Like Growth Factor II: Characterization of the Mouse IGF-II Gene and Identification of Two Pseudo-Exons

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An integrated physical map of 210 markers assigned to the short arm of human chromosome 11.

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Chromosomal mapping of the gene for the type II insulin-like growth factor receptor/cation-independent mannose 6-phosphate receptor in man and mouse

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7 January 2021

Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region

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7 January 2021

Meiosis-induced double-strand break sites determined by yeast chromatin structure

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7 January 2021

Maternal inheritance of atopic IgE responsiveness on chromosome 11q.

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7 January 2021

Association between atopy and variants of the beta subunit of the high-affinity immunoglobulin E receptor

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7 January 2021

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter

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7 January 2021

Parental imprinting of the Mas protooncogene in mouse.

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7 January 2021

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Identifiers

DOI

1 reference

27 March 2018

PubMed ID

8542279

1 reference

27 March 2018