Role of imprinting in abnormal human development (Q41685042)

7 October 2017

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title

Role of imprinting in abnormal human development (English)

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7 October 2017

Mutter GL

1

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7 October 2017

language of work or name

English

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publication date

1 December 1997

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7 October 2017

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7 October 2017

volume

396

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7 October 2017

issue

1-2

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7 October 2017

page(s)

141-147

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Role of paternal and maternal genomes in mouse development

7 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Genomic imprinting in mammalian development: a parental tug-of-war

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

The essentials of DNA methylation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Parental imprinting of the mouse H19 gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

The product of the H19 gene may function as an RNA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Monoallelic expression of the human H19 gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Parental-origin-specific epigenetic modification of the mouse H19 gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Functional imprinting and epigenetic modification of the human SNRPN gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Parental imprinting of the Mas protooncogene in mouse

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Mosaic and polymorphic imprinting of the WT1 gene in humans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Ectopic expression of the H19 gene in mice causes prenatal lethality

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Influence of parental chromosomes on spatial specificity in androgenetic ↔ parthenogenetic chimaeras in the mouse

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Ovarian teratomas in mice are derived from oocytes that have completed the first meiotic division

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

The development of teratomas from parthenogenetically activated ovarian mouse eggs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Totipotency and normal differentiation of single teratocarcinoma cells cloned by injection into blastocysts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Teratocarcinomas and mammalian embryogenesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Epidemiology of gestational trophoblastic disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Androgenetic origin of hydatidiform mole

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Genetic studies on hydatidiform moles II. The origin of complete moles

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Application of gene amplification by polymerase chain reaction to genetic analysis of molar mitochondrial DNA: The detection of anuclear empty ovum as the cause of complete mole

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Complete moles have paternal chromosomes but maternal mitochondrial DNA.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

A prospective genetic study of complete and partial hydatidiform moles

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Dispermic origin of XY hydatidiform moles

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Frequency of heterozygous complete hydatidiform moles, estimated by locus-specific minisatellite and Y chromosome-specific probes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Dads and disomy and disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Placentomegaly with massive hydrops of placental stem villi, diploid DNA content, and fetal omphaloceles: Possible association with Beckwith-Wiedemann syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Molecular biology of Beckwith-Wiedemann syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Wiedemann-Beckwith syndrome, imprinting, IGF2, and H19: implications for hemihyperplasia, associated neoplasms, and overgrowth.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Uniparental disomy in congenital disorders: a prospective study.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

NICHD conference. Robertsonian translocations: clues to imprinting

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Current topic: confined placental mosaicism and intrauterine fetal development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Confined placental mosaicism and stillbirth

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Spontaneous abortion and confined chromosomal mosaicism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

A variety of genetic mechanisms are associated with the Prader-Willi syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Relaxation of imprinted genes in human cancer.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Loss of imprinting in choriocarcinoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Insulin-like growth factor II in uterine smooth-muscle tumors: maintenance of genomic imprinting in leiomyomata and loss of imprinting in leiomyosarcomata.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

Sex chromosome composition of complete hydatidiform moles: relationship to metastasis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2897%2900180-2

10.1016/S0027-5107(97)00180-2

7 January 2021

Identifiers

DOI

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release_xqcya57k5natdezz6xsxyte5um

7 October 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/xqcya57k5natdezz6xsxyte5um

mapped directly with Wikidata item

24 November 2022

based on heuristic

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