Relevance of genomic imprinting in intrauterine human growth expression of CDKN1C, H19, IGF2, KCNQ1 and PHLDA2 imprinted genes (Q34226354)

31 July 2017

Relevance of genomic imprinting in intrauterine human growth expression of CDKN1C, H19, IGF2, KCNQ1 and PHLDA2 imprinted genes (English)

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31 July 2017

Sofia Dória

5

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Filipa Carvalho

object named as

Filipa Carvalho

3

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author name string

Amilcar Cordeiro

1

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31 July 2017

Ana Paula Neto

2

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31 July 2017

Carla Ramalho

4

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31 July 2017

2 July 2014

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Journal of Assisted Reproduction and Genetics

31 July 2017

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31 July 2017

31

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31 July 2017

10

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31 July 2017

1361-1368

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https://scigraph.springernature.com/pub.10.1007/s10815-014-0278-0

31 July 2017

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cites work

Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171407

IGF2 DNA methylation is a modulator of newborn's fetal growth and development

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171407

The role of imprinted genes in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171407

Gain of function in CDKN1C

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171407

Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171407

The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171407

The role of imprinted genes in fetal growth abnormalities

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171407

Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171407

Mechanisms regulating imprinted genes in clusters.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171407

Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171407

Placental-specific insulin-like growth factor 2 (Igf2) regulates the diffusional exchange characteristics of the mouse placenta

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171407

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171407

Causes of intrauterine growth restriction.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171407

5 July 2018

Resourceful imprinting.

1 reference

https://api.crossref.org/works/10.1007%2FS10815-014-0278-0

Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10815-014-0278-0

Unbalanced placental expression of imprinted genes in human intrauterine growth restriction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10815-014-0278-0

Gene expression pattern of IGF2, PHLDA2, PEG10 and CDKN1C imprinted genes in spontaneous miscarriages or fetal deaths.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10815-014-0278-0

Bacterial infection promotes DNA hypermethylation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10815-014-0278-0

The two-domain hypothesis in Beckwith–Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10815-014-0278-0

Fetal growth retardation: associated malformations and chromosomal abnormalities

21 January 2018

1 reference

12 December 2020

Placental IGF2 Expression in Normal and Intrauterine Growth Restricted (IUGR) Pregnancies

1 reference

12 December 2020

MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment

1 reference

12 December 2020

Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci

1 reference

12 December 2020

Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues

1 reference

12 December 2020

10.1007/S10815-014-0278-0

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DOI

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31 July 2017

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31 July 2017

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