Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies (Q59504115)

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22 December 2019

title

Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies (English)

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22 December 2019

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22 December 2019

Ugo Cavallari

7

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22 December 2019

Irene Cetin

9

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22 December 2019

Monica Miozzo

11

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22 December 2019

author name string

Francesca R Grati

1

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22 December 2019

Barbara Gentilin

3

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22 December 2019

Franca Rossella

4

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22 December 2019

Lisetta Ramoscelli

5

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22 December 2019

Patrizio Antonazzo

6

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22 December 2019

Gaetano Bulfamante

8

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22 December 2019

Giuseppe Simoni

10

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publication date

1 April 2004

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European Journal of Human Genetics

22 December 2019

published in

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22 December 2019

volume

12

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issue

4

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22 December 2019

page(s)

272-278

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201121

22 December 2019

exact match

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cites work

Gene action in the X-chromosome of the mouse (Mus musculus L.)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

A first-generation X-inactivation profile of the human X chromosome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

X-chromosome inactivation occurs at different times in different tissues of the post-implantation mouse embryo

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

The causes and consequences of random and non-random X chromosome inactivation in humans

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Paternal X-chromosome inactivation in human trophoblastic cells

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Heterogeneous X inactivation in trophoblastic cells of human full-term female placentas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

X-chromosome inactivation in the human trophoblast of early pregnancy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

X-inactivation patterns in human embryonic and extra-embryonic tissues.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Xist-deficient mice are defective in dosage compensation but not spermatogenesis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

X-chromosome inactivation: counting, choice and initiation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Parental imprinting on the mouse X chromosome: effects on the early development of X0, XXY and XXX embryos

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Maternally inherited X chromosome is not inactivated in mouse blastocysts due to parental imprinting

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Placental-fetal interrelationship in IUGR fetuses--a review.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Placental-specific IGF-II is a major modulator of placental and fetal growth.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

The role of imprinted genes in fetal growth

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Regulation of supply and demand for maternal nutrients in mammals by imprinted genes.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Esx1, a novel X chromosome-linked homeobox gene expressed in mouse extraembryonic tissues and male germ cells.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Esx1 is an X-chromosome-imprinted regulator of placental development and fetal growth

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

ESX1L, a novel X chromosome-linked human homeobox gene expressed in the placenta and testis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Fitting growth curves to head and abdomen measurements of the fetus: a multicentric study.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Diagnostic Value of Blood Sampling in Fetuses with Growth Retardation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Age- and tissue-specific variation of X chromosome inactivation ratios in normal women

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Molecular cytogenetic detection of confined gonadal mosaicism in a conceptus with trisomy 16 placental mosaicism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Divergent evolution in M6P/IGF2R imprinting from the Jurassic to the Quaternary

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201121

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201121

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14673477%20AND%20SRC:MED&resulttype=core&format=json

22 December 2019

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