A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects (Q34979568)

5 August 2017

title

A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects (English)

1 reference

5 August 2017

3

Shaohai Fang

1 reference

5 August 2017

Fei Long

1

1 reference

5 August 2017

Xike Wang

2

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5 August 2017

Yuejuan Xu

4

1 reference

5 August 2017

Kun Sun

5

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5 August 2017

Sun Chen

6

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5 August 2017

Rang Xu

7

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5 August 2017

language of work or name

English

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publication date

29 August 2013

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5 August 2017

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5 August 2017

volume

8

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5 August 2017

issue

8

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5 August 2017

page(s)

e72515

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Creative Commons Attribution 4.0 International

5 August 2017

copyright license

start time

29 August 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Lipid phosphatases identified by screening a mouse phosphatase shRNA library regulate T-cell differentiation and protein kinase B AKT signaling.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Fetal Cardiac Screening and Variation in Prenatal Detection Rates of Congenital Heart Disease: Why Bother With Screening at all?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Human gene copy number spectra analysis in congenital heart malformations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Integrative analysis of array-comparative genomic hybridisation and matched gene expression profiling data reveals novel genes with prognostic significance in oesophageal adenocarcinoma

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Geometric Control of Cardiomyogenic Induction in Human Pluripotent Stem Cells

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Genotype-phenotype correlations in a new case of 8p23.1 deletion and review of the literature

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Endogenous Wnt/beta-catenin signaling is required for cardiac differentiation in human embryonic stem cells

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Genomic profile of copy number variants on the short arm of human chromosome 8.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Haplotyping and copy number estimation of the highly polymorphic human beta-defensin locus on 8p23 by 454 amplicon sequencing

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

The molecular genetics of congenital heart disease: a review of recent developments

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

SoxF genes: Key players in the development of the cardio-vascular system

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Copy number variation of beta-defensins and relevance to disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Lineage specification of Flk-1 progenitors is associated with divergent Sox7 expression in cardiopoiesis.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Allelic recombination between distinct genomic locations generates copy number diversity in human beta-defensins.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Defensins and the dynamic genome: what we can learn from structural variation at human chromosome band 8p23.1.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Sox7 Is an independent checkpoint for beta-catenin function in prostate and colon epithelial cells

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Establishment of endoderm progenitors by SOX transcription factor expression in human embryonic stem cells

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Genetic insights into normal and abnormal heart development

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Psoriasis is associated with increased beta-defensin genomic copy number

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Array-based functional screening for genes that regulate vascular endothelial differentiation of Flk1-positive progenitors derived from embryonic stem cells

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pedia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

SOX7 and SOX18 are essential for cardiogenesis in Xenopus

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

SOX7 is an immediate-early target of VegT and regulates Nodal-related gene expression in Xenopus

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Sox7 plays crucial roles in parietal endoderm differentiation in F9 embryonal carcinoma cells through regulating Gata-4 and Gata-6 expression

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

The application of region-specific probes for the resolution of duplication 8p: a case report and a review of the literature

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Extensive normal copy number variation of a beta-defensin antimicrobial-gene cluster

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Wnt-11 activation of a non-canonical Wnt signalling pathway is required for cardiogenesis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

SOX7 transcription factor: sequence, chromosomal localisation, expression, transactivation and interference with Wnt signalling

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Isolation and characterization of a mouse SRY-related cDNA, mSox7

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Enhanced cardiogenesis in embryonic stem cells overexpressing the GATA-4 transcription factor

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Over-expression of GATA-6 in Xenopus embryos blocks differentiation of heart precursors

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Cloning and characterization of Xenopus laevis xSox7 cDNA.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2.

8 July 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0072515

Association of single-nucleotide polymorphisms in MTMR9 gene with obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0072515

A case of inv dup(8p) with early onset breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0072515

Decreased expression of SOX7 is correlated with poor prognosis in lung adenocarcinoma patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0072515

Embryonic expression of Xenopus laevis SOX7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0072515

Sox7-sustained expression alters the balance between proliferation and differentiation of hematopoietic progenitors at the onset of blood specification

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0072515

SOX7 regulates the expression of VE-cadherin in the haemogenic endothelium at the onset of haematopoietic development

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0072515

Newborn screening for critical congenital heart disease: essential public health roles for birth defects monitoring programs

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0072515

Incidence of congenital heart disease in Beijing, China

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757027

MLPA: A prenatal diagnostic tool for the study of congenital heart defects?

26 October 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0072515

[Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities]

21 January 2018

1 reference

12 December 2020

Fetal echocardiographic screening in twins for congenital heart diseases

1 reference

12 December 2020

Deconstructing DiGeorge syndrome

1 reference

12 December 2020

Cardiovascular anomalies associated with chromosome 22q11.2 deletion

1 reference

12 December 2020

Cytogenetic and molecular genetic study of a case with 8p inverted duplication deletion syndrome

1 reference

12 December 2020

Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1.

1 reference

12 December 2020

The Polish National Registry for Fetal Cardiac Pathology: organization, diagnoses, management, educational aspects and telemedicine endeavors

1 reference

12 December 2020

Complex low-copy repeats associated with a common polymorphic inversion at human chromosome 8p23

1 reference

12 December 2020

Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects

1 reference

12 December 2020

Higher DEFB4 genomic copy number in SLE and ANCA-associated small vasculitis

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0072515

Identifiers

DOI

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5 August 2017

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5 August 2017

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