Abnormal WT1 expression in human fetuses with bilateral renal agenesis and cardiac malformations. (Q38405852)

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20 January 2020

title

Abnormal WT1 expression in human fetuses with bilateral renal agenesis and cardiac malformations (English)

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20 January 2020

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2

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20 January 2020

Tamara N Pereira

series ordinal

3

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20 January 2020

author name string

Christine K C Loo

series ordinal

1

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20 January 2020

Grant A Ramm

series ordinal

4

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20 January 2020

language of work or name

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13 January 2012

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Birth Defects Research Part A: Clinical and Molecular Teratology

20 January 2020

published in

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20 January 2020

volume

94

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20 January 2020

issue

2

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20 January 2020

page(s)

116-122

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Mesenchymal origin of hepatic stellate cells, submesothelial cells, and perivascular mesenchymal cells during mouse liver development

20 January 2020

cites work

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Septum transversum-derived mesothelium gives rise to hepatic stellate cells and perivascular mesenchymal cells in developing mouse liver.

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β-catenin regulates mesenchymal progenitor cell differentiation during hepatogenesis

21 January 2018

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Angioblast-mesenchyme induction of early kidney development is mediated by Wt1 and Vegfa

21 January 2018

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Genomic characterization of Wilms' tumor suppressor 1 targets in nephron progenitor cells during kidney development.

21 January 2018

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The many facets of the Wilms' tumour gene, WT1

21 January 2018

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Wt1 and retinoic acid signaling are essential for stellate cell development and liver morphogenesis

21 January 2018

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WT-1 is required for early kidney development

21 January 2018

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Bilateral preaxial polydactyly in a WAGR syndrome patient.

21 January 2018

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Wt1 and retinoic acid signaling in the subcoelomic mesenchyme control the development of the pleuropericardial membranes and the sinus horns.

21 January 2018

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The candidate Wilms' tumour gene is involved in genitourinary development

21 January 2018

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Fibrogenesis in pediatric cholestatic liver disease: role of taurocholate and hepatocyte-derived monocyte chemotaxis protein-1 in hepatic stellate cell recruitment

21 January 2018

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Transcriptional regulation by WT1 in development.

21 January 2018

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Renal aplasia in humans is associated with RET mutations

21 January 2018

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WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations

21 January 2018

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Paracrine signals from mesenchymal cell populations govern the expansion and differentiation of human hepatic stem cells to adult liver fates

21 January 2018

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Epicardial progenitors contribute to the cardiomyocyte lineage in the developing heart.

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/BDRA.22881

1 reference

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20 January 2020

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