Regulation of the adrenocortical stem cell niche: implications for disease - Test2 - elhamkhani - TriplyDB

Regulation of the adrenocortical stem cell niche: implications for disease

Regulation of the adrenocortical stem cell niche: implications for disease

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Functional Zonation of the Adult Mammalian Adrenal Cortex Adrenocortical zonation, renewal, and remodeling Transplantation of bovine adrenocortical cells encapsulated in alginate.Adrenal histopathology in primary aldosteronism: is it time for a change?Molecular Mechanisms of Stem/Progenitor Cell Maintenance in the Adrenal Cortex.New directions for the treatment of adrenal insufficiency.Regulation of zonation and homeostasis in the adrenal cortex.Genetics of Adrenocortical Development and Tumors.TGF-β/β2-spectrin/CTCF-regulated tumor suppression in human stem cell disorder Beckwith-Wiedemann syndrome.Targeted Disruption of YAP and TAZ Impairs the Maintenance of the Adrenal Cortex.PKA signaling drives reticularis differentiation and sexually dimorphic adrenal cortex renewal.GLI1+ progenitor cells in the adrenal capsule of the adult mouse give rise to heterotopic gonadal-like tissue.Expression of progenitor markers is associated with the functionality of a bioartificial adrenal cortex.Isolation of a multipotent mesenchymal stem cell-like population from human adrenal cortex.

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Regulation of the adrenocortical stem cell niche: implications for disease

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2014 nî lūn-bûn

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NRENDO.2014.166

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Nature Reviews Endocrinology

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Regulation of the adrenocortical stem cell niche: implications for disease

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Elisabeth M Walczak

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Gary D Hammer

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YAC complementation shows a requirement for Wt1 in the development of epicardium, adrenal gland and throughout nephrogenesis

A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans

Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator

DNA binding and transcriptional repression by DAX-1 blocks steroidogenesis

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Receptor specificity of the fibroblast growth factor family

Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome

The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders

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