Decreased Expression of Connexin 43 Blunts the Progression of Experimental GN

Autor: Coralie Poulain, Lise Paule Labéjof, Christos Chatziantoniou, Christos E. Chadjichristos, Florence Authier, Panagiotis Kavvadas, Ahmed Abed, Amelie Calmont, Carlo Afieri, Jean Claude Dussaule, Niki Prakoura

Publikováno v: Journal of the American Society of Nephrology
Journal of the American Society of Nephrology, 2017, 28 (10), pp.2915-2930. ⟨10.1681/ASN.2016111211⟩
Journal of the American Society of Nephrology, American Society of Nephrology, 2017, 28 (10), pp.2915-2930. ⟨10.1681/ASN.2016111211⟩

International audience; GN refers to a variety of renal pathologies that often progress to ESRD, but the molecular mechanisms underlying this progression remain incompletely characterized. Here, we determined whether dysregulated expression of the ga

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bb008003c5b35c9b222c5e2bf59d3bd
https://doi.org/10.1681/asn.2016111211

Defective ciliogenesis, embryonic lethality and severe impairment of the Sonic Hedgehog pathway caused by inactivation of the mouse complex A intraflagellar transport gene Ift122/Wdr10, partially overlapping with the DNA repair gene Med1/Mbd4

Autor: Delphine Champeval, Kenneth S. Zaret, Elena Caretti, Amelie Calmont, John B.E. Burch, Maria Rosaria Bassi, Alfonso Bellacosa, Salvatore Cortellino, Michal Jarnik, Baolin Wang, Lionel Larue, Chengbing Wang

Publikováno v: Developmental Biology. 325:225-237

Primary cilia are assembled and maintained by evolutionarily conserved intraflagellar transport (IFT) proteins that are involved in the coordinated movement of macromolecular cargo from the basal body to the cilium tip and back. The IFT machinery is

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ea379e9469b8c8eb088a39668427bb7
https://doi.org/10.1016/j.ydbio.2008.10.020

22q11 Deletion Syndrome: A Role for Tbx1 in Pharynx and Cardiovascular Development

Autor: Amelie Calmont, Peter J. Scambler

Publikováno v: eLS.

DiGeorge and velocardiofacial syndromes result from a chromosomal deletion involving proximal chromosome 22 and affected individuals commonly present with congenital heart defects, feeding problems, speech delay and learning problems. Psychiatric ill

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ab7ccfda7b8c40f26a6b35e6d64b9141
https://doi.org/10.1002/9780470015902.a0006074.pub2

Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm

Autor: William Andrews, Elizabeth Illingworth, Kelly Lammerts van Bueren, M. Albert Basson, Vanessa Kyriakopoulou, Amelie Calmont, James F. Martin, Sarah Ivins, Irinna Papangeli, Peter J. Scambler, Anne M. Moon

Elucidating the gene regulatory networks that govern pharyngeal arch artery (PAA) development is an important goal, as such knowledge can help to identify new genes involved in cardiovascular disease. The transcription factor Tbx1 plays a vital role

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5d7d2a038f0b55b2db4f64eada903da
http://hdl.handle.net/11386/2292331

Transcriptional control of epithelial differentiation during kidney development

Autor: Evelyne Fischer, Jerome Rossert, Amelie Calmont, David Ribes

Publikováno v: Scopus-Elsevier

In Mammals, kidney development proceeds in three stages (reviewed in [1][1]). The first two stages lead to the formation of transient structures, the pronephros and the mesonephros, and the third stage gives rise to the metanephros, which is the perm

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9db32dfde9dcb47426e45a06abff8a04
https://pubmed.ncbi.nlm.nih.gov/12761232