Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Muriel Umbhauer"'
Autor:
Leticia L. Niborski, Mélanie Paces-Fessy, Pierbruno Ricci, Adeline Bourgeois, Pedro Magalhães, Maria Kuzma-Kuzniarska, Celine Lesaulnier, Martin Reczko, Edwige Declercq, Petra Zürbig, Alain Doucet, Muriel Umbhauer, Silvia Cereghini
Publikováno v:
Disease Models & Mechanisms, Vol 14, Iss 5 (2021)
Heterozygous mutations in HNF1B cause the complex syndrome renal cysts and diabetes (RCAD), characterized by developmental abnormalities of the kidneys, genital tracts and pancreas, and a variety of renal, pancreas and liver dysfunctions. The pathoge
Externí odkaz:
https://doaj.org/article/d6e03fcf8b49477c9eccaaeefc233746
Autor:
Hector Escriva, Stéphanie Bertrand, Pierre Germain, Marc Robinson-Rechavi, Muriel Umbhauer, Jérôme Cartry, Marilyne Duffraisse, Linda Holland, Hinrich Gronemeyer, Vincent Laudet
Publikováno v:
PLoS Genetics, Vol 2, Iss 7, p e102 (2006)
Understanding the role of gene duplications in establishing vertebrate innovations is one of the main challenges of Evo-Devo (evolution of development) studies. Data on evolutionary changes in gene expression (i.e., evolution of transcription factor-
Externí odkaz:
https://doaj.org/article/6b63d52e77ff4c88a952493a6f502b64
Autor:
Jennifer Durant-Vesga, Nanoka Suzuki, Haruki Ochi, Ronan Le Bouffant, Alexis Eschstruth, Hajime Ogino, Muriel Umbhauer, Jean-François Riou
Publikováno v:
Developmental biology. 493
Development of the Xenopus pronephros relies on renal precursors grouped at neurula stage into a specific region of dorso-lateral mesoderm called the kidney field. Formation of the kidney field at early neurula stage is dependent on retinoic (RA) sig
Autor:
Alain Doucet, Adeline Bourgeois, Celine Lesaulnier, Edwige Declercq, Martin Reczko, Silvia Cereghini, Petra Zürbig, Maria Kuzma-Kuzniarska, Muriel Umbhauer, Leticia L. Niborski, Mélanie Paces-Fessy, Pierbruno Ricci, Pedro Magalhães
Publikováno v:
Disease Models & Mechanisms
article-version (VoR) Version of Record
Disease Models & Mechanisms, Vol 14, Iss 5 (2021)
Disease Models & Mechanisms, Cambridge Company of Biologists, 2021, pp.dmm.047498. ⟨10.1242/dmm.047498⟩
Disease Models & Mechanisms, 2021, pp.dmm.047498. ⟨10.1242/dmm.047498⟩
article-version (VoR) Version of Record
Disease Models & Mechanisms, Vol 14, Iss 5 (2021)
Disease Models & Mechanisms, Cambridge Company of Biologists, 2021, pp.dmm.047498. ⟨10.1242/dmm.047498⟩
Disease Models & Mechanisms, 2021, pp.dmm.047498. ⟨10.1242/dmm.047498⟩
Heterozygous mutations in HNF1B cause the complex syndrome renal cysts and diabetes (RCAD), characterized by developmental abnormalities of the kidneys, genital tracts and pancreas, and a variety of renal, pancreas and liver dysfunctions. The pathoge
Autor:
Pierbruno Ricci, Laura Goea, Jens Drube, Joost P. Schanstra, Petra Zürbig, Stéphane Decramer, Giuseppe Remuzzi, Magdalena Krochmal, Franz Schaefer, Martin Pejchinovski, Harald Mischak, Pedro Magalhães, Lars Pape, Muriel Umbhauer, Maria Rosa Caruso, Silvia Cereghini, Iwona Belczacka, Erica Daina
Publikováno v:
Scientific Reports
Scientific Reports, 2019, 9 (1), pp.2225. ⟨10.1038/s41598-019-38713-5⟩
Scientific Reports, Nature Publishing Group, 2019, 9, pp.2225. ⟨10.1038/s41598-019-38713-5⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Scientific Reports, Nature Publishing Group, 2019, 9 (1), pp.2225. ⟨10.1038/s41598-019-38713-5⟩
Scientific Reports, 2019, 9 (1), pp.2225. ⟨10.1038/s41598-019-38713-5⟩
Scientific Reports, Nature Publishing Group, 2019, 9, pp.2225. ⟨10.1038/s41598-019-38713-5⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Scientific Reports, Nature Publishing Group, 2019, 9 (1), pp.2225. ⟨10.1038/s41598-019-38713-5⟩
Renal Cysts and Diabetes Syndrome (RCAD) is an autosomal dominant disorder caused by mutations in the HNF1B gene encoding for the transcriptional factor hepatocyte nuclear factor-1B. RCAD is characterized as a multi-organ disease, with a broad spectr
Publikováno v:
Journal of Cellular Biochemistry
Journal of Cellular Biochemistry, Wiley, 2018, 119 (12), pp.10338-10350. ⟨10.1002/jcb.27376⟩
Journal of Cellular Biochemistry, 2018, 119 (12), pp.10338-10350. ⟨10.1002/jcb.27376⟩
Journal of Cellular Biochemistry, Wiley, 2018, 119 (12), pp.10338-10350. ⟨10.1002/jcb.27376⟩
Journal of Cellular Biochemistry, 2018, 119 (12), pp.10338-10350. ⟨10.1002/jcb.27376⟩
International audience; Transient receptor potential cation channel‐2 (TRPP2) is a nonspecific Ca2+‐dependent cation channel with versatile functions including control of extracellular calcium entry at the plasma membrane, release of intracellula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0786914a9a20e3ee3246086aa43ba2e
https://hal.sorbonne-universite.fr/hal-01981052/document
https://hal.sorbonne-universite.fr/hal-01981052/document
Publikováno v:
Journal of Cellular Biochemistry. 119
Autor:
Laurent Formery, Jean-François Riou, Muriel Umbhauer, Isabelle Gervi, Isabelle Buisson, Ronan Le Bouffant, Michael Schubert, Camille Cosse-Etchepare
Publikováno v:
International Journal of Developmental Biology
International Journal of Developmental Biology, University of the Basque Country Press, 2018, 62 (4-5), pp.325-333. ⟨10.1387/ijdb.170260RL⟩
International Journal of Developmental Biology, University of the Basque Country Press, 2018, 62 (4-5), pp.325-333. ⟨10.1387/ijdb.170260RL⟩
The POU (Pit-Oct-Unc) genes encode a large transcription factor family comprising 6 classes (pou1f to pou6f ) involved in many developmental processes, such as cell commitment and differentiation. The pou3f class contains four members (pou3f1, pou3f2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18eff11abc1872985f8f711006697e3f
https://hal.archives-ouvertes.fr/hal-02117425/file/ft325.pdf
https://hal.archives-ouvertes.fr/hal-02117425/file/ft325.pdf
Autor:
Pier Lorenzo Puri, Sonia Albini, Gregg Duester, Sean Spiering, Pilar Ruiz-Lozano, Paul J. Bushway, Alessandra Sacco, Mark Mercola, Miguel Mano, Jean-François Riou, Wesley L. McKeithan, Mauro Giacca, Michael S. Yu, Chun-Teng Huang, Alexandre R. Colas, Matthew T. Tierney, Florent Carrette, Thomas J. Cunningham, Muriel Umbhauer
Publikováno v:
Genes and Development
Genes and Development, 2017, 31 (13), pp.1325-1338. ⟨10.1101/gad.300400.117⟩
Genes and Development, Cold Spring Harbor Laboratory Press, 2017, 31 (13), pp.1325-1338. ⟨10.1101/gad.300400.117⟩
Genes and Development, 2017, 31 (13), pp.1325-1338. ⟨10.1101/gad.300400.117⟩
Genes and Development, Cold Spring Harbor Laboratory Press, 2017, 31 (13), pp.1325-1338. ⟨10.1101/gad.300400.117⟩
International audience; Deciphering the fundamental mechanisms controlling cardiac specification is critical for our understanding of how heart formation is initiated during embryonic development and for applying stem cell biology to regenerative med
Autor:
Magdalena Krochmal, Maria Rosa Caruso, Muriel Umbhauer, Silvia Cereghini, Stéphane Decramer, Pierbruno Ricci, Joost P. Schanstra, Martin Pejchinovski, Harald Mischak, Pedro Magalhães, Lars Pape, Erica Daina, Petra Zürbig, Giuseppe Remuzzi, Franz Schaefer
Publikováno v:
Nephrology Dialysis Transplantation. 33:i64-i64