Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Sabrina, Martin"'
Autor:
Justyne Feat-Vetel, Nadine Suffee, Florence Bachelot, Morgane Dos Santos, Nathalie Mougenot, Elise Delage, Florian Saliou, Sabrina Martin, Isabelle Brunet, Pierre Sicard, Virginie Monceau
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 17, p 9483 (2024)
Recent epidemiological studies have shown that patients with right-sided breast cancer (RBC) treated with X-ray irradiation (IR) are more susceptible to developing cardiovascular diseases, such as arrhythmias, atrial fibrillation, and conduction dist
Externí odkaz:
https://doaj.org/article/2db2dff300634d73bbd6f3f66e68b661
Publikováno v:
eLife, Vol 11 (2022)
Peripheral nerves are vascularized by a dense network of blood vessels to guarantee their complex function. Despite the crucial role of vascularization to ensure nerve homeostasis and regeneration, the mechanisms governing nerve invasion by blood ves
Externí odkaz:
https://doaj.org/article/1ac1ffadf18349668e7f0519fa873b93
Autor:
Alice Gilbert, Xabier Elorza-Vidal, Armelle Rancillac, Audrey Chagnot, Mervé Yetim, Vincent Hingot, Thomas Deffieux, Anne-Cécile Boulay, Rodrigo Alvear-Perez, Salvatore Cisternino, Sabrina Martin, Sonia Taïb, Aontoinette Gelot, Virginie Mignon, Maryline Favier, Isabelle Brunet, Xavier Declèves, Mickael Tanter, Raul Estevez, Denis Vivien, Bruno Saubaméa, Martine Cohen-Salmon
Publikováno v:
eLife, Vol 10 (2021)
Absence of the astrocyte-specific membrane protein MLC1 is responsible for megalencephalic leukoencephalopathy with subcortical cysts (MLC), a rare type of leukodystrophy characterized by early-onset macrocephaly and progressive white matter vacuolat
Externí odkaz:
https://doaj.org/article/8c131fd67c234cbf982e2d29b237469b
Autor:
Georgios Galaris, Kévin Montagne, Jérémy H. Thalgott, Geoffroy J. P. E. Goujon, Sander van den Driesche, Sabrina Martin, Hans-Jurgen J. Mager, Christine L. Mummery, Ton J. Rabelink, Franck Lebrin
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 16, p 8948 (2021)
Hereditary Hemorrhagic Telangiectasia type 1 (HHT1) is an autosomal dominant inherited disease characterized by arteriovenous malformations and hemorrhage. HHT1 is caused by mutations in ENDOGLIN, which encodes an ancillary receptor for Transforming
Externí odkaz:
https://doaj.org/article/c07ade58f66a4493b1774f42b6b5bf24
Autor:
Emilie Simonnet, Sabrina Martin, José Vilar, Emilie Vessieres, Sonia Taib, Virginie Monceau, Luc Pardanaud, Nadine Bouby, Anne Eichmann, Jean-Sébastien Silvestre, Daniel Henrion, Isabelle Brunet
The autonomic sympathetic nervous system innervates peripheral resistance arteries, thereby controlling arterial diameter and modulating blood supply to organs and arterial tone. Despite its fundamental role in blood flow regulation and adaptive resp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be6d587d26e8933dc0aaedf8e6352902
https://doi.org/10.1101/2023.02.03.526852
https://doi.org/10.1101/2023.02.03.526852
Autor:
Sabrina Martin, Daniela Espósito, Graciela Manzur, Laura Valinotto, Mónica Natale, Graciela Sánchez, María Emilia Villani, Gladys Merola
Publikováno v:
Dermatología Argentina. 28:15-19
La eritroqueratodermia variable y progresiva es una genodermatosis que, en la mayoría de los casos, se hereda de forma autosómica dominante y presenta una expresividad variable. Es producida principalmente por variantes patogénicas en los genes GJ
Autor:
Sabrina Martin
Publikováno v:
Etikk i Praksis: Nordic Journal of Applied Ethics, Vol 10, Iss 2 (2016)
Focusing on the basic structure as the subject of justice has tended to lead theorists to make a choice: either there is no global basic structure and therefore obligations of justice remain domestic only (the statist position) or there is sufficient
Externí odkaz:
https://doaj.org/article/d8d1e0bfd0b342328590b054657a51f6
Autor:
Sabrina Martin
Publikováno v:
Wenn Food Waste sichtbar wird
Sabrina Martin widmet sich in ihrem Beitrag der Frage, welche Werte Food-Waste-Apps konstruieren und hervorheben, um den Verkauf von Nahrungsmittelabfällen zu ermöglichen. Indem die Marktintermediäre »wertlosen« Lebensmittelabfällen neue Werte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4049bcb3a015d015eececc8fb02b8a05
https://doi.org/10.1515/9783839455388-005
https://doi.org/10.1515/9783839455388-005
Autor:
Sonia Taïb, Mickael Tanter, Mervé Yetim, Denis Vivien, Xavier Declèves, Alice Gilbert, Vincent Hingot, Bruno Saubaméa, Martine Cohen-Salmon, Armelle Rancillac, Salvatore Cisternino, Audrey Chagnot, Xabier Elorza-Vidal, Raúl Estévez, Isabelle Brunet, Rodrigo Alvear-Perez, Aontoinette Gelot, Maryline Favier, Virginie Mignon, Sabrina Martin, Thomas Deffieux, Anne-Cécile Boulay
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1652d99103f61f836c47ea81461963e
https://doi.org/10.7554/elife.71379.sa2
https://doi.org/10.7554/elife.71379.sa2
Autor:
Hans-Jurgen J Mager, Sabrina Martin, Georgios Galaris, Geoffroy J P E Goujon, Ton J. Rabelink, Franck Lebrin, Kevin Montagne, Sander van den Driesche, Jérémy H. Thalgott, Christine L. Mummery
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 16
International Journal of Molecular Sciences, Vol 22, Iss 8948, p 8948 (2021)
International Journal of Molecular Sciences, 22(16). MDPI
Volume 22
Issue 16
International Journal of Molecular Sciences, Vol 22, Iss 8948, p 8948 (2021)
International Journal of Molecular Sciences, 22(16). MDPI
Hereditary Hemorrhagic Telangiectasia type 1 (HHT1) is an autosomal dominant inherited disease characterized by arteriovenous malformations and hemorrhage. HHT1 is caused by mutations in ENDOGLIN, which encodes an ancillary receptor for Transforming