Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Raphael Helaers"'
Autor:
Yalda Afshar, Feyiang Ma, Austin Quach, Anhyo Jeong, Hannah L Sunshine, Vanessa Freitas, Yasaman Jami-Alahmadi, Raphael Helaers, Xinmin Li, Matteo Pellegrini, James A Wohlschlegel, Casey E Romanoski, Miikka Vikkula, M Luisa Iruela-Arispe
Publikováno v:
eLife, Vol 12 (2023)
Environmental cues, such as physical forces and heterotypic cell interactions play a critical role in cell function, yet their collective contributions to transcriptional changes are unclear. Focusing on human endothelial cells, we performed broad in
Externí odkaz:
https://doaj.org/article/f5af08e56062488ea026c573d9c0968d
Autor:
Carolina Boucinha, Amanda R Caetano, Helena LC Santos, Raphael Helaers, Miikka Vikkula, Marta Helena Branquinha, André Luis Souza dos Santos, Philippe Grellier, Karina Alessandra Morelli, Claudia Masini d‘Avila-Levy
Publikováno v:
Memorias do Instituto Oswaldo Cruz, Vol 115 (2020)
BACKGROUND Biodiversity screens and phylogenetic studies are dependent on reliable DNA sequences in public databases. Biological collections possess vouchered specimens with a traceable history. Therefore, DNA sequencing of samples available at insti
Externí odkaz:
https://doaj.org/article/6f1d6151b5ff4382a27dbf05ea188866
Autor:
Yalda Afshar, Feyiang Ma, Austin Quach, Anhyo Jeong, Hannah L Sunshine, Vanessa Freitas, Yasaman Jami-Alahmadi, Raphael Helaers, Xinmin Li, Matteo Pellegrini, James A Wohlschlegel, Casey E Romanoski, Miikka Vikkula, M Luisa Iruela-Arispe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f51791b6aa6a7cbbd3846cd98308e97
https://doi.org/10.7554/elife.81370.sa2
https://doi.org/10.7554/elife.81370.sa2
Autor:
Sophie Welsch, Antoine Harvengt, Paola Gallo, Manon Martin, Dominique Beckers, Thierry Mouraux, Nicole Seret, Marie-Christine Lebrethon, Raphaël Helaers, Pascal Brouillard, Miikka Vikkula, Philippe A. Lysy
Publikováno v:
Diabetes & Metabolism Journal, Vol 48, Iss 5, Pp 949-959 (2024)
Background Recent diabetes subclassifications have improved the differentiation between patients with type 1 diabetes mellitus (T1DM) and type 2 diabetes mellitus despite several overlapping features, yet without considering genetic forms of diabetes
Externí odkaz:
https://doaj.org/article/77abe0ff27a345cba7ee84224367e612
Autor:
Vera Lúcia Gil-da-Silva-Lopes, Milena Atique-Tacla, Matheus Copelli, Eleonore Pairet, Isabella Monlleó, Erlane Ribeiro, Elaine Lustosa-Mendes, Raphael Helaers, Tarsis Vieira, Miikka Vikkula
Publikováno v:
re, (2023)
Orofacial clefts (OC) are the most common birth defects in humans and approximately 30% of them form the group of syndromic orofacial clefts (SOCs). Microphthalmia/anophthalmia/coloboma spectrum (MAC) can be associated with OC, however the genetic et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25bad97d612a1067502eb35ad2745876
https://hdl.handle.net/2078.1/274786
https://hdl.handle.net/2078.1/274786
Autor:
Alicia B, Byrne, Pascal, Brouillard, Drew L, Sutton, Jan, Kazenwadel, Saba, Montazaribarforoushi, Genevieve A, Secker, Anna, Oszmiana, Milena, Babic, Kelly L, Betterman, Peter J, Brautigan, Melissa, White, Sandra G, Piltz, Paul Q, Thomas, Christopher N, Hahn, Matthias, Rath, Ute, Felbor, G Christoph, Korenke, Christopher L, Smith, Kathleen H, Wood, Sarah E, Sheppard, Denise M, Adams, Ariana, Kariminejad, Raphael, Helaers, Laurence M, Boon, Nicole, Revencu, Lynette, Moore, Christopher, Barnett, Eric, Haan, Peer, Arts, Miikka, Vikkula, Hamish S, Scott, Natasha L, Harvey
Publikováno v:
Science translational medicine. 14(634)
Central conducting lymphatic anomaly (CCLA), characterized by the dysfunction of core collecting lymphatic vessels including the thoracic duct and cisterna chyli, and presenting as chylothorax, pleural effusions, chylous ascites, and lymphedema, is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5d4178329aba45f643084d569782c198
https://pubmed.ncbi.nlm.nih.gov/35235341
https://pubmed.ncbi.nlm.nih.gov/35235341
Autor:
Alicia B. Byrne, Pascal Brouillard, Drew L. Sutton, Jan Kazenwadel, Saba Montazaribarforoushi, Genevieve A. Secker, Anna Oszmiana, Milena Babic, Kelly L. Betterman, Peter J. Brautigan, Melissa White, Sandra G. Piltz, Paul Q. Thomas, Christopher N. Hahn, Matthias Rath, Ute Felbor, G. Christoph Korenke, Christopher L. Smith, Kathleen H. Wood, Sarah E. Sheppard, Denise M. Adams, Ariana Kariminejad, Raphael Helaers, Laurence M. Boon, Nicole Revencu, Lynette Moore, Christopher Barnett, Eric Haan, Peer Arts, Miikka Vikkula, Hamish S. Scott, Natasha L. Harvey
Publikováno v:
Science Translational Medicine, Vol. 14, no. 634 (2022) (2022)
Central conducting lymphatic anomaly (CCLA), characterized by the dysfunction of core collecting lymphatic vessels including the thoracic duct and cisterna chyli, and presenting as chylothorax, pleural effusions, chylous ascites, and lymphedema, is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a5954867de8c3ef147a7cbf3815f11d
https://hdl.handle.net/2078.1/260107
https://hdl.handle.net/2078.1/260107
Autor:
Ahalieyah Anantharajah, Raphael Helaers, Jean-Philippe Defour, Nathalie Olive, Florence Kabera, Luc Croonen, Françoise Deldime, Jean-Luc Vaerman, Cindy Barbée, Monique Bodéus, Anais Scohy, Alexia Verroken, Hector Rodriguez-Villalobos, Benoît Kabamba-Mukadi
The SARS-CoV-2 pandemic has created an unprecedented need for rapid large-scale diagnostic testing. Currently, several quantitative reverse-transcription polymerase chain reaction (RT-qPCR) assays recommended by the World Health Organization are bein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83b6b3fdabdd9343d60c744a3e3f5968
https://doi.org/10.21203/rs.3.rs-36512/v1
https://doi.org/10.21203/rs.3.rs-36512/v1
Publikováno v:
PLoS Computational Biology, Vol 19, Iss 9, p e1011488 (2023)
The development of high-throughput next-generation sequencing technologies and large-scale genetic association studies produced numerous advances in the biostatistics field. Various aggregation tests, i.e. statistical methods that analyze association
Externí odkaz:
https://doaj.org/article/e36359d2ab3548cd9b7a5869cd08232f
Autor:
Pascal Brouillard, Matthieu J. Schlögel, Nassim Homayun Sepehr, Raphaël Helaers, Angela Queisser, Elodie Fastré, Simon Boutry, Sandra Schmitz, Philippe Clapuyt, Frank Hammer, Anne Dompmartin, Annamaria Weitz-Tuoretmaa, Jussi Laranne, Louise Pasquesoone, Catheline Vilain, Laurence M. Boon, Miikka Vikkula
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-12 (2021)
Abstract Background Theragnostic management, treatment according to precise pathological molecular targets, requests to unravel patients’ genotypes. We used targeted next-generation sequencing (NGS) or digital droplet polymerase chain reaction (ddP
Externí odkaz:
https://doaj.org/article/3222fedb0916439490030c10e72aa9b4