Resultados de búsqueda - Dimitra Micha
- Mostrando 1 - 15 Resultados de 15
-
1
-
2
-
3
-
4
-
5
-
6
Hypoxic human cancer cells are sensitized to BH-3 mimetic–induced apoptosis via downregulation of the Bcl-2 protein Mcl-1 por Luke Harrison, Dimitra Micha, Martin Brandenburg, Kathryn Simpson, Christopher J. Morrow, O. Denneny, Cassandra L. Hodgkinson, Zaira Yunus, Clare Dempsey, Darren L. Roberts, Fiona Blackhall, Guy Makin, Caroline Dive
Publicado 2011Artigo -
7
Is Osteogenesis Imperfecta Associated with Cardiovascular Abnormalities? A Systematic Review of the Literature por Sara J. E. Verdonk, Silvia Storoni, Dimitra Micha, Joost G. van den Aardweg, Paolo Versacci, Luca Celli, Ralph de Vries, Lidiia Zhytnik, Otto Kamp, Marianna Bugiani, Elisabeth M. W. Eekhoff
Publicado 2024Revisão -
8
<i>SMAD2</i>Mutations Are Associated with Arterial Aneurysms and Dissections por Dimitra Micha, Dongchuan Guo, Yvonne Hilhorst‐Hofstee, Fop van Kooten, Dian Atmaja, Eline Overwater, Ferdy Kurniawan Cayami, Ellen S. Regalado, R. Van Uffelen, Hanka Venselaar, Sultana MH Faradz, Gerrit Vriend, Marjan M. Weiss, Erik A. Sistermans, Alessandra Maugeri, Dianna M. Milewicz, Gerard Pals, Fleur S van Dijk
Publicado 2015Artigo -
9
Splice-Site Mutations in the Axonemal Outer Dynein Arm Docking Complex Gene CCDC114 Cause Primary Ciliary Dyskinesia por Alexandros Onoufriadis, Tamara Paff, Dinu Antony, Amelia Shoemark, Dimitra Micha, Bertus Kuyt, Miriam Schmidts, Stavroula Petridi, Jeanette E. Dankert-Roelse, Eric G. Haarman, Johannes M.A. Daniels, Richard D. Emes, Robert Wilson, Claire Hogg, Peter Scambler, Eddie M.K. Chung, Gerard Pals, Hannah M. Mitchison
Publicado 2012Artigo -
10
Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects por Tamara Paff, Niki T. Loges, Isabella Aprea, Kaman Wu, Zeineb Bakey, Eric G. Haarman, Johannes M.A. Daniels, Erik A. Sistermans, Natalija Bogunovic, Gerard W. Dougherty, Inga M. Höben, Jörg Große-Onnebrink, Anja Matter, Heike Olbrich, Claudius Werner, Gerard Pals, Miriam Schmidts, Heymut Omran, Dimitra Micha
Publicado 2016Artigo -
11
Gene Therapy for Fibrodysplasia Ossificans Progressiva: Feasibility and Obstacles por Elisabeth M. W. Eekhoff, Ruben D. de Ruiter, Bernard J. Smilde, Ton Schoenmaker, Teun J. de Vries, Coen Netelenbos, Edward C. Hsiao, Christiaan Scott, Nobuhiko Haga, Zvi Grunwald, Carmen L. De Cunto, Maja Di Rocco, Patricia Delai, Robert J. Diecidue, Vrisha Madhuri, Tae‐Joon Cho, Rolf Morhart, Clive Friedman, Michael Zasloff, Gerard Pals, Jae‐Hyuck Shim, Guangping Gao, Frederick S. Kaplan, Robert J. Pignolo, Dimitra Micha
Publicado 2022Revisão -
12
X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1 por Noriko Miyake, Nicole I. Wolf, Ferdy Kurniawan Cayami, Joanna Crawford, Annette Bley, Dorothy Bulas, Alex Conant, Stephen J. Bent, Karen W. Gripp, Andreas Hahn, Sean Humphray, Shihoko Kimura‐Ohba, Zoya Kingsbury, Bryan R. Lajoie, Dennis Lal, Dimitra Micha, Amy Pizzino, Richard J. Sinke, Deborah A. Sival, Irene Stolte‐Dijkstra, Andrea Superti‐Furga, Nicole Ulrick, Ryan J. Taft, Tsutomu Ogata, Keiichi Ozono, Naomichi Matsumoto, Bernd A. Neubauer, Cas Simons, Adeline Vanderver
Publicado 2017Artigo -
13
<i>PLS3</i> Mutations in X-Linked Osteoporosis with Fractures por Fleur S. van Dijk, M. Carola Zillikens, Dimitra Micha, Markus Rießland, Carlo Marcelis, C E de Die-Smulders, Janine Milbradt, Anton Franken, Arjan J. Harsevoort, Klaske D. Lichtenbelt, Hans E. Pruijs, M. Estela Rubio‐Gozalbo, Rolf Zwertbroek, Youssef Moutaouakil, Jaqueline Egthuijsen, Matthias Hammerschmidt, Renate Bijman, C.M. Semeins, Astrid D. Bakker, Vincent Everts, Jenneke Klein‐Nulend, Natalia Campos‐Obando, Albert Hofman, Gerard J. te Meerman, Annemieke J.M.H. Verkerk, André G. Uitterlinden, Alessandra Maugeri, Erik A. Sistermans, Quinten Waisfisz, Hanne Meijers‐Heijboer, Brunhilde Wirth, Marleen Simon, Gerard Pals
Publicado 2013Artigo -
14
Fibrodysplasia Ossificans Progressiva: What Have We Achieved and Where Are We Now? Follow-up to the 2015 Lorentz Workshop por Ruben D. de Ruiter, Bernard J. Smilde, Gerard Pals, Nathalie Bravenboer, Petra Knaus, Ton Schoenmaker, Esmée Botman, Gonzalo Sánchez‐Duffhues, Maurizio Pacifici, Robert J. Pignolo, Eileen M. Shore, Marjolein van Egmond, Hans Van Oosterwyck, Frederick S. Kaplan, Edward C. Hsiao, Paul B. Yu, Renata Bocciardi, Carmen L. De Cunto, Patricia Delai, Teun J. de Vries, Susanne Hilderbrandt, Richard T. Jaspers, Richard Keen, Peter Koolwijk, Rolf Morhart, J.C. Netelenbos, Thomas Rustemeyer, Christiaan Scott, Clemens Stockklausner, Peter ten Dijke, James T Triffit, Francesc Ventura, Roberto Ravazzolo, Dimitra Micha, Elisabeth M. W. Eekhoff
Publicado 2021Revisão -
15
Interaction between KDELR2 and HSP47 as a Key Determinant in Osteogenesis Imperfecta Caused by Bi-allelic Variants in KDELR2 por Fleur S van Dijk, Oliver Semler, Julia Etich, Anna M. Köhler, Juan A. Jimenez‐Estrada, Nathalie Bravenboer, Lauria Claeys, Elise Riesebos, Sejla Gegic, Sander R. Piersma, Connie R. Jiménez, Quinten Waisfisz, Carmen‐Lisset Flores, Julián Nevado, Arjan J. Harsevoort, Guus Janus, Anton Franken, Astrid M. van der Sar, Hanne Meijers‐Heijboer, Karen E. Heath, Pablo Lapunzina, Peter G. J. Nikkels, Gijs W.E. Santen, Julian Nüchel, Markus Plomann, Raimund Wagener, Mirko Rehberg, Heike Hoyer‐Kuhn, Elisabeth M. W. Eekhoff, Gerard Pals, Matthias Mörgelin, Simon Newstead, Brian T. Wilson, Víctor L. Ruiz‐Pérez, Alessandra Maugeri, Christian Netzer, Frank Zaucke, Dimitra Micha
Publicado 2020Artigo
Herramientas de búsqueda:
Materias Relacionadas
Biology
Gene
Medicine
Genetics
Internal medicine
Anatomy
Disease
Pathology
Bioinformatics
Osteogenesis imperfecta
Phenotype
Surgery
Bronchiectasis
Lung
Mutation
Primary ciliary dyskinesia
Aneurysm
Biochemistry
Cancer research
Cardiology
Cell biology
Chemistry
Cilium
Downregulation and upregulation
Dynein
Exome sequencing
Fibrodysplasia ossificans progressiva
Heterotopic ossification
Microtubule
Abdominal aortic aneurysm