Որոնման արդյունքները - Frederic Tort
- Ցուցադրվում են 1 - 8 արդյունքները 8
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1
ATM gene inactivation in mantle cell lymphoma mainly occurs by truncating mutations and missense mutations involving the phosphatidylinositol-3 kinase domain and is associated with... Emma Camacho, Luís Hernández, Sílvia Hernández, Frederic Tort, Beatríz Bellosillo, Sı́lvia Beà, Francesc Bosch, Emili Montserrat, Antonio Cardesa, Pedro L. Fernández, Elı́as Campo
Հրապարակվել է 2002Artigo -
2
Molecular Characterization of a New ALK Translocation Involving Moesin (MSN-ALK) in Anaplastic Large Cell Lymphoma Frederic Tort, Magda Pinyol, Karen Pulford, Giovanna Roncador, Luís Hernández, Iracema Nayach, Hanneke C. Kluin‐Nelemans, Philip M. Kluin, Christian Touriol, Georges Delsol, David Y. Mason, Elı́as Campo
Հրապարակվել է 2001Artigo -
3
CHK2-decreased protein expression and infrequent genetic alterations mainly occur in aggressive types of non-Hodgkin lymphomas Frederic Tort, Sílvia Hernández, Sı́lvia Beà, Antonio Martı́nez, Manel Esteller, James G. Herman, Xavier Puig, Emma Camacho, Montse Sánchez, Iracema Nayach, Armando López‐Guillermo, Pedro L. Fernández, Dolors Colomer, Luís Hernández, Elı́as Campo
Հրապարակվել է 2002Artigo -
4
Mutations in the lipoyltransferase<i>LIPT1</i>gene cause a fatal disease associated with a specific lipoylation defect of the 2-ketoacid dehydrogenase complexes Frederic Tort, Xènia Ferrer-Cortés, Marta Thió, Aleix Navarro‐Sastre, Leslie Matalonga, Ester Quintana, Núria Bujan, Ángela Arias, Judit García‐Villoria, Cécile Acquaviva, Christine Vianey‐Saban, Rafael Artuch, Àngels García‐Cazorla, Paz Briones, Antònia Ribes
Հրապարակվել է 2013Artigo -
5
Mutations in<i>TRAPPC11</i>are associated with a congenital disorder of glycosylation Leslie Matalonga, Miren Bravo, Carla Serra‐Peinado, Elisabeth García-Pelegrí, Olatz Ugarteburu, Silvia M. Vidal, Maria Llambrich, Ester Quintana, Pedro Fuster-Jorge, Maria Nieves Gonzalez-Bravo, Sergi Beltrán, Joaquı́n Dopazo, Francisco García‐García, François Foulquier, Gert Matthijs, Philippa B. Mills, Antònia Ribes, Gustavo Egea, Paz Briones, Frederic Tort, M. Girós
Հրապարակվել է 2016Artigo -
6
International consensus guidelines for phosphoglucomutase 1 deficiency (<scp>PGM1‐CDG</scp>): Diagnosis, follow‐up, and management Ruqaiah Altassan, Silvia Radenkovic, Andrew C. Edmondson, Rita Barone, Sandra Brasil, Anna Čechová, David Coman, Sarah Donoghue, Kristina Falkenstein, Vanessa dos Reis Ferreira, Carlos R. Ferreira, Agata Fiumara, Rita Francisco, Hudson H. Freeze, Stephanie Grünewald, Tomáš Honzík, Jaak Jaeken, Donna M. Krasnewich, Christina Lam, Joy Lee, Dirk J. Lefeber, Dorinda Marques‐da‐Silva, Carlota Pascoal, Dulce Quelhas, Kimiyo Raymond, Daisy Rymen, Małgorzata Seroczyńska, Mercedes Serrano, Jolanta Sykut‐Cegielska, Christian Thiel, Frederic Tort, Mari‐Anne Vals, Paula A. Videira, Nicol C. Voermans, Peter Witters, Éva Morava
Հրապարակվել է 2020Revisão -
7
Clinical presentation and proteomic signature of patients with <i>TANGO2</i> mutations Nadja Mingirulli, Angela Pyle, Denisa Hathazi, Charlotte L. Alston, Nicolai Kohlschmidt, Gina O’Grady, Leigh B. Waddell, Frances J. Evesson, Sandra B. T. Cooper, Christian Turner, Jennifer Duff, Ana Töpf, Dèlia Yubero, Cristina Jou, A. Nascimento, C. Ortez, Àngels García‐Cazorla, Claudia Groß, María del Mar O’Callaghan, Saikat Santra, M A Preece, Michael Champion, Sergei Korenev, Efsthatia Chronopoulou, Anirban Majumdar, Germaine Pierre, Daniel McArthur, Kyle Thompson, Plácido Navas, Antònia Ribes, Frederic Tort, Agatha Schlüter, Aurora Pujol, Raquel Montero, Geòrgia Sarquella-Brugada, Hanns Lochmüller, C. Jimenez‐Mallebrera, Robert W. Taylor, Rafael Artuch, Janbernd Kirschner, Sarah C. Grünert, Andreas Roos, Rita Horváth
Հրապարակվել է 2019Artigo -
8
Clinical implementation of RNA sequencing for Mendelian disease diagnostics Vicente A. Yépez, Mirjana Gušić, Robert Kopajtich, Christian Mertes, Nicholas H. Smith, Charlotte L. Alston, Rui Ban, Skadi Beblo, Riccardo Berutti, Holger Blessing, Elżbieta Ciara, Felix Distelmaier, Peter Freisinger, Johannes Häberle, Susan J. Hayflick, Maja Hempel, Yulia S. Itkis, Yoshihito Kishita, Thomas Klopstock, Tatiana Krylova, Costanza Lamperti, Dominic Lenz, Christine Makowski, Signe Mosegaard, Michaela Müller, Gerard Muñoz-Pujol, Agnieszka Nadel, Akira Ohtake, Yasushi Okazaki, Elena Procopio, Thomas Schwarzmayr, Joél Smet, Christian Staufner, Sarah L. Stenton, Tim M. Strom, Caterina Terrile, Frederic Tort, Rudy Van Coster, Arnaud Vanlander, Matias Wagner, Manting Xu, Fang Fang, Daniele Ghezzi, Johannes A. Mayr, Dorota Piekutowska‐Abramczuk, Antònia Ribes, Agnès Rötig, Robert W. Taylor, Saskia B. Wortmann, Kei Murayama, Thomas Meitinger, Julien Gagneur, Holger Prokisch
Հրապարակվել է 2022Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Gene
Genetics
Medicine
Cancer research
Immunology
Lymphoma
Molecular biology
Mutation
Biochemistry
Bioinformatics
Enzyme
Human genetics
Internal medicine
Lactic acidosis
Missense mutation
Mitochondrion
Pathology
Phenotype
Respiratory chain
Anaplastic large-cell lymphoma
Anaplastic lymphoma kinase
Antioxidant
Breakpoint
Carcinogenesis
Cell
Cell biology
Chromosomal translocation
Compartment (ship)
Complementation