Resultados de procura - Deepak Vangala

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  1. 1
    Optical Genome Mapping for Cytogenetic Diagnostics in AML

    Optical Genome Mapping for Cytogenetic Diagnostics in AML por Verena Nilius‐Eliliwi, Wanda M. Gerding, Roland Schroers, Huu Phuc Nguyen, Deepak Vangala

    Publicado 2023
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  2. 2
    Optical Genome Mapping Reveals and Characterizes Recurrent Aberrations and New Fusion Genes in Adult ALL

    Optical Genome Mapping Reveals and Characterizes Recurrent Aberrations and New Fusion Genes in Adult ALL por Lisa-Marie Vieler, Verena Nilius‐Eliliwi, Roland Schroers, Deepak Vangala, Huu Phuc Nguyen, Wanda M. Gerding

    Publicado 2023
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  3. 3
    Screening and surveillance in hereditary gastrointestinal cancers: Recommendations from the European Society of Digestive Oncology (ESDO) expert discussion at the 20th European Society for Medical Oncology (ESMO)/World Congress on Gastrointestinal Cancer, Barcelona, June 2018

    Screening and surveillance in hereditary gastrointestinal cancers: Recommendations from the European Society of Digestive Oncology (ESDO) expert discussion at the 20th European Soc... por Deepak Vangala, Estelle Cauchin, Judith Balmañà, Lucjan Wyrwicz, Eric Van Cutsem, Ulrich Güller, Antoni Castells, Fátima Carneiro, Pascal Hammel, Michel Ducreux, Jean‐Luc Van Laethem, Tamara Matysiak‐Budnik, Wolff Schmiegel

    Publicado 2018
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  4. 4
    Optical genome mapping reveals additional prognostic information compared to conventional cytogenetics in <scp>AML</scp>/<scp>MDS</scp> patients

    Optical genome mapping reveals additional prognostic information compared to conventional cytogenetics in <scp>AML</scp>/<scp>MDS</scp> patients por Wanda M. Gerding, Marco Tembrink, Verena Nilius‐Eliliwi, Thomas Mika, Fotios Dimopoulos, Swetlana Ladigan‐Badura, Matthias Eckhardt, Michael Pohl, Max Wünnenberg, Pakhshan Farshi, Peter Reimer, Roland Schroers, Huu Phuc Nguyen, Deepak Vangala

    Publicado 2022
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  5. 5
    Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: a prospective cohort study

    Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: a prospective cohort study por Karolin Bucksch, Silke Zachariae, Stefan Aretz, Reinhard Büttner, Elke Holinski‐Feder, Stefanie Holzapfel, Robert Hüneburg, Matthias Kloor, Magnus von Knebel Doeberitz, Monika Morak, Gabriela Möslein, Jacob Nattermann, Claudia Perne, Nils Rahner, Wolff Schmiegel, Karsten Schulmann, Verena Steinke‐Lange, Christian P. Strassburg, Deepak Vangala, Jürgen Weitz, Markus Loeffler, Christoph Engel

    Publicado 2020
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  6. 6
    Combined inhibition of BET family proteins and histone deacetylases as a potential epigenetics-based therapy for pancreatic ductal adenocarcinoma

    Combined inhibition of BET family proteins and histone deacetylases as a potential epigenetics-based therapy for pancreatic ductal adenocarcinoma por Paweł K. Mazur, Alexander Herner, Stephano S. Mello, Matthias Wirth, Simone Hausmann, Francisco J. Sánchez‐Rivera, Shane Lofgren, Timo Kuschma, Stephan A. Hahn, Deepak Vangala, Marija Trajkovic‐Arsic, Aayush Gupta, Irina Heid, Peter B. Noël, Rickmer Braren, Mert Erkan, Jörg Kleeff, Bence Sipos, Leanne C. Sayles, Mathias Heikenwälder, Elisabeth Heßmann, Volker Ellenrieder, Iréne Esposito, Tyler Jacks, James E. Bradner, Purvesh Khatri, E. Alejandro Sweet‐Cordero, Laura D. Attardi, Roland M. Schmid, Guenter Schneider, Julien Sage, Jens T. Siveke

    Publicado 2015
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  7. 7
    Blood‐based detection of <i><scp>RAS</scp></i> mutations to guide anti‐<scp>EGFR</scp> therapy in colorectal cancer patients: concordance of results from circulating tumor <scp>DNA</scp> and tissue‐based <i><scp>RAS</scp></i> testing

    Blood‐based detection of <i><scp>RAS</scp></i> mutations to guide anti‐<scp>EGFR</scp> therapy in colorectal cancer patients: concordance of results from circulating tumor <scp>DNA... por Wolff Schmiegel, Rodney J. Scott, S Dooley, Wendy Lewis, Cliff Meldrum, Peter Pockney, Brian Draganic, S. Stephen, Chelsee Hewitt, Hazel Philimore, Amanda Lucas, E. Shi, Kateh Namdarian, Timmy Chan, Danilo Acosta, Su Ping‐Chang, Andrea Tannapfel, Anke Reinacher‐Schick, Waldemar Uhl, Christian Teschendorf, Heiner Wolters, J. Stern, Richard Viebahn, Helmut Friess, Klaus‐Peter Janssen, Ulrich Nitsche, Julia Slotta‐Huspenina, Michael Pohl, Deepak Vangala, Alexander Baraniskin, Barbara Dockhorn‐Dworniczak, S. Hegewisch-Becker, Philippe Ronga, Daniel L. Edelstein, Frederick S. Jones, Stephan A. Hahn, Stephen B. Fox

    Publicado 2017
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  8. 8
    Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome

    Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome por Christoph Engel, Aysel Ahadova, Toni T. Seppälä, Stefan Aretz, Marloes Bigirwamungu-Bargeman, Hendrik Bläker, Karolin Bucksch, Reinhard Büttner, Wouter T. de Vos tot Nederveen Cappel, Volker Endris, Elke Holinski‐Feder, Stefanie Holzapfel, Robert Hüneburg, Maarten Jacobs, Jan J. Koornstra, Alexandra M. J. Langers, Anna Lepistö, Monika Morak, Gabriela Möslein, Païvi Peltomäki, Kirsi Pylvänäinen, Nils Rahner, Laura Renkonen‐Sinisalo, Karsten Schulmann, Verena Steinke‐Lange, Albrecht Stenzinger, Christian P. Strassburg, Paul C. van de Meeberg, Mariëtte van Kouwen, Monique E. van Leerdam, Deepak Vangala, J. van der Vecht, Marie–Louise Verhulst, Magnus von Knebel Doeberitz, Jürgen Weitz, Silke Zachariae, Markus Loeffler, Jukka‐Pekka Mecklin, Matthias Kloor, Hans F. A. Vasen

    Publicado 2020
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  9. 9
    Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report

    Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report por Toni T. Seppälä, Aysel Ahadova, Mev Dominguez–Valentin, Finlay Macrae, D. Gareth Evans, Christina Therkildsen, Julian R. Sampson, Rodney J. Scott, John Burn, Gabriela Möslein, Inge Bernstein, Elke Holinski‐Feder, Kirsi Pylvänäinen, Laura Renkonen‐Sinisalo, Anna Lepistö, Charlotte Kvist Lautrup, Annika Lindblom, John‐Paul Plazzer, Ingrid Winship, Douglas Tjandra, Lior H. Katz, Stefan Aretz, Robert Hüneburg, Stefanie Holzapfel, Karl Heinimann, Adriana Della Valle, Florencia Neffa, Nathan Gluck, Wouter H. de Vos tot Nederveen Cappel, Hans F. A. Vasen, Monika Morak, Verena Steinke‐Lange, Christoph Engel, Nils Rahner, Wolff Schmiegel, Deepak Vangala, Huw Thomas, Kate Green, Fiona Lalloo, Emma J. Crosbie, James Hill, Gabriel Capellà, Marta Pineda, Matilde Navarro, Ignacio Blanco, Sanne W. ten Broeke, Maartje Nielsen, Ken Ljungmann, Sigve Nakken, Noralane M. Lindor, Ian M. Frayling, Eivind Hovig, Lone Sunde, Matthias Kloor, Jukka‐Pekka Mecklin, Mette Kalager, Pål Møller

    Publicado 2019
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  10. 10
    Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

    Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database por Mev Dominguez–Valentin, Julian R. Sampson, Toni T. Seppälä, Sanne W. ten Broeke, John‐Paul Plazzer, Sigve Nakken, Christoph Engel, Stefan Aretz, Mark A. Jenkins, Lone Sunde, Inge Bernstein, Gabriel Capellà, Francesc Balaguer, Huw Thomas, D. Gareth Evans, John Burn, Marc S. Greenblatt, Eivind Hovig, Wouter H. de Vos tot Nederveen Cappel, Rolf H. Sijmons, Lucio Bertario, Maria Grazia Tibiletti, Giulia Martina Cavestro, Annika Lindblom, Adriana Della Valle, Francisco López‐Köstner, Nathan Gluck, Lior H. Katz, Karl Heinimann, Carlos Vaccaro, Reinhard Büttner, Heike Görgens, Elke Holinski‐Feder, Monika Morak, Stefanie Holzapfel, Robert Hüneburg, Magnus von Knebel Doeberitz, Markus Loeffler, Nils Rahner, Hans K. Schackert, Verena Steinke‐Lange, Wolff Schmiegel, Deepak Vangala, Kirsi Pylvänäinen, Laura Renkonen‐Sinisalo, John L. Hopper, Aung Ko Win, Robert W. Haile, Noralane M. Lindor, Steven Gallinger, Loı̈c Le Marchand, Polly A. Newcomb, Jane C. Figueiredo, Stephen N. Thibodeau, Karin Wadt, Christina Therkildsen, Henrik Okkels, Zohreh Ketabi, Leticia Moreira, Ariadna Sánchez, Miquel Serra‐Burriel, Marta Pineda, Matilde Navarro, Ignacio Blanco, Kate Green, Fiona Lalloo, Emma J. Crosbie, James Hill, Oliver G. Denton, Ian M. Frayling, Einar Andreas Rødland, Hans F. A. Vasen, Miriam Mints, Florencia Neffa, Patricia Esperón, Karin Álvarez, Revital Kariv, Guy Rosner, Tamara Alejandra Piñero, María Laura González, Pablo Kalfayan, Douglas Tjandra, Ingrid Winship, Finlay Macrae, Gabriela Möslein, Jukka‐Pekka Mecklin, Maartje Nielsen, Pål Møller

    Publicado 2019
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  11. 11
    Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database

    Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospec... por Mev Dominguez–Valentin, Saskia Haupt, Toni T. Seppälä, Julian R. Sampson, Lone Sunde, Inge Bernstein, Mark A. Jenkins, Christoph Engel, Stefan Aretz, Maartje Nielsen, Gabriel Capellà, Francesc Balaguer, D. Gareth Evans, John Burn, Elke Holinski‐Feder, Lucio Bertario, Bernardo Bonanni, Annika Lindblom, Zohar Levi, Finlay Macrae, Ingrid Winship, John‐Paul Plazzer, Rolf H. Sijmons, Luigi Laghi, Adriana Della Valle, Karl Heinimann, Tadeusz Dębniak, Robert Fruscio, Francisco Lopez-Koestner, Karin Alvarez-Valenzuela, Lior H. Katz, Ido Laish, E Vainer, Carlos Vaccaro, Dirce Maria Carraro, Kevin Monahan, Elizabeth Half, Áine Stakelum, D. C. Winter, Rory Kennelly, Nathan Gluck, Harsh Sheth, Naim Abu‐Freha, Marc S. Greenblatt, Bernard Rossi, Mábel Bohórquez, Giulia Martina Cavestro, Leonardo S. Lino‐Silva, Karoline Horisberger, Maria Grazia Tibiletti, Ivana do Nascimento, Huw Thomas, Norma Rossi, Leandro Apolinário da Silva, Attila Zaránd, Juan Ruiz‐Bañobre, Vincent Heuveline, Jukka‐Pekka Mecklin, Kirsi Pylvänäinen, Laura Renkonen‐Sinisalo, Anna Lepistö, Païvi Peltomäki, Christina Therkildsen, Mia Gebauer Madsen, Stefan Kobbelgaard Burgdorf, John L. Hopper, Aung Ko Win, Robert W. Haile, Noralane M. Lindor, Steven Gallinger, Loı̈c Le Marchand, Polly A. Newcomb, Jane C. Figueiredo, Daniel D. Buchanan, Stephen N. Thibodeau, Magnus von Knebel Doeberitz, Markus Loeffler, Nils Rahner, Evelin Schröck, Verena Steinke‐Lange, Wolff Schmiegel, Deepak Vangala, Claudia Perne, Robert Hüneburg, Silke Redler, Reinhard Büttner, Jürgen Weitz, Marta Pineda, Núria Dueñas, Joan Brunet, Leticia Moreira, Ariadna Sánchez, Eivind Hovig, Sigve Nakken, Kate Green, Fiona Lalloo, James Hill, Emma J. Crosbie, Miriam Mints, Yael Goldberg

    Publicado 2023
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  12. 12
    Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

    Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium por Pål Møller, Toni T. Seppälä, James G. Dowty, Saskia Haupt, Mev Dominguez–Valentin, Lone Sunde, Inge Bernstein, Christoph Engel, Stefan Aretz, Maartje Nielsen, Gabriel Capellà, D. Gareth Evans, John Burn, Elke Holinski‐Feder, Lucio Bertario, Bernardo Bonanni, Annika Lindblom, Zohar Levi, Finlay Macrae, Ingrid Winship, John‐Paul Plazzer, Rolf H. Sijmons, Luigi Laghi, Adriana Della Valle, Karl Heinimann, Elizabeth Half, Francisco Lopez-Koestner, Karin Alvarez-Valenzuela, Rodney J. Scott, Lior H. Katz, Ido Laish, E Vainer, Carlos Vaccaro, Dirce Maria Carraro, Nathan Gluck, Naim Abu‐Freha, Áine Stakelum, Rory Kennelly, D. C. Winter, Bernard Rossi, Marc S. Greenblatt, Mábel Bohórquez, Harsh Sheth, Maria Grazia Tibiletti, Leonardo S. Lino‐Silva, Karoline Horisberger, Carmen Portenkirchner, Ivana do Nascimento, Norma Rossi, Leandro Apolinário da Silva, Huw Thomas, Attila Zaránd, Jukka‐Pekka Mecklin, Kirsi Pylvänäinen, Laura Renkonen‐Sinisalo, Anna Lepistö, Païvi Peltomäki, Christina Therkildsen, Lars Joachim Lindberg, Ole Thorlacius‐Ussing, Magnus von Knebel Doeberitz, Markus Loeffler, Nils Rahner, Verena Steinke‐Lange, Wolff Schmiegel, Deepak Vangala, Claudia Perne, Robert Hüneburg, Aı́da Falcón de Vargas, Andrew Latchford, Anne‐Marie Gerdes, A Bäckman, Carmen Guillén‐Ponce, Carrie Snyder, Charlotte Kvist Lautrup, David J. Amor, Edenir Inêz Palmero, Elena M. Stoffel, Floor A.M. Duijkers, Michael J. Hall, Heather Hampel, Heinric Williams, Henrik Okkels, Jan Lubiński, Jeanette C. Reece, Joanne Ngeow, José G. Guillem, Julie Arnold, Karin Wadt, Kevin Monahan, Leigha Senter, Lene Juel Rasmussen, Liselotte P. van Hest, Luigi Ricciardiello, Maija Kohonen‐Corish, Marjolijn J. L. Ligtenberg, Melissa C. Southey, Melyssa Aronson, Mohd Nizam Zahary, N. Jewel Samadder

    Publicado 2022
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