Resultados de procura - Anne‐Marie Gerdes
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Toward mechanistic models for genotype–phenotype correlations in phenylketonuria using protein stability calculations por Rasmus Scheller, Amelie Stein, Sofie V. Nielsen, Frederikke I. Marin, Anne‐Marie Gerdes, Miriam Di Marco, Elena Papaleo, Kresten Lindorff‐Larsen, Rasmus Hartmann‐Petersen
Publicado 2019Artigo -
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A BAP1 Mutation in a Danish Family Predisposes to Uveal Melanoma and Other Cancers por Lauren G. Aoude, Karin Wadt, Anders Bojesen, Dorthe Gylling Crüger, Åke Borg, Jeffrey M. Trent, Kevin M. Brown, Anne‐Marie Gerdes, Göran Jönsson, Nicholas K. Hayward
Publicado 2013Artigo -
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A cryptic <scp><i>BAP1</i></scp> splice mutation in a family with uveal and cutaneous melanoma, and paraganglioma por Karin Wadt, Jiyeon Choi, Joon‐Yong Chung, Jens Folke Kiilgaard, Steffen Heegaard, Krzysztof T. Drzewiecki, Jeffrey M. Trent, Stephen M. Hewitt, Nicholas K. Hayward, Anne‐Marie Gerdes, Kevin M. Brown
Publicado 2012Artigo -
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Classifications within Molecular Subtypes Enables Identification of BRCA1/BRCA2 Mutation Carriers by RNA Tumor Profiling por Martin J. Larsen, Torben A. Kruse, Qihua Tan, Anne‐Vibeke Lænkholm, Martin Bak, Anne E. Lykkesfeldt, Kristina P. Sørensen, Thomas van Overeem Hansen, Bent Ejlertsen, Anne‐Marie Gerdes, Mads Thomassen
Publicado 2013Artigo -
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Computational and cellular studies reveal structural destabilization and degradation of MLH1 variants in Lynch syndrome por Amanda B. Abildgaard, Amelie Stein, Sofie V. Nielsen, Katrine Schultz-Knudsen, Elena Papaleo, Amruta Shrikhande, Eva R. Hoffmann, Inge Bernstein, Anne‐Marie Gerdes, Masanobu Takahashi, Chikashi Ishioka, Kresten Lindorff‐Larsen, Rasmus Hartmann‐Petersen
Publicado 2019Artigo -
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Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium ‘Care for CMMRD’ (C4CMMRD) por Katharina Wimmer, Christian P. Kratz, Hans F. A. Vasen, Olivier Caron, Chrystelle Colas, Natacha Entz‐Werlé, Anne‐Marie Gerdes, Yael Goldberg, Denisa Ilenčíková, Martine Muleris, Alex Duval, Noémie Lavoine, Clara Ruíz-Ponte, Irene Slavc, B Burkhardt, Laurence Brugières
Publicado 2014Revisão -
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Germline TERT promoter mutations are rare in familial melanoma por Mark Harland, Mia Petljak, Carla Daniela Robles‐Espinoza, Zhihao Ding, Nelleke A. Gruis, Remco van Doorn, Karen A. Pooley, Alison M. Dunning, Lauren G. Aoude, Karin Wadt, Anne‐Marie Gerdes, Kevin M. Brown, Nicholas K. Hayward, Julia Newton‐Bishop, David J. Adams, D. Timothy Bishop
Publicado 2015Artigo -
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Deep sequencing of uveal melanoma identifies a recurrent mutation in <i>PLCB4</i> por Peter A. Johansson, Lauren G. Aoude, Karin Wadt, William Glasson, Sunil Warrier, Alex W. Hewitt, Jens Folke Kiilgaard, Steffen Heegaard, Tim Isaacs, Maria Franchina, Christian Ingvar, Tersia Vermeulen, Kevin J. Whitehead, Christopher Schmidt, Jane M. Palmer, Judith Symmons, Anne‐Marie Gerdes, Göran Jönsson, Nicholas K. Hayward
Publicado 2015Artigo -
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Oral Contraceptives and Breast Cancer Risk in the International <i>BRCA1/2</i> Carrier Cohort Study: A Report From EMBRACE, GENEPSO, GEO-HEBON, and the IBCCS Collaborating Group por Richard M. Brohet, David E. Goldgar, Douglas F. Easton, Antonis C. Antoniou, Nadine Andrieu, Jenny Chang‐Claude, Susan Peock, Rosalind A. Eeles, Margaret Cook, Carol Chu, Catherine Noguès, Christine Lasset, Pascaline Berthet, Hanne Meijers‐Heijboer, Anne‐Marie Gerdes, Håkan Olsson, Miguel de la Hoya, Flora E. van Leeuwen, Matti A. Rookus
Publicado 2007Artigo -
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Cancer Prevention with Resistant Starch in Lynch Syndrome Patients in the CAPP2-Randomized Placebo Controlled Trial: Planned 10-Year Follow-up por John C. Mathers, Faye Elliott, Finlay Macrae, Jukka‐Pekka Mecklin, Gabriela Möslein, Fiona E. McRonald, Lucio Bertario, D. Gareth Evans, Anne‐Marie Gerdes, Judy Ho, Annika Lindblom, Patrick J. Morrison, Jem Rashbass, Raj Ramesar, Toni T. Seppälä, Huw Thomas, Harsh Sheth, Kirsi Pylvänäinen, Lynn Reed, Gillian M. Borthwick, D. Timothy Bishop, John Burn
Publicado 2022Artigo -
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Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromes por Anna Byrjalsen, Thomas van Overeem Hansen, Ulrik Kristoffer Stoltze, Mana M. Mehrjouy, Nanna Moeller Barnkob, Lisa Lyngsie Hjalgrim, René Mathiasen, Charlotte Kvist Lautrup, Pernille A. Gregersen, Henrik Hasle, Peder Skov Wehner, Ruta Tuckuviene, Peter Wad Sackett, Adrian Otamendi Laspiur, Maria Rossing, Rasmus L. Marvig, Niels Tommerup, Tina Elisabeth Olsen, David Scheie, Ramneek Gupta, Anne–Marie Gerdes, Kjeld Schmiegelow, Karin Wadt
Publicado 2020Artigo -
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Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial por John C. Mathers, Mohammad Movahedi, Finlay Macrae, Jukka‐Pekka Mecklin, Gabriela Möslein, Sylviane Olschwang, Diana Eccles, D. Gareth Evans, Eamonn R. Maher, Lucio Bertario, Marie-Luise Bisgaard, Malcolm G. Dunlop, Judy Ho, Shirley Hodgson, Annika Lindblom, Jan Lubiński, Patrick J. Morrison, Victoria Murday, Raj Ramesar, Lucy Side, Rodney J. Scott, Huw Thomas, Hans F. A. Vasen, Anne‐Marie Gerdes, G Barker, Gillian Crawford, Faye Elliott, Kirsi Pylvänäinen, Juul Wijnen, Riccardo Fodde, Henry T. Lynch, D. Timothy Bishop, John Burn
Publicado 2012Artigo -
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Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial por John Burn, Anne‐Marie Gerdes, Finlay Macrae, Jukka‐Pekka Mecklin, Gabriela Möslein, Sylviane Olschwang, Diana Eccles, D. Gareth Evans, Eamonn R. Maher, Lucio Bertario, Marie-Luise Bisgaard, Malcolm G. Dunlop, Judy Ho, Shirley V. Hodgson, Annika Lindblom, Jan Lubiński, Patrick J. Morrison, Victoria Murday, Raj Ramesar, Lucy Side, Rodney J. Scott, Huw Thomas, Hans F. A. Vasen, G Barker, Gillian Crawford, Faye Elliott, Mohammad Movahedi, Kirsi Pylvänäinen, Juul Wijnen, Riccardo Fodde, Henry T. Lynch, John C. Mathers, D. Timothy Bishop
Publicado 2011Artigo
Ferramentas de procura:
Materias Relacionadas
Medicine
Cancer
Internal medicine
Biology
Genetics
Gene
Oncology
Mutation
Breast cancer
Germline mutation
Cancer research
Gynecology
Genotype
Germline
Ovarian cancer
Allele
Colorectal cancer
DNA mismatch repair
Environmental health
Population
Single-nucleotide polymorphism
BRCA2 Protein
Confidence interval
Lynch syndrome
Melanoma
Cohort
Missense mutation
Pathology
Physics
Blood pressure