Results
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4361.
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4362.
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Mutational analysis of OGG1, MYH, MTH1 in FAP, HNPCC and sporadic colorectal cancer patients: R154H OGG1 polymorphism is associated with sporadic colorectal cancer patients. [electronic resource] by
- Kim, I-J
- Ku, J-L
- Kang, H C
- Park, J-H
- Yoon, K-A
- Shin, Y
- Park, H-W
- Jang, S G
- Lim, S-K
- Han, S Y
- Shin, Y-K
- Lee, M R
- Jeong, S-Y
- Shin, H-R
- Lee, J S
- Kim, W-H
- Park, J-G
Producer: 20050223
In:
Human genetics vol. 115
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4363.
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4364.
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4365.
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4366.
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The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations. [electronic resource] by
- Senter, Leigha
- Clendenning, Mark
- Sotamaa, Kaisa
- Hampel, Heather
- Green, Jane
- Potter, John D
- Lindblom, Annika
- Lagerstedt, Kristina
- Thibodeau, Stephen N
- Lindor, Noralane M
- Young, Joanne
- Winship, Ingrid
- Dowty, James G
- White, Darren M
- Hopper, John L
- Baglietto, Laura
- Jenkins, Mark A
- de la Chapelle, Albert
Producer: 20080902
In:
Gastroenterology vol. 135
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4367.
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EPCAM germ line deletions as causes of Lynch syndrome in Spanish patients. [electronic resource] by
- Guarinos, Carla
- Castillejo, Adela
- Barberá, Víctor-Manuel
- Pérez-Carbonell, Lucía
- Sánchez-Heras, Ana-Beatriz
- Segura, Angel
- Guillén-Ponce, Carmen
- Martínez-Cantó, Ana
- Castillejo, María-Isabel
- Egoavil, Cecilia-Magdalena
- Jover, Rodrigo
- Payá, Artemio
- Alenda, Cristina
- Soto, José-Luís
Producer: 20110228
In:
The Journal of molecular diagnostics : JMD vol. 12
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4368.
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4369.
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Comparative effectiveness research in cancer genomics and precision medicine: current landscape and future prospects. [electronic resource] by
- Simonds, Naoko I
- Khoury, Muin J
- Schully, Sheri D
- Armstrong, Katrina
- Cohn, Wendy F
- Fenstermacher, David A
- Ginsburg, Geoffrey S
- Goddard, Katrina A B
- Knaus, William A
- Lyman, Gary H
- Ramsey, Scott D
- Xu, Jianfeng
- Freedman, Andrew N
Producer: 20130916
In:
Journal of the National Cancer Institute vol. 105
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4370.
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Association of a let-7 miRNA binding region of TGFBR1 with hereditary mismatch repair proficient colorectal cancer (MSS HNPCC). [electronic resource] by
- Xicola, Rosa M
- Bontu, Sneha
- Doyle, Brian J
- Rawson, Jamie
- Garre, Pilar
- Lee, Esther
- de la Hoya, Miguel
- Bessa, Xavier
- Clofent, Joan
- Bujanda, Luis
- Balaguer, Francesc
- Castellví-Bel, Sergi
- Alenda, Cristina
- Jover, Rodrigo
- Ruiz-Ponte, Clara
- Syngal, Sapna
- Andreu, Montserrat
- Carracedo, Angel
- Castells, Antoni
- Newcomb, Polly A
- Lindor, Noralane
- Potter, John D
- Baron, John A
- Ellis, Nathan A
- Caldes, Trinidad
- LLor, Xavier
Producer: 20170515
In:
Carcinogenesis vol. 37
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4371.
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4372.
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Clinical impact of molecular genetic diagnosis, genetic counseling, and management of hereditary cancer. Part II: Hereditary nonpolyposis colorectal carcinoma as a model. [electronic resource] by
- Lynch, H T
- Watson, P
- Shaw, T G
- Lynch, J F
- Harty, A E
- Franklin, B A
- Kapler, C R
- Tinley, S T
- Liu, B
- Lerman, C
Producer: 20000120
In:
Cancer vol. 86
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4373.
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Low rate of microsatellite instability in young patients with adenomas: reassessing the Bethesda guidelines. [electronic resource] by
- Velayos, Fernando S
- Allen, Brian A
- Conrad, Peggy G
- Gum, James
- Kakar, Sanjay
- Chung, Daniel C
- Truta, Brindusa
- Sleisenger, Marvin H
- Kim, Young S
- Terdiman, Jonathan P
Producer: 20050601
In:
The American journal of gastroenterology vol. 100
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4374.
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4375.
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Assessing the pathogenicity of MLH1 missense mutations in patients with suspected hereditary nonpolyposis colorectal cancer: correlation with clinical, genetic and functional features. [electronic resource] by
- Belvederesi, Laura
- Bianchi, Francesca
- Loretelli, Cristian
- Gagliardini, Daniela
- Galizia, Eva
- Bracci, Raffaella
- Rosati, Saverio
- Bearzi, Italo
- Viel, Alessandra
- Cellerino, Riccardo
- Porfiri, Emilio
Producer: 20060822
In:
European journal of human genetics : EJHG vol. 14
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4376.
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4377.
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Prevalence of adenomas and hyperplastic polyps in mismatch repair mutation carriers among CAPP2 participants: report by the colorectal adenoma/carcinoma prevention programme 2. [electronic resource] by
- Liljegren, Annelie
- Barker, Gail
- Elliott, Faye
- Bertario, Lucio
- Bisgaard, Marie Luise
- Eccles, Diana
- Evans, Gareth
- Macrae, Finlay
- Maher, Eamonn
- Lindblom, Annika
- Rotstein, Samuel
- Nilsson, Bo
- Mecklin, Jukka-Pekka
- Möslein, Gabriela
- Jass, Jeremy
- Fodde, Riccardo
- Mathers, John
- Burn, John
- Bishop, D Timothy
Producer: 20080813
In:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology vol. 26
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4378.
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4379.
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Functional characterization of MLH1 missense variants identified in Lynch syndrome patients. [electronic resource] by
- Andersen, Sofie Dabros
- Liberti, Sascha Emilie
- Lützen, Anne
- Drost, Mark
- Bernstein, Inge
- Nilbert, Mef
- Dominguez, Mev
- Nyström, Minna
- Hansen, Thomas Van Overeem
- Christoffersen, Janus Wiese
- Jäger, Anne Charlotte
- de Wind, Niels
- Nielsen, Finn Cilius
- Tørring, Pernille M
- Rasmussen, Lene Juel
Producer: 20130416
In:
Human mutation vol. 33
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4380.
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Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery. [electronic resource] by
- Parry, Susan
- Win, Aung Ko
- Parry, Bryan
- Macrae, Finlay A
- Gurrin, Lyle C
- Church, James M
- Baron, John A
- Giles, Graham G
- Leggett, Barbara A
- Winship, Ingrid
- Lipton, Lara
- Young, Graeme P
- Young, Joanne P
- Lodge, Caroline J
- Southey, Melissa C
- Newcomb, Polly A
- Le Marchand, Loïc
- Haile, Robert W
- Lindor, Noralane M
- Gallinger, Steven
- Hopper, John L
- Jenkins, Mark A
Producer: 20110912
In:
Gut vol. 60
Availability: No items available.
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