Results
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32161.
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32162.
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32163.
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32164.
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Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status. [electronic resource] by
- Oliveira, Carla
- Westra, Jantine L
- Arango, Diego
- Ollikainen, Miina
- Domingo, Enric
- Ferreira, Ana
- Velho, Sérgia
- Niessen, Renee
- Lagerstedt, Kristina
- Alhopuro, Pia
- Laiho, Paivi
- Veiga, Isabel
- Teixeira, Manuel R
- Ligtenberg, Marjolijn
- Kleibeuker, Jan H
- Sijmons, Rolf H
- Plukker, John T
- Imai, Kohzoh
- Lage, Pedro
- Hamelin, Richard
- Albuquerque, Cristina
- Schwartz, Simo
- Lindblom, Annika
- Peltomaki, Päivi
- Yamamoto, Hiroyuki
- Aaltonen, Lauri A
- Seruca, Raquel
- Hofstra, Robert M W
Producer: 20050217
In:
Human molecular genetics vol. 13
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32165.
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32166.
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32167.
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RBSP3 (HYA22) is a tumor suppressor gene implicated in major epithelial malignancies. [electronic resource] by
- Kashuba, Vladimir I
- Li, Jingfeng
- Wang, Fuli
- Senchenko, Vera N
- Protopopov, Alexey
- Malyukova, Alena
- Kutsenko, Alexey S
- Kadyrova, Elena
- Zabarovska, Veronika I
- Muravenko, Olga V
- Zelenin, Alexander V
- Kisselev, Lev L
- Kuzmin, Igor
- Minna, John D
- Winberg, Gösta
- Ernberg, Ingemar
- Braga, Eleonora
- Lerman, Michael I
- Klein, George
- Zabarovsky, Eugene R
Producer: 20040610
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 101
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32168.
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MSH2 c.1452-1455delAATG is a founder mutation and an important cause of hereditary nonpolyposis colorectal cancer in the southern Chinese population. [electronic resource] by
- Chan, Tsun Leung
- Chan, Yee Wai
- Ho, Judy W C
- Chan, Celine
- Chan, Annie S Y
- Chan, Emily
- Lam, Polly W Y
- Tse, Chun Wah
- Lee, Kam Cheong
- Lau, Chi Waii
- Gwi, Elaine
- Leung, Suet Yi
- Yuen, Siu Tsan
Producer: 20040603
In:
American journal of human genetics vol. 74
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32169.
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32170.
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32171.
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Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis. Molecular genetic study. [electronic resource] by
- Ivanov, D
- Kirov, G
- Norton, N
- Williams, H J
- Williams, N M
- Nikolov, I
- Tzwetkova, R
- Stambolova, S M
- Murphy, K C
- Toncheva, D
- Thapar, A
- O'Donovan, M C
- Owen, M J
Producer: 20040116
In:
The British journal of psychiatry : the journal of mental science vol. 183
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32172.
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Genome-wide scan for prostate cancer susceptibility genes using families from the University of Michigan prostate cancer genetics project finds evidence for linkage on chromosome 17 near BRCA1. [electronic resource] by
- Lange, Ethan M
- Gillanders, Elizabeth M
- Davis, Cralen C
- Brown, W Mark
- Campbell, Joel K
- Jones, MaryPat
- Gildea, Derek
- Riedesel, Erica
- Albertus, Julie
- Freas-Lutz, Diana
- Markey, Carol
- Giri, Veda
- Dimmer, Jennifer Beebe
- Montie, James E
- Trent, Jeffrey M
- Cooney, Kathleen A
Producer: 20040106
In:
The Prostate vol. 57
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32173.
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32174.
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32175.
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Frequent p16-independent inactivation of p14ARF in human melanoma. [electronic resource] by
- Freedberg, Daniel E
- Rigas, Sushila H
- Russak, Julie
- Gai, Weiming
- Kaplow, Margarita
- Osman, Iman
- Turner, Faye
- Randerson-Moor, Juliette A
- Houghton, Alan
- Busam, Klaus
- Timothy Bishop, D
- Bastian, Boris C
- Newton-Bishop, Julia A
- Polsky, David
Producer: 20080702
In:
Journal of the National Cancer Institute vol. 100
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32176.
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A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity. [electronic resource] by
- Conte, Maria Luisa
- Bertoli-Avella, Aida M
- de Graaf, Bianca M
- Punzo, Francesca
- Lama, Giuliana
- La Manna, Angela
- Grassia, Carolina
- Rambaldi, Pier Francesco
- Oostra, Ben A
- Perrotta, Silverio
Producer: 20080626
In:
Pediatric nephrology (Berlin, Germany) vol. 23
Availability: No items available.
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32177.
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TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. [electronic resource] by
- Sreedharan, Jemeen
- Blair, Ian P
- Tripathi, Vineeta B
- Hu, Xun
- Vance, Caroline
- Rogelj, Boris
- Ackerley, Steven
- Durnall, Jennifer C
- Williams, Kelly L
- Buratti, Emanuele
- Baralle, Francisco
- de Belleroche, Jacqueline
- Mitchell, J Douglas
- Leigh, P Nigel
- Al-Chalabi, Ammar
- Miller, Christopher C
- Nicholson, Garth
- Shaw, Christopher E
Producer: 20080402
In:
Science (New York, N.Y.) vol. 319
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32178.
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Detection of urothelial bladder cancer cells in voided urine can be improved by a combination of cytology and standardized microsatellite analysis. [electronic resource] by
- Wild, Peter J
- Fuchs, Thomas
- Stoehr, Robert
- Zimmermann, Dieter
- Frigerio, Simona
- Padberg, Barbara
- Steiner, Inbal
- Zwarthoff, Ellen C
- Burger, Maximilian
- Denzinger, Stefan
- Hofstaedter, Ferdinand
- Kristiansen, Glen
- Hermanns, Thomas
- Seifert, Hans-Helge
- Provenzano, Maurizio
- Sulser, Tullio
- Roth, Volker
- Buhmann, Joachim M
- Moch, Holger
- Hartmann, Arndt
Producer: 20090908
In:
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology vol. 18
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32179.
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Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia. [electronic resource] by
- Kurian, Manju A
- Zhen, Juan
- Cheng, Shu-Yuan
- Li, Yan
- Mordekar, Santosh R
- Jardine, Philip
- Morgan, Neil V
- Meyer, Esther
- Tee, Louise
- Pasha, Shanaz
- Wassmer, Evangeline
- Heales, Simon J R
- Gissen, Paul
- Reith, Maarten E A
- Maher, Eamonn R
Producer: 20090724
In:
The Journal of clinical investigation vol. 119
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32180.
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A nosocomial outbreak of Candida parapsilosis in southern Sweden verified by genotyping. [electronic resource] by
- Brillowska-Dabrowska, Anna
- Schön, T
- Pannanusorn, S
- Lönnbro, N
- Bernhoff, L
- Bonnedal, J
- Haggstrom, J
- Wistedt, A
- Fernandez, V
- Arendrup, M C
Producer: 20090406
In:
Scandinavian journal of infectious diseases vol. 41
Availability: No items available.
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