EPCAM deletions, Lynch syndrome, and cancer risk

被引：13
|
作者：
Lynch, Henry T. [1 ]
Lynch, Jane F. [1 ]
Snyder, Carrie L. [1 ]
Riegert-Johnson, Douglas [2 ]
机构：
[1] Creighton Univ, Dept Prevent Med & Publ Hlth, Omaha, NE 68178 USA
[2] Mayo Clin, Jacksonville, FL 32224 USA
来源：
LANCET ONCOLOGY | 2011年 / 12卷 / 01期
关键词：
FAMILIES; TACSTD1;
D O I：
10.1016/S1470-2045(10)70291-6
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
引用
收藏
页码：5 / 6
页数：2
相关论文
共 50 条
  • [1] Recurrence and Variability of Germline EPCAM Deletions in Lynch Syndrome
    Kuiper, Roland P.
    Vissers, Lisenka E. L. M.
    Venkatachalam, Ramprasath
    Bodmer, Danielle
    Hoenselaar, Eveline
    Goossens, Monique
    Haufe, Aline
    Kamping, Eveline
    Niessen, Renee C.
    Hogervorst, Frans B. L.
    Gille, Johan J. P.
    Redeker, Bert
    Tops, Carli M. J.
    van Gijn, Marielle E.
    van den Ouweland, Ans M. W.
    Rahner, Nils
    Steinke, Verena
    Kahl, Philip
    Holinski-Feder, Elke
    Morak, Monika
    Kloor, Matthias
    Stemmler, Susanne
    Betz, Beate
    Hutter, Pierre
    Bunyan, David J.
    Syngal, Sapna
    Culver, Julie O.
    Graham, Tracy
    Chan, Tsun L.
    Nagtegaal, Iris D.
    van Krieken, J. Han J. M.
    Schackert, Hans K.
    Hoogerbrugge, Nicoline
    van Kessel, Ad Geurts
    Ligtenberg, Marjolijn J. L.
    [J]. HUMAN MUTATION, 2011, 32 (04) : 407 - 414
  • [2] Do EPCAM full deletions have a role in Lynch Syndrome?
    Sonnini, Elena
    Cordisco, Emanuela Lucci
    Orteschi, Daniela
    Pomponi, Maria Grazia
    Amenta, Simona
    Rivera, Daniela
    Gismondi, Viviana
    Varesco, Liliana
    Genuardi, Maurizio
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 590 - 591
  • [3] PHENOTYPE OF TWO ITALIAN LYNCH SYNDROME FAMILIES WITH EPCAM DELETIONS
    Tabuso, M.
    Canzonieri, V.
    Viel, A.
    Belluco, C.
    Cannizzaro, R.
    Fornasarig, M.
    [J]. DIGESTIVE AND LIVER DISEASE, 2014, 46 : S102 - S102
  • [4] Germline deletions in the EPCAM gene as a cause of Lynch syndrome - literature review
    Tutlewska, Katarzyna
    Lubinski, Jan
    Kurzawski, Grzegorz
    [J]. HEREDITARY CANCER IN CLINICAL PRACTICE, 2013, 11
  • [5] EPCAM Germ Line Deletions as Causes of Lynch Syndrome in Spanish Patients
    Guarinos, Carla
    Castillejo, Adela
    Barbera, Victor-Manuel
    Perez-Carbonell, Lucia
    Sanchez-Heras, Ana-Beatriz
    Segura, Angel
    Guillen-Ponce, Carmen
    Martinez-Canto, Ana
    Castillejo, Maria-Isabel
    Egoavil, Cecilia-Magdalena
    Jover, Rodrigo
    Paya, Artemio
    Alenda, Cristina
    Soto, Jose-Luis
    [J]. JOURNAL OF MOLECULAR DIAGNOSTICS, 2010, 12 (06): : 765 - 770
  • [6] Germline deletions in the EPCAM gene as a cause of Lynch syndrome – literature review
    Katarzyna Tutlewska
    Jan Lubinski
    Grzegorz Kurzawski
    [J]. Hereditary Cancer in Clinical Practice, 11
  • [7] Germline Hypermethylation of MLH1 and EPCAM Deletions Are a Frequent Cause of Lynch Syndrome
    Niessen, Renee C.
    Hofstra, Robert M. W.
    Westers, Helga
    Ligtenberg, Marjolijn J. L.
    Kooi, Krista
    Jager, Paul O. J.
    de Groote, Marloes L.
    Dijkhuizen, Trijnie
    Olderode-Berends, Maran J. W.
    Hollema, Harry
    Kleibeuker, Jan H.
    Sijmons, Rolf H.
    [J]. GENES CHROMOSOMES & CANCER, 2009, 48 (08): : 737 - 744
  • [8] Frequency of Deletions of EPCAM (TACSTD1) in MSH2-Associated Lynch Syndrome Cases
    Rumilla, Kandelaria
    Schowalter, Karen V.
    Lindor, Noralane M.
    Thomas, Brittany C.
    Mensink, Kara A.
    Gallinger, Steven
    Holter, Spring
    Newcomb, Polly A.
    Potter, John D.
    Jenkins, Mark A.
    Hopper, John L.
    Long, Tiffany I.
    Weisenberger, Daniel J.
    Haile, Robert W.
    Casey, Graham
    Laird, Peter W.
    Le Marchand, Loic
    Thibodeau, Stephen N.
    [J]. JOURNAL OF MOLECULAR DIAGNOSTICS, 2011, 13 (01): : 93 - 99
  • [9] Cancer risk in Lynch Syndrome
    Barrow, Emma
    Hill, James
    Evans, D. Gareth
    [J]. FAMILIAL CANCER, 2013, 12 (02) : 229 - 240
  • [10] Cancer risk in Lynch Syndrome
    Emma Barrow
    James Hill
    D. Gareth Evans
    [J]. Familial Cancer, 2013, 12 : 229 - 240
12345