BAP1 germline mutations in Finnish uveal melanoma patients

被引：0
|
作者：
Turunen, J. [1 ,2 ]
Markkinen, S. [2 ]
Wilska, R. [1 ]
Muona, M. [2 ,3 ]
Raivio, V. [1 ]
Tall, M. [1 ]
Lindh, S. [2 ]
Lehesjoki, A. E. [2 ,4 ,5 ]
Kivela, T. [1 ]
机构：
[1] Univ Helsinki, Cent Hosp, Dept Ophthalmol, Helsinki, Finland
[2] Folkhalsan Inst Genet, Helsinki, Finland
[3] Univ Helsinki, Inst Mol Med Finland, Helsinki, Finland
[4] Univ Helsinki, Neurosci Ctr, Helsinki, Finland
[5] Univ Helsinki, Res Programs Unit, Mol Neurol, Helsinki, Finland
来源：
ACTA OPHTHALMOLOGICA | 2014年 / 92卷
关键词：
D O I：
10.1111/j.1755-3768.2014.4242.x
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
4242
引用
收藏
页数：3
相关论文
共 50 条
  • [21] BAP1 mutations are associated with metastasis in polyploid uveal melanoma
    Verdijk, R. M.
    Yavuzyigitoglu, S.
    Mensink, H. W.
    Vaarwater, J.
    Naus, N. C.
    Bruggenwirth, H. T.
    Paridaens, D.
    de Klein, A.
    Kilic, E.
    VIRCHOWS ARCHIV, 2016, 469 : S10 - S10
  • [22] Lack of BAP1 germline gene mutation in patients with early onset uveal melanoma
    Binkley, Elaine Michele
    Cebulla, Colleen M.
    Pilarski, Robert
    Massengill, James B.
    Marino, Meghan J.
    Singh, Arun D.
    Abdel-Rahman, Mohamed H.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2014, 55 (13)
  • [23] Population-based analysis of BAP1 germline variations in patients with uveal melanoma
    Repo, Pauliina
    Jarvinen, Reetta-Stiina
    Jantti, Johannes E.
    Markkinen, Salla
    Tall, Martin
    Raivio, Virpi
    Turunen, Joni A.
    Kivela, Tero T.
    HUMAN MOLECULAR GENETICS, 2019, 28 (14) : 2415 - 2426
  • [24] Germline mutations in BAP1 predispose to melanocytic nevi and melanoma
    Wiesner, Thomas
    Obenauf, Anna
    Murali, Rajmohan
    Fried, Isabella
    Griewank, Klaus
    Ulz, Peter
    Windpassinger, Christian
    Loy, Shea
    Wackernagel, Werner
    Wolf, Ingrid
    Becker, Juergen
    Viale, Agnes
    Lash, Alex
    Pirun, Mono
    Socci, Nick
    Ruetten, Arno
    Palmedo, Gabrielle
    Ott, Arthur
    Abramson, David
    Offit, Kenneth
    Cerroni, Lorenzo
    Kutzner, Heinz
    Bastian, Boris
    Speicher, Michael
    CANCER RESEARCH, 2011, 71
  • [25] Population-based analysis of germline variations in the BAP1 gene in patients with uveal melanoma
    Repo, P. E.
    Jarvinen, R.
    Jantti, J. E.
    Markkinen, S.
    Tall, M.
    Raivio, V.
    Turunen, J. A.
    Kivela, T. T.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 1604 - 1605
  • [26] Response to "BAP1 Germline Mutation Associated with Bilateral Primary Uveal Melanoma"
    Herwig-Carl, Martina C.
    Sharma, Amit
    Melzer, Charlotte
    Holz, Frank G.
    Loeffler, Karin U.
    OCULAR ONCOLOGY AND PATHOLOGY, 2021, 7 (03) : 233 - 234
  • [27] BAP1 germline variants in Finnish patients with malignant mesothelioma
    Repo, Pauliina
    Staskiewicz, Aleksandra
    Sutinen, Eva
    Ronty, Mikko
    Kivela, Tero T.
    Myllarniemi, Marjukka
    Turunen, Joni A.
    LUNG CANCER, 2022, 165 : 102 - 107
  • [28] BAP1 germline variations in Finnish patients with malignant mesothelioma
    Repo, Pauliina
    Staskiewicz, Aleksandra
    Sutinen, Eva
    Ronty, Mikko
    Kivela, Tero T.
    Myllarniemi, Marjukka
    Turunen, Joni A.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (SUPPL 1) : 372 - 372
  • [29] Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma
    Verdijk, R.
    Koopmans, A.
    Brouwer, R.
    van den Bosch, T.
    van den Berg, M.
    Vaarwater, J.
    Paridaens, D.
    Naus, N.
    Kilic, E.
    de Klein, A.
    VIRCHOWS ARCHIV, 2014, 465 : S44 - S44
  • [30] Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma
    Koopmans, Anna E.
    Verdijk, Robert M.
    Brouwer, Rutger W. W.
    van den Bosch, Thierry P. P.
    van den Berg, Mike M. P.
    Vaarwater, Jolanda
    Kockx, Christel E. M.
    Paridaens, Dion
    Naus, Nicole C.
    Nellist, Mark
    van IJcken, Wilfred F. J.
    Kilic, Emine
    de Klein, Annelies
    MODERN PATHOLOGY, 2014, 27 (10) : 1321 - 1330
12345