FINE TUMOR DELETION MAPPING LOCALIZES A PUTATIVE 17Q25 GENE INVOLVED IN BREAST CARCINOGENESIS

被引：0
|
作者：
KALIKIN, LM
OU, X
FRANK, TS
CADUFF, RF
SVOBODA, SM
LAW, DJ
PETTY, EM
机构：
[1] UNIV MICHIGAN,SCH MED,DEPT INTERNAL MED,ANN ARBOR,MI 48109
[2] UNIV MICHIGAN,SCH MED,DEPT PATHOL,ANN ARBOR,MI 48109
[3] UNIV MICHIGAN,SCH MED,DEPT HUMAN GENET,ANN ARBOR,MI 48109
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1995年 / 57卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：361 / 361
页数：1
相关论文
共 50 条
  • [31] ASSIGNMENT OF A POLYCOMB-LIKE CHROMOBOX GENE (CBX2) TO HUMAN-CHROMOSOME 17Q25
    GECZ, J
    GAUNT, SJ
    PASSAGE, E
    BURTON, RD
    CUDREY, C
    PEARCE, JJH
    FONTES, M
    GENOMICS, 1995, 26 (01) : 130 - 133
  • [32] The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25
    Ladanyi, M
    Lui, MY
    Antonescu, CR
    Krause-Boehm, A
    Meindl, A
    Argani, P
    Healey, JH
    Ueda, T
    Yoshikawa, H
    Meloni-Ehrig, A
    Sorensen, PHB
    Mertens, F
    Mandahl, N
    van den Berghe, H
    Sciot, R
    Dal Cin, P
    Bridge, J
    ONCOGENE, 2001, 20 (01) : 48 - 57
  • [33] The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25
    Marc Ladanyi
    Man Yee Lui
    Cristina R Antonescu
    Amber Krause-Boehm
    Alfons Meindl
    Pedram Argani
    John H Healey
    Takafumi Ueda
    Hideki Yoshikawa
    Aurelia Meloni-Ehrig
    Poul H B Sorensen
    Fredrik Mertens
    Nils Mandahl
    Herman van den Berghe
    Raf Sciot
    Paola Dal Cin
    Julia Bridge
    Oncogene, 2001, 20 : 48 - 57
  • [34] Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region
    Paschou, P
    Feng, Y
    Pakstis, AJ
    Speed, WC
    DeMille, MM
    Kidd, JR
    Jaghori, B
    Kurlan, R
    Pauls, DL
    Sandor, P
    Barr, CL
    Kidd, KK
    AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 75 (04) : 545 - 560
  • [35] Common variants on 17q25 and gene–gene interactions conferring risk of schizophrenia in Han Chinese population and regulating gene expressions in human brain
    L Guan
    Q Wang
    L Wang
    B Wu
    Y Chen
    F Liu
    F Ye
    T Zhang
    K Li
    B Yan
    C Lu
    L Su
    G Jin
    H Wang
    H Tian
    L Wang
    Z Chen
    Y Wang
    J Chen
    Y Yuan
    W Cong
    J Zheng
    J Wang
    X Xu
    H Liu
    W Xiao
    C Han
    Y Zhang
    F Jia
    X Qiao
    D Zhang
    M Zhang
    H Ma
    Molecular Psychiatry, 2016, 21 : 1244 - 1250
  • [36] Identification and mapping of a putative bombesin receptor gene on human chromosome 17q21.3
    Kelavkar, U
    Abel, K
    Miller, D
    Murtagh, J
    Shah, K
    GENETIC ANALYSIS-BIOMOLECULAR ENGINEERING, 1996, 13 (04): : 99 - 103
  • [37] Mapping an endometrial cancer tumor suppressor gene at 10q25 and development of a bacterial clone contig for the consensus deletion interval
    Peiffer-Schneider, S
    Noonan, FC
    Mutch, DG
    Simpkins, SB
    Herzog, T
    Rader, J
    Elbendary, A
    Gersell, DJ
    Call, K
    Goodfellow, PJ
    GENOMICS, 1998, 52 (01) : 9 - 16
  • [38] Common variants on 17q25 and gene-gene interactions conferring risk of schizophrenia in Han Chinese population and regulating gene expressions in human brain
    Guan, L.
    Wang, Q.
    Wang, L.
    Wu, B.
    Chen, Y.
    Liu, F.
    Ye, F.
    Zhang, T.
    Li, K.
    Yan, B.
    Lu, C.
    Su, L.
    Jin, G.
    Wang, H.
    Tian, H.
    Wang, L.
    Chen, Z.
    Wang, Y.
    Chen, J.
    Yuan, Y.
    Cong, W.
    Zheng, J.
    Wang, J.
    Xu, X.
    Liu, H.
    Xiao, W.
    Han, C.
    Zhang, Y.
    Jia, F.
    Qiao, X.
    Zhang, D.
    Zhang, M.
    Ma, H.
    MOLECULAR PSYCHIATRY, 2016, 21 (09) : 1244 - 1250
  • [39] Genomic and expression analyses of alternatively spliced transcripts of the MLL septin-like fusion gene (MSF) that map to a 17q25 region of loss in breast and ovarian tumors
    Kalikin, LM
    Sims, HL
    Petty, EM
    GENOMICS, 2000, 63 (02) : 165 - 172
  • [40] The human plakoglobin gene localizes on chromosome 17q21 and is subjected to loss of heterozygosity in breast and ovarian cancers
    Aberle, H.
    Bierkamp, C.
    Torchard, D.
    Serova, O.
    Proceedings of the National Academy of Sciences of the United States of America, 92 (14):
12345