About the mechanism of chromosoma mutations.

被引：0
|
作者：
Jordan, P
机构：
来源：
NATURWISSENSCHAFTEN | 1938年 / 26卷
关键词：
D O I：
10.1007/BF01774306
中图分类号：
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号：
07 ; 0710 ; 09 ;
摘要：
引用
收藏
页码：839 / 839
页数：1
相关论文
共 50 条
  • [41] Volume-sensing mechanism of CLC-3 Cl- channel revealed by point mutations.
    Duan, D
    Cowley, S
    Horowitz, B
    Hume, JR
    BIOPHYSICAL JOURNAL, 1998, 74 (02) : A221 - A221
  • [42] Regarding the cultural gemmary mutations of Solanum Maglia and the first cultural results of these mutations.
    Heckel, E
    COMPTES RENDUS HEBDOMADAIRES DES SEANCES DE L ACADEMIE DES SCIENCES, 1911, 153 : 417 - 420
  • [43] From the writing to the screen. Popular literature: generic mutations, mediatic mutations.
    Thiesse, AM
    REVUE D HISTOIRE LITTERAIRE DE LA FRANCE, 2005, 105 (04): : 1060 - 1061
  • [44] Mitochondrial mutations in non syndromic sensorineural hearing impairement:: A large spectrum of mutations.
    Marlin, S
    Feldmann, D
    Chapiro, E
    Denoyelle, F
    Sternberg, D
    Weil, D
    Petit, C
    Garabédian, EN
    Couderc, R
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2002, 10 : 243 - 243
  • [45] Common and Rare EGFR Mutations. The Challenge of Their Cytological Detection
    Rossi, E. D.
    Gerhard, R.
    Cirnes, L.
    Machado, J. C.
    Schmitt, F. C.
    MODERN PATHOLOGY, 2013, 26 : 102A - 102A
  • [46] Somatic and/or germline mosaicism for recurrent APC gene mutations.
    Bakker, E
    Bik, EC
    Hendricks, YMC
    Vossen, RHAM
    Tops, CMJ
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 96 - 96
  • [47] Increased spontaneous in vitro apoptosis in humans with Fas mutations.
    Haas, PJ
    Hieronymus, T
    Dirnecker, D
    Frank, C
    Kolowos, W
    Lorenz, HM
    Leipold, G
    Gruenke, M
    Herrmann, M
    ARTHRITIS AND RHEUMATISM, 1997, 40 (09): : 890 - 890
  • [48] Prions may act as the gain-of-function mutations.
    Nizhnikov, A. A.
    Antonets, K. S.
    Kliver, S. F.
    Polev, D. E.
    Shuvalova, A. R.
    Andreeva, E. A.
    Inge-Vechtomov, S. G.
    MOLECULAR BIOLOGY OF THE CELL, 2017, 28
  • [49] Familial hypocalciuric hypercalcemia: Four novel inactivating mutations.
    Cetani, F.
    Borsari, S.
    Pardi, E.
    Ambrogini, E.
    Cianferotti, L.
    Lemmi, M.
    Vignali, E.
    Viccica, G.
    Pinchera, A.
    Marcocci, C.
    JOURNAL OF BONE AND MINERAL RESEARCH, 2006, 21 : S447 - S447
  • [50] Characterization of urinary bladder paragangliomas in patients with germline mutations.
    Rayn, Kareem
    Weintraub, Michael Daniel
    Pena-La Grave, Gustavo R.
    Hale, Graham R.
    Gold, Samuel
    Bloom, Jonathan
    Brancato, Sam Joseph
    Agarwal, Piyush K.
    JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (06)
12345