Molecular characterization of somatic gene mutations arising in vivo in humans
Albertini, R.J.; Nicklas, J.A.; O'Neill, J.P.
Progress in Clinical and Biological Research 207: 77-85
1986
ISSN/ISBN: 0361-7742 PMID: 3008192 Document Number: 281179
Document emailed within 1 workday
Related Documents
Jayandharan, G.R.; Shaji, R.V.; Baidya, S.; Nair, S.C.; Chandy, M.; Srivastava, A. 2005: Molecular characterization of factor IX gene mutations in 53 patients with haemophilia B in India Thrombosis and Haemostasis 94(4): 883-886Khalizev, A.E.; Pyzhov, A.P.; Shapiro, N.I. 1976: Development of spontaneous mutations in somatic mamalian cells and DNA replication. II. Expression of gene mutations in cultured cells Genetika 12(11): 51-60
Zhuang, Z.; Vortmeyer, A.O.; Pack, S.; Huang, S.; Pham, T.A.; Wang, C.; Park, W.S.; Agarwal, S.K.; Debelenko, L.V.; Kester, M.; Guru, S.C.; Manickam, P.; Olufemi, S.E.; Yu, F.; Heppner, C.; Crabtree, J.S.; Skarulis, M.C.; Venzon, D.J.; Emmert-Buck, M.R.; Spiegel, A.M.; Chandrasekharappa, S.C.; Collins, F.S.; Burns, A.L.; Marx, S.J.; Lubensky, I.A. 1997: Somatic mutations of the MEN1 tumor suppressor gene in sporadic gastrinomas and insulinomas Cancer Research 57(21): 4682-4686
Gimm, O.; Armanios, M.; Dziema, H.; Neumann, H.P.; Eng, C. 2000: Somatic and occult germ-line mutations in SDHD, a mitochondrial complex Ii gene, in nonfamilial pheochromocytoma Cancer Research 60(24): 6822-6825
Vorechovský, I.; Undén, A.B.; Sandstedt, B.; Toftgård, R.; Ståhle-Bäckdahl, M. 1997: Trichoepitheliomas contain somatic mutations in the overexpressed PTCH gene: support for a gatekeeper mechanism in skin tumorigenesis Cancer Research 57(21): 4677-4681
Bignell, G.R.; Barfoot, R.; Seal, S.; Collins, N.; Warren, W.; Stratton, M.R. 1998: Low frequency of somatic mutations in the LKB1/Peutz-Jeghers syndrome gene in sporadic breast cancer Cancer Research 58(7): 1384-1386
Kanno, H.; Kondo, K.; Ito, S.; Yamamoto, I.; Fujii, S.; Torigoe, S.; Sakai, N.; Hosaka, M.; Shuin, T.; Yao, M. 1994: Somatic mutations of the von Hippel-Lindau tumor suppressor gene in sporadic central nervous system hemangioblastomas Cancer Research 54(18): 4845-4847
Miyaki, M.; Konishi, M.; Kikuchi-Yanoshita, R.; Enomoto, M.; Tanaka, K.; Takahashi, H.; Muraoka, M.; Mori, T.; Konishi, F.; Iwama, T. 1993: Coexistence of somatic and germ-line mutations of APC gene in desmoid tumors from patients with familial adenomatous polyposis Cancer Research 53(21): 5079-5082
Kanno, H.; Shuin, T.; Kondo, K.; Yamamoto, I.; Ito, S.; Shinonaga, M.; Yoshida, M.; Yao, M. 1997: Somatic mutations of the von Hippel-Lindau tumor suppressor gene and loss of heterozygosity on chromosome 3p in human glial tumors Cancer Research 57(6): 1035-1038
Gong, K.; Zhang, Z.; Xin, D. 2001: Frequent somatic mutations of the von Hippel-Lindau tumor suppressor gene in primary sporadic human renal clear cell carcinomas Zhonghua Yi Xue Za Zhi 81(3): 142-144
Seidel, J.; Caca, K.; Schwab, S.G.; Berr, F.; Wildenauer, D.B.; Mentzel, H.J.; Horn, N.; Kauf, E. 2001: Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD) Cellular and Molecular Biology 47 Online Pub: Ol149-Ol157
Helmy, M.M.F.; Rashed, L.A.; el-Garhy, M.F. 2004: Molecular characterization of Cryptosporidium parvum isolates obtained from humans Journal of the Egyptian Society of Parasitology 34(2): 447-458
Solov'ev, V.V.; Rogozin, I.V.; Kolchanov, N.A. 1989: Somatic hypermutagenesis in immunoglobulin genes. I. Connection of somatic mutations with repeats. a statistical weighting method Molekuliarnaia Biologiia 23(3): 783-794
Nohmi, T.; Masumura, K-Ichi. 2004: Gpt delta transgenic mouse: A novel approach for molecular dissection of deletion mutations in vivo Advances in Biophysics 38(Complete): 97-121
Cao, F.; Xia, J.; Chen, Y.-p.; Zhang, M.; Xiang, L.-e.; Zeng, J.-l.; Chen, M.; Lan, X.-z.; Liao, Z.-h. 2016: Molecular cloning and functional characterization of the gene encoding hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate reductase gene from Artemisia annua L Yao Xue Xue Bao 51(11): 1791-1798
Wulff, K.; Bykowska, K.; Lopaciuk, S.; Herrmann, F.H. 1999: Molecular analysis of hemophilia B in Poland: 12 novel mutations of the factor IX gene Acta Biochimica Polonica 46(3): 721-726
Bancone, G.; Menard, D.; Khim, N.; Kim, S.; Canier, L.; Nguong, C.; Phommasone, K.; Mayxay, M.; Dittrich, S.; Vongsouvath, M.; Fievet, N.; Le Hesran, J.-Y.; Briand, V.; Keomany, S.; Newton, P.N.; Gorsawun, G.; Tardy, K.; Chu, C.S.; Rattanapalroj, O.; Dong, L.T.; Quang, H.H.; Tam-Uyen, N.; Thuy-Nhien, N.; Hien, T.T.; Kalnoky, M.; Nosten, F. 2019: Molecular characterization and mapping of glucose-6-phosphate dehydrogenase (G6PD) mutations in the Greater Mekong Subregion Malaria Journal 18(1): 20
Espinós, C.; Casaña, P.; Haya, S.; Cid, A.R.; Aznar, J.A. 2003: Molecular analyses in hemophilia B families: identification of six new mutations in the factor IX gene Haematologica 88(2): 235-236
González, N.; Torres, M.J.; Palomares, J.C.; Aznar, J. 1998: Characterization of the rpoB gene mutations in clinical isolates of rifampicin-resistant Mycobacterium tuberculosis Enfermedades Infecciosas y Microbiologia Clinica 16(9): 404-407
Greenblatt, M.S.; Bennett, W.P.; Hollstein, M.; Harris, C.C. 1994: Mutations in the p53 tumor suppressor gene: clues to cancer etiology and molecular pathogenesis Cancer Research 54(18): 4855-4878