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Chromosome fusion

Stodolsky, M.

Genetics 73 73 65-73: 66

1973

ISSN/ISBN: 0016-6731
PMID: 4711553
Document Number: 62454

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Stobetskiĭ, V.I. 1991: Telomeric chromosome fusion in cells with micronuclei under the combined action of hyperthermia and hypothermia and halogenated analogs of thymidine Biulleten' Eksperimental'noi Biologii i Meditsiny 112(7): 72-73
Demmer, L.A.; Chaplin, D.D. 1993: Simultaneous transfer of four functional genes from the HLA class II region into mammalian cells by fusion with yeast spheroplasts carrying an artificial chromosome Journal of Immunology 150(12): 5371-5378
Long, H.; Kazunasa, U.; Liu, S.; Akio, S.; Taito, I. 2007: Preliminary application of one-level posterior lumbar interbody fusion with prospace and facet fusion using local autograft Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi 21(11): 1155-1159
Galante Romo, M.ía.I.; Ciappara Paniagua, M.; Moreno Sierra, J.ús. 2019: Fusion biopsy. Analysis of fusion software platforms Archivos Espanoles de Urologia 72(8): 794-803
Leufvén, C.; Nordwall, A. 1999: Management of chronic disabling low back pain with 360 degrees fusion. Results from pain provocation test and concurrent posterior lumbar interbody fusion, posterolateral fusion, and pedicle screw instrumentation in patients with chronic disabling low back pain Spine 24(19): 2042-2045
Kim, N.H.; Lee, J.W. 1999: Anterior interbody fusion versus posterolateral fusion with transpedicular fixation for isthmic spondylolisthesis in adults. A comparison of clinical results Spine 24(8): 812
Lovett, M.; Goldgaber, D.; Ashley, P.; Cox, D.R.; Gajdusek, D.C.; Epstein, C.J. 1987: The mouse homolog of the human amyloid beta protein (AD-AP) gene is located on the distal end of mouse chromosome 16: further extension of the homology between human chromosome 21 and mouse chromosome 16 Biochemical and Biophysical Research Communications 144(2): 1069-1075
Zhu, Y.; Liu, H-ying.; Wang, B.; Wang, H-min.; Qian, Y-long.; Zhu, Z-qi.; Miao, K-nan. 2013: Long-term clinical outcomes of selective segmental transforaminal lumbar interbody fusion and posterior spinal fusion for degenerative lumbar scoliosis Zhonghua Yi Xue Za Zhi 93(45): 3577-3581
Ohgimoto, S.; Tabata, N.; Suga, S.; Nishio, M.; Ohta, H.; Tsurudome, M.; Komada, H.; Kawano, M.; Watanabe, N.; Ito, Y. 1995: Molecular characterization of fusion regulatory protein-1 (FRP-1) that induces multinucleated giant cell formation of monocytes and HIV gp160-mediated cell fusion. FRP-1 and 4F2/CD98 are identical molecules Journal of Immunology 155(7): 3585-3592
Wild, J. 1986: Gene fusion in studies on gene expression regulation and protein analysis. use of lac fusion Postepy Biochemii 32(4): 421-443
Sakazume, S. 2014: Spread of X-chromosome inactivation into chromosome 15 is associated with Prader Willi syndrome phenotype in a boy with a t (X ; 15) (p21.1 ; q11.2) translocation No to Hattatsu 46(2): 121-124
Terzoudi, G.I.; Singh, S.K.; Pantelias, G.E.; Iliakis, G. 2008: Premature chromosome condensation reveals DNA-PK independent pathways of chromosome break repair International Journal of Oncology 33(4): 871-879
Verma, R.S.; Dosik, H.; Wexler, I.B. 1977: Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q Journal de Genetique Humaine 25(4): 295-301
Yakut, S.; Cetin, Z.; Sanhal, C.; Karauzum, S.B.; Karaman, B.; Simsek, M. 2015: Prenatal Diagnosis of de Novo Supernumerary Marker Chromosome Originated from Chromosome 16 by Array-Cgh Genetic Counseling 26(3): 299-305
Noutoshi, Y.; Arai, R.; Fujie, M.; Yamada, T. 1997: Designing of plant artificial chromosome (PAC) by using the Chlorella smallest chromosome as a model system Nucleic Acids Symposium Series 37: 143-144
Prieto, F.; Badia, L.; Mayans, J.; Besalduch, J.; Marty, M.L. 1978: Trysomy of chromosome 1 long arms plus chromosome 9 inversion in leukaemic cells Sangre 23(1): 64-68
Rao, L.; Murthy, K.; Babu, A.; Venkata, P.; Deenadayal, M.; Singh, L. 2005: Chromosome inversions and a novel chromosome insertion associated with recurrent miscarriages in South India Archives of Gynecology and Obstetrics 272(4): 273-277
Zollinger, A.; Schmid, W.; Vilan, J.; Sorg, B.; Knoblauch, M. 1983: X chromosome-linked mental retardation with fragile X chromosome and macro-orchidism Schweizerische Medizinische Wochenschrift 113(7): 238-244
Steinbach, P.; Drews, K.; Horstmann, W.; Barbi, G.; Scholz, W. 1981: Two cases of ring chromosome 13. Chromosome banding patterns and mosaic configuration Annales de Genetique 24(3): 152-157
Doco-Fenzy, M.; Navrocki, B.; Cornillet, P.; Sabouraud, P.; Robillard, P.; Gruson, N.; Gaillard, D.; Adnet, J.J. 1994: Use of chromosome painting for marker chromosome identification in two children with congenital disorders Bulletin de l'Association des Anatomistes 78(241): 9-13