85 related articles for article (PubMed ID: 7656587)
41. Ubiquitin-activating enzyme, E1, is phosphorylated in mammalian cells by the protein kinase Cdc2.
Nagai Y; Kaneda S; Nomura K; Yasuda H; Seno T; Yamao F
J Cell Sci; 1995 Jun; 108 ( Pt 6)():2145-52. PubMed ID: 7673335
[TBL] [Abstract][Full Text] [Related]
42. The t(X;18)(p11.2;q11.2) translocation found in human synovial sarcomas involves two distinct loci on the X chromosome.
Shipley JM; Clark J; Crew AJ; Birdsall S; Rocques PJ; Gill S; Chelly J; Monaco AP; Abe S; Gusterson BA
Oncogene; 1994 May; 9(5):1447-53. PubMed ID: 8152806
[TBL] [Abstract][Full Text] [Related]
43. Two categories of synovial sarcoma defined by divergent chromosome translocation breakpoints in Xp11.2, with implications for the histologic sub-classification of synovial sarcoma.
Renwick PJ; Reeves BR; Dal Cin P; Fletcher CD; Kempski H; Sciot R; Kazmierczak B; Jani K; Sonobe H; Knight JC
Cytogenet Cell Genet; 1995; 70(1-2):58-63. PubMed ID: 7736791
[TBL] [Abstract][Full Text] [Related]
44. Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short arm.
Lafreniere RG; Geraghty MT; Valle D; Shows TB; Willard HF
Genomics; 1991 May; 10(1):276-9. PubMed ID: 1675195
[TBL] [Abstract][Full Text] [Related]
45. An evolutionary rearrangement of the Xp11.3-11.23 region in 3p21.3, a region frequently deleted in a variety of cancers.
Timmer T; Terpstra P; van den Berg A; Veldhuis PM; Ter Elst A; van der Veen AY; Kok K; Naylor SL; Buys CH
Genomics; 1999 Sep; 60(2):238-40. PubMed ID: 10486216
[TBL] [Abstract][Full Text] [Related]
46. The physical location of genes cdc2 and prh1 in maize (Zea mays L.).
Ren N; Song YC; Bi XZ; Ding Y; Liu LH
Hereditas; 1997; 126(3):211-7. PubMed ID: 9350135
[TBL] [Abstract][Full Text] [Related]
47. The human NFKB3 gene encoding the p65 subunit of transcription factor NF-kappa B is located on chromosome 11q12.
Deloukas P; Dauwerse JG; van Ommen GJ; van Loon AP
Genomics; 1994 Feb; 19(3):592-4. PubMed ID: 8188306
[TBL] [Abstract][Full Text] [Related]
48. Does the human X contain a third evolutionary block? Origin of genes on human Xp11 and Xq28.
Delbridge ML; Patel HR; Waters PD; McMillan DA; Marshall Graves JA
Genome Res; 2009 Aug; 19(8):1350-60. PubMed ID: 19439513
[TBL] [Abstract][Full Text] [Related]
49. [Some YAC contig construction and long range physical mapping at human X chromosome Xp11.3-21.3].
Miao WM; Wei Y; Deng W; Zhou W; Li HJ; Chal J; Tan J
Yi Chuan Xue Bao; 1997 Apr; 24(2):99-108. PubMed ID: 9254964
[TBL] [Abstract][Full Text] [Related]
50. Physical analysis of the terminal 240 kb of DNA from human chromosome 7q.
Riethman HC; Spais C; Buckingham J; Grady D; Moyzis RK
Genomics; 1993 Jul; 17(1):25-32. PubMed ID: 8406463
[TBL] [Abstract][Full Text] [Related]
51. Interphase fluorescence in situ hybridization and reverse transcription polymerase chain reaction as a diagnostic aid for synovial sarcoma.
Shipley J; Crew J; Birdsall S; Gill S; Clark J; Fisher C; Kelsey A; Nojima T; Sonobe H; Cooper C; Gusterson B
Am J Pathol; 1996 Feb; 148(2):559-67. PubMed ID: 8579118
[TBL] [Abstract][Full Text] [Related]
52. Identification of YAC and cosmid clones encompassing the ZFX-POLA region using irradiation hybrid cell lines.
Francis F; Benham F; See CG; Fox M; Ishikawa-Brush Y; Monaco AP; Weiss B; Rappold G; Hamvas RM; Lehrach H
Genomics; 1994 Mar; 20(1):75-83. PubMed ID: 8020959
[TBL] [Abstract][Full Text] [Related]
53. Assignment of an anonymous DNA sequence IB/D22 (DXS371) to XP11.1-11.4.
Spurr NK; Mitchell C; Gough AC; Rooke L; Cowell JK
Dis Markers; 1989; 7(4):247-51. PubMed ID: 2573448
[TBL] [Abstract][Full Text] [Related]
54. Isolation of a candidate gene for Norrie disease by positional cloning.
Berger W; Meindl A; van de Pol TJ; Cremers FP; Ropers HH; Döerner C; Monaco A; Bergen AA; Lebo R; Warburg M
Nat Genet; 1992 Jun; 1(3):199-203. PubMed ID: 1303235
[TBL] [Abstract][Full Text] [Related]
55. Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp.
Lindsay S; Thiselton DL; Bateman JB; Ngo JT; Sparkes RS; Coleman M; Davies KE; Bhattacharya SS
Hum Genet; 1992 Jan; 88(3):349-50. PubMed ID: 1733838
[TBL] [Abstract][Full Text] [Related]
56. Cosmids map two incontinentia pigmenti type 1 (IP1) translocation breakpoints to a 180-kb region within a 1.2-Mb YAC contig.
Gorski JL; Bialecki MD; McDonald MT; Massa HF; Trask BJ; Burright EN
Genomics; 1996 Jul; 35(2):338-45. PubMed ID: 8661147
[TBL] [Abstract][Full Text] [Related]
57. Molecular cloning, sequence, and tissue distribution of the human ubiquitin-activating enzyme E1.
Proc Natl Acad Sci U S A; 1991 Aug; 88(16):7456. PubMed ID: 1871145
[No Abstract] [Full Text] [Related]
58. Complementation by a cloned human ubiquitin-activating enzyme E1 of the S-phase-arrested mouse FM3A cell mutant with thermolabile E1.
Ayusawa D; Kaneda S; Itoh Y; Yasuda H; Murakami Y; Sugasawa K; Hanaoka F; Seno T
Cell Struct Funct; 1992 Apr; 17(2):113-22. PubMed ID: 1606621
[TBL] [Abstract][Full Text] [Related]
59. tsBN75 and tsBN423, temperature-sensitive x-linked mutants of the BHK21 cell line, can be complemented by the ubiquitin-activating enzyme E1 cDNA.
Nishitani H; Goto H; Kaneda S; Yamao F; Seno T; Handley P; Schwartz AL; Nishimoto T
Biochem Biophys Res Commun; 1992 Apr; 184(2):1015-21. PubMed ID: 1575720
[TBL] [Abstract][Full Text] [Related]
60. A gene in the chromosomal region 3p21 with greatly reduced expression in lung cancer is similar to the gene for ubiquitin-activating enzyme.
Kok K; Hofstra R; Pilz A; van den Berg A; Terpstra P; Buys CH; Carritt B
Proc Natl Acad Sci U S A; 1993 Jul; 90(13):6071-5. PubMed ID: 8327486
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
