77 related articles for article (PubMed ID: 8125014)
1. Assignment of the human moesin gene (MSN) to chromosome region Xq11.2-->q12.
Kishino T; Ariga T; Soejima H; Tamura T; Ohta T; Jinno Y; Yonemura S; Sato N; Tsukita S; Tsukita S
Cytogenet Cell Genet; 1994; 66(3):167-9. PubMed ID: 8125014
[TBL] [Abstract][Full Text] [Related]
2. Structure and localization on the X chromosome of the gene coding for the human filopodial protein moesin (MSN).
Wilgenbus KK; Hsieh CL; Lankes WT; Milatovich A; Francke U; Furthmayr H
Genomics; 1994 Jan; 19(2):326-33. PubMed ID: 8188263
[TBL] [Abstract][Full Text] [Related]
3. Mapping of 50 cosmid clones isolated from a flow-sorted human X chromosome library by fluorescence in situ hybridization.
Fan YS; Sasi R; Lee C; Court D; Lin CC
Genomics; 1992 Oct; 14(2):542-5. PubMed ID: 1427877
[TBL] [Abstract][Full Text] [Related]
4. Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint.
Weterman MA; Wilbrink M; Janssen I; Janssen HA; van den Berg E; Fisher SE; Craig I; Geurts van Kessel A
Cytogenet Cell Genet; 1996; 75(1):2-6. PubMed ID: 8995477
[TBL] [Abstract][Full Text] [Related]
5. The UDP-galactose translocator gene is mapped to band Xp11.23-p11.22 containing the Wiskott-Aldrich syndrome locus.
Hara T; Yamauchi M; Takahashi E; Hoshino M; Aoki K; Ayusawa D; Kawakita M
Somat Cell Mol Genet; 1993 Nov; 19(6):571-5. PubMed ID: 8128316
[TBL] [Abstract][Full Text] [Related]
6. Isolation and chromosomal mapping of genomic clones encoding the human fatty acid synthase gene.
Jayakumar A; Chirala SS; Chinault AC; Baldini A; Abu-Elheiga L; Wakil SJ
Genomics; 1994 Sep; 23(2):420-4. PubMed ID: 7835891
[TBL] [Abstract][Full Text] [Related]
7. Isolation of cDNA clones mapping around DXS178: a search for human X-linked agammaglobulinaemia gene using yeast artificial chromosomes, cosmids and direct cDNA selection.
Vorechovský I; Holland J; Sideras P; Dunham I; Hammarström L; Smith CI; Bentley DR; Vetrie D
Immunodeficiency; 1993; 4(1-4):221-4. PubMed ID: 8167705
[TBL] [Abstract][Full Text] [Related]
8. Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22).
Trent JM; Flink IL; Morkin E; van Tuinen P; Ledbetter DH
Am J Hum Genet; 1987 Sep; 41(3):428-35. PubMed ID: 3115094
[TBL] [Abstract][Full Text] [Related]
9. Isolation and fluorescence in situ hybridization mapping of 60 cosmid clones on human chromosome 18.
Nakashima H; Sakai M; Inaba R; Imamura T
Genomics; 1994 Feb; 19(3):577-80. PubMed ID: 8188303
[TBL] [Abstract][Full Text] [Related]
10. Sublocalization of the synovial sarcoma-associated t(X;18) chromosomal breakpoint in Xp11.2 using cosmid cloning and fluorescence in situ hybridization.
de Leeuw B; Suijkerbuijk RF; Balemans M; Sinke RJ; de Jong B; Molenaar WM; Meloni AM; Sandberg AA; Geraghty M; Hofker M
Oncogene; 1993 Jun; 8(6):1457-63. PubMed ID: 8389029
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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 PH; Mertens F; Mandahl N; van den Berghe H; Sciot R; Dal Cin P; Bridge J
Oncogene; 2001 Jan; 20(1):48-57. PubMed ID: 11244503
[TBL] [Abstract][Full Text] [Related]
13. Cosmid clones from microdissected human chromosomal region 15q11-q13.
Tohma T; Tamura T; Ohta T; Soejima H; Kubota T; Jinno Y; Tsukamoto K; Nakamura Y; Naritomi K; Niikawa N
Jpn J Hum Genet; 1993 Sep; 38(3):267-75. PubMed ID: 8260719
[TBL] [Abstract][Full Text] [Related]
14. FISH mapping of 22 novel X chromosome cosmids and the isolation of a novel microsatellite on proximal Xp.
Kamakari S; Thiselton D; Lindsay S; Hardcastle A; Bhattacharya S
Cytogenet Cell Genet; 1995; 71(2):151-4. PubMed ID: 7656586
[TBL] [Abstract][Full Text] [Related]
15. A fluorescence in situ hybridization map of human chromosome 21 consisting of 30 genetic and physical markers on the chromosome: localization of 137 additional YAC and cosmid clones with respect to this map.
Gingrich JC; Shadravan F; Lowry SR
Genomics; 1993 Jul; 17(1):98-105. PubMed ID: 8406476
[TBL] [Abstract][Full Text] [Related]
16. Characterization of a flow-sorted human chromosome 10 cosmid library by FISH.
Ma NS; Zheng C; Benchekroun Y; Deaven LL; Longmire JL; Moir DT; Mao J
Cytogenet Cell Genet; 1996; 74(4):266-71. PubMed ID: 8976382
[TBL] [Abstract][Full Text] [Related]
17. Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp.
Fisher SE; Ciccodicola A; Tanaka K; Curci A; Desicato S; D'urso M; Craig IW
Genomics; 1997 Oct; 45(2):340-7. PubMed ID: 9344658
[TBL] [Abstract][Full Text] [Related]
18. The human vigilin gene: identification, chromosomal localization and expression pattern.
Plenz G; Kügler S; Schnittger S; Rieder H; Fonatsch C; Müller PK
Hum Genet; 1994 May; 93(5):575-82. PubMed ID: 8168838
[TBL] [Abstract][Full Text] [Related]
19. Radiation hybrids for the proximal long arm of the X chromosome and their use in the derivation of an ordered set of cosmid markers from a defined subregion in proximal Xq13.1.
Röhme D; Sidén T; van der Maarel SM; Cremers FP; Tantravahi U; Marinoni JC; Ropers HH; Schwartz CE
Somat Cell Mol Genet; 1994 Jan; 20(1):1-10. PubMed ID: 8197472
[TBL] [Abstract][Full Text] [Related]
20. A high-resolution map of genes, microsatellite markers, and new dinucleotide repeats from UBE1 to the GATA locus in the region Xp11.23.
Kwan SP; Hagemann TL; Blaese RM; Rosen FS
Genomics; 1995 Sep; 29(1):247-52. PubMed ID: 8530079
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
