178 related articles for article (PubMed ID: 2014801)
1. A t(4;22) in a meningioma points to the localization of a putative tumor-suppressor gene.
Lekanne Deprez RH; Groen NA; van Biezen NA; Hagemeijer A; van Drunen E; Koper JW; Avezaat CJ; Bootsma D; Zwarthoff EC
Am J Hum Genet; 1991 Apr; 48(4):783-90. PubMed ID: 2014801
[TBL] [Abstract][Full Text] [Related]
2. Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma.
Tanaka N; Nishisho I; Yamamoto M; Miya A; Shin E; Karakawa K; Fujita S; Kobayashi T; Rouleau GA; Mori T
Genes Chromosomes Cancer; 1992 Nov; 5(4):399-403. PubMed ID: 1283329
[TBL] [Abstract][Full Text] [Related]
3. Mapping the breakpoint of a constitutional translocation on chromosome 22 in a patient with NF2.
Arai E; Tokino T; Imai T; Inazawa J; Ikeuchi T; Tonomura A; Nakamura Y
Genes Chromosomes Cancer; 1993 Apr; 6(4):235-8. PubMed ID: 7685627
[TBL] [Abstract][Full Text] [Related]
4. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
Laureys GG
Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670
[TBL] [Abstract][Full Text] [Related]
5. Deletion mapping of the long arm of chromosome 22 in human meningiomas.
Akagi K; Kurahashi H; Arita N; Hayakawa T; Monden M; Mori T; Takai S; Nishisho I
Int J Cancer; 1995 Jan; 60(2):178-82. PubMed ID: 7829212
[TBL] [Abstract][Full Text] [Related]
6. Combined molecular genetic studies of chromosome 22q and the neurofibromatosis type 2 gene in central nervous system tumors.
Ng HK; Lau KM; Tse JY; Lo KW; Wong JH; Poon WS; Huang DP
Neurosurgery; 1995 Oct; 37(4):764-73. PubMed ID: 8559307
[TBL] [Abstract][Full Text] [Related]
7. Abnormalities of chromosome 22 in meningiomas and confirmation of the origin of a dicentric 22 by in situ hybridization.
Tonk V; Osella P; Delasmorenas A; Wyandt HE; Milunsky A
Cancer Genet Cytogenet; 1992 Nov; 64(1):65-8. PubMed ID: 1458452
[TBL] [Abstract][Full Text] [Related]
8. The molecular genetics of meningiomas.
Collins VP; Nordenskjöld M; Dumanski JP
Brain Pathol; 1990 Sep; 1(1):19-24. PubMed ID: 1688296
[TBL] [Abstract][Full Text] [Related]
9. The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus.
Zhang FR; Delattre O; Rouleau G; Couturier J; Lefrançois ; Thomas G; Aurias A
Genomics; 1990 Jan; 6(1):174-7. PubMed ID: 2303258
[TBL] [Abstract][Full Text] [Related]
10. Cosmid mapping and locus linkage within the human chromosomal region 22q13.1.
Blin N; Müllenbach R; Suijkerbuijk R; Herzog R; Meese E
Cancer Genet Cytogenet; 1993 Oct; 70(2):108-11. PubMed ID: 8242588
[TBL] [Abstract][Full Text] [Related]
11. Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers.
Laureys G; Speleman F; Versteeg R; van der Drift P; Chan A; Leroy J; Francke U; Opdenakker G; Van Roy N
Oncogene; 1995 Mar; 10(6):1087-93. PubMed ID: 7700633
[TBL] [Abstract][Full Text] [Related]
12. Molecular characterization of a variant Ph1 translocation t(9;22;11) (q34;q11;q13) in chronic myelogenous leukemia (CML) reveals the translocation of the 3'-part of BCR gene to the chromosome band 11q13.
Koduru PR; Goh JC; Pergolizzi RG; Lichtman SM; Broome JD
Oncogene; 1993 Dec; 8(12):3239-47. PubMed ID: 8247527
[TBL] [Abstract][Full Text] [Related]
13. Analysis of chromosome 22 loci in meningioma. Alterations in the leukemia inhibitory factor (LIF) locus.
Pergolizzi RG; Erster SH
Mol Chem Neuropathol; 1994; 21(2-3):189-217. PubMed ID: 7916188
[TBL] [Abstract][Full Text] [Related]
14. BCR expression is decreased in meningiomas showing loss of heterozygosity of 22q within a new minimal deletion region.
Wozniak K; Piaskowski S; Gresner SM; Golanska E; Bieniek E; Bigoszewska K; Sikorska B; Szybka M; Kulczycka-Wojdala D; Zakrzewska M; Zawlik I; Papierz W; Stawski R; Jaskolski DJ; Och W; Sieruta M; Liberski PP; Rieske P
Cancer Genet Cytogenet; 2008 May; 183(1):14-20. PubMed ID: 18474292
[TBL] [Abstract][Full Text] [Related]
15. Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis.
Lockwood DH; Farrier A; Hecht F; Allanson J
Hum Genet; 1989 Oct; 83(3):287-8. PubMed ID: 2793173
[TBL] [Abstract][Full Text] [Related]
16. Sublocalization of von Willebrand factor pseudogene to 22q11.22-q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocation.
Patracchini P; Calzolari E; Aiello V; Palazzi P; Banin P; Marchetti G; Bernardi F
Hum Genet; 1989 Oct; 83(3):264-6. PubMed ID: 2793170
[TBL] [Abstract][Full Text] [Related]
17. Red cell dimorphism in a young man with a constitutional chromosomal translocation t(11;22)(p15.5;q11.21).
Rees MI; Worwood M; Thompson PW; Gilbertson C; May A
Br J Haematol; 1994 Jun; 87(2):386-95. PubMed ID: 7947283
[TBL] [Abstract][Full Text] [Related]
18. Cloning and characterization of MN1, a gene from chromosome 22q11, which is disrupted by a balanced translocation in a meningioma.
Lekanne Deprez RH; Riegman PH; Groen NA; Warringa UL; van Biezen NA; Molijn AC; Bootsma D; de Jong PJ; Menon AG; Kley NA
Oncogene; 1995 Apr; 10(8):1521-8. PubMed ID: 7731706
[TBL] [Abstract][Full Text] [Related]
19. Characterization of a complex Philadelphia translocation (1p-;9q+;22q-) by gene mapping.
Geurts van Kessel AH; van Agthoven AJ; de Groot PG; Hagemeijer A
Hum Genet; 1981; 58(2):162-5. PubMed ID: 6945288
[TBL] [Abstract][Full Text] [Related]
20. Loss of heterozygosity on chromosome 22q and 17p correlates with aggressiveness of meningiomas.
Kim JH; Lee SH; Rhee CH; Park SY; Lee JH
J Neurooncol; 1998 Nov; 40(2):101-6. PubMed ID: 9892091
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
