The t(8;13) atypical myeloproliferative disorder: Further analysis of the ZNF198 gene and lack of evidence for multiple genes disrupted on chromosome 13

被引：36

作者：

Still, IH ^{[1
]}

Cowell, JK ^{[1
]}

机构：

[1] Cleveland Clin Fdn, Lerner Res Inst, Dept Neurosci NC30, Cleveland, OH 44195 USA

来源：

BLOOD | 1998年 / 92卷 / 04期

关键词：

D O I：

10.1182/blood.V92.4.1456.splL3_1456_1458

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1456 / 1458

页数：3

共 15 条

[1] t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12 [J].

Chaffanet, M ;

Popovici, C ;

Leroux, D ;

Jacrot, M ;

Adélaïde, J ;

Dastugue, N ;

Grégoire, MJ ;

Hagemeijer, A ;

Lafage-Pochitaloff, M ;

Birnbaum, D ;

Pébusque, MJ .

ONCOGENE, 1998, 16 (07) :945-949

[2]

Chernova O, 1998, GENE CHROMOSOME CANC, V21, P160, DOI 10.1002/(SICI)1098-2264(199802)21:2<160::AID-GCC12>3.0.CO

[3]

2-V

[4] NOVEL RECIPROCAL TRANSLOCATION BETWEEN CHROMOSOME-8 AND CHROMOSOME-9 FOUND IN A PATIENT WITH MYELOPROLIFERATIVE DISORDER [J].

FRIEDHOFF, F ;

RAJENDRA, B ;

MOODY, R ;

ALAPATT, T .

CANCER GENETICS AND CYTOGENETICS, 1983, 9 (04) :391-394

[5] A YAC CONTIG AND AN EST MAP IN THE PERICENTROMERIC REGION OF CHROMOSOME-13 SURROUNDING THE LOCI FOR NEUROSENSORY NONSYNDROMIC DEAFNESS (DFNB1 AND DFNA3) AND LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2C (LGMD2C) [J].

GUILFORD, P ;

DODE, C ;

CROZET, F ;

BLANCHARD, S ;

CHAIB, H ;

LEVILLIERS, J ;

LEVIACOBAS, F ;

WEIL, D ;

WEISSENBACH, J ;

COHEN, D ;

LEPASLIER, D ;

KAPLAN, JC ;

PETIT, C .

GENOMICS, 1995, 29 (01) :163-169

[6] A SYNDROME OF LYMPHOBLASTIC LYMPHOMA, EOSINOPHILIA, AND MYELOID HYPERPLASIA MALIGNANCY ASSOCIATED WITH T(8-13) (P11-Q11) - DESCRIPTION OF A DISTINCTIVE CLINICOPATHOLOGICAL ENTITY [J].

INHORN, RC ;

ASTER, JC ;

ROACH, SA ;

SLAPAK, CA ;

SOIFFER, R ;

TANTRAVAHI, R ;

STONE, RM .

BLOOD, 1995, 85 (07) :1881-1887

[7] LOCALIZATION OF THE 8-13 TRANSLOCATION BREAKPOINT ASSOCIATED WITH MYELOPROLIFERATIVE DISEASE TO A 1.5 MBP REGION OF CHROMOSOME-13 [J].

KEMPSKI, H ;

MACDONALD, D ;

MICHALSKI, AJ ;

ROBERTS, T ;

GOLDMAN, JM ;

CROSS, NCP ;

COWELL, JK .

GENES CHROMOSOMES & CANCER, 1995, 12 (04) :283-287

[8]

LEWIS JP, 1983, AM J PEDIAT HEMATOL, V5, P265

[9] RECIPROCAL TRANSLOCATION BETWEEN CHROMOSOME-8 AND CHROMOSOME-9 IN ATYPICAL CHRONIC MYELOID-LEUKEMIA [J].

OSCIER, DG ;

MUFTI, GJ ;

GARDINER, A ;

HAMBLIN, TJ .

JOURNAL OF MEDICAL GENETICS, 1985, 22 (05) :398-401

[10] Fibroblast growth factor receptor 1 is used to FIM in stem-cell myeloproliferative disorder with t(8;13)(p12;q12) [J].

Popovici, C ;

Adélaïde, J ;

Ollendorff, V ;

Chaffanet, M ;

Guasch, G ;

Jacrot, M ;

Leroux, D ;

Birnbaum, D ;

Pébusque, MJ .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (10) :5712-5717

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