J Derre
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Explore the profile of J Derre including associated specialties, affiliations and a list of published articles.
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Citations
237
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Recent Articles
11.
Berger R, Derre J, Le Coniat M, Hebert J, Romana P, Jonveaux P
Genes Chromosomes Cancer
. 1995 Jan;
12(1):58-62.
PMID: 7534112
Cytogenetic studies of three acute myelomonocytic leukemias with bone marrow eosinophilia (M4EO) revealed chromosome 16 inversion associated with additional abnormalities. The inverted chromosome 16 was involved in two patients. Fluorescence...
12.
Jonveaux P, Hillion J, Bernard O, Le Coniat M, Derre J, Flexor M, et al.
Leukemia
. 1994 Dec;
8(12):2224-7.
PMID: 7808011
A patient with acute monocytic leukemia (AMoL) and t(6;11)(q27;q23) developed acute lymphoblastic leukemia (ALL) and t(4;11)(q21;23), 10 months after complete remission of the AMoL. The MLL gene, normally located at...
13.
Leblanc T, Hillion J, Derre J, Le Coniat M, Baruchel A, Daniel M, et al.
Leukemia
. 1994 Oct;
8(10):1646-8.
PMID: 7934159
A child with acute myelomonocytic leukemia, bone marrow eosinophilia and inv(16) received first-line therapy including etoposide (VP-16). Cytopenia and monocytosis appeared 7 months after complete remission while the child was...
14.
Baranger L, Szapiro N, Gardais J, Hillion J, Derre J, Francois S, et al.
Br J Haematol
. 1994 Oct;
88(2):343-7.
PMID: 7803280
A t(5;12)(q33;p13) translocation has been detected in two patients with myeloid disorder and eosinophilia. Six other patients with haematological disease with eosinophilia with similar translocation have been published previously. The...
15.
Jonveaux P, Derre J, Berger R
Leukemia
. 1993 Dec;
7(12):1987-9.
PMID: 8255097
Whole arm translocation t(17;18) was detected in two patients, one with acute monocytic leukemia and the other with acute transformation of chronic myelocytic leukemia. Dual-color fluorescence in situ hybridization (FISH)...
16.
Romana S, Cherif D, Le Coniat M, Derre J, Flexor M, Berger R
Genes Chromosomes Cancer
. 1993 Oct;
8(2):98-103.
PMID: 7504523
Numerical chromosome abnormalities were studied in 17 acute lymphoblastic leukemias and one hyperdiploid acute myeloblastic leukemia by fluorescence in situ hybridization (FISH) using YAC clones specific to chromosomes 21 and...
17.
Chen S, Zelent A, Tong J, Yu H, Wang Z, Derre J, et al.
J Clin Invest
. 1993 May;
91(5):2260-7.
PMID: 8387545
Cytogenetic study of a patient with acute promyelocytic leukemia (APL) showed an unusual karyotype 46,xy,t(11;17) (q23;21) without apparent rearrangement of chromosome 15. Molecular studies showed rearrangements of the retinoic acid...
18.
Berger R, Le Coniat M, Derre J, Flexor M, Hillion J
Cancer Genet Cytogenet
. 1992 Oct;
63(2):97-9.
PMID: 1423238
Monosomy 18 and partial deletion of 18q are nonrandom events in myelodysplastic syndromes (MDS) and secondary acute myeloblastic leukemia (sAML). They are part of complex chromosome abnormalities, as shown in...
19.
Pugliatti L, Derre J, Berger R, Ucla C, Reith W, MACH B
Genomics
. 1992 Aug;
13(4):1307-10.
PMID: 1505960
RFX1 is a transacting DNA-binding regulatory factor involved in the control of MHC class II gene expression. RFX2 is a structurally very similar protein with identical DNA binding features. A...
20.
Berger R, Le Coniat M, Derre J, Flexor M
Cancer Genet Cytogenet
. 1992 Jul;
61(2):210-2.
PMID: 1638507
We report studies of 12 patients with refractory anemia and excess of blasts in transformation (RAEB-t) and 17 with acute myeloblastic leukemia (AML) after RAEB. Besides chromosome 5 and 7...