M Le Coniat
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Explore the profile of M Le Coniat including associated specialties, affiliations and a list of published articles.
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Articles
71
Citations
509
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Recent Articles
11.
Leblanc T, Le Coniat M, Flexor M, Baruchel A, Daniel M, Berger R
Leukemia
. 1996 Nov;
10(11):1844-6.
PMID: 8892693
Chromosome studies of an infant with acute myeloblastic leukemia (AML), classified as M2 in the FAB nomenclature revealed an unusual karyotype with del(11)(q23) and a marker chromosome resembling a small...
12.
Maarek O, Jonveaux P, Le Coniat M, Derre J, Berger R
Leukemia
. 1996 Nov;
10(11):1700-4.
PMID: 8892670
Clonal chromosome abnormalities were detected in bone marrow cells of 20 patients with Fanconi anemia investigated at various stages of the disease. Two presented with acute leukemia, six with myelodysplastic...
13.
Della Valle V, Le Coniat M, Soulard M, Nguyen V, Berger R, Larsen C
Hum Genet
. 1996 Aug;
98(2):210-3.
PMID: 8698345
A cDNA probe representative of the human hnRNP I/PTB gene was used to perform fluorescence in situ hybridization (FISH) on metaphases of human chromosomes. A new localization was found on...
14.
Monte D, Coutte L, DeWITTE F, Defossez P, Le Coniat M, Stehelin D, et al.
Genomics
. 1996 Jul;
35(1):236-40.
PMID: 8661127
The ERM protein belongs to the family of Ets transcription factors. We show here that the human ERM gene is organized into 14 exons distributed along 65 kb of genomic...
15.
Berger R, Le Coniat M, Romana S, Jonveaux P
Hematol Cell Ther
. 1996 Apr;
38(2):183-6.
PMID: 8932000
A t(16;21) (q24;122) translocation was detected by fluorescence in situ hybridization in a patient with acute myeloblastic leukemia previously treated for malignant lymphoma. While the breakpoint on chromosome 21 was...
16.
Le Coniat M, Choi D, Maroteaux L, Launay J, Berger R
Genomics
. 1996 Feb;
32(1):172-3.
PMID: 8786115
No abstract available.
17.
Berger R, Le Coniat M, Flexor M, Leblanc T
Ann Genet
. 1996 Jan;
39(3):147-51.
PMID: 8839887
Fluorescence in situ hybridization analysis in an infant with acute monocytic leukemia revealed a complex translocation, t(10;11;4) (p12; q23;q26). Southern blot analysis confirmed the existence of rearrangement of the MLL...
18.
Jonveaux P, Le Coniat M, Derre J, Flexor M, Daniel M, Berger R
Genes Chromosomes Cancer
. 1996 Jan;
15(1):26-33.
PMID: 8824722
In many human cancers the presence of marker chromosomes or unbalanced translocations prevents complete karyotypic analysis. Chromosome microdissection has become an increasingly important method for assessing chromosome rearrangements. However, most...
19.
Berger R, Flexor M, Le Coniat M, Larsen C
Cancer Genet Cytogenet
. 1996 Jan;
86(1):76-9.
PMID: 8616793
A complex chromosomal abnormality associating three recurrent rearrangements, t(2;3)((p12;q37), del (8)(q24) and t(14;18)(q32;q21), was detected in a patient with acute lymphoblastic leukemia of the Burkitt type. Southern blot studies showed...
20.
Romana S, Le Coniat M, Poirel H, Marynen P, Bernard O, Berger R
Leukemia
. 1996 Jan;
10(1):167-70.
PMID: 8558923
Translocation t(12;21) has been described as a nonrandom event in acute lymphoblastic leukemia (ALL) in patients with deletion of the short arm of chromosome 12, using fluorescence in situ hybridization...