Viegas-Pequignot E - Search Results

1

Hypomethylation of classical satellite DNA and chromosome instability in lymphoblastoid cell lines.

Almeida A, Kokalj-Vokac N, Lefrancois D, Viegas-Pequignot E, Jeanpierre M, Dutrillaux B, Malfoy B. Almeida A, et al. Hum Genet. 1993 Jul;91(6):538-46. doi: 10.1007/BF00205077. Hum Genet. 1993. PMID: 8340107

2

High recurrence of rearrangements involving chromosome 14 in an ataxia telangiectasia lymphoblastoid cell line and in its mutagen-treated derivatives.

Lefrançois D, Kokalj N, Viegas-Péquignot E, Montagnier L, Dutrillaux B. Lefrançois D, et al. Hum Genet. 1991 Mar;86(5):475-80. doi: 10.1007/BF00194636. Hum Genet. 1991. PMID: 1849869

3

A t(X;15)(q23;q25) with Xq reactivation in a lymphoblastoid cell line from Fanconi anemia.

Kokalj-Vokac N, Saint-Ruf C, Lefrançois D, Viegas-Péquignot E, Lemieux N, Malfoy B, Dutrillaux B. Kokalj-Vokac N, et al. Cytogenet Cell Genet. 1991;57(1):11-5. doi: 10.1159/000133103. Cytogenet Cell Genet. 1991. PMID: 1855386

4

Detection of 1q polysomy in interphase nuclei of human solid tumors with a biotinylated probe.

Viegas-Péquignot E, Jeanpierre M, Dutrillaux AM, Gerbault-Seureau M, Muleris M, Dutrillaux B. Viegas-Péquignot E, et al. Hum Genet. 1989 Mar;81(4):311-4. doi: 10.1007/BF00283681. Hum Genet. 1989. PMID: 2539324

5

Assignment of human desmin gene to band 2q35 by nonradioactive in situ hybridization.

Viegas-Péquignot E, Li ZL, Dutrillaux B, Apiou F, Paulin D. Viegas-Péquignot E, et al. Hum Genet. 1989 Aug;83(1):33-6. doi: 10.1007/BF00274143. Hum Genet. 1989. PMID: 2670738

6

Studies on the human chromosome 3 centromere with a newly cloned alphoid DNA probe.

Delattre O, Bernard A, Malfoy B, Marlhens F, Viegas-Pequignot E, Brossard C, Haguenauer O, Creau-Goldberg N, N'guyen VC, Dutrillaux B, et al. Delattre O, et al. Hum Hered. 1988;38(3):156-67. doi: 10.1159/000153777. Hum Hered. 1988. PMID: 2899543

7

Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatin.

Kokalj-Vokac N, Almeida A, Viegas-Péquignot E, Jeanpierre M, Malfoy B, Dutrillaux B. Kokalj-Vokac N, et al. Cytogenet Cell Genet. 1993;63(1):11-5. doi: 10.1159/000133492. Cytogenet Cell Genet. 1993. PMID: 7680606

8

Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients.

Miniou P, Jeanpierre M, Blanquet V, Sibella V, Bonneau D, Herbelin C, Fischer A, Niveleau A, Viegas-Péquignot E. Miniou P, et al. Hum Mol Genet. 1994 Dec;3(12):2093-102. doi: 10.1093/hmg/3.12.2093. Hum Mol Genet. 1994. PMID: 7881405

9

An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome.

Jeanpierre M, Turleau C, Aurias A, Prieur M, Ledeist F, Fischer A, Viegas-Pequignot E. Jeanpierre M, et al. Hum Mol Genet. 1993 Jun;2(6):731-5. doi: 10.1093/hmg/2.6.731. Hum Mol Genet. 1993. PMID: 8102570

10

No relationship between genetic instability in Bloom's syndrome and DNA hypomethylation of some major repetitive sequences.

Noguiez P, Jaulin C, Praz F, Khelil M, Jeanpierre M, Viegas-Pequignot E, Amor-Gueret M. Noguiez P, et al. Hum Genet. 1993 Aug;92(1):57-60. doi: 10.1007/BF00216145. Hum Genet. 1993. PMID: 8365727

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