Jeanpierre M - 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. Among authors: jeanpierre m. Hum Genet. 1993 Jul;91(6):538-46. doi: 10.1007/BF00205077. Hum Genet. 1993. PMID: 8340107

2

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. Among authors: jeanpierre m. Cytogenet Cell Genet. 1993;63(1):11-5. doi: 10.1159/000133492. Cytogenet Cell Genet. 1993. PMID: 7680606

3

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. Among authors: jeanpierre m. Hum Mol Genet. 1994 Dec;3(12):2093-102. doi: 10.1093/hmg/3.12.2093. Hum Mol Genet. 1994. PMID: 7881405

4

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

5

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. Among authors: jeanpierre m. Hum Genet. 1993 Aug;92(1):57-60. doi: 10.1007/BF00216145. Hum Genet. 1993. PMID: 8365727

6

alpha-satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues.

Miniou P, Jeanpierre M, Bourc'his D, Coutinho Barbosa AC, Blanquet V, Viegas-Péquignot E. Miniou P, et al. Among authors: jeanpierre m. Hum Genet. 1997 Jun;99(6):738-45. doi: 10.1007/s004390050441. Hum Genet. 1997. PMID: 9187666

7

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. Among authors: jeanpierre m. Hum Genet. 1989 Mar;81(4):311-4. doi: 10.1007/BF00283681. Hum Genet. 1989. PMID: 2539324

8

Undermethylation of Alu sequences in ICF syndrome: molecular and in situ analysis.

Miniou P, Bourc'his D, Molina Gomes D, Jeanpierre M, Viegas-Péquignot E. Miniou P, et al. Among authors: jeanpierre m. Cytogenet Cell Genet. 1997;77(3-4):308-13. doi: 10.1159/000134605. Cytogenet Cell Genet. 1997. PMID: 9284945

9

Abnormal methylation does not prevent X inactivation in ICF patients.

Bourc'his D, Miniou P, Jeanpierre M, Molina Gomes D, Dupont J, De Saint-Basile G, Maraschio P, Tiepolo L, Viegas-Péquignot E. Bourc'his D, et al. Among authors: jeanpierre m. Cytogenet Cell Genet. 1999;84(3-4):245-52. doi: 10.1159/000015269. Cytogenet Cell Genet. 1999. PMID: 10393442

10

De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy.

Chelly J, Marlhens F, Le Marec B, Jeanpierre M, Lambert M, Hamard G, Dutrillaux B, Kaplan JC. Chelly J, et al. Among authors: jeanpierre m. Hum Genet. 1986 Oct;74(2):193-6. doi: 10.1007/BF00282093. Hum Genet. 1986. PMID: 2876949

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