Buresi C - Search Results

1

Structural analysis of the minisatellite present at the 3' end of the human apolipoprotein B gene: new definition of the alleles and evolutionary implications.

Buresi C, Desmarais E, Vigneron S, Lamarti H, Smaoui N, Cambien F, Roizes G. Buresi C, et al. Hum Mol Genet. 1996 Jan;5(1):61-8. doi: 10.1093/hmg/5.1.61. Hum Mol Genet. 1996. PMID: 8789440

2

Variant mapping of the Apo(B) AT rich minisatellite. Dependence on nucleotide sequence of the copy number variations. Instability of the non-canonical alleles.

Desmarais E, Vigneron S, Buresi C, Cambien F, Cambou JP, Roizes G. Desmarais E, et al. Among authors: buresi c. Nucleic Acids Res. 1993 May 11;21(9):2179-84. doi: 10.1093/nar/21.9.2179. Nucleic Acids Res. 1993. PMID: 8502559 Free PMC article.

3

Polymorphism at VNTR locus 3 to the apolipoprotein B gene in a Tunisian population: difference from other ethnic groups.

Buresi C, Desmarais E, Vigneron S, Ben Rayana C, Chaabouni H, Roizes G. Buresi C, et al. Genet Epidemiol. 1995;12(4):381-9. doi: 10.1002/gepi.1370120406. Genet Epidemiol. 1995. PMID: 8536955

4

DNA polymorphisms in linkage disequilibrium at the 3' end of the human APO AII gene: relationships with lipids, apolipoproteins and coronary heart disease.

Dupuy-Gorce AM, Desmarais E, Vigneron S, Buresi C, Nicaud V, Evans A, Luc G, Arveiler D, Marqués-Vidal P, Cambien F, Tiret L, Crastes de Paulet A, Roizés G. Dupuy-Gorce AM, et al. Among authors: buresi c. Clin Genet. 1996 Oct;50(4):191-8. doi: 10.1111/j.1399-0004.1996.tb02624.x. Clin Genet. 1996. PMID: 9001797

5

Structure and function of alleles in the 3' end region of human apoB gene.

Chen B, Guo Z, He P, Ye P, Buresi C, Roizes G. Chen B, et al. Among authors: buresi c. Chin Med J (Engl). 1999 Mar;112(3):221-3. Chin Med J (Engl). 1999. PMID: 11593553

6

Defective, deleted or converted CYP21B gene and negative association with a rare restriction fragment length polymorphism allele of the factor B gene in congenital adrenal hyperplasia.

Ghanem N, Lobaccaro JM, Buresi C, Abbal M, Halaby G, Sultan C, Lefranc G. Ghanem N, et al. Among authors: buresi c. Hum Genet. 1990 Dec;86(2):117-25. doi: 10.1007/BF00197691. Hum Genet. 1990. PMID: 1979956

7

Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations.

Moulard B, Genton P, Grid D, Jeanpierre M, Ouazzani R, Mrabet A, Morris M, LeGuern E, Dravet C, Mauguière F, Utermann B, Baldy-Moulinier M, Belaidi H, Bertran F, Biraben A, Ali Chérif A, Chkili T, Crespel A, Darcel F, Dulac O, Geny C, Humbert-Claude V, Kassiotis P, Buresi C, Malafosse A. Moulard B, et al. Among authors: buresi c. Hum Genet. 2002 Sep;111(3):255-62. doi: 10.1007/s00439-002-0755-x. Epub 2002 Jul 23. Hum Genet. 2002. PMID: 12215838

8

HindIII/EcoRI RFLP of the human immunoglobulin IGHE gene detected with a C epsilon probe in the French and Tunisian populations.

Bernard F, Ducret F, Buresi C, Lefranc G, Lefranc MP. Bernard F, et al. Among authors: buresi c. Hum Genet. 1991 May;87(1):101. doi: 10.1007/BF01213105. Hum Genet. 1991. PMID: 1674713

9

The monoamine oxidase A gene may influence the means used in suicide attempts.

Courtet P, Jollant F, Buresi C, Castelnau D, Mouthon D, Malafosse A. Courtet P, et al. Among authors: buresi c. Psychiatr Genet. 2005 Sep;15(3):189-93. doi: 10.1097/00041444-200509000-00009. Psychiatr Genet. 2005. PMID: 16094253

10

Deletion, insertion, and restriction site polymorphism of the T-cell receptor gamma variable locus in French, Lebanese, Tunisian, and black African populations.

Ghanem N, Buresi C, Moisan JP, Bensmana M, Chuchana P, Huck S, Lefranc G, Lefranc MP. Ghanem N, et al. Among authors: buresi c. Immunogenetics. 1989;30(5):350-60. doi: 10.1007/BF02425275. Immunogenetics. 1989. PMID: 2572547

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