Loux N - Search Results

1

Two new polymorphisms in the coding sequence of the LDL receptor (LDLR) gene.

Saint-Jore B, Loux N, Junien C, Boileau C. Saint-Jore B, et al. Among authors: loux n. Hum Genet. 1993 Jun;91(5):511-2. doi: 10.1007/BF00217783. Hum Genet. 1993. PMID: 8100212

2

Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism method.

Loux N, Saint-Jore B, Collod G, Dairou F, Benlian P, Truffert J, Dastugue B, Douste-Blazy P, de Gennes JL, Junien C, et al. Loux N, et al. Hum Mutat. 1992;1(4):325-32. doi: 10.1002/humu.1380010411. Hum Mutat. 1992. PMID: 1301940

3

Extended haplotypes and linkage disequilibrium between 11 markers at the APOA1-C3-A4 gene cluster on chromosome 11.

Benlian P, Boileau C, Loux N, Pastier D, Masliah J, Coulon M, Nigou M, Ragab A, Guimard J, Ruidavets JB, et al. Benlian P, et al. Among authors: loux n. Am J Hum Genet. 1991 May;48(5):903-10. Am J Hum Genet. 1991. PMID: 1673288 Free PMC article.

4

Recurrent mutation at aa 792 in the LDL receptor gene in a French patient.

Loux N, Benlian P, Pastier D, Boileau C, Cambou JP, Monnier L, Percheron C, Junien C. Loux N, et al. Hum Genet. 1991 Jul;87(3):373-5. doi: 10.1007/BF00200923. Hum Genet. 1991. PMID: 1677927

5

Identification of the haplotype associated with the APOB-3500 mutation in a French hypercholesterolemic subject: further support for a unique European ancestral mutation.

Loux N, Saint-Jore B, Collod G, Benlian P, Cambou JP, Denat M, Junien C, Boileau C. Loux N, et al. Hum Mutat. 1993;2(2):145-7. doi: 10.1002/humu.1380020216. Hum Mutat. 1993. PMID: 8318993 No abstract available.

6

Anderson's disease: genetic exclusion of the apolipoprotein-B gene in two families.

Pessah M, Benlian P, Beucler I, Loux N, Schmitz J, Junien C, Infante R. Pessah M, et al. Among authors: loux n. J Clin Invest. 1991 Jan;87(1):367-70. doi: 10.1172/JCI114996. J Clin Invest. 1991. PMID: 1985110 Free PMC article.

7

Genetic exclusion of apo-B gene in recessive abetalipoproteinemia.

Pessah M, Beucler I, Loux N, Navarro J, Guillerd X, Dulac O, Lequeux J, Junien C, Infante R. Pessah M, et al. Among authors: loux n. Biochem Biophys Res Commun. 1993 Jan 15;190(1):97-103. doi: 10.1006/bbrc.1993.1016. Biochem Biophys Res Commun. 1993. PMID: 8422264

8

A LDL receptor gene homozygous mutation: PCR amplification, direct genomic sequencing, associated haplotype, rapid screening for frequency.

Benlian P, Amselem S, Loux N, Pastier D, Giraud G, de Gennes JL, Turpin G, Monnier L, Rieu D, Douste-Blazy P, et al. Benlian P, et al. Among authors: loux n. Ann Genet. 1990;33(2):65-9. Ann Genet. 1990. PMID: 1978630

9

[Towards gene therapy in familial hypercholesterolemia].

Pagès JC, Andreoletti M, Loux N, Vons C, Mahieu D, Bargy F, Chapman J, Briand P, Franco D, Weber A. Pagès JC, et al. Among authors: loux n. C R Seances Soc Biol Fil. 1996;190(1):53-65. C R Seances Soc Biol Fil. 1996. PMID: 8881269 French.

10

Engraftment of autologous retrovirally transduced hepatocytes after intraportal transplantation into nonhuman primates: implication for ex vivo gene therapy.

Andreoletti M, Loux N, Vons C, Nguyen TH, Lorand I, Mahieu D, Simon L, Di Rico V, Vingert B, Chapman J, Briand P, Schwall R, Hamza J, Capron F, Bargy F, Franco D, Weber A. Andreoletti M, et al. Among authors: loux n. Hum Gene Ther. 2001 Jan 20;12(2):169-79. doi: 10.1089/104303401750061230. Hum Gene Ther. 2001. PMID: 11177554

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