Borot N - Search Results

1

Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosis.

Boretto J, Jouanolle AM, Yaouanq J, el Kahloun A, Mauvieux V, Blayau M, Perichon M, Le Treut A, Clayton J, Borot N, et al. Boretto J, et al. Among authors: borot n. Hum Genet. 1992 Apr;89(1):33-6. doi: 10.1007/BF00207038. Hum Genet. 1992. PMID: 1349563

2

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis Consortium.

Merryweather-Clarke AT, Pointon JJ, Shearman JD, Robson KJ, Jouanolle AM, Mosser A, David V, Le Gall JY, Halsall DJ, Elsey TS, Kelly A, Cox TM, Clare M, Bomford A, Vandwalle JL, Rochette J, Borot N, Coppin H, Roth MP, Ryan E, Crowe J, Totaro A, Gasparini P, Roetto A, Walker AP, et al. Merryweather-Clarke AT, et al. Among authors: borot n. Nat Genet. 1999 Nov;23(3):271. doi: 10.1038/15452. Nat Genet. 1999. PMID: 10545942 No abstract available.

3

Three highly polymorphic microsatellites at the human myelin oligodendrocyte glycoprotein locus, 100 kb telomeric to HLA-F. Characterization and relation to HLA haplotypes.

Roth MP, Dolbois L, Borot N, Amadou C, Clanet M, Pontarotti P, Coppin H. Roth MP, et al. Among authors: borot n. Hum Immunol. 1995 Aug;43(4):276-82. doi: 10.1016/0198-8859(95)91033-t. Hum Immunol. 1995. PMID: 7499175

4

Polymorphic tri- and tetranucleotide repeats in exons 1 and 8 of the myelin oligodendrocyte glycoprotein (MOG) gene.

Malfroy L, Viratelle C, Coppin H, Borot N, Roth MP. Malfroy L, et al. Among authors: borot n. Hum Genet. 1995 Dec;96(6):737-8. doi: 10.1007/BF00210310. Hum Genet. 1995. PMID: 8522338

5

Selection, hitchhiking and disequilibrium analysis at three linked loci with application to HLA data.

Robinson WP, Cambon-Thomsen A, Borot N, Klitz W, Thomson G. Robinson WP, et al. Among authors: borot n. Genetics. 1991 Nov;129(3):931-48. doi: 10.1093/genetics/129.3.931. Genetics. 1991. PMID: 1752429 Free PMC article.

6

Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients.

Borot N, Roth M, Malfroy L, Demangel C, Vinel JP, Pascal JP, Coppin H. Borot N, et al. Immunogenetics. 1997;45(5):320-4. doi: 10.1007/s002510050211. Immunogenetics. 1997. PMID: 9038104

7

Heterogeneity in rates of recombination in the 6-Mb region telomeric to the human major histocompatibility complex.

Malfroy L, Roth MP, Carrington M, Borot N, Volz A, Ziegler A, Coppin H. Malfroy L, et al. Among authors: borot n. Genomics. 1997 Jul 15;43(2):226-31. doi: 10.1006/geno.1997.4800. Genomics. 1997. PMID: 9244441

8

Phosphoglucomutase-1 subtypes in two populations in Adriatic islands: presence of PGM1*W3 (PGM1*7+) allele.

Borot N, Arnaud J, Rudan P, Chaventré A, Sevin J. Borot N, et al. Hum Hered. 1991;41(5):309-15. doi: 10.1159/000154018. Hum Hered. 1991. PMID: 1838099

9

Recombination fractions in the HLA system based on the data set 'provinces Françaises': indications of haplotype-specific recombination rates.

Thomsen M, Neugebauer M, Arnaud J, Borot N, Sevin A, Baur M, Cambon-Thomsen A. Thomsen M, et al. Among authors: borot n. Eur J Immunogenet. 1994 Feb;21(1):33-43. doi: 10.1111/j.1744-313x.1994.tb00174.x. Eur J Immunogenet. 1994. PMID: 9098418

10

The human myelin oligodendrocyte glycoprotein (MOG) gene: complete nucleotide sequence and structural characterization.

Roth MP, Malfroy L, Offer C, Sevin J, Enault G, Borot N, Pontarotti P, Coppin H. Roth MP, et al. Among authors: borot n. Genomics. 1995 Jul 20;28(2):241-50. doi: 10.1006/geno.1995.1137. Genomics. 1995. PMID: 8530032

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