Blanché H - Search Results

1

A short tandem repeat polymorphism at the endothelin 1 (EDN1) locus.

Pages JC, Drieu C, Blanché H, Beckmann J, Cann HM. Pages JC, et al. Among authors: blanche h. Hum Mol Genet. 1993 Jan;2(1):90. doi: 10.1093/hmg/2.1.90. Hum Mol Genet. 1993. PMID: 8490632 No abstract available.

2

Genetic mapping of three human homologues of murine t-complex genes localizes TCP10 to 6q27, 15 cM distal to TCP1 and PLG.

Blanché H, Wright LG, Vergnaud G, de Gouyon B, Lauthier V, Silver LM, Dausset J, Cann HM, Spielman RS. Blanché H, et al. Genomics. 1992 Apr;12(4):826-8. doi: 10.1016/0888-7543(92)90317-l. Genomics. 1992. PMID: 1572657

3

A centromere-based genetic map of the short arm of human chromosome 6.

Blanché H, Zoghbi HY, Jabs EW, de Gouyon B, Zunec R, Dausset J, Cann HM. Blanché H, et al. Genomics. 1991 Mar;9(3):420-8. doi: 10.1016/0888-7543(91)90407-6. Genomics. 1991. PMID: 2032717

4

A subclone of the autosomal phosphoglycerate kinase pseudogene (HGM8 gene symbol PGK1P2), localized to 6p23-q12, detects moderately polymorphic RFLP.

Blanché H, Szabo P, Cohen D, Dausset J, Cann HM. Blanché H, et al. Nucleic Acids Res. 1987 May 11;15(9):3941. doi: 10.1093/nar/15.9.3941. Nucleic Acids Res. 1987. PMID: 2884642 Free PMC article. No abstract available.

5

A human anonymous low copy number clone, 4c11 (D6S4), localized to 6p12-6p21, detects 2 RFLPs, one of which is moderately polymorphic.

Blanché H, Zunec R, Gilliam C, Hartley D, Williamson R, Dausset J, Cann HM. Blanché H, et al. Nucleic Acids Res. 1987 Jul 24;15(14):5902. doi: 10.1093/nar/15.14.5902. Nucleic Acids Res. 1987. PMID: 2886978 Free PMC article. No abstract available.

6

A fragment of the human c-Ki-ras1 pseudogene (HGM9 gene symbol KRAS1P), localized to 6p12-p11, detects 3 allele, RFLP.

Blanché H, Chang EH, Dausset J, Cann HM. Blanché H, et al. Nucleic Acids Res. 1988 Feb 25;16(4):1652. doi: 10.1093/nar/16.4.1652. Nucleic Acids Res. 1988. PMID: 2894641 Free PMC article. No abstract available.

7

Exhaustive screening of the 21-hydroxylase gene in a population of hyperandrogenic women.

Blanché H, Vexiau P, Clauin S, Le Gall I, Fiet J, Mornet E, Dausset J, Bellanné-Chantelot C. Blanché H, et al. Hum Genet. 1997 Nov;101(1):56-60. doi: 10.1007/s004390050586. Hum Genet. 1997. PMID: 9385370

8

Significant linkage to spondyloarthropathy on 9q31-34.

Miceli-Richard C, Zouali H, Said-Nahal R, Lesage S, Merlin F, De Toma C, Blanche H, Sahbatou M, Dougados M, Thomas G, Breban M, Hugot JP; Groupe Français d'Etude Génétique des Spondylarthropathies. Miceli-Richard C, et al. Among authors: blanche h. Hum Mol Genet. 2004 Aug 1;13(15):1641-8. doi: 10.1093/hmg/ddh179. Hum Mol Genet. 2004. PMID: 15234954

9

Positive selection in the chromosome 16 VKORC1 genomic region has contributed to the variability of anticoagulant response in humans.

Patillon B, Luisi P, Blanché H, Patin E, Cann HM, Génin E, Sabbagh A. Patillon B, et al. Among authors: blanche h. PLoS One. 2012;7(12):e53049. doi: 10.1371/journal.pone.0053049. Epub 2012 Dec 28. PLoS One. 2012. PMID: 23285254 Free PMC article.

10

The complete genome sequence of a Neanderthal from the Altai Mountains.

Prüfer K, Racimo F, Patterson N, Jay F, Sankararaman S, Sawyer S, Heinze A, Renaud G, Sudmant PH, de Filippo C, Li H, Mallick S, Dannemann M, Fu Q, Kircher M, Kuhlwilm M, Lachmann M, Meyer M, Ongyerth M, Siebauer M, Theunert C, Tandon A, Moorjani P, Pickrell J, Mullikin JC, Vohr SH, Green RE, Hellmann I, Johnson PL, Blanche H, Cann H, Kitzman JO, Shendure J, Eichler EE, Lein ES, Bakken TE, Golovanova LV, Doronichev VB, Shunkov MV, Derevianko AP, Viola B, Slatkin M, Reich D, Kelso J, Pääbo S. Prüfer K, et al. Among authors: blanche h. Nature. 2014 Jan 2;505(7481):43-9. doi: 10.1038/nature12886. Epub 2013 Dec 18. Nature. 2014. PMID: 24352235 Free PMC article.

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