Lathrop M - Search Results

1

ADAM33, a new candidate for psoriasis susceptibility.

Lesueur F, Oudot T, Heath S, Foglio M, Lathrop M, Prud'homme JF, Fischer J. Lesueur F, et al. Among authors: lathrop m. PLoS One. 2007 Sep 19;2(9):e906. doi: 10.1371/journal.pone.0000906. PLoS One. 2007. PMID: 17878941 Free PMC article.

2

Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1.

Jobard F, Lefèvre C, Karaduman A, Blanchet-Bardon C, Emre S, Weissenbach J, Ozgüc M, Lathrop M, Prud'homme JF, Fischer J. Jobard F, et al. Among authors: lathrop m. Hum Mol Genet. 2002 Jan 1;11(1):107-13. doi: 10.1093/hmg/11.1.107. Hum Mol Genet. 2002. PMID: 11773004

3

Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome.

Jobard F, Bouadjar B, Caux F, Hadj-Rabia S, Has C, Matsuda F, Weissenbach J, Lathrop M, Prud'homme JF, Fischer J. Jobard F, et al. Among authors: lathrop m. Hum Mol Genet. 2003 Apr 15;12(8):925-35. doi: 10.1093/hmg/ddg097. Hum Mol Genet. 2003. PMID: 12668616

4

Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.

Lefévre C, Audebert S, Jobard F, Bouadjar B, Lakhdar H, Boughdene-Stambouli O, Blanchet-Bardon C, Heilig R, Foglio M, Weissenbach J, Lathrop M, Prud'homme JF, Fischer J. Lefévre C, et al. Among authors: lathrop m. Hum Mol Genet. 2003 Sep 15;12(18):2369-78. doi: 10.1093/hmg/ddg235. Epub 2003 Jul 15. Hum Mol Genet. 2003. PMID: 12915478

5

Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis.

Lefèvre C, Bouadjar B, Karaduman A, Jobard F, Saker S, Ozguc M, Lathrop M, Prud'homme JF, Fischer J. Lefèvre C, et al. Among authors: lathrop m. Hum Mol Genet. 2004 Oct 15;13(20):2473-82. doi: 10.1093/hmg/ddh263. Epub 2004 Aug 18. Hum Mol Genet. 2004. PMID: 15317751

6

L-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1.

Topçu M, Jobard F, Halliez S, Coskun T, Yalçinkayal C, Gerceker FO, Wanders RJ, Prud'homme JF, Lathrop M, Ozguc M, Fischer J. Topçu M, et al. Among authors: lathrop m. Hum Mol Genet. 2004 Nov 15;13(22):2803-11. doi: 10.1093/hmg/ddh300. Epub 2004 Sep 22. Hum Mol Genet. 2004. PMID: 15385440

7

Exhaustive genotyping of the CEM15 (APOBEC3G) gene and absence of association with AIDS progression in a French cohort.

Do H, Vasilescu A, Diop G, Hirtzig T, Heath SC, Coulonges C, Rappaport J, Therwath A, Lathrop M, Matsuda F, Zagury JF. Do H, et al. Among authors: lathrop m. J Infect Dis. 2005 Jan 15;191(2):159-63. doi: 10.1086/426826. Epub 2004 Dec 15. J Infect Dis. 2005. PMID: 15609224

8

Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3.

Lefèvre C, Bouadjar B, Ferrand V, Tadini G, Mégarbané A, Lathrop M, Prud'homme JF, Fischer J. Lefèvre C, et al. Among authors: lathrop m. Hum Mol Genet. 2006 Mar 1;15(5):767-76. doi: 10.1093/hmg/ddi491. Epub 2006 Jan 25. Hum Mol Genet. 2006. PMID: 16436457

9

Associations of the IL2Ralpha, IL4Ralpha, IL10Ralpha, and IFN (gamma) R1 cytokine receptor genes with AIDS progression in a French AIDS cohort.

Do H, Vasilescu A, Diop G, Hirtzig T, Coulonges C, Labib T, Heath SC, Spadoni JL, Therwath A, Lathrop M, Matsuda F, Zagury JF. Do H, et al. Among authors: lathrop m. Immunogenetics. 2006 Apr;58(2-3):89-98. doi: 10.1007/s00251-005-0072-3. Epub 2006 Feb 21. Immunogenetics. 2006. PMID: 16491350

10

Identification of distinct quantitative trait Loci affecting length or weight variability at birth in humans.

Fradin D, Heath S, Lepercq J, Lathrop M, Bougnères P. Fradin D, et al. Among authors: lathrop m. J Clin Endocrinol Metab. 2006 Oct;91(10):4164-70. doi: 10.1210/jc.2006-0529. Epub 2006 Jul 18. J Clin Endocrinol Metab. 2006. PMID: 16849411

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