1 - 25 of 28 results for author:"Elion J." in Literature citations
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| Genetic variation among major human geographic groups supports a peculiar evolutionary trend in PAX9. Paixao-Cortes V.R., Meyer D., Pereira T.V., Mazieres S., Elion J., Krishnamoorthy R., Zago M.A., Silva W.A. Jr., Salzano F.M., Bortolini M.C. PLoS ONE 6:e15656-e15656(2011) · Mapped (6) |
| Activation state of alpha4beta1 integrin on sickle red blood cells is linked to the duffy antigen receptor for chemokines (DARC) expression. Durpes M.C., Hardy-Dessources M.D., El Nemer W., Picot J., Lemonne N., Elion J., Decastel M. J. Biol. Chem. 286:3057-3064(2011) · Mapped (15) |
| Alpha-thalassemia is associated with a decreased occurrence and a delayed age-at-onset of albuminuria in sickle cell anemia patients. Nebor D., Broquere C., Brudey K., Mougenel D., Tarer V., Connes P., Elion J., Romana M. Blood Cells Mol. Dis. 45:154-158(2010) · Mapped (52) |
| Phenotypic expression and origin of the rare beta-thalassemia splice site mutation HBB:c.315 + 1G>T. Broquere C., Brudey K., Harteveld C.L., Saint-Martin C., Elion J., Giordano P.C., Romana M. Hemoglobin 34:322-326(2010) · Mapped (38) |
| Variants of the mannose-binding lectin gene in the Benin population: heterozygosity for the p.G57E allele may confer a selective advantage. 2007. Dossou-Yovo O.P., Lapoumeroulie C., Hauchecorne M., Zaccaria I., Ducrocq R., Krishnamoorthy R., Rahimy M.C., Elion J. Hum. Biol. 81:899-909(2009) · Mapped (3) |
| Association between Duffy antigen receptor for chemokines expression and levels of inflammation markers in sickle cell anemia patients. Nebor D., Durpes M.C., Mougenel D., Mukisi-Mukaza M., Elion J., Hardy-Dessources M.D., Romana M. Clin. Immunol. 136:116-122(2010) · Mapped (15) |
| Effect of interleukin-8 and RANTES on the Gardos channel activity in sickle human red blood cells: role of the Duffy antigen receptor for chemokines. Durpes M.C., Nebor D., du Mesnil P.C., Mougenel D., Decastel M., Elion J., Hardy-Dessources M.D. Blood Cells Mol. Dis. 44:219-223(2010) · Mapped (15) |
| Genotype-phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease. Denamur E., Delezoide A.L., Alberti C., Bourillon A., Gubler M.C., Bouvier R., Pascaud O., Elion J., Grandchamp B., Michel-Calemard L. et al. Kidney Int. 77:350-358(2010) · Mapped (2) |
| Effects of RANTES and MBL2 gene polymorphisms in sickle cell disease clinical outcomes: association of the g.In1.1T>C RANTES variant with protection against infections. Dossou-Yovo O.P., Zaccaria I., Benkerrou M., Hauchecorne M., Alberti C., Rahimy M.C., Elion J., Lapoumeroulie C. Am. J. Hematol. 84:378-380(2009) · Mapped (7) |
| Variants of the mannose-binding lectin gene in the Benin population: heterozygosity for the p.G57E allele may confer a selective advantage. Dossou-Yovo O.P., Lapoumeroulie C., Hauchecorne M., Zaccaria I., Ducrocq R., Krishnamoorthy R., Rahimy M.C., Elion J. Hum. Biol. 79:687-697(2007) · Mapped (3) |
| Modulation of erythroid adhesion receptor expression by hydroxyurea in children with sickle cell disease. Odievre M.H., Bony V., Benkerrou M., Lapoumeroulie C., Alberti C., Ducrocq R., Jacqz-Aigrain E., Elion J., Cartron J.P. Haematologica 93:502-510(2008) · Mapped (2) |
| The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 gene. Sznajer Y., Keren B., Baumann C., Pereira S., Alberti C., Elion J., Cave H., Verloes A. Pediatrics 119:e1325-31(2007) · Mapped (6) |
| ET-1 and ecNOS gene polymorphisms andsusceptibility to acute chest syndrome and painful vaso-occlusive crises in children with sickle cell anemia. Chaar V., Tarer V., Etienne-Julan M., Diara J.P., Elion J., Romana M. Haematologica 91:1277-1278(2006) · Mapped (9) |
| Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP-B) deficiency. Tredano M., Cooper D.N., Stuhrmann M., Christodoulou J., Chuzhanova N.A., Roudot-Thoraval F., Boelle P.Y., Elion J., Jeanpierre M., Feingold J. et al. Am. J. Med. Genet. A 140:62-69(2006) · Mapped (5) |
| Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia. Chaar V., Keclard L., Diara J.P., Leturdu C., Elion J., Krishnamoorthy R., Clayton J., Romana M. Haematologica 90:188-199(2005) · Mapped (15) |
| Molecular basis of methylmalonyl-CoA mutase apoenzyme defect in 40 European patients affected by mut(o) and mut- forms of methylmalonic acidemia: identification of 29 novel mutations in the MUT gene. Acquaviva C., Benoist J.-F., Pereira S., Callebaut I., Koskas T., Porquet D., Elion J. |
| Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease. Tredano M., Griese M., Brasch F., Schumacher S., de Blic J., Marque S., Houdayer C., Elion J., Couderc R., Bahuau M. Am. J. Med. Genet. A 126:18-26(2004) · UniProtKB (1) · Mapped (2) |
| Analysis of 40 sporadic or familial neonatal and pediatric cases with severe unexplained respiratory distress: relationship to SFTPB. Tredano M., Griese M., de Blic J., Lorant T., Houdayer C., Schumacher S., Cartault F., Capron F., Boccon-Gibod L., Lacaze-Masmonteil T. et al. Am. J. Med. Genet. A 119A:324-339(2003) · Mapped (5) |
| Infectious complications in sickle cell disease are influenced by HLA class II alleles. Tamouza R., Neonato M.G., Busson M., Marzais F., Girot R., Labie D., Elion J., Charron D. Hum. Immunol. 63:194-199(2002) · Mapped (481) |
| Evolutionary implications of the frequent horizontal transfer of mismatch repair genes. Denamur E., Lecointre G., Darlu P., Tenaillon O., Acquaviva C., Sayada C., Sunjevaric I., Rothstein R., Elion J., Taddei F. et al. Cell 103:711-721(2000) · UniProtKB (9) |
| Ethnic heterogeneity of the factor XIII Val34Leu polymorphism. Attie-Castro F.A., Zago M.A., Lavinha J., Elion J., Rodriguez-Delfin L., Guerreiro J.F., Franco R.F. Thromb. Haemost. 84:601-603(2000) · Mapped (12) |
| Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database. Jeanpierre C., Denamur E., Henry I., Cabanis M.-O., Luce S., Cecille A., Elion J., Peuchmaur M., Loirat C., Niaudet P. et al. Am. J. Hum. Genet. 62:824-833(1998) · UniProtKB (1) |
| Novel mutation (A141D) in exon 4 of the CFTR gene identified in an Algerian patient. Gouya L., Pascaud O., Munck A., Elion J., Denamur E. Hum. Mutat. 10:86-87(1997) · UniProtKB (1) |
| Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: identification of two novel mutations. Messaoud T., Verlingue C., Denamur E., Pascaud O., Quere I., Fattoum S., Elion J., Ferec C. Eur. J. Hum. Genet. 4:20-24(1996) · UniProtKB (1) |
| Heterogeneity within the first constant segment of the major outer membrane protein gene in Chlamydia trachomatis serovar D/Da distinguishes 2 lineages. Sayada C., Vretou E., Orfila J., Elion J., Denamur E. C. R. Acad. Sci. III, Sci. Vie 318:943-949(1995) · UniProtKB (2) |