AAAAAA

   
Results: 1-11 |
Results: 11
ORGANIZATION OF THE HUMAN RH50A GENE (RHAG) AND EVOLUTION OF BASE COMPOSITION OF THE RH GENE FAMILY
Authors: MATASSI G CHERIFZAHAR B RAYNAL V ROUGER P CARTRON JP
Citation: G. Matassi et al., ORGANIZATION OF THE HUMAN RH50A GENE (RHAG) AND EVOLUTION OF BASE COMPOSITION OF THE RH GENE FAMILY, Genomics, 47(2), 1998, pp. 286-293
SHIFT FROM RH-POSITIVE TO RH-NEGATIVE PHENOTYPE CAUSED BY A SOMATIC MUTATION WITHIN THE RHD GENE IN A PATIENT WITH CHRONIC MYELOCYTIC-LEUKEMIA
Authors: CHERIFZAHAR B BONY V STEFFENSEN R GANE P RAYNAL V GOOSENS D LAURSEN JS VARMING K JERSILD G CARTRON JP
Citation: B. Cherifzahar et al., SHIFT FROM RH-POSITIVE TO RH-NEGATIVE PHENOTYPE CAUSED BY A SOMATIC MUTATION WITHIN THE RHD GENE IN A PATIENT WITH CHRONIC MYELOCYTIC-LEUKEMIA, British Journal of Haematology, 102(5), 1998, pp. 1263-1270
RH-DEFICIENCY OF THE REGULATOR TYPE CAUSED BY SPLICING MUTATIONS IN THE HUMAN RH50 GENE
Authors: CHERIFZAHAR B MATASSI G RAYNAL V GANE P DELAUNAY J ARRIZABALAGA B CARTRON JP
Citation: B. Cherifzahar et al., RH-DEFICIENCY OF THE REGULATOR TYPE CAUSED BY SPLICING MUTATIONS IN THE HUMAN RH50 GENE, Blood, 92(7), 1998, pp. 2535-2540
MOLECULAR DEFECTS OF THE RHCE GENE IN RH-DEFICIENT INDIVIDUALS OF THEAMORPH TYPE
Authors: CHERIFZAHAR B MATASSI G RAYNAL V GANE P MEMPEL W PEREZ C CARTRON JP
Citation: B. Cherifzahar et al., MOLECULAR DEFECTS OF THE RHCE GENE IN RH-DEFICIENT INDIVIDUALS OF THEAMORPH TYPE, Blood, 92(2), 1998, pp. 639-646
A NOVEL SINGLE MISSENSE MUTATION IDENTIFIED ALONG THE RH50 GENE IN A COMPOSITE HETEROZYGOUS RH-NULL BLOOD-DONOR OF THE REGULATOR TYPE
Authors: HYLAND CA CHERIFZAHAR B COWLEY N RAYNAL V PARKES J SAUL A CARTRON JP
Citation: Ca. Hyland et al., A NOVEL SINGLE MISSENSE MUTATION IDENTIFIED ALONG THE RH50 GENE IN A COMPOSITE HETEROZYGOUS RH-NULL BLOOD-DONOR OF THE REGULATOR TYPE, Blood, 91(4), 1998, pp. 1458-1463
RH GENE STRUCTURE - REASSIGNMENT OF 2 EXON-EXON JUNCTIONS
Authors: CHERIFZAHAR B RAYNAL V CARTRON JP
Citation: B. Cherifzahar et al., RH GENE STRUCTURE - REASSIGNMENT OF 2 EXON-EXON JUNCTIONS, Blood, 89(12), 1997, pp. 4661-4662
CANDIDATE GENE ACTING AS A SUPPRESSOR OF THE RH LOCUS IN MOST CASES OF RH-DEFICIENCY
Authors: CHERIFZAHAR B RAYNAL V GANE P MATTEI MG BAILLY P GIBBS B COLIN Y CARTRON JP
Citation: B. Cherifzahar et al., CANDIDATE GENE ACTING AS A SUPPRESSOR OF THE RH LOCUS IN MOST CASES OF RH-DEFICIENCY, Nature genetics, 12(2), 1996, pp. 168-173
LACK OF RHCE-ENCODED PROTEINS IN THE D-- PHENOTYPE MAY RESULT FROM HOMOLOGOUS RECOMBINATION BETWEEN THE 2 RH GENES
Authors: CHERIFZAHAR B RAYNAL V CARTRON JP
Citation: B. Cherifzahar et al., LACK OF RHCE-ENCODED PROTEINS IN THE D-- PHENOTYPE MAY RESULT FROM HOMOLOGOUS RECOMBINATION BETWEEN THE 2 RH GENES, Blood, 88(4), 1996, pp. 1518-1520
ORGANIZATION OF THE GENE (RHCE) ENCODING THE HUMAN BLOOD-GROUP RHCCEEANTIGENS AND CHARACTERIZATION OF THE PROMOTER REGION
Authors: CHERIFZAHAR B LEVANKIM C ROUILLAC C RAYNAL V CARTRON JP COLIN Y
Citation: B. Cherifzahar et al., ORGANIZATION OF THE GENE (RHCE) ENCODING THE HUMAN BLOOD-GROUP RHCCEEANTIGENS AND CHARACTERIZATION OF THE PROMOTER REGION, Genomics, 19(1), 1994, pp. 68-74
MOLECULAR ANALYSIS OF THE STRUCTURE AND EXPRESSION OF THE RH LOCUS ININDIVIDUALS WITH D--, DC-, AND DCW- GENE COMPLEXES
Authors: CHERIFZAHAR B RAYNAL V DAMBROSIO AM CARTRON JP COLIN Y
Citation: B. Cherifzahar et al., MOLECULAR ANALYSIS OF THE STRUCTURE AND EXPRESSION OF THE RH LOCUS ININDIVIDUALS WITH D--, DC-, AND DCW- GENE COMPLEXES, Blood, 84(12), 1994, pp. 4354-4360
STRUCTURE AND EXPRESSION OF THE RH LOCUS IN THE RH-DEFICIENCY SYNDROME
Authors: CHERIFZAHAR B RAYNAL V LEVANKIM C DAMBROSIO AM BAILLY P CARTRON JP COLIN Y
Citation: B. Cherifzahar et al., STRUCTURE AND EXPRESSION OF THE RH LOCUS IN THE RH-DEFICIENCY SYNDROME, Blood, 82(2), 1993, pp. 656-662
Risultati: 1-11 |