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Results: 1-25 | 26-50 | 51-51
Results: 26-50/51
CYTOGENETIC ANALYSIS OF BC2, A NEW HUMAN HEPATOMA-CELL LINE, BY FLUORESCENT IN-SITU HYBRIDIZATION
Authors: INGSTER O HAMONBENAIS C COUTURIERTURPIN MH GUGUENGUILLOUZO C LUCAS J BERNHEIM A FELDMANN G
Citation: O. Ingster et al., CYTOGENETIC ANALYSIS OF BC2, A NEW HUMAN HEPATOMA-CELL LINE, BY FLUORESCENT IN-SITU HYBRIDIZATION, Annales de genetique, 39(3), 1996, pp. 123-128
MAPPING OF 22 YACS ON HUMAN-CHROMOSOMES BY FISH USING YEAST DNA ALU-PCR PRODUCTS FOR COMPETITION
Authors: GOGUEL AF PULCINI F DANGLOT G FAUVET D DEVIGNES MD BERNHEIM A
Citation: Af. Goguel et al., MAPPING OF 22 YACS ON HUMAN-CHROMOSOMES BY FISH USING YEAST DNA ALU-PCR PRODUCTS FOR COMPETITION, Annales de genetique, 39(2), 1996, pp. 64-68
NEUROFIBROMATOSIS-1 (NF1) MESSENGER-RNAS EXPRESSED IN THE CENTRAL-NERVOUS-SYSTEM ARE DIFFERENTIALLY SPLICED IN THE 5' PART OF THE GENE
Authors: DANGLOT G REGNIER V FAUVET D VASSAL G KUJAS M BERNHEIM A
Citation: G. Danglot et al., NEUROFIBROMATOSIS-1 (NF1) MESSENGER-RNAS EXPRESSED IN THE CENTRAL-NERVOUS-SYSTEM ARE DIFFERENTIALLY SPLICED IN THE 5' PART OF THE GENE, Human molecular genetics, 4(5), 1995, pp. 915-920
FISH DIAGNOSIS OF T(8-21) IN A MYELODYSPLASIA SECONDARY TO HODGKIN LYMPHOMA
Authors: BERNHEIM A DUVERGER A FOUQUET F BAYLE C OBERLIN O
Citation: A. Bernheim et al., FISH DIAGNOSIS OF T(8-21) IN A MYELODYSPLASIA SECONDARY TO HODGKIN LYMPHOMA, Leukemia, 9(1), 1995, pp. 107-108
A TSP509I VARIANT IN EXON-13 OF THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE ALLOWS THE IDENTIFICATION OF BOTH ALLELES AT THE MESSENGER-RNA LEVEL (VOL 96, PG 131, 1995)
Authors: REGNIER V DANGLOT G NGUYEN VC BERNHEIM A
Citation: V. Regnier et al., A TSP509I VARIANT IN EXON-13 OF THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE ALLOWS THE IDENTIFICATION OF BOTH ALLELES AT THE MESSENGER-RNA LEVEL (VOL 96, PG 131, 1995), Human genetics, 96(6), 1995, pp. 744-744
A TSP509I VARIANT IN EXON-13 OF THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE ALLOWS THE IDENTIFICATION OF BOTH ALLELES AT THE MESSENGER-RNA LEVEL
Authors: REGNIER V DANGLOT G NGUYEN VG BERNHEIM A
Citation: V. Regnier et al., A TSP509I VARIANT IN EXON-13 OF THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE ALLOWS THE IDENTIFICATION OF BOTH ALLELES AT THE MESSENGER-RNA LEVEL, Human genetics, 96(1), 1995, pp. 131-132
CYTOGENETIC STUDY OF A CASE OF SYNCHRONOUS BILATERAL SEMINOMA
Authors: VENUAT AM DROZ JP TERRIERLACOMBE MJ MACHAVOINE C BERNHEIM A
Citation: Am. Venuat et al., CYTOGENETIC STUDY OF A CASE OF SYNCHRONOUS BILATERAL SEMINOMA, Cancer genetics and cytogenetics, 81(1), 1995, pp. 17-19
EVOLUTION OF CHROMOSOMAL ALTERATIONS AND BIOLOGIC FEATURES IN 2 SMALL-CELL LUNG-CARCINOMA CELL-LINES ESTABLISHED FROM ONE PATIENT DURING THE COURSE OF THE DISEASE
Authors: GOGUEL AF FOUQUET F DUVERGER A ARVELO F JACROT M POUPON MF BERNHEIM A
Citation: Af. Goguel et al., EVOLUTION OF CHROMOSOMAL ALTERATIONS AND BIOLOGIC FEATURES IN 2 SMALL-CELL LUNG-CARCINOMA CELL-LINES ESTABLISHED FROM ONE PATIENT DURING THE COURSE OF THE DISEASE, Cancer genetics and cytogenetics, 80(1), 1995, pp. 47-54
GONADAL-DYSGENESIS IN DEL(18P) SYNDROME
Authors: TELVI L BERNHEIM A ION A FOUQUET F LEBOUC Y CHAUSSAIN JL
Citation: L. Telvi et al., GONADAL-DYSGENESIS IN DEL(18P) SYNDROME, American journal of medical genetics, 57(4), 1995, pp. 598-600
MORPHOLOGIC AND MOLECULAR CYTOGENETICS IN NEUROBLASTOMA
Authors: AVETLOISEAU H VENUAT AM BENARD J LEIBOVITCH MP HARTMANN O BERNHEIM A
Citation: H. Avetloiseau et al., MORPHOLOGIC AND MOLECULAR CYTOGENETICS IN NEUROBLASTOMA, Cancer, 75(7), 1995, pp. 1694-1699
GENISTEIN RESISTANCE IN HUMAN LEUKEMIC CCRF-CEM CELLS - SELECTION OF A DIPLOID-CELL LINE WITH REDUCED DNA TOPOISOMERASE-II BETA-ISOFORM
Authors: MARKOVITS J JUNQUA S GOLDWASSER F VENUAT AM LUCCIONI C BEAUMATIN J SAUCIER JM BERNHEIM A JACQUEMINSABLON A
Citation: J. Markovits et al., GENISTEIN RESISTANCE IN HUMAN LEUKEMIC CCRF-CEM CELLS - SELECTION OF A DIPLOID-CELL LINE WITH REDUCED DNA TOPOISOMERASE-II BETA-ISOFORM, Biochemical pharmacology, 50(2), 1995, pp. 177-186
A NEW HYBRID CELL-LINE CONTAINING ONLY HUMAN-CHROMOSOME-15 SELECTED THROUGH FLUORESCENCE IN-SITU HYBRIDIZATION AND CHARACTERIZED BY ALU-PCRAMPLIFICATION OP THE HUMAN DNA
Authors: DIRIONG S DANGLOT G BERNHEIM A NGUYEN VC
Citation: S. Diriong et al., A NEW HYBRID CELL-LINE CONTAINING ONLY HUMAN-CHROMOSOME-15 SELECTED THROUGH FLUORESCENCE IN-SITU HYBRIDIZATION AND CHARACTERIZED BY ALU-PCRAMPLIFICATION OP THE HUMAN DNA, Annales de genetique, 38(1), 1995, pp. 27-31
EPIDERMOLYTIC PALMOPLANTAR KERATODERMA COSEGREGATES WITH A KERATIN-9 MUTATION IN A PEDIGREE WITH BREAST AND OVARIAN-CANCER
Authors: TORCHARD D BLANCHETBARDON C SEROVA O LANGBEIN L NAROD S JANIN N GOGUEL AF BERNHEIM A FRANKE WW LENOIR GM FEUNTEUN J
Citation: D. Torchard et al., EPIDERMOLYTIC PALMOPLANTAR KERATODERMA COSEGREGATES WITH A KERATIN-9 MUTATION IN A PEDIGREE WITH BREAST AND OVARIAN-CANCER, Nature genetics, 6(1), 1994, pp. 106-110
A 1.7-MB YAC CONTIG AROUND THE HUMAN BDNF GENE (11P13) - INTEGRATION OF THE PHYSICAL, GENETIC, AND CYTOGENETIC MAPS IN RELATION TO WAGR SYNDROME
Authors: ROSIER MF GOGUEL AF MARTIN A LEPASLIER D COUILLIN P HOULGATTE R BERNHEIM A AUFFRAY C DEVIGNES MD
Citation: Mf. Rosier et al., A 1.7-MB YAC CONTIG AROUND THE HUMAN BDNF GENE (11P13) - INTEGRATION OF THE PHYSICAL, GENETIC, AND CYTOGENETIC MAPS IN RELATION TO WAGR SYNDROME, Genomics, 24(1), 1994, pp. 69-77
TISSUE-SPECIFIC ALTERNATIVE SPLICING OF NEUROFIBROMATOSIS-1 (NF1) MESSENGER-RNA
Authors: DANGLOT G TEINTURIER C DUVERGER A BERNHEIM A
Citation: G. Danglot et al., TISSUE-SPECIFIC ALTERNATIVE SPLICING OF NEUROFIBROMATOSIS-1 (NF1) MESSENGER-RNA, Biomedicine & pharmacotherapy, 48(8-9), 1994, pp. 365-372
IN-VITRO PARAMETERS AND TREATMENT OUTCOME IN HEAD AND NECK CANCERS TREATED WITH SURGERY AND OR RADIATION - CELL CHARACTERIZATION AND CORRELATIONS WITH LOCAL-CONTROL AND OVERALL SURVIVAL/
Authors: GIRINSKY T BERNHEIM A LUBIN R TAVAKOLIRAZAVI T BAKER F JANOT F WIBAULT P COSSET JM DUVILLARD P DUVERGER A FERTIL B
Citation: T. Girinsky et al., IN-VITRO PARAMETERS AND TREATMENT OUTCOME IN HEAD AND NECK CANCERS TREATED WITH SURGERY AND OR RADIATION - CELL CHARACTERIZATION AND CORRELATIONS WITH LOCAL-CONTROL AND OVERALL SURVIVAL/, International journal of radiation oncology, biology, physics, 30(4), 1994, pp. 789-794
ASSIGNMENT OF THE HUMAN 8.5-H GENE TO CHROMOSOME-5, REGION-5Q35
Authors: DIRIONG S SABERANDJONEIDI D LEVISTRAUSS M BERNHEIM A NGUYEN VC
Citation: S. Diriong et al., ASSIGNMENT OF THE HUMAN 8.5-H GENE TO CHROMOSOME-5, REGION-5Q35, Human genetics, 93(6), 1994, pp. 703-706
ASSIGNMENT OF 2 YAC CLONES TO CHROMOSOME-14 BY FLUORESCENT IN-SITU HYBRIDIZATION TO R-BANDED CHROMOSOMES
Authors: BERNHEIM A GOGUEL AF SLIM R
Citation: A. Bernheim et al., ASSIGNMENT OF 2 YAC CLONES TO CHROMOSOME-14 BY FLUORESCENT IN-SITU HYBRIDIZATION TO R-BANDED CHROMOSOMES, Cytogenetics and cell genetics, 66(1), 1994, pp. 10-10
ASSIGNMENTS OF 37 YAC CLONES TO R-BANDED CHROMOSOMES BY FLUORESCENT IN-SITU HYBRIDIZATION
Authors: SLIM R MACHAVOINE C BERNHEIM A
Citation: R. Slim et al., ASSIGNMENTS OF 37 YAC CLONES TO R-BANDED CHROMOSOMES BY FLUORESCENT IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 65(1-2), 1994, pp. 104-107
PRENATAL IDENTIFICATION OF AN ISOCHROMOSOME FOR THE SHORT ARM OF THE Y I(YP), BY CYTOGENETIC AND MOLECULAR ANALYSES
Authors: SLIM R SOULIE J HOTMAR J LECOLIER B BERCAU G BERNHEIM A
Citation: R. Slim et al., PRENATAL IDENTIFICATION OF AN ISOCHROMOSOME FOR THE SHORT ARM OF THE Y I(YP), BY CYTOGENETIC AND MOLECULAR ANALYSES, Prenatal diagnosis, 14(1), 1994, pp. 23-28
NUMERICAL ABERRATIONS, INCLUDING TRISOMY-22 AS THE SOLE ANOMALY, ARE RECURRENT IN FOLLICULAR THYROID ADENOMAS
Authors: ANTONINI P LEVY N CAILLOU B VENUAT AM SCHLUMBERGER M PARMENTIER C BERNHEIM A
Citation: P. Antonini et al., NUMERICAL ABERRATIONS, INCLUDING TRISOMY-22 AS THE SOLE ANOMALY, ARE RECURRENT IN FOLLICULAR THYROID ADENOMAS, Genes, chromosomes & cancer, 8(1), 1993, pp. 63-66
ISOLATION OF COSMIDS AND FETAL BRAIN CDNAS FROM THE PROXIMAL LONG ARMOF HUMAN CHROMOSOME-22
Authors: LAMOUR V LEVY N DESMAZE C BAUDE V LECLUSE Y DELATTRE O BERNHEIM A THOMAS G AURIAS A LIPINSKI M
Citation: V. Lamour et al., ISOLATION OF COSMIDS AND FETAL BRAIN CDNAS FROM THE PROXIMAL LONG ARMOF HUMAN CHROMOSOME-22, Human molecular genetics, 2(5), 1993, pp. 535-540
CONSTRUCTION OF A YEAST ARTIFICIAL CHROMOSOME CONTIG SPANNING THE PSEUDOAUTOSOMAL REGION AND ISOLATION OF 25 NEW SEQUENCE-TAGGED SITES
Authors: SLIM R LEPASLIER D COMPAIN S LEVILLIERS J OUGEN P BILLAULT A DONOHUE SJ KLEIN DC MINTZ L BERNHEIM A COHEN D WEISSENBACH J PETIT C
Citation: R. Slim et al., CONSTRUCTION OF A YEAST ARTIFICIAL CHROMOSOME CONTIG SPANNING THE PSEUDOAUTOSOMAL REGION AND ISOLATION OF 25 NEW SEQUENCE-TAGGED SITES, Genomics, 16(3), 1993, pp. 691-697
LOCALIZATION OF 15 COSMIDS ON HUMAN CHROMOSOME-22 BY FLUORESCENCE INSITU HYBRIDIZATION
Authors: LEVY N LAMOUR V DANGLOT G SLIM R LIPINSKI M BERNHEIM A
Citation: N. Levy et al., LOCALIZATION OF 15 COSMIDS ON HUMAN CHROMOSOME-22 BY FLUORESCENCE INSITU HYBRIDIZATION, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 316(5), 1993, pp. 482-486
REARRANGEMENTS BETWEEN IRRADIATED CHROMOSOMES IN 3-SPECIES RADIATION HYBRID CELL-LINES REVEALED BY 2-COLOR IN-SITU HYBRIDIZATION
Authors: PHILIPPE C NGUYEN VC SLIM R HOLVOETVERMAUT L HORSCAYLA MC BERNHEIM A
Citation: C. Philippe et al., REARRANGEMENTS BETWEEN IRRADIATED CHROMOSOMES IN 3-SPECIES RADIATION HYBRID CELL-LINES REVEALED BY 2-COLOR IN-SITU HYBRIDIZATION, Human genetics, 92(1), 1993, pp. 11-17
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