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La ricerca find articoli where authors phrase all words ' Taine, L' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 41 riferimenti
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    1. Richard, E; Mendez, M; Mazurier, F; Morel, C; Costet, P; Xia, P; Fontanellas, A; Geronimi, F; Cario-Andre, M; Taine, L; Ged, C; Malik, P; de Verneuil, H; Moreau-Gaudry, F
      Gene therapy of a mouse model of protoporphyria with a self-inactivating erythroid-specific lentiviral vector without preselection

      MOLECULAR THERAPY
    2. Mangione, R; Guyon, F; Taine, L; Wen, ZQ; Roux, D; Vergnaud, A; Maugey-Laulom, B; Horovitz, J; Saura, R
      Pregnancy outcome and prognosis in fetuses with increased first-trimester nuchal translucency

      FETAL DIAGNOSIS AND THERAPY
    3. Fontanellas, A; Mendez, M; Mazurier, F; Cario-Andre, M; Navarro, S; Ged, C; Taine, L; Geronimi, F; Richard, E; Moreau-Gaudry, F; de Salamanca, RE; de Verneuil, H
      Successful therapeutic effect in a mouse model of erythropoietic protoporphyria by partial genetic correction and fluorescence-based selection of hematopoietic cells

      GENE THERAPY
    4. Giraudeau, F; Taine, L; Biancalana, V; Delobel, B; Journel, H; Missirian, C; Lacombe, D; Bonneau, D; Parent, P; Aubert, D; Hauck, Y; Croquette, MF; Toutain, A; Mattei, MG; Loiseau, HA; David, A; Vergnaud, G
      Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation

      JOURNAL OF MEDICAL GENETICS
    5. Coupry, I; Taine, L; Goizet, C; Soriano, C; Mortemousque, B; Arveiler, B; Lacombe, D
      Leucodystrophy and oculocutaneous albinism in a child with an 11q14 deletion

      JOURNAL OF MEDICAL GENETICS
    6. Frengen, E; Rocca-Serra, P; Shaposhnikov, S; Taine, L; Thorsen, J; Bepoldin, C; Krekling, M; Lafon, D; Aas, KK; Abd El Moneim, A; Johansen, H; Longy, M; Prydz, H; Dorion-Bonnet, F
      High-resolution integrated map encompassing the breast cancer loss of heterozygosity region on human chromosome 16q22.1

      GENOMICS
    7. Dupuy, D; Aubert, I; Duperat, VG; Petit, J; Taine, L; Stef, M; Bloch, B; Arveiler, B
      Mapping, characterization, and expression analysis of the SM-20 human homologue, C1orf12, and identification of a novel related gene, SCAND2

      GENOMICS
    8. Fontanellas, A; Mazurier, F; Landry, M; Taine, L; Morel, C; Larou, M; Daniel, JY; Montagutelli, X; de Salamanca, RE; de Verneuil, H
      Reversion of hepatobiliary alterations by bone marrow transplantation in amurine model of erythropoietic protoporphyria

      HEPATOLOGY
    9. Goizet, C; Excoffier, E; Taine, L; Taupiac, E; El Moneim, AA; Arveiler, B; Bouvard, M; Lacombe, D
      Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH

      AMERICAN JOURNAL OF MEDICAL GENETICS
    10. Bahuau, M; Laurendeau, I; Pelet, A; Assouline, B; Lamireau, T; Taine, L; Bail, B; Vergnes, P; Gallet, S; Vidaud, M; Lyonnet, S; Lacombe, D; Vidaud, D
      Tandem duplication within the neurofibromatosis type 1 gene (NF1) and reciprocal t(15;16)(q26.3;q12.1) translocation in familial association of NF1 with intestinal neuronal dysplasia type B (IND B)

      JOURNAL OF MEDICAL GENETICS
    11. Battin, J; Lacombe, D; Taine, L; Goizet, C
      Williams syndrome and behavioral phenotypes in human microdeletion syndromes

      BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE
    12. Fontanellas, A; Mazurier, F; Belloc, F; Taine, L; Dumain, P; Morel, C; Ged, C; de Verneuil, H; Moreau-Gaudry, F
      Fluorescence-based selection of retrovirally transduced cells in congenital erythropoietic porphyria: Direct selection based on the expression of thetherapeutic gene

      JOURNAL OF GENE MEDICINE
    13. Mazurier, F; Fontanellas, A; Salesse, S; Taine, L; Landriau, S; Moreau-Gaudry, F; Reiffers, J; Peault, B; Di Santo, JP; de Verneuil, H
      A novel immunodeficient mouse model - RAG2 x common cytokine receptor gamma chain double mutants - Requiring exogenous cytokine administration for human hematopoietic stem cell engraftment

      JOURNAL OF INTERFERON AND CYTOKINE RESEARCH
    14. Petit, J; Boisseau, P; Taine, L; Gauthier, B; Arveiler, B
      A YAC contig encompassing the 11q14.3 breakpoint of a translocation associated with schizophrenia, and including the tyrosinase gene

      MAMMALIAN GENOME
    15. LACOMBE D; TAINE L; SAURA R
      SECKEL-SYNDROME WITH GONADAL-DYSGENESIS, DYSMYELOPOIESIS, RADIAL RAY DEFECT AND CHROMOSOME INSTABILITY

      European journal of human genetics
    16. TAINE L; COUPRY I; BOISSEAU P; SAURA R; LACOMBE D; ARVEILER B
      REFINED LOCALIZATION OF THE VOLTAGE-GATED CHLORIDE CHANNEL, CLCN3, TO4Q33

      Human genetics
    17. SAURA R; ROUX D; MAUGEYLAULON B; TAINE L; WEN ZQ; VERGNAUD A; HOROVITZ J
      FALSE-NEGATIVE RESULTS OF TRISOMY-21 ON DIRECT ANALYSIS ON CHORIONIC VILLUS SAMPLING

      Prenatal diagnosis
    18. TAINE L; GOIZET C; WEN ZQ; PETRIJ F; BREUNING MH; AYME S; SAURA R; ARVEILER B; LACOMBE D
      SUBMICROSCOPIC DELETION OF CHROMOSOME 16P13.3 IN PATIENTS WITH RUBINSTEIN-TAYBI-SYNDROME

      American journal of medical genetics
    19. SAURA R; TAINE L; GUYON F; MANGIONE R; HOROVITZ J
      SAFETY AND FETAL-OUTCOME OF EARLY AND MIDTRIMESTER AMNIOCENTESIS

      Lancet
    20. SAURA R; LECHAT X; TAINE L; WEN ZQ; GUYON F; HOROVITZ J
      FIRST-TRIMESTER NUCHAL TRANSLUCENCY AND CYSTIC HYGROMA - A RISK A RISK ANALYSIS ON FETAL CHROMOSOME ABNORMALITY - A REPORT ON 183 CASES

      Cytogenetics and cell genetics
    21. SAURA R; TAINE L; WEN ZQ; GUYON F; HOROVITZ J
      FETOPLACENTAL DISCREPANCIES - LITERATURE-REVIEW (CONCERNING 36,981 TESTS)

      Cytogenetics and cell genetics
    22. SAURA R; TAINE L; WEN ZQ; GUYON F; HOROVITZ J
      MATERNAL HETERODISOMY-16 AND INTRAUTERINE GROWTH-RETARDATION (IUGR)

      Cytogenetics and cell genetics
    23. SAURA R; RUIZ B; TAINE L; WEN ZQ; GUYON F; HOROVITZ J
      CHORIONIC VILLUS SAMPLING AND MATERNAL CELL CONTAMINATION ON LONG-TERM CULTURE

      Cytogenetics and cell genetics
    24. TAINE L; GOIZET C; WEN ZQ; PETRIJ F; BREUNING M; SAURA R; ARVEILER B; LACOMBE D
      FREQUENCY OF 16P13.3 SUBMICROSCOPIC DELETIONS IN FRENCH PATIENTS WITHRUBINSTEIN-TAYBI-SYNDROME

      Cytogenetics and cell genetics
    25. ARVEILER B; BOISSEAU P; PETIT J; TAINE L
      GENE-MAPPING IN REGION 1Q42.1 AROUND A TRANSLOCATION BREAKPOINT ASSOCIATED WITH SCHIZOPHRENIA

      American journal of medical genetics
    26. TAINE L; GOIZET C; WEN ZQ; CHATEIL JF; BATTIN J; SAURA R; LACOMBE D
      18P MONOSOMY WITH MIDLINE DEFECTS AND A DE-NOVO SATELLITE IDENTIFIED BY FISH

      Annales de genetique
    27. LACOMBE D; TAINE L; SAURA R
      SECKEL-SYNDROME WITH GONADAL-DYSGENESIS, DYSMYELOPOIESIS, RADIAL RAY DEFECT, AND CHROMOSOME INSTABILITY

      American journal of human genetics
    28. COUPRY I; IMBERT G; TAINE L; BOISSEAU P; BIANCALANA V; SAURA R; BATTIN J; MANDEL JL; LACOMBE D; ARVEILER B
      A 2ND CHOREA LOCUS ON CHROMOSOME-4

      American journal of human genetics
    29. GED C; MOREAUGAUDRY F; TAINE L; HOMBRADOS I; CALVAS P; COLOMBIES P; DEVERNEUIL H
      PRENATAL-DIAGNOSIS IN CONGENITAL ERYTHROPOIETIC PORPHYRIA BY METABOLIC MEASUREMENT AND DNA MUTATION ANALYSIS

      Prenatal diagnosis
    30. BIANCALANA V; TAINE L; BOUIX JC; FINCK S; CHAUVIN A; DEVERNEUIL H; KNIGHT SJL; STOLL C; LACOMBE D; MANDEL JL
      EXPANSION AND METHYLATION STATUS AT FRAXE CAN BE DETECTED ON ECORI BLOTS USED FOR FRAXA DIAGNOSIS - ANALYSIS OF 4 FRAXE FAMILIES WITH MILD MENTAL-RETARDATION IN MALES

      American journal of human genetics
    31. SAURA R; TRAORE W; TAINE L; WEN ZQ; ROUX D; MAUGEYLAULOM B; RUFFIE M; VERGNAUD A; HOROVITZ J
      PRENATAL-DIAGNOSIS OF TRISOMY-9 - 6 CASES AND A REVIEW OF THE LITERATURE

      Prenatal diagnosis
    32. BRUN JL; SAURA R; HOROVITZ J; MAUGEY B; TAINE L; ROUX D; VERGNAUD A
      FIRST TRIMESTER DIAGNOSIS OF FETAL NUCHAL EDEMA - REPORT OF 29 CASES

      Fetal diagnosis and therapy
    33. SAURA R; TAINE L; WEN ZQ; TRAORE W; HOROVITZ J
      AMNIOTIC-FLUID LEAKAGE AND MISCARRIAGES AFTER TA-CVS

      Prenatal diagnosis
    34. SAURA R; BRUN JL; TAINE L; HOROVITZ J; MAUGEY B; ROUX D
      IS NON-ECHOGENIC NUCHAL EDEMA A MARKER IN TRISOMY-21 SCREENING

      Prenatal diagnosis
    35. SAURA R; GAUTHIER B; TAINE L; WEN ZQ; HOROVITZ J; ROUX D; LAULOM B; VERGNAUD A
      OPERATOR EXPERIENCE AND FETAL LOSS RATE IN TRANSABDOMINAL CVS

      Prenatal diagnosis
    36. SAURA R; ROUX D; TAINE L; MAUGEY B; LAULON D; LAPLACE JP; HOROVITZ J
      EARLY AMNIOCENTESIS VERSUS CHORIONIC VILLUS SAMPLING FOR FETAL KARYOTYPING

      Lancet
    37. SAURA R; TAINE L; HOROVITZ J; VERDIER G; WEN ZQ; ROUX D; MAUGEY B; VERGNAUD A
      WHY CONFINE CHORIONIC VILLUS BIOPSY TO SINGLE PREGNANCIES

      Prenatal diagnosis
    38. LONGY M; SAURA R; DUMAS F; LESEVE JF; TAINE L; GOUSSOT JF; COUZIGOU P
      CHROMOSOME ANALYSIS OF ADENOMATOUS POLYPS OF THE COLON - POSSIBLE EXISTENCE OF 2 DIFFERENTLY EVOLVING CYTOGENETIC GROUPS

      Cancer genetics and cytogenetics
    39. SAURA R; GAUTHIER B; TAINE L; WEN ZQ; HOROVITZ J; ROUX D; LAULOM B; VERGNAUD A
      EXPERIENCE AND FETAL LOSS RATE IN TACVS

      American journal of human genetics
    40. SAURA R; BRUN JL; TAINE L; WEN ZQ; HOROVITZ J; MAUGEY B; ROUX D
      IS NON-ECHOGENIC NUCHAL EDEMA A MARKER IN TRISOMY-21 SCREENING

      American journal of human genetics
    41. SAURA R; TAINE L; HOROVITZ J; VERDIER G; WEN ZQ; ROUX D; MAUGEY B; VERGNAUD A
      WHY CONFINE CHORIONIC VILLUS BIOPSY TO SINGLE PREGNANCIES

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 25/10/20 alle ore 23:21:53