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    1. Mathieu, A; Asfari, Z; Thuery, P; Nierlich, M; Faure, S; Vicens, J
      Water-soluble para-sulfonated 1,2;3,4-calix[4]arene-biscrowns in the 1,2-alternate conformation

      JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY
    2. Faure, S; Piva, O
      Application of chiral tethers to intramolecular [2+2] photocycloadditions:synthetic approach to (-)-italicene and (+)-isoitalicene

      TETRAHEDRON LETTERS
    3. Enders, D; Faure, S; Potthoff, M; Runsink, J
      Diastereoselective electrophilic fluorination of enantiopure alpha-silylketones using N-fluoro-benzosulfonimide: Regio- and enantioselective synthesis of alpha-fluoroketones

      SYNTHESIS-STUTTGART
    4. Blanchet, S; Desgranges, B; Denise, P; Lechevalier, B; Eustache, F; Faure, S
      New questions on the hemispheric encoding/retrieval asymmetry (HERA) modelassessed by divided visual-field tachistoscopy in normal subjects

      NEUROPSYCHOLOGIA
    5. Moatti, D; Faure, S; Fumeron, F; Amara, ME; Seknadji, P; McDermott, DH; Debre, P; Aumont, MC; Murphy, PM; de Prost, D; Combadiere, C
      Polymorphism in the fractalkine receptor CX3CR1 as a genetic risk factor for coronary artery disease

      BLOOD
    6. Grafte-Faure, S; Leveque, C; Ketata, E; Jean, P; Vasse, M; Soria, C; Vannier, JP
      Recruitment of primitive peripheral blood cells: Synergism of interleukin 12 with interleukin 6 and stromal cell-derived factor-1

      CYTOKINE
    7. Faure, S; Lee, MA; Keller, T; ten Dijke, P; Whitman, M
      Endogenous patterns of TGF beta superfamily signaling during early Xenopusdevelopment

      DEVELOPMENT
    8. Tiret, L; Kessler, JL; Bentolila, S; Faure, S; Bach, JM; Weissenbach, J; Panthier, JJ
      Assignation of highly polymorphic markers on a canine purebred pedigree

      MAMMALIAN GENOME
    9. Chauvin, J; Nakatani, K; Delaire, JA; Faure, S; Mercier, R; Sillion, B
      Subglass transition and relaxation of oriented chromophores in polyimides for second order nonlinear optics

      SYNTHETIC METALS
    10. Caillot-Augusseau, A; Lafage-Proust, MH; Margaillan, P; Vergely, N; Faure, S; Paillet, S; Lang, F; Alexandre, C; Estour, B
      Weight gain reverses bone turnover and restores circadian variation of bone resorption in anorexic patients

      CLINICAL ENDOCRINOLOGY
    11. Querne, L; Eustache, F; Faure, S
      Interhemispheric inhibition, intrahemispheric activation, and lexical capacities of the right hemisphere: A tachistoscopic, divided visual-field study in normal subjects

      BRAIN AND LANGUAGE
    12. Faure, S; Connolly, JD; Fakunle, CO; Piva, O
      Structure and synthesis of anhydrobisfarnesol from Euphorbia lateriflora and asymmetric synthesis of (R)-sesquilavandulol

      TETRAHEDRON
    13. Faure, S; Meyer, L; Costagliola, D; Vaneensberghe, C; Genin, E; Autran, B; Delfraissy, JF; McDermott, DH; Murphy, PM; Debre, P; Theodorou, I; Combadiere, C
      Rapid progression to AIDS in HIV+ individuals with a structural variant ofthe chemokine receptor CX(3)CR1

      SCIENCE
    14. Cau, J; Faure, S; Vigneron, S; Labbe, JC; Delsert, C; Morin, N
      Regulation of xenopus p21-activated kinase (X-PAK2) by Cdc42 and maturation-promoting factor controls Xenopus oocyte maturation

      JOURNAL OF BIOLOGICAL CHEMISTRY
    15. Faure, S; Valentin, B; Rouzaud, J; Gornitzka, H; Castel, A; Riviere, P
      Synthesis and characterization of Group 14 elements - dithienylsulfur cycloadducts and oligomers

      INORGANICA CHIMICA ACTA
    16. Gory-Faure, S; Prandini, MH; Pointu, H; Roullot, V; Pignot-Paintrand, I; Vernet, M; Huber, P
      Role of vascular endothelial-cadherin in vascular morphogenesis

      DEVELOPMENT
    17. Grafte-Faure, S; Leveque, C; Vasse, M; Soria, C; Norris, V; Vannier, JP
      Effects of glucocorticoids and mineralocorticoids on proliferation and maturation of human peripheral blood stem cells

      AMERICAN JOURNAL OF HEMATOLOGY
    18. Blanchet, S; Faure, S; Desgranges, B; Denise, P; Lechevalier, B; Eustache, F
      Hemispheric asymmetry in encoding and retrieval processes in short-term memory and long-term memory: A tachistoscopic and divided visual field study in normal subjects

      BRAIN AND COGNITION
    19. Tiret, L; Kessler, JL; Bentolila, S; Faure, S; Bach, JM; Weissenbach, J; Panthier, JJ
      Characterization and mapping of canine polymorphic markers

      ANIMAL GENETICS
    20. Faure, S; Piva-Le Blanc, S; Piva, O
      Synthesis of vinyl spirolactones and lactams by sequential cross-coupling metathesis, [2+2] photocycloaddition and cyclobutane ring-opening

      TETRAHEDRON LETTERS
    21. Faure, S; Vigneron, S; Galas, S; Brassac, T; Delsert, C; Morin, N
      Control of G(2)/M transition in Xenopus by a member of the p21-activated kinase (PAK) family: A link between protein kinase a and PAK signaling pathways?

      JOURNAL OF BIOLOGICAL CHEMISTRY
    22. Faure, S; Bordelais, I; Marquette, C; Rittey, C; Campos-Castello, J; Goutieres, F; Ponsot, G; Weissenbach, J; Lebon, P
      Aicardi-Goutieres syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?

      CLINICAL GENETICS
    23. Grafte-Faure, S; Leveque, C; Vasse, M; Soria, C; Vannier, JP
      Recruitment of primitive peripheral blood cells: synergism of interleukin 12 with interleukin 6 and stem cell factor

      BRITISH JOURNAL OF HAEMATOLOGY
    24. DELPEDRO AD; BARJAVEL MJ; MAMDOUH Z; FAURE S; BAKOUCHE O
      SIGNAL-TRANSDUCTION IN LPS-ACTIVATED AGED AND YOUNG MONOCYTES

      Journal of interferon & cytokine research
    25. FAURE S; MORIN N; DOREE M
      INACTIVATION OF PROTEIN-KINASE-A IS NOT REQUIRED FOR C-MOS TRANSLATION DURING MEIOTIC MATURATION OF XENOPUS OOCYTES

      Oncogene
    26. Faure, S; Piva, O
      Asymmetric alpha-alkylation of alpha,beta-unsaturated esters. Application to the synthesis of (R)-lavandulol, (R)-sesquilavandulol and related trifluoromethyl compounds

      SYNLETT
    27. QUERNE L; FAURE S
      ACTIVATION-INHIBITION PROCESSES AND IMPLEMENTATION OF HEMISPHERIC LEXICAL COMPETENCE

      Brain and cognition
    28. FAURE S; CLIQUET JB; THEPHANY G; BOUCAUD J
      NITROGEN ASSIMILATION IN LOLIUM-PERENNE COLONIZED BY THE ARBUSCULAR MYCORRHIZAL FUNGUS GLOMUS-FASCICULATUM

      New phytologist
    29. CORNELIS F; FAURE S; MARTINEZ M; PRUDHOMME JF; FRITZ P; DIB C; ALVES H; BARRERA P; DEVRIES N; BALSA A; PASCUALSALCEDO D; MAENAUT K; WESTHOVENS R; MIGLIORINI P; TRAN TH; DELAYE A; PRINCE N; LEFEVRE C; THOMAS G; POIRIER M; SOUBIGOU S; ALIBERT O; LASBLEIZ S; FOUIX S; BOUCHIER C; LIOTE F; LOSTE MN; LEPAGE V; CHARRON D; GYAPAY G; LOPESVAZ A; KUNTZ D; BARDIN T; WEISSENBACH J
      NEW SUSCEPTIBILITY LOCUS FOR RHEUMATOID-ARTHRITIS SUGGESTED BY A GENOME-WIDE LINKAGE STUDY

      Proceedings of the National Academy of Sciences of the United Statesof America
    30. NEYROUD N; TESSON F; DENJOY I; LEIBOVICI M; DONGER C; BARHANIN J; FAURE S; GARY F; COUMEL P; PETIT C; SCHWARTZ K; GUICHENEY P
      A NOVEL MUTATION IN THE POTASSIUM CHANNEL GENE KVLQT1 CAUSES THE JERVELL AND LANGE-NIELSEN CARDIOAUDITORY SYNDROME

      Nature genetics
    31. FAURE S; VIGNERON S; DOREE M; MORIN N
      A MEMBER OF THE STE20 PAK FAMILY OF PROTEIN-KINASES IS INVOLVED IN BOTH ARREST OF XENOPUS OOCYTES AT G(2)/PROPHASE OF THE FIRST MEIOTIC CELL-CYCLE AND IN PREVENTION OF APOPTOSIS/

      EMBO journal
    32. FAURE S; PIVALEBLANC S; PIVA O; PETE JP
      HYDROXYACIDS AS EFFICIENT CHIRAL SPACERS FOR ASYMMETRIC INTRAMOLECULAR [2+2] PHOTOCYCLOADDITIONS

      Tetrahedron letters
    33. VIGOUROUX C; KHALLOUF E; BOURUT C; ROBERT JJ; DEKERDANET M; TUBIANARUFI N; FAURE S; WEISSENBACH J; CAPEAU J; MAGRE J
      GENETIC EXCLUSION OF 14 CANDIDATE GENES IN LIPOATROPIC DIABETES USINGLINKAGE ANALYSIS IN 10 CONSANGUINEOUS FAMILIES

      The Journal of clinical endocrinology and metabolism
    34. LAFONT V; FISCHER T; ZUMBIHL R; FAURE S; HIVROZ C; ROUOT B; FAVERO J
      EVIDENCE FOR A CD4-ASSOCIATED CALCIUM INFLUX INDEPENDENT OF THE PHOSPHOINOSITIDE TRANSDUCTION PATHWAY IN HUMAN T-CELLS

      European Journal of Immunology
    35. CORNELIS F; FAURE S; MARTINEZ M; PRUDHOMME JF; FRITZ P; DIB C; ALVES H; BARRERA P; DEVRIES N; BALSA A; PASCUALSALCIDO D; MAENAUT K; WESTHOEVENS B; MIGLIORINI P; TRAN TH; DELAYE A; PRINCE N; LEFEVRE C; THOMAS G; POIRIER M; SOUBIGOU S; ALIBERT O; LASBLEIZ S; FOUIX S; BOUCHIER C; LLOTE F; LOSTE MN; LEPAGE V; CHARRON D; GYAPAV G; LOPEZVAZ A; KUNTZ D; BARDIN T; WEISSENBACH J
      RHEUMATOID-ARTHRITIS GENOME SCAN AND PUTATIVE AUTOIMMUNITY LOCUS

      Arthritis and rheumatism
    36. KWIATKOWSKI DJ; HUMPHREY D; VANSLEGTENHORST M; ATTWOOD J; HAINES JL; BURLEY MW; HORNIGOLD N; SMITH M; NAHMIAS J; FAURE S; POVEY S
      A DENSE STR-MAP OF 1.5-MB OF 9Q34 - SMALL REDUCTION IN THE TSC1-CRITICAL-REGION

      Annals of Human Genetics
    37. REBELLO M; ATTWOOD J; EKONG R; FOX M; ROUSSEAUX S; FAURE S; POVEY S
      GENETIC AND PHYSICAL MAPPING IN THE DISTAL PORTION OF CHROMOSOME 9P -TOWARD A MORE DETAILED AND RELIABLE MAP OF THE REGION

      Annals of Human Genetics
    38. NEUFELD EJ; MANDEL H; RAZ T; SZARGEL R; YANDAVA CN; STAGG A; FAURE S; BARRETT T; BUIST N; COHEN N
      LOCALIZATION OF THE GENE FOR THIAMINE-RESPONSIVE MEGALOBLASTIC-ANEMIASYNDROME, ON THE LONG ARM OF CHROMOSOME-1, BY HOMOZYGOSITY MAPPING

      American journal of human genetics
    39. NEUFELD EJ; MANDEL H; RAZ T; YANDAVA CN; SZARGEL R; STAGG A; FAURE S; BARRETT TG; COHEN N
      LOCALIZATION OF THE GENE FOR THE SYNDROME OF THIAMINE-RESPONSIVE MEGALOBLASTIC-ANEMIA WITH DIABETES AND DEAFNESS TO CHROMOSOME 1Q23 BY HOMOZYGOSITY MAPPING

      American journal of human genetics
    40. CORNELIS F; FAURE S; MARTINEZ M; PRUDHOMME JF; FRITZ P; DIB C; ALVES H; BARRERA P; DEVRIES N; BALSA A; PASCUALSALCIDO D; MAENAUT K; WESTHOEVENS R; MIGLIORINI P; TRAN T; DELAYE A; PRINCE N; LEFEVRE C; THOMAS G; POIRIER M; SOUBIGOU S; ALIBERT O; LASBLEIZ S; FOUIX S; BOUCHIER C; LIOTE F; LOSTE MN; LEPAGE V; CHARRON D; GYAPAY G; LOPESVAZ A; KUNTZ D; BARDIN T; WEISSENBACH J
      RHEUMATOID-ARTHRITIS GENOME SCAN AND PUTATIVE AUTOIMMUNITY LOCUS

      American journal of human genetics
    41. AVELA K; LIPSANENNYMAN M; PERHEENTUPA J; WALLGRENPETTERSSON C; MARCHAND S; FAURE S; SISTONEN P; DELACHAPELLE A; LEHESJOKI AE
      ASSIGNMENT OF THE MULIBREY NANISM GENE TO 17Q BY LINKAGE AND LINKAGE-DISEQUILIBRIUM ANALYSIS

      American journal of human genetics
    42. FOISSAC A; CROUAUROY B; FAURE S; THOMSEN M; CAMBONTHOMSEN A
      MICROSATELLITES IN THE HLA REGION - AN OVERVIEW

      Tissue antigens
    43. FAURE S; JEBRAK M; ANGELIER J
      STRUCTURAL EVOLUTION OF LES-MINES-SELBAIE, NORTHERN ABITIBI BELT, QUEBEC, CANADA

      Exploration and mining geology
    44. RILEY BP; TAHIR E; MOGUDICARTER M; RAJAGOPALAN S; FAURE S; WEISSENBACH J; JENKINS T; WILLIAMSON R
      PRELIMINARY-RESULTS FROM A LINKAGE STUDY OF THE N-METHYL-D-ASPARTATE (NMDA) RECEPTOR SUBUNIT GENES IN A SAMPLE OF SOUTHERN AFRICAN BANTU-SPEAKING FAMILIES MULTIPLY AFFECTED WITH SCHIZOPHRENIA

      Schizophrenia research
    45. REGUIGNEARNOULD I; FAURE S; CHERY M; MOTAVIEIRA L; MOLLICONE R; CANDELIER JJ; ORIOL R; COUILLIN P
      PHYSICAL MAPPING OF 49 MICROSATELLITE MARKERS ON CHROMOSOME-19 AND CORRELATION WITH THE GENETIC-LINKAGE MAP

      Genomics
    46. GEDDEDAHL T; TRYGSTAD O; VANMALDERGEM L; MAGRE J; VANDERHAGEN C; OLAISEN B; STENERSEN M; MEVAG B; COPEAU J; DESBOISMOUTHON C; VIGOUROUX C; HILBERT P; FAURE S; WEISSENBACH J
      GENETICS OF THE BERARDINELLI-SEIP SYNDROME (CONGENITAL GENERALIZED LIPODYSTROPHY) IN NORWAY - EPIDEMIOLOGY AND GENE-MAPPING

      Acta paediatrica
    47. REGUIGNEARNOULD I; WOLFE J; HORNIGOLD N; FAURE S; MOLLICONE R; ORIOL R; COULLIN P
      FUCOSYL-TRANSFERASE GENES ARE DISPERSED IN THE GENOME - FUT7 IS LOCATED ON 9Q34.3 DISTAL TO D9S1830

      Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie
    48. GELB BD; SPENCER E; OBAD S; EDELSON GJ; FAURE S; WEISSENBACH J; DESNICK RJ
      PYCNODYSOSTOSIS - REFINED LINKAGE AND RADIATION HYBRID ANALYSES REDUCE THE CRITICAL REGION TO 2 CM AT 1Q21 AND MAP-2 CANDIDATE GENES

      Human genetics
    49. WALLGRENPETTERSSON C; AVELA R; MARCHAND S; KOLEHMAINEN J; TAHVANAINEN E; HANSEN FJ; MUNTONI F; DUBOWITZ V; DEVISSER M; VANLANGEN IM; LAING NG; FAURE S; DELACHAPELLE A
      A GENE FOR AUTOSOMAL RECESSIVE NEMALINE MYOPATHY ASSIGNED TO CHROMOSOME 2Q BY LINKAGE ANALYSIS

      Cytogenetics and cell genetics
    50. GIBSON RA; PRONK JC; SAVOIA A; MORGAN NV; WIJKER M; HASSOCK S; VETRIE D; OLAVESEN M; KENDALL E; FAURE S; WEISSENBACH J; DOGGETT NA; JOENJE H; ARWERT F; MATHEW CG
      LOCALIZATION OF THE FANCONI-ANEMIA COMPLEMENTATION GROUP-A GENE TO CHROMOSOME 16Q24.3

      Cytogenetics and cell genetics
    51. GSCHWEND M; LEVRAN O; KRUGLYAK L; RANDADE K; VERLANDER PC; SHEN S; FAURE S; WEISSENBACH J; ALTAY C; LANDER ES; AUERBACH AD; BOTSTEIN D
      A LOCUS FOR FANCONI-ANEMIA ON 16Q DETERMINED BY HOMOZYGOSITY MAPPING

      Cytogenetics and cell genetics
    52. QUERNE L; FAURE S
      ACTIVATING THE RIGHT-HEMISPHERE BY A PRIOR SPATIAL TASK - EQUAL LEXICAL DECISION ACCURACY IN LEFT AND RIGHT VISUAL-FIELDS IN NORMAL SUBJECTS

      Brain and cognition
    53. CARDEBAT D; DEMONET JF; VIALLARD G; FAURE S; PUEL M; CELSIS P
      BRAIN FUNCTIONAL PROFILES IN FORMAL AND SEMANTIC FLUENCY TASKS - A SPECT STUDY IN NORMALS

      Brain and language
    54. FAURE S; TREMBLAY A; ANGELIER J
      STATE OF INTRAPLATE STRESS AND TECTONISM OF NORTHEASTERN AMERICA SINCE CRETACEOUS TIMES, WITH PARTICULAR EMPHASIS ON THE NEW-ENGLAND QUEBECIGNEOUS PROVINCE

      Tectonophysics
    55. FARDEAU M; TOME FMS; HELBLINGLECLERC A; EVANGELISTA T; OTTOLINI A; CHEVALLAY M; BAROIS A; ESTOURNET B; HARPEY JP; FAURE S; GUICHENEY P; HILLAIRE D
      CONGENITAL MUSCULAR-DYSTROPHY WITH MEROSI N DEFICIENCY - CLINICAL, HISTOPATHOLOGICAL, IMMUNOCYTOCHEMICAL AND GENETIC-STUDY

      Revue neurologique
    56. DIB C; FAURE S; FIZAMES C; SAMSON D; DROUOT N; VIGNAL A; MILLASSEAU P; MARC S; HAZAN J; SEBOUN E; LATHROP M; GYAPAY G; MORISSETTE J; WEISSENBACH J
      A COMPREHENSIVE GENETIC-MAP OF THE HUMAN GENOME BASED ON 5,264 MICROSATELLITES

      Nature
    57. DAUSSE E; BERTHET M; DENJOY I; ANDREFOUET X; CRUAUD C; BENNACEUR M; FAURE S; COUMEL P; SCHWARTZ K; GUICHENEY P
      A MUTATION IN HERG ASSOCIATED WITH NOTCHED T-WAVES IN LONG QT SYNDROME

      Journal of Molecular and Cellular Cardiology
    58. FAURE S; TREMBLAY A; ANGELIER J
      ALLEGHANIAN PALEOSTRESS RECONSTRUCTION IN THE NORTHERN APPALACHIANS -INTRAPLATE DEFORMATION BETWEEN LAURENTIA AND GONDWANA

      Geological Society of America bulletin
    59. FORISSIER JF; CARRIER L; FARZA H; BONNE G; BERCOVICI J; RICHARD P; HAINQUE B; TOWNSEND PJ; YACOUB MH; FAURE S; DUBOURG O; MILLAIRE A; HAGEGE AA; DESNOS M; KOMAJDA M; SCHWARTZ K
      CODON-102 OF THE CARDIAC TROPONIN-T GENE IS A PUTATIVE HOT-SPOT FOR MUTATIONS IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY

      Circulation
    60. CORNELIS F; FAURE S; MARTINEZ M; FRITZ P; DIB C; PRUDHOMME JF; TRAN TH; DELAYE A; PRINCE N; LEFEVRE C; THOMAS G; POIRIER M; SOUBIGOU S; ALIBERT O; LASBLEIZ S; FOUIX S; LIOTE F; LOSTE MN; LEPAGE V; CHARRON D; GYAPAY G; KUNTZ D; BARDIN T; WEISSENBACH J
      SYSTEMATIC SCREENING OF THE ENTIRE GENOME IN RHEUMATOID-ARTHRITIS FAMILIES REVEALS 3 MAJOR SUSCEPTIBILITY LOCI

      Arthritis and rheumatism
    61. PLATEL H; FAURE S; EUSTACHE F
      NEUROPSYCHOLOGY AND FUNCTIONAL CEREBRAL I MAGING

      Annee Psychologique
    62. COX SA; ATTWOOD J; BRYANT SP; BAINS R; POVEY R; POVEY S; REBELLO M; KAPSETAKI M; MOSCHONAS NK; GRZESCHIK KH; OTTO M; DIXON M; SUDWORTH HE; KOOY RF; WRIGHT A; TEAGUE P; TERRENATO L; VERGNAUD G; MONFOUILLOUX S; WEISSENBACH J; ALIBERT O; DIB C; FAURE S; BAKKER E; PEARSON NM; VOSSEN RHAM; GAL A; MUELLERMYHSOK B; CANN HM; SPURR NK
      EUROPEAN GENE-MAPPING PROJECT (EUROGEM) - BREAKPOINT PANELS FOR HUMAN-CHROMOSOMES BASED ON THE CEPH REFERENCE FAMILIES

      Annals of Human Genetics
    63. TOUITOU I; REY JM; DROSS C; DUPONT M; BRUN O; CIANO M; DEMAILLE J; SMAOUI N; NEDELEC B; HAMIDI L; CATTAN D; MERY JP; PRIER A; CABANE J; CHOUKROUN G; GODEAU P; DELPECH M; GRATEAU G; FAURE S; PRUDHOMME JF; CLEPET C; WEISSENBACH J; AKOPIAN K; KOUYOUMDJIAN JC; AMSELEM S; DERVICHIAN M; GOOSSENS M
      LOCALIZATION OF THE FAMILIAL MEDITERRANEAN FEVER GENE (FMF) TO A 250-KB INTERVAL IN NON-ASHKENAZI JEWISH FOUNDER HAPLOTYPES

      American journal of human genetics
    64. GSCHWEND M; LEVRAN O; KRUGLYAK L; RANADE K; VERLANDER PC; SHEN S; FAURE S; WEISSENBACH J; ALTAY C; LANDER ES; AUERBACH AD; BOTSTEIN D
      A LOCUS FOR FANCONI-ANEMIA ON 16Q DETERMINED BY HOMOZYGOSITY MAPPING

      American journal of human genetics
    65. VINCENT P; PLAUCHU H; HAZAN J; FAURE S; WEISSENBACH J; GODET J
      A 3RD LOCUS FOR HEREDITARY HEMORRHAGIC TELANGIECTASIA MAPS TO CHROMOSOME 12Q (VOL 4, PG 945, 1995)

      Human molecular genetics
    66. VINCENT P; PLAUCHU H; HAZAN J; FAURE S; WEISSENBACH J; GODET J
      A 3RD LOCUS FOR HEREDITARY HEMORRHAGIC TELANGIECTASIA MAPS TO CHROMOSOME 12Q

      Human molecular genetics
    67. WALLGRENPETTERSSON C; AVELA K; MARCHAND S; KOLEHMAINEN J; TAHVANAINEN E; HANSEN FJ; MUNTONI F; DUBOWITZ V; DEVISSER M; VANLANGEN IM; LAING NG; FAURE S; DELACHAPELLE A
      A GENE FOR AUTOSOMAL RECESSIVE NEMALINE MYOPATHY ASSIGNED TO CHROMOSOME 2Q BY LINKAGE ANALYSIS

      Neuromuscular disorders
    68. DAUSSE E; DENJOY I; KAHLEM P; BENNACEUR M; FAURE S; WEISSENBACH J; COUMEL P; SCHWARTZ K; GUICHENEY P
      READJUSTING THE LOCALIZATION OF LONG QT SYNDROME GENE ON CHROMOSOME 11P15

      Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie
    69. REGUIGNEARNOULD I; COUILLIN P; MOLLICONE R; FAURE S; FLETCHER A; KELLY RJ; LOWE JB; ORIOL R
      RELATIVE POSITIONS OF 2 CLUSTERS OF HUMAN ALPHA-L-FUCOSYL-TRANSFERASES IN 19Q (FUT1-FUT2) AND 19P (FUT6-FUT3-FUT5) WITHIN THE MICROSATELLITE GENETIC-MAP OF CHROMOSOME-19

      Cytogenetics and cell genetics
    70. FAURE S; CECCALDI M; ALEXIS S; PONCET M
      ACQUIRED LEFT HAND AGRAPHIA IN A NON-RIGHT-HANDED PATIENT

      Brain and cognition
    71. HUDSON TJ; STEIN LD; GERETY SS; MA JL; CASTLE AB; SILVA J; SLONIM DK; BAPTISTA R; KRUGLYAK L; XU SH; HU XT; COLBERT AME; ROSENBERG C; REEVEDALY MP; ROZEN S; HUI L; WU XY; VESTERGAARD C; WILSON KM; BAE JS; MAITRA S; GANIATSAS S; EVANS CA; DEANGELIS MM; INGALLS KA; NAHF RW; HORTON LT; ANDERSON MO; COLLYMORE AJ; YE WJ; KOUYOUMJIAN V; ZEMSTEVA IS; TAM J; DEVINE R; COURTNEY DF; RENAUD MT; NGUYEN H; OCONNOR TJ; FIZAMES C; FAURE S; GYAPAY G; DIB C; MORISSETTE J; ORLIN JB; BIRREN BW; GOODMAN N; WEISSENBACH J; HAWKINS TL; FOOTE S; PAGE DC; LANDER ES
      AN STS-BASED MAP OF THE HUMAN GENOME

      Science
    72. CHUMAKOV IM; RIGAULT P; LEGALL I; BELLANNECHANTELOT C; BILLAULT A; GUILLOU S; SOULARUE P; GUASCONI G; POULLIER E; GROS I; BELOVA M; SAMBUCY JL; SUSINI L; GERVY P; GLIBERT F; BEAUFILS S; BUI H; MASSART C; DETAND MF; DUKASZ F; LECOULANT S; OUGEN P; PERROT V; SAUMLER M; SORAVITO C; BAHOUAYILA R; COHENAKENINE A; BARILLOT E; BERTRAND S; CODANI JJ; CATERINA D; GEORGES I; LACROIX B; LUCOTTE G; SAHBATOU M; SCHMIT C; SANGOUARD M; TUBACHER E; DIB C; FAURE S; FIZAMES C; GYAPAY G; MILLASSEAU P; NGUYEN S; MUSELET D; VIGNAL A; MORISSETTE J; MENNINGER J; LIEMAN J; DESAI T; BANKS A; BRAYWARD P; WARD D; HUDSON T; GERETY S; FOOTE S; STEIN L; PAGE DC; LANDER ES; WEISSENBACH J; LEPASLIER D; COHEN D
      A YAC CONTIG MAP OF THE HUMAN GENOME

      Nature
    73. CORNELIS F; FAURE S; HAMZA M; PRINCE N; TRAN TH; WEISSENBACH J; PRUDHOMME JF; BARDIN T
      ABSENCE OF LINKAGE WITH CHROMOSOME 8Q MARKERS IN A CHONDROCALCINOSIS FAMILY

      Arthritis and rheumatism
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      American journal of human genetics
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      Nature genetics
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/01/21 alle ore 14:12:56