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La ricerca find articoli where authors phrase all words 'Lucotte, G' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 84 riferimenti
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    1. Lucotte, G; Mercier, G
      Meta-analysis of GJB2 mutation 35delG frequencies in Europe

      GENETIC TESTING
    2. Lucotte, G
      Study of the mutation M694V of familial Mediterranean fever in Jews

      GENETIC TESTING
    3. Lucotte, G; Mercier, G
      Population genetics of factor V Leiden in Europe

      BLOOD CELLS MOLECULES AND DISEASES
    4. Lucotte, G; Mercier, G
      Population genetics of factor V Leiden in Europe

      BLOOD CELLS MOLECULES AND DISEASES
    5. Lucotte, G
      Frequency analysis and allele map in favor of the Celtic origin of the C282Y mutation of hemochromatosis

      BLOOD CELLS MOLECULES AND DISEASES
    6. Lucotte, G; Semonin, O; Mercier, G
      Presymptomatic testing for autosomal dominant spinocerebellar ataxia type 1 in a French family

      GENETIC COUNSELING
    7. Lucotte, G; Bathelier, C; Champenois, T
      PCR test for diagnosis of the common CJB2 (connexin 26) 35delG mutation ondried blood spots and determination of the carrier frequency in France

      MOLECULAR AND CELLULAR PROBES
    8. Lucotte, G; Gerard, N; Mercier, G
      North African genes in Iberia studied by Y-chromosome DNA haplotype V

      HUMAN IMMUNOLOGY
    9. Lucotte, G
      Distribution of the CCR5 gene 32-basepair deletion in West Europe. A hypothesis about the possible dispersion of the mutation by the Vikings in historical times

      HUMAN IMMUNOLOGY
    10. Semonin, O; Fontaine, K; Daviaud, C; Ayuso, C; Lucotte, G
      Identification of three novel mutations of the noggin gene in patients with fibrodysplasia ossificans progressiva

      AMERICAN JOURNAL OF MEDICAL GENETICS
    11. Lucotte, G; Gerard, N; Mercier, G
      North African genes in Iberia studied by Y-chromosome DNA haplotype 5

      HUMAN BIOLOGY
    12. Mercier, G; Lucotte, G
      Apolipoprotein E epsilon 4 allele, the major risk factor for Alzheimer's disease, is also involved in temporal lobe epilepsy

      ALZHEIMERS REPORTS
    13. Oddoze, C; Michel, BF; Lucotte, G
      Apolipoprotein E epsilon 4 allele predicts a better response to donepezil therapy in Alzheimer's disease

      ALZHEIMERS REPORTS
    14. Lucotte, G; Mercier, G; Clavel, C
      Apolipoprotein E epsilon 4 allele, the major risk factor for Alzheimer's disease, is also involved in the severity of multiple sclerosis

      ALZHEIMERS REPORTS
    15. Rasmussen, HB; Lucotte, G; Clausen, T
      Endogenous retroviruses and multiple sclerosis

      JOURNAL OF NEUROVIROLOGY
    16. Lucotte, G; Bathelier, C; Mercier, G
      TNF-alpha polymorphisms in multiple sclerosis: no association with-238 and-308 promoter alleles, but the microsatellite allele a11 is associated withthe disease in French patients

      MULTIPLE SCLEROSIS
    17. Lucotte, G; Mercier, G
      Celtic origin of the C282Y mutation of hemochromatosis

      GENETIC TESTING
    18. Lucotte, G; Bathelier, C; Mercier, G; Gerard, N; Lenoir, G; Semonin, O; Fontaine, K
      Localization of the gene for fibrodysplasia ossificans progressiva (FOP) to chromosome 17q21-22

      GENETIC COUNSELING
    19. Lucotte, G; Bathelier, C; Champenois, T
      Genotyping the hemochromatosis mutation of the HFE gene in a series of more than one thousand patients with seric iron overload

      GASTROENTEROLOGIE CLINIQUE ET BIOLOGIQUE
    20. Lucotte, G; Aouizerate, A; Berriche, S
      Y-chromosome DNA haplotypes in North African populations

      HUMAN BIOLOGY
    21. Zouali, H; Faure-Delanef, L; Lucotte, G
      Chromosome 19 locus apolipoprotein C-II association with multiple sclerosis

      MULTIPLE SCLEROSIS
    22. Lucotte, G; Sesboue, R
      Polymerase chain reaction detection of S and Z alpha-1-antitrypsin variants by duplex PCR assay

      MOLECULAR AND CELLULAR PROBES
    23. Lucotte, G; Mercier, G; Smets, P
      Elevated frequencies of the mutant allele Delta 32 at the CCR5 gene in Ashkenazic Jews

      AIDS RESEARCH AND HUMAN RETROVIRUSES
    24. Dupret, JM; Longuemaux, S; Lucotte, G
      Acetylator genotype for N-acetyltransferase 2 and Parkinson's disease

      ANNALS OF NEUROLOGY
    25. Mercier, G; Turpin, JC; Lucotte, G
      Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease: no association found

      JOURNAL OF NEUROLOGY
    26. Lucotte, G; Smets, P
      Origins of Falasha Jews studied by haplotypes of the Y chromosome

      HUMAN BIOLOGY
    27. Lucotte, G; Loirat, F
      Y-chromosome DNA haplotype 15 in Europe

      HUMAN BIOLOGY
    28. Lucotte, G; Semonin, O; Lutz, P
      A de novo heterozygous deletion of 42 base-pairs in the noggin gene of a fibrodysplasia ossificans progressiva patient

      CLINICAL GENETICS
    29. Lucotte, G; Mercier, G; Burckel, A
      The vitamin D receptor FokI start codon polymorphism and bone mineral density in osteoporotic postmenopausal French women

      CLINICAL GENETICS
    30. Lucotte, G; Mercier, G; Burckel, A
      FokI polymorphism at the human vitamin D receptor gene locus in Europeans and Africans

      CLINICAL GENETICS
    31. Ducros, A; Denier, C; Joutel, A; Vahedi, K; Michel, A; Darcel, F; Madigand, M; Guerouaou, D; Tison, F; Julien, J; Hirsch, E; Chedru, F; Bisgard, C; Lucotte, G; Despres, P; Billard, C; Barthez, MA; Ponsot, G; Bousser, MG; Tournier-Lasserve, E
      Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia

      AMERICAN JOURNAL OF HUMAN GENETICS
    32. Lucotte, G
      Apolipoprotein E epsilon 4 allele frequencies in Europe in relation to Alzheimer's disease

      ALZHEIMERS REPORTS
    33. Lucotte, G; Mercier, G; Burckel, A
      Apolipoprotein E epsilon 4 allele, the major risk factor in Alzheimer's disease, is not involved in osteoporosis

      ALZHEIMERS REPORTS
    34. Oddoze, C; Michel, BF; Berthezene, P; Clavel, C; Lucotte, G
      Apolipoprotein E epsilon 4 allele predicts a positive response to tacrine in Alzheimer's disease

      ALZHEIMERS REPORTS
    35. MERCIER G; BATHELIER C; LUCOTTE G
      FREQUENCY OF THE C282Y MUTATION OF HEMOCHROMATOSIS IN 5 FRENCH POPULATIONS

      Blood cells, molecules, & diseases
    36. LUCOTTE G
      CELTIC ORIGIN OF THE C282Y MUTATION OF HEMOCHROMATOSIS

      Blood cells, molecules, & diseases (Print)
    37. LUCOTTE G; MERCIER G
      DISTRIBUTION OF THE CCR5 GENE 32-BP DELETION IN EUROPE

      Journal of acquired immune deficiency syndromes and human retrovirology
    38. Spurr, NK; Autrup, H; Bishop, T; Haugen, A; Lang, M; Lafuente, A; Lechner, MC; Lucotte, G; Rane, A; Regateiro, FJ; Strange, RC; Wolf, CR
      Metabolic polymorphism of drug metabolising enzymes as markers of susceptibility in cancer and neurological disorders

      CANCER RESEARCH SUPPORTED UNDER BIOMED I
    39. BATHELIER C; CHAMPENOIS T; LUCOTTE G
      ARMS TEST FOR DIAGNOSIS OF FACTOR-V-LEIDEN MUTATION AND ALLELE FREQUENCIES IN FRANCE

      Molecular and cellular probes
    40. Lucotte, G; Mercier, G; Burckel, A
      The use of nested RT-PCR of prostate-specific membrane antigen in blood cells: implications for the detection of haematogenous neoplastic cells in patients with prostate adenocarcinoma

      MOLECULAR AND CELLULAR PROBES
    41. LUCOTTE G; MERCIER G
      DELTA-32 MUTATION FREQUENCIES OF THE CCR5 CORECEPTOR IN DIFFERENT FRENCH REGIONS

      Comptes rendus de l'Academie des Sciences. Serie III, Sciences de lavie
    42. Lucotte, G; Bathelier, C; Pillet, A; Bali, C; Turpin, JC
      Genetic susceptibility to multiple sclerosis carried by Class II HLA DR alleles 15 and 4.

      SEMAINE DES HOPITAUX
    43. Lucotte, G; Mercier, G; Turpin, JC
      Lack of mutation G209A in the alpha-synuclein gene in French patients withfamilial and sporadic Parkinson's disease

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    44. ROUX C; DOUGADOS M; ABEL L; MERCIER G; LUCOTTE G
      ASSOCIATION OF A POLYMORPHISM IN THE COLLAGEN-I ALPHA-GENE WITH OSTEOPOROSIS IN FRENCH WOMEN

      Arthritis and rheumatism
    45. LOIRAT F; LUCOTTE G
      FREQUENCY OF THE CYSTIC-FIBROSIS MUTATION DELTA-F508 IN FRANCE - RESULTS FROM 2.617 FAMILIES

      Archives de pediatrie
    46. LUCOTTE G; BURCKEL A
      DNA TYPING OF HLA-B27 BY POLYMERASE CHAIN-REACTION

      Molecular and cellular probes
    47. MERCIER G; BURCKEL A; LUCOTTE G
      DETECTION OF BORRELIA-BURGDORFERI DNA BY POLYMERASE CHAIN-REACTION INURINE SPECIMENS OF PATIENTS WITH ERYTHEMA MIGRANS LESIONS

      Molecular and cellular probes
    48. LUCOTTE G
      FREQUENCIES OF THE CC-CHEMOKINE RECEPTOR-5 DELTA-32 ALLELE IN VARIOUSPOPULATIONS OF DEFINED RACIAL BACKGROUND

      Biomedicine & pharmacotherapy
    49. LUAUTE JP; TURPIN JC; LUCOTTE G
      SCHIZOPHRENIA AND HUNTINGTONS-DISEASE - C LINICAL AND MOLECULAR-BIOLOGY DATA IN FRENCH FAMILIES

      La Semaine des hopitaux de Paris
    50. LUCOTTE G; AOUIZERATE A; GERARD N; MERCIER G; TURPIN JC
      EXPERIENCE WITH THE PRESYMPTOMATIC DIAGNO SIS OF HUNTINGTONS-DISEASE

      La Semaine des hopitaux de Paris
    51. ZEKRAOUI L; LAGARDE JP; RAISONNIER A; GERARD N; AOUIZERATE A; LUCOTTE G
      HIGH-FREQUENCY OF THE APOLIPOPROTEIN-E ASTERISK-4 ALLELE IN AFRICAN PYGMIES AND MOST OF THE AFRICAN POPULATIONS IN SUB-SAHARAN AFRICA

      Human biology
    52. LOIRAT F; HAZOUT S; LUCOTTE G
      G542X AS A PROBABLE PHOENICIAN CYSTIC-FIBROSIS MUTATION

      Human biology
    53. LUCOTTE G; LOIRAT F; HAZOUT S
      PATTERN OF GRADIENT OF APOLIPOPROTEIN-E ALLELE ASTERISK-4 FREQUENCIESIN WESTERN-EUROPE

      Human biology
    54. LUCOTTE G; MERCIER G
      FREQUENCY OF FACTOR-V-LEIDEN (ARG506GLN) IN FRANCE

      British Journal of Haematology
    55. MACEK M; MACKOVA A; HAMOSH A; HILMAN BC; SELDEN RF; LUCOTTE G; FRIEDMAN KJ; KNOWLES MR; ROSENSTEIN BJ; CUTTING GR
      IDENTIFICATION OF COMMON CYSTIC-FIBROSIS MUTATIONS IN AFRICAN-AMERICANS WITH CYSTIC-FIBROSIS INCREASES THE DETECTION RATE TO 75-PERCENT

      American journal of human genetics
    56. LOIRAT F; LUCOTTE G
      FREQUENCY OF THE CYSTIC-FIBROSIS MUTATION DELTA-F508 IN FRANCE - NEW RESULTS FROM 1656 UNRELATED FAMILIES

      Archives de pediatrie
    57. BATHELIER C; MERCIER G; LUCOTTE G
      A SIMPLIFIED SEMIQUANTITATIVE DETERMINATION OF HEPATITIS-C VIRUS GENOME MOLECULES BY THE END-POINT DILUTION METHOD

      Molecular and cellular probes
    58. LUCOTTE G; TURPIN JC; GERARD N; PANSERAT S; KRISHNAMOORTHY R
      MUTATION FREQUENCIES OF THE CYTOCHROME CYP2D6 GENE IN PARKINSON DISEASE PATIENTS AND IN FAMILIES

      American journal of medical genetics
    59. LUCOTTE G; HAZOUT S
      Y-CHROMOSOME DNA HAPLOTYPES IN BASQUES

      Journal of molecular evolution
    60. LUCOTTE G; DAVID F; BERRICHE S
      HAPLOTYPE-VIII OF THE Y-CHROMOSOME IS THE ANCESTRAL HAPLOTYPE IN JEWS

      Human biology
    61. LUCOTTE G
      DELTA-F508 FREQUENCY IN FRANCE - A STUDY OF 1030 UNRELATED FAMILIES

      Archives de pediatrie
    62. LUCOTTE G; BATHELIER C; LESPIAUX V; BALI C; CHAMPENOIS T
      DETECTION AND GENOTYPING OF HERPES-SIMPLEX VIRUS TYPE-1 AND TYPE-2 BYPOLYMERASE CHAIN-REACTION

      Molecular and cellular probes
    63. LUCOTTE G; TURPIN JC; RIESS O; EPPLEN JT; SIEDLACZK I; LOIRAT F; HAZOUT S
      CONFIDENCE-INTERVALS FOR PREDICTED AGE-OF-ONSET, GIVEN THE SIZE OF (GAG)(N) REPEAT, IN HUNTINGTONS-DISEASE

      Human genetics
    64. LUCOTTE G; AOUIZERATE A; GERARD N; TURPIN JC; LANDAIS P
      ALLELE DOSES OF APOLIPOPROTEIN-E TYPE EPSILON-4 IN SPORADIC LATE-ONSET ALZHEIMERS-DISEASE

      American journal of medical genetics
    65. 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
    66. LUCOTTE G; HAZOUT S; DEBRAEKELEER M
      COMPLETE MAP OF CYSTIC-FIBROSIS MUTATION DF508 FREQUENCIES IN WESTERN-EUROPE AND CORRELATION BETWEEN MUTATION FREQUENCIES AND INCIDENCE OF DISEASE

      Human biology
    67. LUCOTTE G; HAZOUT S
      GEOGRAPHIC AND ETHNIC DISTRIBUTIONS OF THE MORE FREQUENT CYSTIC-FIBROSIS MUTATIONS IN EUROPE SHOW THAT A FOUNDER EFFECT IS APPARENT FOR SEVERAL MUTANT ALLELES

      Human biology
    68. LUCOTTE G; GALZOT P; LU CY; BATHELIER C; CHAMPENOIS T
      DETECTION OF SERUM HEPATITIS-B VIRUS USING A NESTED POLYMERASE CHAIN-REACTION ASSAY

      Molecular and cellular probes
    69. LUCOTTE G
      CAG TRINUCLEOTIDE REPEATS IN HUNTINGTON D ISEASE - A WORLDWIDE STUDY

      MS. Medecine sciences
    70. LUCOTTE G; TURPIN JC; LANDAIS P
      APOLIPOPROTEIN E-EPSILON-4 ALLELE DOSES IN LATE-ONSET ALZHEIMERS-DISEASE

      Annals of neurology
    71. LUCOTTE G; VISVIKIS S; LEININGERMULER B; DAVID F; BERRICHE S; REVEILLEAU S; COUDERC R; BABRON MC; AGUILLON D; SIEST G
      ASSOCIATION OF APOLIPOPROTEIN-E ALLELE EPSILON-4 WITH LATE-ONSET SPORADIC ALZHEIMERS-DISEASE

      American journal of medical genetics
    72. TURPIN JC; LUCOTTE G
      HUNTINGTONS-DISEASE PROCEEDINGS OF THE 1S T FRENCH SYMPOSIUM ON HUNTINGTONS-DISEASE - REIMS, FRANCE, SEPTEMBER 24, 1993 - INTRODUCTION

      La Semaine des hopitaux de Paris
    73. LUCOTTE G; BERRICHE S; AOUIZERATE A; LOREILLE O; GERARD N
      NUMBER OF TRIPLET REPEATS IN FRENCH FAMIL IES WITH HUNTINGTONS-DISEASE

      La Semaine des hopitaux de Paris
    74. TURPIN JC; LUCOTTE G
      MULTIDISCIPLINARY APPROACH TO THE PRESYMP TOMATIC DIAGNOSIS OF HUNTINGTONS-DISEASE

      La Semaine des hopitaux de Paris
    75. LUCOTTE G; GERARD N; KRISHNAMOORTHY R; DAVID F; AOUIZERATE A; GALZOT P
      REDUCED VARIABILITY IN Y-CHROMOSOME-SPECIFIC HAPLOTYPES FOR SOME CENTRAL AFRICAN POPULATIONS

      Human biology
    76. ANDREW SE; GOLDBERG YP; KREMER B; SQUITIERI F; THEILMANN J; ZEISLER J; TELENIUS H; ADAM S; ALMQUIST E; ANVRET M; LUCOTTE G; STOESS AJ; CAMPANELLA G; HAYDEN MR
      HUNTINGTON DISEASE WITHOUT CAG EXPANSION - PHENOCOPIES OR ERRORS IN ASSIGNMENT

      American journal of human genetics
    77. TELENIUS H; KREMER HPH; THEILMANN J; ANDREW SE; ALMQVIST E; ANVRET M; GREENBERG C; GREENBERG J; LUCOTTE G; SQUITIERI F; STARR E; GOLDBERG YP; HAYDEN MR
      MOLECULAR ANALYSIS OF JUVENILE HUNTINGTON DISEASE - THE MAJOR INFLUENCE ON (CAG)(N) REPEAT LENGTH IS THE SEX OF THE AFFECTED PARENT

      Human molecular genetics
    78. LUCOTTE G; FRANCOIS MH; PETIT MC; BERRICHE S; REVEILLEAU S
      A MULTIPLE PRIMER PAIRS POLYMERASE CHAIN-REACTION FOR THE DETECTION OF HUMAN GENITAL PAPILLOMAVIRUS TYPES

      Molecular and cellular probes
    79. LUCOTTE G; BERRICHE S; TURPIN JC
      A RECOMBINANT FRIEDREICHS ATAXIA FAMILY

      Human genetics
    80. LUCOTTE G; DAVID F; VISVIKIS S; LEININGERMULLER B; SIEST G; BABRON MC; COUDERC R
      APOLIPOPROTEIN-E-SIGMA-4 ALLELE AND ALZHEIMERS-DISEASE

      Lancet
    81. LUCOTTE G; SMETS P; RUFFIE J
      Y-CHROMOSOME-SPECIFIC HAPLOTYPE DIVERSITY IN ASHKENAZIC AND SEPHARDICJEWS

      Human biology
    82. LUCOTTE G; LOIRAT F
      A MORE DETAILED MAP OF THE CYSTIC-FIBROSIS MUTATION DF508 FREQUENCIESIN EUROPE

      Human biology
    83. ANDREW S; THEILMANN J; ALMQVIST E; NORREMOLLE A; LUCOTTE G; ANVRET M; SORENSEN SA; TURPIN JC; HAYDEN MR
      DNA ANALYSIS OF DISTINCT POPULATIONS SUGGESTS MULTIPLE ORIGINS FOR THE MUTATION CAUSING HUNTINGTON DISEASE

      Clinical genetics
    84. TELENIUS H; KREMER B; ADAM S; THEILMAN J; ANDREW SE; GOLDBERG YP; SQUITIERI F; STARR E; ALMQUIST E; ANVRET M; GREENBERG J; LUCOTTE G; HAYDEN MR
      EFFECT OF PARENTAL TRANSMISSION ON TRINUCLEOTIDE EXPANSION AND AGE ATONSET OF SYMPTOMS IN JUVENILE HUNTINGTON DISEASE

      American journal of human genetics


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Documento generato il 30/05/20 alle ore 02:44:12