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    1. Pailhoux, E; Vigier, B; Chaffaux, S; Servel, N; Taourit, S; Furet, JP; Fellous, M; Grosclaude, F; Cribiu, EP; Cotinot, C; Vaiman, D
      A 11.7-kb deletion triggers intersexuality and polledness in goats

      NATURE GENETICS
    2. De Baere, E; Dixon, MJ; Small, KW; Jabs, EW; Leroy, BP; Devriendt, K; Gillerot, Y; Mortier, G; Meire, F; Van Maldergem, L; Courtens, W; Hjalgrim, H; Huang, S; Liebaers, I; Van Regemorter, N; Touraine, P; Praphanphoj, V; Verloes, A; Udar, N; Yellore, V; Chalukya, M; Yelchits, S; De Paepe, A; Kuttenn, F; Fellous, M; Veitia, R; Messiaen, L
      Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation

      HUMAN MOLECULAR GENETICS
    3. Nunes, M; Blanc, I; Maes, J; Fellous, M; Robert, B; McElreavey, K
      NSPc1, a novel mammalian Polycomb gene, is expressed in neural crest-derived structures of the peripheral nervous system

      MECHANISMS OF DEVELOPMENT
    4. Jamain, S; Girondot, M; Leroy, P; Clergue, M; Quach, H; Fellous, M; Bourgeron, T
      Transduction of the human gene FAM8A1 by endogenous retrovirus during primate evolution

      GENOMICS
    5. Jamain, S; Quach, H; Fellous, M; Bourgeron, T
      Identification of the human KIF13A gene homologous to Drosophila kinesin-73 and candidate for schizophrenia

      GENOMICS
    6. Quintana-Murci, T; Jamain, S; Fellous, M
      The origin and evolution of mammalian sex chromosomes.

      COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES
    7. Veitia, RA; Salas-Cortes, L; Ottolenghi, C; Pailhoux, E; Cotinot, C; Fellous, M
      Testis determination in mammals: more questions than answers

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    8. Lennon-Dumenil, AM; Barbouche, MR; Vedrenne, J; Prod'Homme, T; Bejaoui, M; Ghariani, S; Charron, D; Fellous, M; Dellagi, K; Alcaide-Loridan, C
      Uncoordinated HLA-D gene expression in a RFXANK-defective patient with MHCclass II deficiency

      JOURNAL OF IMMUNOLOGY
    9. Pailhoux, E; Vigier, B; Vaiman, D; Schibler, L; Vaiman, A; Cribiu, E; Nezer, C; Georges, M; Sundstrom, J; Pelliniemi, LJ; Fellous, M; Cotinot, C
      Contribution of domestic animals to the identification of new genes involved in sex determination

      JOURNAL OF EXPERIMENTAL ZOOLOGY
    10. Salas-Cortes, L; Jaubert, F; Bono, MR; Fellous, M; Rosemblatt, M
      Expression of the human SRY protein during development in normal male gonadal and sex-reversed tissues

      JOURNAL OF EXPERIMENTAL ZOOLOGY
    11. Ottolenghi, C; Moreira, C; Mendonca, BB; Barbieri, M; Fellous, M; Berkovitz, GD; McElreavey, K
      Absence of mutations involving the lim homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    12. El Khil, HK; Marrakchi, RT; Loueslati, BY; Langaney, A; Fellous, M; Elgaaied, AB
      Y chromosome microsatellite variation in three populations of Jerba Island(Tunisia)

      ANNALS OF HUMAN GENETICS
    13. Krausz, C; Quintana-Murci, L; Fellous, M; Siffroi, JP; McElreavey, K
      Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism

      MOLECULAR HUMAN REPRODUCTION
    14. Ottolenghi, C; Veitia, R; Quintana-Murci, L; Torchard, D; Scapoli, L; Souleyreau-Therville, N; Beckmann, J; Fellous, M; McElreavey, K
      The region on 9p associated with 46,XY sex reversal contains several transcripts expressed in the urogenital system and a novel doublesex-related domain

      GENOMICS
    15. Ottolenghi, C; Veitia, R; Barbieri, M; Fellous, M; McElreavey, K
      The human doublesex-related gene, DMRT2 is homologous to a gene involved in somitogenesis and encodes a potential bicistronic transcript

      GENOMICS
    16. Siffroi, JP; Le Bourhis, C; Krausz, C; Dadoune, JP; Fellous, M
      Male infertility: molecular pathologies and new therapeutic approaches

      M S-MEDECINE SCIENCES
    17. Salas-Cortes, L; Jaubert, F; Nihoul-Fekete, C; Brauner, R; Rosemblatt, M; Fellous, M
      SRY protein is expressed in ovotestis and streak gonads from human sex-reversal

      CYTOGENETICS AND CELL GENETICS
    18. Siffroi, JP; Le Bourhis, C; Krausz, C; Barbaux, S; Quintana-Murci, L; Kanafani, S; Rouba, H; Bujan, L; Bourrouillou, G; Seifer, I; Boucher, D; Fellous, M; McElreavey, K; Dadoune, JP
      Sex chromosome mosaicism in males carrying Y chromosome long arm deletions

      HUMAN REPRODUCTION
    19. Denamur, E; Bocquet, N; Baudouin, V; Da Silva, F; Veitia, R; Peuchmaur, M; Elion, J; Gubler, MC; Fellous, M; Niaudet, P; Loirat, C
      WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis

      KIDNEY INTERNATIONAL
    20. Saifi, GM; Veitia, R; El Khil, HK; Barbaux, S; Tilak, P; Thomas, IM; Fellous, M
      sY116, a human Y-linked polymorphic STS

      JOURNAL OF GENETICS
    21. Fouchet, C; Gane, P; Huet, M; Fellous, M; Rouger, P; Banting, G; Cartron, JP; Lopez, C
      A study of the coregulation and tissue specificity of XG and MIC2 gene expression in eukaryotic cells

      BLOOD
    22. Fellous, M
      A tribute to Donald Pious (1930-1998)

      MICROBES AND INFECTION
    23. Alcaide-Loridan, C; Lennon, AM; Bono, MR; Barbouche, R; Dellagi, K; Fellous, M
      Differential expression of MHC class II isotype chains

      MICROBES AND INFECTION
    24. Barbosa, AS; Hadjiathanasiou, CG; Theodoridis, C; Papathanasiou, A; Tar, A; Merksz, M; Gyorvari, B; Sultan, C; Dumas, R; Jaubert, F; Niaudet, P; Moreira, CA; Cotinot, C; Fellous, M
      The same mutation affecting the splicing of WT1 gene is present on Frasiersyndrome patients with or without Wilms' tumor

      HUMAN MUTATION
    25. Vaiman, D; Schibler, L; Oustry-Vaiman, A; Pailhoux, E; Goldammer, T; Stevanovic, M; Furet, JP; Schwerin, M; Cotinot, C; Fellous, M; Cribiu, EP
      High-resolution human/goat comparative map of the goat polled/intersex syndrome (PIS): The human homologue is contained in a human YAC from HSA3q23

      GENOMICS
    26. Quintana-Murci, L; Veitia, R; Santachiara-Benerecetti, S; McElreavey, K; Fellous, M; Bourgeron, T
      Mitochondrial DNA, Y chromosome and human population history

      M S-MEDECINE SCIENCES
    27. Damiani, D; Guedes, DR; Fellous, M; Barbaux, S; McElreavey, K; Kalil, J; Goldberg, ACK; Moreira, CA; Barbosa, A; Manna, TD; Dichtchekenian, V; Setian, N
      Ullrich-Turner syndrome: Relevance of searching for Y chromosome fragments

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    28. Salas-Cortes, L; Jaubert, F; Barbaux, S; Nessmann, C; Bono, MR; Fellous, M; McElreavey, K; Rosemblatt, M
      The human SRY protein is present in fetal and adult Sertoli cells and germcells

      INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY
    29. McElreavey, K; Fellous, M
      Sex determination and the Y chromosome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    30. Saifi, GM; Tilak, P; Veitia, R; Thomas, IM; Tharapel, A; McElreavey, K; Fellous, M; Chandra, HS
      A novel mutation 5 ' to the HMG box of the SRY gene in a case of Swyer syndrome

      JOURNAL OF GENETICS
    31. Krausz, C; Quintana-Murci, L; Barbaux, S; Siffroi, JP; Rouba, H; Delafontaine, D; Souleyreau-Therville, N; Arvis, G; Antoine, JM; Erdei, E; Taar, JP; Tar, A; Jeandidier, E; Plessis, G; Bourgeron, T; Dadoune, JP; Fellous, M; McElreavey, K
      A high frequency of Y chromosome deletions in males with nonidiopathic infertility

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    32. BOURGERON T; FELLOUS M; MCELREAVEY K
      FAMILIAL PREMATURE OVARIAN FAILURE

      European journal of human genetics
    33. VEITIA R; GONCALVES J; SILVA M; RODRIGUES JC; BOIEIRO F; MARQUES R; LAVINHA J; CASPURRO M; NUNES M; RAPPAPORT R; THIBAUD E; JAUBERT F; FELLOUS M; MCELREAVEY K
      46,XY COMPLETE GONADAL-DYSGENESIS (SYWERS-SYNDROME) AND 46,XY PARTIALGONADAL-DYSGENESIS ASSOCIATED WITH DELETIONS OF 9P

      European journal of human genetics
    34. QUINTANAMURCI L; BARBAUX S; SIFFROI JP; DELAFONTAINE D; ROUBA H; KRAUSZ C; SOULEYREAUTHERVILLE N; JEANDIDIER E; PLESSIS G; BOURGERON T; FELLOUS M; MCELREAVEY K; FELLOUS M; MCELREAVEY K
      MOLECULAR ANALYSIS OF THE Y-CHROMOSOME IN INFERTILE MEN

      European journal of human genetics
    35. BOURGERON T; LEROY P; FELLOUS M; MCELREAVEY K
      IDENTIFICATION OF HCP, A NOVEL HIGHLY CONSERVED GENE ON HUMAN-CHROMOSOME-6, TRANSPOSED TO THE Y-CHROMOSOME DURING PRIMATE EVOLUTION AND A CANDIDATE FOR GENETIC PREDISPOSITION TO SCHIZOPHRENIA

      European journal of human genetics
    36. ION R; TELVI L; CHAUSSAIN JL; BARBET JP; NUNES M; SAFAR A; RETHORE MO; FELLOUS M; MCELREAVEY K
      FAILURE OF TESTICULAR DEVELOPMENT ASSOCIATED WITH A REARRANGEMENT OF 9P24.1 PROXIMAL TO THE SNF2 GENE

      Human genetics
    37. VEITIA R; LAURENT A; QUINTANAMURCI L; OTTOLENGHI C; FELLOUS M; VIDAUD M; MCELREAVEY K
      THE INSL4 GENE MAPS CLOSE TO WI-5527 AT 9P24.1-]P23.3 CLUSTERED WITH 2 RELAXIN GENES AND OUTSIDE THE CRITICAL REGION FOR THE MONOSOMY 9P SYNDROME

      Cytogenetics and cell genetics
    38. LENNON AM; OTTONE C; ROSEMBLATT M; FELLOUS M; BONO MR; ALCAIDELORIDAN C
      CIITA B-CELL-SPECIFIC PROMOTER SUPPRESSION IN MHC CLASS II-SILENCED CELL HYBRIDS

      Immunogenetics (New York)
    39. DUMENIL G; OLIVO JC; PELLEGRINI S; FELLOUS M; SANSONETTI PJ; VANNHIEU GT
      INTERFERON-ALPHA INHIBITS A SRC-MEDIATED PATHWAY NECESSARY FOR SHIGELLA-INDUCED CYTOSKELETAL REARRANGEMENTS IN EPITHELIAL-CELLS

      The Journal of cell biology
    40. RICHTER MF; DUMENIL G; UZE G; FELLOUS M; PELLEGRINI S
      SPECIFIC CONTRIBUTION OF TYK2 JH REGIONS TO THE BINDING AND THE EXPRESSION OF THE INTERFERON-ALPHA BETA RECEPTOR COMPONENT IFNAR1/

      The Journal of biological chemistry
    41. VEITIA RA; NUNES M; QUINTANAMURCI L; RAPPAPORT R; THIBAUD E; JAUBERT E; FELLOUS M; MCELREAVEY K; GONCALVES J; SILVA M; RODRIGUES JC; CASPURRO M; BOIEIRO F; MARQUES R; LAVINHA J
      SWYER-SYNDROME AND 46,XY PARTIAL GONADAL-DYSGENESIS ASSOCIATED WITH 9P DELETIONS IN THE ABSENCE OF MONOSOMY-9P SYNDROME

      American journal of human genetics
    42. BARBAUX S; FELLOUS M
      STERILITY AND HEREDITARY

      Contraception fertilite sexualite
    43. BARBAUX S; NIAUDET P; GUBLER MC; GRUNFELD JP; JAUBERT F; KUTTENN F; FEKETE CN; SOULEYREAUTHERVILLE N; THIBAUD E; FELLOUS M; MCELREAVEY K
      DONOR SPLICE-SITE MUTATIONS IN WT1 ARE RESPONSIBLE FOR FRASIER-SYNDROME

      Nature genetics
    44. MCELREAVEY K; FELLOUS M
      SEX-DETERMINING GENES

      Trends in endocrinology and metabolism
    45. VEITIA R; NUNES M; MCELREAVEY K; FELLOUS M
      SEXUAL DETERMINISM AND DIFFERENTIATION IN MEN - FROM PATHOLOGY TO GENES

      Archives de pediatrie
    46. SEBOUN E; BARBAUX S; BOURGERON T; NISHI S; ALGONIK A; EGASHIRA M; NIKKAWA N; BISHOP C; FELLOUS M; MCELREAVEY K; KASAHARA M
      GENE SEQUENCE, LOCALIZATION, AND EVOLUTIONARY CONSERVATION OF DAZLA, A CANDIDATE MALE-STERILITY GENE (VOL 41, PG 227, 1997)

      Genomics
    47. SEBOUN E; BARBAUX S; BOURGERON T; NISHI S; ALGONIK A; EGASHIRA M; NIKKAWA N; BISHOP C; FELLOUS M; MCELREAVEY K; KASAHARA M
      GENE SEQUENCE, LOCALIZATION, AND EVOLUTIONARY CONSERVATION OF DAZLA, A CANDIDATE MALE-STERILITY GENE

      Genomics
    48. VEITIA R; NUNES M; BRAUNER R; DOCOFENZY M; JOANNYFLINOIS O; JAUBERT F; LORTATJACOB S; FELLOUS M; MCELREAVEY K
      DELETIONS OF DISTAL 9P ASSOCIATED WITH 46,XY MALE TO FEMALE SEX REVERSAL - DEFINITION OF THE BREAKPOINTS AT 9P23.3-P24.1

      Genomics
    49. DAMIANI D; FELLOUS M; MCELREAVEY K; BARBAUX S; BARRETO ESA; DICHTCHEKENIAN V; SETIAN N
      TRUE HERMAPHRODITISM - CLINICAL ASPECTS AND MOLECULAR STUDIES IN 16 CASES

      European journal of endocrinology
    50. VEITIA RA; FELLOUS M; MCELREAVEY K
      CONSERVATION OF Y-CHROMOSOME-SPECIFIC SEQUENCES IMMEDIATELY 5' TO THETESTIS-DETERMINING GENE IN PRIMATES

      Gene
    51. VEITIA R; ION A; BARBAUX S; JOBLING MA; SOULEYREAU N; ENNIS K; OSTRER H; TOSI M; MEO T; CHIBANI J; FELLOUS M; MCELREAVEY K
      MUTATIONS AND SEQUENCE VARIANTS IN THE TESTIS-DETERMINING REGION OF THE Y-CHROMOSOME IN INDIVIDUALS WITH A 46,XY FEMALE PHENOTYPE

      Human genetics
    52. TAR A; ION A; SOLYOM J; GYORVARI B; STEPHENSON C; BARBAUX S; NUNES M; FELLOUS M; MCELREAVEY K
      HYPERTELORISM AND HYPOSPADIAS ASSOCIATED WITH A DE-NOVO APPARENTLY BALANCED TRANSLOCATION BETWEEN 8Q22.3-23 AND 20P13

      American journal of medical genetics
    53. LENNON AM; OTTONE C; RIGAUD G; DEAVEN LL; LONGMIRE J; FELLOUS M; BONO R; ALCAIDELORIDAN C
      ISOLATION OF A B-CELL-SPECIFIC PROMOTER FOR THE HUMAN CLASS-II TRANSACTIVATOR

      Immunogenetics
    54. VEITIA RA; NUNES M; MCELREAVEY K; FELLOUS M
      GENETIC-BASIS OF HUMAN SEX DETERMINATION - AN OVERVIEW

      Theriogenology
    55. VAIMAN D; PAILHOUX E; SCHIBLER L; OUSTRY A; CHAFFAUX S; COTINOT C; FELLOUS M; CRIBIU EP
      GENETIC-MAPPING OF THE POLLED INTERSEX LOCUS (PIS) IN GOATS/

      Theriogenology
    56. GAUZZI MC; BARBIERI G; RICHTER MF; UZE G; LING L; FELLOUS M; PELLEGRINI S
      THE AMINO-TERMINAL REGION OF TYK2 SUSTAINS THE LEVEL OF INTERFERON-ALPHA RECEPTOR-1, A COMPONENT OF THE INTERFERON-ALPHA BETA RECEPTOR/

      Proceedings of the National Academy of Sciences of the United Statesof America
    57. DUMENIL G; RUBINI M; DUBOIS G; BASERGA R; FELLOUS M; PELLEGRINI S
      IDENTIFICATION OF SIGNALING COMPONENTS IN TYROSINE KINASE CASCADES USING PHOSPHOPEPTIDE AFFINITY-CHROMATOGRAPHY

      Biochemical and biophysical research communications
    58. VEITIA R; NUNES M; BRAUNER R; JOANNYFLINOIS O; FELLOUS M; MCELREAVEY K
      TERMINAL DELETIONS OF DISTAL 9P DEFINE A MINIMUM REGION ASSOCIATED WITH MALE TO FEMALE SEX REVERSAL

      Annals of Human Genetics
    59. BARBAUX S; NIAUDET P; GUBLER MC; GRUNFELD JP; JAUBERT F; KUTTENN F; FEKETE CN; SOULEYREAUTHERVILLE N; THIBAUD E; FELLOUS M; MCELREAVEY K
      DONOR SPLICE-SITE MUTATIONS IN THE WILMS-TUMOR GENE, WT1 ARE RESPONSIBLE FOR FRAZIER-SYNDROME

      American journal of human genetics
    60. COTINOT C; PAILHOUX E; VAIMAN D; BARBOSA A; CRIBIU E; FELLOUS M
      XX MALENESS - CONTRIBUTION OF ANIMAL-MODE LS

      Contraception fertilite sexualite
    61. VAIMAN D; KOUTITA O; OUSTRY A; ELSEN JM; MANFREDI E; FELLOUS M; CRIBIU EP
      GENETIC-MAPPING OF THE AUTOSOMAL REGION INVOLVED IN XX SEX-REVERSAL AND HORN DEVELOPMENT IN GOATS

      Mammalian genome
    62. BOURGERON T; BARBAUX S; MCELREAVEY K; FELLOUS M
      GENETICS OF MALE-INFERTILITY

      MS. Medecine sciences
    63. LENNON AM; OTTONE C; PEIJNENBURG A; HAMONBENAIS C; COLLAND F; GOBIN S; VANDENELSEN P; FELLOUS M; BONO R; ALCAIDELORIDAN C
      THE RAG CELL-LINE DEFINES A NEW COMPLEMENTATION GROUP OF MHC CLASS-IIDEFICIENCY

      Immunogenetics
    64. MCELREAVEY K; VILAIN E; BARBAUX S; FUQUA JS; FECHNER PY; SOULEYREAU N; DOCOFENZY M; GABRIEL R; QUEREUX C; FELLOUS M; BERKOVITZ GD
      LOSS OF SEQUENCE-3' TO THE TESTIS-DETERMINING GENE, SRY, INCLUDING THE Y-PSEUDOAUTOSOMAL BOUNDARY ASSOCIATED WITH PARTIAL TESTICULAR DETERMINATION

      Proceedings of the National Academy of Sciences of the United Statesof America
    65. TELVI L; ION A; CAREL JC; DESGUERRE I; PIRAUD M; BOUTIN AM; FEINGOLD J; PONSOT G; FELLOUS M; MCELREAVEY K
      A DUPLICATION OF DISTAL XP ASSOCIATED WITH HYPOGONADOTROPIC HYPOGONADISM, HYPOPLASTIC EXTERNAL GENITALIA, MENTAL-RETARDATION, AND MULTIPLE CONGENITAL-ABNORMALITIES

      Journal of Medical Genetics
    66. GAUZZI MC; VELAZQUEZ L; MCKENDRY R; MOGENSEN KE; FELLOUS M; PELLEGRINI S
      INTERFERON-ALPHA-DEPENDENT ACTIVATION OF TYK2 REQUIRES PHOSPHORYLATION OF POSITIVE REGULATORY TYROSINES BY ANOTHER KINASE

      The Journal of biological chemistry
    67. SEMINO O; PASSARINO G; BREGA A; FELLOUS M; SANTACHIARABENERECETTI AS
      A VIEW OF THE NEOLITHIC DEMIC DIFFUSION IN EUROPE THROUGH 2 Y-CHROMOSOME-SPECIFIC MARKERS

      American journal of human genetics
    68. ION A; TELVI L; CHAUSSAIN JL; GALACTEROS F; VALAYER J; FELLOUS M; MCELREAVEY K
      NOVEL MUTATION IN THE PUTATIVE DNA HELICASE XH2 IS RESPONSIBLE FOR MALE-TO-FEMALE SEX REVERSAL ASSOCIATED WITH AN ATYPICAL FORM OF THE ATR-X SYNDROME

      American journal of human genetics
    69. BARBAUX S; VILAIN E; RAOUL O; GILGENKRANTZ S; JEANDIDIER E; CHADENAS D; SOULEYREAU N; FELLOUS M; MCELREAVEY K
      PROXIMAL DELETIONS OF THE LONG ARM OF THE Y-CHROMOSOME SUGGEST A CRITICAL REGION ASSOCIATED WITH A SPECIFIC SUBSET OF CHARACTERISTIC TURNERSTIGMATA

      Human molecular genetics
    70. SPEZIA F; JULIEN P; THIENAUBERT H; FELLOUS M; VANNIER B; BODE G
      A WHOLE-EMBRYO CULTURE SYSTEM PROPOSED TO STUDY MOUSE SEXUAL DETERMINATION

      Toxicology in vitro
    71. FELLOUS M
      TAVLITZKI,JEAN

      MS. Medecine sciences
    72. BARBAUX S; VILAIN E; MCELREAVEY K; FELLOUS M
      A VIEW ON SEX DETERMINATION IN MAMMALS

      MS. Medecine sciences
    73. GOBIN SJP; ALCAIDELORIDAN C; BONO MR; OTTONE C; CHUMAKOV I; ROTHSTEIN R; FELLOUS M
      TRANSFER OF YEAST ARTIFICIAL CHROMOSOMES INTO MAMMALIAN-CELLS AND COMPARATIVE-STUDY OF THEIR INTEGRITY

      Gene
    74. TAR A; SOLYOM J; GYORVARI B; ION A; TELVI L; BARBAUX S; SOULEYREAU N; VILAIN E; FELLOUS M; MCELREAVEY K
      TESTICULAR DEVELOPMENT IN AN SRY-NEGATIVE 46,XX INDIVIDUAL HARBORING A DISTAL XP DELETION

      Human genetics
    75. VELAZQUEZ L; MOGENSEN KE; BARBIERI G; FELLOUS M; UZE G; PELLEGRINI S
      DISTINCT DOMAINS OF THE PROTEIN-TYROSINE KINASE TYK2 REQUIRED FOR BINDING OF INTERFERON-ALPHA BETA AND FOR SIGNAL-TRANSDUCTION/

      The Journal of biological chemistry
    76. MCELREAVEY K; BARBAUX S; ION A; FELLOUS M
      THE GENETIC-BASIS OF MURINE AND HUMAN SEX DETERMINATION - A REVIEW

      Heredity
    77. ION A; TELVI L; NUNES M; RETHORE MO; CHAUSSAIN JL; FELLOUS M; MCELREAVEY K
      A MALE TO FEMALE AUTOSOMAL SEX-REVERSING LOCUS AT DISTAL 9P

      American journal of human genetics
    78. MCELREAVEY K; BARBAUX S; VEITIA R; FELLOUS M
      MUTATIONS IN THE TESTIS-DETERMINING REGION OF THE Y-CHROMOSOME IN 46,XY INDIVIDUALS ARE ASSOCIATED WITH A SPECTRUM OF SEX-REVERSED PHENOTYPES

      American journal of human genetics
    79. FELLOUS M; KORCZYN A
      SPECIAL ISSUE ON HUMAN-GENETICS - EDITORIAL

      Biomedicine & pharmacotherapy
    80. MCELREAVEY K; BARBAUX S; VILAIN E; ION R; TELVI L; FELLOUS M
      DELETIONS OF YQ11 ASSOCIATED WITH INFERTILITY, SHORT STATURE AND THE TURNER-SYNDROME - TENTATIVE MAPPING OF A REGION ASSOCIATED WITH TURNERSTIGMATA TO PROXIMAL INTERVAL-5

      Cytogenetics and cell genetics
    81. BOUCEKKINE C; TOUBLANC JE; ABBAS N; CHAABOUNI S; OUAHID S; SEMROUNI M; JAUBERT F; TOUBLANC M; MCELREAVEY K; VILAIN E; FELLOUS M
      CLINICAL AND ANATOMICAL SPECTRUM IN XX SEX REVERSED PATIENTS - RELATIONSHIP TO THE PRESENCE OF Y-SPECIFIC DNA-SEQUENCES

      Clinical endocrinology
    82. PAILHOUX E; POPESCU PC; PARMA P; BOSCHER J; LEGAULT C; MOLTENI L; FELLOUS M; COTINOT C
      GENETIC-ANALYSIS OF 38XX MALES WITH GENITAL AMBIGUITIES AND TRUE HERMAPHRODITES IN PIGS

      Animal genetics
    83. MENDONCA BB; BARBOSA AS; ARNHOLD IJP; MCELREAVEY K; FELLOUS M; MOREIRAFILHO CA
      GONADAL AGENESIS IN XX-SISTER AND XY-SISTER - EVIDENCE FOR THE INVOLVEMENT OF AN AUTOSOMAL GENE

      American journal of medical genetics
    84. VILAIN E; LEFIBLEC B; MORICHONDELVALLEZ N; BRAUNER R; DOMMERGUES M; DUMEZ Y; JAUBERT F; BOUCEKKINE C; MCELREAVEY K; VEKEMANS M; FELLOUS M
      SRY-NEGATIVE XX FETUS WITH COMPLETE MALE PHENOTYPE

      Lancet
    85. PIERGA JY; GIACCHETTI S; VILAIN E; EXTRA JM; BRICE P; ESPIE M; MARAGI JA; FELLOUS M; MARTY M
      DYSGERMINOMA IN A PURE 45,X TURNER SYNDROME - REPORT OF A CASE AND REVIEW OF THE LITERATURE

      Gynecologic oncology
    86. PAILHOUX E; CRIBIU EP; CHAFFAUX S; DARRE R; FELLOUS M; COTINOT C
      MOLECULAR ANALYSIS OF 60,XX PSEUDOHERMAPHRODITE POLLED GOATS FOR THE PRESENCE OF SRY AND ZFY GENES

      Journal of Reproduction and Fertility
    87. HADJIATHANASIOU CG; BRAUNER R; LORTATJACOB S; NIVOT S; JAUBERT F; FELLOUS M; NIHOULFEKETE C; RAPPAPORT R
      TRUE HERMAPHRODITISM - GENETIC-VARIANTS AND CLINICAL MANAGEMENT

      The Journal of pediatrics
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      HORMONAL AND MOLECULAR-GENETIC FINDINGS IN 46,XX SUBJECTS WITH SEXUALAMBIGUITY AND TESTICULAR-DIFFERENTIATION

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    91. MCELREAVEY K; VILAIN E; ABBAS N; HERSKOWITZ I; FELLOUS M
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      Proceedings of the National Academy of Sciences of the United Statesof America
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 24/01/21 alle ore 04:30:35