Marc Fellous

Articles in Scholarly Journals [Incomplete List]

  1. Potential targets of FOXL2, a transcription factor involved in craniofacial and follicular development, identified by transcriptomics
    Proceedings of the National Academy of Sciences, vol. 104, no. 9, pp. 3330–3335, 2007
  2. Mutations in the NOG gene are not a common cause of nonsyndromic premature ovarian failure
    Clinical Endocrinology, vol. 66, no. 6, pp. 900–900, 2007
  3. Recovery of Female Fertility After Chemotherapy, Irradiation, and Bone Marrow Allograft: Further Evidence Against Massive Oocyte Regeneration by Bone Marrow-Derived Germline Stem Cells
    Stem Cells, vol. 25, no. 5, pp. 1334–1335, 2007
  4. Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure
    European Journal of Endocrinology, vol. 154, no. 5, pp. 739–744, 2006
  5. Partial defects in transcriptional activity of two novel DAX-1 mutations in childhood-onset adrenal hypoplasia congenita
    Clinical Endocrinology, vol. 65, no. 5, pp. 681–686, 2006
  6. Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation
    Human Molecular Genetics, vol. 14, no. 23, pp. 3557–3564, 2005
  7. Familial Occurrence of the IMAGe Association: Additional Clinical Variants and a Proposed Mode of Inheritance
    Journal of Clinical Endocrinology & Metabolism, vol. 90, no. 6, pp. 3186–3190, 2005
  8. Foxl2 gene and the development of the ovary: a story about goat, mouse, fish and woman
    Reproduction Nutrition Development, vol. 45, no. 6, p. 729, 2005
  9. Foxl2 gene and the development of the ovary: a story about goat, mouse, fish and woman
    Reproduction Nutrition Development, vol. 45, no. 3, pp. 377–382, 2005
  10. Distribution of Y chromosome lineages in Jerba island population
    Forensic Science International, vol. 148, no. 2-3, pp. 211–218, 2005
  11. The transcription factor Sox9 is degraded by the ubiquitin?proteasome system and stabilized by a mutation in a ubiquitin-target site
    Matrix Biology, vol. 23, no. 8, pp. 499–505, 2005
  12. Sense and antisense transcripts in mouse
    Genomics, vol. 85, no. 5, pp. 531–541, 2005
  13. Cloacal exstrophy in an infant with 9q34.1-qter deletion resulting from a de novo unbalanced translocation between chromosome 9q and Yq
    American Journal of Medical Genetics, vol. 126A, no. 3, pp. 303–307, 2004
  14. Interspecific Chromosome-Wide Transcription Profiles Reveal the Existence of Mammalian-Specific and Species-Specific Chromosome Domains
    Journal of Molecular Evolution, vol. 59, no. 3, pp. 317–328, 2004
  15. An evolutionary and functional analysis of FoxL2 in rainbow trout gonad differentiation
    Journal of Molecular Endocrinology, vol. 33, no. 3, pp. 705–715, 2004
  16. Structure, evolution and expression of the FOXL2 transcription unit
    Cytogenetic and Genome Research, vol. 101, no. 3-4, pp. 206–211, 2003
  17. FOXL2 and BPES: Mutational Hotspots, Phenotypic Variability, and Revision of the Genotype-Phenotype Correlation
    The American Journal of Human Genetics, vol. 72, no. 2, pp. 478–487, 2003
  18. Characterization of a putative type IV aminophospholipid transporter P-type ATPase
    Mammalian Genome, vol. 14, no. 1, pp. 21–30, 2003
  19. Genetic structure of Mediterranean populations revealed by Y-chromosome haplotype analysis
    American Journal of Physical Anthropology, vol. 121, no. 2, pp. 157–171, 2003
  20. GermOnline, a new cross-species community annotation database on germ-line development and gametogenesis
    Nature Genetics, vol. 35, no. 4, Article ID ng1203-291, 1 pages, 2003
  21. CATSPER2, a human autosomal nonsyndromic male infertility gene
    European Journal of Human Genetics, vol. 11, no. 7, Article ID 5200991, 5 pages, 2003
  22. Molecular Genetics of Sex Determination
    Seminars in Reproductive Medicine, vol. 20, no. 3, pp. 157–168, 2002
  23. Infertilité masculine et les microdélétions du chromosome YMale infertility and microdeletions of the Y chromosome.
    Gynécologie Obstétrique & Fertilité, vol. 30, no. 5, pp. 405–412, 2002
  24. Novel Paralogy Relations Among Human Chromosomes Support a Link between the Phylogeny of doublesex-Related Genes and the Evolution of Sex Determination
    Genomics, vol. 79, no. 3, pp. 333–343, 2002
  25. MHC class II-deficient tumor cell lines with a defective expression of the class II transactivator
    International Immunology, vol. 14, no. 5, pp. 481–491, 2002
  26. Evolution and expression of FOXL2
    Journal of Medical Genetics, vol. 39, no. 12, pp. 916–921, 2002
  27. Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses
    Journal of Medical Genetics, vol. 39, no. 7, pp. 514–518, 2002
  28. The Human Y Chromosome: The Biological Role of a “Functional Wasteland”
    Journal of Biomedicine and Biotechnology, vol. 1, no. 1, pp. 18–24, 2001
  29. The Human Genome Revolution or Evolution?
    Journal of Biomedicine and Biotechnology, vol. 1, no. 3, pp. 96–96, 2001
  30. Absence of Mutations Involving the Lim Homeobox Domain Gene LHX9 in 46,XY Gonadal Agenesis and Dysgenesis
    Journal of Clinical Endocrinology & Metabolism, vol. 86, no. 6, pp. 2465–2469, 2001
  31. Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation
    Human Molecular Genetics, vol. 10, no. 15, pp. 1591–1600, 2001
  32. Identification of the Human KIF13A Gene Homologous to Drosophila kinesin-73 and Candidate for Schizophrenia
    Genomics, vol. 74, no. 1, pp. 36–44, 2001
  33. Transduction of the Human Gene FAM8A1 by Endogenous Retrovirus During Primate Evolution
    Genomics, vol. 78, no. 1-2, pp. 38–45, 2001
  34. Expression of the human SRY protein during development in normal male gonadal and sex-reversed tissues
    Journal of Experimental Zoology, vol. 290, no. 6, pp. 607–615, 2001
  35. Contribution of domestic animals to the identification of new genes involved in sex determination
    Journal of Experimental Zoology, vol. 290, no. 7, pp. 700–708, 2001
  36. Testis determination in mammals: more questions than answers
    Molecular and Cellular Endocrinology, vol. 179, no. 1-2, pp. 3–16, 2001
  37. Origine et évolution des chromosomes sexuels des mammifèresThe origin and evolution of mammalian sex chromosomes.
    Comptes Rendus de l'Académie des Sciences - Series III - Sciences de la Vie, vol. 324, no. 1, pp. 1–11, 2001
  38. NSPc1, a novel mammalian Polycomb gene, is expressed in neural crest-derived structures of the peripheral nervous system
    Mechanisms of Development, vol. 102, no. 1-2, pp. 219–222, 2001
  39. Nature Genetics, vol. 29, no. 4, pp. 453–458, 2001
  40. WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis
    Kidney International, vol. 57, no. 5, pp. 1868–1872, 2000
  41. The Human Doublesex-Related Gene, DMRT2, Is Homologous to a Gene Involved in Somitogenesis and Encodes a Potential Bicistronic Transcript
    Genomics, vol. 64, no. 2, pp. 179–186, 2000
  42. 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, vol. 64, no. 2, pp. 170–178, 2000
  43. Sex chromosome mosaicism in males carrying Y chromosome long arm deletions
    Human Reproduction, vol. 15, no. 12, pp. 2559–2562, 2000
  44. Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism
    Molecular Human Reproduction, vol. 6, no. 4, pp. 298–302, 2000
  45. SRY protein is expressed in ovotestis and streak gonads from human sex-reversal
    Cytogenetic and Genome Research, vol. 91, no. 1-4, pp. 212–216, 2000
  46. A High Frequency of Y Chromosome Deletions in Males with Nonidiopathic Infertility
    Journal of Clinical Endocrinology & Metabolism, vol. 84, no. 10, pp. 3606–3612, 1999
  47. The same mutation affecting the splicing ofWT1 gene is present on Frasier syndrome patients with or without Wilms' tumor
    Human Mutation, vol. 13, no. 2, pp. 146–153, 1999
  48. 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, vol. 56, no. 1, pp. 31–39, 1999
  49. Differential expression of MHC class II isotype chains
    Microbes and Infection, vol. 1, no. 11, pp. 929–934, 1999
  50. Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene
    Human Genetics, vol. 102, no. 2, pp. 151–156, 1998
  51. CIITA B-cell-specific promoter suppression in MHC class II-silenced cell hybrids
    Immunogenetics, vol. 48, no. 4, pp. 283–291, 1998
  52. The INSL4 gene maps close to WI-5527 at 9p24.1→p23.3 clustered with two relaxin genes and outside the critical region for the monosomy 9p syndrome
    Cytogenetic and Genome Research, vol. 81, no. 3-4, pp. 275–277, 1998
  53. Swyer Syndrome and 46,XY Partial Gonadal Dysgenesis Associated with 9p Deletions in the Absence of Monosomy-9p Syndrome
    The American Journal of Human Genetics, vol. 63, no. 3, pp. 901–905, 1998
  54. Specific Contribution of Tyk2 JH Regions to the Binding and the Expression of the Interferon alpha /beta Receptor Component IFNAR1
    Journal of Biological Chemistry, vol. 273, no. 38, pp. 24723–24729, 1998
  55. Interferon alpha Inhibits a Src-mediated Pathway Necessary for Shigella-induced Cytoskeletal Rearrangements in Epithelial Cells
    The Journal of Cell Biology, vol. 143, no. 4, pp. 1003–1012, 1998
  56. Isolation of a B-cell-specific promoter for the human class II transactivator
    Immunogenetics, vol. 45, no. 4, pp. 266–273, 1997
  57. Hypertelorism and hypospadias associated with a de novo apparently balanced translocation between 8q22.3-23 and 20p13
    American Journal of Medical Genetics, vol. 68, no. 2, pp. 231–235, 1997
  58. Identification of Signalling Components in Tyrosine Kinase Cascades Using Phosphopeptide Affinity Chromatography*1
    Biochemical and Biophysical Research Communications, vol. 234, no. 3, pp. 748–753, 1997
  59. Deletions of Distal 9p Associated with 46,XY Male to Female Sex Reversal: Definition of the Breakpoints at 9p23.3–p24.1
    Genomics, vol. 41, no. 2, pp. 271–274, 1997
  60. Donor splice-site mutations in WT1 are responsible for Frasier syndrome
    Nature Genetics, vol. 17, no. 4, Article ID ng1297-467, 3 pages, 1997
  61. 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, vol. 94, no. 22, pp. 11839–11844, 1997
  62. Déterminisme et différenciation sexuels chez l'homme: de la pathologie aux gènes
    Archives de Pédiatrie, vol. 4, pp. 118s–120s, 1997
  63. Sex-Determining Genes
    Trends in Endocrinology and Metabolism, vol. 8, no. 9, pp. 342–346, 1997
  64. Conservation of Y chromosome-specific sequences immediately 5' to the testis determining gene in primates
    Gene, vol. 199, no. 1-2, pp. 63–70, 1997
  65. Genetic basis of human sex determination: An overview
    Theriogenology, vol. 47, no. 1, pp. 83–91, 1997
  66. Genetic mapping of the polled/intersex locus (PIS) in goats
    Theriogenology, vol. 47, no. 1, pp. 103–109, 1997
  67. Genetic mapping of the autosomal region involved in XX sex-reversal and horn development in goats
    Mammalian Genome, vol. 7, no. 2, pp. 133–137, 1996
  68. The RAG cell line defines a new complementation group of MHC class II deficiency
    Immunogenetics, vol. 43, no. 6, pp. 352–359, 1996
  69. Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination
    Proceedings of the National Academy of Sciences, vol. 93, no. 16, pp. 8590–8594, 1996
  70. Interferon-alpha -dependent Activation of Tyk2 Requires Phosphorylation of Positive Regulatory Tyrosines by Another Kinase
    Journal of Biological Chemistry, vol. 271, no. 34, pp. 20494–20500, 1996
  71. Distinct Domains of the Protein Tyrosine Kinase tyk2 Required for Binding of Interferon-alpha/beta and for Signal Transduction
    Journal of Biological Chemistry, vol. 270, no. 7, pp. 3327–3334, 1995
  72. SRY-negative XX fetus with complete male phenotype
    The Lancet, vol. 343, no. 8891, pp. 240–241, 1994
  73. Activation of the protein tyrosine kinase tyk2 by interferon alpha/beta
    European Journal of Biochemistry, vol. 223, no. 2, pp. 427–435, 1994
  74. Pathology of 46, XY pure gonadal dysgenesis: absence of testis differentiation associated with mutations in the testis-determining factor
    Differentiation, vol. 52, no. 2, pp. 151–159, 1993
  75. A Regulatory Cascade Hypothesis for Mammalian Sex Determination: SRY Represses a Negative Regulator of Male Development
    Proceedings of the National Academy of Sciences, vol. 90, no. 8, pp. 3368–3372, 1993
  76. A protein tyrosine kinase in the interferon $alpha;/$beta; signaling pathway
    Cell, vol. 70, no. 2, pp. 313–322, 1992
  77. The recombinant human interferon-? receptor is fully functional in a human × murine hybrid containing human chromosome 21Le récepteur de l'interféron-? humain recombinant est totalement fonctionnel dans les cellules hybrides homme × souris contenant le chromosome 21 humain
    Research in Immunology, vol. 142, no. 9, pp. 765–772, 1991
  78. The protein encoded by a murine male germ cell-specific transcript is a putative ATP-dependent RNA helicase
    Cell, vol. 57, no. 4, pp. 549–559, 1989
  79. Further cytologic evidence for Xp-Yp translocation in XX males using in situ hybridization with Y-derived probe
    Human Genetics, vol. 75, no. 3, pp. 228–233, 1987
  80. HLA-DR-specific monoclonal antibodies cross-react with several self and nonself non-MHC molecules
    Immunogenetics, vol. 24, no. 2, pp. 118–121, 1986
  81. Presence of an abnormal ? 2-microglobulin mRNA in Daudi cells: Induction by interferon
    Immunogenetics, vol. 17, no. 2, pp. 125–131, 1983
  82. A monoclonal antibody with anti-burkitt lymphoma specificity. I. Analysis of human haematopoietic and lymphoid cell lines
    International Journal of Cancer, vol. 29, no. 6, pp. 653–658, 1982
  83. A five-generation family with sacral agenesis and spina bifida: Possible similarities with the mouse T-locus
    American Journal of Medical Genetics, vol. 12, no. 4, pp. 465–487, 1982
  84. Interferon-Dependent Induction of mRNA for the Major Histocompatibility Antigens in Human Fibroblasts and Lymphoblastoid Cells
    Proceedings of the National Academy of Sciences, vol. 79, no. 10, pp. 3082–3086, 1982
  85. Preferential effect of ? interferon on the synthesis of HLA antigens and their mRNAs in human cells
    Nature, vol. 299, no. 5886, Article ID 299833a0, 3 pages, 1982
  86. Monoclonal Antibody against a Burkitt Lymphoma-Associated Antigen
    Proceedings of the National Academy of Sciences, vol. 78, no. 10, pp. 6485–6488, 1981
  87. Production d'anticorps monoclonaux anti-HBs
    Annales de l'Institut Pasteur. Immunologie, vol. 132, no. 3, pp. 319–326, 1981
  88. Interferon enhances the amount of membrane-bound ß2-microglobulin and its release from human Burkitt cells
    European Journal of Immunology, vol. 11, no. 6, pp. 524–526, 1981
  89. CHARACTERIZATION OF HUMAN TERATOMA CELL LINES FOR THEIR IN VITRO DEVELOPMENTAL PROPERTIES AND EXPRESSION OF EMBRYONIC AND MAJOR HISTOCOMPATIBILITY LOCUS-ASSOCIATED ANTIGENS
    European Journal of Immunogenetics, vol. 8, no. 2, pp. 151–162, 1981
  90. Reactivity of Human Lymphoid and Lymphoblastoid Cells with Peanut Agglutinin: Detection of a Blood Cell Subset which Lacks Detectable Membrane HLA
    Scandinavian Journal of Immunology, vol. 11, no. 5, pp. 555–560, 1980
  91. Enhanced expression of HLA antigens and ß2-microglobulin on interferon-treated human lymphoid cells
    European Journal of Immunology, vol. 9, no. 6, pp. 446–449, 1979
  92. Distinctive properties of fucosyl glycopeptides on human teratoma cells
    Somatic Cell Genetics, vol. 5, no. 6, pp. 753–761, 1979
  93. Association of the H-Y male antigen with beta2-microglobulin on human lymphoid and differentiated mouse teratocarcinoma cell lines
    Journal of Experimental Medicine, vol. 148, no. 1, pp. 58–70, 1978
  94. PRESENCE OF SLA AND Ia-LIKE ANTIGEN ON BOAR SPERMATOZOA
    European Journal of Immunogenetics, vol. 5, no. 2, pp. 135–142, 1978
  95. ABSORPTION ANALYSIS OF H-2D AND K ANTIGENS ON SPERMATOZOA
    European Journal of Immunogenetics, vol. 4, no. 1, pp. 47–51, 1977
  96. The Study of Human Ia-Like Specificities Using Antibody Eluates from Human Lymphoblastoid Cell Lines
    Scandinavian Journal of Immunology, vol. 6, no. 5, pp. 409–412, 1977
  97. The expression and relation of HLA, ß2 -microglobulin and receptor for marmoset red blood cells on man/mouse and man/Chinese hamster hybrid cells
    European Journal of Immunology, vol. 7, no. 1, pp. 22–26, 1977
  98. Isolation of a human teratoma cell line which expresses F9 antigen
    Nature, vol. 270, no. 5637, Article ID 270515a0, 3 pages, 1977
  99. The expression of human beta2 microglobulin on human spermatozoa
    European Journal of Immunology, vol. 6, no. 1, pp. 21–24, 1976
  100. Developmental expression of an early embryonic antigen common to mouse spermatozoa and cleavage embryos, and to human spermatozoa: Its expression during spermatogenesis*1
    Developmental Biology, vol. 50, no. 2, pp. 310–320, 1976
  101. Similar location of an early embryonic antigen on mouse and human spermatozoa
    Developmental Biology, vol. 41, no. 2, pp. 331–337, 1974
  102. Studies of human alloantigens on man-mouse hybrids: possible syntheny between hl-a and p systems
    European Journal of Immunology, vol. 3, no. 9, pp. 543–548, 1973
  103. Probable Haploid Expression of HL-A Antigens on Human Spermatozoon
    Nature, vol. 225, no. 5228, Article ID 225191a0, 2 pages, 1970