N. Ayraud

发表

Characterization of centromere alterations in liposarcomas

O. Myklebost, J. Vermeesch, J. Coindre, 2000, Genes, chromosomes & cancer.

Translocation, t(17;22)(q22;q13), in dermatofibrosarcoma protuberans: a new tumor-associated chromosome rearrangement.

G. Sozzi, C. Turc‐Carel, M. Terrier-Lacombe, 1996, Cytogenetics and cell genetics.

Distribution of neutral maltase activity in mononuclear cells from different human lymphoid organs.

N. Ayraud, J. Giudicelli, P. Sudaka, 1983, Clinica chimica acta; international journal of clinical chemistry.

Another case of t(17;22)(q22;q13) in an infantile dermatofibrosarcoma protuberans.

C. Turc‐Carel, F. Pedeutour, N. Ayraud, 1996, Cancer genetics and cytogenetics.

Antibody Transfer Mechanisms From Mother to Fetus Across Rat Yolk Sac Endoderm *

N. Ayraud, F. Laliberté, R. Masseyeff, 1981 .

HLA in families with Down's syndrome children.

J. Lambert, S. Benzaken, N. Ayraud, 2008, Tissue antigens.

Neutral maltase: the first human B-cell enzymatic marker reflecting terminal differentiation of mature B cells into plasma cells.

J. Cassuto, N. Ayraud, J. Giudicelli, 1983, Blood.

Arthrogryposis-like signs in trisomy 18

J. Lambert, N. Ayraud, M. Donzeau, 2004, Human Genetics.

Cytogenetic study of 88 cases of refractory anemia.

J. Lambert, N. Ayraud, S. Raynaud, 1983, Cancer genetics and cytogenetics.

T PROLYMPHOCYTOID LEUKAEMIC TRANSFORMATION OF A T CHRONIC LYMPHOID LEUKAEMIA CHARACTERIZED BY SURFACE MARKERS AS HELPER T CELLS FOR B CELL IMMUNOGLOBULIN SYNTHESIS

N. Ayraud, J. Bayle, N. Gratecos, 1988, British journal of haematology.

Variant translocation t(8;21;15) in an acute myeloblastic leukemia with phenotypic differential evolution.

S. Raynaud, N. Ayraud, J. Bayle, 1985, Cancer genetics and cytogenetics.

Supernumerary ring chromosomes containing chromosome 17 sequences. A specific feature of dermatofibrosarcoma protuberans?

F. Hecht, A. Leroux, J. Coindre, 1994, Cancer genetics and cytogenetics.

Dynamics of human sperm acrosome reaction: relation with in vitro fertilization.

N. Ayraud, P. Fénichel, B. Hsi, 1991, Fertility and sterility.

Ultrastructural localization of alpha-fetoprotein in the immature rat uterus with use of the immunoperoxidase technique.

N. Ayraud, F. Laliberté, R. Masseyeff, 1981, Journal of steroid biochemistry.

Immunolocalization of alpha-fetoprotein in the ovary and hypophysis of immature female rats

N. Ayraud, M. Lafaurie, D. Castelli, 1982, The Histochemical Journal.

[Trisomy 11 q (q23.1 - qter) through maternal translocation t(11;22) (q23.1;q11.1). A new case].

N. Ayraud, A. Galiana, M. Llyod, 1976, Annales de genetique.

Neutral maltase: a marker of cell differentiation in human myeloid leukaemias?

J. Cassuto, N. Ayraud, J. Giudicelli, 1982, British journal of haematology.

[Comparative cytogenetic study of 7 types of mammary cancer].

J. Lambert, N. Ayraud, B. Basteris, 1977, Annales de Genetique.

Triploidy with cyclopia and identical HLA alleles in the parents.

G. Charpentier, J. Lambert, N. Ayraud, 1984, Journal of medical genetics.

Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromes.

P. Marynen, J. Grosgeorge, S. Raynaud, 1996, Blood.

[4p monosomy with paternal t(13;14) (p11;p11) translocation].

J. Lambert, N. Ayraud, J. Mattéi, 1979, Pediatrie.

myelodysplastic syndromes in recurring chromosomal abnormality involving the TEL gene (ETV6) Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a

P. Marynen, J. Grosgeorge, N. Ayraud, 2011 .

Rearrangement of proximal 11q13 band in a CMML in acute transformation.

C. Larsson, J. Grosgeorge, N. Ayraud, 1995, Leukemia.

18q- Syndrome resulting from a tdic(14p;18q)

J. Lambert, N. Ayraud, M. Ferrari, 1979, Human Genetics.

Recurrent cytogenetic abnormalities observed in complete remission of acute myeloid leukemia do not necessarily mark preleukemic cells.

G. Flandrin, A. Pesce, N. Ayraud, 1994, Leukemia.

[Interstitial deletion of the long arm of chromosome 7 in a female child with leprechaunism].

J. Lambert, N. Ayraud, J. Rovinski, 1976, Annales de genetique.

tetrasomy 22 pter leads to q 11 . Cat eye syndrome owing to

G. Charpentier, J. Lambert, N. Ayraud, 2022 .

[Identification by means of heat denaturation of chromosome aberrations in 6 human metastatic tumors].

N. Ayraud, 1975, Biomedicine / [publiee pour l'A.A.I.C.I.G.].

[18p- syndrome. A further case].

N. Ayraud, G. Darcourt, C. Capdeville, 1969, Annales de Genetique.

Transfer, tissue localization and proliferation of fetal cells in pregnant mice.

N. Ayraud, R. Masseyeff, P. Philip, 1982, Immunology letters.

[Cytogenetic effects of anticonvulsants. Apropos of an observation of abnormalities transmitted during intra-uterine life].

N. Ayraud, J. Martínón, J. Kermarec, 1968, Annales de genetique.

[45,X-46,XX-47,XXX karyotype and tumor of the nervous system. 2 cases].

J. Duplay, N. Ayraud, P. Grellier, 1972, La Nouvelle presse medicale.

Ring chromosomes in dermatofibrosarcoma protuberans contain chromosome 17 sequences: fluorescence in situ hybridization.

J. Coindre, F. Pedeutour, N. Ayraud, 1993, Cancer genetics and cytogenetics.

Inversion (14)(q11q32) in a case of acute myeloid leukemia expressing lymphoid-associated antigens.

F. Monpoux, N. Ayraud, J. Bayle, 1993, Cancer genetics and cytogenetics.