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Wyświetlanie 1-20 z 20
Tytuł :
Common features of myeloproliferative disorders with t(8;9)(p12;q33) and CEP110-FGFR1 fusion: report of a new case and review of the literature.
Autorzy :
Mozziconacci MJ; Laboratoire d'Oncologie Moléculaire, Centre de Recherche en Cancérologie de Marseille, UMR599 Inserm, Institut Paoli-Calmettes, Marseille, France. />Carbuccia N
Prebet T
Charbonnier A
Murati A
Vey N
Chaffanet M
Birnbaum D
Pokaż więcej
Źródło :
Leukemia research [Leuk Res] 2008 Aug; Vol. 32 (8), pp. 1304-8. Date of Electronic Publication: 2007 Dec 21.
Typ publikacji :
Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms :
Chromosomes, Human, Pair 8*
Chromosomes, Human, Pair 9*
Translocation, Genetic*
Leukemia, Myelomonocytic, Acute/*genetics
Myeloproliferative Disorders/*genetics
Oncogene Proteins, Fusion/*metabolism
Receptor, Fibroblast Growth Factor, Type 1/*metabolism
Aged ; Humans ; Male
Czasopismo naukowe
Tytuł :
Rearrangements involving 12q in myeloproliferative disorders: possible role of HMGA2 and SOCS2 genes.
Autorzy :
Etienne A; UMR599 INSERM, Institut Paoli-Calmettes, Laboratoire d'Oncologie Moléculaire, Centre de Recherche en Cancérologie de Marseille, 232 Bd. de Sainte-Marguerite, 13009 Marseille, France.
Carbuccia N
Adélaïde J
Bekhouche I
Rémy V
Sohn C
Sainty D
Gastaut JA
Olschwang S
Birnbaum D
Mozziconacci MJ
Chaffanet M
Pokaż więcej
Źródło :
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2007 Jul 01; Vol. 176 (1), pp. 80-8.
Typ publikacji :
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 12*
Translocation, Genetic*
HMGA2 Protein/*genetics
Myeloproliferative Disorders/*genetics
Suppressor of Cytokine Signaling Proteins/*genetics
Aged ; Chromosomes, Human, Pair 3 ; Chromosomes, Human, Pair 9 ; Humans ; In Situ Hybridization, Fluorescence ; Male ; Middle Aged ; Oligonucleotide Array Sequence Analysis ; Reverse Transcriptase Polymerase Chain Reaction
Czasopismo naukowe
Tytuł :
Combined translocation with ZNF198-FGFR1 gene fusion and deletion of potential tumor suppressors in a myeloproliferative disorder.
Autorzy :
Etienne A; Centre de Recherche en Cancérologie de Marseille, Départements d'Oncologie Moléculaire et d'Hématologie Moléculaire, UMR599 INSERM, Institut Paoli-Calmettes, 27 Bd. Leï Roure, 13009, Marseille, France.
Gelsi-Boyer V
Carbuccia N
Adélaïde J
Barba G
La Starza R
Murati A
Eclache V
Birg F
Birnbaum D
Mozziconacci MJ
Mecucci C
Chaffanet M
Pokaż więcej
Źródło :
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2007 Mar; Vol. 173 (2), pp. 154-8.
Typ publikacji :
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Deletion*
Genes, Tumor Suppressor*
Translocation, Genetic*
Carrier Proteins/*genetics
DNA-Binding Proteins/*genetics
Myeloproliferative Disorders/*genetics
Receptor, Fibroblast Growth Factor, Type 1/*genetics
Adolescent ; Adult ; Chromosome Painting ; Chromosomes, Human, Pair 13 ; Chromosomes, Human, Pair 8 ; Female ; Gene Fusion ; Humans ; Karyotyping ; Male ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; Transcription Factors ; Transcription, Genetic
Czasopismo naukowe
Tytuł :
A t(8;9) translocation with PCM1-JAK2 fusion in a patient with T-cell lymphoma.
Autorzy :
Adélaïde J
Pérot C
Gelsi-Boyer V
Pautas C
Murati A
Copie-Bergman C
Imbert M
Chaffanet M
Birnbaum D
Mozziconacci MJ
Pokaż więcej
Źródło :
Leukemia [Leukemia] 2006 Mar; Vol. 20 (3), pp. 536-7.
Typ publikacji :
Case Reports; Letter; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 8*
Chromosomes, Human, Pair 9*
Gene Fusion*
Translocation, Genetic*
Cell Cycle Proteins/*genetics
Lymphoma, T-Cell/*genetics
Protein-Tyrosine Kinases/*genetics
Proto-Oncogene Proteins/*genetics
Adult ; Autoantigens ; Humans ; Janus Kinase 2 ; Lymphoma, T-Cell/enzymology ; Male
Raport
Tytuł :
Dual lympho-myeloproliferative disorder in a patient with t(8;22) with BCR-FGFR1 gene fusion.
Autorzy :
Murati A; Department of Molecular Oncology, Marseille Cancer Institute, UMR599 Inserm and Paoli-Calmettes Institute, Marseille, France.
Arnoulet C
Lafage-Pochitaloff M
Adélaide J
Derré M
Slama B
Delaval B
Popovici C
Vey N
Xerri L
Mozziconacci MJ
Boulat O
Sainty D
Birnbaum D
Chaffanet M
Pokaż więcej
Źródło :
International journal of oncology [Int J Oncol] 2005 Jun; Vol. 26 (6), pp. 1485-92.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 8*
Translocation, Genetic*
Lymphoproliferative Disorders/*genetics
Myeloproliferative Disorders/*genetics
Protein-Tyrosine Kinases/*genetics
Proto-Oncogene Proteins/*genetics
Receptor Protein-Tyrosine Kinases/*genetics
Receptors, Fibroblast Growth Factor/*genetics
Aged ; Chromosomes, Human, Pair 22 ; Humans ; Immunophenotyping ; Male ; Proto-Oncogene Proteins c-bcr ; Receptor, Fibroblast Growth Factor, Type 1
Czasopismo naukowe
Tytuł :
Variant MYST4-CBP gene fusion in a t(10;16) acute myeloid leukaemia.
Autorzy :
Murati A; Département d'Oncologie Moléculaire, Institut Paoli-Calmettes and JMR 599 Inserm, Marseille, France.
Adélaïde J
Mozziconacci MJ
Popovici C
Carbuccia N
Letessier A
Birg F
Birnbaum D
Chaffanet M
Pokaż więcej
Źródło :
British journal of haematology [Br J Haematol] 2004 Jun; Vol. 125 (5), pp. 601-4.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 10/*genetics
Chromosomes, Human, Pair 16/*genetics
Leukemia, Myeloid/*genetics
Translocation, Genetic/*genetics
Acute Disease ; Artificial Gene Fusion ; Chimera/genetics ; Female ; Gene Rearrangement/genetics ; Humans
Czasopismo naukowe
Tytuł :
A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 gene.
Autorzy :
Adélaïde J; Département d'Oncologie Moléculaire, Laboratoires de Cytogénétique Moléculaire et de Pathologie Moléculaire, U119 Institut National de la Santé et de la Recherche Médicale (INSERM) and Institut Paoli-Calmettes (IPC), Marseille, France.
Huang HE
Murati A
Alsop AE
Orsetti B
Mozziconacci MJ
Popovici C
Ginestier C
Letessier A
Basset C
Courtay-Cahen C
Jacquemier J
Theillet C
Birnbaum D
Edwards PA
Chaffanet M
Pokaż więcej
Źródło :
Genes, chromosomes & cancer [Genes Chromosomes Cancer] 2003 Aug; Vol. 37 (4), pp. 333-45.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Breast Neoplasms/*genetics
Chromosome Breakage/*genetics
Neuregulin-1/*genetics
Pancreatic Neoplasms/*genetics
Translocation, Genetic/*genetics
Breast Neoplasms/chemistry ; Breast Neoplasms/pathology ; Chromosome Mapping ; Codon, Initiator/genetics ; Exons/genetics ; Humans ; Neuregulin-1/biosynthesis ; Pancreatic Neoplasms/chemistry ; Pancreatic Neoplasms/pathology ; Protein Isoforms/biosynthesis ; Protein Isoforms/genetics ; RNA, Messenger/biosynthesis ; RNA, Messenger/genetics ; RNA, Neoplasm/biosynthesis ; RNA, Neoplasm/genetics ; Tumor Cells, Cultured
Czasopismo naukowe
Tytuł :
Endogenous retroviral sequence is fused to FGFR1 kinase in the 8p12 stem-cell myeloproliferative disorder with t(8;19)(p12;q13.3).
Autorzy :
Guasch G; INSERM U119, the Institut de Cancérologie et d'Immunologie de Marseille, France.
Popovici C
Mugneret F
Chaffanet M
Pontarotti P
Birnbaum D
Pébusque MJ
Pokaż więcej
Źródło :
Blood [Blood] 2003 Jan 01; Vol. 101 (1), pp. 286-8. Date of Electronic Publication: 2002 Jun 28.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 19*
Chromosomes, Human, Pair 8*
Translocation, Genetic*
Endogenous Retroviruses/*genetics
Myeloproliferative Disorders/*genetics
Oncogene Proteins, Fusion/*genetics
Receptor Protein-Tyrosine Kinases/*genetics
Receptors, Fibroblast Growth Factor/*genetics
3' Flanking Region ; 5' Flanking Region ; Cloning, Molecular ; Cytogenetic Analysis ; Humans ; Receptor, Fibroblast Growth Factor, Type 1 ; Terminal Repeat Sequences
Czasopismo naukowe
Tytuł :
[FGFR1 and MOZ, two key genes involved in malignant hemopathies linked to rearrangements within the chromosomal region 8p11-12].
Autorzy :
Pébusque MJ; Laboratoire d'oncologie moléculaire, Inserm U. 119, IFR57, 27, boulevard Leï-Roure, 13009 Marseille, France.
Chaffanet M
Popovici C
Birnbaum D
Pokaż więcej
Transliterated Title :
FGFR1 et MOZ, deux gènes clés dans les hémopathies malignes associées à des réarrangements de la région chromosomique 8p11-12.
Źródło :
Bulletin du cancer [Bull Cancer] 2000 Dec; Vol. 87 (12), pp. 887-94.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms :
Acetyltransferases/*genetics
Chromosomes, Human, Pair 8/*genetics
Leukemia, Myeloid/*genetics
Myeloproliferative Disorders/*genetics
Oncogene Proteins, Fusion/*genetics
Receptor Protein-Tyrosine Kinases/*genetics
Receptors, Fibroblast Growth Factor/*genetics
Translocation, Genetic/*genetics
Acetyltransferases/physiology ; Acute Disease ; Gene Rearrangement/genetics ; Hematopoiesis/physiology ; Histone Acetyltransferases ; Humans ; Leucine/genetics ; Neoplasm Proteins/genetics ; Proto-Oncogene Proteins ; Receptor Protein-Tyrosine Kinases/physiology ; Receptor, Fibroblast Growth Factor, Type 1 ; Receptors, Fibroblast Growth Factor/physiology ; Zinc Fingers/genetics
Czasopismo naukowe
Tytuł :
The 8p12 myeloproliferative disorder. t(8;19)(p12;q13.3): a novel translocation involving the FGFR1 gene.
Autorzy :
Mugneret F; Laboratoires de Cytogénétique et d'Hématologie, Hématologie clinique, Hôpital du Bocage, Dijon, France.
Chaffanet M
Maynadié M
Guasch G
Favre B
Casasnovas O
Birnbaum D
Pébusque MJ
Pokaż więcej
Źródło :
British journal of haematology [Br J Haematol] 2000 Nov; Vol. 111 (2), pp. 647-9.
Typ publikacji :
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 19*
Chromosomes, Human, Pair 8*
Translocation, Genetic*
Myeloproliferative Disorders/*genetics
Receptor Protein-Tyrosine Kinases/*genetics
Receptors, Fibroblast Growth Factor/*genetics
Aged ; Humans ; In Situ Hybridization, Fluorescence ; Male ; Receptor, Fibroblast Growth Factor, Type 1
Czasopismo naukowe
Tytuł :
Translocation and coamplification of loci from chromosome arms 8p and 11q in the MDA-MB-175 mammary carcinoma cell line.
Autorzy :
Adélaïde J; Laboratoire de Biologie des Tumeurs, Institut Paoli-Calmettes (IPC), Marseille, France.
Chaffanet M
Mozziconacci MJ
Popovici C
Conte N
Fernandez F
Sobol H
Jacquemier J
Pébusque M
Ron D
Lafage-Pochitaloff M
Birnbaum D
Pokaż więcej
Źródło :
International journal of oncology [Int J Oncol] 2000 Apr; Vol. 16 (4), pp. 683-8.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 11*
Chromosomes, Human, Pair 8*
Translocation, Genetic*
Breast Neoplasms/*genetics
Chromosome Mapping ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Membrane Proteins ; Neuregulin-1/genetics ; Nuclear Proteins/genetics ; Polymerase Chain Reaction ; Tumor Cells, Cultured
Czasopismo naukowe
Tytuł :
gamma-heregulin is the product of a chromosomal translocation fusing the DOC4 and HGL/NRG1 genes in the MDA-MB-175 breast cancer cell line.
Autorzy :
Wang XZ; Department of Medicine, Skirball Institute of Biomolecular Medicine, Kaplan Cancer Center, NYU Medical Center, New York, NY 10016, USA.
Jolicoeur EM
Conte N
Chaffanet M
Zhang Y
Mozziconacci MJ
Feiner H
Birnbaum D
Pébusque MJ
Ron D
Pokaż więcej
Źródło :
Oncogene [Oncogene] 1999 Oct 07; Vol. 18 (41), pp. 5718-21.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
MeSH Terms :
Translocation, Genetic*
Breast Neoplasms/*genetics
Carcinoma/*genetics
Carrier Proteins/*genetics
Chromosomes, Human, Pair 11/*genetics
Chromosomes, Human, Pair 8/*genetics
Neuregulin-1/*genetics
Nuclear Proteins/*genetics
Oncogene Proteins, Fusion/*genetics
Breast Neoplasms/pathology ; Carcinoma/pathology ; Chromosomes, Human, Pair 11/ultrastructure ; Chromosomes, Human, Pair 8/ultrastructure ; Female ; Gene Expression Regulation, Neoplastic ; Humans ; In Situ Hybridization, Fluorescence ; Membrane Proteins ; Receptor, ErbB-2/physiology ; Signal Transduction ; Tumor Cells, Cultured
Czasopismo naukowe
Tytuł :
A case of inv(8)(p11q24) associated with acute myeloid leukemia involves the MOZ and CBP genes in a masked t(8;16).
Autorzy :
Chaffanet M; Laboratoire d'Oncologie Moléculaire, U.119 INSERM, Marseille, France.
Mozziconacci MJ
Fernandez F
Sainty D
Lafage-Pochitaloff M
Birnbaum D
Pébusque MJ
Pokaż więcej
Źródło :
Genes, chromosomes & cancer [Genes Chromosomes Cancer] 1999 Oct; Vol. 26 (2), pp. 161-5.
Typ publikacji :
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Inversion*
Acetyltransferases/*genetics
Chromosomes, Human, Pair 16/*genetics
Chromosomes, Human, Pair 8/*genetics
Leukemia, Myeloid, Acute/*genetics
Nuclear Proteins/*genetics
Trans-Activators/*genetics
Translocation, Genetic/*genetics
CREB-Binding Protein ; Cyclic AMP Response Element-Binding Protein/genetics ; Female ; Histone Acetyltransferases ; Humans ; Middle Aged
Czasopismo naukowe
Tytuł :
Identification of a YAC spanning the translocation breakpoint t(8;22) associated with acute monocytic leukemia.
Autorzy :
Soenen V; Laboratoire d'Hématologie, Höpital Calmettes, Lille, France.
Chaffanet M
Preudhomme C
Dib A
Lai JL
Fletcher JA
Birnbaurn D
Pébusque MJ
Pokaż więcej
Źródło :
Genes, chromosomes & cancer [Genes Chromosomes Cancer] 1996 Mar; Vol. 15 (3), pp. 191-4.
Typ publikacji :
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 22*
Chromosomes, Human, Pair 8*
Translocation, Genetic*
Leukemia, Monocytic, Acute/*genetics
Leukemia, Myelomonocytic, Acute/*genetics
Bone Marrow/pathology ; Chromosome Banding ; Chromosome Mapping ; Chromosomes, Artificial, Yeast ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Leukemia, Monocytic, Acute/pathology ; Leukemia, Myelomonocytic, Acute/pathology
Czasopismo naukowe
Tytuł :
Regional assignment of seven loci to 12p13.2-pter by PCR analysis of somatic cell hybrids containing the der(12) or the der(X) chromosome from a mesothelioma showing t(X;12)(q22;p13).
Autorzy :
Aerssens J; Arthritis and Metabolic Bone Disease Research Unit, Center for Human Genetics-K.U., Leuven, Belgium.
Chaffanet M
Baens M
Matthijs G
Van den Berghe H
Cassiman JJ
Marynen P
Pokaż więcej
Źródło :
Genomics [Genomics] 1994 Mar 01; Vol. 20 (1), pp. 119-21.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 12*
Translocation, Genetic*
X Chromosome*
Mesothelioma/*genetics
Animals ; Chromosome Mapping ; Genetic Markers ; Humans ; Hybrid Cells/ultrastructure ; In Situ Hybridization, Fluorescence ; Mice ; Polymerase Chain Reaction ; Sequence Tagged Sites
Czasopismo naukowe
    Wyświetlanie 1-20 z 20

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