Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Przeglądasz jako GOŚĆ

Wyszukujesz frazę ""Chaffanet, M"" wg kryterium: Autor


Wyświetlanie 1-17 z 17
Tytuł :
Genomic analysis of myeloproliferative neoplasms in chronic and acute phases.
Autorzy :
Courtier F; Centre de Recherche en Cancérologie de Marseille, (CRCM), Inserm, U1068, CNRS UMR7258, France.; Institut Paoli-Calmettes (IPC), Département d'Oncologie Moléculaire, UM 105, Marseille, F-13284, France.; Aix-Marseille Université, UM 105, Marseille, F-13284, France.
Carbuccia N; Centre de Recherche en Cancérologie de Marseille, (CRCM), Inserm, U1068, CNRS UMR7258, France.; Institut Paoli-Calmettes (IPC), Département d'Oncologie Moléculaire, UM 105, Marseille, F-13284, France.
Garnier S; Centre de Recherche en Cancérologie de Marseille, (CRCM), Inserm, U1068, CNRS UMR7258, France.; Institut Paoli-Calmettes (IPC), Département d'Oncologie Moléculaire, UM 105, Marseille, F-13284, France.
Guille A; Centre de Recherche en Cancérologie de Marseille, (CRCM), Inserm, U1068, CNRS UMR7258, France.; Institut Paoli-Calmettes (IPC), Département d'Oncologie Moléculaire, UM 105, Marseille, F-13284, France.
Adélaïde J; Centre de Recherche en Cancérologie de Marseille, (CRCM), Inserm, U1068, CNRS UMR7258, France.; Institut Paoli-Calmettes (IPC), Département d'Oncologie Moléculaire, UM 105, Marseille, F-13284, France.
Cervera N; Centre de Recherche en Cancérologie de Marseille, (CRCM), Inserm, U1068, CNRS UMR7258, France.; Institut Paoli-Calmettes (IPC), Département d'Oncologie Moléculaire, UM 105, Marseille, F-13284, France.
Gelsi-Boyer V; Centre de Recherche en Cancérologie de Marseille, (CRCM), Inserm, U1068, CNRS UMR7258, France.; Institut Paoli-Calmettes (IPC), Département d'Oncologie Moléculaire, UM 105, Marseille, F-13284, France.; IPC, Département de Biopathologie, Marseille, UM 105, Marseille, F-13284, France.; Aix-Marseille Université, UM 105, Marseille, F-13284, France.
Mozziconacci MJ; Centre de Recherche en Cancérologie de Marseille, (CRCM), Inserm, U1068, CNRS UMR7258, France.; Institut Paoli-Calmettes (IPC), Département d'Oncologie Moléculaire, UM 105, Marseille, F-13284, France.; IPC, Département de Biopathologie, Marseille, UM 105, Marseille, F-13284, France.
Rey J; Centre de Recherche en Cancérologie de Marseille, (CRCM), Inserm, U1068, CNRS UMR7258, France.; IPC, Département d'Hématologie, UM 105, Marseille, F-13284, France.; Aix-Marseille Université, UM 105, Marseille, F-13284, France.
Vey N; Centre de Recherche en Cancérologie de Marseille, (CRCM), Inserm, U1068, CNRS UMR7258, France.; IPC, Département d'Hématologie, UM 105, Marseille, F-13284, France.; Aix-Marseille Université, UM 105, Marseille, F-13284, France.
Chaffanet M; Centre de Recherche en Cancérologie de Marseille, (CRCM), Inserm, U1068, CNRS UMR7258, France.; Institut Paoli-Calmettes (IPC), Département d'Oncologie Moléculaire, UM 105, Marseille, F-13284, France.; Aix-Marseille Université, UM 105, Marseille, F-13284, France.
Birnbaum D; Centre de Recherche en Cancérologie de Marseille, (CRCM), Inserm, U1068, CNRS UMR7258, France.; Institut Paoli-Calmettes (IPC), Département d'Oncologie Moléculaire, UM 105, Marseille, F-13284, France.; Aix-Marseille Université, UM 105, Marseille, F-13284, France.
Murati A; Centre de Recherche en Cancérologie de Marseille, (CRCM), Inserm, U1068, CNRS UMR7258, France .; Institut Paoli-Calmettes (IPC), Département d'Oncologie Moléculaire, UM 105, Marseille, F-13284, France.; IPC, Département de Biopathologie, Marseille, UM 105, Marseille, F-13284, France.; Aix-Marseille Université, UM 105, Marseille, F-13284, France.
Pokaż więcej
Źródło :
Haematologica [Haematologica] 2017 Jan; Vol. 102 (1), pp. e11-e14. Date of Electronic Publication: 2016 Oct 14.
Typ publikacji :
Letter; Research Support, Non-U.S. Gov't
MeSH Terms :
Genomics*
Mutation*
Cell Transformation, Neoplastic/*genetics
Hematologic Neoplasms/*genetics
Myeloproliferative Disorders/*genetics
Neoplasm Proteins/*genetics
Acute Disease ; Cell Transformation, Neoplastic/metabolism ; Cell Transformation, Neoplastic/pathology ; Chronic Disease ; Female ; Hematologic Neoplasms/metabolism ; Hematologic Neoplasms/pathology ; Humans ; Male ; Myeloproliferative Disorders/metabolism ; Myeloproliferative Disorders/pathology ; Neoplasm Proteins/metabolism
Raport
Tytuł :
Epigenetically centered evolution in an example of myeloid malignancy.
Autorzy :
Adélaide J; Centre de Recherche en Cancérologie de Marseille, Laboratoire D'Oncologie Moléculaire, UMR1068 Inserm, Institut Paoli-Calmettes, CNRS UMR725, Marseille, France.
Cervera N; Centre de Recherche en Cancérologie de Marseille, Laboratoire D'Oncologie Moléculaire, UMR1068 Inserm, Institut Paoli-Calmettes, CNRS UMR725, Marseille, France.
Carbuccia N; Centre de Recherche en Cancérologie de Marseille, Laboratoire D'Oncologie Moléculaire, UMR1068 Inserm, Institut Paoli-Calmettes, CNRS UMR725, Marseille, France.
Garnier S; Centre de Recherche en Cancérologie de Marseille, Laboratoire D'Oncologie Moléculaire, UMR1068 Inserm, Institut Paoli-Calmettes, CNRS UMR725, Marseille, France.
Guille A; Centre de Recherche en Cancérologie de Marseille, Laboratoire D'Oncologie Moléculaire, UMR1068 Inserm, Institut Paoli-Calmettes, CNRS UMR725, Marseille, France.
Mozziconnaci MJ; Département de BioPathologie, Institut Paoli-Calmettes, Marseille, France.
Devillier R; Aix-Marseille Université, Marseille, France.; Département d'Hématologie, Institut Paoli-Calmettes, Marseille, France.
Chaffanet M; Centre de Recherche en Cancérologie de Marseille, Laboratoire D'Oncologie Moléculaire, UMR1068 Inserm, Institut Paoli-Calmettes, CNRS UMR725, Marseille, France.
Vey N; Aix-Marseille Université, Marseille, France.; Département d'Hématologie, Institut Paoli-Calmettes, Marseille, France.
Birnbaum D; Centre de Recherche en Cancérologie de Marseille, Laboratoire D'Oncologie Moléculaire, UMR1068 Inserm, Institut Paoli-Calmettes, CNRS UMR725, Marseille, France.
Gelsi-Boyer V; Centre de Recherche en Cancérologie de Marseille, Laboratoire D'Oncologie Moléculaire, UMR1068 Inserm, Institut Paoli-Calmettes, CNRS UMR725, Marseille, France.; Département de BioPathologie, Institut Paoli-Calmettes, Marseille, France.; Aix-Marseille Université, Marseille, France.
Pokaż więcej
Źródło :
American journal of hematology [Am J Hematol] 2016 Sep; Vol. 91 (9), pp. E361-2. Date of Electronic Publication: 2016 Jul 04.
Typ publikacji :
Case Reports; Letter; Research Support, Non-U.S. Gov't
MeSH Terms :
Epigenesis, Genetic*
Cell Transformation, Neoplastic/*genetics
Cell Transformation, Neoplastic/*pathology
Myeloproliferative Disorders/*diagnosis
Myeloproliferative Disorders/*genetics
Adult ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Bone Marrow/pathology ; Comparative Genomic Hybridization ; Disease Progression ; Humans ; Immunophenotyping ; Leukemia, Myeloid, Acute/diagnosis ; Leukemia, Myeloid, Acute/drug therapy ; Leukemia, Myeloid, Acute/genetics ; Male ; Mutation ; Myeloproliferative Disorders/drug therapy ; Translocation, Genetic ; Treatment Outcome
Raport
Tytuł :
Alterations of polycomb gene BMI1 in human myeloproliferative neoplasms.
Autorzy :
Brecqueville M
Adélaïde J
Bertucci F
Finetti P
Chaffanet M
Birnbaum D
Murati A
Pokaż więcej
Źródło :
Cell cycle (Georgetown, Tex.) [Cell Cycle] 2012 Aug 15; Vol. 11 (16), pp. 3141-2. Date of Electronic Publication: 2012 Jul 24.
Typ publikacji :
Letter; Research Support, Non-U.S. Gov't
MeSH Terms :
Myeloproliferative Disorders/*genetics
Neoplasms/*genetics
Polycomb Repressive Complex 1/*genetics
Chromosome Deletion ; Chromosomes, Human, Pair 10/genetics ; Chromosomes, Human, Pair 10/metabolism ; Comparative Genomic Hybridization ; Genetic Loci ; Humans ; Male ; Middle Aged ; Myeloproliferative Disorders/pathology ; Neoplasms/pathology ; Polycomb Repressive Complex 1/metabolism
Raport
Tytuł :
Gain of CBL-interacting protein, a possible alternative to CBL mutations in myeloid malignancies.
Autorzy :
Adélaïde J
Gelsi-Boyer V
Rocquain J
Carbuccia N
Birnbaum DJ
Finetti P
Bertucci F
Mozziconacci MJ
Vey N
Birnbaum D
Chaffanet M
Pokaż więcej
Źródło :
Leukemia [Leukemia] 2010 Aug; Vol. 24 (8), pp. 1539-41. Date of Electronic Publication: 2010 Jun 17.
Typ publikacji :
Letter; Research Support, Non-U.S. Gov't
MeSH Terms :
Mutation*
Myeloproliferative Disorders/*genetics
Proto-Oncogene Proteins c-cbl/*metabolism
Aged ; Humans ; Male ; Proto-Oncogene Proteins c-cbl/genetics
Raport
Tytuł :
Mutations of ASXL1 gene in myeloproliferative neoplasms.
Autorzy :
Carbuccia N
Murati A
Trouplin V
Brecqueville M
Adélaïde J
Rey J
Vainchenker W
Bernard OA
Chaffanet M
Vey N
Birnbaum D
Mozziconacci MJ
Pokaż więcej
Źródło :
Leukemia [Leukemia] 2009 Nov; Vol. 23 (11), pp. 2183-6. Date of Electronic Publication: 2009 Jul 16.
Typ publikacji :
Letter; Research Support, Non-U.S. Gov't
MeSH Terms :
Frameshift Mutation*
Myeloproliferative Disorders/*genetics
Repressor Proteins/*genetics
Base Sequence ; Humans ; Molecular Sequence Data
Raport
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 :
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 :
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 :
Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13).
Autorzy :
Popovici C; Laboratoire d'Oncologie Moléculaire, Unité 119, Institut National de la Santé et de la Recherche Médicale, Institut de Cancérologie et Immunologie, 232 Boulevard Sainte-Marguerite, 13009 Marseille, France.
Adélaïde J
Ollendorff V
Chaffanet M
Guasch G
Jacrot M
Leroux D
Birnbaum D
Pébusque MJ
Pokaż więcej
Źródło :
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 1998 May 12; Vol. 95 (10), pp. 5712-7.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 8*
Receptor Protein-Tyrosine Kinases*
Fibroblast Growth Factors/*metabolism
Myeloproliferative Disorders/*genetics
Plant Proteins/*genetics
Receptors, Fibroblast Growth Factor/*genetics
3T3 Cells ; Amino Acid Sequence ; Animals ; Base Sequence ; Catalysis ; Humans ; In Situ Hybridization, Fluorescence ; Introns ; Mice ; Molecular Sequence Data ; Receptor, Fibroblast Growth Factor, Type 1 ; Recombinant Fusion Proteins/genetics ; Sequence Alignment ; Translocation, Genetic ; Tumor Cells, Cultured ; Zinc Fingers
Czasopismo naukowe
Tytuł :
t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12.
Autorzy :
Chaffanet M; Laboratoire d'Oncologie Moléculaire, U.119 INSERM, Institut de Cancérologie et d'Immunologie de Marseille, France.
Popovici C
Leroux D
Jacrot M
Adélaïde J
Dastugue N
Grégoire MJ
Hagemeijer A
Lafage-Pochitaloff M
Birnbaum D
Pébusque MJ
Pokaż więcej
Źródło :
Oncogene [Oncogene] 1998 Feb 19; Vol. 16 (7), pp. 945-9.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 8*
Receptor Protein-Tyrosine Kinases*
Myeloproliferative Disorders/*genetics
Receptors, Fibroblast Growth Factor/*genetics
Adult ; Aged ; Chromosome Mapping ; Chromosomes, Human, Pair 13 ; Chromosomes, Human, Pair 6 ; Chromosomes, Human, Pair 9 ; Female ; Genes ; Humans ; In Situ Hybridization, Fluorescence ; Male ; Middle Aged ; Myeloproliferative Disorders/pathology ; Receptor, Fibroblast Growth Factor, Type 1 ; Restriction Mapping ; Translocation, Genetic
Czasopismo naukowe
    Wyświetlanie 1-17 z 17

    Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies