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


Tytuł:
Amplification and Expression of Viral Sequences and Oncogenes in Human Brain Tumors
Autorzy:
Benabid, A. L.
Chauvin, C.
Foote, A. M.
Suh, M.
Danik, M.
Laine, M.
Chaffanet, M.
Mercier, C.
Rost, N.
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Źródło:
Brain Oncology Biology, diagnosis and therapy : An international meeting on brain oncology, Rennes, France, September 4–5, 1986, held under the auspices of the Ministry of National Education, the University of Rennes and the Regional Hospital Rennes. 52:15-19
Książka elektroniczna
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
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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
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
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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:
Chromosome arm 8p and cancer: a fragile hypothesis.
Autorzy:
Birnbaum D (AUTHOR)
Adélaïde J (AUTHOR)
Popovici C (AUTHOR)
Charafe-Jauffret E (AUTHOR)
Mozziconacci M (AUTHOR)
Chaffanet M (AUTHOR)
Birnbaum, Daniel (AUTHOR)
Adélaïde, José (AUTHOR)
Popovici, Cornel (AUTHOR)
Charafe-Jauffret, Emmanuelle (AUTHOR)
Mozziconacci, Marie-Joelle (AUTHOR)
Chaffanet, Max (AUTHOR)
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Źródło:
Lancet Oncology. Oct2003, Vol. 4 Issue 10, p639-642. 4p.
Czasopismo naukowe
Tytuł:
Multicolour-banding fluorescence in situ hybridisation (mbanding-FISH) to identify recurrent chromosomal alterations in breast tumour cell lines.
Autorzy:
Letessier A; Laboratory of Molecular Cytogenetics, Department of Molecular Oncology, Paoli-Calmettes Institute-UMR599 INSERM, Marseille Cancer Research Institute, Marseille, France.
Mozziconacci MJ
Murati A
Juriens J
Adélaïde J
Birnbaum D
Chaffanet M
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Źródło:
British journal of cancer [Br J Cancer] 2005 Jan 31; Vol. 92 (2), pp. 382-8.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Aberrations*
In Situ Hybridization, Fluorescence*
Breast Neoplasms/*genetics
Cell Line, Tumor ; Humans ; Karyotyping
Czasopismo naukowe
Tytuł:
Frequency, prognostic impact, and subtype association of 8p12, 8q24, 11q13, 12p13, 17q12, and 20q13 amplifications in breast cancers.
Autorzy:
Letessier A; Centre de Recherche en Cancérologie de Marseille, Département d'Oncologie Moléculaire, UMR599 Inserm/Institut Paoli-Calmettes, Marseille, France. <>
Sircoulomb F
Ginestier C
Cervera N
Monville F
Gelsi-Boyer V
Esterni B
Geneix J
Finetti P
Zemmour C
Viens P
Charafe-Jauffret E
Jacquemier J
Birnbaum D
Chaffanet M
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Źródło:
BMC cancer [BMC Cancer] 2006 Oct 13; Vol. 6, pp. 245. Date of Electronic Publication: 2006 Oct 13.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 11*
Chromosomes, Human, Pair 12*
Chromosomes, Human, Pair 17*
Chromosomes, Human, Pair 20*
Chromosomes, Human, Pair 8*
Gene Amplification*
Breast Neoplasms/*genetics
Carcinoma/*genetics
Adult ; Aged ; Aged, 80 and over ; Biomarkers ; Female ; Gene Frequency ; Humans ; Middle Aged ; Models, Biological ; Neoplasm Metastasis/diagnosis ; Prognosis ; Statistics as Topic
Czasopismo naukowe
Tytuł:
Genome profiling of chronic myelomonocytic leukemia: frequent alterations of RAS and RUNX1 genes.
Autorzy:
Gelsi-Boyer V; Centre de Recherche en Cancérologie de Marseille, Laboratoire d'Oncologie Moléculaire, UMR891 Inserm, Institut Paoli-Calmettes, Marseille, France. />Trouplin V
Adélaïde J
Aceto N
Remy V
Pinson S
Houdayer C
Arnoulet C
Sainty D
Bentires-Alj M
Olschwang S
Vey N
Mozziconacci MJ
Birnbaum D
Chaffanet M
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Źródło:
BMC cancer [BMC Cancer] 2008 Oct 16; Vol. 8, pp. 299. Date of Electronic Publication: 2008 Oct 16.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Profiling*
Core Binding Factor Alpha 2 Subunit/*genetics
Genes, ras/*genetics
Leukemia, Myelomonocytic, Chronic/*genetics
Chromosomes, Human, Pair 21 ; Comparative Genomic Hybridization ; Humans ; Leukemia, Myelomonocytic, Chronic/pathology ; Mutation ; Oncogene Proteins, Fusion/genetics ; Sequence Analysis, DNA ; Signal Transduction/genetics ; Ubiquitin Thiolesterase/genetics
Czasopismo naukowe
Tytuł:
Genome profiling of acute myelomonocytic leukemia: alteration of the MYB locus in MYST3-linked cases.
Autorzy:
Murati A; Département d'Oncologie Moléculaire, Centre de Recherche en Cancérologie de Marseille, Institut Paoli-Calmettes, Marseille, France.
Gervais C
Carbuccia N
Finetti P
Cervera N
Adélaïde J
Struski S
Lippert E
Mugneret F
Tigaud I
Penther D
Bastard C
Poppe B
Speleman F
Baranger L
Luquet I
Cornillet-Lefebvre P
Nadal N
Nguyen-Khac F
Pérot C
Olschwang S
Bertucci F
Chaffanet M
Lessard M
Mozziconacci MJ
Birnbaum D
Pokaż więcej
Corporate Authors:
Groupe Francophone de Cytogénétique Hématologique
Źródło:
Leukemia [Leukemia] 2009 Jan; Vol. 23 (1), pp. 85-94. Date of Electronic Publication: 2008 Sep 25.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Profiling/*methods
Genes, myb/*genetics
Histone Acetyltransferases/*genetics
Leukemia, Myelomonocytic, Acute/*genetics
CD4 Antigens/genetics ; Comparative Genomic Hybridization ; Gene Expression Regulation, Neoplastic ; Genome, Human ; Homeodomain Proteins/genetics ; Humans ; Oligonucleotide Array Sequence Analysis ; Proto-Oncogene Proteins c-myb/genetics
Czasopismo naukowe

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