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


Tytuł :
EGF receptor amplification and expression in human brain tumours.
Autorzy :
Chaffanet M; Inserm U. 318 Neurobiophysique, Université J. Fourier, Grenoble, France.
Chauvin C
Lainé M
Berger F
Chédin M
Rost N
Nissou MF
Benabid AL
Pokaż więcej
Źródło :
European journal of cancer (Oxford, England : 1990) [Eur J Cancer] 1992; Vol. 28 (1), pp. 11-7.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Amplification*
Gene Expression*
Brain Neoplasms/*genetics
ErbB Receptors/*genetics
Adolescent ; Adult ; Aged ; Blotting, Northern ; Female ; Gene Rearrangement ; Glioma/genetics ; Humans ; Male ; Meningioma/genetics ; Middle Aged ; Protein Binding
Czasopismo naukowe
Tytuł :
A study of the expression of four chemoresistance-related genes in human primary and metastatic brain tumours.
Autorzy :
Mousseau M; Unité d'Oncologie Médicale, C.H.U.R.G., Grenoble, France.
Chauvin C
Nissou MF
Chaffanet M
Plantaz D
Pasquier B
Schaerer R
Benabid A
Pokaż więcej
Źródło :
European journal of cancer (Oxford, England : 1990) [Eur J Cancer] 1993; Vol. 29A (5), pp. 753-9.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Brain Neoplasms/*genetics
Drug Resistance/*genetics
Blotting, Northern ; DNA Topoisomerases, Type II/genetics ; Gene Expression Regulation, Neoplastic ; Glutathione Transferase/genetics ; Humans ; RNA, Messenger/analysis ; RNA, Neoplasm/analysis ; Tetrahydrofolate Dehydrogenase/genetics
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
Tytuł :
Assignment of the gene for the human proliferating cell nucleolar protein P120 (NOL1) to chromosome 12p13 by fluorescence in situ hybridization and polymerase chain reaction with somatic cell hybrids.
Autorzy :
Baens M; Human Genome Laboratory, University of Leuven, Belgium.
Chaffanet M
Aerssens J
Cassiman JJ
Marynen P
Pokaż więcej
Źródło :
Genomics [Genomics] 1994 May 01; Vol. 21 (1), pp. 296-7.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 12*
Nuclear Proteins/*genetics
Base Sequence ; Cell Cycle ; Chromosome Mapping ; Genes ; Humans ; Hybrid Cells ; In Situ Hybridization, Fluorescence ; Molecular Sequence Data ; Polymerase Chain Reaction ; tRNA Methyltransferases
Czasopismo naukowe
Tytuł :
Mapping of an ordered set of 14 cosmids to human chromosome 12p by two-color in situ hybridization.
Autorzy :
Chaffanet M; Center for Human Genetics, University of Leuven, Belgium.
Baens M
Aerssens J
Schoenmakers E
Cassiman JJ
Marynen P
Pokaż więcej
Źródło :
Cytogenetics and cell genetics [Cytogenet Cell Genet] 1995; Vol. 69 (1-2), pp. 27-32.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Aberrations*
Chromosomes, Human, Pair 12*
Cosmids*
Hominidae/*genetics
Animals ; Cell Nucleus/ultrastructure ; Cells, Cultured ; Chromosome Mapping ; Humans ; In Situ Hybridization, Fluorescence/methods ; Interphase ; Lymphocytes/cytology ; Male
Czasopismo naukowe
Tytuł :
A 3.1-Mb YAC contig within the Werner syndrome region, on the short arm of human chromosome 8.
Autorzy :
Chaffanet M; Laboratoire d'Oncologie Moléculaire, U.119 INSERM, Marseille, France.
Imbert A
Adélaïde J
Le Paslier D
Wagner MJ
Wells DE
Birnbaum D
Pébusque MJ
Pokaż więcej
Źródło :
Cytogenetics and cell genetics [Cytogenet Cell Genet] 1996; Vol. 72 (1), pp. 63-8.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Artificial, Yeast*
Chromosomes, Human, Pair 8*
Werner Syndrome/*genetics
Chromosome Mapping ; Genetic Markers ; Humans ; In Situ Hybridization, Fluorescence ; Restriction Mapping
Czasopismo naukowe
Tytuł :
Integrated map of the chromosome 8p12-p21 region, a region involved in human cancers and Werner syndrome.
Autorzy :
Imbert A; Laboratoire d'Oncologie Moléculaire, U. 119 INSERM, Marseille, France.
Chaffanet M
Essioux L
Noguchi T
Adélaïde J
Kerangueven F
Le Paslier D
Bonaïti-Pellié C
Sobol H
Birnbaum D
Pébusque MJ
Pokaż więcej
Źródło :
Genomics [Genomics] 1996 Feb 15; Vol. 32 (1), pp. 29-38.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Mapping*
Chromosomes, Human, Pair 8/*genetics
Neoplasms/*genetics
Werner Syndrome/*genetics
Base Sequence ; Breast Neoplasms/genetics ; Chromosomes, Artificial, Yeast/genetics ; DNA Primers/genetics ; Female ; Gene Deletion ; Genetic Linkage ; Genome, Human ; Humans ; Male ; Molecular Sequence Data ; Oncogenes
Czasopismo naukowe
Tytuł :
Regional assignment of 64 human gene transcripts on chromosome 8.
Autorzy :
Ugolini F; Laboratoire d'Oncologie Moléculaire, U.119 INSERM, Marseille, France.
Chaffanet M
Houlgatte R
Patterson D
Wells D
Auffray C
Birnbaum D
Pébusque MJ
Pokaż więcej
Źródło :
Cytogenetics and cell genetics [Cytogenet Cell Genet] 1997; Vol. 77 (3-4), pp. 197-200.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Mapping*
Chromosomes, Human, Pair 8/*genetics
Animals ; Chromosomes, Human, Pair 8/ultrastructure ; Cricetinae ; Gene Expression ; Genetic Markers ; Humans ; Hybrid Cells ; Mice ; Polymerase Chain Reaction ; Rats ; Transcription, Genetic
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
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 :
Chromosome region 8p11-p21: refined mapping and molecular alterations in breast cancer.
Autorzy :
Adélaïde J; Laboratoire de Biologie des Tumeurs, Institut Paoli-Calmettes, Marseille, France.
Chaffanet M
Imbert A
Allione F
Geneix J
Popovici C
van Alewijk D
Trapman J
Zeillinger R
Børresen-Dale AL
Lidereau R
Birnbaum D
Pébusque MJ
Pokaż więcej
Źródło :
Genes, chromosomes & cancer [Genes Chromosomes Cancer] 1998 Jul; Vol. 22 (3), pp. 186-99.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Breast Neoplasms/*genetics
Chromosome Mapping/*methods
Chromosomes, Human, Pair 8/*genetics
Chromosome Aberrations/genetics ; Chromosome Disorders ; DNA, Complementary/isolation & purification ; Gene Amplification ; Humans ; Loss of Heterozygosity ; Restriction Mapping ; Sequence Tagged Sites ; Transcription, Genetic
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 :
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 :
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 :
[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 :
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 :
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 :
Chromosome arm 8p and cancer: a fragile hypothesis.
Autorzy :
Birnbaum D; Department of Molecular Oncology, Institut Paoli-Calmettes and U119 Inserm, IFR57, Marseille, France. />Adélaïde J
Popovici C
Charafe-Jauffret E
Mozziconacci MJ
Chaffanet M
Pokaż więcej
Źródło :
The Lancet. Oncology [Lancet Oncol] 2003 Oct; Vol. 4 (10), pp. 639-42.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Acid Anhydride Hydrolases*
Chromosome Fragility*
Chromosomes, Human, Pair 8*
Neoplasms/*genetics
Breast Neoplasms ; Chromosome Breakage ; Chromosome Fragile Sites ; Humans ; Neoplasm Proteins/genetics ; Neuregulin-1/genetics ; Pancreatic Neoplasms/genetics
Czasopismo naukowe
Tytuł :
Loss of FHIT protein expression is a marker of adverse evolution in good prognosis localized breast cancer.
Autorzy :
Ginestier C; Département d'Oncologie Moléculaire, Institut Paoli-Calmettes and U119 INSERM, IFR57, Marseille, France.
Bardou VJ
Popovici C
Charafe-Jauffret E
Bertucci F
Geneix J
Adélaïde J
Chaffanet M
Hassoun J
Viens P
Jacquemier J
Birnbaum D
Pokaż więcej
Źródło :
International journal of cancer [Int J Cancer] 2003 Dec 10; Vol. 107 (5), pp. 854-62.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Acid Anhydride Hydrolases*
Gene Deletion*
Genes, Tumor Suppressor*
Breast Neoplasms/*genetics
Breast Neoplasms/*pathology
Neoplasm Proteins/*genetics
Adult ; Biomarkers, Tumor/analysis ; Breast Neoplasms/mortality ; Breast Neoplasms/therapy ; Female ; Humans ; Lymphatic Metastasis ; Middle Aged ; Neoplasm Invasiveness ; Oligonucleotide Array Sequence Analysis ; Prognosis ; Reproducibility of Results ; Survival Analysis ; Time Factors
Czasopismo naukowe

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