Informacja

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

Przeglądasz jako GOŚĆ

Wyszukujesz frazę ""Delattre, O."" wg kryterium: Autor


Tytuł :
An aggressive Ewing sarcoma associated with a new variant translocation, t(4;11;22)(q25;q24;q12), hyperdiploid karyotype, and tetrasomy 8.
Autorzy :
Abdelmoula NB
Landman-Parker J
Tourniaire B
Josset P
Boccon-Gibod L
Peter M
Delattre O
Perot C
Taillemite JL
Portnoi MF
Van den Akker J
Pokaż więcej
Źródło :
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Dec; Vol. 163 (2), pp. 186-8.
Typ publikacji :
Case Reports; Letter
MeSH Terms :
Chromosome Aberrations*
Chromosomes, Human, Pair 11*
Chromosomes, Human, Pair 22*
Chromosomes, Human, Pair 4*
Chromosomes, Human, Pair 8*
Diploidy*
Translocation, Genetic*
Sarcoma, Ewing/*genetics
Adolescent ; Combined Modality Therapy ; Fatal Outcome ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Sarcoma, Ewing/drug therapy ; Sarcoma, Ewing/surgery
Raport
Tytuł :
hSNF5/INI1 inactivation is mainly associated with homozygous deletions and mitotic recombinations in rhabdoid tumors.
Autorzy :
Rousseau-Merck MF; Pathologie Moléculaire des cancers INSERM U509, Institut Curie, Paris, France.
Versteege I
Legrand I
Couturier J
Mairal A
Delattre O
Aurias A
Pokaż więcej
Źródło :
Cancer research [Cancer Res] 1999 Jul 01; Vol. 59 (13), pp. 3152-6.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Aberrations*
Chromosomes, Human, Pair 22*
Gene Deletion*
Mutation*
Recombination, Genetic*
DNA-Binding Proteins/*genetics
Rhabdoid Tumor/*genetics
Chromosomal Proteins, Non-Histone ; Chromosome Mapping ; Consensus Sequence ; Genes, Tumor Suppressor ; Genetic Markers ; Homozygote ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Microsatellite Repeats ; Mitosis ; Polymorphism, Genetic ; SMARCB1 Protein ; Transcription Factors ; Translocation, Genetic ; Tumor Cells, Cultured
Czasopismo naukowe
Tytuł :
VPREB3: cDNA characterization and expression in human and chromosome mapping in human and mouse.
Autorzy :
Rosnet O; Centre d'Immunologie INSERM-CNRS de Marseille-Luminy, Marseille, France. />Mattéi MG
Delattre O
Schiff C
Pokaż więcej
Źródło :
Cytogenetics and cell genetics [Cytogenet Cell Genet] 1999; Vol. 87 (3-4), pp. 205-8.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Expression*
Physical Chromosome Mapping*
Chromosomes, Human, Pair 22/*genetics
Membrane Glycoproteins/*genetics
Amino Acid Sequence ; Animals ; B-Lymphocytes/cytology ; B-Lymphocytes/metabolism ; Base Sequence ; Cell Differentiation ; Cell Line ; Cloning, Molecular ; DNA, Complementary/genetics ; Gene Expression Profiling ; Hematopoietic Stem Cells/cytology ; Hematopoietic Stem Cells/metabolism ; Humans ; In Situ Hybridization, Fluorescence ; Membrane Glycoproteins/chemistry ; Mice ; Molecular Sequence Data ; Pre-B Cell Receptors ; RNA, Messenger/analysis ; RNA, Messenger/genetics ; Receptors, Antigen, B-Cell
Czasopismo naukowe
Tytuł :
Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer.
Autorzy :
Versteege I; Laboratoire de Pathologie Moléculaire des Cancers, Section de Recherche, Institut Curie, Paris, France.
Sévenet N
Lange J
Rousseau-Merck MF
Ambros P
Handgretinger R
Aurias A
Delattre O
Pokaż więcej
Źródło :
Nature [Nature] 1998 Jul 09; Vol. 394 (6689), pp. 203-6.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Mapping*
Chromosomes, Human, Pair 22*
DNA-Binding Proteins/*genetics
Rhabdoid Tumor/*genetics
Transcription Factors/*genetics
Child ; Chromosomal Proteins, Non-Histone ; Chromosome Deletion ; Frameshift Mutation ; Humans ; Infant ; Infant, Newborn ; Mutation ; SMARCB1 Protein ; Tumor Cells, Cultured
Czasopismo naukowe
Tytuł :
Cytogenetic and molecular analysis of a t(1;22)(p36;q11.2) in a rhabdoid tumor with a putative homozygous deletion of chromosome 22.
Autorzy :
Rosty C; Laboratoire de Génétique de Tumeurs, Institut Curie, Paris, France.
Peter M
Zucman J
Validire P
Delattre O
Aurias A
Pokaż więcej
Źródło :
Genes, chromosomes & cancer [Genes Chromosomes Cancer] 1998 Feb; Vol. 21 (2), pp. 82-9.
Typ publikacji :
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 1/*genetics
Chromosomes, Human, Pair 22/*genetics
Rhabdoid Tumor/*genetics
Thoracic Neoplasms/*genetics
Translocation, Genetic/*genetics
Humans ; In Situ Hybridization, Fluorescence ; Infant ; Karyotyping ; Loss of Heterozygosity ; Male ; Rhabdoid Tumor/pathology ; Thoracic Neoplasms/pathology ; Tumor Cells, Cultured
Czasopismo naukowe
Tytuł :
Assignment of the beta B1 crystallin gene (CRYBB1) to human chromosome 22 and mouse chromosome 5.
Autorzy :
Hulsebos TJ; Institute of Human Genetics, Academic Medical Center, University of Amsterdam, The Netherlands.
Gilbert DJ
Delattre O
Smink LJ
Dunham I
Westerveld A
Thomas G
Jenkins NA
Copeland NG
Pokaż więcej
Źródło :
Genomics [Genomics] 1995 Oct 10; Vol. 29 (3), pp. 712-8.
Typ publikacji :
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
MeSH Terms :
Chromosome Mapping*
Chromosomes, Human, Pair 22*
Crystallins/*genetics
Mice/*genetics
Animals ; Base Sequence ; Cattle ; Cosmids ; Crystallins/biosynthesis ; Exons ; Gene Library ; Genetic Complementation Test ; Humans ; Hybrid Cells ; Molecular Sequence Data ; Rats ; Sequence Homology, Nucleic Acid ; Species Specificity
Czasopismo naukowe
Tytuł :
Physical mapping of 30 CA repeats on human chromosome 22.
Autorzy :
Demczuk S; Laboratoire de Génétique des Tumeurs, INSERM, U434, Institut Curie, Paris, France.
Delattre O
Vignal A
Weissenbach J
Thomas G
Aurias A
Pokaż więcej
Źródło :
Genomics [Genomics] 1995 May 20; Vol. 27 (2), pp. 345-7.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Mapping*
Chromosomes, Human, Pair 22*
Repetitive Sequences, Nucleic Acid*
Base Sequence ; DNA, Satellite/chemistry ; Genetic Markers ; Humans ; Molecular Sequence Data ; Polymerase Chain Reaction
Czasopismo naukowe
Tytuł :
Analysis of the NF2 tumor-suppressor gene and of chromosome 22 deletions in gliomas.
Autorzy :
Hoang-Xuan K; Laboratoire de Génétique des Tumeurs, INSERM CJF 9201, Institut Curie, Paris, France.
Merel P
Vega F
Hugot JP
Cornu P
Delattre JY
Poisson M
Thomas G
Delattre O
Pokaż więcej
Źródło :
International journal of cancer [Int J Cancer] 1995 Feb 08; Vol. 60 (4), pp. 478-81.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Deletion*
Genes, Neurofibromatosis 2*
Chromosomes, Human, Pair 22/*genetics
Glioma/*genetics
Base Sequence ; Blotting, Northern ; DNA Mutational Analysis ; DNA Primers ; DNA, Neoplasm/genetics ; DNA, Satellite/genetics ; Electrophoresis, Polyacrylamide Gel/methods ; Gene Deletion ; Heterozygote ; Humans ; Molecular Sequence Data ; Polymerase Chain Reaction/methods
Czasopismo naukowe
Tytuł :
Refined mapping of eight cosmid markers on human chromosome 22.
Autorzy :
Kurahashi H; Department of Medical Genetics, Osaka University Medical School, Japan.
Akagi K
Yana I
Melot T
Delattre O
Thomas G
Okada S
Takai S
Nishisho I
Pokaż więcej
Źródło :
The Japanese journal of human genetics [Jpn J Hum Genet] 1994 Jun; Vol. 39 (2), pp. 243-8.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 22*
Cosmids*
Chromosome Mapping/methods ; Genetic Markers ; Humans ; Polymorphism, Restriction Fragment Length
Czasopismo naukowe
Tytuł :
DNA-binding and transcriptional activation properties of the EWS-FLI-1 fusion protein resulting from the t(11;22) translocation in Ewing sarcoma.
Autorzy :
Bailly RA; Laboratoire d'Oncologie Virale et Cellulaire, Centre National de la Recherche Scientifique, URA 1443, Institut Curie, Orsay, France.
Bosselut R
Zucman J
Cormier F
Delattre O
Roussel M
Thomas G
Ghysdael J
Pokaż więcej
Źródło :
Molecular and cellular biology [Mol Cell Biol] 1994 May; Vol. 14 (5), pp. 3230-41.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
MeSH Terms :
Chromosomes, Human, Pair 11*
Chromosomes, Human, Pair 22*
Genes*
Translocation, Genetic*
Bone Neoplasms/*genetics
DNA-Binding Proteins/*metabolism
Recombinant Fusion Proteins/*metabolism
Sarcoma, Ewing/*genetics
Trans-Activators/*metabolism
Transcription Factors/*metabolism
Amino Acid Sequence ; Base Sequence ; Chromosome Mapping ; DNA Primers ; DNA-Binding Proteins/biosynthesis ; DNA-Binding Proteins/genetics ; Humans ; Molecular Sequence Data ; Plasmids ; Polymerase Chain Reaction ; Proto-Oncogene Protein c-fli-1 ; Proto-Oncogene Proteins/isolation & purification ; Proto-Oncogene Proteins/metabolism ; Proto-Oncogene Proteins c-ets ; Recombinant Fusion Proteins/biosynthesis ; Restriction Mapping ; Trans-Activators/biosynthesis ; Trans-Activators/genetics ; Transcription, Genetic
Czasopismo naukowe
Tytuł :
Interphase molecular cytogenetics of Ewing's sarcoma and peripheral neuroepithelioma t(11;22) with flanking and overlapping cosmid probes.
Autorzy :
Desmaze C; Laboratoire de Génétique des Tumeurs, INSERM CJF 9201, Institut Curie, Paris, France.
Zucman J
Delattre O
Melot T
Thomas G
Aurias A
Pokaż więcej
Źródło :
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1994 May; Vol. 74 (1), pp. 13-8.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 11*
Chromosomes, Human, Pair 22*
Translocation, Genetic*
Neuroectodermal Tumors, Primitive, Peripheral/*genetics
Sarcoma, Ewing/*genetics
Cell Line ; Cosmids ; Humans ; In Situ Hybridization, Fluorescence ; Tumor Cells, Cultured
Czasopismo naukowe
Tytuł :
Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas.
Autorzy :
Ruttledge MH; Centre for research in Neuroscience, McGill University, Montreal, Quebec, Canada.
Sarrazin J
Rangaratnam S
Phelan CM
Twist E
Merel P
Delattre O
Thomas G
Nordenskjöld M
Collins VP
et. al.
Pokaż więcej
Źródło :
Nature genetics [Nat Genet] 1994 Feb; Vol. 6 (2), pp. 180-4.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 22*
Genes, Neurofibromatosis 2/*genetics
Meningeal Neoplasms/*genetics
Meningioma/*genetics
Adult ; Aged ; Base Sequence ; DNA Mutational Analysis ; DNA, Neoplasm/analysis ; Female ; Heterozygote ; Humans ; Middle Aged ; Molecular Sequence Data ; Nucleic Acid Conformation ; Point Mutation/genetics ; Suppression, Genetic/genetics
Czasopismo naukowe
Tytuł :
The neurofibromatosis type 2 gene is inactivated in schwannomas.
Autorzy :
Twist EC; Centre for Research in Neuroscience, McGill University, Montreal, Canada.
Ruttledge MH
Rousseau M
Sanson M
Papi L
Merel P
Delattre O
Thomas G
Rouleau GA
Pokaż więcej
Źródło :
Human molecular genetics [Hum Mol Genet] 1994 Jan; Vol. 3 (1), pp. 147-51.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 22*
Genes, Neurofibromatosis 2*
Point Mutation*
Membrane Proteins/*genetics
Neoplasm Proteins/*genetics
Neurilemmoma/*genetics
Base Sequence ; Chromosome Deletion ; DNA Primers ; DNA, Neoplasm/genetics ; Exons ; Humans ; Incidence ; Meningeal Neoplasms/genetics ; Meningioma/genetics ; Molecular Sequence Data ; Neurilemmoma/blood ; Neurilemmoma/pathology ; Neurilemmoma/surgery ; Neurofibromatosis 2/blood ; Neurofibromatosis 2/epidemiology ; Neurofibromatosis 2/genetics ; Neurofibromin 2 ; Polymerase Chain Reaction
Czasopismo naukowe
Tytuł :
Physical mapping of the NF2/meningioma region on human chromosome 22q12.
Autorzy :
Ruttledge MH; Ludwig Institute for Cancer Research, Karolinska Hospital, Stockholm, Sweden.
Xie YG
Han FY
Giovannini M
Janson M
Fransson I
Werelius B
Delattre O
Thomas G
Evans G
et. al.
Pokaż więcej
Źródło :
Genomics [Genomics] 1994 Jan 01; Vol. 19 (1), pp. 52-9.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 22*
Genes*
Genes, Neurofibromatosis 2*
Meningeal Neoplasms/*genetics
Meningioma/*genetics
Cell Line, Transformed ; Chromosome Mapping ; Electrophoresis, Gel, Pulsed-Field ; Fibroblasts ; Genetic Markers ; Humans ; Hybrid Cells ; In Situ Hybridization, Fluorescence
Czasopismo naukowe
Tytuł :
Genetic alterations in the chromosome 22q12 region associated with development of neuroectodermal tumors.
Autorzy :
Thomas G; Laboratoire de Génétique des Tumeurs, Institut Curie, Paris, France.
Delattre O
Zucman J
Merel P
Desmaze C
Melot T
Sanson M
Hoang-Xuan K
Plougastel B
Dejong P
et. al.
Pokaż więcej
Źródło :
Cold Spring Harbor symposia on quantitative biology [Cold Spring Harb Symp Quant Biol] 1994; Vol. 59, pp. 555-64.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 22/*genetics
Neuroectodermal Tumors/*genetics
Chromosome Mapping ; Cosmids ; Genes, Neurofibromatosis 2 ; Humans ; Oncogenes ; Point Mutation ; Sarcoma, Ewing/genetics ; Translocation, Genetic
Czasopismo naukowe
Tytuł :
Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases.
Autorzy :
Desmaze C; Laboratoire de Génétique des Tumeurs INSERM CJF9201 and CNRS URA 620, Institut Curie, France.
Prieur M
Amblard F
Aikem M
LeDeist F
Demczuk S
Zucman J
Plougastel B
Delattre O
Croquette MF
et. al.
Pokaż więcej
Źródło :
American journal of human genetics [Am J Hum Genet] 1993 Dec; Vol. 53 (6), pp. 1239-49.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Mapping*
Chromosomes, Human, Pair 22*
DiGeorge Syndrome/*genetics
Adult ; Cell Line ; Child ; Chromosome Deletion ; Cosmids ; DiGeorge Syndrome/pathology ; Female ; Humans ; Hybrid Cells ; In Situ Hybridization, Fluorescence ; Infant ; Infant, Newborn ; Male ; Molecular Probes ; Pedigree ; Phenotype ; Pregnancy ; Translocation, Genetic
Czasopismo naukowe
Tytuł :
Genomic structure of the EWS gene and its relationship to EWSR1, a site of tumor-associated chromosome translocation.
Autorzy :
Plougastel B; Laboratoire de Génétique des Tumeurs, Inserm CJF 9201, Institut Curie, Paris, France.
Zucman J
Peter M
Thomas G
Delattre O
Pokaż więcej
Źródło :
Genomics [Genomics] 1993 Dec; Vol. 18 (3), pp. 609-15.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 11*
Chromosomes, Human, Pair 22*
Translocation, Genetic*
Bone Neoplasms/*genetics
Neuroectodermal Tumors/*genetics
Sarcoma, Ewing/*genetics
Amino Acid Sequence ; Base Sequence ; Chromosome Mapping ; Chromosome Walking ; Cloning, Molecular ; Cosmids ; DNA Primers ; DNA, Complementary ; Exons ; Genomic Library ; Humans ; Introns ; Molecular Sequence Data ; Polymerase Chain Reaction ; Promoter Regions, Genetic ; RNA Splicing ; Restriction Mapping
Czasopismo naukowe
Tytuł :
Regional fine mapping of the beta crystallin genes on chromosome 22 excludes these genes as physically linked markers for neurofibromatosis type 2.
Autorzy :
Bijlsma EK; Institute of Human Genetics, University of Amsterdam, The Netherlands.
Delattre O
Juyn JA
Melot T
Westerveld A
Dumanski JP
Thomas G
Hulsebos TJ
Pokaż więcej
Źródło :
Genes, chromosomes & cancer [Genes Chromosomes Cancer] 1993 Oct; Vol. 8 (2), pp. 112-8.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Mapping*
Chromosomes, Human, Pair 22*
Genetic Linkage*
Crystallins/*genetics
Neurofibromatosis 2/*genetics
Animals ; Base Sequence ; Blotting, Southern ; DNA Primers/chemistry ; DNA Probes/chemistry ; DNA, Neoplasm/analysis ; Electrophoresis, Gel, Pulsed-Field ; Eye Diseases/etiology ; Humans ; Hybrid Cells ; Molecular Sequence Data ; Multigene Family ; Neurofibromatosis 2/complications ; Polymerase Chain Reaction ; Rodentia ; Sequence Homology, Nucleic Acid
Czasopismo naukowe
Tytuł :
Isolation and mapping of 45 NotI linking clones to chromosome 22.
Autorzy :
Sanson M; Centre for Research in Neuroscience, McGill University, Montreal, Canada.
Zhang F
Demczuk S
Delattre O
DeJong P
Aurias A
Thomas G
Rouleau GA
Pokaż więcej
Źródło :
Genomics [Genomics] 1993 Sep; Vol. 17 (3), pp. 776-9.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 22*
Deoxyribonucleases, Type II Site-Specific*
Base Sequence ; Chromosome Mapping ; Cloning, Molecular ; Cosmids ; DNA/genetics ; Gene Library ; Humans ; Hybrid Cells ; Oligodeoxyribonucleotides/genetics ; Repetitive Sequences, Nucleic Acid
Czasopismo naukowe
Tytuł :
Mapping of human gamma-glutamyl transpeptidase genes on chromosome 22 and other human autosomes.
Autorzy :
Figlewicz DA; Department of Neurology, Montreal General Hospital, Canada.
Delattre O
Guellaen G
Krizus A
Thomas G
Zucman J
Rouleau GA
Pokaż więcej
Źródło :
Genomics [Genomics] 1993 Aug; Vol. 17 (2), pp. 299-305.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 19*
Chromosomes, Human, Pair 20*
Chromosomes, Human, Pair 22*
gamma-Glutamyltransferase/*genetics
Animals ; Base Sequence ; Cell Line ; Chromosome Mapping ; Humans ; Kidney/enzymology ; Liver/enzymology ; Molecular Sequence Data ; Oligodeoxyribonucleotides ; Polymerase Chain Reaction/methods ; Pseudogenes ; Rats
Czasopismo naukowe
Tytuł :
Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus.
Autorzy :
Sanson M; Center for Research in Neuroscience, McGill University, Montreal, Canada.
Marineau C
Desmaze C
Lutchman M
Ruttledge M
Baron C
Narod S
Delattre O
Lenoir G
Thomas G
et. al.
Pokaż więcej
Źródło :
Human molecular genetics [Hum Mol Genet] 1993 Aug; Vol. 2 (8), pp. 1215-20.
Typ publikacji :
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 22*
Gene Deletion*
Genes, Neurofibromatosis 2*
Meningeal Neoplasms/*genetics
Meningioma/*genetics
Neurilemmoma/*genetics
Neurofibromatosis 2/*genetics
Cells, Cultured ; Chromosome Mapping ; Cosmids ; Female ; Genetic Markers ; Humans ; In Situ Hybridization, Fluorescence ; Lymphocytes/metabolism ; Male ; Neurofilament Proteins/genetics ; Oligonucleotide Probes ; Pedigree ; Restriction Mapping
Czasopismo naukowe
Tytuł :
The genes for oncostatin M (OSM) and leukemia inhibitory factor (LIF) are tightly linked on human chromosome 22.
Autorzy :
Rose TM; Fred Hutchinson Cancer Research Center, Seattle, Washington 98104.
Lagrou MJ
Fransson I
Werelius B
Delattre O
Thomas G
de Jong PJ
Todaro GJ
Dumanski JP
Pokaż więcej
Źródło :
Genomics [Genomics] 1993 Jul; Vol. 17 (1), pp. 136-40.
Typ publikacji :
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 22*
Genes*
Interleukin-6*
Growth Inhibitors/*genetics
Lymphokines/*genetics
Peptides/*genetics
Animals ; Blotting, Southern ; Cosmids ; Cricetinae ; DNA Probes ; DNA, Complementary/genetics ; Humans ; Hybrid Cells ; Leukemia Inhibitory Factor ; Multigene Family ; Oncostatin M ; Restriction Mapping
Czasopismo naukowe
Tytuł :
Ewing sarcoma 11;22 translocation produces a chimeric transcription factor that requires the DNA-binding domain encoded by FLI1 for transformation.
Autorzy :
May WA; Department of Pediatrics, Gwynne Hazen Cherry Memorial Laboratories, University of California, Los Angeles 90024.
Gishizky ML
Lessnick SL
Lunsford LB
Lewis BC
Delattre O
Zucman J
Thomas G
Denny CT
Pokaż więcej
Źródło :
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 1993 Jun 15; Vol. 90 (12), pp. 5752-6.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
MeSH Terms :
Chromosomes, Human, Pair 11*
Chromosomes, Human, Pair 22*
Transformation, Genetic*
Translocation, Genetic*
DNA-Binding Proteins/*genetics
Recombinant Proteins/*genetics
Sarcoma, Ewing/*genetics
Transcription Factors/*biosynthesis
Transcription Factors/*genetics
Amino Acid Sequence ; Animals ; Base Sequence ; Cell Line ; Friend murine leukemia virus/genetics ; Gene Library ; Humans ; Molecular Sequence Data ; Oligodeoxyribonucleotides ; Polymerase Chain Reaction ; Recombinant Proteins/biosynthesis ; Restriction Mapping ; Sarcoma, Ewing/metabolism ; Transcription Factors/metabolism ; Tumor Cells, Cultured ; Virus Integration
Czasopismo naukowe
Tytuł :
Isolation of cosmids and fetal brain cDNAs from the proximal long arm of human chromosome 22.
Autorzy :
Lamour V; Laboratoire de Biologie des Tumeurs Humaines, CNRS URA 1156, Institut Gustave Roussy, Villejuif, France.
Lévy N
Desmaze C
Baude V
Lécluse Y
Delattre O
Bernheim A
Thomas G
Aurias A
Lipinski M
Pokaż więcej
Źródło :
Human molecular genetics [Hum Mol Genet] 1993 May; Vol. 2 (5), pp. 535-40.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 22*
Cosmids/*isolation & purification
DNA/*isolation & purification
Animals ; Brain/metabolism ; Cosmids/genetics ; Cricetinae ; DNA/genetics ; DiGeorge Syndrome/genetics ; Fetus/metabolism ; Gene Library ; Genetic Vectors ; Genome, Human ; Humans ; Hybrid Cells ; Mice
Czasopismo naukowe

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