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Increased fatty acid synthase is a therapeutic target in mesothelioma
CLINICAL CANCER RESEARCH
Genomic imbalances in human lung adenocarcinomas and squamous cell carcinomas
GENES CHROMOSOMES & CANCER
Human hepatocellular carcinoma is characterized by a highly consistent pattern of genomic imbalances, including frequent loss of 16q23.1-24.1
GENES CHROMOSOMES & CANCER
Absence of post-transcription RNA modifications of BCL10 in human malignant mesothelioma and colorectal cancer
GENES CHROMOSOMES & CANCER
SV40 and cell cycle perturbations in malignant mesothelioma
SEMINARS IN CANCER BIOLOGY
Loss of heterozygosity analysis defines a 3-cM region of 15q commonly deleted in human malignant mesothelioma
ONCOGENE
Cloning and chromosomal localization of a gene encoding a novel serine/threonine kinase belonging to the subfamily of testis-specific kinases
GENOMICS
Analysis of the structure and expression pattern of MRP7 (ABCC10), a new member of the MRP subfamily
CANCER LETTERS
Familial malignant mesothelioma - Reply
LANCET
Genetic susceptibility and familial malignant mesothelioma - Reply
LANCET
Genetic-susceptibility factor and malignant mesothelioma in the Cappadocian region of Turkey
LANCET
Commentary - AKT plays a central role in tumorigenesis
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Anti-apoptotic signaling by hepatocyte growth factor/Met via the phosphatidylinositol 3-kinase/Akt and mitogen-activated protein kinase pathways
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Cyclin T2A gene maps on human chromosome 2q21
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY
AKT activation up-regulates insulin-like growth factor I receptor expression and promotes invasiveness of human pancreatic cancer cells
CANCER RESEARCH
Loss of heterozygosity analysis of 13q and 14q in human malignant mesothelioma
GENES CHROMOSOMES & CANCER
Expression of GPC3, an X-linked recessive overgrowth gene, is silenced in malignant mesothelioma
ONCOGENE
Identification and structural analysis of human RBM8A and RBM8B: Two highly conserved RNA-binding motif proteins that interact with OVCA1, a candidate tumor suppressor
GENOMICS
Mapping of AKT3, encoding a member of the Akt/protein kinase B family, to human and rodent chromosomes by fluorescence in situ hybridization
CYTOGENETICS AND CELL GENETICS
Loss of chromosomes 1 and X in a renal oncocytoma: implications for a possible pseudoautosomal tumor suppressor locus
CANCER GENETICS AND CYTOGENETICS
Human mesothelial cells are unusually susceptible to simian virus 40-mediated transformation and asbestos cocarcinogenicity
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
The phosphatidylinositol 3-kinase/AKT signal transduction pathway plays a critical role in the expression of p21(WAF1/CIP1/SDI1) induced by cisplatinand paclitaxel
CANCER RESEARCH
The Fn14 immediate-early response gene is induced during liver regeneration and highly expressed in both human and murine hepatocellular carcinomas
AMERICAN JOURNAL OF PATHOLOGY
The p16 status of tumor cell lines identifies small molecule inhibitors specific for cyclin-dependent kinase 4
CLINICAL CANCER RESEARCH
Genome scanning detects amplification of the cathepsin B gene (CtsB) in transformed rat ovarian surface epithelial cells
JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION
The DNA repair gene MBD4 (MED1) is mutated in human carcinomas with microsatellite instability
NATURE GENETICS
Frequent mutations of NF2 and allelic loss from chromosome band 22q12 in malignant mesothelioma: Evidence for a two-hit mechanism of NF2 inactivation
GENES CHROMOSOMES & CANCER
Somatic genetic alterations in human malignant mesothelioma (Review)
INTERNATIONAL JOURNAL OF ONCOLOGY
Localization of human NQO1 gene to chromosome 16q22 and NQO2-6p25 and associated polymorphisms
PHARMACOGENETICS
Identification of a chromosome 3p14.3-21.1 gene, APPL, encoding an adaptormolecule that interacts with the oncoprotein-serine/threonine kinase AKT2
ONCOGENE
Novel human and mouse annexin A10 are linked to the genome duplications during early chordate evolution
GENOMICS
Human annexin 31 genetic mapping and origin
GENE
Cell cycle withdrawal promotes myogenic induction of Akt, a positive modulator of myocyte survival
MOLECULAR AND CELLULAR BIOLOGY
Coexisting myelodysplasia and myeloproliferative features in a single clone containing 5q-, Ph and i(17q)
LEUKEMIA RESEARCH
Absence of BCL10 mutations in human malignant mesothelioma
CELL
Asbestos, chromosomal deletions, and tumor suppressor gene alterations in human malignant mesothelioma
JOURNAL OF CELLULAR PHYSIOLOGY
A new human synovial sarcoma cell line, HS-SY-3, with a truncated form of hybrid SYT/SSX1 gene
INTERNATIONAL JOURNAL OF CANCER
Emerging translational therapies for mesothelioma
CHEST
Comparative genomic hybridization and loss of heterozygosity analyses identify a common region of deletion at 15q11.1-15 in human malignant mesothelioma
CANCER RESEARCH
AKT2 MESSENGER-RNA IS HIGHLY EXPRESSED IN EMBRYONIC BROWN FAT AND THEAKT2 KINASE IS ACTIVATED BY INSULIN
Oncogene
AMPLIFICATION AND OVEREXPRESSION OF THE AKT2 ONCOGENE IN A SUBSET OF HUMAN PANCREATIC DUCTAL ADENOCARCINOMAS
Molecular carcinogenesis
CLONING AND LOCALIZATION OF A HUMAN DIPHTHAMIDE BIOSYNTHESIS-LIKE PROTEIN-2 GENE, DPH2L2
Genomics (San Diego, Calif.)
IDENTIFICATION AND MAPPING OF HUMAN HISTONE ACETYLATION MODIFIER GENEHOMOLOGS
Genomics (San Diego, Calif.)
GENOMIC LOCATIONS OF ANX11 AND ANX13 AND THE EVOLUTIONARY GENETICS OFHUMAN ANNEXINS
Genomics
TRANSLOCATION AND ACTIVATION OF AKT2 IN RESPONSE TO STIMULATION BY INSULIN
Journal of cellular biochemistry
ANALYSIS OF THE INTERACTION OF THE NOVEL RNA-POLYMERASE-II (POL-II) SUBUNIT HSRPB4 WITH ITS PARTNER HSRPB7 AND WITH POL-II
Molecular and cellular biology
CLINICAL RELEVANCE OF CHROMOSOME-ABNORMALITIES IN NONSMALL CELL LUNG-CANCER
Cancer genetics and cytogenetics
B cells malignantly transformed by human immunodeficiency virus are polyclonal
VIROLOGY
OCI-5 GPC3, A GLYPICAN ENCODED BY A GENE THAT IS MUTATED IN THE SIMPSON-GOLABI-BEHMEL OVERGROWTH SYNDROME, INDUCES APOPTOSIS IN A CELL LINE-SPECIFIC MANNER/
The Journal of cell biology
AMPLIFICATION OF THE ATP-BINDING CASSETTE-2 TRANSPORTER GENE IS FUNCTIONALLY LINKED WITH ENHANCED EFFLUX OF ESTRAMUSTINE IN OVARIAN-CARCINOMA CELLS
Cancer research
A MULTIINSTITUTIONAL STUDY CONFIRMS THE PRESENCE AND EXPRESSION OF SIMIAN-VIRUS-40 IN HUMAN-MALIGNANT MESOTHELIOMAS
Cancer research
AKT2, A MEMBER OF THE PROTEIN-KINASE-B FAMILY, IS ACTIVATED BY GROWTH-FACTORS, V-HA-RAS, AND V-SRC THROUGH PHOSPHATIDYLINOSITOL 3-KINASE INHUMAN OVARIAN EPITHELIAL CANCER-CELLS
Cancer research
ISOLATION OF MOAT-B, A WIDELY EXPRESSED MULTIDRUG RESISTANCE-ASSOCIATED PROTEIN CANALICULAR MULTISPECIFIC ORGANIC ANION TRANSPORTER-RELATEDTRANSPORTER
Cancer research
CHARACTERIZATION OF MOAT-C AND MOAT-D, NEW MEMBERS OF THE MRP CMOAT SUBFAMILY OF TRANSPORTER PROTEINS/
Journal of the National Cancer Institute
PROGNOSTIC VALUE OF SPECIFIC KRAS MUTATIONS IN LUNG ADENOCARCINOMAS
Cancer epidemiology, biomarkers & prevention
COMPARATIVE GENOMIC HYBRIDIZATION DETECTS FREQUENT OVERREPRESENTATIONOF CHROMOSOMAL MATERIAL FROM 3Q26, 8Q24, AND 20Q13 IN HUMAN OVARIAN CARCINOMAS
Genes, chromosomes & cancer
COMBINED CHROMOSOME MICRODISSECTION AND COMPARATIVE GENOMIC HYBRIDIZATION DETECT MULTIPLE SITES OF AMPLIFIED DNA IN A HUMAN LUNG-CARCINOMA CELL-LINE
Genes, chromosomes & cancer
DETECTION OF DNA GAINS AND LOSSES IN PRIMARY ENDOMETRIAL CARCINOMAS BY COMPARATIVE GENOMIC HYBRIDIZATION
Genes, chromosomes & cancer
CHARACTERIZATION OF UNCONVENTIONAL MYO6, THE HUMAN HOMOLOG OF THE GENE RESPONSIBLE FOR DEAFNESS IN SNELLS-WALTZER MICE
Human molecular genetics
ASSOCIATION OF KREV-1 RAPLA WITH KRIT1, A NOVEL ANKYRIN REPEAT-CONTAINING PROTEIN ENCODED BY A GENE-MAPPING TO 7Q21-22/
Oncogene
TRANSFORMING ACTIVITY AND MITOSIS-RELATED EXPRESSION OF THE AKT2 ONCOGENE - EVIDENCE SUGGESTING A LINK BETWEEN CELL-CYCLE REGULATION AND ONCOGENESIS
Oncogene
IDENTIFICATION OF A ZINC-FINGER GENE AT 6Q25 - A CHROMOSOMAL REGION IMPLICATED IN DEVELOPMENT OF MANY SOLID TUMORS
Oncogene
MAPPING OF THE SIMPSON-GOLABI-BEHMEL OVERGROWTH SYNDROME GENE (GPC3) TO CHROMOSOME-X IN HUMAN AND RAT BY FLUORESCENCE IN-SITU HYBRIDIZATION
Mammalian genome
ADVANCES IN THE ANALYSIS OF CHROMOSOME ALTERATIONS IN HUMAN LUNG CARCINOMAS
Cancer genetics and cytogenetics
MEMBRANE TRANSLOCATION AND ACTIVATION OF THE AKT KINASE IN GROWTH FACTOR-STIMULATED HEMATOPOIETIC-CELLS
Leukemia research
DETECTION OF LOW-FRACTION K-RAS MUTATIONS IN PRIMARY LUNG-TUMORS USING A SENSITIVE METHOD
International journal of cancer
THE CLONING AND CHARACTERIZATION OF HUMAN MYD88 - A MEMBER OF AN IL-1RECEPTOR-RELATED FAMILY
FEBS letters
ASSOCIATION OF IMMUNOREACTIVE HEPATOCYTE GROWTH-FACTOR WITH POOR SURVIVAL IN RESECTABLE NONSMALL CELL LUNG-CANCER
Cancer research
MULTIPLE REGIONS OF ALLELIC LOSS FROM CHROMOSOME ARM 6Q IN MALIGNANT MESOTHELIOMA
Cancer research
COMPARATIVE GENOMIC HYBRIDIZATION ANALYSIS DETECTS FREQUENT, OFTEN HIGH-LEVEL, OVERREPRESENTATION OF DNA-SEQUENCES AT 3Q, 5P, 7P, AND 8Q INHUMAN NONSMALL CELL LUNG CARCINOMAS
Cancer research
IDENTIFICATION OF A GENE CONTAINING ZINC-FINGER MOTIFS BASED ON LOST EXPRESSION IN MALIGNANTLY TRANSFORMED RAT OVARIAN SURFACE EPITHELIAL-CELLS
Cancer research
GPC3, THE GLYPICAN GENE MUTATED IN THE SIMPSON-GOLABI-BEHMEL-OVERGROWTH-SYNDROME, IS DOWN-REGULATED IN MALIGNANT MESOTHELIOMAS
American journal of human genetics
FREQUENT ALTERATIONS OF NF2 AND DELETION OF CHROMOSOME 22Q12 IN MALIGNANT MESOTHELIOMA - EVIDENCE FOR A 2-HIT MECHANISM OF NF2 INACTIVATION
American journal of human genetics
IDENTIFICATION OF ARGBP1, AN ARG PROTEIN-TYROSINE KINASE BINDING-PROTEIN THAT IS THE HUMAN HOMOLOG OF A CNS-SPECIFIC XENOPUS GENE
Oncogene
A GENETIC, PHYSICAL, AND COMPARATIVE MAP OF RAT CHROMOSOME-10
Mammalian genome
THE VPREB1 AND COMT GENES ARE CLOSELY LINKED AND SUBLOCALIZED TO RAT CHROMOSOME 11Q23
Mammalian genome
THE HUMAN GATA-6 GENE - STRUCTURE, CHROMOSOMAL LOCATION, AND REGULATION OF EXPRESSION BY TISSUE-SPECIFIC AND MITOGEN-RESPONSIVE SIGNALS
Genomics
MYBL2 (BMYB) MAPS TO MOUSE CHROMOSOME-2 AND HUMAN-CHROMOSOME 20Q13.1
Genomics
CHROMOSOMAL LOCALIZATION OF TIL, A GENE ENCODING A PROTEIN RELATED TOTHE DROSOPHILA TRANSMEMBRANE RECEPTOR TOLL, TO HUMAN-CHROMOSOME 4P14
Genomics
CHROMOSOME MAPPING OF THE MOUSE AKT2 GENE AND AKT2 PSEUDOGENE
Cytogenetics and cell genetics
STRUCTURES AND CHROMOSOME LOCATIONS OF THE HUMAN MEF2A GENE AND A PSEUDOGENE MEF2AP
Cytogenetics and cell genetics
ISOLATION, CHARACTERIZATION, AND MAPPING TO HUMAN-CHROMOSOME 11Q24-25OF A CDNA-ENCODING A HIGHLY CONSERVED PUTATIVE TRANSMEMBRANE PROTEIN,TMC
Biochimica et biophysica acta, N. Gene structure and expression
DETECTION OF ANEUPLOIDY IN INTERPHASE NUCLEI FROM NONSMALL CELL LUNG CARCINOMAS BY FLUORESCENCE IN-SITU HYBRIDIZATION USING CHROMOSOME-SPECIFIC REPETITIVE DNA PROBES
Cancer genetics and cytogenetics
CYTOGENETIC FINDINGS IN A BREAST STROMAL SARCOMA - APPLICATION OF FLUORESCENCE IN-SITU HYBRIDIZATION TO CHARACTERIZE THE BREAKPOINT REGIONSIN AN 11-19 TRANSLOCATION (VOL 63, PG 47, 1992)
Cancer genetics and cytogenetics
AMPLIFICATION OF AKT2 IN HUMAN PANCREATIC-CANCER CELLS AND INHIBITIONOF ATK2 EXPRESSION AND TUMORIGENICITY BY ANTISENSE RNA
Proceedings of the National Academy of Sciences of the United Statesof America
MOLECULAR-CLONING OF THE CDNA AND CHROMOSOME LOCALIZATION OF THE GENEFOR HUMAN UBIQUITIN-CONJUGATING ENZYME-9
The Journal of biological chemistry
CLONING OF A PUTATIVE LIGAND FOR THE T1 ST2 RECEPTOR/
The Journal of biological chemistry
LOSS OF HETEROZYGOSITY ANALYSIS DEFINES A CRITICAL REGION IN CHROMOSOME 1P22 COMMONLY DELETED IN HUMAN-MALIGNANT MESOTHELIOMA
Cancer research
IDENTIFICATION OF ZINC-FINGER MESSENGER-RNAS USING DOMAIN-SPECIFIC DIFFERENTIAL DISPLAY
Analytical biochemistry
CLONING, CHROMOSOMAL LOCALIZATION AND EXPRESSION ANALYSIS OF THE MOUSE AKT2 ONCOGENE
Oncogene
MAPPING OF GUANYLIN TO MURINE CHROMOSOME-4 AND HUMAN-CHROMOSOME 1P34-P35
Genomics
CHROMOSOMAL LOCALIZATION OF A GENE, GFI1, ENCODING A NOVEL ZINC-FINGER PROTEIN REVEALS A NEW SYNTENIC REGION BETWEEN MAN AND RODENTS
Cytogenetics and cell genetics
A MICRODISSECTION LIBRARY OF THE RAT RENAL-CARCINOMA GENE REGION
Cytogenetics and cell genetics
CLONING AND REGIONAL ASSIGNMENT OF THE HUMAN MYOSIN HEAVY-CHAIN-12 (MYH12) GENE TO CHROMOSOME BAND-15Q21
Cytogenetics and cell genetics
HIGH-FREQUENCY OF INACTIVATING MUTATIONS IN THE NEUROFIBROMATOSIS TYPE-2 GENE (NF2) IN PRIMARY MALIGNANT MESOTHELIOMAS
Proceedings of the National Academy of Sciences of the United Statesof America
MOLECULAR ALTERATIONS OF THE AKT2 ONCOGENE IN OVARIAN AND BREAST CARCINOMAS
International journal of cancer
RETROVIRAL-LIKE SEQUENCES SPECIFICALLY EXPRESSED IN THE RAT OVARY DETECT GENETIC-DIFFERENCES BETWEEN NORMAL AND TRANSFORMED RAT OVARIAN SURFACE EPITHELIAL-CELLS
Endocrinology
MOLECULAR CHARACTERIZATION OF 16P DELETIONS ASSOCIATED WITH INVERSION-16 DEFINES THE CRITICAL FUSION FOR LEUKEMOGENESIS
Blood
DELETION MAPPING OF THE SHORT ARM OF CHROMOSOME-3 IN HUMAN-MALIGNANT MESOTHELIOMA
Genes, chromosomes & cancer
CYTOGENETIC ANALYSIS OF 63 NONSMALL CELL LUNG CARCINOMAS - RECURRENT CHROMOSOME ALTERATIONS AMID FREQUENT AND WIDESPREAD GENOMIC UPHEAVAL
Genes, chromosomes & cancer