Lancet Oncology, The, ISSN 1470-2045, 2017, Volume 18, Issue 7, pp. 958 - 971
Summary Background International consensus recognises four medulloblastoma molecular subgroups: WNT (MBWNT ), SHH (MBSHH ), group 3 (MBGrp3 ), and group 4...
Hematology, Oncology and Palliative Medicine | TUMOR | ONCOLOGY | PATHWAY | GENETIC PROFILES | EXPRESSION | BETA-CATENIN STATUS | Risk Assessment - methods | Age Factors | Humans | Zinc Finger Protein Gli2 | Transcriptome | Child, Preschool | N-Myc Proto-Oncogene Protein - genetics | Infant | Male | Patched-1 Receptor - genetics | Smoothened Receptor - genetics | Tumor Suppressor Protein p53 - genetics | DNA Methylation | Medulloblastoma - radiotherapy | Telomerase - genetics | Medulloblastoma - pathology | Female | Retrospective Studies | Cerebellar Neoplasms - pathology | Cerebellar Neoplasms - classification | Medulloblastoma - genetics | Nuclear Proteins - genetics | Child | Infant, Newborn | Risk Factors | Repressor Proteins - genetics | Survival Rate | Cerebellar Neoplasms - genetics | beta Catenin - genetics | Disease-Free Survival | Gene Amplification | Adolescent | Proto-Oncogene Proteins c-myc - genetics | Mutation | Cerebellar Neoplasms - radiotherapy | Kruppel-Like Transcription Factors - genetics | Medulloblastoma - classification | Medulloblastoma | Children's hospitals | Genomics | DNA microarrays | Brain tumors | Leukemia | Oncology, Experimental | Research | Methylation | Cancer
Hematology, Oncology and Palliative Medicine | TUMOR | ONCOLOGY | PATHWAY | GENETIC PROFILES | EXPRESSION | BETA-CATENIN STATUS | Risk Assessment - methods | Age Factors | Humans | Zinc Finger Protein Gli2 | Transcriptome | Child, Preschool | N-Myc Proto-Oncogene Protein - genetics | Infant | Male | Patched-1 Receptor - genetics | Smoothened Receptor - genetics | Tumor Suppressor Protein p53 - genetics | DNA Methylation | Medulloblastoma - radiotherapy | Telomerase - genetics | Medulloblastoma - pathology | Female | Retrospective Studies | Cerebellar Neoplasms - pathology | Cerebellar Neoplasms - classification | Medulloblastoma - genetics | Nuclear Proteins - genetics | Child | Infant, Newborn | Risk Factors | Repressor Proteins - genetics | Survival Rate | Cerebellar Neoplasms - genetics | beta Catenin - genetics | Disease-Free Survival | Gene Amplification | Adolescent | Proto-Oncogene Proteins c-myc - genetics | Mutation | Cerebellar Neoplasms - radiotherapy | Kruppel-Like Transcription Factors - genetics | Medulloblastoma - classification | Medulloblastoma | Children's hospitals | Genomics | DNA microarrays | Brain tumors | Leukemia | Oncology, Experimental | Research | Methylation | Cancer
Journal Article
Nature Communications, ISSN 2041-1723, 01/2017, Volume 8, Issue 1, p. 13932
Microsporidians are obligate intracellular parasites that have minimized their genome content and sub-cellular structures by reductive evolution. Here, we...
CFD1-NBP35 COMPLEX | MONOTHIOL GLUTAREDOXINS | PROTEIN | SULFHYDRYL OXIDASE | BIOGENESIS | MULTIDISCIPLINARY SCIENCES | EUKARYOTES | MATURATION | MULTIPLE SEQUENCE ALIGNMENT | MITOCHONDRIAL REMNANT | SCAFFOLD | Biological Evolution | Cell Nucleus - metabolism | Fungal Proteins - biosynthesis | Iron-Sulfur Proteins - genetics | Cytosol - metabolism | Iron-Sulfur Proteins - biosynthesis | Mitochondria - metabolism | Pansporablastina - genetics | Fungal Proteins - genetics | Pansporablastina - metabolism | Phylogeny
CFD1-NBP35 COMPLEX | MONOTHIOL GLUTAREDOXINS | PROTEIN | SULFHYDRYL OXIDASE | BIOGENESIS | MULTIDISCIPLINARY SCIENCES | EUKARYOTES | MATURATION | MULTIPLE SEQUENCE ALIGNMENT | MITOCHONDRIAL REMNANT | SCAFFOLD | Biological Evolution | Cell Nucleus - metabolism | Fungal Proteins - biosynthesis | Iron-Sulfur Proteins - genetics | Cytosol - metabolism | Iron-Sulfur Proteins - biosynthesis | Mitochondria - metabolism | Pansporablastina - genetics | Fungal Proteins - genetics | Pansporablastina - metabolism | Phylogeny
Journal Article
Molecular cancer research : MCR, ISSN 1541-7786, 06/2019, Volume 17, Issue 6, pp. 1264 - 1278
The androgen receptor (AR) is a key driver of prostate cancer development. Antiandrogens effectively inactivate the AR, but subsequent AR reactivation...
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2012, Volume 7, Issue 1, p. e30287
The mucosal microbiota is recognised as an important factor for our health, with many disease states linked to imbalances in the normal community structure....
BACILLUS-THURINGIENSIS | TRICHOMONAS-VAGINALIS | GENOME SEQUENCE | CARBOHYDRATE-BINDING MODULES | MULTIDISCIPLINARY SCIENCES | PARASITE ENTAMOEBA-HISTOLYTICA | ESCHERICHIA-COLI | BIOLOGICAL ROLES | INTESTINAL MUCIN | VIBRIO-CHOLERAE | PAENIBACILLUS-LARVAE | Amino Acid Sequence | Invertebrates - microbiology | Adaptation, Biological - genetics | Humans | Invertebrates - enzymology | Invertebrates - genetics | Metalloproteases - genetics | Molecular Sequence Data | Protein Structure, Tertiary - genetics | Adaptation, Biological - physiology | Symbiosis - genetics | Digestive System - pathology | Sequence Homology, Amino Acid | Animals | Host-Pathogen Interactions - genetics | Base Sequence | Digestive System - microbiology | Metalloproteases - chemistry | Amino acids | Peptides | Microbiota (Symbiotic organisms) | Proteases | Genomics | Mucins | Commensals | Mucosa | Genomes | Cell surface | Data bases | Proteins | Microorganisms | Microbiota | Work capacity | User interface | Phylogenetics | Metalloproteinase | Bioinformatics | Digestive tract | Anchoring | Recombinant | Biomedical engineering | Binding | Biodegradation | Community structure | Carbohydrates | Enzymes | Pathogens | Peptidase | Glycoproteins | Industrial applications | Mucinase | Zinc | Glycan | Peptidases | Acids | Molecular biology | Colonization | Signal peptides
BACILLUS-THURINGIENSIS | TRICHOMONAS-VAGINALIS | GENOME SEQUENCE | CARBOHYDRATE-BINDING MODULES | MULTIDISCIPLINARY SCIENCES | PARASITE ENTAMOEBA-HISTOLYTICA | ESCHERICHIA-COLI | BIOLOGICAL ROLES | INTESTINAL MUCIN | VIBRIO-CHOLERAE | PAENIBACILLUS-LARVAE | Amino Acid Sequence | Invertebrates - microbiology | Adaptation, Biological - genetics | Humans | Invertebrates - enzymology | Invertebrates - genetics | Metalloproteases - genetics | Molecular Sequence Data | Protein Structure, Tertiary - genetics | Adaptation, Biological - physiology | Symbiosis - genetics | Digestive System - pathology | Sequence Homology, Amino Acid | Animals | Host-Pathogen Interactions - genetics | Base Sequence | Digestive System - microbiology | Metalloproteases - chemistry | Amino acids | Peptides | Microbiota (Symbiotic organisms) | Proteases | Genomics | Mucins | Commensals | Mucosa | Genomes | Cell surface | Data bases | Proteins | Microorganisms | Microbiota | Work capacity | User interface | Phylogenetics | Metalloproteinase | Bioinformatics | Digestive tract | Anchoring | Recombinant | Biomedical engineering | Binding | Biodegradation | Community structure | Carbohydrates | Enzymes | Pathogens | Peptidase | Glycoproteins | Industrial applications | Mucinase | Zinc | Glycan | Peptidases | Acids | Molecular biology | Colonization | Signal peptides
Journal Article
Oncogene, ISSN 0950-9232, 08/2018, Volume 37, Issue 34, pp. 4679 - 4691
The TP53-MDM2-AR-AKT signalling network plays a critical role in the development and progression of prostate cancer. However, the molecular mechanisms...
ANDROGEN RECEPTOR | PHOSPHORYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CISPLATIN RESISTANCE | AKT | INDEPENDENT PROSTATE-CANCER | CELL BIOLOGY | CELL LUNG-CANCER | DEUBIQUITINATING ENZYME USP12 | ONCOLOGY | PATHWAY | GENETICS & HEREDITY | MDM2 | INHIBITORS | Prostatic Neoplasms - metabolism | Neoplasm Recurrence, Local - metabolism | Humans | Receptors, Androgen - metabolism | Tumor Suppressor Protein p53 - metabolism | Cercopithecus aethiops | Male | Animals | Cell Line, Tumor | Ubiquitin Thiolesterase - metabolism | Signal Transduction - physiology | Proto-Oncogene Proteins c-akt - metabolism | COS Cells | Proto-Oncogene Proteins c-mdm2 - metabolism | Molecular targeted therapy | Care and treatment | Proteases | Innovations | Development and progression | Cellular signal transduction | Genetic aspects | Health aspects | Prostate cancer | MDM2 protein | Molecular modelling | Therapeutic applications | p53 Protein | AKT protein | Gene expression | Prostate | Tumors
ANDROGEN RECEPTOR | PHOSPHORYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CISPLATIN RESISTANCE | AKT | INDEPENDENT PROSTATE-CANCER | CELL BIOLOGY | CELL LUNG-CANCER | DEUBIQUITINATING ENZYME USP12 | ONCOLOGY | PATHWAY | GENETICS & HEREDITY | MDM2 | INHIBITORS | Prostatic Neoplasms - metabolism | Neoplasm Recurrence, Local - metabolism | Humans | Receptors, Androgen - metabolism | Tumor Suppressor Protein p53 - metabolism | Cercopithecus aethiops | Male | Animals | Cell Line, Tumor | Ubiquitin Thiolesterase - metabolism | Signal Transduction - physiology | Proto-Oncogene Proteins c-akt - metabolism | COS Cells | Proto-Oncogene Proteins c-mdm2 - metabolism | Molecular targeted therapy | Care and treatment | Proteases | Innovations | Development and progression | Cellular signal transduction | Genetic aspects | Health aspects | Prostate cancer | MDM2 protein | Molecular modelling | Therapeutic applications | p53 Protein | AKT protein | Gene expression | Prostate | Tumors
Journal Article
PLoS Pathogens, ISSN 1553-7366, 10/2012, Volume 8, Issue 10, p. e1002979
The dynamics of reductive genome evolution for eukaryotes living inside other eukaryotic cells are poorly understood compared to well-studied model systems...
TRANSPORTER SUPERFAMILY | ENCEPHALITOZOON-CUNICULI | TRYPANOSOMA-BRUCEI | TRANSPOSABLE ELEMENTS | MICROBIOLOGY | ENTAMOEBA-HISTOLYTICA | SPOROGONIAL STAGES | VIROLOGY | CHITIN-SYNTHASE | BACILLUS-SUBTILIS | PROTEIN FAMILIES | PARASITOLOGY | RNA-POLYMERASE | Proteome - genetics | Humans | Acquired Immunodeficiency Syndrome - microbiology | Phylogeny | Sequence Analysis, DNA | Biological Evolution | Mitochondria | Genome, Fungal | RNA Interference | Microsporidia - isolation & purification | Proteomics | Microsporidia - genetics | RNA, Small Interfering | Energy Metabolism - genetics | Evolution, Molecular | Microbial genetics | Genomics | Physiological aspects | Genetic aspects | Research | Microsporidia | Health aspects | Proteins | Eukaryotes | Parasites | Acquired immune deficiency syndrome--AIDS | AIDS | Acquired immune deficiency syndrome
TRANSPORTER SUPERFAMILY | ENCEPHALITOZOON-CUNICULI | TRYPANOSOMA-BRUCEI | TRANSPOSABLE ELEMENTS | MICROBIOLOGY | ENTAMOEBA-HISTOLYTICA | SPOROGONIAL STAGES | VIROLOGY | CHITIN-SYNTHASE | BACILLUS-SUBTILIS | PROTEIN FAMILIES | PARASITOLOGY | RNA-POLYMERASE | Proteome - genetics | Humans | Acquired Immunodeficiency Syndrome - microbiology | Phylogeny | Sequence Analysis, DNA | Biological Evolution | Mitochondria | Genome, Fungal | RNA Interference | Microsporidia - isolation & purification | Proteomics | Microsporidia - genetics | RNA, Small Interfering | Energy Metabolism - genetics | Evolution, Molecular | Microbial genetics | Genomics | Physiological aspects | Genetic aspects | Research | Microsporidia | Health aspects | Proteins | Eukaryotes | Parasites | Acquired immune deficiency syndrome--AIDS | AIDS | Acquired immune deficiency syndrome
Journal Article
Blood, ISSN 0006-4971, 12/2014, Volume 124, Issue 21, pp. 3582 - 3582
Abstract Acute lymphoblastic leukemia (ALL) is characterized by the expansion of immature hematopoietic cells in the bone marrow and blood. It is the most...
Journal Article
PLoS Pathogens, ISSN 1553-7366, 12/2014, Volume 10, Issue 12, p. e1004547
Microsporidia are obligate intracellular parasites of most animal groups including humans, but despite their significant economic and medical importance there...
ATP/ADP | GENOME SEQUENCE | EVOLUTION | VIROLOGY | SPECIFICITY | ALIGNMENT | MICROBIOLOGY | RICKETTSIA-PROWAZEKII | DIVERSITY | MITOCHONDRIAL REMNANT | PARASITOLOGY | DNA, Fungal - genetics | Humans | RNA, Fungal - biosynthesis | Acquired Immunodeficiency Syndrome - microbiology | Fungal Proteins - genetics | Microsporidia - metabolism | Purine Nucleotides - metabolism | Carrier Proteins - genetics | DNA, Fungal - biosynthesis | Carrier Proteins - metabolism | Biological Transport, Active - physiology | Microsporidia - isolation & purification | Microsporidia - genetics | RNA, Fungal - genetics | Fungal Proteins - metabolism | Microbiological research | Protein research | Carrier proteins | Host-parasite relationships | Cell membranes | Purine nucleotides | Research | Health aspects | Microsporidia | Plasma | AIDS | Biosynthesis | Genomes | Parasites | Metabolism | Experiments | Proteins | Acquired immune deficiency syndrome | HIV | E coli | Microscopy | Protein synthesis | Deoxyribonucleic acid | DNA | Human immunodeficiency virus | Cytoplasm
ATP/ADP | GENOME SEQUENCE | EVOLUTION | VIROLOGY | SPECIFICITY | ALIGNMENT | MICROBIOLOGY | RICKETTSIA-PROWAZEKII | DIVERSITY | MITOCHONDRIAL REMNANT | PARASITOLOGY | DNA, Fungal - genetics | Humans | RNA, Fungal - biosynthesis | Acquired Immunodeficiency Syndrome - microbiology | Fungal Proteins - genetics | Microsporidia - metabolism | Purine Nucleotides - metabolism | Carrier Proteins - genetics | DNA, Fungal - biosynthesis | Carrier Proteins - metabolism | Biological Transport, Active - physiology | Microsporidia - isolation & purification | Microsporidia - genetics | RNA, Fungal - genetics | Fungal Proteins - metabolism | Microbiological research | Protein research | Carrier proteins | Host-parasite relationships | Cell membranes | Purine nucleotides | Research | Health aspects | Microsporidia | Plasma | AIDS | Biosynthesis | Genomes | Parasites | Metabolism | Experiments | Proteins | Acquired immune deficiency syndrome | HIV | E coli | Microscopy | Protein synthesis | Deoxyribonucleic acid | DNA | Human immunodeficiency virus | Cytoplasm
Journal Article
9.
Full Text
Characterisation of the genomic landscape of CRLF2‐rearranged acute lymphoblastic leukemia
Genes, Chromosomes and Cancer, ISSN 1045-2257, 05/2017, Volume 56, Issue 5, pp. 363 - 372
Deregulated expression of the type I cytokine receptor, CRLF2, is observed in 5–15% of precursor B‐cell acute lymphoblastic leukaemia (B‐ALL). We aimed to...
REARRANGEMENT | ONCOLOGY | USP9X | JAK | GENETICS & HEREDITY | ADULTS | MUTATIONS | IKZF1 | B-PROGENITOR | IGH-AT TRANSLOCATIONS | GENETIC ALTERATIONS | CRLF2 | Prognosis | Follow-Up Studies | Humans | Middle Aged | Child, Preschool | In Situ Hybridization, Fluorescence | Infant | Male | Mutation - genetics | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Young Adult | Oncogene Proteins, Fusion - genetics | Gene Rearrangement | Adolescent | Adult | Female | Biomarkers, Tumor - genetics | High-Throughput Nucleotide Sequencing | Genome, Human | Neoplasm Staging | Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology | Child | Receptors, Cytokine - genetics | Genetic aspects | Down syndrome | Analysis | Cancer
REARRANGEMENT | ONCOLOGY | USP9X | JAK | GENETICS & HEREDITY | ADULTS | MUTATIONS | IKZF1 | B-PROGENITOR | IGH-AT TRANSLOCATIONS | GENETIC ALTERATIONS | CRLF2 | Prognosis | Follow-Up Studies | Humans | Middle Aged | Child, Preschool | In Situ Hybridization, Fluorescence | Infant | Male | Mutation - genetics | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Young Adult | Oncogene Proteins, Fusion - genetics | Gene Rearrangement | Adolescent | Adult | Female | Biomarkers, Tumor - genetics | High-Throughput Nucleotide Sequencing | Genome, Human | Neoplasm Staging | Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology | Child | Receptors, Cytokine - genetics | Genetic aspects | Down syndrome | Analysis | Cancer
Journal Article
Blood, ISSN 0006-4971, 11/2019, Volume 134, Issue Supplement_1, pp. 3952 - 3952
Acute lymphoblastic leukemia (ALL) is the most common type of childhood leukaemia. Recently improved risk stratification resulted in therapy optimization and...
Journal Article
11.
Full Text
The SF3b Splicing Complex Regulates DNA Damage Response in Acute Lymphoblastic Leukemia
Blood, ISSN 0006-4971, 11/2019, Volume 134, Issue Supplement_1, pp. 1237 - 1237
To identify potential regulators of propagation and self-renewal of Acute Lymphoblastic Leukaemia (ALL), we performed an explorative genome-wide RNAi screen...
Journal Article
Molecular Cancer Therapeutics, ISSN 1535-7163, 03/2016, Volume 15, Issue 3, pp. 379 - 391
Sensitivity to MDM2 inhibitors is widely different among responsive TP53 wild-type cell lines and tumors. Understanding the determinants of MDM2 inhibitor...
DRUG-SENSITIVITY | APOPTOSIS | PPM1D MUTATIONS | ONCOLOGY | PHOSPHORYLATION | DNA-DAMAGE | GENE-EXPRESSION | WIP1 PHOSPHATASE | P53 PATHWAY | CANCER | G1 CHECKPOINT | Caspase 7 - metabolism | Neoplasms - metabolism | Apoptosis - drug effects | Protein Phosphatase 2C - metabolism | para-Aminobenzoates - pharmacology | Humans | Caspase 3 - metabolism | Ubiquitin - metabolism | Apoptosis - genetics | Drug Resistance, Neoplasm | Tumor Suppressor Protein p53 - genetics | Pyrrolidines - pharmacology | Dose-Response Relationship, Drug | Proteolysis - drug effects | Protein Phosphatase 2C - antagonists & inhibitors | Neoplasms - genetics | Transcription, Genetic | Antineoplastic Agents - pharmacology | Proto-Oncogene Proteins c-mdm2 - antagonists & inhibitors | Cell Survival - drug effects | Dipeptides - pharmacology | Tumor Suppressor Protein p53 - metabolism | Imidazoles - pharmacology | Piperazines - pharmacology | Drug Synergism | Catalysis - drug effects | Aminopyridines - pharmacology | Cell Line, Tumor | Mutation | Protein Phosphatase 2C - genetics | Potentiation | GSK2830371 | WIP1 | PPM1D | TP53 | MDM2 inhibitor
DRUG-SENSITIVITY | APOPTOSIS | PPM1D MUTATIONS | ONCOLOGY | PHOSPHORYLATION | DNA-DAMAGE | GENE-EXPRESSION | WIP1 PHOSPHATASE | P53 PATHWAY | CANCER | G1 CHECKPOINT | Caspase 7 - metabolism | Neoplasms - metabolism | Apoptosis - drug effects | Protein Phosphatase 2C - metabolism | para-Aminobenzoates - pharmacology | Humans | Caspase 3 - metabolism | Ubiquitin - metabolism | Apoptosis - genetics | Drug Resistance, Neoplasm | Tumor Suppressor Protein p53 - genetics | Pyrrolidines - pharmacology | Dose-Response Relationship, Drug | Proteolysis - drug effects | Protein Phosphatase 2C - antagonists & inhibitors | Neoplasms - genetics | Transcription, Genetic | Antineoplastic Agents - pharmacology | Proto-Oncogene Proteins c-mdm2 - antagonists & inhibitors | Cell Survival - drug effects | Dipeptides - pharmacology | Tumor Suppressor Protein p53 - metabolism | Imidazoles - pharmacology | Piperazines - pharmacology | Drug Synergism | Catalysis - drug effects | Aminopyridines - pharmacology | Cell Line, Tumor | Mutation | Protein Phosphatase 2C - genetics | Potentiation | GSK2830371 | WIP1 | PPM1D | TP53 | MDM2 inhibitor
Journal Article
Frontiers in Plant Science, ISSN 1664-462X, 04/2014, Volume 5
The loss of key biosynthetic pathways is a common feature of important parasitic protists, making them heavily dependent on scavenging nutrients from their...
Protozoa | Hexose | Amino acid | Parasite | Purine | Transport | Transporter | Protist | amino acid | INOSINE-GUANOSINE TRANSPORTER | CONFER DRUG-RESISTANCE | FUNCTIONAL-CHARACTERIZATION | transport | protozoa | PLANT SCIENCES | BINDING CASSETTE TRANSPORTER | PFNT1 NUCLEOSIDE TRANSPORTER | parasite | GLUCOSE-TRANSPORTER | PLASMODIUM-FALCIPARUM | transporter | protist | purine | hexose | MALARIA PARASITE | TOXOPLASMA-GONDII | LEISHMANIA-DONOVANI | nutrient
Protozoa | Hexose | Amino acid | Parasite | Purine | Transport | Transporter | Protist | amino acid | INOSINE-GUANOSINE TRANSPORTER | CONFER DRUG-RESISTANCE | FUNCTIONAL-CHARACTERIZATION | transport | protozoa | PLANT SCIENCES | BINDING CASSETTE TRANSPORTER | PFNT1 NUCLEOSIDE TRANSPORTER | parasite | GLUCOSE-TRANSPORTER | PLASMODIUM-FALCIPARUM | transporter | protist | purine | hexose | MALARIA PARASITE | TOXOPLASMA-GONDII | LEISHMANIA-DONOVANI | nutrient
Journal Article