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1. Full Text Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia
by Gunnarsson, Rebeqa and Dilorenzo, Sebastian and Lundin-Ström, Kristina B and Olsson, Linda and Biloglav, Andrea and Lilljebjörn, Henrik and Rissler, Marianne and Wahlberg, Per and Lundmark, Anders and Castor, Anders and Behrendtz, Mikael and Fioretos, Thoas and Paulsson, Kajsa and Isaksson, Anders and Johansson, Bertil and Region Östergötland and Medicinska fakulteten and Linköpings universitet and H.K.H. Kronprinsessan Victorias barn- och ungdomssjukhus and Institutionen för klinisk och experimentell medicin and Barn- och kvinnocentrum and Avdelningen för barns och kvinnors hälsa
Leukemia, ISSN 0887-6924, 10/2018, Volume 32, Issue 10, pp. 2117 - 2125
High-throughput sequencing was applied to investigate the mutation/methylation patterns on 1q and gene expression profiles in pediatric B-cell precursor acute... 
MULTIPLE-MYELOMA | ONCOLOGY | CHROMOSOME-1 ABNORMALITIES | IN-SITU HYBRIDIZATION | TANDEM DUPLICATION | ACUTE MYELOID-LEUKEMIA | COMPARATIVE GENOMIC HYBRIDIZATION | SEQUENCING DATA | HEMATOLOGY | CANCER | DIFFERENTIAL DNA METHYLATION | DEATH-ASSOCIATED PROTEIN-3 | Care and treatment | Gene mutations | Development and progression | Genetic aspects | Acute lymphocytic leukemia | Gene expression | Health aspects | Pediatrics | Gene dosage | Deregulation | Acute lymphatic leukemia | Exons | Leukemia | Genes | Catalytic activity | Lymphatic leukemia | Ribonucleic acid--RNA | Biological activity | Chromosome 1 | Gene sequencing | Proteins | Poly(ADP-ribose) Polymerase 1 | Next-generation sequencing | Lymphocytes B | Precursors | DNA methylation | Mutation | Catalysis | Methylation | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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2. Full Text Imatinib after induction for treatment of children and adolescents with Philadelphia-chromosome-positive acute lymphoblastic leukaemia (EsPhALL): a randomised, open-label, intergroup study
by Biondi, Andrea, Prof and Schrappe, Martin, Prof and De Lorenzo, Paola, PhD and Castor, Anders, PhD and Lucchini, Giovanna, MD and Gandemer, Virginie, MD and Pieters, Rob, Prof and Stary, Jan, MD and Escherich, Gabriele, MD and Campbell, Myriam, MD and Li, Chi-Kong, MD and Vora, Ajay, MD and Aricò, Maurizio, MD and Röttgers, Silja, PhD and Saha, Vaskar, Prof and Valsecchi, Maria Grazia, Prof and Paediatrics (Lund) and Lund University and Lunds universitet and Pediatrik, Lund
Lancet Oncology, The, ISSN 1470-2045, 2012, Volume 13, Issue 9, pp. 936 - 945
Summary Background Trials of imatinib have provided evidence of activity in adults with Philadelphia-chromosome-positive acute lymphoblastic leukaemia (ALL),... 
Hematology, Oncology and Palliative Medicine | MESYLATE | THERAPY | INHIBITION | ONCOLOGY | AIEOP-BFM | TYROSINE KINASE | T-CELL | STEM-CELL TRANSPLANTATION | COMBINATION | CHEMOTHERAPY | STRATIFICATION | Piperazines - administration & dosage | Precursor Cell Lymphoblastic Leukemia-Lymphoma - surgery | Risk Assessment | Pyrimidines - administration & dosage | Humans | Child, Preschool | Infant | Male | Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality | Survival Rate | Imatinib Mesylate | Incidence | Neoplasm, Residual | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Stem Cell Transplantation | Disease-Free Survival | Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Adolescent | Female | Neoplasm Recurrence, Local - epidemiology | Benzamides | Child | Philadelphia Chromosome | Antimitotic agents | Preventive health services for children | Chemotherapy | Stem cells | Transplantation | Children | Antineoplastic agents | Medicine, Preventive | Cancer | Preventive health services | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Cancer and Oncology | Medicin och hälsovetenskap | Cancer och onkologi
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3. Full Text Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia
by Gunnarsson, Rebeqa and Dilorenzo, Sebastian and Lundin-Ström, Kristina B and Olsson, Linda and Biloglav, Andrea and Lilljebjörn, Henrik and Rissler, Marianne and Wahlberg, Per and Lundmark, Anders and Castor, Anders and Behrendtz, Mikael and Fioretos, Thoas and Paulsson, Kajsa and Isaksson, Anders and Johansson, Bertil and Paediatrics (Lund) and Lund University and Division of Clinical Genetics and Avdelningen för klinisk genetik and Pediatrik, Lund and Lunds universitet
Leukemia, ISSN 0887-6924, 03/2018, Volume 32, Issue 10, p. 2117
High-throughput sequencing was applied to investigate the mutation/methylation patterns on 1q and gene expression profiles in pediatric B-cell precursor acute... 
Clinical Medicine | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Klinisk medicin | Cancer and Oncology | Cancer och onkologi
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4. Full Text Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia
by Gunnarsson, Rebeqa and DiLorenzo, Sebastian and Lundin-Ström, Kristina B and Olsson, Linda and Biloglav, Andrea and Lilljebjörn, Henrik and Rissler, Marianne and Wahlberg, Per and Lundmark, Anders and Castor, Anders and Behrendtz, Mikael and Fioretos, Thoas and Paulsson, Kajsa and Isaksson, Anders and Johansson, Bertil and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för medicinsk biokemi och mikrobiologi and Molekylär medicin and Uppsala universitet and Institutionen för medicinska vetenskaper
Leukemia, ISSN 1476-5551, 2018, Volume 32, Issue 10, p. 2117
High-throughput sequencing was applied to investigate the mutation/methylation patterns on 1q and gene expression profiles in pediatric B-cell precursor acute... 
Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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5. Full Text Transmission of HIV Drug Resistance and the Predicted Effect on Current First-line Regimens in Europe
by Hofstra, L. Marije and Sauvageot, Nicolas and Albert, Jan and Alexiev, Ivailo and Garcia, Federico and Struck, Daniel and van de Vijver, David A. M. C and Åsjö, Birgitta and Beshkov, Danail and Coughlan, Suzie and Descamps, Diane and Griskevicius, Algirdas and Hamouda, Osamah and Horban, Anzej and van Kasteren, Marjo and Kolupajeva, Tatjana and Kostrikis, Leondios G and Liitsola, Kirsi and Linka, Marek and Mor, Orna and Nielsen, Claus and Otelea, Dan and Paraskevis, Dimitrios and Paredes, Roger and Poljak, Mario and Puchhammer-Stöckl, Elisabeth and Sönnerborg, Anders and Staneková, Danica and Stanojevic, Maja and van Laethem, Kristel and Zazzi, Maurizio and Zidovec Lepej, Snjezana and Boucher, Charles A. B and Schmit, Jean-Claude and Wensing, Annemarie M. J and Puchhammer-Stockl, E and Sarcletti, M and Schmied, B and Geit, M and Balluch, G and Vandamme, A.-M and Vercauteren, J and Derdelinckx, I and Sasse, A and Bogaert, M and Ceunen, H and de Roo, A and de Wit, S and Echahidi, F and Langebeek, N and SPREAD Program
Clinical infectious diseases, ISSN 1058-4838, 2016, Volume 62, Issue 5, pp. 655 - 663
Background. Numerous studies have shown that baseline drug resistance patterns may influence the outcome of antiretroviral therapy. Therefore, guidelines... 
HIV-1 | Drug resistance | Europe | Antiretroviral therapy | Transmission | INFECTIOUS DISEASES | INTEGRASE | antiretroviral therapy | MICROBIOLOGY | PREVALENCE | IMMUNOLOGY | INDIVIDUALS | transmission | REVERSE-TRANSCRIPTASE INHIBITORS | EFAVIRENZ | INFECTION | drug resistance | RILPIVIRINE | MUTATIONS | ANTIRETROVIRAL TREATMENT | ETRAVIRINE | Anti-HIV Agents - pharmacology | Prevalence | HIV-1 - drug effects | HIV Infections - virology | Humans | Middle Aged | Reverse Transcriptase Inhibitors - pharmacology | Male | HIV-1 - genetics | HIV Protease Inhibitors - pharmacology | Microbial Sensitivity Tests | Drug Resistance, Viral - genetics | Adult | Female | HIV Infections - drug therapy | Mutation | Prevention | Antiviral agents | Control | Care and treatment | Disease transmission | Analysis | Dosage and administration | HIV infection | HIV | AIDS
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6. Full Text The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia
by Paulsson, Kajsa and Lilljebjörn, Henrik and Biloglav, Andrea and Olsson, Linda and Rissler, Marianne and Castor, Anders and Barbany, Gisela and Fogelstrand, Linda and Nordgren, Ann and Sjögren, Helene and Fioretos, Thoas and Johansson, Bertil and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Institutionen för biomedicin, avdelningen för klinisk kemi och transfusionsmedicin and Institute of Biomedicine, Department of Clinical Chemistry and Transfusion Medicine and Sahlgrenska Academy
Nature Genetics, ISSN 1061-4036, 05/2015, Volume 47, Issue 6, pp. 672 - 676
High hyperdiploid (51-67 chromosomes) acute lymphoblastic leukemia (ALL) is one of the most common childhood malignancies, comprising 30% of all pediatric B... 
REARRANGEMENT | FREQUENT | TWINS | RAS | FLT3 | GENES | GENETICS & HEREDITY | KRAS | MUTATIONS | EXPRESSION | CANCER | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Diploidy | Humans | Adolescent | Child, Preschool | Female | Infant | Male | Polymorphism, Single Nucleotide | Mutation | Genome, Human | Child | Genetic susceptibility | Oncology, Experimental | Genetic research | Development and progression | Genetic aspects | Acute lymphocytic leukemia | Research | Identification and classification | Health aspects | Cancer | Studies | Pediatrics | Genomics | Cell division | Genomes | Grants | Gene expression | Chromosomes | Genetics & Heredity | Genetik | Genetics
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7. Full Text Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia
by Lilljebjörn, Henrik and Henningsson, Rasmus and Hyrenius-Wittsten, Axel and Olsson, Linda and Orsmark-Pietras, Christina and Von Palffy, Sofia and Askmyr, Maria and Rissler, Marianne and Schrappe, Martin and Cario, Gunnar and Castor, Anders and Pronk, Cornelis J.H and Behrendtz, Mikael and Mitelman, Felix and Johansson, Bertil and Paulsson, Kajsa and Andersson, Anna K and Fontes, Magnus and Fioretos, Thoas and Division of Molecular Hematology (DMH) and Mathematics (Faculty of Engineering) and Division of Clinical Genetics and Aneuploidy in cancer and Avdelningen för klinisk genetik and Translational Genomic and Functional Studies of Leukemia and The pathogenetic mechanisms behind MLL-rearranged acute leukemia in infancy and Hematopoetisk och immunologisk utveckling and Hematopoietic and immunologic developement and Lunds universitet and MLL-rearrangerad leukemi hos spädbarn and Avdelningen för molekylär hematologi and Paediatrics (Lund) and Lund University and Matematik LTH and Translationella genomiska och funktionella studier av leukemi and Pediatrik, Lund and Aneuploidi i cancer and BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation
Nature Communications, ISSN 2041-1723, 06/2016, Volume 7, Issue 1, p. 11790
Fusion genes are potent driver mutations in cancer. In this study, we delineate the fusion gene landscape in a consecutive series of 195 paediatric B-cell... 
GENOMIC LANDSCAPE | FUSION | ERG DELETION | MULTIDISCIPLINARY SCIENCES | IKZF1 DELETION | TRANSCRIPTION | CLASSIFICATION | MUTATIONS | EXPRESSION | GENETIC ALTERATIONS | CHILDREN | Alternative Splicing - genetics | Humans | Gene Expression Regulation, Neoplastic | Gene Regulatory Networks | Homeodomain Proteins - genetics | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - genetics | DNA Mutational Analysis | Oncogene Proteins, Fusion - genetics | Gene Rearrangement - genetics | Child | Principal Component Analysis | Chromosome Breakage | Cluster Analysis | Cohort Studies | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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8. Full Text Adherence to childhood cancer treatment: a prospective cohort study from Northern Vietnam
by Lan, Bui Ngoc and Castor, Anders and Wiebe, Thomas and Toporski, Jacek and Moëll, Christian and Hagander, Lars
BMJ Open, ISSN 2044-6055, 08/2019, Volume 9, Issue 8, p. e026863
ObjectivesGlobal incidence and attention to childhood cancer is increasing and treatment abandonment is a major cause of treatment failure in low- and... 
Low income groups | Health risk assessment | Cancer therapies | Developing countries--LDCs
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9. Full Text Whole-exome sequencing exploration of acquired uniparental disomies in B-cell precursor acute lymphoblastic leukemia
by Lundin-Ström, Kristina B and Biloglav, Andrea and Lilljebjörn, Henrik and Rissler, Marianne and Fioretos, Thoas and Hansson, Markus and Behrendtz, Mikael and Castor, Anders and Olsson, Linda and Johansson, Bertil and Medicinska fakulteten and Region Östergötland and Linköpings universitet and Institutionen för klinisk och experimentell medicin and H.K.H. Kronprinsessan Victorias barn- och ungdomssjukhus and Barn- och kvinnocentrum and Avdelningen för barns och kvinnors hälsa
Leukemia, ISSN 0887-6924, 09/2018, Volume 32, Issue 9, pp. 2058 - 2062
PROLIFERATION | ONCOLOGY | HEMATOLOGY | ACUTE MYELOID LEUKEMIAS | MUTATION | SUSCEPTIBILITY | Computational Biology - methods | Genetic Predisposition to Disease | Genetic Association Studies | Humans | Databases, Genetic | Genotype | Whole Exome Sequencing | Genetic Variation | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - genetics | Uniparental Disomy - genetics | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - diagnosis | Alleles | Chromosome Aberrations | Polymorphism, Single Nucleotide | Usage | Gene mutations | Exome sequencing | Cytogenetics | Genetic aspects | B cells | Research | Single nucleotide polymorphisms | Acute lymphocytic leukemia | Diagnosis | Exploration | Acute lymphatic leukemia | Lymphatic leukemia | Lymphocytes B | Leukemia | Brief Communication | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
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10. Full Text Improved cytogenetic characterization and risk stratification of pediatric acute lymphoblastic leukemia using single nucleotide polymorphism array analysis: A single center experience of 296 cases
by Olsson, Linda and Lundin‐Ström, Kristina B and Castor, Anders and Behrendtz, Mikael and Biloglav, Andrea and Norén‐Nyström, Ulrika and Paulsson, Kajsa and Johansson, Bertil and Region Östergötland and Medicinska fakulteten and Linköpings universitet and H.K.H. Kronprinsessan Victorias barn- och ungdomssjukhus and Institutionen för klinisk och experimentell medicin and Barn- och kvinnocentrum and Avdelningen för barns och kvinnors hälsa
Genes, Chromosomes and Cancer, ISSN 1045-2257, 11/2018, Volume 57, Issue 11, pp. 604 - 607
Single nucleotide polymorphism array (SNP‐A) analyses are increasingly being introduced in routine genetic diagnostics of acute lymphoblastic leukemia (ALL).... 
array analysis | single nucleotide polymorphism | clinical genetic diagnostics | pediatric acute lymphoblastic leukemia | PATHWAYS | ONCOLOGY | GENETICS & HEREDITY | CHILDHOOD | LESIONS | REVEALS | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Precursor Cell Lymphoblastic Leukemia-Lymphoma - epidemiology | Humans | Adolescent | Child, Preschool | Polymorphism, Single Nucleotide - genetics | Infant | Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis | Cytogenetic Analysis | Child | Infant, Newborn | Cohort Studies | Pediatrics | Medical research | Medicine, Experimental | Genetic aspects | Acute lymphocytic leukemia | Single nucleotide polymorphisms | T cells | Chromosomes | Acute lymphatic leukemia | Copy number | Leukemia | Karyotypes | Minimal residual disease | Risk | Single-nucleotide polymorphism | Lymphocytes T | Lymphatic leukemia | Pax5 protein | Gene polymorphism | Banding | Lymphocytes B | Diagnostic systems | Polymorphism | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | array analysis; clinical genetic diagnostics; pediatric acute lymphoblastic leukemia; single nucleotide polymorphism
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11. Full Text Proteogenomics and Hi-C reveal transcriptional dysregulation in high hyperdiploid childhood acute lymphoblastic leukemia
by Yang, M and Vesterlund, M and Siavelis, I and Moura-Castro, LH and Castor, A and Fioretos, T and Jafari, R and Lilljebjorn, H and Odom, DT and Olsson, L and Ravi, N and Woodward, EL and Harewood, L and Lehtio, J and Paulsson, K and Paediatrics (Lund) and Lund University and Aneuploidy in cancer and Translationella genomiska och funktionella studier av leukemi and Pediatrik, Lund and Genetic and epigenetic studies of pediatric leukemia and Translational Genomic and Functional Studies of Leukemia and Aneuploidi i cancer and BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation and Lunds universitet and Genetiska och epigenetiska studier av barnleukemi
NATURE COMMUNICATIONS, ISSN 2041-1723, 04/2019, Volume 10, Issue 1, pp. 1519 - 15
Hyperdiploidy, i.e. gain of whole chromosomes, is one of the most common genetic features of childhood acute lymphoblastic leukemia (ALL), but its pathogenetic... 
TOPOLOGY | COPY-NUMBER | LANDSCAPE | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | COHESIN | ARCHITECTURE | MUTATIONS | CTCF | IDENTIFICATION | GENOME | Insulation | Regulators | Chromatin | Profiling | Acute lymphatic leukemia | Transcription | Leukemia | Runx1 protein | Mass spectroscopy | Genomes | Lymphatic leukemia | Gene expression | Ribonucleic acid--RNA | Gene sequencing | Proteins | Cohesin | Children | Mass spectrometry | Chromosomes | Borders | Medicinsk genetik | Basic Medicine | Medical Genetics | Clinical Medicine | Pediatrics | Medical and Health Sciences | Medicin och hälsovetenskap | Pediatrik | Medicinska och farmaceutiska grundvetenskaper | Klinisk medicin | Cancer and Oncology | Cancer och onkologi
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12. Full Text Distinct patterns of hematopoietic stem cell involvement in acute lymphoblastic leukemia
by Castor, A and Nilsson, L and Astrand-Grundstrom, [No Value] and Buitenhuis, M and Ramirez, C and Anderson, K and Strombeck, B and Garwicz, S and Bekassy, AN and Schmiegelow, K and Lausen, B and Hokland, P and Lehmann, S and Juliusson, G and Johansson, B and Jacobsen, SEW
Nature Medicine, ISSN 1078-8956, 06/2005, Volume 11, Issue 6, pp. 630 - 637
The cellular targets of primary mutations and malignant transformation remain elusive in most cancers. Here, we show that clinically and genetically different... 
PHILADELPHIA-CHROMOSOME | IN-SITU HYBRIDIZATION | MYELOGENOUS LEUKEMIA | PROGENITOR/STEM CELLS | ACUTE MYELOID-LEUKEMIA | IDENTIFICATION | EXPRESSION | CANCER | MYELODYSPLASTIC SYNDROMES | CHILDREN | MEDICINE, RESEARCH & EXPERIMENTAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL BIOLOGY | Antigens, CD34 | Translocation, Genetic | Precursor Cell Lymphoblastic Leukemia-Lymphoma - immunology | Humans | ADP-ribosyl Cyclase | ADP-ribosyl Cyclase 1 | Oncogene Proteins, Fusion - physiology | Repressor Proteins - physiology | Flow Cytometry | Core Binding Factor Alpha 2 Subunit | Hematopoietic Stem Cells - physiology | Adult | Membrane Glycoproteins | Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology | Child | Chromosomes, Human, Pair 21 | Proto-Oncogene Proteins c-ets | DNA-Binding Proteins - physiology | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Fusion Proteins, bcr-abl - genetics | Phenotype | Fusion Proteins, bcr-abl - physiology | Antigens, CD19 | Nuclear Proteins - physiology | Chromosomes, Human, Pair 12 | Mutation | Precursor Cell Lymphoblastic Leukemia-Lymphoma - classification | Antigens, CD | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
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13. Full Text Cooperative genetic changes in pediatric B‐cell precursor acute lymphoblastic leukemia with deletions or mutations of IKZF1
by Olsson, Linda and Albitar, Ferras and Castor, Anders and Behrendtz, Mikael and Biloglav, Andrea and Paulsson, Kajsa and Johansson, Bertil and Medicinska fakulteten and Region Östergötland and Barn- och ungdomskliniken i Linköping and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Avdelningen för kliniska vetenskaper and Barn- och kvinnocentrum
Genes, Chromosomes and Cancer, ISSN 1045-2257, 05/2015, Volume 54, Issue 5, pp. 315 - 325
In contrast to IKZF1 deletions (ΔIKZF1), IKZF1 sequence mutations (mutIKZF1) have been reported to be rare in B‐cell precursor acute lymphoblastic leukemia and... 
IKAROS GENE | IMPACT | ERG DELETION | ONCOLOGY | KINASE | GENETICS & HEREDITY | DIFFERENTIATION | MINIMAL RESIDUAL DISEASE | TRANSCRIPTION FACTOR | EXPRESSION | CHILDRENS ONCOLOGY GROUP | CRLF2 | Ikaros Transcription Factor - genetics | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - genetics | Sequence Deletion | Prognosis | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - diagnosis | Base Sequence | Humans | Adolescent | Polymorphism, Single Nucleotide | Mutation | Child | Clinical Medicine | Pediatrics | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Pediatrik
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