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Clinical Chemistry, ISSN 0009-9147, 02/2019, Volume 65, Issue 2, pp. 345 - 347
[...]we successfully quantified the target sequences in diagnostic bone marrow samples as ranging between 17% and 29% (Table 1). [...]we quantified the load of... 
MEDICAL LABORATORY TECHNOLOGY | Neonates | Pediatrics | Medical research | Leukemia | Cloning | Childrens health | Genomes | Chromosome rearrangements | Patients | Gene sequencing | Children & youth | Hospitals | Councils | Bone marrow | Diagnostic systems | Children | Thermal cycling | Deoxyribonucleic acid--DNA | Cancer
Journal Article
Journal Article
Journal Article
Journal Article
Journal of Neuroimmunology, ISSN 0165-5728, 03/2019, Volume 328, pp. 5 - 19
We evaluated the importance of histocompatibility of transplanted MSCs in terms of therapeutic potential. Mouse syngeneic MSCs or allogeneic MSCs were... 
Mesenchymal stem cell | Graft survival | Hind limb function | Immune response | Neuroinflammation | Spinal cord injury | Histocompatibility | BONE-MARROW | IMMUNOLOGY | SUPPRESSION | NEUROSCIENCES | TRANSPLANTATION | PROMOTES FUNCTIONAL RECOVERY | IMMUNOGENICITY | LOCOMOTOR RECOVERY | DIPHTHERIA-TOXIN RECEPTOR | GROWTH-FACTOR | STROMAL CELLS | EXPRESSION
Journal Article
Human Mutation, ISSN 1059-7794, 02/2017, Volume 38, Issue 2, pp. 180 - 192
ABSTRACT Most balanced translocations are thought to result mechanistically from nonhomologous end joining or, in rare cases of recurrent events, by nonallelic... 
balanced chromosomal aberration | whole‐genome sequencing | reciprocal translocation | nonhomologous end joining | microhomology | replication‐based repair mechanisms | replication-based repair mechanisms | whole-genome sequencing | DIAGNOSIS | COMPLEX | REARRANGEMENTS | BREAKPOINTS | DELETION | INTELLECTUAL DISABILITY | ALIGNMENT | GENETICS & HEREDITY | ARCHITECTURE | MUTATIONS | RECEPTORS | Translocation, Genetic | Genetic Association Studies | Humans | Genotype | Homologous Recombination | In Situ Hybridization, Fluorescence | Male | Chromosome Mapping | DNA Copy Number Variations | Whole Genome Sequencing | Phenotype | Comparative Genomic Hybridization | Base Sequence | Female | Genomics - methods | Chromosome Breakage | Karyotype | Tourette's syndrome | Analysis | Genes | Genomics | Genetic research | Genetic aspects | Genomes | Nucleotide sequencing | DNA sequencing | whole genome sequencing | non-homologous end joining | Medical Biotechnology | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinsk bioteknologi | Medical Biotechnology (with a focus on Cell Biology (including Stem Cell Biology), Molecular Biology, Microbiology, Biochemistry or Biopharmacy) | Medicinsk bioteknologi (med inriktning mot cellbiologi (inklusive stamcellsbiologi), molekylärbiologi, mikrobiologi, biokemi eller biofarmaci)
Journal Article
British Journal of Haematology, ISSN 0007-1048, 09/2015, Volume 170, Issue 6, pp. 847 - 858
Summary Paediatric B‐cell precursor acute lymphoblastic leukaemias (BCP ALL) with IKZF1 deletions (∆IKZF1) are associated with a poor outcome. However, there... 
risk‐stratifying factors | paediatric B‐cell precursor acute lymphoblastic leukaemia | IKZF1 deletion | P2RY8‐CRLF2, minimal residual disease | P2RY8-CRLF2, minimal residual disease | Paediatric B-cell precursor acute lymphoblastic leukaemia | Risk-stratifying factors | risk-stratifying factors | ERG DELETION | GENE DELETIONS | IKAROS | RISK | P2RY8-CRLF2 | CHILDHOOD | CHILDREN | POOR-PROGNOSIS | minimal residual disease | paediatric B-cell precursor acute lymphoblastic leukaemia | FLOW-CYTOMETRY | HEMATOLOGY | CRLF2 | REVEALS | Transcriptional Regulator ERG | Translocation, Genetic | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - pathology | Prognosis | Age Factors | Humans | Child, Preschool | Infant | Ikaros Transcription Factor - genetics | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - drug therapy | Sweden | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - mortality | Gene Deletion | Trans-Activators - genetics | Child | Chromosomes, Human, Pair 21 | Gene Expression | Patient Outcome Assessment | Neoplasm, Residual - genetics | Receptor, PAR-1 - genetics | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - genetics | Proto-Oncogene Proteins c-rel - genetics | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Adolescent | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 12 | Cohort Studies | Cytogenetics | Pediatrics | Single nucleotide polymorphisms | minimal sidual disease | Medical and Health Sciences | Medicin och hälsovetenskap | Pediatrik | Klinisk medicin | Clinical Medicine | Cancer and Oncology | Cancer och onkologi
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2016, Volume 98, Issue 2, pp. 373 - 381
Journal Article
Leukemia & Lymphoma, ISSN 1042-8194, 09/2016, Volume 57, Issue 9, pp. 2161 - 2170
Journal Article