M Nilsson

Summary

Affiliation: University Hospital
Country: Sweden

Publications

  1. ncbi Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors
    M Nilsson
    Department of Clinical Genetics, University Hospital, 221 85 Lund, Sweden
    Virchows Arch 441:475-80. 2002
  2. ncbi Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12
    Malin Nilsson
    Department of Clinical Genetics, University Hospital, SE 221 85 Lund, Sweden
    Oncol Rep 13:649-52. 2005
  3. ncbi Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32-->q33 and 12q14-->q15
    M Nilsson
    Department of Clinical Genetics, University Hospital, Lund, Sweden
    Cytogenet Genome Res 112:60-6. 2006
  4. ncbi Fusion of the HMGA2 and NFIB genes in lipoma
    M Nilsson
    Department of Clinical Genetics, University Hospital, 221 85 Lund, Sweden
    Virchows Arch 447:855-8. 2005
  5. ncbi PDGF-A signaling is a critical event in lung alveolar myofibroblast development and alveogenesis
    H Bostrom
    Department of Medical Biochemistry, University of Goteborg, Sweden
    Cell 85:863-73. 1996
  6. ncbi Expression of classical cadherins in thyroid development: maintenance of an epithelial phenotype throughout organogenesis
    H Fagman
    Institute of Anatomy and Cell Biology, Goteborg University, SE 40530 Goteborg, Sweden
    Endocrinology 144:3618-24. 2003
  7. ncbi Multiplex PCR amplification assay for the detection of blaSHV, blaTEM and blaCTX-M genes in Enterobacteriaceae
    H J Monstein
    Division of Clinical Microbiology, University Hospital Linkoping, Linkoping, Sweden
    APMIS 115:1400-8. 2007
  8. ncbi Single-nucleotide sequence discrimination in situ using padlock probes
    M Nilsson
    Uppsala University, Uppsala, Sweden
    Curr Protoc Cytom . 2001

Collaborators

Detail Information

Publications8

  1. ncbi Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors
    M Nilsson
    Department of Clinical Genetics, University Hospital, 221 85 Lund, Sweden
    Virchows Arch 441:475-80. 2002
    ..In four of seven cases there was a breakpoint within the sequence covered by probe 260J21, where the RDC1 gene is located, a gene reported to fuse with HMGIC in lipomas with a 2;12 translocation...
  2. ncbi Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12
    Malin Nilsson
    Department of Clinical Genetics, University Hospital, SE 221 85 Lund, Sweden
    Oncol Rep 13:649-52. 2005
    ..Whether ALTs with these types of aberrations have a lower risk of tumor progression than ALTs with the notoriously mitotically unstable ring and giant marker chromosomes remains to be investigated...
  3. ncbi Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32-->q33 and 12q14-->q15
    M Nilsson
    Department of Clinical Genetics, University Hospital, Lund, Sweden
    Cytogenet Genome Res 112:60-6. 2006
    ....
  4. ncbi Fusion of the HMGA2 and NFIB genes in lipoma
    M Nilsson
    Department of Clinical Genetics, University Hospital, 221 85 Lund, Sweden
    Virchows Arch 447:855-8. 2005
    ..Since similar 9;12 translocations have been described also in rare cases of hamartoma and uterine leiomyoma, the occurrence of HMGA2/NFIB could be postulated in these tumors as well...
  5. ncbi PDGF-A signaling is a critical event in lung alveolar myofibroblast development and alveogenesis
    H Bostrom
    Department of Medical Biochemistry, University of Goteborg, Sweden
    Cell 85:863-73. 1996
    ..The two PDGF null phenotypes also reveal analogous morphogenetic functions for myofibroblast-type cells in lung and kidney organogenesis...
  6. ncbi Expression of classical cadherins in thyroid development: maintenance of an epithelial phenotype throughout organogenesis
    H Fagman
    Institute of Anatomy and Cell Biology, Goteborg University, SE 40530 Goteborg, Sweden
    Endocrinology 144:3618-24. 2003
    ....
  7. ncbi Multiplex PCR amplification assay for the detection of blaSHV, blaTEM and blaCTX-M genes in Enterobacteriaceae
    H J Monstein
    Division of Clinical Microbiology, University Hospital Linkoping, Linkoping, Sweden
    APMIS 115:1400-8. 2007
    ..Apparently, the universal well-established CTX-M primer pair used here to reveal plasmid-encoded (bla)CTX-M genes would also amplify the chromosomally located K-1 enzyme gene in all Klebsiella oxytoca strains included in the study...
  8. ncbi Single-nucleotide sequence discrimination in situ using padlock probes
    M Nilsson
    Uppsala University, Uppsala, Sweden
    Curr Protoc Cytom . 2001
    ..The discussion of probe synthesis has been greatly expanded and an Alternate Protocol 1 added for enzymatic probe ligation at low probe concentration. A new Support Protocol describes enzymatic probe synthesis...