Marilyn Li

Summary

Affiliation: Tulane University
Country: USA

Publications

  1. ncbi request reprint Advanced molecular and cytogenetic technologies in birth defect diagnosis and prevention
    Marilyn M Li
    Hayward Genetics Center and Department of Pediatrics, Tulane University Health Science Center, New Orleans, LA 70112, USA
    Beijing Da Xue Xue Bao 37:14-9. 2005
  2. pmc Clinical cytogenetics and molecular cytogenetics
    Marilyn Li
    Medical School, Tulane University, New Orleans, LA 70112 2699, USA
    J Zhejiang Univ Sci B 7:162-3. 2006
  3. pmc Human cancer genetics
    Marilyn Li
    Medical School, Tulane University, New Orleans, LA 70112 2699, USA
    J Zhejiang Univ Sci B 7:164. 2006
  4. pmc Characterization of a cryptic 3.3 Mb deletion in a patient with a "balanced t(15;22) translocation" using high density oligo array CGH and gene expression arrays
    Marilyn M Li
    Hayward Genetics Center, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA
    Am J Med Genet A 146:368-75. 2008
  5. ncbi request reprint Imatinib (ST1571) provides only limited selectivity for CML cells and treatment might be complicated by silent BCR-ABL genes
    Guanchao Jiang
    Tulane Cancer Center and Humon Genetics Program, Tulane Medical School, New Orleans, Lousiana 70112, USA
    Cancer Biol Ther 2:103-8. 2003
  6. pmc Fluorescence in situ hybridization using an old world monkey Y chromosome specific probe combined with immunofluorescence staining on rhesus monkey tissues
    Xiujin Xia
    Department of Pharmacologiy, Tulane University Health Sciences Center, New Orleans, LA, USA
    J Histochem Cytochem 55:1115-21. 2007
  7. doi request reprint Classification of multicolor fluorescence in situ hybridization (M-FISH) images with sparse representation
    Hongbao Cao
    Department of Biomedical Engineering, Tulane University, New Orleans, LA 70118, USA
    IEEE Trans Nanobioscience 11:111-8. 2012
  8. ncbi request reprint Trisomy 4 as the sole cytogenetic abnormality in a Waldenström macroglobulinemia
    Ada I Rivera
    Department of Pathology and Laboratory Medicine, Tulane Health Sciences Center, New Orleans, LA 70131, USA
    Cancer Genet Cytogenet 133:172-3. 2002
  9. ncbi request reprint A novel interstitial deletion on the long arm of chromosome 16 in a patient with chronic myelomonocytic leukemia
    Lukasz K Kozon
    Cancer Genet Cytogenet 162:92-4. 2005

Collaborators

Detail Information

Publications9

  1. ncbi request reprint Advanced molecular and cytogenetic technologies in birth defect diagnosis and prevention
    Marilyn M Li
    Hayward Genetics Center and Department of Pediatrics, Tulane University Health Science Center, New Orleans, LA 70112, USA
    Beijing Da Xue Xue Bao 37:14-9. 2005
    ....
  2. pmc Clinical cytogenetics and molecular cytogenetics
    Marilyn Li
    Medical School, Tulane University, New Orleans, LA 70112 2699, USA
    J Zhejiang Univ Sci B 7:162-3. 2006
    ....
  3. pmc Human cancer genetics
    Marilyn Li
    Medical School, Tulane University, New Orleans, LA 70112 2699, USA
    J Zhejiang Univ Sci B 7:164. 2006
    ..They will also review presymptomatic testing of hereditary cancers, and the application of expression profiling to identify patients likely to benefit from particular therapeutic approaches...
  4. pmc Characterization of a cryptic 3.3 Mb deletion in a patient with a "balanced t(15;22) translocation" using high density oligo array CGH and gene expression arrays
    Marilyn M Li
    Hayward Genetics Center, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA
    Am J Med Genet A 146:368-75. 2008
    ..Both approaches can assist in the elucidation of the etiology of unexplained phenotypic differences in cases such as this one...
  5. ncbi request reprint Imatinib (ST1571) provides only limited selectivity for CML cells and treatment might be complicated by silent BCR-ABL genes
    Guanchao Jiang
    Tulane Cancer Center and Humon Genetics Program, Tulane Medical School, New Orleans, Lousiana 70112, USA
    Cancer Biol Ther 2:103-8. 2003
    ..Our results indicate that IM is only partially specific for CML progenitor cells compared to normal hematopoietic progenitor cells and suggest that some CML cells may have a silent BCR-ABL oncogene that could interfere with therapy...
  6. pmc Fluorescence in situ hybridization using an old world monkey Y chromosome specific probe combined with immunofluorescence staining on rhesus monkey tissues
    Xiujin Xia
    Department of Pharmacologiy, Tulane University Health Sciences Center, New Orleans, LA, USA
    J Histochem Cytochem 55:1115-21. 2007
    ..These studies indicate that our FISH immunofluorescence technique can be reliably used to identify and phenotype male cells in paraffin-embedded rhesus monkey tissues...
  7. doi request reprint Classification of multicolor fluorescence in situ hybridization (M-FISH) images with sparse representation
    Hongbao Cao
    Department of Biomedical Engineering, Tulane University, New Orleans, LA 70118, USA
    IEEE Trans Nanobioscience 11:111-8. 2012
    ....
  8. ncbi request reprint Trisomy 4 as the sole cytogenetic abnormality in a Waldenström macroglobulinemia
    Ada I Rivera
    Department of Pathology and Laboratory Medicine, Tulane Health Sciences Center, New Orleans, LA 70131, USA
    Cancer Genet Cytogenet 133:172-3. 2002
    ..Trisomy 4 has been reported in other hematologic malignancies including acute myeloid and lymphoid leukemias...
  9. ncbi request reprint A novel interstitial deletion on the long arm of chromosome 16 in a patient with chronic myelomonocytic leukemia
    Lukasz K Kozon
    Cancer Genet Cytogenet 162:92-4. 2005