Fern F. Tsien, Ph.D.
Affiliations: | 2002 | Tulane University, New Orleans, LA, United States |
Area:
Genetics, Molecular BiologyGoogle:
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Sign in to add mentor| Melanie Ehrlich | grad student | 2002 | Tulane | |
| (DNA methylation and constitutive heterochromatin in the ICF syndrome, FSHD syndrome, and normal human embryonic cell cultures.) | ||||
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| Gleditsch K, Peñas J, Mercer D, et al. (2020) Intratumoral Translocation Positive Heterogeneity in Pediatric Alveolar Rhabdomyosarcoma Tumors Correlates to Patient Survival Prognosis Frontiers in Cell and Developmental Biology. 8 |
| Mercer D, Hurley A, Tsien F. (2017) Detailed Audiological Evaluation of a Patient with Xeroderma Pigmentosum with Neural Degeneration. Journal of the American Academy of Audiology. 28: 80-90 |
| Loupe JM, Miller PJ, Bonner BP, et al. (2016) Acquisition of an oncogenic fusion protein serves as an initial driving mutation by inducing aneuploidy and overriding proliferative defects. Oncotarget |
| Howe B, Umrigar A, Tsien F. (2014) Chromosome preparation from cultured cells. Journal of Visualized Experiments : Jove. e50203 |
| Izadpanah R, Kaushal D, Kriedt C, et al. (2008) Long-term in vitro expansion alters the biology of adult mesenchymal stem cells. Cancer Research. 68: 4229-38 |
| Tsien F, Morava E, Talarski A, et al. (2005) Phenotypic features of a boy with trisomy of 16q22-->qter due to paternal Y; 16 translocation. Clinical Dysmorphology. 14: 177-181 |
| Tsien F, Fiala ES, Youn B, et al. (2002) Prolonged culture of normal chorionic villus cells yields ICF syndrome-like chromatin decondensation and rearrangements Cytogenetic and Genome Research. 98: 13-21 |
| Ehrlich M, Tsien F, Herrera D, et al. (2001) High frequencies of ICF syndrome-like pericentromeric heterochromatin decondensation and breakage in chromosome 1 in a chorionic villus sample. Journal of Medical Genetics. 38: 882-884 |
| Ehrlich M, Buchanan KL, Tsien F, et al. (2001) DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes Human Molecular Genetics. 10: 2917-2931 |
| Tsien F, Sun B, Hopkins NE, et al. (2001) Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues. Molecular Genetics and Metabolism. 74: 322-31 |