| Year |
Citation |
Score |
| 2020 |
Gleditsch K, Peñas J, Mercer D, Umrigar A, Briscoe J, Stark M, Tsien F, Hollenbach AD. Intratumoral Translocation Positive Heterogeneity in Pediatric Alveolar Rhabdomyosarcoma Tumors Correlates to Patient Survival Prognosis Frontiers in Cell and Developmental Biology. 8. DOI: 10.3389/Fcell.2020.564136 |
0.349 |
|
| 2017 |
Mercer D, Hurley A, Tsien F. Detailed Audiological Evaluation of a Patient with Xeroderma Pigmentosum with Neural Degeneration. Journal of the American Academy of Audiology. 28: 80-90. PMID 28054914 DOI: 10.3766/Jaaa.15112 |
0.324 |
|
| 2016 |
Loupe JM, Miller PJ, Bonner BP, Maggi EC, Vijayaraghavan J, Zabaleta J, Taylor CM, Tsien F, Crabtree JS, Hollenbach AD. Acquisition of an oncogenic fusion protein serves as an initial driving mutation by inducing aneuploidy and overriding proliferative defects. Oncotarget. PMID 27588498 DOI: 10.18632/Oncotarget.11716 |
0.341 |
|
| 2014 |
Howe B, Umrigar A, Tsien F. Chromosome preparation from cultured cells. Journal of Visualized Experiments : Jove. e50203. PMID 24513647 DOI: 10.3791/50203 |
0.583 |
|
| 2008 |
Izadpanah R, Kaushal D, Kriedt C, Tsien F, Patel B, Dufour J, Bunnell BA. Long-term in vitro expansion alters the biology of adult mesenchymal stem cells. Cancer Research. 68: 4229-38. PMID 18519682 DOI: 10.1158/0008-5472.Can-07-5272 |
0.327 |
|
| 2005 |
Tsien F, Morava E, Talarski A, Marble M. Phenotypic features of a boy with trisomy of 16q22-->qter due to paternal Y; 16 translocation. Clinical Dysmorphology. 14: 177-181. PMID 16155418 DOI: 10.1097/00019605-200510000-00002 |
0.505 |
|
| 2002 |
Tsien F, Fiala ES, Youn B, Long TI, Laird PW, Weissbecker K, Ehrlich M. Prolonged culture of normal chorionic villus cells yields ICF syndrome-like chromatin decondensation and rearrangements Cytogenetic and Genome Research. 98: 13-21. PMID 12584436 DOI: 10.1159/000068543 |
0.656 |
|
| 2001 |
Ehrlich M, Tsien F, Herrera D, Blackman V, Roggenbuck J, Tuck-Muller CM. 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. PMID 11768395 DOI: 10.1136/Jmg.38.12.882 |
0.7 |
|
| 2001 |
Ehrlich M, Buchanan KL, Tsien F, Jiang G, Sun B, Uicker W, Weemaes CMR, Smeets D, Sperling K, Belohradsky BH, Tommerup N, Misek DE, Rouillard JM, Kuick R, Hanash SM. DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes Human Molecular Genetics. 10: 2917-2931. PMID 11741835 DOI: 10.1093/Hmg/10.25.2917 |
0.569 |
|
| 2001 |
Tsien F, Sun B, Hopkins NE, Vedanarayanan V, Figlewicz D, Winokur S, Ehrlich M. Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues. Molecular Genetics and Metabolism. 74: 322-31. PMID 11708861 DOI: 10.1006/Mgme.2001.3219 |
0.688 |
|
| 2000 |
Jackson KE, Tsien F, Marble M. Phenotypic features in a boy with monosomy 18 mosaicism. American Journal of Medical Genetics. 95: 229-32. PMID 11102928 DOI: 10.1002/1096-8628(20001127)95:3<229::Aid-Ajmg8>3.0.Co;2-3 |
0.436 |
|
| 2000 |
Tuck-Muller CM, Narayan A, Tsien F, Smeets DF, Sawyer J, Fiala ES, Sohn OS, Ehrlich M. DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients. Cytogenetics and Cell Genetics. 89: 121-8. PMID 10894953 DOI: 10.1159/000015590 |
0.57 |
|
| 1998 |
Marble M, Morava E, Tsien F, Amedee R, Pierce M. Subglottic web in a mother and son with 22q11.2 deletion. American Journal of Medical Genetics. 75: 537-537. PMID 9489801 DOI: 10.1002/(Sici)1096-8628(19980217)75:5<537::Aid-Ajmg16>3.0.Co;2-L |
0.384 |
|
| 1997 |
Gill JI, Varela M, Tsien F, Krause JR. der(1)t(1;19)(p12;p11): A new nonrandom chromosomal abnormality in myelodysplastic syndrome Cancer Genetics and Cytogenetics. 94: 85-87. PMID 9109932 DOI: 10.1016/S0165-4608(96)00188-4 |
0.452 |
|
| 1995 |
Varela M, Aydin F, Tsien F, Johnson J. Extensive cytogenetic evaluation of a sacral chordoma (including fluorescent in situ hybridization) Cancer Genetics and Cytogenetics. 84: 154. DOI: 10.1016/0165-4608(96)85301-5 |
0.321 |
|
| Show low-probability matches. |