☰

Yingying Tang, Ph.D. - Publications

Affiliations: 
2000 Columbia University, New York, NY 
Area:
Genetics
Tree Info Similar researchers PubMed Report error

7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2002 Shanske S, Tang Y, Hirano M, Nishigaki Y, Tanji K, Bonilla E, Sue C, Krishna S, Carlo JR, Willner J, Schon EA, DiMauro S. Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with pearson syndrome. American Journal of Human Genetics. 71: 679-83. PMID 12152148 DOI: 10.1086/342482  0.544
2001 Umeda S, Tang Y, Okamoto M, Hamasaki N, Schon EA, Kang D. Both heavy strand replication origins are active in partially duplicated human mitochondrial DNAs. Biochemical and Biophysical Research Communications. 286: 681-7. PMID 11520050 DOI: 10.1006/Bbrc.2001.5436  0.534
2000 Tang Y, Manfredi G, Hirano M, Schon EA. Maintenance of human rearranged mitochondrial DNAs in long-term cultured transmitochondrial cell lines. Molecular Biology of the Cell. 11: 2349-58. PMID 10888673 DOI: 10.1091/Mbc.11.7.2349  0.566
2000 Tang Y, Schon EA, Wilichowski E, Vazquez-Memije ME, Davidson E, King MP. Rearrangements of human mitochondrial DNA (mtDNA): new insights into the regulation of mtDNA copy number and gene expression. Molecular Biology of the Cell. 11: 1471-85. PMID 10749943 DOI: 10.1091/Mbc.11.4.1471  0.562
1999 Bruno C, Martinuzzi A, Tang Y, Andreu AL, Pallotti F, Bonilla E, Shanske S, Fu J, Sue CM, Angelini C, DiMauro S, Manfredi G. A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV. American Journal of Human Genetics. 65: 611-20. PMID 10441567 DOI: 10.1086/302546  0.373
1998 Bruno C, Minetti C, Tang Y, Magalhães PJ, Santorelli FM, Shanske S, Bado M, Cordone G, Gatti R, DiMauro S. Primary adrenal insufficiency in a child with a mitochondrial DNA deletion Journal of Inherited Metabolic Disease. 21: 155-161. PMID 9584267 DOI: 10.1023/A:1005347826664  0.429
1997 Bruno C, Tang Y, Santorelli FM, Minetti C, Bado M, Cordone G, Shanske S, Gatti R, DeVivo DC, DiMauro S. A novel mtDNA deletion associated with primary adrenal insufficiency.† 594 Pediatric Research. 41: 101-101. DOI: 10.1203/00006450-199704001-00614  0.307
Show low-probability matches.