Larsson, Catharina

Human mitochondrial DNA deletions associated with mutations in the gene encoding twinkle, a phage T7 gene 4-like protein localized in mitochondria

Spelbrink, J. N., Li, F.-Y., Tiranti, V., Nikali, K., Yuan, Q.-P., Tariq, M., Wanrooij, S., Garrido, N., Comi, G., Morandi, L., et al. (2001) · Nature Genetics

Mitochondrial Function and PathologyDNA Repair Mechanisms

Cited by 882

Mechanisms underlying the activation of TERT transcription and telomerase activity in human cancer: Old actors and new players

Yuan, X., Larsson, C., & Xu, D. (2019) · Oncogene

Telomeres, Telomerase, and SenescenceGenetics, Aging, and Longevity in Model Organisms

Cited by 450

Adrenal lesion in multiple endocrine neoplasia type 1

Skogseid, B., Rastad, J., Gobl, A., Larsson, C., Backlin, K., Juhlin, C., Åkerström, G., & Öberg, K. (1995) · Surgery

Neuroendocrine Tumor Research AdvancesAdrenal and Paraganglionic Tumors

Cited by 111

Characterization of chromosomal abnormalities in prostate cancer cell lines by spectral karyotyping

Pan, Y., Kytölä, S., Farnebo, F., Wang, N., Lui, W. O., Nupponen, N., Isola, J., Visakorpi, T., Bergerheim, U. S. R., & Larsson, C. (1999) · Cytogenetic and Genome Research

Genomic variations and chromosomal abnormalitiesProstate Cancer Treatment and Research

Cited by 63