Shulin Zhang, Ph.D.
Affiliations: | 2001 | University of Victoria, Victoria, British Columbia, Canada |
Area:
Molecular BiologyGoogle:
"Shulin Zhang"Parents
Sign in to add mentor| Barry W. Glickman | grad student | 2001 | University of Victoria | |
| (The role of Msh2 DNA mismatch repair and p27kip1 cell cycle regulation on mutagenesis and carcinogenesis.) | ||||
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Publications
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| Lin L, Li M, Luo J, et al. (2021) A high proportion of novel ACAN mutations and their prevalence in a large cohort of Chinese short stature children. The Journal of Clinical Endocrinology and Metabolism |
| Wong LC, Chen T, Schmitt ES, et al. (2020) Clinical and Laboratory Interpretation of Mitochondrial mRNA Variants. Human Mutation |
| Bedoyan JK, Hecht L, Zhang S, et al. (2019) A novel null mutation in the pyruvate dehydrogenase phosphatase catalytic subunit gene () causing pyruvate dehydrogenase complex deficiency. Jimd Reports. 48: 26-35 |
| Xu Z, Zhou A, Wu J, et al. (2018) Transcriptional Approach for Decoding the Mechanism of Compensatory Mutations for the Fitness Cost in Rifampicin-Resistant . Frontiers in Microbiology. 9: 2895 |
| Goldstein JH, Tim-Aroon T, Shieh J, et al. (2015) Novel SMC1A frameshift mutations in children with developmental delay and epilepsy. European Journal of Medical Genetics |
| Deeb KK, Metcalf JD, Sesock KM, et al. (2015) The c.1364C>A (p.A455E) Mutation in the CFTR Pseudogene Results in an Incorrectly Assigned Carrier Status by a Commonly Used Screening Platform. The Journal of Molecular Diagnostics : Jmd. 17: 360-5 |
| Deeb KK, Bedoyan JK, Wang R, et al. (2014) Somatic mosaicism for a novel PDHA1 mutation in a male with severe pyruvate dehydrogenase complex deficiency. Molecular Genetics and Metabolism Reports. 1: 362-367 |
| Guda K, Fink SP, Milne GL, et al. (2014) Inactivating mutation in the prostaglandin transporter gene, SLCO2A1, associated with familial digital clubbing, colon neoplasia, and NSAID resistance. Cancer Prevention Research (Philadelphia, Pa.). 7: 805-12 |
| Coughlin CR, Krantz ID, Schmitt ES, et al. (2010) Somatic mosaicism for PDHA1 mutation in a male with pyruvate dehydrogenase complex deficiency. Molecular Genetics and Metabolism. 100: 296-9 |
| El-Hattab AW, Li FY, Schmitt E, et al. (2010) MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: new patients and novel mutations. Molecular Genetics and Metabolism. 99: 300-8 |