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Shulin Zhang, Ph.D. - Publications

Affiliations: 
2001 University of Victoria, Victoria, British Columbia, Canada 
Area:
Molecular Biology
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19 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
2021 Lin L, Li M, Luo J, Li P, Zhou S, Yang Y, Chen K, Weng Y, Ge X, Mireguli M, Wei H, Yang H, Li G, Sun Y, Cui L, ... Zhang S, et al. 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. PMID 33606014 DOI: 10.1210/clinem/dgab088  0.335
2020 Wong LC, Chen T, Schmitt ES, Wang J, Tang S, Landsverk M, Li F, Zhang S, Wang Y, Zhang VW, Craigen WJ. Clinical and Laboratory Interpretation of Mitochondrial mRNA Variants. Human Mutation. PMID 32652755 DOI: 10.1002/Humu.24082  0.307
2019 Bedoyan JK, Hecht L, Zhang S, Tarrant S, Bergin A, Demirbas D, Yang E, Shin HK, Grahame GJ, DeBrosse SD, Hoppel CL, Kerr DS, Berry GT. A novel null mutation in the pyruvate dehydrogenase phosphatase catalytic subunit gene () causing pyruvate dehydrogenase complex deficiency. Jimd Reports. 48: 26-35. PMID 31392110 DOI: 10.1002/jmd2.12054  0.337
2018 Xu Z, Zhou A, Wu J, Zhou A, Li J, Zhang S, Wu W, Karakousis PC, Yao YF. Transcriptional Approach for Decoding the Mechanism of Compensatory Mutations for the Fitness Cost in Rifampicin-Resistant . Frontiers in Microbiology. 9: 2895. PMID 30555440 DOI: 10.3389/fmicb.2018.02895  0.337
2015 Goldstein JH, Tim-Aroon T, Shieh J, Merrill M, Deeb KK, Zhang S, Bass NE, Bedoyan JK. Novel SMC1A frameshift mutations in children with developmental delay and epilepsy. European Journal of Medical Genetics. PMID 26386245 DOI: 10.1016/j.ejmg.2015.09.007  0.32
2015 Deeb KK, Metcalf JD, Sesock KM, Shen J, Wensel CA, Rippel LI, Smith M, Chapman MS, Zhang S. 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. PMID 25956447 DOI: 10.1016/j.jmoldx.2015.02.005  0.328
2014 Deeb KK, Bedoyan JK, Wang R, Sremba L, Schroeder MC, Grahame GJ, Boyer M, McCandless SE, Kerr DS, Zhang S. Somatic mosaicism for a novel PDHA1 mutation in a male with severe pyruvate dehydrogenase complex deficiency. Molecular Genetics and Metabolism Reports. 1: 362-367. PMID 27896109 DOI: 10.1016/J.Ymgmr.2014.08.001  0.481
2014 Guda K, Fink SP, Milne GL, Molyneaux N, Ravi L, Lewis SM, Dannenberg AJ, Montgomery CG, Zhang S, Willis J, Wiesner GL, Markowitz SD. 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. PMID 24838973 DOI: 10.1158/1940-6207.Capr-14-0108  0.33
2010 Coughlin CR, Krantz ID, Schmitt ES, Zhang S, Wong LJ, Kerr DS, Ganesh J. Somatic mosaicism for PDHA1 mutation in a male with pyruvate dehydrogenase complex deficiency. Molecular Genetics and Metabolism. 100: 296-9. PMID 20462777 DOI: 10.1016/J.Ymgme.2010.04.004  0.424
2010 El-Hattab AW, Li FY, Schmitt E, Zhang S, Craigen WJ, Wong LJ. MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: new patients and novel mutations. Molecular Genetics and Metabolism. 99: 300-8. PMID 20074988 DOI: 10.1016/j.ymgme.2009.10.003  0.386
2010 Zhang S, Li FY, Bass HN, Pursley A, Schmitt ES, Brown BL, Brundage EK, Mardach R, Wong LJ. Application of oligonucleotide array CGH to the simultaneous detection of a deletion in the nuclear TK2 gene and mtDNA depletion. Molecular Genetics and Metabolism. 99: 53-7. PMID 19815440 DOI: 10.1016/J.Ymgme.2009.09.003  0.45
2010 Wong L, Shaibani A, Shchelochkov OA, Zhang S, Katsonis P, Lichtarge O, Shinawi M. 114 Expanding clinical spectrum of RRM2B mutations to include MNGIE Mitochondrion. 10: 232. DOI: 10.1016/J.Mito.2009.12.106  0.443
2010 El-Hattab AW, Li F, Schmitt E, Zhang S, Craigen W, Wong L. 78 MPV17—Associated hepatocerebral mitochondrial DNA depletion syndrome: New patients and novel mutations Mitochondrion. 10: 222. DOI: 10.1016/J.Mito.2009.12.073  0.38
2009 Wang FX, Yang LJ, Li M, Zhang SL, Zhu XH. A novel missense mutation of CYLD gene in a Chinese family with multiple familial trichoepithelioma. Archives of Dermatological Research. 302: 67-70. PMID 19911186 DOI: 10.1007/s00403-009-1003-1  0.33
2009 Shaibani A, Shchelochkov OA, Zhang S, Katsonis P, Lichtarge O, Wong LJ, Shinawi M. Mitochondrial neurogastrointestinal encephalopathy due to mutations in RRM2B. Archives of Neurology. 66: 1028-32. PMID 19667227 DOI: 10.1001/Archneurol.2009.139  0.358
2002 Zhang S, Lloyd R, Bowden G, Glickman BW, de Boer JG. Msh2 deficiency increases the mutation frequency in all parts of the mouse colon. Environmental and Molecular Mutagenesis. 40: 243-50. PMID 12489114 DOI: 10.1002/Em.10113  0.605
2002 Zhang S, Lloyd R, Bowden G, Glickman BW, de Boer JG. Thymic lymphomas arising in Msh2 deficient mice display a large increase in mutation frequency and an altered mutational spectrum. Mutation Research. 500: 67-74. PMID 11890935 DOI: 10.1016/S0027-5107(01)00297-4  0.603
2001 Zhang S, Lloyd R, Bowden G, Glickman BW, de Boer JG. Msh2 DNA mismatch repair gene deficiency and the food-borne mutagen 2-amino-1-methy1-6-phenolimidazo [4,5-b] pyridine (PhIP) synergistically affect mutagenesis in mouse colon. Oncogene. 20: 6066-72. PMID 11593414 DOI: 10.1038/Sj.Onc.1204730  0.571
2001 Zhang S, Glickman BW, de Boer JG. Spontaneous mutation of the lacI transgene in rodents: absence of species, strain, and insertion-site influence. Environmental and Molecular Mutagenesis. 37: 141-6. PMID 11246220 DOI: 10.1002/Em.1021  0.568
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