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Marija Tadin-Strapps, Ph.D. - Publications

Affiliations: 
2003 Columbia University, New York, NY 
Area:
Genetics
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18 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
2019 Jiao Y, Ahmed U, Sim MFM, Bejar A, Zhang X, Talukder MMU, Rice R, Flannick J, Podgornaia AI, Reilly DF, Engreitz JM, Kost-Alimova M, Hartland K, Mercader JM, Georges S, ... ... Tadin-Strapps M, et al. Discovering metabolic disease gene interactions by correlated effects on cellular morphology. Molecular Metabolism. PMID 30940487 DOI: 10.1016/J.Molmet.2019.03.001  0.33
2018 McLaren DG, Han S, Murphy BA, Wilsie L, Stout SJ, Zhou H, Roddy TP, Gorski JN, Metzger DE, Shin MK, Reilly DF, Zhou HH, Tadin-Strapps M, Bartz SR, Cumiskey AM, et al. DGAT2 Inhibition Alters Aspects of Triglyceride Metabolism in Rodents but Not in Non-human Primates. Cell Metabolism. PMID 29706567 DOI: 10.1016/J.Cmet.2018.04.004  0.318
2017 Murphy BA, Tadin-Strapps M, Jensen K, Mogg R, Liaw A, Herath K, Bhat G, McLaren DG, Previs SF, Pinto S. siRNA-mediated inhibition of SREBP cleavage-activating protein reduces dyslipidemia in spontaneously dysmetabolic rhesus monkeys. Metabolism: Clinical and Experimental. 71: 202-212. PMID 28521874 DOI: 10.1016/J.Metabol.2017.02.015  0.351
2016 Jensen KK, Tadin-Strapps M, Wang SP, Hubert J, Kan Y, Ma Y, McLaren DG, Previs SF, Herath KB, Mahsut A, Liaw A, Wang S, Stout SJ, Keohan C, Forrest G, et al. Dose-dependent effects of siRNA-mediated inhibition of SCAP on PCSK9, LDLR and plasma lipids in mouse and rhesus monkey. Journal of Lipid Research. PMID 27707816 DOI: 10.1194/Jlr.M071498  0.391
2015 Hamza MS, Kumar C, Chia SM, Anandalakshmi V, Boo N, Strapps W, Robinson M, Caguyong M, Bartz S, Tadin-Strapps M, van Gool A, Shih SJ. Alterations in the hepatic transcriptional landscape after RNAi mediated ApoB silencing in cynomolgus monkeys. Atherosclerosis. 242: 383-95. PMID 26275376 DOI: 10.1016/J.Atherosclerosis.2015.07.032  0.399
2015 Metzger JM, Tadin-Strapps M, Thankappan A, Strapps WR, DiPietro M, Leander K, Zhang Z, Shin MK, Levorse J, Desai K, Xu Y, Lai K, Wu W, Chen Z, Cai TQ, et al. Titrating haemophilia B phenotypes using siRNA strategy: evidence that antithrombotic activity is separated from bleeding liability. Thrombosis and Haemostasis. 113: 1300-11. PMID 25790442 DOI: 10.1160/Th14-06-0505  0.378
2015 Chen Z, Luo B, Cai TQ, Thankappan A, Xu Y, Wu W, DiMuzio J, Lifsted T, DiPietro M, Disa J, Ng B, Leander K, Clark S, Hoos L, Zhou Y, ... ... Tadin-Strapps M, et al. Proof-of-concept Studies for siRNA-mediated Gene Silencing for Coagulation Factors in Rat and Rabbit. Molecular Therapy. Nucleic Acids. 4: e224. PMID 25625614 DOI: 10.1038/Mtna.2014.75  0.333
2014 DeStefano GM, Kurban M, Anyane-Yeboa K, Dall'Armi C, Di Paolo G, Feenstra H, Silverberg N, Rohena L, López-Cepeda LD, Jobanputra V, Fantauzzo KA, Kiuru M, Tadin-Strapps M, Sobrino A, Vitebsky A, et al. Mutations in the cholesterol transporter gene ABCA5 are associated with excessive hair overgrowth. Plos Genetics. 10: e1004333. PMID 24831815 DOI: 10.1371/Journal.Pgen.1004333  0.711
2013 DeStefano GM, Fantauzzo KA, Petukhova L, Kurban M, Tadin-Strapps M, Levy B, Warburton D, Cirulli ET, Han Y, Sun X, Shen Y, Shirazi M, Jobanputra V, Cepeda-Valdes R, Cesar Salas-Alanis J, et al. Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis. Proceedings of the National Academy of Sciences of the United States of America. 110: 7790-5. PMID 23603273 DOI: 10.1073/Pnas.1216412110  0.677
2012 Tep S, Mihaila R, Freeman A, Pickering V, Huynh F, Huyhn F, Tadin-Strapps M, Stracks A, Hubbard B, Caldwell J, Flanagan WM, Kuklin NA, Ason B. Rescue of Mtp siRNA-induced hepatic steatosis by DGAT2 siRNA silencing. Journal of Lipid Research. 53: 859-67. PMID 22355095 DOI: 10.1194/Jlr.M021063  0.309
2011 Castro-Perez JM, Roddy TP, Shah V, Wang SP, Ouyang X, Ogawa A, McLaren DG, Tadin-Strapps M, Robinson MJ, Bartz SR, Ason B, Chen Y, Previs SF, Wong KK, Vreeken RJ, et al. Attenuation of Slc27a5 gene expression followed by LC-MS measurement of bile acid reconjugation using metabolomics and a stable isotope tracer strategy. Journal of Proteome Research. 10: 4683-91. PMID 21819150 DOI: 10.1021/Pr200475G  0.305
2011 Tadin-Strapps M, Peterson LB, Cumiskey AM, Rosa RL, Mendoza VH, Castro-Perez J, Puig O, Zhang L, Strapps WR, Yendluri S, Andrews L, Pickering V, Rice J, Luo L, Chen Z, et al. siRNA-induced liver ApoB knockdown lowers serum LDL-cholesterol in a mouse model with human-like serum lipids. Journal of Lipid Research. 52: 1084-97. PMID 21398511 DOI: 10.1194/Jlr.M012872  0.353
2008 Fantauzzo KA, Tadin-Strapps M, You Y, Mentzer SE, Baumeister FA, Cianfarani S, Van Maldergem L, Warburton D, Sundberg JP, Christiano AM. A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice. Human Molecular Genetics. 17: 3539-51. PMID 18713754 DOI: 10.1093/Hmg/Ddn247  0.684
2004 Tadin-Strapps M, Warburton D, Baumeister FA, Fischer SG, Yonan J, Gilliam TC, Christiano AM. Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome. Cytogenetic and Genome Research. 107: 68-76. PMID 15305058 DOI: 10.1159/000079573  0.564
2004 Moss C, Martinez-Mir A, Lam H, Tadin-Strapps M, Kljuic A, Christiano AM. A recurrent intragenic deletion in the desmoglein 4 gene underlies localized autosomal recessive hypotrichosis. The Journal of Investigative Dermatology. 123: 607-10. PMID 15304105 DOI: 10.1111/J.0022-202X.2004.23311.X  0.653
2004 Tadin-Strapps M, Warburton D, Salas-Alanis JC, Lopez-Cepeda LD, Christiano AM. Fishing for new genes in skin biology: impact of cytogenetics on gene discovery. Clinical Genetics. 66: 94-106. PMID 15253757 DOI: 10.1111/J.0009-9163.2004.00301.X  0.557
2003 Tadin-Strapps M, Salas-Alanis JC, Moreno L, Warburton D, Martinez-Mir A, Christiano AM. Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X-linked trait. Clinical Genetics. 63: 418-22. PMID 12752576 DOI: 10.1034/J.1399-0004.2003.00069.X  0.583
2003 Horev L, Waran Lalin T, Martinez-Mir A, Bagheri BA, Tadin-Strapps M, Schneiderman PI, Grossman ME, Bickers DR, Christiano AM. Identification of mutations in the COL7A1 gene in a proband with mild recessive dystrophic epidermolysis bullosa and aortic insufficiency. Clinical and Experimental Dermatology. 28: 80-4. PMID 12558638 DOI: 10.1046/J.1365-2230.2003.01190.X  0.52
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