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Teddi Adler, Ed.D. - Publications

Affiliations: 
2008 East Tennessee State University, Johnson City, TN, United States 
Area:
Special Education, Curriculum and Instruction Education
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13 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
2016 Kumar S, Rathkolb B, Kemter E, Sabrautzki S, Michel D, Adler T, Becker L, Beckers J, Busch DH, Garrett L, Hans W, Hölter SM, Horsch M, Klingenspor M, Klopstock T, et al. Generation and Standardized, Systemic Phenotypic Analysis of Pou3f3L423P Mutant Mice. Plos One. 11: e0150472. PMID 27003440 DOI: 10.1371/journal.pone.0150472  0.476
2015 de Angelis MH, Nicholson G, Selloum M, White JK, Morgan H, Ramirez-Solis R, Sorg T, Wells S, Fuchs H, Fray M, Adams DJ, Adams NC, Adler T, Aguilar-Pimentel A, Ali-Hadji D, et al. Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics. Nature Genetics. PMID 26214591 DOI: 10.1038/Ng.3360  0.477
2013 Kemter E, Prückl P, Rathkolb B, Micklich K, Adler T, Becker L, Beckers J, Busch DH, Götz AA, Hans W, Horsch M, Ivandic B, Klingenspor M, Klopstock T, Rozman J, et al. Standardized, systemic phenotypic analysis of Umod(C93F) and Umod(A227T) mutant mice. Plos One. 8: e78337. PMID 24205203 DOI: 10.1371/journal.pone.0078337  0.398
2013 Sabrautzki S, Janas E, Lorenz-Depiereux B, Calzada-Wack J, Aguilar-Pimentel JA, Rathkolb B, Adler T, Cohrs C, Hans W, Diener S, Fuchs H, Gailus-Durner V, Busch DH, Höfler H, Ollert M, et al. An ENU mutagenesis-derived mouse model with a dominant Jak1 mutation resembling phenotypes of systemic autoimmune disease. The American Journal of Pathology. 183: 352-68. PMID 23791841 DOI: 10.1016/j.ajpath.2013.04.027  0.331
2013 Ju L, Wing J, Taylor E, Brandt R, Slijepcevic P, Horsch M, Rathkolb B, Rácz I, Becker L, Hans W, Adler T, Beckers J, Rozman J, Klingenspor M, Wolf E, et al. SMC6 is an essential gene in mice, but a hypomorphic mutant in the ATPase domain has a mild phenotype with a range of subtle abnormalities. Dna Repair. 12: 356-66. PMID 23518413 DOI: 10.1016/J.Dnarep.2013.02.006  0.383
2012 Klymiuk I, Kenner L, Adler T, Busch DH, Boersma A, Irmler M, Fridrich B, Gailus-Durner V, Fuchs H, Leitner N, Müller M, Kühn R, Schlederer M, Treise I, de Angelis MH, et al. In vivo functional requirement of the mouse Ifitm1 gene for germ cell development, interferon mediated immune response and somitogenesis. Plos One. 7: e44609. PMID 23115618 DOI: 10.1371/journal.pone.0044609  0.351
2012 Staropoli JF, Haliw L, Biswas S, Garrett L, Hölter SM, Becker L, Skosyrski S, Da Silva-Buttkus P, Calzada-Wack J, Neff F, Rathkolb B, Rozman J, Schrewe A, Adler T, Puk O, et al. Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous system. Plos One. 7: e38310. PMID 22701626 DOI: 10.1371/Journal.Pone.0038310  0.329
2011 Fuchs H, Gailus-Durner V, Adler T, Aguilar-Pimentel JA, Becker L, Calzada-Wack J, Da Silva-Buttkus P, Neff F, Götz A, Hans W, Hölter SM, Horsch M, Kastenmüller G, Kemter E, Lengger C, et al. Mouse phenotyping. Methods (San Diego, Calif.). 53: 120-35. PMID 20708688 DOI: 10.1016/j.ymeth.2010.08.006  0.42
2010 Rosemann M, Ivashkevich A, Favor J, Dalke C, Hölter SM, Becker L, Rácz I, Bolle I, Klempt M, Rathkolb B, Kalaydjiev S, Adler T, Aguilar A, Hans W, Horsch M, et al. Microphthalmia, parkinsonism, and enhanced nociception in Pitx3 ( 416insG ) mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 21: 13-27. PMID 20033184 DOI: 10.1007/S00335-009-9235-0  0.383
2009 Grzmil P, Konietzko J, Boehm D, Hölter SM, Hoelter SM, Aguilar-Pimentel A, Aguilar A, Javaheri A, Kalaydjiev S, Adler T, Bolle I, Adham I, Dixkens C, Wolf S, Fuchs H, et al. Targeted disruption of the mouse Npal3 gene leads to deficits in behavior, increased IgE levels, and impaired lung function. Cytogenetic and Genome Research. 125: 186-200. PMID 19738379 DOI: 10.1159/000230003  0.375
2009 Gailus-Durner V, Fuchs H, Adler T, Aguilar Pimentel A, Becker L, Bolle I, Calzada-Wack J, Dalke C, Ehrhardt N, Ferwagner B, Hans W, Hölter SM, Hölzlwimmer G, Horsch M, Javaheri A, et al. Systemic first-line phenotyping. Methods in Molecular Biology (Clifton, N.J.). 530: 463-509. PMID 19266331 DOI: 10.1007/978-1-59745-471-1_25  0.369
2009 Fuchs H, Gailus-Durner V, Adler T, Pimentel JA, Becker L, Bolle I, Brielmeier M, Calzada-Wack J, Dalke C, Ehrhardt N, Fasnacht N, Ferwagner B, Frischmann U, Hans W, Hölter SM, et al. The German Mouse Clinic: a platform for systemic phenotype analysis of mouse models. Current Pharmaceutical Biotechnology. 10: 236-43. PMID 19199957 DOI: 10.2174/138920109787315051  0.402
2008 Marx I, Lenting PJ, Adler T, Pendu R, Christophe OD, Denis CV. Correction of bleeding symptoms in von Willebrand factor-deficient mice by liver-expressed von Willebrand factor mutants Arteriosclerosis, Thrombosis, and Vascular Biology. 28: 419-424. PMID 18187670 DOI: 10.1161/ATVBAHA.107.159442  0.311
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