نتائج البحث - Mychaleckyj, Josyf C
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Expression Profiling Reveals Differential Gene Induction Underlying Specific and Non-Specific Memory for Pheromones in Mice حسب Upadhya, Sudarshan C., Smith, Thuy K., Brennan, Peter A., Mychaleckyj, Josyf C., Hegde, Ashok N.
منشور في 2011نص -
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Gene Expression Differences in Skin Fibroblasts in Identical Twins Discordant for Type 1 Diabetes حسب Caramori, M. Luiza, Kim, Youngki, Moore, Jason H., Rich, Stephen S., Mychaleckyj, Josyf C., Kikyo, Nobuaki, Mauer, Michael
منشور في 2012نص -
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Genetic analysis of the GLUT10 glucose transporter (SLC2A10) polymorphisms in Caucasian American type 2 diabetes حسب Bento, Jennifer L, Bowden, Donald W, Mychaleckyj, Josyf C, Hirakawa, Shohei, Rich, Stephen S, Freedman, Barry I, Segade, Fernando
منشور في 2005نص -
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Synergism Between Circulating Tumor Necrosis Factor Receptor 2 and HbA(1c) in Determining Renal Decline During 5–18 Years of Follow-up in Patients With Type 1 Diabetes and Proteinu... حسب Skupien, Jan, Warram, James H., Niewczas, Monika A., Gohda, Tomohito, Malecki, Maciej, Mychaleckyj, Josyf C., Galecki, Andrzej T., Krolewski, Andrzej S.
منشور في 2014نص -
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Genome-Wide Analysis in Brazilians Reveals Highly Differentiated Native American Genome Regions حسب Mychaleckyj, Josyf C., Havt, Alexandre, Nayak, Uma, Pinkerton, Relana, Farber, Emily, Concannon, Patrick, Lima, Aldo A., Guerrant, Richard L.
منشور في 2017نص -
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POLYMORPHISMS NEAR SOCS3 ARE ASSOCIATED WITH OBESITY AND GLUCOSE HOMEOSTASIS TRAITS IN HISPANIC AMERICANS FROM THE INSULIN RESISTANCE ATHEROSCLEROSIS FAMILY STUDY حسب Talbert, Matthew E, Langefeld, Carl D, Ziegler, Julie, Mychaleckyj, Josyf C, Haffner, Steven M, Norris, Jill M, Bowden, Donald W
منشور في 2008نص -
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Evaluation of DLG2 as a Positional Candidate for Disposition Index in African Americans from the IRAS Family Study حسب Palmer, Nicholette D., Mychaleckyj, Josyf C., Langefeld, Carl. D., Ziegler, Julie T., Williams, Adrienne. H., Bryer-Ash, Michael., Bowden, Donald. W.
منشور في 2009نص -
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Buffy coat specimens remain viable as a DNA source for highly multiplexed genome-wide genetic tests after long term storage حسب Mychaleckyj, Josyf C, Farber, Emily A, Chmielewski, Jessica, Artale, Jamie, Light, Laney S, Bowden, Donald W, Hou, Xuanlin, Marcovina, Santica M
منشور في 2011نص -
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Family-Based Association Analysis Confirms the Role of the Chromosome 9q21.32 Locus in the Susceptibility of Diabetic Nephropathy حسب Pezzolesi, Marcus G., Jeong, Jackson, Smiles, Adam M., Skupien, Jan, Mychaleckyj, Josyf C., Rich, Stephen S., Warram, James H., Krolewski, Andrzej S.
منشور في 2013نص -
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An intergenic region on chromosome 13q33.3 is associated with the susceptibility to kidney disease in type 1 and 2 diabetes حسب Pezzolesi, Marcus G., Poznik, G. David, Skupien, Jan, Smiles, Adam, Mychaleckyj, Josyf C., Rich, Stephen S., Warram, James H., Krolewski, Andrzej S.
منشور في 2011نص -
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Significant linkage at chromosome 19q for otitis media with effusion and/or recurrent otitis media (COME/ROM) حسب Chen, Wei-Min, Allen, E Kaitlynn, Mychaleckyj, Josyf C, Chen, Fang, Hou, Xuanlin, Rich, Stephen S, Daly, Kathleen A, Sale, Michèle M
منشور في 2011نص -
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Differential Response to High Glucose in Skin Fibroblasts of Monozygotic Twins Discordant for Type 1 Diabetes حسب Caramori, M. Luiza, Kim, Youngki, Natarajan, Rama, Moore, Jason H., Rich, Stephen S., Mychaleckyj, Josyf C., Kuriyama, Ryoko, Kirkpatrick, David, Mauer, Michael
منشور في 2015نص -
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Confirmation of Genetic Associations at ELMO1 in the GoKinD Collection Supports Its Role as a Susceptibility Gene in Diabetic Nephropathy حسب Pezzolesi, Marcus G., Katavetin, Pisut, Kure, Masahiko, Poznik, G. David, Skupien, Jan, Mychaleckyj, Josyf C., Rich, Stephen S., Warram, James H., Krolewski, Andrzej S.
منشور في 2009نص -
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Genetic Variation in the Matrix Metalloproteinase Genes and Diabetic Nephropathy in Type 1 Diabetes حسب Kure, Masahiko, Pezzolesi, Marcus G., Poznik, G. David, Katavetin, Pisut, Skupien, Jan, Dunn, Jonathon S., Mychaleckyj, Josyf C., Warram, James H., Krolewski, Andrzej S.
منشور في 2011نص -
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Association of the proprotein convertase subtilisin/kexin-type 2 (PCSK2) gene with type 2 diabetes in an African American population حسب Leak, Tennille S., Keene, Keith L., Langefeld, Carl D., Gallagher, Carla J., Mychaleckyj, Josyf C., Freedman, Barry I., Bowden, Donald W., Rich, Stephen S., Sale, Michèle M.
منشور في 2007نص -
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Analysis of Family- and Population-Based Samples in Cohort Genome-Wide Association Studies حسب Manichaikul, Ani, Chen, Wei-Min, Williams, Kayleen, Wong, Quenna, Sale, Michèle M., Pankow, James S., Tsai, Michael Y., Rotter, Jerome I., Rich, Stephen S., Mychaleckyj, Josyf C.
منشور في 2011نص