Zobrazeno 1 - 10
of 28
pro vyhledávání: '"B. Sarkis"'
Autor:
Howard J. Jacob, James D. Shull, Michael B. Dwinell, Peter S. LaViolette, Paula E. North, Jozef Lazar, Zelmira Lazarova, Scott C. Fahrenkrug, Wenfang Tan, Daniel F. Carlson, Jeffery De Pons, Shirng-Wern Tsaih, Sophia Ran, Carol Moreno, Aron M. Geurts, Angela Lemke, Ishan Roy, Stephanie Santarriaga, Allison B. Sarkis, Nathan Rudemiller, Bradley T. Endres, Michael J. Flister
Expanded Materials and Methods, Supplemental Figures, and Supplemental Tables Figure S1. Flow cytometric analysis of peripheral blood from SS, SS.BN3, SSIL2Rγ, and SS.BN3IL2Rγ rats. Figure S2.SH2B3 specifically marks CD31+ blood vessels, but not LY
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6c154ffd6a88cb5cd68a80a135811e4
https://doi.org/10.1158/0008-5472.22401336
https://doi.org/10.1158/0008-5472.22401336
Autor:
Howard J. Jacob, James D. Shull, Michael B. Dwinell, Peter S. LaViolette, Paula E. North, Jozef Lazar, Zelmira Lazarova, Scott C. Fahrenkrug, Wenfang Tan, Daniel F. Carlson, Jeffery De Pons, Shirng-Wern Tsaih, Sophia Ran, Carol Moreno, Aron M. Geurts, Angela Lemke, Ishan Roy, Stephanie Santarriaga, Allison B. Sarkis, Nathan Rudemiller, Bradley T. Endres, Michael J. Flister
The majority of causative variants in familial breast cancer remain unknown. Of the known risk variants, most are tumor cell autonomous, and little attention has been paid yet to germline variants that may affect the tumor microenvironment. In this s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e0154732934a5924ba7a91c179c2905
https://doi.org/10.1158/0008-5472.c.6505833
https://doi.org/10.1158/0008-5472.c.6505833
Autor:
Howard J. Jacob, Peter S. LaViolette, James D. Shull, Jozef Lazar, Zelmira Lazarova, Sophia Ran, Carol Moreno, Ishan Roy, Jeffery De Pons, Aron M. Geurts, Wenfang Tan, Scott C. Fahrenkrug, Angela Lemke, Allison B. Sarkis, Michael J. Flister, Daniel F. Carlson, Michael B. Dwinell, Paula E. North, Stephanie Santarriaga, Shirng-Wern Tsaih, Nathan P. Rudemiller, Bradley T. Endres
Publikováno v:
Cancer Research. 74:6419-6429
The majority of causative variants in familial breast cancer remain unknown. Of the known risk variants, most are tumor cell autonomous, and little attention has been paid yet to germline variants that may affect the tumor microenvironment. In this s
Autor:
Nan Cher Yeo, Howard J. Jacob, Sasha Z. Prisco, Allison B. Sarkis, Jeremy W. Prokop, Colin Hansen, Matthew Hoffman, Jozef Lazar, Michael J. Flister
Publikováno v:
Hypertension. 64:883-890
Previously, we found that transferring 6.1 Mb of salt-sensitive (SS) chromosome 12 (13.4–19.5 Mb) onto the consomic SS-12 BN background significantly elevated mean arterial pressure in response to an 8% NaCl diet (178±7 versus 144±2 mm Hg; P BN c
Autor:
Pamela J. Kaisaki, Edwin Cuppen, Anna Dominiczak, Ana Garcia Diaz, Kathirvel Gopalakrishnan, Paul Flicek, Kathrin Saar, Timothy J. Aitman, Tadao Serikawa, David J. Adams, Georg W. Otto, Laurence Game, Dominique Gauguier, Michael Tschannen, Santosh S. Atanur, Giuseppe Bianchi, Lorena Citterio, Thomas M. Keane, Bina Joe, Oliver Hummel, Enrico Petretto, Anne E. Kwitek, Wei-Wei Chen, Norbert Hubner, Klio Maratou, Howard J. Jacob, Allison B. Sarkis, Victor Guryev, Michael R. Garrett, Man Chun John Ma, Maxime Rotival, Martin W. McBride
Publikováno v:
Atanur, S, Diaz, A G, Maratou, K, Sarkis, A, Rotival, M, Game, L, Tschannen, M, Kaisaki, P, Otto, G, Ma, M C J, Keane, T, Hummel, O, Saar, K, Chen, W, Guryev, V, Gopalakrishnan, K, Garrett, M, Joe, B, Citterio, L, Bianchi, G, Mcbride, M, Dominiczak, A, Adams, D, Serikawa, T, Flicek, P, Cuppen, E, Hubner, N, Petretto, E, Gauguier, D, Kwitek, A, Jacob, H & Aitman, T 2013, ' Genome Sequencing Reveals Loci under Artificial Selection that Underlie Disease Phenotypes in the Laboratory Rat ', Cell, vol. 154, no. 3, pp. 691-703 . https://doi.org/10.1016/j.cell.2013.06.040
Cell, 154(3), 691-703. CELL PRESS
Cell
Cell, 154(3), 691-703. Elsevier B.V.
Cell, 154(3), 691-703. CELL PRESS
Cell
Cell, 154(3), 691-703. Elsevier B.V.
Summary Large numbers of inbred laboratory rat strains have been developed for a range of complex disease phenotypes. To gain insights into the evolutionary pressures underlying selection for these phenotypes, we sequenced the genomes of 27 rat strai
Autor:
Allison B. Sarkis, Haiyan Xu, Jozef Lazar, Caitlin C. O'Meara, Matthew Hoffman, Howard J. Jacob, Niloofar M. Tabatabai, Michelle M. Lutz, Carol Moreno, Rajendra K. Kothinti, Richard J. Roman
Publikováno v:
Journal of the American Society of Nephrology. 23:825-833
The majority of ESRD cases are associated with diabetes, hypertension, or both; however, numerous studies in both humans and animal models suggest that renal disease susceptibility genes exist that are independent of the initiating factor.1–6 The d
Autor:
Timothy J. Stodola, Andrew S. Greene, Micheline Resende, Norbert Huebner, Carol Moreno, Howard J. Jacob, Oliver Hummel, Allison B. Sarkis, Daniela N. Didier, Kathrin Saar
Publikováno v:
Physiological Genomics. 43:808-817
Impaired regulation of renin in Dahl salt-sensitive rats (SS/JRHsdMcwi, SS) contributes to attenuated angiogenesis in this strain. This study examined angiogenic function and genomic structure of regions surrounding the renin gene using subcongenic s
Autor:
Donna K. Arnett, Howard J. Jacob, Abraham P. Provoost, Ming-Huei Chen, Jozef Lazar, Caroline S. Fox, Allison B. Sarkis, Haiyan Xu, Carol Moreno, Ulrich Broeckel, Caitlin C. O'Meara, Sasha Z. Prisco
Publikováno v:
Physiological genomics. 45(16)
Many lines of evidence demonstrate that genetic variability contributes to chronic kidney disease susceptibility in humans as well as rodent models. Little progress has been made in discovering causal kidney disease genes in humans mainly due to gene
Autor:
Jan M. Williams, Howard J. Jacob, Richard J. Roman, Marilyn Burke, Fan Fan, Malikarjuna R. Pabbidi, Jozef Lazar, Allison B. Sarkis, Ruisheng Liu, Ying Ge
Publikováno v:
American journal of physiology. Renal physiology. 304(5)
This study examined the effect of substitution of a 2.4-megabase pair (Mbp) region of Brown Norway (BN) rat chromosome 1 (RNO1) between 258.8 and 261.2 Mbp onto the genetic background of fawn-hooded hypertensive (FHH) rats on autoregulation of renal
Autor:
Michael J Flister, Shirng-Wern Tsaih, Bradley Endres, Allison B Sarkis, Aron M Geurts, Jozef Lazar, Carol Moreno, Melinda R Dwinell, Howard J Jacob
Publikováno v:
Hypertension. 60
Background: Genome-wide association studies (GWAS) are frequently used to nominate candidate genes for complex diseases, but are largely unable to identify the causative variant(s). One example: the AGTRAP-PLOD1 locus contains 6 genes in close proxim