Zobrazeno 1 - 10
of 20
pro vyhledávání: '"D W Bowden"'
Autor:
Michael D. W. Bowden, Steven A. Clarke, Kathryn E. Brown, Christopher J. Snyder, Patrick R. Bowden
Publikováno v:
SHOCK COMPRESSION OF CONDENSED MATTER - 2019: Proceedings of the Conference of the American Physical Society Topical Group on Shock Compression of Condensed Matter.
Iron(II) tris(3-amino-6-pyrazolyl-1,2,4-triazolo[4,3-b][1,2,4,5]-tetrazine) perchlorate (FATP) is an energetic material that has low sensitivity to mechanical stimuli [impact, electrostatic discharge (ESD), and friction] and is also capable of being
Publikováno v:
Nephrology Dialysis Transplantation. 27:3660-3662
Autor:
D. W. Bowden, M. Sale, T. D. Howard, A. Qadri, B. J. Spray, C. B. Rothschild, G. Akots, S. S. Rich, B. I. Freedman
Publikováno v:
Diabetes. 46:882-886
Publikováno v:
Diabetic medicine : a journal of the British Diabetic Association. 29(6)
Although current American Heart Association guidelines address C-reactive protein concentration and cardiovascular disease risk, it remains unclear whether this paradigm is consistent across populations with differing disease burdens. Individuals wit
Publikováno v:
Diabetes. 41:88-92
Autor:
M. Budgett, L. Hernandez, Eli Ipp, Carol Fondran, A. Pickens, B. S. Kasinath, Michael F. Seldin, V. Turner, R. Juan, H. Abboud, J. Schelling, Philip G Zager, C. Brown, B. Kessing, C. Winkler, Y. D I Chen, S. J. O'Brien, D. W. Bowden, Gyungah Jun, L. Jones, J. Gonzalez, E. Zaletel, Katrina A.B. Goddard, M. W. Smith, Amanda Horvath, L. Getz-Fradley, X. Guo, T. Whitehead, H. Li, L. M. Phillips, Jane M. Olson, J. Chester, Robert L. Hanson, T. Abboud, Michael J. Klag, Marina Scavini, K. Ngo, K. Taylor, L. Mead, O. Kohn, R. Lovelace, Paul L. Kimmel, William C. Knowler, R. Spielman, B. Waseta, C. Muro, L. Humbert, Mohammed F. Saad, R. Young, Vallabh O. Shah, I. Sili, C. Garcia, Madeleine V. Pahl, C. Jefferson, Sharon G. Adler, Robert C. Elston, Rulan S. Parekh, Sudha K. Iyengar, J. R. Sedor, Jerome I. Rotter, Denyse Thornley-Brown, Janine La Page, M. Thompson, J. Wolford, Josephine P. Briggs, L. Ingram-Drake, J. Sewemaenewa, D. Leehey, A. Bobelu, R. Chakraborty, C. Goyes, N. Arar, H. E. Collins-Schramm, R. G. Nelson, C. Pagliasotti, S. C. Satko, S. Viverette, R. L. Hanson, F. Hariri, S. Warren, S. Nicholas, J. Loebel, M. Slaughter, R. Plaetke, G. Brooks, G. Barone, Sarah Ialacci, M. Spainhour, G. M. Dunston, V. Sartorio, M. Stern, S. Edwards-Quade, David G. Warnock, W. H. Linda Kao, Kristopher Kramp, S. S. Rich, B. I. Freedman, B. Walker, C. Jenkinson, Lucy A. Meoni, R. Duggirala, C. Luethe, Rebekah S. Rasooly
Publikováno v:
Clinical journal of the American Society of Nephrology : CJASN. 2(6)
Background and objectives: This study investigated the effect of long-term storage at 70°C on urinary albumin, protein, and creatinine measurements in the Family Investigation of Nephropathy and Diabetes, a multicenter study designed to identify gen
Autor:
T C, Hart, P S, Hart, D W, Bowden, M D, Michalec, S A, Callison, S J, Walker, Y, Zhang, E, Firatli
Publikováno v:
Journal of medical genetics. 36(12)
Papillon-Lefèvre syndrome (PLS) is an autosomal recessive disorder characterised by palmoplantar hyperkeratosis and severe early onset periodontitis that results in the premature loss of the primary and secondary dentitions. A major gene locus for P
Autor:
T C, Hart, D W, Bowden, K A, Ghaffar, W, Wang, C W, Cutler, I, Cebeci, A, Efeoglu, E, Firatli
Publikováno v:
American journal of medical genetics. 79(2)
Papillon-Lefevre syndrome (PLS) is an autosomal recessive form of palmoplantar ectodermal dysplasia, characterized by palmoplantar hyperkeratosis and severe early-onset periodontitis. The presence of severe periodontitis distinguishes PLS from other
Autor:
M M, Sale, T, Akamizu, T D, Howard, T, Yokota, K, Nakao, T, Mori, H, Iwasaki, S S, Rich, J E, Jennings-Gee, M, Yamada, D W, Bowden
Publikováno v:
Proceedings of the Association of American Physicians. 109(5)
To examine the genetic contribution of the thyroid-stimulating hormone receptor (TSHR, or thyrotropin receptor) gene to autoimmune thyroid disease (AITD), we identified a dinucleotide repeat polymorphism near the TSHR gene that mapped to an 8.6 cM in
Publikováno v:
Diabetic medicine : a journal of the British Diabetic Association. 13(9 Suppl 6)
MODY is a sub-type of NIDDM. It is characterized by an early age of onset and autosomal dominant mode of inheritance. These features, and the availability of large multigenerational pedigrees, make MODY useful for genetic studies of diabetes. In the