Zobrazeno 1 - 10
of 996
pro vyhledávání: '"E T, Young"'
Autor:
J. Rodriguez, V. Torossian, A. Woodmansee, M. Hart, A. Balady, Sylvain Guiriec, T. C. Chang, A. J. van der Horst, R. O. Morris, P. Willems, R. Sambruna, David M. Russell, E. T. Young, N. E. White, M. Rud, R. Dyer, R. Terrile, Peter W. A. Roming, H. Fausey, M. Seiffert
The Photo-z InfraRed Telescope (PIRT) is an instrument on the Gamow Explorer, currently proposed for a NASA Astrophysics Medium Explorer. PIRT works in tandem with a companion wide-field instrument, the Lobster Eye X-ray Telescope (LEXT), that will i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01b343b1785154e3c08e9bc85f9235d7
Publikováno v:
SPIE Proceedings.
Autor:
Nazli, Recep Irfan1 (AUTHOR) cerenaslankaciran@gmail.com, Aslankaciran, Ceren1 (AUTHOR) waqasliaqat789@gmail.com, Yang, Dongsheng2 (AUTHOR) inazli@cu.edu.tr, Liaqat, Waqas1 (AUTHOR) mihrabpolat@gmail.com, Polat, Mihrab1 (AUTHOR) ascavdar@cu.edu.tr, Cavdar, Asiye Sena1 (AUTHOR) veyis@cu.edu.tr, Tansi, Veyis1 (AUTHOR), Baloch, Faheem Shehzad3,4 (AUTHOR) balochfaheem13@gmail.com
Publikováno v:
Agronomy. Nov2024, Vol. 14 Issue 11, p2626. 27p.
Autor:
Pat Kendall-Taylor, William F. Kelly, Helen Imrie, Petros Perros, Anthony Toft, E. T. Young, Simon H. S. Pearce, Bijayeswar Vaidya
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 86:626-630
Graves’ disease (GD), which has a strong female preponderance (female/male ratio, >5:1), is inherited as a complex genetic trait. Loci for GD have started to be defined using genome-wide approaches for genetic linkage. To date, 3 loci have been con
Autor:
R. A. James, P. H. Baylis, Petros Perros, E. T. Young, William F. Kelly, Steve Ball, Pat Kendall-Taylor, Shs Pearce, Bijay Vaidya, D. R. Geatch, David H. Carr, Anthony P. Weetman, Helen Imrie, E.H. Kemp, S. J. Hurel
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 85:688-691
Although autoimmune Addison's disease (AAD) may occur as a component of the monogenic autoimmune polyendocrinopathy type 1 syndrome (APS1), it is most commonly found as an isolated disorder or associated with the autoimmune polyendocrinopathy type 2
Autor:
Anthony Toft, Pat Kendall-Taylor, E. T. Young, David M. Large, Helen Imrie, David Carr, Petros Perros, Bijayeswar Vaidya, William F. Kelly, Mark I. McCarthy, Simon H. S. Pearce
Publikováno v:
Human Molecular Genetics. 8:1195-1199
Graves' disease (GD) is an autoimmune thyroid disorder that is inherited as a complex trait. We have genotyped 77 affected sib-pairs with autoimmune thyroid disease for eight polymorphic markers spanning the cytotoxic T lymphocyte antigen-4 ( CTLA-4
Autor:
Fuller, Rachel1 (AUTHOR) Rachel.fuller@marketingscience.info, Hogan, Samantha2 (AUTHOR), Pervan, Simon3 (AUTHOR)
Publikováno v:
International Journal of Market Research. Jan2024, Vol. 66 Issue 1, p91-114. 24p.
Autor:
F. Tunbridge, D. Appleton, F. Clark, David W. Bates, W.M.G. Tunbridge, E. T. Young, J.M. French, Helen Rodgers, J. Grimley Evans, M. P. J. Vanderpump
Publikováno v:
Diabetic Medicine. 13:741-747
The original Whickham Survey documented the prevalence of diabetes and lipid disorders in a sample of 2779 adults aged 18 years and over, which matched the British population structure. The aim of the 20-year follow-up study was to determine the inci
Publikováno v:
Molecular and Cellular Biology. 13:4391-4399
In Saccharomyces cerevisiae, expression of the ADH2 gene is undetectable during growth on glucose. The transcription factor ADR1 is required to fully activate expression when glucose becomes depleted. Partial activation during growth on glucose occur
Mutations in the zinc fingers of ADR1 that change the specificity of DNA binding and transactivation
Publikováno v:
Molecular and Cellular Biology. 12:2784-2792
ADR1 is a yeast transcription factor that contains two zinc fingers of the Cys-2-His-2 (C2H2) class. Mutations that change the specificity of DNA binding of ADR1 to its target site, upstream activation sequence 1 (UAS1), have been identified at three