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Page 1
The Spectrum of the Universe.
Hill R, Masui KW, Scott D. Hill R, et al. Among authors: scott d. Appl Spectrosc. 2018 May;72(5):663-688. doi: 10.1177/0003702818767133. Epub 2018 Apr 4. Appl Spectrosc. 2018. PMID: 29617155
Can we avoid dark energy?
Zibin JP, Moss A, Scott D. Zibin JP, et al. Among authors: scott d. Phys Rev Lett. 2008 Dec 19;101(25):251303. doi: 10.1103/PhysRevLett.101.251303. Epub 2008 Dec 18. Phys Rev Lett. 2008. PMID: 19113691
First direct measurement of the 17O(p,γ)18F reaction cross section at Gamow energies for classical novae.
Scott DA, Caciolli A, Di Leva A, Formicola A, Aliotta M, Anders M, Bemmerer D, Broggini C, Campeggio M, Corvisiero P, Elekes Z, Fülöp Z, Gervino G, Guglielmetti A, Gustavino C, Gyürky G, Imbriani G, Junker M, Laubenstein M, Menegazzo R, Marta M, Napolitani E, Prati P, Rigato V, Roca V, Somorjai E, Salvo C, Straniero O, Strieder F, Szücs T, Terrasi F, Trezzi D; LUNA Collaboration. Scott DA, et al. Phys Rev Lett. 2012 Nov 16;109(20):202501. doi: 10.1103/PhysRevLett.109.202501. Epub 2012 Nov 13. Phys Rev Lett. 2012. PMID: 23215474
Hair loss and quality of life in muslim American women.
Ziad A, Al-Zubi L, Santiago-Soltero K, Li YH, Huang KP, Scott DA, Mostaghimi A, Girmay Y, Charrow A. Ziad A, et al. Among authors: scott da. Arch Dermatol Res. 2024 May 25;316(6):257. doi: 10.1007/s00403-024-02950-0. Arch Dermatol Res. 2024. PMID: 38795172 No abstract available.
Large-scale mutational analysis identifies UNC93B1 variants that drive TLR-mediated autoimmunity in mice and humans.
Rael VE, Yano JA, Huizar JP, Slayden LC, Weiss MA, Turcotte EA, Terry JM, Zuo W, Thiffault I, Pastinen T, Farrow EG, Jenkins JL, Becker ML, Wong SC, Stevens AM, Otten C, Allenspach EJ, Bonner DE, Bernstein JA, Wheeler MT, Saxton RA; Undiagnosed Diseases Network; Liu B, Majer O, Barton GM. Rael VE, et al. J Exp Med. 2024 Aug 5;221(8):e20232005. doi: 10.1084/jem.20232005. Epub 2024 May 23. J Exp Med. 2024. PMID: 38780621 Free PMC article.
Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder.
Kohler JN, Legro NR, Baldridge D, Shin J, Bowman A, Ugur B, Jackstadt MM, Shriver LP, Patti GJ, Zhang B, Feng W, McAdow AR, Goddard P, Ungar RA, Jensen T, Smith KS, Fresard L, Alvarez R, Bonner D, Reuter CM, McCormack C, Kravets E, Marwaha S, Holt JM; Undiagnosed Diseases Network; Worthey E, Ashley EA, Montgomery SB, Fisher P, Postlethwait J, De Camilli P, Solnica-Krezel L, Bernstein JA, Wheeler MT. Kohler JN, et al. Genet Med. 2024 May 16:101166. doi: 10.1016/j.gim.2024.101166. Online ahead of print. Genet Med. 2024. PMID: 38767059
6,530 results