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pro vyhledávání: '"M. C. King"'
Autor:
R. J. Elsworthy, J. A. Crowe, M. C. King, C. Dunleavy, E. Fisher, A. Ludlam, H. R. Parri, E. J. Hill, S. Aldred
Publikováno v:
Translational Psychiatry, Vol 12, Iss 1, Pp 1-7 (2022)
Abstract Selective Serotonin Reuptake Inhibitors (SSRIs) may hold therapeutic benefits for people with Alzheimer’s disease (AD). SSRIs may perturb AD progression, or the conversion from MCI to AD, via increased neurogenesis, reduced oxidative stres
Externí odkaz:
https://doaj.org/article/e7f1b746a8ae4a16b4933a228980608e
Akademický článek
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Publikováno v:
Organisms Diversity & Evolution. 22:131-140
Animals of the intertidal zone tolerate substantial environmental fluctuations. Survival under such unstable conditions requires specific adaptations. Several intertidal species have evolved endogenous mechanisms that follow tidal rhythms permitting
Autor:
ASSEN JABLENSKY1, VERA MORGAN2
Publikováno v:
Psychological Medicine. Jun2007, Vol. 37 Issue 6, p905-906. 2p.
Publikováno v:
OENO One, Vol 36, Iss 1, Pp 21-30 (2002)
One-hundred and eighty-nine commercial red wines from four vintages (1996-1999), four varieties (Pinot noir, Merlot, Cabernet franc, Cabernet Sauvignon) and 13 vineyard locations within the Okanagan Valley of British Columbia were analysed for total
Externí odkaz:
https://doaj.org/article/2e7d191c5f4543f2b3cb6ee8771d8985
Autor:
I, Kedar, L, Walsh, G Reznick, Levi, S, Lieberman, A Abu, Shtaya, S Naftaly, Nathan, I, Lagovsky, R, Tomashov-Matar, M, Goldenberg, L, Basel-Salmon, L, Katz, O, Aleme, T Yablonski, Peretz, A, Hubert, D, Rothstein, S, Castellvi-Bel, T, Walsh, M C, King, C C, Pritchard, Z, Levi, E, Half, I, Laish, Y, Goldberg
Publikováno v:
Familial cancer. 21(2)
Lynch syndrome is an inherited cancer predisposition syndrome caused by germline defects in any of the mismatch repair (MMR) genes. Diagnosis of carriers makes precision prevention, early detection, and tailored treatment possible. Herein we report a
Autor:
Sébastien Barbarot, M. Denis-Musquer, A. Shimamura, E. Chasseuil, Nonhlanhla P. Khumalo, H. Chasseuil, Dan Lipsker, Eve Puzenat, Arti Nanda, Nathalie Bodak, Aaron Seo, Stéphane Bézieau, Sandra Mercier, Alice Goldenberg, Xavier Balguerie, Alan D. Irvine, M.-C. King, Robert Sidbury, John A. McGrath, R. Goussot, Emmanuelle Salort-Campana, Bongani M. Mayosi, Sébastien Küry, Stéphanie Mallet
Publikováno v:
British Journal of Dermatology
British Journal of Dermatology, Wiley, 2019, ⟨10.1111/bjd.17996⟩
British Journal of Dermatology, Wiley, 2019, ⟨10.1111/bjd.17996⟩
International audience; Dear Editor, Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy and Pulmonary Fibrosis (POIKTMP [MIM 615704]) is a recently described autosomal dominant disorder due to missense mutations in the FAM111B gene.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe4903a34e6507ce7bc7dd8d68679d28
https://hal.archives-ouvertes.fr/hal-02098832
https://hal.archives-ouvertes.fr/hal-02098832
Akademický článek
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Written by a range of international industry practitioners, this book offers a comprehensive overview of the essence and nature of airline operations in terms of an operational and regulatory framework, the myriad of planning activities leading up to