Výsledky vyhledávání - "Pettigrew, K. A."

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Entry of Opioid Peptides into the Central Nervous System

Autor: Rapoport, S. I., Klee, W. A., Pettigrew, K. D., Ohno, K.

Publikováno v: Science, 1980 Jan 01. 207(4426), 84-86.

Externí odkaz: https://www.jstor.org/stable/1683216

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Lack of replication for the myosin- 18B association with mathematical ability in independent cohorts.

Autor: Pettigrew, K. A.¹, Fajutrao Valles, S. F.¹, Moll, K.^2,3, Northstone, K.⁴, Ring, S.⁴, Pennell, C.⁵, Wang, C.⁵, Leavett, R.³, Hayiou‐Thomas, M. E.³, Thompson, P.⁶, Simpson, N. H.⁷, Fisher, S. E.^8,9, Whitehouse, A. J. O.¹⁰, Snowling, M. J.^6,11, Newbury, D. F.^7,11, Paracchini, S.¹

Publikováno v: Genes, Brain & Behavior. Apr2015, Vol. 14 Issue 4, p369-376. 8p.

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The widespread use of topical antimicrobials enriches for resistance in Staphylococcus aureus isolated from atopic dermatitis patients

Autor: Harkins, C P, McAleer, M A, Bennett, D, McHugh, M, Fleury, O M, Pettigrew, K A, Oravcová, K., Parkhill, J, Proby, C M, Dawe, R S, Geoghegan, J A, Irvine, A D, Holden, M T G

This work was supported by grants from the Wellcome Trust (104241/z/14/z to C.P.H., and 098731/z/11/z to St Andrews University Bioinformatics Unit), and the Chief Scientists Office (SIRN10 to M.T.G.H.). Background Carriage rates of Staphylococcus aur

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e2d5d7227be8d3cf9432f58494e11811
https://eprints.gla.ac.uk/161990/1/161990.pdf

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Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes

Autor: Pettigrew, K, Frinton, E, Nudel, R, Chan, M, Thompson, P, Hayiou-Thomas, M, Talcott, J, Stein, J, Newbury, D, Paracchini, S

Background: Specific Language Impairment (SLI) is a common neurodevelopmental disorder, observed in 5-10% of children. Family and twin studies suggest a strong genetic component, but relatively few candidate genes have been reported to date. A recent

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=r3110ae70d66::7d24b19939aa0ec14af5cbccf76f332f
https://radar.brookes.ac.uk/radar/items/2ffc182d-1ca5-4273-9714-252e193a7ba0/1/

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Copy number variation screen identifies a rare de Novo deletion at chromosome 15q13.1-13.3 in a child with language impairment

Autor: Pettigrew, K. A., Reeves, E., Leavett, R., Hayious-Thomas, Emma, Sharma, A., Simpson, N. H., Martinelli, A., Thompson, Paul A., Hulme, Charles, Snowling, Margaret J., Newbury, D. F., Paracchini, S.

A significant proportion of children (up to 7% in the UK) present with pronounced language difficulties that cannot be explained by obvious causes like other neurological and medical conditions. A substantial genetic component is predicted to underli

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3651::0290a224154e857b2bd481fc95b639bf
https://acuresearchbank.acu.edu.au/item/8qx7x/copy-number-variation-screen-identifies-a-rare-de-novo-deletion-at-chromosome-15q13-1-13-3-in-a-child-with-language-impairment

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