Výsledky vyhledávání - "Griffiths LR."

Akademický článek

Exploring the Hereditary Nature of Migraine

Autor: Bron C, Sutherland HG, Griffiths LR

Publikováno v: Neuropsychiatric Disease and Treatment, Vol Volume 17, Pp 1183-1194 (2021)

Charlene Bron, Heidi G Sutherland, Lyn R Griffiths Queensland University of Technology (QUT), Centre for Genomics and Personalised Health, Genomics Research Centre, School of Biomedical Sciences, Institute of Health and Biomedical Innovation, Queensl

Externí odkaz: https://doaj.org/article/a5539f4f574541b9b81b48858753ed3f

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Association of polymorphisms in ARRB2 and clinical response to methadone for pain in advanced cancer

Autor: Ozberk, D, Haywood, A, Sutherland, HG, Yu, C, Albury, CL, Zunk, M, George, R, Good, P, Griffiths, LR, Hardy, J, Haupt, LM

Background: The prescription of methadone in advanced cancer poses multiple challenges due to the considerable interpatient variation seen in effective dose and toxicity. Previous reports have suggested that ARRB2 influences the response to methadone

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______363::e1e76860910f02e8acbdcafca8519a8a
https://hdl.handle.net/10453/162782

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HSPGs glypican-1 and glypican-4 are human neuronal proteins characteristic of different neural phenotypes

Autor: Oikari LE, Yu C, Okolicsanyi RK, Avgan N, Peall IW, Griffiths LR, Haupt LM

Generating neurons from human stem cells has potential for brain damage therapy and neurogenesis modeling, but current efficacy is limited by culture heterogeneity and the lack of markers. We have previously reported the heparan sulfate proteoglycans

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______363::b2abb5112350e7677f041891fde48298
https://hdl.handle.net/10453/144734

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Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene

Autor: Esposito T, Lea RA, Maher BH, Moses D, Cox HC, Magliocca S, Angius A, Nyholt DR, Titus T, Kay T, Gray NA, Rastaldi MP, Parnham A, Gianfrancesco F, Griffiths LR.

Publikováno v: Human molecular genetics
(2013).
info:cnr-pdr/source/autori:Esposito T, Lea RA, Maher BH, Moses D, Cox HC, Magliocca S, Angius A, Nyholt DR, Titus T, Kay T, Gray NA, Rastaldi MP, Parnham A, Gianfrancesco F, Griffiths LR./titolo:Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene./doi:/rivista:Human molecular genetics (Print)/anno:2013/pagina_da:/pagina_a:/intervallo_pagine:/volume

Focal segmental glomerulosclerosis (FSGS) is the consequence of a disease process that attacks the kidney's filtering system, causing serious scarring. More than half of FSGS patients develop chronic kidney failure within 10 years, ultimately requiri

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::2658802f4ed103680446076a7de80497
http://www.cnr.it/prodotto/i/224081

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X-linked familial typical migraine: genetic and physical refinement of the locus and molecular analysis of candidate genes

Autor: Esposito T, Miano MG, Griffiths LR, Squitieri F, Gianfrancesco F

Publikováno v: VIII Società Italiana Genetica Umana, Cagliari, 28-30 Settembre, 2005
info:cnr-pdr/source/autori:Esposito T, Miano MG, Griffiths LR, Squitieri F, Gianfrancesco F/congresso_nome:VIII Società Italiana Genetica Umana/congresso_luogo:Cagliari/congresso_data:28-30 Settembre, 2005/anno:2005/pagina_da:/pagina_a:/intervallo_pagine

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::df9df9c2d78306a3f24fb8ece2d6df1d
https://publications.cnr.it/doc/244311

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