Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Robert H Wallis"'
Autor:
Robert H Wallis, Stephan C Collins, Pamela J Kaisaki, Karène Argoud, Steven P Wilder, Karin J Wallace, Massimiliano Ria, Alain Ktorza, Patrik Rorsman, Marie-Thérèse Bihoreau, Dominique Gauguier
Publikováno v:
PLoS ONE, Vol 3, Iss 8, p e2962 (2008)
BACKGROUND:Complex etiology and pathogenesis of pathophysiological components of the cardio-metabolic syndrome have been demonstrated in humans and animal models. METHODOLOGY/PRINCIPAL FINDINGS:We have generated extensive physiological, genetic and g
Externí odkaz:
https://doaj.org/article/1872e1fd71ef4dab85caf745480c854a
Autor:
Pamela J. Kaisaki, Georg W. Otto, Karène Argoud, Stephan C. Collins, Robert H. Wallis, Steven P. Wilder, Anthony C. Y. Yau, Christophe Hue, Sophie Calderari, Marie-Thérèse Bihoreau, Jean-Baptiste Cazier, Richard Mott, Dominique Gauguier
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 6, Iss 11, Pp 3671-3683 (2016)
To test the impact of genetic heterogeneity on cis- and trans-mediated mechanisms of gene expression regulation, we profiled the transcriptome of adipose tissue in 20 inbred congenic strains derived from diabetic Goto–Kakizaki (GK) rats and Brown
Externí odkaz:
https://doaj.org/article/6bcff2133149453ca150abb910cd16f2
Autor:
Janice Sarmiento, Åke Lernmark, Leili Marandi, Philippe Poussier, Robert H. Wallis, Gary Chao, André Veillette, Terri Ning, Andrew D. Paterson
Publikováno v:
The Journal of Immunology. 194:615-629
The R620W variant of PTPN22 is one of the major genetic risk factors for several autoimmune disorders including type 1 diabetes (T1D) in humans. In the BioBreeding T1D-prone (BBDP) rat, a single nucleotide polymorphism in Ptpn22 results in an A629T s
Autor:
Stephan C. Collins, Dominique Gauguier, Marie-Thérèse Bihoreau, Robert H. Wallis, Richard Mott, Sophie Calderari, Jean-Baptiste Cazier, Steven P. Wilder, Anthony C. Y. Yau, Christophe Hue, Karène Argoud, Georg W. Otto, Pamela J. Kaisaki
Publikováno v:
G3
G3, 2016, 6 (11), pp.3671-3683. ⟨10.1534/g3.116.033274⟩
G3, Genetics Society of America, 2016, 6 (11), pp.3671-3683. ⟨10.1534/g3.116.033274⟩
G3: Genes, Genomes, Genetics, Vol 6, Iss 11, Pp 3671-3683 (2016)
G3, Genetics Society of America, 2016, 6 (11), pp.3671-3683. 〈10.1534/g3.116.033274〉
G3: Genes|Genomes|Genetics
G3, 2016, 6 (11), pp.3671-3683. ⟨10.1534/g3.116.033274⟩
G3, Genetics Society of America, 2016, 6 (11), pp.3671-3683. ⟨10.1534/g3.116.033274⟩
G3: Genes, Genomes, Genetics, Vol 6, Iss 11, Pp 3671-3683 (2016)
G3, Genetics Society of America, 2016, 6 (11), pp.3671-3683. 〈10.1534/g3.116.033274〉
G3: Genes|Genomes|Genetics
To test the impact of genetic heterogeneity on cis- and trans-mediated mechanisms of gene expression regulation, we profiled the transcriptome of adipose tissue in 20 inbred congenic strains derived from diabetic Goto–Kakizaki (GK) rats and Brown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8eeafc5e60b0592260cc6a2a9de71ea6
https://hal.sorbonne-universite.fr/hal-01425993
https://hal.sorbonne-universite.fr/hal-01425993
Autor:
Pamela J. Kaisaki, Mark Lathrop, Robert H. Wallis, Peng Y. Woon, Dominique Gauguier, Anthony P. Monaco
Uncoupling proteins (UCP) 2 and UCP3 are closely related to themitochondrial membrane protein UCP1, which can dissociate res-piration from ATP synthesis, resulting in the generation of heat(Fleury et al. 1997; Boss et al. 1997; Vidal-Puig et al. 1997
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a21565449dc8226ef87066f77d25d98c
https://doi.org/10.1007/s003359900895
https://doi.org/10.1007/s003359900895
Autor:
Philippe Poussier, Leili Marandi, Gary Y.C. Chao, Robert H. Wallis, Terri Ning, Janice Sarmiento, Eugene Hsieh, Kesheng Wang, Andrew D. Paterson
Publikováno v:
Diabetes
OBJECTIVE Two type 1 diabetes susceptibility genes have been identified in the spontaneously diabetic biobreeding diabetes-prone (BBDP) rat, the major histocompatibility complex (MHC) (RT1) class II u haplotype (Iddm1) and Gimap5 (Iddm2). The strong
Autor:
Ulla G. Sidelmann, Lisa D'Amato, Robert H. Wallis, Christine Blancher, Jane F. Fearnside, Richard H. Barton, Hector C. Keun, Karène Argoud, Marc-Emmanuel Dumas, Dominique Gauguier, Jeremy K. Nicholson, Steven P. Wilder, Dorrit Baunsgaard, James Scott, Marie-Thérèse Bihoreau
Publikováno v:
Nature Genetics. 39:666-672
Characterizing the relationships between genomic and phenotypic variation is essential to understanding disease etiology. Information-dense data sets derived from pathophysiological1, proteomic2,3 and transcriptomic4 profiling have been applied to ma
Autor:
M. T. Bihoreau, Alain Ktorza, Dominique Gauguier, Peng Y. Woon, Steven P. Wilder, Karène Argoud, Robert H. Wallis, F. Ouali, M. A. McAteer
Publikováno v:
Diabetologia. 49:2679-2688
AIMS/HYPOTHESIS: Dyslipidaemia is a main component of the insulin resistance syndrome. The inbred Goto-Kakizaki (GK) rat is a model of spontaneous type 2 diabetes and insulin resistance, which has been used to identify diabetes-related susceptibility
Autor:
Marie-Thérèse Bihoreau, Karin J. Wallace, Steven P. Wilder, Karène Argoud, Stephan C. Collins, Robert H. Wallis, Dominique Gauguier, Pamela J. Kaisaki
Publikováno v:
Mammalian Genome. 17:538-547
Genetic studies in experimental crosses derived from the inbred Goto-Kakizaki (GK) rat model of spontaneous diabetes mellitus have identified quantitative trait loci (QTL) for diabetes phenotypes in a large region of rat Chromosome (RNO) 1. To test t
Publikováno v:
Mammalian Genome. 14:350-356
Over the past decades, genetic studies in rodent models of human multifactorial disorders have led to the detection of numerous chromosomal regions associated with disease phenotypes. Owing to the complex control of these phenotypes and the size of t