Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Evi Aerts"'
Autor:
An Verrijken, M. Ruppert, Evi Aerts, Peter Michielsen, Sven Francque, Fenna de Freitas, Wim Van Hul, Luc Van Gaal, Sigri Beckers, Doreen Zegers, Guy Hubens
Publikováno v:
Clinics and research in hepatology and gastroenterology
Background: Previous research has clearly implicated the PNPLA3 gene in the etiology of nonalcoholic fatty liver disease as a polymorphism in the gene was found to be robustly associated to the disease. However, data on the involvement of rare PNPLA3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1086f37393041a1694cf56e761168b2
https://doi.org/10.1016/j.clinre.2016.05.004
https://doi.org/10.1016/j.clinre.2016.05.004
Autor:
An Verrijken, Guy Massa, Laure Sorber, Stijn Verhulst, Luc Van Gaal, Sigri Beckers, Evi Aerts, Ellen Geets, Wim Van Hul, Kim Van Hoorenbeeck
Publikováno v:
Annals of human genetics
Summary Neuropeptide Y (NPY) and its G protein–coupled NPY Y2 Receptor (NPY2R) are highly expressed in orexigenic NPY/Agouti-related peptide neurons within the arcuate nucleus, a major integrator of appetite control in the hypothalamus. As NPY and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df45cb9289072163dec6844541c0ae3c
https://hdl.handle.net/10067/1484850151162165141
https://hdl.handle.net/10067/1484850151162165141
Autor:
Wim Van Hul, Kim Van Hoorenbeeck, An Verrijken, Ellen Geets, Evi Aerts, Stijn Verhulst, Luc Van Gaal
Publikováno v:
Obesity research & clinical practice
Background: Prader Willi Syndrome (PWS) is a syndromic form of obesity caused by a chromosomal aberration on chromosome 15q11.2-q13. Patients with a comparable phenotype to PWS not carrying the 15q11.2q13 defect are classified as Prader Willi like (P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9557e01c68e06b57db782ca1a6bc505d
https://hdl.handle.net/10067/1516050151162165141
https://hdl.handle.net/10067/1516050151162165141
Autor:
Evi, Aerts, Sigri, Beckers, Doreen, Zegers, Kim, Van Hoorenbeeck, Guy, Massa, An, Verrijken, Stijn L, Verhulst, Luc F, Van Gaal, Wim, Van Hul
Publikováno v:
Obesity (Silver Spring, Md.). 24(4)
Genome-wide copy number variation (CNV) analyses have associated the 10q11.22 CNV with obesity. As the NPY4R gene is the most interesting candidate gene in this region, it was hypothesized that both genetic and structural variation in NPY4R might be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::297034cf265ef6cc7d12a0f45908cbb8
https://pubmed.ncbi.nlm.nih.gov/26921218
https://pubmed.ncbi.nlm.nih.gov/26921218
Autor:
Ilse Mertens, Stijn Verhulst, An Verrijken, Guy Massa, Doreen Zegers, Jasmijn K. Van Camp, Evi Aerts, Luc Van Gaal, Sigri Beckers, Raoul R. Rooman, Wim Van Hul, Kim Van Hoorenbeeck
Publikováno v:
Molecular genetics and metabolism
Objective: Animal studies, genome-wide association and genomic structural variation studies have identified the SH2B1 gene as a candidate gene for obesity. Therefore, we have designed an extensive mutation and copy number variation (CNV) analysis inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cac8830a263f1563233bc4f9ce3285de
https://hdl.handle.net/10067/1272200151162165141
https://hdl.handle.net/10067/1272200151162165141