Genetics, genomics, and diet interactions in obesity in the Latin American environment.
Frontiers In Nutrition
Guevara-Ramírez, Patricia P; Cadena-Ullauri, Santiago S; Ruiz-Pozo, Viviana A VA; Tamayo-Trujillo, Rafael R; Paz-Cruz, Elius E; Simancas-Racines, Daniel D; Zambrano, Ana Karina AK
Peroxisome proliferator-activated receptor gamma gene variants modify human airway and systemic responses to indoor dibutyl phthalate exposure.
Respiratory Research
Leung, Clarus C; Ryu, Min Hyung MH; Bølling, Anette Kocbach AK; Maestre-Batlle, Danay D; Rider, Christopher F CF; Hüls, Anke A; Urtatiz, Oscar O; MacIsaac, Julie L JL; Lau, Kevin Soon-Keen KS; Lin, David Tse Shen DTS; Kobor, Michael S MS; Carlsten, Chris C
Publication Date: 2022-09-16
Variant appearance in text: PPARG: His449His; rs3856806
G Allele of the rs1801282 Polymorphism in PPARγ Gene Confers an Increased Risk of Obesity and Hypercholesterolemia, While T Allele of the rs3856806 Polymorphism Displays a Protective Role Against Dyslipidemia: A Systematic Review and Meta-Analysis.
Genomic, transcriptomic, and metabolomic profiles of hiPSC-derived dopamine neurons from clinically discordant brothers with identical PRKN deletions.
Npj Parkinson'S Disease
Cukier, Holly N HN; Kim, Hyunjin H; Griswold, Anthony J AJ; Codreanu, Simona G SG; Prince, Lisa M LM; Sherrod, Stacy D SD; McLean, John A JA; Dykxhoorn, Derek M DM; Ess, Kevin C KC; Hedera, Peter P; Bowman, Aaron B AB; Neely, M Diana MD
Publication Date: 2022-06-29
Variant appearance in text: PPARG: H449H; rs3856806
Personalized Dietary Recommendations Based on Lipid-Related Genetic Variants: A Systematic Review.
Frontiers In Nutrition
Pérez-Beltrán, Yolanda E YE; Rivera-Iñiguez, Ingrid I; Gonzalez-Becerra, Karina K; Pérez-Naitoh, Naomi N; Tovar, Juscelino J; Sáyago-Ayerdi, Sonia G SG; Mendivil, Edgar J EJ
Associations among perfluorooctanesulfonic/perfluorooctanoic acid levels, nuclear receptor gene polymorphisms, and lipid levels in pregnant women in the Hokkaido study.
Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss.
Bmc Medical Genomics
Yang, Guangxian G; Yin, Yi Y; Tan, Zhiping Z; Liu, Jian J; Deng, Xicheng X; Yang, Yifeng Y
Publication Date: 2021-01-21
Variant appearance in text: PPARG: H449H; rs3856806