Guo, Qi Wei Si, Yan Jun Shen, Yi Lin Chen, Xu Yang, Mei Fang, Ding Zhi Lin, Jia
Published in
Journal of molecular neuroscience : MN
The association of apolipoprotein AIV (APOA4) with depression or plasma levels of lipids and glucose has been inconsistently reported. However, interplays between APOA4 and depression on the levels have not been explored yet. The present study aimed to investigate plasma levels of APOA4, lipids, and glucose in adolescents with different genotypes o...
Cabodevila, Victoria Guadalupe Cambiaso, Vladimir Rodríguez, Gustavo Rubén Picardi, Liliana Amelia Pratta, Guillermo Raúl Capel, Carmen Lozano, Rafael Capel, Juan
Published in
Euphytica
The domestication process of tomato (Solanum lycopersium L.) resulted in very low variability for most agronomic interesting traits. In this work we explore the variability present in an unusual segregating population obtained by selfing a second cycle hybrid to identify and mapping novel Quantitative Trait Loci (QTL) for fruit quality traits. With...
Sadhukhan, Ayan Agrahari, Raj Kishan Wu, Liujie Watanabe, Toshihiro Nakano, Yuki Panda, Sanjib Kumar Koyama, Hiroyuki Kobayashi, Yuriko
Published in
Plant science : an international journal of experimental plant biology
To identify unknown regulatory mechanisms leading to aluminium (Al)-induction of the Al tolerance gene ALS3, we conducted an expression genome-wide association study (eGWAS) for ALS3 in the shoots of 95 Arabidopsis thaliana accessions in the presence of Al. The eGWAS was conducted using a mixed linear model with 145,940 genome-wide single nucleotid...
Zheng, Peng-Fei Yin, Rui-Xing Guan, Yao-Zong Wei, Bi-Liu Liu, Chun-Xiao Deng, Guo-Xiong
Published in
Nutrition & Metabolism
BackgroundThe current research was to assess the relationship of the solute carrier family 44 member 4 (SLC44A4) rs577272, notch receptor 4 (NOTCH4) rs3134931 SNPs and serum lipid levels in the Han and Maonan ethnic groups.MethodsThe genetic makeup of the SLC44A4 rs577272 and NOTCH4 rs3134931 SNPs in 2467 unrelated subjects (Han, 1254; Maonan,1213)...
Pan, Xuefeng Wei, Benjie Wang, Hong Ma, Lingyu Du, Zhaoli Chen, Ying
Published in
BMC Pregnancy and Childbirth
BackgroundBoth genetic susceptibility and dysregulated lipid metabolism are important susceptibilities to preeclampsia. In the study, we devote to investigate the associations of FOXO3 and TLR7 genetic polymorphisms with preeclampsia in a Chinese population.MethodsThis case-control study involved 335 Han Chinese pregnant women, including 177 pregna...
Strenn, Nina Pålsson, Erik Liberg, Benny Landén, Mikael Ekman, Agneta
Published in
Psychiatry research
Involvement of the immune system has been implicated in the etiology and pathophysiology of mood disorders, including bipolar disorder. Neuroimaging studies have reported structural brain pathology in bipolar disorder patients, and both levels of and genetic variants in cytokines have been associated with altered volumes of brain regions. The aim o...
OLIVEIRA, J. C. de
O amendoim forrageiro (Arachis pintoi Krapov. e W.C. Greg.) tem apresentado resultados importantes na pecuária por seu alto valor nutritivo, o que tem contribuído no aumento da produção de leite, ganho de peso no gado de corte e redução no tempo de abate em até nove meses. Além disso, seu uso como cobertura verde em consórcios com culturas comercia...
Ikezu, Tsuneya Koro, Lacin Wolozin, Benjamin Farraye, Francis A Strongosky, Audrey J Wszolek, Zbigniew K
Published in
Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology
The Leucine Rich Repeat Kinase 2 (LRRK2) is one of causative genes of familial Parkinson's disease (PD). The M2397T polymorphism in LRRK2 is genetically associated with sporadic Crohn's disease (CD). LRRK2 is expressed in human CD14+ monocytes, induced by interferon-γ (IFN-γ) and suppresses inflammatory activation. We hypothesize that IFN-γ-induced...
Dhorne-Pollet, Sophie Barrey, Eric Pollet, Nicolas
Published in
BMC Genomics
BackgroundMitochondrial DNA is remarkably polymorphic. This is why animal geneticists survey mitochondrial genomes variations for fundamental and applied purposes. We present here an approach to sequence whole mitochondrial genomes using nanopore long-read sequencing. Our method relies on the selective elimination of nuclear DNA using an exonucleas...
Bezerra, João Felipe Silva, Heglayne Pereira Vital da Bortolin, Raul Hernandes Luchessi, André Ducati Ururahy, Marcela Abbott Galvão Loureiro, Melina Bezerra Gil-da-Silva-Lopes, Vera Lúcia Almeida, Maria das Graças Amaral, Viviane Souza do Rezende, Adriana Augusto de
...
Abstract Introduction: Non-syndromic orofacial clefts have a complex etiology due to the contribution from both genetic and environmental risk factors, as well as the interaction between them. Among the more than 15 susceptibility loci for non-syndromic orofacial clefts with considerable statistical and biological support, the IRF6 is the most vali...
