Zobrazeno 1 - 10
of 111
pro vyhledávání: '"Homozygous genotype"'
Publikováno v:
Hematology, Transfusion and Cell Therapy. 44:95-99
Hemochromatosis is currently characterized by the iron overload caused by hepcidin deficiency. Large advances in the knowledge on the hemochromatosis pathophysiology have occurred due to a better understanding of the protein of the iron metabolism, t
Publikováno v:
Molecular Biology Reports. 48:6911-6921
The aim of this study is to investigate of the relationship between GSTM1 gene variations and serum trace elements, plasma malondialdehyde levels in patient with colorectal cancer. Mateials and Methods. Genotype distributions of GSTM1 gene variations
Autor:
Yuqian Wang, Lijin Zhu, Rui Chen, Xingfan Zhou, Min Zhang, Guangyi Li, Min Yu, Shichuan Tang, Li Rong, Huahuang Dong, Hailing Xia
Publikováno v:
Biomarkers. 26:335-342
Dyslipidemia is an emerging metabolic disorder among pesticide-exposed agricultural workers, and this study was aimed to explore biomarkers of hypertriglyceridaemia susceptibility.This cross-sectional study recruited 72 pesticide-exposed subjects and
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-6 (2021)
Scientific Reports
Scientific Reports
Retinitis pigmentosa (RP) is a heterogenous hereditary disorder leading to blindness. Despite using next-generation sequencing technologies, causal variants in about 60% of RP cases remain unknown. The heterogeneous genetic inheritance pattern makes
International Transaction Journal of Engineering, Management, & Applied Sciences & Technologies, 13, 3, 13A3J: 1-11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::181f891b7990cacea8853800ad304c98
Publikováno v:
Patologìâ, Vol 16, Iss 3, Pp 401-407 (2019)
Purpose. The study of the distribution patterns of allelic genes and genotypes of the C/A polymorphism of the collagen COL1A1_1 gene (rs1107946) in children with bronchial asthma, taking into account the indicators of external respiration function. M
Autor:
Phuntila Tharabenjasin, Panan Suntornsaratoon, Chatchai Muanprasat, Noel Pabalan, Hamdi Jarjanazi
Publikováno v:
Infection, Genetics and Evolution
Background The reported association between an insertion/deletion (I/D) polymorphism in the angiotensin-converting enzyme (ACE) gene and the risk for acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) remains controversial despite the
Autor:
Tainor de Mesquita Tisotti, Ananda da Rocha Pires, Priscila B S Serpa, Daniel Guimarães Gerardi, Claudio Correa Natalini
Publikováno v:
Ciência Rural, Volume: 51, Issue: 10, Article number: e20200690, Published: 14 JUN 2021
Ciência Rural, Vol 51, Iss 10 (2021)
Ciência Rural v.51 n.10 2021
Ciência Rural
Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Ciência Rural, Vol 51, Iss 10 (2021)
Ciência Rural v.51 n.10 2021
Ciência Rural
Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
The P-glycoprotein (P-gp) is a transmembrane protein encoded by the MDR1 gene that functions as a biological barrier by extruding toxins and xenobiotics out of cells. The MDR1 gene can carry a mutation called nt230(del4), which is a deletion of four
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdec8ee4dae1b65475952da0b876d371
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-84782021001000602&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-84782021001000602&lng=en&tlng=en
Autor:
Jarosław Gorący, Anna Bogacz, Daniel Kotrych, Małgorzata Łochyńska, Izabela Uzar, Bogusław Czerny, Adam Kamiński, Agnieszka Seremak-Mrozikiewicz
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
The UDP-glucuronosyltransferase 1A1 (UGT1A1) is involved in the process of estrogen conjugation and elimination. The aim of the study was to analyze whether the UGT1A1 genetic variants are associated with the development of osteopenia and osteoporosi
Autor:
Judy R. Shary, Carol L. Wagner, Danforth A. Newton, Bruce W. Hollis, John E. Baatz, Mark S. Kindy, Sebastiano Gattoni-Celli
Publikováno v:
Pediatric Research
Background Polymorphic alleles of the vitamin D (vitD)-binding protein (VDBP) gene are associated with discriminatory differences in circulating concentrations of 25-hydroxyvitamin D (25-D), the indicator of vitD status (sufficiency defined by the En