Results 301 to 310 of about 758,578 (355)

CYP2C19 gene polymorphism in Ningxia

Pharmacological Reports, 2023
Poor metabolizer (PM) status of CYP2C19 can be a predisposing factor for developing gastric cancer in H. pylori-infected patients. It is unclear whether PM status of CYP2C19 can also be a potential factor for H.pylori infection in healthy people.We used high-throughput sequencing to detect single nucleotide polymorphisms (SNPs) at just three loci ...
Zhen Yang, Yunqian Xie, Daya Zhang, Yan Zou, Ximei Li, Runxiang Chen, Xiaodong Zhang, Shiju Chen, Feihu Bai   +8 more
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Gene Polymorphisms in Female Reproduction

2014
This chapter presents an overview of the gene polymorphisms underlying the functions of ovarian receptors and their clinical implications in the female fecundity. A selection of genetic studies revealing significant associations between receptor polymorphisms, gene mutations, and some pathological conditions (i.e., female infertility, premature ovarian
CASARINI, Livio, SIMONI, Manuela
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Gene polymorphisms and behavior

Pediatric Blood & Cancer, 2007
AbstractGenetics has a entered golden post genomic era that promises to greatly improve our understanding of the etiology of complex familial disorders. Many forms of behavior are familial but Mendelian disorders are rare, and common conditions have complex inheritance.
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Gene Polymorphisms in Renal Transplantation

Seminars in Nephrology, 2010
A vast majority of gene polymorphism studies in renal transplantation focus on short-term outcomes such as acute rejection. The main purpose of this article is to review the literature available and studies that have examined the association between the gene polymorphisms and long-term renal allograft functions.
Monica, Grafals, Leila, Kamal, Daniel, Chung, Reza, Abdi   +3 more
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Gene polymorphisms in childhood ALL

Pediatric Blood & Cancer, 2009
AbstractAcute lymphoblastic leukemia (ALL) is the most common malignancy diagnosed in children. Inherited predisposition and exposure to exogenous leukemogenic agents have been investigated as potential risk factors. Current therapy results in 5‐year event‐free survival exceeding 80% in children in developed countries.
Nikolaos V, Karathanasis, Despoina M, Choumerianou, Maria, Kalmanti   +2 more
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Selector Genes, Polymorphisms, and Evolution

Science, 1996
Evolution has been thought to act on small changes in the characteristics of organisms coded by genes called realizator genes. D. Tautz explains how a new result in this issue of Science by Gibson and Hogness ( p. 200 ) shows that this may not always be true. A small phenotypic variation in
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Degradome Gene Polymorphisms

2008
DNA sequence variations contribute to inter-individual variability in susceptibility to and/or severity of common diseases such as cancer, diabetes, and asthma. About 90% of all sequence variations in the human genome are single nucleotide polymorphisms.
Ross Laxton, Shu Ye
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Gene polymorphisms in bladder cancer

Urologic Oncology: Seminars and Original Investigations, 2008
In Europe, cancer of the bladder is the fourth most common cancer among men, accounting for 7% of total cancers. In the USA, bladder cancer is the fifth most common cancer in men and seventh in women. This disease is three times more common in men than in women.
Maria, Franekova, Erika, Halasova, Eva, Bukovska, Jan, Luptak, Dusan, Dobrota   +4 more
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FOXP3 gene polymorphisms in preeclampsia

American Journal of Obstetrics and Gynecology, 2012
To determine whether polymorphisms in the FOXP3 gene are associated with preeclampsia.Case-control study in which 120 women with preeclampsia were compared with 120 healthy normotensive controls. Genetic variants (single nucleotide polymorphisms and microsatellites) in the FOXP3 gene were analyzed.
Torri D, Metz, Lesa M, Nelson, Gregory J, Stoddard, Robert M, Silver   +3 more
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Cytokine gene polymorphisms in Taiwan

Tissue Antigens, 2004
Abstract:  Cytokine gene polymorphisms may affect their transcription, influence their level of production, and may be implicated in inducing susceptibility or resistance to diseases. Cytokine single‐nucleotide polymorphisms (SNPs) were used to determine allelic and genotypic frequencies in the Minnan, the Hakka, and in four indigenous tribes: the Ami,
J A, Trejaut, Z-U, Tsai, H-L, Lee, Z-X, Chen, M, Lin   +4 more
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