Results 181 to 190 of about 22,958 (200)

Molecular study of vitamin D metabolism-related single nucleotide polymorphisms in cardiovascular risk: a case-control study. [PDF]

open access: yesJ Physiol Biochem
Gálvez-Navas JM   +11 more
europepmc   +1 more source

The integrated stress response drives MET oncogene overexpression in cancers. [PDF]

open access: yesEMBO J
Cerqua M   +4 more
europepmc   +1 more source
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Point Mutations in FgSdhC2 or in the 5' Untranslated Region of FgSdhC1 Confer Resistance to a Novel Succinate Dehydrogenase Inhibitor Flubeneteram in Fusarium graminearum.

Journal of Agricultural and Food Chemistry, 2021
Fusarium graminearum is one of the phytopathogenic fungi causing cereal fusarium head blight worldwide. Flubeneteram (Flu) is a novel succinate dehydrogenase inhibitor (SDHI) which exhibits strong fungicidal activity against F. graminearum. In this study,
Wenchan Chen   +11 more
semanticscholar   +1 more source

The genetic diversity of heat shock protein 70 gene at promoter and 5' untranslated region in beef cattle

, 2021
This study was aimed to identify genetic diversity in the promoter area and 5' UTR (untranslated region) HSP70 (heat shock protein 70) gene in several beef cattle in Indonesia. A total of 86 blood samples of Bali, Madura, PO (Peranakan Ongole), Limousine,
I. Suhendro, J. Jakaria, R. R. Noor
semanticscholar   +1 more source

A Polymorphism at the microRNA Binding Site in the 3' Untranslated Region of KRT81 Is Associated with Breast Cancer.

DNA and Cell Biology, 2020
Single nucleotide polymorphisms in miRNA binding sites (miR-SNPs) are associated with cancer risk. We assessed the relationship between five miR-SNPs in the 3' untranslated region (3'-UTR) of RYR3 (rs1044129), KIAA0423 (rs1053667), C14orf101 (rs4901706),
Z. Sha   +6 more
semanticscholar   +1 more source

Genetic Studies of Familial Myeloproliferative Disorders

, 2007
Hereditary thrombocythemia (HT) is an autosomal dominant disorder with clinical features resembling sporadic essential thrombocythemia. HT families share similar clinical symptoms caused by heterogeneous genetic alterations.
Kun Liu
semanticscholar   +1 more source

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