نتایج جستجو برای: exon gene

تعداد نتایج: 1147509  

ایزدی, امیر, فرامرزی, حسین, مسلمی, الهام,

Background: The molecular studies indicate some of the genes in the promoter region itself, will undergo methylation. Methylation of CpG islands in the promoter region of that cause silence or reduced expression of genes involved in cell growth pathways, which are colorectal cancer causing agents. Detection of methylation status can be used as a marker for cancer diagnosis and prediction of dis...

Journal: :Biodiversitas 2022

Abstract. Ermawati D, Panjono, Bintara S, Hartatik T. 2022. Diversity of partial sequence leptin gene (Exon 3) in crossbred cattle compared to GenBank database. Biodiversitas 23: 5614-5620. Genetic marker method that is often used select Single Polymorphism Nucleotide (SNP). Polymorphisms (SNP) has been found various candidate genes, one which the gene. Leptin a affects reproduction and weight....

Journal: :Indian Journal of Animal Sciences 2023

The study aimed to identify polymorphism of LEP, and STAT5A milk-producing genes their association with production traits in Rathi cattle. An overall 160 animals were selected from a population cattle Livestock Research Station, Rajasthan University Veterinary Animals Sciences, Bikaner (Rajasthan). phenotypic information on total milk yield, peak yield lactation length recorded the years 2012- ...

Journal: :Indian Journal of Animal Sciences 2022

Information on the camel leptin gene when compared to other domestic livestock species is very limited. Hence, thepresent study was undertaken characterize of Indian dromedary (Camelus dromedarius).Five overlapping primer pairs were designed utilizing available Lama Glama sequence. Through theassembly, alignment, and editing five nucleotide sequences, a 2425 bp long sequence(Accession no. MT103...

Journal: :Xinan Jiaotong Daxue Xuebao 2023

Colorectal cancer is a major cause of cancer-related deaths globally, and the disease arises from genetic mutations that impair cellular signaling pathways involved in proliferation, differentiation, apoptosis. This study aimed to determine prevalence, describe, establish correlation between different types KRAS exon 2 patients with colorectal cancer. The used cross-sectional investigation on c...

A Vaziri Gohar GH Mohammadi M Baghaie M.R Shakibaie

Introduction: Despite improvements in the diagnosis and treatment of lung cancer in the past two decades, it has remained the most common cause of death from cancer worldwide. Among all genes that are mutated in lung cancer, TP53 located on chromosome 17P13/1 has a significant diagnostic and prognostic value. TP53 mutations have been extensively studied in lung cancer and TP53 mutational spectr...

2016
Kazuhiro Fukumura Shunichi Wakabayashi Naoyuki Kataoka Hiroshi Sakamoto Yutaka Suzuki Kenta Nakai Akila Mayeda Kunio Inoue

The exon junction complex (EJC) that is deposited onto spliced mRNAs upstream of exon-exon junctions plays important roles in multiple post-splicing gene expression events, such as mRNA export, surveillance, localization, and translation. However, a direct role for the human EJC in pre-mRNA splicing has not been fully understood. Using HeLa cells, we depleted one of the EJC core components, Y14...

Information theory is a branch of mathematics. Information theory is used in genetic and bioinformatics analyses and can be used for many analyses related to the biological structures and sequences. Bio-computational grouping of genes facilitates genetic analysis, sequencing and structural-based analyses. In this study, after retrieving gene and exon DNA sequences affecting milk yield in dairy ...

E. O. Unal O. Ozmen, S. Kul

The purpose of the study was to detect the AluI and DdeI polymorphisms within POU1F1 gene exon 6 and 3'UTR region in Turkish sheep breeds, and their association with milk productive traits. Jugular blood samples were collected from 50 Sakiz, 50 White Karaman, and 50 Awassi sheep using EDTA as an anticoagulant. PCR-RFLP and sequencing analysis were performed to investigate possible polymorphisms...

A Mohseni Meybodi H Hosseini, H Hosseinifar MA Sadighi Gilani, T Modarresi

Background One of the main causes of male infertility is defect in structure and function of sperm cells. Infertile men with oligoasthenoteratospermia (OAT) defect, have sperms with abnormalities in count, motility and morphology. Patients with immotile short tail sperm (ISTS) disorder have immotile short-tailed sperm with disorganized axonem, and a significant decrease in sperm counts. Numerou...

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