Results 191 to 200 of about 2,712,849 (369)

Evaluation of P53 protein expression in gingival tissues of patients with chronic periodontitis by immunohistochemistry methods

open access: yesClinical and Experimental Dental Research, Volume 8, Issue 6, Page 1348-1353, December 2022., 2022
Abstract Objective Periodontitis is one of the most important periodontal diseases that can be affected by many factors. Although the mechanism of periodontitis development is not yet fully understood, previous studies suggest that apoptosis may be one of the pathological factors that can affect the process of the disease by destroying old and damaged ...
Samaneh Minabian   +4 more
wiley   +1 more source

Beyond Structure: Methylation Fine‐Tunes Stability and Folding Kinetics of bcl2Mid G‐Quadruplex

open access: yesAngewandte Chemie, EarlyView.
The introduction of a single 5‐methylcytosine into a G‐rich sequence originating from the B‐cell lymphoma 2 (BCL2) gene promoter affects both the folding kinetics and thermodynamics of the two G4 structures and thus plays a crucial role in regulating G4 folding pathways, which has significant implications for the control of gene expression.
Nataša Medved   +5 more
wiley   +2 more sources

Next generation genetics

open access: yesFrontiers in Genetics, 2014
Mogens eFenger
doaj   +1 more source

Advancing allergic rhinitis research through phenome-wide association studies: Insights from known genetic loci

open access: yesWorld Allergy Organization Journal
Background: Allergic rhinitis (AR) is a common chronic respiratory disease that can lead to the development of various other conditions. Although genetic risk loci associated with AR have been reported, the connections between these loci and AR ...
Xingling Tan, MD   +4 more
doaj  

Gene-associated Disease Discovery Powered by Large Language Models [PDF]

open access: yesarXiv
The intricate relationship between genetic variation and human diseases has been a focal point of medical research, evidenced by the identification of risk genes regarding specific diseases. The advent of advanced genome sequencing techniques has significantly improved the efficiency and cost-effectiveness of detecting these genetic markers, playing a ...
arxiv  

An investigation of the progression from Barrett's esophagus to adenocarcinoma [PDF]

open access: yes, 2016
Barrett's esophagus is a metaplasia of the epithelium of the lower esophagus from a normal squamous appearance to a columnar appearance more typically found in the stomach. It is normally caused by prolonged gastric reflux. While Barrett's esophagus is
Palmese, Scott Joseph
core   +1 more source

Genomics Review of Selective RET Inhibitors Sensitivity in Thyroid Cancer Clinical Trials

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT RET gene is a driver of thyroid cancer (TC) tumorigenesis. The incidence of TC has increased worldwide in the last few decades, both in medullary and follicular‐derived subtypes. Several drugs, including multikinase and selective inhibitors, have been explored.
Sara Gil‐Bernabé   +5 more
wiley   +1 more source

Superficial radiation therapy for nonmelanoma skin cancer: A review

open access: yesDermatological Reviews, Volume 3, Issue 6, Page 409-417, December 2022., 2022
Abstract Background The high prevalence of nonmelanoma skin cancer (NMSC) has become a global health‐care burden. Various modalities have been established to treat NMSC, with surgery being the mainstay approach. Superficial radiation therapy (SRT) has been in use for over a century to treat various conditions. Recent discussion among the dermatological
Haowei Han   +5 more
wiley   +1 more source

Genetic predisposition to cardiovascular disease potentiates delayed doxorubicin cardiotoxicity during pregnancy

open access: bronze, 2006
Pamela Fettig   +4 more
openalex   +1 more source

Genetic Predisposition of Atherosclerotic Cardiovascular Disease in Ancient Human Remains

open access: yesAnnals of Global Health
Background: Several computed tomographic studies have shown the presence of atherosclerosis in ancient human remains. However, while it is important to understand the development of atherosclerotic cardiovascular disease (ASCVD), genetic data concerning the prevalence of the disease-associated single nucleotide polymorphisms (SNPs) in our ancestors are
Christina Wurst   +7 more
openaire   +3 more sources

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