[HTML][HTML] Prostate cancer review: genetics, diagnosis, treatment options, and alternative approaches

M Sekhoacha, K Riet, P Motloung, L Gumenku… - Molecules, 2022 - mdpi.com
Simple Summary Prostate cancer affects men of all racial and ethnic groups and leads to
higher rates of mortality in those belonging to a lower socioeconomic status due to late …

Transcriptional regulatory elements in the human genome

GA Maston, SK Evans, MR Green - Annu. Rev. Genomics Hum …, 2006 - annualreviews.org
The faithful execution of biological processes requires a precise and carefully orchestrated
set of steps that depend on the proper spatial and temporal expression of genes. Here we …

Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants

A Wang, J Shen, AA Rodriguez, EJ Saunders, F Chen… - Nature …, 2023 - nature.com
The transferability and clinical value of genetic risk scores (GRSs) across populations
remain limited due to an imbalance in genetic studies across ancestrally diverse …

Genetic lesions associated with chronic lymphocytic leukemia transformation to Richter syndrome

G Fabbri, H Khiabanian, AB Holmes, J Wang… - Journal of Experimental …, 2013 - rupress.org
Richter syndrome (RS) derives from the rare transformation of chronic lymphocytic leukemia
(CLL) into an aggressive lymphoma, most commonly of the diffuse large B cell lymphoma …

Signatures of archaic adaptive introgression in present-day human populations

F Racimo, D Marnetto… - Molecular biology and …, 2017 - academic.oup.com
Comparisons of DNA from archaic and modern humans show that these groups interbred,
and in some cases received an evolutionary advantage from doing so. This process …

Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

MRP Baca, EZ Jacobs, L Vantomme, P Leblanc… - The American Journal of …, 2024 - cell.com
Neurodevelopmental disorders (NDDs) result from impaired development and functioning of
the brain. Here, we identify loss-of-function (LoF) variation in ZFHX3 as a cause for …

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry

EJ Benjamin, KM Rice, DE Arking, A Pfeufer… - Nature …, 2009 - nature.com
We conducted meta-analyses of genome-wide association studies for atrial fibrillation (AF)
in participants from five community-based cohorts. Meta-analyses of 896 prevalent (15,768 …

The complexity of prostate cancer: genomic alterations and heterogeneity

LK Boyd, X Mao, YJ Lu - Nature reviews urology, 2012 - nature.com
Although prostate cancer is the most common malignancy to affect men in the Western
world, the molecular mechanisms underlying its development and progression remain …

Long non-coding RNA HNF1A-AS1 regulates proliferation and migration in oesophageal adenocarcinoma cells

X Yang, JH Song, Y Cheng, W Wu, T Bhagat, Y Yu… - Gut, 2014 - gut.bmj.com
Objectives Long non-coding RNAs (lncRNA) have been shown to play important roles in the
development and progression of cancer. However, functional lncRNAs and their …

Prevalent mutations in prostate cancer

JT Dong - Journal of cellular biochemistry, 2006 - Wiley Online Library
Quantitative and structural genetic alterations cause the development and progression of
prostate cancer. A number of genes have been implicated in prostate cancer by genetic …