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 …

Influence of CAG repeat polymorphism on the targets of testosterone action

G Tirabassi, A Cignarelli, S Perrini… - International journal …, 2015 - Wiley Online Library
In the last decade, ample evidence has demonstrated the growing importance of androgen
receptor (AR) CAG repeat polymorphism in andrology. This genetic parameter is able to …

Design, synthesis and biological evaluation of nuclear receptor-degradation inducers

Y Itoh, R Kitaguchi, M Ishikawa, M Naito… - Bioorganic & medicinal …, 2011 - Elsevier
Compounds that regulate the function (s) of nuclear receptors (NRs) are useful for biological
studies and as candidate therapeutic agents. Most such compounds are agonists or …

[HTML][HTML] Association of sex hormone receptor gene polymorphisms with recurrent pregnancy loss: a systematic review and meta-analysis

MT Su, SH Lin, YC Chen - Fertility and sterility, 2011 - Elsevier
OBJECTIVE: To investigate the genetic association between estrogen and progesterone
receptor polymorphisms (ER, PR) and skewed X chromosome inactivation (XCI) and …

Poly-glutamine-dependent self-association as a potential mechanism for regulation of androgen receptor activity

CM Roggero, V Esser, L Duan, AM Rice, S Ma, GV Raj… - PloS one, 2022 - journals.plos.org
The androgen receptor (AR) plays a central role in prostate cancer. Development of
castration resistant prostate cancer (CRPC) requires androgen-independent activation of …

Incidence and prevalence of Spinal and bulbar muscular atrophy in South Korea: a nationwide population-based study

JM Park, M Kang, JS Park - Journal of Neurology, 2023 - Springer
Spinal and bulbar muscular atrophy (SBMA), or Kennedy's disease, is a rare X-linked
neuromuscular disorder predominantly affecting males and caused by a mutation in the …

A Potential Novel Spontaneous Preterm Birth Gene, AR, Identified by Linkage and Association Analysis of X Chromosomal Markers

MK Karjalainen, JM Huusko, J Ulvila, J Sotkasiira… - PloS one, 2012 - journals.plos.org
Preterm birth is the major cause of neonatal mortality and morbidity. In many cases, it has
severe life-long consequences for the health and neurological development of the newborn …

Polyglutamine repeats are associated to specific sequence biases that are conserved among eukaryotes

M Ramazzotti, E Monsellier, C Kamoun… - PLoS …, 2012 - journals.plos.org
Nine human neurodegenerative diseases, including Huntington's disease and several
spinocerebellar ataxia, are associated to the aggregation of proteins comprising an …

[HTML][HTML] The influence of microsatellite polymorphisms in sex steroid receptor genes ESR1, ESR2 and AR on sex differences in brain structure

GCY Tan, C Chu, YT Lee, CCK Tan, J Ashburner… - NeuroImage, 2020 - Elsevier
The androgen receptor (AR), oestrogen receptor alpha (ESR1) and oestrogen receptor beta
(ESR2) play essential roles in mediating the effect of sex hormones on sex differences in the …

Cancer: from wild-type to mutant huntingtin

MS Thion, S Humbert - Journal of Huntington's disease, 2018 - content.iospress.com
Huntingtin (HTT) is a scaffold protein mostly known because it gives rise to the severe and
incurable inherited neurological disorder Huntington's disease (HD) when mutated. The …