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Finasteride helps treat skin issues like acne and baldness by blocking testosterone conversion.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Reduced AR gene methylation may cause early pubic hair growth in girls.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

Longer CAG repeat lengths in the androgen receptor gene are linked to higher testosterone levels in women with PCOS.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

Vitamin D receptor helps control hair growth genes in skin cells.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

Certain gene variations might be linked to severe acne in women but not in men.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

The document concludes that stem cells and their environments are crucial for skin and hair health and have potential for medical treatments.