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Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Birth control pills increase certain receptor activities in female gerbil prostate glands and can lead to prostate changes.

Testosterone can both promote hair growth and cause baldness by affecting hair growth signals.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Different substances that activate or block the androgen receptor can affect male development and treat conditions like prostate cancer.

No clear link between specific gene and hair loss in Mexican brothers.

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

Understanding skin structure and development helps diagnose and treat skin disorders.

The document concludes that identifying the specific cells where skin cancers begin is important for creating better prevention, detection, and treatment methods.

PF-05314882 selectively activates androgen receptors without much effect on prostate and may help in prostate cancer treatment and hair loss prevention.

Androgen receptors in the mouse brain may explain cognitive and mood changes in prostate cancer treatment.

Vav2 changes how hair follicle stem cells' genes work as they age, which might improve regeneration but also raise cancer risk.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

The HR protein's role as a repressor is essential for controlling hair growth.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

The document explains how to identify different hair problems using a microscope.

The Androgen Receptor could be a target for treating diseases like cancer, but more research is needed to confirm the effectiveness of potential treatments.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Understanding how androgens work is key for creating new treatments for prostate issues and hair/skin conditions.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Oestrogens are key for bone growth during puberty in both boys and girls.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.