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Key genes linked to hair growth and cancer were identified in hairless mice.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Targeting FGFR-1 with antisense oligonucleotides may help treat baldness by increasing hair follicle activity.

Frontal Fibrosing Alopecia might be an autoimmune disease.

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

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

The study concluded that changing the culture conditions can cause sika deer skin cells to switch from a flat to a 3D pattern, which is important for creating hair follicles.

Certain gene variations may increase the risk and severity of alopecia areata.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

The document concludes that while some organisms can regenerate body parts, mammals generally cannot, and cancer progression is complex, involving mutations rather than a strict stem cell hierarchy.

Using radiation to make mice's hair turn gray helps study and find ways to prevent or reverse hair graying.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

Vitamin D receptor interacts with certain dietary components to help prevent diseases and regulate hair growth.

Androgens can both increase and decrease hair growth in different parts of the body.

High levels of male hormones, insulin resistance, and obesity are closely linked and worsen polycystic ovary syndrome, but more research is needed to improve treatments.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Men's sensitivity to male hormones might affect how severe COVID-19 gets for them.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Interferon, especially alfa interferon, is an effective treatment for cutaneous T-cell lymphoma with manageable side effects.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

Changes to the Foxp3 protein affect how well regulatory T cells can control the immune system, which could help treat immune diseases and cancer.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

Hair greying is caused by oxidative stress damaging hair follicles and melanocytes.

The document concludes that alopecia areata is an autoimmune disease without a definitive cure, but treatments like corticosteroids are commonly used.

Alisertib was found to be an effective and tolerable treatment for children with recurrent brain tumors.

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

Prolactin may play a significant role in skin and hair health and could be a target for treating skin and hair disorders.