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Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.

Retinoic acid affects skin and hair health by working with specific receptors, and its absence can lead to hair loss and skin changes.

Different factors help diagnose and treat hair loss accurately.

Isotretinoin's effects and side effects, like birth defects and depression, might be due to it causing cell death in various cells.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

Alopecia Areata is an autoimmune condition causing hair loss with no cure and treatments that often don't work well.

Oxidative stress may contribute to hair loss in alopecia areata and antioxidants could potentially help as a treatment.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Different genes cause Female Pattern Hair Loss compared to male hair loss, and treatments vary, but more research is needed to understand it fully.

The project created a standardized system for classifying skin lesions in lab rats and mice.

The Middle East and Africa need better data, treatment consensus, and support for Alopecia Areata.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Hair loss gene found on chromosome 3q26.

Insulin resistance and obesity are key factors in the development and worsening of polycystic ovary syndrome, and lifestyle changes are important for managing it.

Hair loss may indicate a higher risk of heart disease and other health issues related to metabolism.

Women with alopecia often experience high levels of anxiety and depression, needing psychiatric help.

iPSCs can help treat genetic skin disorders by creating healthy skin cells from a small biopsy.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Long-Acting Platelet Rich Plasma therapy can effectively reduce hair shedding, thicken hair, and promote new growth in women with pattern hair loss.

The skin's layers protect, sense, and regulate the body's internal balance, but can be prone to cancer.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

A cat with ear infection and skin issues was successfully treated for Demodex mites using imidacloprid and moxidectin.

A 12-year-old girl's hair loss was linked to a rare genetic condition called ALX4-related frontonasal dysplasia.